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Yendamuri, S.; Nitsche, L.; Mukherjee, S.; Cheruvu, K.; , . Obesity and Cancer. Encyclopedia. Available online: https://encyclopedia.pub/entry/21581 (accessed on 16 June 2024).
Yendamuri S, Nitsche L, Mukherjee S, Cheruvu K,  . Obesity and Cancer. Encyclopedia. Available at: https://encyclopedia.pub/entry/21581. Accessed June 16, 2024.
Yendamuri, Sai, Lindsay Nitsche, Sarbajit Mukherjee, Kareena Cheruvu,  . "Obesity and Cancer" Encyclopedia, https://encyclopedia.pub/entry/21581 (accessed June 16, 2024).
Yendamuri, S., Nitsche, L., Mukherjee, S., Cheruvu, K., & , . (2022, April 11). Obesity and Cancer. In Encyclopedia. https://encyclopedia.pub/entry/21581
Yendamuri, Sai, et al. "Obesity and Cancer." Encyclopedia. Web. 11 April, 2022.
Obesity and Cancer
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The obesity is associated with many adverse health effects, including worse cancer outcomes. It has been established that obesity (BMI > 30 kg/m2) is a major risk factor for many types of cancer.

obesity cancer

1. Obesity and Cancer Development

Obesity is an epidemiologic problem that will continue to grow in the coming years. CDC data reported that 42.4% of American adults were obese in 2018, and that number increased from 30.5% in 2000 [1]. As well as the negative public health care impacts, obesity is a significant strain on health care spending, with 147 billion dollars spent in 2008 [1]. Much of this spending is secondary to the diseases often concomitant with obesity, such as heart disease [2], type 2 diabetes [3], hypertension [4], asthma [5][6], and cancers [7][8]. When the costs of inpatient care, outpatient care, emergency care, dental care, and prescriptions were analyzed, it was found that obesity (BMI > 30) accounted for 149.4 billion dollars in 2014 [7].
An early association between obesity and cancer risk was made in 1966 by analyzing trends in endometrial cancer [9]. The authors proposed increased estrogen exposure as the pathogenesis of the heightened oncologic risk in obese women [9]. Since that time, many groups have shown associations between increased BMI and the development of cancer. Obesity is a major cause of the non-alcoholic fatty liver disease (NAFLD), a leading cause of hepatocellular carcinoma (HCC) [10][11][12]. Obesity increases the risk of non-Hodgkin lymphomas [13][14], particularly diffuse large B-cell lymphomas (DLBCL) [15]. Obesity showed a significant increase in the incidence of gastric cardia cancer [16], thyroid cancer [17], colon cancer [18], renal cancer [19][20][21], liver cancer [22], malignant melanoma [23], multiple myeloma [24], rectal cancer [18], gallbladder cancer [25], leukemia [26], esophageal cancer [16], and, as previously mentioned, non-Hodgkin lymphoma [27].
It has been suggested that childhood obesity contributes to increased cancer risk and cardiovascular disease risk in adulthood [28]. This is concerning because childhood obesity was pronounced an epidemic affecting 17% of the children [29] in the US. It is likely related to the fact that if a person is obese as a child, they also tend to be obese as an adult. Increased BMI as a teen was associated with a higher risk for leukemia (OR = 1.32, 95% CI 1.15–1.53) [30][31], Hodgkin’s disease (HR = 1.25, 95% CI 1.13–1.37) [28][32], and colon cancer (39% increase in men and 19% increase in women) [33].
The increase in cancer development has been proposed to be secondary to immunologic and metabolic derangements in the tumor microenvironment [34]. Obesity has been said to create a “meta-inflammatory” state through the body, leading to impaired immunologic recruitment, coordination, and response [35]. Obesity has been shown to contribute to increased cytokine production, aberrant macrophage activity, and increased exhaustion phenotypes shown by immune cells [36]. Obesity-associated inflammation contributes to increased myeloid-derived suppressors cells (MDSCs), which suppress innate and adaptive immune responses [37][38]. Usually, cells of myeloid lineage progress to become macrophages, granulocytes, and dendritic cells [39]. If these cells instead become MDSCs, they may inhibit natural killer cells and T-cell cytotoxicity and increase regulatory T cells by liberating factors such as arginase-1 and inducible nitric oxide synthase [40]. Natural killer cells defend the body against foreign matter and neoplasms by releasing cytoplasmic mediators or cytotoxic activity [41][42]. When the tumor microenvironment is altered so that there is an abundance of pro-inflammatory phenotypes and increased TGF-β, the natural killer cells are less protective against carcinogenesis [43]. In particular, it has been shown that the natural killer cells in an obese patient struggle to activate glycolysis [44], which is essential for activating their cytotoxic machinery. It was postulated that this is due to increased lipid uptake by the natural killer cells [44]. It has been shown that adipose tissue serves as a reservoir for cytokines, including TNF-α, leading to inflammation [45]. This effect is seen in animal models, with obese dogs exhibiting higher IL-6 and TNF-α levels and lower T-cell proliferation than healthy weight dogs [46]. It has been suggested that increased adipose tissue promotes that pivoting of a Th2 phenotype to a Th1 and Th17 predominant phenotype [47]. This shift and the increase in liberated cytokines contribute to a pro-inflammatory state [34].
Obesity increases the liberation of leptin and other adipokines due to an increase in adipose tissue volume [48]. Leptin has been shown to promote cancer growth in mice [48]. Obesity decreases adiponectin levels, an adipokine that counters the cancer-promoting effects of leptin [48]. In conjunction with increased leptin release, the downregulation of adiponectin allows increased growth and metastasis. Obesity alters levels of steroid hormones which can contribute to cancer growth [48]. Estrogen can be produced by adipose tissue [49]; in fact, it is the primary way estrogen is produced in postmenopausal women [48]. Estrogen has been shown to induce cancer-promoting effects, such as inhibiting apoptosis and inducing angiogenesis [48]. It has been shown that estrogen promotes tumor growth and angiogenesis in mice, even in cancer cells lacking the 17β-estradiol receptor [49]. Obesity also reduces the sequestration of estrogen by downregulating levels of sex hormone-binding globulin, leading to increased circulating unbound estrogen [50]. Obesity leads to the dysregulation of insulin signaling, negatively impacting cellular signaling pathways and promoting cancer growth. Obesity causes increased insulin release due to decreased insulin responsiveness [51]. In addition to its metabolic effects, insulin promotes mitosis [48]. Cancer cells exposed to insulin divide faster, leading to increased tumor growth [52]. Insulin signals through the PI3K and MAPK pathways are common to many crucial signaling cascades that regulate cellular functioning and metabolism [48]. Consequently, dysfunction in these pathways secondary to improper insulin signaling can lead to derangements in normal cell development and cancer [48]. Increased levels of IGF-2 (insulin-like growth factor 2) methylation are correlated with obesity and insulin resistance [53][54]. IGF-2 may bind to IR-A (insulin receptor A) or IGF1R (insulin-like growth factor 1 receptor) to increase glucose uptake and activate anabolic pathways, leading to energy production, cell growth, and division [48]. Furthermore, high-fat diet-induced obesity leads to a metabolic competition between tumor and CD8 T cells for lipids, leading to increased lipid uptake by tumor cells than T cells, thereby impairing CD8 T-cell infiltration and function [55].

2. Obesity and Cancer Prognosis

Along with increasing the incidence of cancers, obese patients tend to have compromised survival and increased complications following cancer treatment. Prostate cancer-specific mortality and biochemical recurrence were increased by 15% and 21%, respectively, with a 5 kg/m2 weight gain [56]. In colorectal cancer, obese patients have elevated all-cause mortality, cancer-specific mortality, disease recurrence, and decreased disease-free survival [57]. These negative prognostic factors were not seen when analyzing patients with BMIs characterized as overweight [57]. Obesity compromised survival and post-operative outcomes of recurrent hepatocellular carcinoma [58]. When operated on for hepatic metastasis of colorectal cancer, obese patients spent a longer time in the operating room and had higher estimated blood loss, morbidity, and reintervention rates when compared to non-obese peers [59]. A higher BMI was associated with extrathyroidal and vascular invasion of papillary thyroid carcinoma, suggesting obesity leads to a more aggressive phenotype [60]. Obesity was associated with increased wound dehiscence, incisional site hernia, and stoma complications following colorectal surgery, and these patients were at higher risk for conversion to an open surgery [61]. Obese patients were found to present with melanomas that were twice as thick as their non-obese peers [62]. Following surgical resection of squamous cell carcinoma (SCC) of the tongue, obese patients had worse disease-specific survival (DSS), recurrence-free survival (RFS), and overall survival (OS) [63]. Elderly female patients with B-cell lymphomas treated with RCHOP had a worse prognosis if they were obese [64]. Following resection of gastric cancer, patients with a BMI > 30 experienced increased hospital length of stay (LOS), OR time, post-operative morbidity, and post-operative mortality [65]. It was shown that the inflammation and desmoplasia caused by obesity led to a more aggressive phenotype of pancreatic adenocarcinoma that was resistant to chemotherapy and was prone to progression [66]. It was also found that patients with a BMI >35 kg/m2 were 12-fold more likely to have lymph node-positive disease and decreased DFS and OS [67]. Obesity leads to poor prognosis in patients undergoing surgical resection of extremity soft-tissue sarcoma resection. This is likely due to poor wound healing, increased dehiscence, and increased infections [68].

3. Obesity Paradox in Other Cancers

3.1. Renal

It has been hypothesized that there is an obesity paradox in renal cell carcinoma (RCC) patients. RCC is the most common type of kidney cancer and is 2.4% of all adult cancers [69]. Adiposity is a significant risk factor for developing RCC but may improve prognosis [69]. The increased incidence is thought to be secondary to insulin resistance and the increase in IGF-1. This elevated IGF-1 suppresses Bcl-2 to decrease apoptosis while simultaneously increasing proliferative and angiogenic factors [70]. Possible explanations for the improved prognosis echo many of the same sentiments cited in lung cancer, namely the use of BMI for patient categorization and alterations of the tumor immune microenvironment, with obese patients exhibiting higher levels of IL-6 TNF-α and c-peptide [71]. Multiple studies have shown an increase in overall survival and progression-free survival in obese patients [72]. This effect was seen in patients with metastatic disease [73] and those who underwent nephrectomy [74][75]. Similar to how obese patients respond better to PD-1 inhibitor therapy, obese RCC patients tend to respond better and have longer OS when treated with anti-VEGF therapies such as sunitinib, sorafenib, and bevacizumab, and axitinib [76][77]. Therefore, there is an apparent obesity paradox seen in RCC when patients are treated with immunotherapy.

3.2. Melanoma

Similar to NSCLC and RCC, obese melanoma patients treated with immunotherapy tended to have increased survival and better checkpoint inhibitor response than their normal-weight peers [78]. Obese patients were observed to respond more robustly to immune checkpoint inhibitors and have increased OS [79]. Significantly better reactions to dabrafenib, ipilimumab, trametinib, the BRAF inhibitor vemurafenib, and PD-1 therapies have been observed in obese patients [80][81]. Similar to the mice experiments performed in lung cancer, obese mice with melanoma treated with PD-1 therapy showed a better response than normal-weight mice [82] Therefore, there is an apparent obesity paradox in melanoma patients that becomes apparent when they are treated with immunotherapy.

4. Obesity Paradox in Lung Cancer

4.1. Obesity and Survival in Lung Cancer

The notion that obesity may be protective against lung cancer or contribute to improved outcomes has been a paradoxical clinical conundrum. Part of this controversy involves its absolute deviation from data obtained in animal experiments which show obesity is negatively associated with NSCLC survival [83][84]. It was thought that when undergoing surgery for lung cancer, obese patients would experience more complications. This was thought to be secondary to having less excursion of the diaphragm, lower lung volumes due to restriction, and relative immobility, but this has been disproven [85]. A relationship was found between being underweight and compromised post-operative outcomes, with these patients experiencing more surgical and infectious complications [86][87]. It has also been shown that in-hospital morbidity and mortality are significantly decreased in obese patients and can be a predictor for long-term survival [88] (Table 1). Obesity improves prognosis in operable NSCLC as shown by an increased OS [89][90][91]. When mortality in the years following surgical resection of locally advanced lung cancer was analyzed, obesity confirmed a survival benefit [92]. In a large metanalysis of 76,086 patients, obesity increased lung cancer survival [93]. This effect was seen in patients receiving carboplatin-paclitaxel chemotherapy, with obese patients experiencing no decreased survival or increased toxicity [94]. When 676 patients were treated with docetaxel in the OAK and POPLAR trials, BMI did not affect overall survival (HR = 0.96, 95% CI 0.78–1.18) for overweight and (HR = 0.92, CI 95% 0.70–1.21) for obese patients [95]. When patients with a BMI of 18.5–25 where compared to patients with a BMI above 25, the higher-BMI patients had better overall survival (HR = 1.42 95% CI 1.14–1.78) [96]. When a BMI of 25 kg/m2 was used as a cutoff, higher-BMI patients were at a 5.3-fold increased risk of post-operative respiratory complications [97] (Table 1).
Table 1. Published Literature.
Author BMI Definition (kg/m2) Number of Patients Conclusions
Ferguson [85] Overweight (25–29.9)
Obese (30–34.9)
Very obese (>35)
1369 Patients in the overweight, obese, and very obese categories had a lower rate of complications than patients with a BMI < 25 (OR: 0.72 p = 0.048)
Thomas [86] Overweight (25–30)
Obese (>30)
19,635 Overweight patients had lower mortality (OR: 0.72 p = 0.002) and obese patients had lower mortality (OR: 0.52 p < 0.001) compared to normal-weight patients and a statistically significant protective effect of obesity was observed in surgical complications
Williams [87] Overweight (25–29.9)
Obese I (30–34.9)
Obese II (35–39.9)
Obese III (>40)
41,466 Obese III patients had significantly higher rates of pulmonary complications (p < 0.001), but overweight, Obese I and Obese II patients had a lower risk of pulmonary complications and any post-operative event
Matsunaga [88] Overweight (25–30)
Obese (>30)
1518 Overweight and obese patients did not experience higher rates of pulmonary complications
Nakagawa [89] Underweight (<18.5)
Normal (18.5–25)
Overweight (25–30)
Obese (>30)
1311 Only underweight BMI was a poor prognostic factor for DFS (p = 0.03) OS (p = 0.03)
Lam [92] Overweight (25–30)
Obese (>30)
291 Increasing BMI was associated with improved survival (p = 0.011) and Obese individuals had a decrease of 31–58% (HR = 0.68 ± 0.21)
Attaran [91] Obese (BMI > 30) 337 Survival rate was higher for obese patients (p = 0.02) on univariate analysis and (p = 0.04) on multivariate analysis
Petrella [97] Obese (>25) 154 The high BMI group had a higher incidence of respiratory complications (p = 0.002) but there was no significant difference in ICU admission, LOS, and 30 day mortality

4.2. Enhanced PD-1 Checkpoint Inhibitor Therapy Response

PD-1 is present on all activated T cells and binds to PD-L1 [98]. When tumor cells express PD-L1, the local T cells in the microenvironment become exhausted, dysfunctional, and neutralized and can no longer contribute to host defense [98]. PD-1 inhibitors include monoclonal antibodies such as pembrolizumab and nivolumab that target the PD-1 receptor on T cells to release the negative regulator control [99]. This is typically in place to allow for anergy and mitigate autoimmune insults. By removing this control, the goal is to increase neoplasm destruction [99]. These medications have also been beneficial to reactivate and recruit cytotoxic T cells [99].
It has been shown that patients with a BMI > 25 (kg/m2) had a significantly better overall survival [100] and a better immunologic response [101][95] following treatment with a PD-1 inhibitor, pembrolizumab. This phenomenon was also seen in melanoma [79][81] and renal cell carcinoma patients [100][102].
In animal experiments, diet-induced obesity (DIO) mice treated with a PD-1 inhibitor experienced less B16-F0 melanoma and 3LL lung carcinoma tumor growth (expressed as lower tumor volume) and increased tumor PD-1 inhibitor response (shown by decreasing tumor size) compared to their average weight counter-parts. [82]. The DIO mice had less tumor growth at days 11 and 16 [82], and this effect was additionally seen when DIO mice were inoculated with lung tumors. The DIO mice had higher T-cell infiltration and increased CD8 to CD4 ratio [82]. There were also fewer PDL1+ T cells in the TME, proving that T cells were rescued from an exhausted state [103]. Increased expression of PD-1 may be why obese mice and people fare better [103]. This increase may be secondary to an increase in leptin [82], often elevated in obesity [104], leading to increased CD8+ T cells and STAT3, which is both a signal transducer and activator of transcription [105]. The increased expression of STAT leads to a higher PD-1 expression [82] and the phenotype of T-cell exhaustion seen in obese patients [82]. This survival advantage for obese patients is not seen when treated with conventional chemotherapy such as docetaxel, suggesting that the survival advantage is due to better PD-1 checkpoint inhibitor response [106][107].

5. Measurements of Adiposity

5.1. BMI

Body mass index (BMI) is the most common form of measurement for obesity [108]. To calculate BMI, one must divide weight in kilograms by height in meters squared. Obesity is further stratified into risk groups.
Some advantages of using BMI to measure obesity are that it is inexpensive, allows risk stratification, is strongly correlated with body fat levels, and is easy to measure [108]. BMI is not a reliable measurement of obesity because it measures total body mass, not only adipose tissue [109], and fails to identify abdominal obesity. This impacts patients because some adiposity patterns predispose them to more adverse sequelae than others. For example, increased visceral fat carries a worse prognosis than increased subcutaneous fat [110]. In a study examining the effect of obesity on lung cancer risk, BMI was inversely associated with the risk of lung cancer, but two other measures of obesity, the waist-to-hip ratio (WHR) and A Body Size Index (ABSI), showed positive correlations with lung cancer risk [111].

5.2. Underwater Weighing

To measure body habitus using underwater weighing, individuals are weighed in air and submerged in a tank with an underwater seat hanging from a scale [112]. Researchers then calculate body volume, body density, and body fat percentage due to the difference in densities [112]. Underwater weighing is accurate but is inaccessible to children, older adults, people with a BMI of 40+, and health-related problems due to the requirement of complete submersion [112].

5.3. Dual-Energy X-ray Absorptiometry

Dual-energy X-ray absorptiometry uses two low-level X-ray beams to estimate fat-free mass, fat mass, and bone mineral density [112]. Though incredibly accurate, the method is expensive and cumbersome and is suboptimal for patients with a BMI > 35 kg/m [113] and those who are pregnant due to radiation exposure [112].

5.4. Bioelectric Impedance

Bioelectric impedance utilizes the differences in resistance between tissue types when bombarded with electric current to estimate body water from which body fat is computed [114]. The method is convenient, safe, relatively inexpensive, and fast [114]. Limitations include device calibration and the inaccuracy introduced during illness, dehydration, weight loss, and a BMI of approximately 35 or higher [114].

5.5. The Waist-to-Hip Ratio

The waist-to-hip ratio measures obesity by dividing the waist measurement (cm) by the hip measurement (cm) [115]. Like BMI, it is inexpensive and convenient but is prone to measurement error and is less accurate to measure in individuals with a BMI of 35 kg/m2 or greater [115]. Turning the measured data into a ratio leads to a loss of information mathematically; two people with very different BMIs can have the same waist-to-hip ratio.
Although the waist-to-hip ratio and waist circumference are easy to measure and validate, a detriment to these methods is that they need to be performed prospectively and add additional burden on the patient [116]. There may be additional challenges getting subsequent measurements, and patients may be lost to follow up or pass away before the data can be collected [116]. The waist-to-hip ratio has the advantage of detecting abdominal obesity, which may be a better predictor of the development of lung cancer [117].

5.6. Visceral Fat Index

Visceral fat index (VFI) utilizes densitometry analysis of the routine computer tomography (CT) scans at the level of L3 to quantify visceral and subcutaneous adiposity [116]. The visceral adiposity area is then normalized to the patient’s height to allow comparative analysis [116]. This method can be performed retrospectively, does not require additional work by the patient, and mitigates many of the current qualms pertaining to BMI [116]. An additional advantage of this method is that the scans are frozen when taken, so it can accurately analyze patients retrospectively, unlike the other methods. It also allows for more granulated data that can be subsequently analyzed, and higher-level conclusions may be drawn about the impact of adiposity distributions [116]. This method has been shown to highly correlate with volumetric determinations of subcutaneous and visceral adipose tissue [118]. By utilizing VFI, it has been able to definitively show that increased visceral fat compromises overall survival and recurrence-free survival in NSCLC [116]. it was able to show that visceral obesity, as defined by a relatively high VFI, was inversely associated with inflammatory genes within the tumor microenvironment [116]. This suggests that visceral adiposity may downregulate the anti-tumor immune response and lead to progression and advanced disease [116].

5.7. Abdominal Obesity

Abdominal obesity is a known risk factor for both cardiovascular disease and the development of many cancers [119][120][121]. The age-adjusted prevalence of abdominal obesity increased from 46.4% of adults in 1999–2000 to 54.2% in 2011–2012, and this trend is consistent regardless of gender and ethnicity [122]. This increase occurred independently of an increase in the average BMI as seen by the increase in the average waist circumference by 0.2 cm in men and 2.4 cm in women in the same time span [122]. It has been shown that for each 0.1 unit increase in the waist-to-hip ratio, there was a 5% increased rate of developing lung cancer [117]. Abdominal obesity has more clearly been associated with an increased risk of NSCLC than general obesity [123][124][125]. This association’s proposed mechanisms include hyperinsulinemia, increased unbound androgen level, increased estrogens, and lower levels of sex hormone-binding globulin [125][126][127][128][129]. All of the characteristics above are explicitly seen in association with abdominal obesity. Abdominal obesity also predisposes patients to the development of insulin-resistant diabetes, contributing to inflammatory and immune sequala [122].

6. Confounding Factors

6.1. Metformin

It has been shown that type 2 diabetes is associated with a higher risk of developing lung cancer [130][131]. When analyzing the obesity paradox, a major confounding factor is the use of the anti-diabetic agent metformin. It was found that 52% of patients with type 2 diabetes mellitus were found to be obese (BMI > 30 kg/m2), and 8.1% of patients were found to be morbidly obese (BMI > 40 kg/m2) [132]. Commonly used in type 2 diabetes, metformin has been associated with decreased cancer development [133]. A major protective mechanism of metformin is decreasing the development of tobacco-associated cancer development [134]. It has been shown that the protective effects of metformin are disproportionately seen in obese or overweight patients [135][136].
Women diagnosed with early-stage breast cancer taking metformin had 22% lower fasting insulin levels and had several improved metabolic factors such as lower total cholesterol [137]. These metabolic benefits also extended to patients with metabolic syndrome secondary to androgen deprivation therapy for prostate cancer [138]. In addition to its metabolic benefits, metformin has also been shown to inhibit cancer cell proliferation; therefore, it may have utility as an adjuvant therapy [138].
A study investigating the impact of metformin on chemotherapy patients found that its anti-tumor behavior is secondary to the activation of adenosine monophosphate kinase (AMPK), the modulation of adenosine A1 receptors, a reduction in insulin/insulin growth factors, and its role in blocking endogenous reactive oxygen species [139].
Metformin appears to decrease the proliferation and growth of certain forms of cancer in preclinical studies [140][141]. Metformin achieves these effects by decreasing the biosynthetic activity of mitochondria by decreasing Krebs cycle activity and lipid synthesis, effectively starving it for nutrients [141]. Given the potential for differences in metformin responses in cancer patients, its therapeutic uses may be limited to target populations, and advantageous genetic polymorphisms remain unknown [142]. Metformin’s efficacy as neoadjuvant therapy in cancer patients has yet to be proven [142].

6.2. Statins

The statin class of medications treats high cholesterol and works by blocking HMG-CoA reductase. Statins lower LDL and raise HDL. Advantages of these medications include a reduction in atherosclerosis lower coronary artery disease [143]. They can be used for primary or secondary prevention [143]. Similar to how metformin is more likely to be on the medication list of a patient who has diabetes, statins are more likely to be used by those with hypercholesteremia. Both diabetes and high cholesterol are associated with obesity.
Statins have improved overall survival in stage four esophageal cancer patients [144]. Other studies showed improved outcomes in statin users when used after diagnosis [145][146]. This group was able to show an overall and cancer-specific survival benefit of statins when they were used prior to esophageal adenocarcinoma diagnosis [144].
This benefit has also been seen in stage IV lung cancer [147]. In patients who are overweight or obese, statin use was associated with improved recurrence-free survival [148]. These higher-BMI patients who used statin were found to have higher expression of granzyme A and interferon-γ, which are tumoricidal [148].
The likely mechanism of this survival advantage is the pro-apoptotic and anti-proliferative effects caused by the statin medications [144]. Multiple mechanisms have been proposed, including endoplasmic reticulum stress, caspase induction, NF-kB blockade, and mTOR inhibition [144].

6.3. Sex

It has been shown that there are sex-specific differences in adipocyte storage and tissue metabolism [149]. Biological males tend to experience android adipose deposition, with concentrations in the upper body and abdominal areas [149]. Biological females tend to deposit adipose in a gynoid pattern, with higher concentrations in their lower bodies. The differences in deposition are thought to be due to the relative differences in concentration of sex hormones which also explains the reason for these changes to be more pronounced prior to menopause [150]. An additional explanation that has been shown in mice hypothesizes that the changes may be due to the sex chromosomes themselves [151]. In mice, it was observed that mice with XYY had increased visceral adiposity [152].
In addition to affecting the way adiposity deposits, recent data have suggested that there may be a differential response to immunotherapy due to a patient’s sex [153]. This has been explained by the differences in sex hormone levels and genes whose expression is based on sex chromosomes [154]. Females often mount more aggressive immune responses than men, as displayed by the much higher rate of autoimmune diseases in females than men [155][156]. When immunotherapy is used alone, men often fair better than women [157]. These results have been seen in PD-1 and CTLA-4 inhibitors [158][159].
In male NSCLC patients, immunotherapy using anti-PDL1 inhibitors vs. chemotherapy showed improved outcomes while the same effect was not seen in female patients [160]. The trend of men benefitting more from immunotherapy was supported by a 2018 analysis of RCTs, with men showing significantly improved survival and efficacy when compared to women [161]. It was found that when metastatic melanoma patients were treated with immunotherapy, those who had the best long-term survival were male patients who were overweight or obese compared to average BMI patients and women who were overweight and obese [81].
Interestingly, when combined with chemotherapy in advanced lung cancer, female patients had larger benefits from immune checkpoint inhibitors than men. A possible mechanism is that chemotherapy influences the tumor to accumulate more mutations to survive, and therefore the immunotherapy has more targets to attack in an already strong female immune system [153]. Another potential explanation for these differences could be the sex-associated differences in the gut microbiota composition [162]. Finally, male-derived tumors often have higher tumor mutational burden (TMB) and cancer germline antigen expression than those from females, and therefore males may benefit more from immunotherapy [147].

6.4. Smoking

It has been extensively proven that smoking dramatically increases the risk for the development of lung cancer [163][164], with even passive smoking, or secondhand smoke, significantly increasing people’s risk [165][166]. Obese people have lower rates of smoking [167][168]. Smoking is an appetite suppressant due to the activating effects of nicotine on the hypothalamic pro-opiomelanocortin neuron pathway [169]. Nicotine does this by leading to α3β4 nicotinic acetylcholine receptor activation, which may contribute to smokers having lower BMIs [169][170][171]. Smokers tend to have greater abdominal obesity, suggesting that smoking may impact BMI and patients’ adipose tissue [172][173][174]. This increase in abdominal obesity is hypothesized to be secondary to increased cortisol levels, leading to downstream sequence such as insulin-resistant diabetes [175]. Therefore, using BMI, which does not have the sensitivity to detect abdominal obesity, these patients who are abdominally obese and whose weight is not enough to categorize them as generally obese can be missed [176][177].

References

  1. Adult Obesity Facts. 2021. Available online: https://www.cdc.gov/obesity/data/adult.html (accessed on 21 August 2021).
  2. Benjamin, E.J.; Muntner, P.; Alonso, A.; Bittencourt, M.S.; Callaway, C.W.; Carson, A.P.; Chamberlain, A.M.; Chang, A.R.; Cheng, S.; Das, S.R. Heart Disease and Stroke Statistics-2019 Update: A Report from the American Heart Association. Circulation 2019, 139, e56–e528.
  3. Chobot, A.; Górowska-Kowolik, K.; Sokołowska, M.; Jarosz-Chobot, P. Obesity and diabetes-Not only a simple link between two epidemics. Diabetes Metab. Res. Rev. 2018, 34, e3042.
  4. Saliba, L.J.; Maffett, S. Hypertensive Heart Disease and Obesity: A Review. Heart Fail Clin. 2019, 15, 509–517.
  5. Garcia-Rio, F.; Alvarez-Puebla, M.J.; Esteban-Gorgojo, I.; Barranco, P.; Olaguibel, J.M. Obesity and Asthma: Key Clinical Questions. J. Investig. Allergol. Clin. Immunol. 2019, 29, 262–271.
  6. Peters, U.; Dixon, A.E.; Forno, E. Obesity and asthma. J. Allergy Clin. Immunol. 2018, 141, 1169–1179.
  7. Kim, D.D.; Basu, A. Estimating the Medical Care Costs of Obesity in the United States: Systematic Review, Meta-Analysis, and Empirical Analysis. Value Health 2016, 19, 602–613.
  8. Avgerinos, K.I.; Spyrou, N.; Mantzoros, C.S.; Dalamaga, M. Obesity and cancer risk: Emerging biological mechanisms and perspectives. Metabolism 2019, 92, 121–135.
  9. Wynder, E.L.; Escher, G.C.; Mantel, N. An epidemiological investigation of cancer of the endometrium. Cancer 1966, 19, 489–520.
  10. Bertot, L.C.; Adams, L.A. Trends in hepatocellular carcinoma due to non-alcoholic fatty liver disease. Expert Rev. Gastroenterol. Hepatol. 2019, 13, 179–187.
  11. Pocha, C.; Kolly, P.; Dufour, J.F. Nonalcoholic Fatty Liver Disease-Related Hepatocellular Carcinoma: A Problem of Growing Magnitude. Semin. Liver Dis. 2015, 35, 304–317.
  12. Saitta, C.; Pollicino, T.; Raimondo, G. Obesity and liver cancer. Ann. Hepatol. 2019, 18, 810–815.
  13. Calle, E.E.; Rodriguez, C.; Walker-Thurmond, K.; Thun, M.J. Overweight, obesity, and mortality from cancer in a prospectively studied cohort of US adults. N. Engl. J. Med. 2003, 348, 1625–1638.
  14. Larsson, S.C.; Wolk, A. Body mass index and risk of non-Hodgkin’s and Hodgkin’s lymphoma: A meta-analysis of prospective studies. Eur. J. Cancer 2011, 47, 2422–2430.
  15. Morton, L.M.; Slager, S.L.; Cerhan, J.R.; Wang, S.S.; Vajdic, C.M.; Skibola, C.F.; Bracci, P.M.; de Sanjose, S.; Smedby, K.E.; Chiu, B.C.H.; et al. Etiologic heterogeneity among non-Hodgkin lymphoma subtypes: The InterLymph non-Hodgkin lymphoma subtypes project. J. Natl. Cancer Inst. Monogr. 2014, 2014, 130–144.
  16. Kubo, A.; Corley, D.A. Body mass index and adenocarcinomas of the esophagus or gastric cardia: A systematic review and meta-analysis. Cancer Epidemiol. Prev. Biomark. 2006, 15, 872–878.
  17. Dal Maso, L.; La Vecchia, C.; Franceschi, S.; Preston-Martin, S.; Ron, E.; Levi, F.; Mack, W.; Mark, S.D.; McTieran, A.; Kolonel, L.; et al. A pooled analysis of thyroid cancer studies. V. Anthropometric factors. Cancer Causes Control 2000, 11, 137–144.
  18. Larsson, S.C.; Wolk, A. Obesity and colon and rectal cancer risk: A meta-analysis of prospective studies. Am. J. Clin. Nutr. 2007, 86, 556–565.
  19. Bergström, A.; Hsieh, C.; Lindblad, P.; Lu, C.; Cook, N.; Wolk, A. Obesity and renal cell cancer—A quantitative review. Br. J. Cancer 2001, 85, 984–990.
  20. Marshall, F.F. Obesity and Renal Cell Cancer—A Quantitative Review. J. Urol. 2002, 168, 877.
  21. Setiawan, V.W.; Stram, D.O.; Nomura, A.M.; Kolonel, L.N.; Henderson, B.E. Risk factors for renal cell cancer: The multiethnic cohort. Am. J. Epidemiol. 2007, 166, 932–940.
  22. Larsson, S.; Wolk, A. Overweight, obesity and risk of liver cancer: A meta-analysis of cohort studies. Br. J. Cancer 2007, 97, 1005–1008.
  23. Friedman, G.D.; Herrinton, L.J. Obesity and multiple myeloma. Cancer Causes Control. 1994, 5, 479–483.
  24. Larsson, S.C.; Wolk, A. Body mass index and risk of multiple myeloma: A meta-analysis. Int. J. Cancer 2007, 121, 2512–2516.
  25. Larsson, S.; Wolk, A. Obesity and the risk of gallbladder cancer: A meta-analysis. Br. J. Cancer 2007, 96, 1457–1461.
  26. Larsson, S.C.; Wolk, A. Overweight and obesity and incidence of leukemia: A meta-analysis of cohort studies. Int. J. Cancer 2008, 122, 1418–1421.
  27. Larsson, S.C.; Wolk, A. Obesity and risk of non-Hodgkin’s lymphoma: A meta-analysis. Int. J. Cancer 2007, 121, 1564–1570.
  28. Weihrauch-Blüher, S.; Schwarz, P.; Klusmann, J.-H. Childhood obesity: Increased risk for cardiometabolic disease and cancer in adulthood. Metabolism 2019, 92, 147–152.
  29. Sanyaolu, A.; Okorie, C.; Qi, X.; Locke, J.; Rehman, S. Childhood and Adolescent Obesity in the United States: A Public Health Concern. Glob. Pediatr. Health 2019, 6, 12333794X19891305.
  30. Dushnicky, M.J.; Nazarali, S.; Mir, A.; Portwine, C.; Samaan, M.C. Is There a Causal Relationship between Childhood Obesity and Acute Lymphoblastic Leukemia? A Review. Cancers 2020, 12, 3082.
  31. Ghosh, T.; Richardson, M.; Ryder, J.; Spector, L.; Turcotte, L. Abstract 3118: Obesity as a risk factor for pediatric acute lymphoblastic leukemia: A report from the Children’s Oncology Group. Cancer Res. 2019, 79 (Suppl. 13), 3118.
  32. Leiba, M.; Leiba, A.; Keinan-Boker, L.; Avigdor, A.; Derazne, E.; Levine, H.; Kark, J.D. Adolescent weight and height are predictors of specific non-Hodgkin lymphoma subtypes among a cohort of 2,352,988 individuals aged 16 to 19 years. Cancer 2016, 122, 1068–1077.
  33. Garcia, H.; Song, M. Early-life obesity and adulthood colorectal cancer risk: A meta-analysis. Rev. Panam Salud. Publica 2019, 43, e3.
  34. Naik, A.; Monjazeb, A.M.; Decock, J. The Obesity Paradox in Cancer, Tumor Immunology, and Immunotherapy: Potential Therapeutic Implications in Triple Negative Breast Cancer. Front. Immunol. 2019, 10, 1940.
  35. De Heredia, F.P.; Gómez-Martínez, S.; Marcos, A. Obesity, inflammation and the immune system. Proc Nutr Soc. 2012, 71, 332–338.
  36. Kanneganti, T.-D.; Dixit, V.D. Immunological complications of obesity. Nat. Immunol. 2012, 13, 707–712.
  37. Ostrand-Rosenberg, S. Myeloid derived-suppressor cells: Their role in cancer and obesity. Curr. Opin. Immunol. 2018, 51, 68–75.
  38. Ostrand-Rosenberg, S. Myeloid-Derived Suppressor Cells: Facilitators of Cancer and Obesity-Induced Cancer. Annu. Rev. Cancer Biol. 2021, 5, 17–38.
  39. De Kleer, I.; Willems, F.; Lambrecht, B.; Goriely, S. Ontogeny of Myeloid Cells. Front. Immunol. 2014, 5, 423.
  40. Gantt, S.; Gervassi, A.; Jaspan, H.; Horton, H. The role of myeloid-derived suppressor cells in immune ontogeny. Front. Immunol. 2014, 5, 387.
  41. Fauriat, C.; Long, E.O.; Ljunggren, H.-G.; Bryceson, Y.T. Regulation of human NK-cell cytokine and chemokine production by target cell recognition. Blood J. Am. Soc. Hematol. 2010, 115, 2167–2176.
  42. Vivier, E.; Tomasello, E.; Baratin, M.; Walzer, T.; Ugolini, S. Functions of natural killer cells. Nat. Immunol. 2008, 9, 503–510.
  43. Elaraby, E.; Malek, A.I.; Abdullah, H.W.; Elemam, N.M.; Saber-Ayad, M.; Talaat, I.M. Natural Killer Cell Dysfunction in Obese Patients with Breast Cancer: A Review of a Triad and Its Implications. J. Immunol. Res. 2021, 2021, 9972927.
  44. Michelet, X.; Dyck, L.; Hogan, A.; Loftus, R.M.; Duquette, D.; Wei, K.; Beyaz, S.; Tavakkoli, A.; Foley, C.; Donnelly, R. Metabolic reprogramming of natural killer cells in obesity limits antitumor responses. Nat. Immunol. 2018, 19, 1330–1340.
  45. Hotamisligil, G.S.; Shargill, N.S.; Spiegelman, B.M. Adipose expression of tumor necrosis factor-alpha: Direct role in obesity-linked insulin resistance. Science 1993, 259, 87–91.
  46. Frank, L.; Mann, S.; Levine, C.B.; Cummings, B.P.; Wakshlag, J.J. Increasing body condition score is positively associated interleukin-6 and monocyte chemoattractant protein-1 in Labrador retrievers. Vet. Immunol. Immunopathol. 2015, 167, 104–109.
  47. Deng, T.; Liu, J.; Deng, Y.; Minze, L.; Xiao, X.; Wright, V.; Yu, R.; Li, X.C.; Blaszczak, A.; Bergin, S.; et al. Adipocyte adaptive immunity mediates diet-induced adipose inflammation and insulin resistance by decreasing adipose Treg cells. Nat. Commun. 2017, 8, 15725.
  48. Hopkins, B.D.; Goncalves, M.; Cantley, L.C. Obesity and cancer mechanisms: Cancer metabolism. J. Clin. Oncol. 2016, 34, 4277.
  49. Péqueux, C.; Raymond-Letron, I.; Blacher, S.; Boudou, F.; Adlanmerini, M.; Fouque, M.J.; Rochaix, P.; Noël, A.; Foidart, J.-M.; Krust, A.; et al. Stromal estrogen receptor-α promotes tumor growth by normalizing an increased angiogenesis. Cancer Res. 2012, 72, 3010–3019.
  50. Kaaks, R.; Lukanova, A.; Kurzer, M.S. Obesity, endogenous hormones, and endometrial cancer risk: A synthetic review. Cancer Epidemiol. Prev. Biomark. 2002, 11, 1531–1543.
  51. Kahn, B.B.; Flier, J.S. Obesity and insulin resistance. J. Clin. Investig. 2000, 106, 473–481.
  52. Ryu, T.Y.; Park, J.; Scherer, P.E. Hyperglycemia as a risk factor for cancer progression. Diabetes Metab. J. 2014, 38, 330–336.
  53. Frystyk, J.; Skjaerbaek, C.; Vestbo, E.; Fisker, S.; Ørskov, H. Circulating levels of free insulin-like growth factors in obese subjects: The impact of type 2 diabetes. Diabetes/Metab. Res. Rev. 1999, 15, 314–322.
  54. Murrell, A.; Heeson, S.; Cooper, W.N.; Douglas, E.; Apostolidou, S.; Moore, G.E.; Maher, E.; Reik, W. An association between variants in the IGF2 gene and Beckwith–Wiedemann syndrome: Interaction between genotype and epigenotype. Hum. Mol. Genet. 2004, 13, 247–255.
  55. Ringel, A.E.; Drijvers, J.M.; Baker, G.J.; Catozzi, A.; García-Cañaveras, J.C.; Gassaway, B.M.; Miller, B.C.; Juneja, V.R.; Nguyen, T.H.; Joshi, S.; et al. Obesity Shapes Metabolism in the Tumor Microenvironment to Suppress Anti-Tumor Immunity. Cell 2020, 183, 1848–1866.e1826.
  56. Cao, Y.; Ma, J. Body mass index, prostate cancer-specific mortality, and biochemical recurrence: A systematic review and meta-analysis. Cancer Prev. Res. 2011, 4, 486–501.
  57. Doleman, B.; Mills, K.T.; Lim, S.; Zelhart, M.D.; Gagliardi, G. Body mass index and colorectal cancer prognosis: A systematic review and meta-analysis. Tech. Coloproctol. 2016, 20, 517–535.
  58. Utsunomiya, T.; Okamoto, M.; Kameyama, T.; Matsuyama, A.; Yamamoto, M.; Fujiwara, M.; Mori, M.; Aimitsu, S.; Ishida, T. Impact of obesity on the surgical outcome following repeat hepatic resection in Japanese patients with recurrent hepatocellular carcinoma. World J. Gastroenterol. 2008, 14, 1553–1558.
  59. Langella, S.; Russolillo, N.; Forchino, F.; Lo Tesoriere, R.; D’Eletto, M.; Ferrero, A. Impact of obesity on postoperative outcome of hepatic resection for colorectal metastases. Surgery 2015, 158, 1521–1529.
  60. Feng, J.W.; Yang, X.H.; Wu, B.Q.; Sun, D.L.; Jiang, Y.; Qu, Z. Influence of Body Mass Index on the Clinicopathologic Features of Papillary Thyroid Carcinoma. Ann. Otol. Rhinol. Laryngol. 2019, 128, 625–632.
  61. Gendall, K.A.; Raniga, S.; Kennedy, R.; Frizelle, F.A. The impact of obesity on outcome after major colorectal surgery. Dis. Colon. Rectum. 2007, 50, 2223–2237.
  62. Harrell Shreckengost, C.S.; Tariq, M.; Farley, C.R.; Zhang, C.; Delman, K.A.; Kudchadkar, R.R.; Lowe, M.C. The Impact of Obesity on Surgically Treated Locoregional Melanoma. Ann. Surg. Oncol. 2021, 28, 6140–6151.
  63. Iyengar, N.M.; Kochhar, A.; Morris, P.G.; Zhou, X.K.; Ghossein, R.A.; Pino, A.; Fury, M.G.; Pfister, D.G.; Patel, S.G.; Boyle, J.O. Impact of obesity on the survival of patients with early-stage squamous cell carcinoma of the oral tongue. Cancer 2014, 120, 983–991.
  64. Hohloch, K.; Altmann, B.; Pfreundschuh, M.; Loeffler, M.; Schmitz, N.; Zettl, F.; Ziepert, M.; Trumper, L. Obesity negatively impacts outcome in elderly female patients with aggressive B-cell lymphomas treated with R-CHOP: Results from prospective trials of the German high grade non-Hodgkin’s lymphoma trial group. Br. J. Haematol. 2018, 180, 236–245.
  65. Struecker, B.; Biebl, M.; Dadras, M.; Chopra, S.; Deneche, C.; Spenke, J.; Heilmann, A.C.; Bahra, M.; Sauer, I.M.; Pratschke, J.; et al. The Impact of Obesity on Outcomes Following Resection for Gastric Cancer. Dig. Surg. 2017, 34, 133–141.
  66. Incio, J.; Liu, H.; Suboj, P.; Chin, S.M.; Chen, I.X.; Pinter, M.; Ng, M.R.; Nia, H.T.; Grahovac, J.; Kao, S. Obesity-Induced Inflammation and Desmoplasia Promote Pancreatic Cancer Progression and Resistance to Chemotherapy. Cancer Discov. 2016, 6, 852–869.
  67. Fleming, J.B.; Gonzalez, R.J.; Petzel, M.Q.; Lin, E.; Morris, J.S.; Gomez, H.; Lee, J.E.; Crane, C.H.; Pisters, W.T.; Evans, D.B. Influence of obesity on cancer-related outcomes after pancreatectomy to treat pancreatic adenocarcinoma. Arch. Surg. 2009, 144, 216–221.
  68. Houdek, M.T.; Griffin, A.M.; Ferguson, P.C.; Wunder, J.S. Morbid Obesity Increases the Risk of Postoperative Wound Complications, Infection, and Repeat Surgical Procedures Following Upper Extremity Limb Salvage Surgery for Soft Tissue Sarcoma. Hand 2019, 14, 114–120.
  69. Li, M.; Bu, R. Biological Support to Obesity Paradox in Renal Cell Carcinoma: A Review. Urol. Int. 2020, 104, 837–848.
  70. Björndahl, M.; Cao, R.; Nissen, L.J.; Clasper, S.; Johnson, L.A.; Xue, Y.; Zhou, Z.; Jackson, D.; Hansen, A.J.; Cao, Y. Insulin-like growth factors 1 and 2 induce lymphangiogenesis in vivo. Proc. Natl. Acad. Sci. USA 2005, 102, 15593–15598.
  71. Wang, Q.; Tu, H.; Zhu, M.; Liang, D.; Ye, Y.; Chang, D.W.; Lng, Y.; Wu, X. Circulating obesity-driven biomarkers are associated with risk of clear cell renal cell carcinoma: A two-stage, case-control study. Carcinogenesis 2019, 40, 1191–1197.
  72. Kamat, A.M.; Shock, R.P.; Naya, Y.; Rosser, C.J.; Slaton, J.W.; Pisters, L.L. Prognostic value of body mass index in patients undergoing nephrectomy for localized renal tumors. Urology 2004, 63, 46–50.
  73. Albiges, L.; Hakimi, A.A.; Xie, W.; McKay, R.R.; Simantov, R.; Lin, X.; Lee, J.L.; Rini, B.I.; Srinvas, S.; Bjarnason, G.A. Body Mass Index and Metastatic Renal Cell Carcinoma: Clinical and Biological Correlations. J. Clin. Oncol. 2016, 34, 3655–3663.
  74. Choi, Y.; Park, B.; Jeong, B.C.; Seo, S.I.; Jeon, S.S.; Choi, H.Y.; Adami, H.O.; Lee, J.E.; Lee, H.M. Body mass index and survival in patients with renal cell carcinoma: A clinical-based cohort and meta-analysis. Int. J. Cancer 2013, 132, 625–634.
  75. Jeon Hwang, G.; Jeong In, G.; Lee June, H.; Lee Chang, J.; Kwak, C.; Kim Hyeon, H.; Lee Sang, E.; Lee, E. Prognostic Value of Body Mass Index in Korean Patients with Renal Cell Carcinoma. J. Urol. 2010, 183, 448–454.
  76. Choueiri, T.K.; Xie, W.; Kollmannsberger, C.K.; Rini, B.I.; McDermott, D.F.; Knox, J.J.; Heng, Y. The impact of body mass index (BMI) and body surface area (BSA) on treatment outcome to vascular endothelial growth factor (VEGF)-targeted therapy in metastatic renal cell carcinoma: Results from a large international collaboration. J. Clin. Oncol. 2010, 28 (Suppl. S15), 4524.
  77. Steffens, S.; Grünwald, V.; Ringe, K.I.; Seidel, C.; Eggers, H.; Schrader, M.; Wacker, F.; Kuczyk, M.A.; Schrader, A.J. Does Obesity Influence the Prognosis of Metastatic Renal Cell Carcinoma in Patients Treated with Vascular Endothelial Growth Factor–Targeted Therapy? Oncologist 2011, 16, 1565–1571.
  78. Naik, G.S.; Waikar, S.S.; Johnson, A.E.W.; Buchbinder, E.I.; Haq, R.; Hodi, F.S.; Schoenfeld, J.D.; Ott, P.A. Complex inter-relationship of body mass index, gender and serum creatinine on survival: Exploring the obesity paradox in melanoma patients treated with checkpoint inhibition. J. Immunother. Cancer 2019, 7, 89.
  79. Donnelly, D.; Bajaj, S.; Yu, J.; Hsu, M.; Balar, A.; Pavlick, A.; Weber, J.; Osman, I.; Zhong, J. The complex relationship between body mass index and response to immune checkpoint inhibition in metastatic melanoma patients. J. Immunother. Cancer 2019, 7, 222.
  80. Pencheva, N.; Buss, C.; Posada, J.; Merghoub, T.; Tavazoie, S.F. Broad-spectrum therapeutic suppression of metastatic melanoma through nuclear hormone receptor activation. Cell 2014, 156, 986–1001.
  81. McQuade, J.L.; Daniel, C.R.; Hess, K.R.; Mak, C.; Wang, D.Y.; Rai, R.R.; Park, J.J.; Haydu, L.E.; Spencer, C.; Wongchenko, M.; et al. Association of body-mass index and outcomes in patients with metastatic melanoma treated with targeted therapy, immunotherapy, or chemotherapy: A retrospective, multicohort analysis. Lancet Oncol. 2018, 19, 310–322.
  82. Wang, Z.; Aguilar, E.G.; Luna, J.I.; Dunai, C.; Khuat, L.T.; Le, C.; Mirsoian, A.; Minnar, C.M.; Stoffel, K.M.; Sturgill, I.R.; et al. Paradoxical effects of obesity on T cell function during tumor progression and PD-1 checkpoint blockade. Nat. Med. 2019, 25, 141–151.
  83. Xie, J.; Lesaffre, E.; Kesteloot, H. The relationship between animal fat intake, cigarette smoking, and lung cancer. Cancer Causes Control. 1991, 2, 79–83.
  84. Shi, D.; Wu, J.; Wu, Y.; Lin, X.; Xu, C.; Lian, X. High-Fat Diet-Related Obesity Promotes Urethane-Induced Lung Tumorigenesis in C57BL/6J Mice. Front. Oncol. 2021, 11, 100.
  85. Ferguson, M.K.; Im, H.K.; Watson, S.; Johnson, E.; Wigfield, C.H.; Vigneswaran, W.T. Association of body mass index and outcomes after major lung resection. Eur. J. Cardio-Thorac. Surg. 2014, 45, e94–e99.
  86. Thomas, P.; Berbis, J.; Falcoz, P.-E.; Le Pimpec-Barthes, F.; Bernard, A.; Jougon, J.; Porte, H.; Alifano, M.; Dahan, M.; Alauzen, M.; et al. National perioperative outcomes of pulmonary lobectomy for cancer: The influence of nutritional status. Eur. J. Cardio-Thorac. Surg. 2014, 45, 652–659.
  87. Williams, T.; Gulack, B.C.; Kim, S.; Fernandez, F.G.; Ferguson, M.K. Operative risk for major lung resection increases at extremes of body mass index. Ann. Thorac. Surg. 2017, 103, 296–302.
  88. Matsunaga, T.; Imashimizu, K.; Banno, T.; Takamochi, K.; Oh, S.; Suzuki, K. Body mass index as a prognostic factor in resected lung cancer: Obesity or underweight, which is the risk factor? Thorac. Cardiovasc. Surg. 2015, 63, 551–557.
  89. Nakagawa, T.; Toyazaki, T.; Chiba, N.; Ueda, Y.; Gotoh, M. Prognostic value of body mass index and change in body weight in postoperative outcomes of lung cancer surgery. Interact. Cardiovasc. Thorac. Surg. 2016, 23, 560–566.
  90. Li, S.; Wang, Z.; Huang, J.; Fan, J.; Du, H.; Liu, L.; Che, G. Systematic review of prognostic roles of body mass index for patients undergoing lung cancer surgery: Does the ‘obesity paradox’ really exist? Eur. J. Cardio-Thorac. Surg. 2017, 51, 817–828.
  91. Attaran, S.; McShane, J.; Whittle, I.; Poullis, M.; Shackcloth, M. A propensity-matched comparison of survival after lung resection in patients with a high versus low body mass index. Eur. J. Cardio-Thorac. Surg. 2012, 42, 653–658.
  92. Lam, V.K.; Bentzen, S.M.; Mohindra, P.; Nichols, E.M.; Bhooshan, N.; Vyfhuis, M.; Scilla, K.A.; Feigenberg, S.J.; Edelman, M.J.; Feliciano, J.L. Obesity is associated with long-term improved survival in definitively treated locally advanced non-small cell lung cancer (NSCLC). Lung Cancer 2017, 104, 52–57.
  93. Yang, R.; Cheung, M.C.; Pedroso, F.E.; Byrne, M.M.; Koniaris, L.G.; Zimmers, T.A. Obesity and weight loss at presentation of lung cancer are associated with opposite effects on survival. J. Surg. Res. 2011, 170, e75–e83.
  94. Kashiwabara, K.; Yamane, H.; Tanaka, H. Toxicity and prognosis in overweight and obese women with lung cancer receiving carboplatin-paclitaxel doublet chemotherapy. Cancer Investig. 2013, 31, 251–257.
  95. Kichenadasse, G.; Miners, J.O.; Mangoni, A.A.; Rowland, A.; Hopkins, A.; Sorich, M. Association Between Body Mass Index and Overall Survival with Immune Checkpoint Inhibitor Therapy for Advanced Non-Small Cell Lung Cancer. JAMA Oncol. 2020, 6, 512–518.
  96. Yap, W.-K.; Shih, M.-C.; Kuo, C.; Pai, P.-C.; Chou, W.-C.; Chang, K.-P.; Tsai, M.-H.; Tsang, N.-M. Development and Validation of a Nomogram for Assessing Survival in Patients with Metastatic Lung Cancer Referred for Radiotherapy for Bone Metastases. JAMA Netw. Open 2018, 1, 183242.
  97. Petrella, F.; Radice, D.; Borri, A.; Galetta, D.; Gasparri, R.; Solli, P.; Veronesi, G.; Spaggiari, L. The impact of preoperative body mass index on respiratory complications after pneumonectomy for non-small-cell lung cancer. Results from a series of 154 consecutive standard pneumonectomies. Eur. J. Cardio-Thorac. Surg. 2011, 39, 738–744.
  98. Sun, Z.; Fourcade, J.; Pagliano, O.; Chauvin, J.-M.; Sander, C.; Kirkwood, J.M.; Zarour, H.M. IL10 and PD-1 Cooperate to Limit the Activity of Tumor-Specific CD8+ T Cells. Cancer Res. 2015, 75, 1635–1644.
  99. Alsaab, H.O.; Sau, S.; Alzhrani, R.; Tatiparti, K.; Bhise, K.; Kashaw, S.K.; Iyer, A.K. PD-1 and PD-L1 Checkpoint Signaling Inhibition for Cancer Immunotherapy: Mechanism, Combinations, and Clinical Outcome. Front. Pharmacol. 2017, 8, 561.
  100. Cortellini, A.; Bersanelli, M.; Buti, S.; Cannita, K.; Santini, D.; Perrone, F.; Giusti, R.; Tiseo, M.; Michiara, M.; Marino, P.D. A multicenter study of body mass index in cancer patients treated with anti-PD-1/PD-L1 immune checkpoint inhibitors: When overweight becomes favorable. J. Immunother. Cancer 2019, 7, 57.
  101. Ten Haaf, K.; Jeon, J.; Tammemägi, M.C.; Han, S.S.; Kong, C.Y.; Plevritis, S.K.; Feuer, E.J.; de Koning, H.J.; Steyerberg, E.W.; Meza, R. Risk prediction models for selection of lung cancer screening candidates: A retrospective validation study. PLoS Med. 2017, 14, e1002277.
  102. Sánchez-Jiménez, F.; Pérez, A.P.; de la Cruz-Merino, L.; Sánchez-Margalet, V. Obesity and Breast Cancer: Role of Leptin. Front. Oncol. 2019, 9, 596.
  103. Murphy, W.J.; Longo, D.L. The Surprisingly Positive Association Between Obesity and Cancer Immunotherapy Efficacy. Jama 2019, 321, 1247–1248.
  104. Münzberg, H.; Myers, M.G., Jr. Molecular and anatomical determinants of central leptin resistance. Nat. Neurosci. 2005, 8, 566–570.
  105. Aggarwal, B.B.; Kunnumakkara, A.B.; Harikumar, K.B.; Gupta, S.R.; Tharakan, S.T.; Koca, C.; Dey, S.; Sung, B. Signal transducer and activator of transcription-3, inflammation, and cancer: How intimate is the relationship? Ann. N. Y. Acad. Sci. 2009, 1171, 59–76.
  106. Fehrenbacher, L.; Spira, A.; Ballinger, M.; Kowanetz, M.; Vansteenkiste, J.; Mazieres, J.; Park, K.; Smith, D.; Artal-Cortes, A.; Lewanski, C.; et al. Atezolizumab versus docetaxel for patients with previously treated non-small-cell lung cancer (POPLAR): A multicentre, open-label, phase 2 randomised controlled trial. Lancet 2016, 387, 1837–1846.
  107. Peters, S.; Gettinger, S.; Johnson, M.L.; Jänne, P.A.; Garassino, M.C.; Christoph, D.; Toh, C.K.; Rizvi, N.A.; Chaft, J.E.; Costa, E.C.; et al. Phase II trial of atezolizumab as first-line or subsequent therapy for patients with programmed death-ligand 1–selected advanced non–small-cell lung cancer (BIRCH). J. Clin. Oncol. 2017, 35, 2781.
  108. Ghesmaty Sangachin, M.; Cavuoto, L.A.; Wang, Y. Use of various obesity measurement and classification methods in occupational safety and health research: A systematic review of the literature. BMC Obes. 2018, 5, 28.
  109. Donini, L.M.; Pinto, A.; Giusti, A.M.; Lenzi, A.; Poggiogalle, E. Obesity or BMI paradox? Beneath the tip of the iceberg. Front. Nutr. 2020, 7, 53.
  110. Neeland, I.J.; Poirier, P.; Després, J.-P. Cardiovascular and metabolic heterogeneity of obesity: Clinical challenges and implications for management. Circulation 2018, 137, 1391–1406.
  111. Ardesch, F.H.; Ruiter, R.; Mulder, M.; LaHousse, L.; Stricker, B.H.C.; Jong, J.C.K.-D. The obesity paradox in lung cancer: Associations with body size versus body shape. Front. Oncol. 2020, 10, 2430.
  112. Heymsfield, S.B.; Smith, B.; Wong, M.; Bennett, J.; Ebbeling, C.; Wong, J.M.W.; Strauss, B.J.G.; Shepherd, J. Multicomponent density models for body composition: Review of the dual energy X-ray absorptiometry volume approach. Obes. Rev. 2021, 22, e13274.
  113. Ogden, C.L.; Fakhouri, T.H.; Carroll, M.D.; Hales, C.M.; Fryar, C.D.; Li, X.; Freedman, D.S. Prevalence of obesity among adults, by household income and education—United States, 2011–2014. MMWR Morb. Mortal. Wkly. Rep. 2017, 66, 1369.
  114. de-Mateo-Silleras, B.; de-la-Cruz-Marcos, S.; Alonso-Izquierdo, L.; Camina-Martín, M.A.; Marugán-de-Miguelsanz, J.M.; Redondo-del-Río, M.P. Bioelectrical impedance vector analysis in obese and overweight children. PLoS ONE 2019, 14, e0211148.
  115. Czernichow, S.; Kengne, A.-P.; Huxley, R.; Batty, G.; De Galan, B.; Grobbee, D.; Pillai, A.; Zoungas, S.; Marre, M.; Woodward, M.; et al. Comparison of waist-to-hip ratio and other obesity indices as predictors of cardiovascular disease risk in people with type-2 diabetes: A prospective cohort study from ADVANCE. Eur. J. Prev. Cardiol. 2011, 18, 312–319.
  116. Barbi, J.; Patnaik, S.K.; Pabla, S.; Zollo, R.; Smith, R.J., Jr.; Sass, S.N.; Srinivasan, A.; Petrucci, C.; Seager, R.; Conroy, J.; et al. Visceral Obesity Promotes Lung Cancer Progression-Toward Resolution of the Obesity Paradox in Lung Cancer. J. Thorac. Oncol. 2021, 16, 1333–1348.
  117. Hidayat, K.; Du, X.; Chen, G.; Shi, M.; Shi, B. Abdominal Obesity and Lung Cancer Risk: Systematic Review and Meta-Analysis of Prospective Studies. Nutrients 2016, 8, 810.
  118. Irlbeck, T.; Massaro, J.; Bamberg, F.; O’Donnell, C.J.; Hoffmann, U.; Fox, C.S. Association between single-slice measurements of visceral and abdominal subcutaneous adipose tissue with volumetric measurements: The Framingham Heart Study. Int. J. Obes. 2010, 34, 781–787.
  119. Zhang, C.; Rexrode, K.M.; van Dam, R.M.; Li, T.Y.; Hu, F.B. Abdominal obesity and the risk of all-cause, cardiovascular, and cancer mortality: Sixteen years of follow-up in US women. Circulation 2008, 117, 1658–1667.
  120. Barberio, A.M.; Alareeki, A.; Viner, B.; Pader, J.; Vena, J.E.; Arora, P.; Friedenreich, C.M.; Brenner, D.R. Central body fatness is a stronger predictor of cancer risk than overall body size. Nat. Commun. 2019, 10, 383.
  121. Agurs-Collins, T.; Ross, S.A.; Dunn, B.K. The Many Faces of Obesity and Its Influence on Breast Cancer Risk. Front. Oncol. 2019, 9, 765.
  122. Bhupathiraju, S.N.; Hu, F.B. Epidemiology of Obesity and Diabetes and Their Cardiovascular Complications. Circ. Res. 2016, 118, 1723–1735.
  123. Kabat, G.C.; Kim, M.; Hunt, J.R.; Chlebowski, R.T.; Rohan, T.E. Body mass index and waist circumference in relation to lung cancer risk in the Women’s Health Initiative. Am. J. Epidemiol. 2008, 168, 158–169.
  124. Lam, T.K.; Moore, S.C.; Brinton, L.A.; Smith, L.; Hollenbeck, A.R.; Gierach, G.L.; Freedman, N.D. Anthropometric measures and physical activity and the risk of lung cancer in never-smokers: A prospective cohort study. PLoS ONE 2013, 8, e70672.
  125. Olson, J.E.; Yang, P.; Schmitz, K.; Vierkant, R.A.; Cerhan, J.R.; Sellers, T.A. Differential association of body mass index and fat distribution with three major histologic types of lung cancer: Evidence from a cohort of older women. Am. J. Epidemiol. 2002, 156, 606–615.
  126. Drinkard, C.R.; Sellers, T.A.; Potter, J.D.; Zheng, W.; Bostlck, R.M.; Nelson, C.L.; Folsom, A.R. Association of body mass index and body fat distribution with risk of lung cancer in older women. Am. J. Epidemiol. 1995, 142, 600.
  127. Soler, J.T.; Folsom, A.R.; Kaye, S.A.; Prineas, R.J. Associations of abdominal adiposity, fasting insulin, sex hormone binding globulin, and estrone with lipids and lipoproteins in post-menopausal women. Atherosclerosis 1989, 79, 21–27.
  128. Mohamed-Ali, V.; Pinkney, J.; Coppack, S. Adipose tissue as an endocrine and paracrine organ. Int. J. Obes. Relat. Metab. Disord. 1998, 22, 1145–1158.
  129. Wajchenberg, B.L. Subcutaneous and visceral adipose tissue: Their relation to the metabolic syndrome. Endocr. Rev. 2000, 21, 697–738.
  130. Tseng, C.H. Diabetes but not insulin increases the risk of lung cancer: A Taiwanese population-based study. PLoS ONE 2014, 9, e101553.
  131. Tseng, C.H. Higher risk of mortality from lung cancer in Taiwanese people with diabetes. Diabetes Res. Clin. Pract. 2013, 102, 193–201.
  132. Daousi, C.; Casson, I.F.; Gill, G.V.; MacFarlane, I.A.; Wilding, J.P.; Pinkney, J.H. Prevalence of obesity in type 2 diabetes in secondary care: Association with cardiovascular risk factors. Postgrad. Med. J. 2006, 82, 280–284.
  133. Dowling, R.J.O.; Niraula, S.; Stambolic, V.; Goodwin, P.J. Metformin in cancer: Translational challenges. J. Mol. Endocrinol. 2012, 48, R31–R43.
  134. Thakkar, B.; Aronis, K.N.; Vamvini, M.T.; Shields, K.; Mantzoros, C.S. Metformin and sulfonylureas in relation to cancer risk in type II diabetes patients: A meta-analysis using primary data of published studies. Metabolism 2013, 62, 922–934.
  135. Dhillon, S.S.; Groman, A.; Meagher, A.; Demmy, T.; Warren, G.W.; Yendamuri, S. Metformin and Not Diabetes Influences the Survival of Resected Early Stage NSCLC Patients. J. Cancer Sci. Ther. 2014, 6, 217–222.
  136. Currie, C.J.; Poole, C.D.; Jenkins-Jones, S.; Gale, E.A.; Johnson, J.A.; Morgan, C.L. Mortality after incident cancer in people with and without type 2 diabetes: Impact of metformin on survival. Diabetes Care 2012, 35, 299–304.
  137. Goodwin, P.J.; Pritchard, K.I.; Ennis, M.; Clemons, M.; Graham, M.; Fantus, I.G. Insulin-lowering effects of metformin in women with early breast cancer. Clin. Breast Cancer 2008, 8, 501–505.
  138. Whitburn, J.; Edwards, C.M.; Sooriakumaran, P. Metformin and prostate cancer: A new role for an old drug. Curr. Urol. Rep. 2017, 18, 46.
  139. Ugwueze, C.V.; Ogamba, O.J.; Young, E.E.; Onyenekwe, B.M.; Ezeokpo, B.C. Metformin: A possible option in cancer chemotherapy. Anal. Cell. Pathol. 2020, 2020, 1–10.
  140. Xiong, Z.S.; Gong, S.F.; Si, W.; Jiang, T.; Li, Q.L.; Wang, T.J.; Wang, W.J.; Wu, R.Y.; Jiang, K. Effect of metformin on cell proliferation, apoptosis, migration and invasion in A172 glioma cells and its mechanisms. Mol. Med. Rep. 2019, 20, 887–894.
  141. Griss, T.; Vincent, E.; Egnatchik, R.; Chen, J.; Ma, E.H.; Faubert, B.; Viollet, B.; DeBerardinis, R.J.; Jones, R.G. Metformin Antagonizes Cancer Cell Proliferation by Suppressing Mitochondrial-Dependent Biosynthesis. PLoS Biol. 2015, 13, e1002309.
  142. Morales, D.R.; Morris, A.D. Metformin in cancer treatment and prevention. Annu. Rev. Med. 2015, 66, 17–29.
  143. Alenghat, F.J.; Davis, A.M. Management of Blood Cholesterol. JAMA 2019, 321, 800–801.
  144. Dighe, S.G.; Yan, L.; Mukherjee, S.; McGillicuddy, C.S.; Hulme, K.L.; Hochwald, S.N.; Yendamuri, S.; Bain, A.J.; Robillard, K.T.; Moysich, K.B.; et al. Clinical and Lifestyle-Related Prognostic Indicators among Esophageal Adenocarcinoma Patients Receiving Treatment at a Comprehensive Cancer Center. Cancers 2021, 13, 4653.
  145. Alexandre, L.; Clark, A.B.; Bhutta, H.Y.; Chan, S.S.; Lewis, M.P.; Hart, A.R. Association between statin use after diagnosis of esophageal cancer and survival: A population-based cohort study. Gastroenterology 2016, 150, 854–865.e851.
  146. Nguyen, T.; Khan, A.; Liu, Y.; El-Serag, H.B.; Thrift, A.P. The association between statin use after diagnosis and mortality risk in patients with esophageal cancer: A retrospective cohort study of United States veterans. Off. J. Am. Coll. Gastroenterol. ACG 2018, 113, 1310.
  147. Lin, J.J.; Ezer, N.; Sigel, K.; Mhango, G.; Wisnivesky, J.P. The effect of statins on survival in patients with stage IV lung cancer. Lung Cancer 2016, 99, 137–142.
  148. Patnaik, S.K.; Petrucci, C.; Barbi, J.; Seager, R.J.; Pabla, S.; Yendamuri, S. Obesity-Specific Association of Statin Use and Reduced Risk of Recurrence of Early Stage NSCLC. JTO Clin. Res. Rep. 2021, 2, 100254.
  149. Karastergiou, K.; Smith, S.R.; Greenberg, A.S.; Fried, S.K. Sex differences in human adipose tissues–the biology of pear shape. Biol. Sex Differ. 2012, 3, 1–12.
  150. Fuente-Martín, E.; Argente-Arizón, P.; Ros, P.; Argente, J.; Chowen, J.A. Sex differences in adipose tissue: It is not only a question of quantity and distribution. Adipocyte 2013, 2, 128–134.
  151. Chen, X.; McClusky, R.; Chen, J.; Beaven, S.W.; Tontonoz, P.; Arnold, A.P.; Reue, K. The number of x chromosomes causes sex differences in adiposity in mice. PLoS Genet. 2012, 8, e1002709.
  152. Bardsley, M.Z.; Kowal, K.; Levy, C.; Gosek, A.; Ayari, N.; Tartaglia, N.; Lahlou, N.; Winder, B.; Grimes, S.; Ross, J.L. 47, XYY syndrome: Clinical phenotype and timing of ascertainment. J. Pediatr. 2013, 163, 1085–1094.
  153. Wang, S.; Cowley, L.A.; Liu, X.-S. Sex Differences in Cancer Immunotherapy Efficacy, Biomarkers, and Therapeutic Strategy. Molecules 2019, 24, 3214.
  154. Klein, S.L.; Flanagan, K.L. Sex differences in immune responses. Nat. Rev. Immunol. 2016, 16, 626–638.
  155. Jacobson, D.L.; Gange, S.J.; Rose, N.R.; Graham, N.M. Epidemiology and estimated population burden of selected autoimmune diseases in the United States. Clin. Immunol. Immunopathol. 1997, 84, 223–243.
  156. Voskuhl, R. Sex differences in autoimmune diseases. Biol. Sex Differ. 2011, 2, 1.
  157. Wang, C.; Qiao, W.; Jiang, Y.; Zhu, M.; Shao, J.; Ren, P.; Liu, D.; Li, W. Effect of sex on the efficacy of patients receiving immune checkpoint inhibitors in advanced non-small cell lung cancer. Cancer Med. 2019, 8, 4023–4031.
  158. Wu, Y.; Ju, Q.; Jia, K.; Yu, J.; Shi, H.; Wu, H.; Jiang, M. Correlation between sex and efficacy of immune checkpoint inhibitors (PD-1 and CTLA-4 inhibitors). Int. J. Cancer. 2018, 143, 45–51.
  159. Grassadonia, A.; Sperduti, I.; Vici, P.; Iezzi, L.; Brocco, D.; Gamucci, T.; Pizzuti, L.; Maugeri-Saccà, M.; Marchetti, P.; Cognetti, G.; et al. Effect of Gender on the Outcome of Patients Receiving Immune Checkpoint Inhibitors for Advanced Cancer: A Systematic Review and Meta-Analysis of Phase III Randomized Clinical Trials. J. Clin. Med. 2018, 7, 542.
  160. Pinto, J.A.; Vallejos, C.S.; Raez, L.E.; Mas, L.A.; Ruiz, R.; Torres-Roman, J.S.; Morante, Z.; Araujo, J.M.; Gomez, H.L.; Aguilar, A. Gender and outcomes in non-small cell lung cancer: An old prognostic variable comes back for targeted therapy and immunotherapy? ESMO Open 2018, 3, e000344.
  161. Conforti, F.; Pala, L.; Bagnardi, V.; De Pas, T.; Martinetti, M.; Viale, G.; Gelber, R.D.; Goldhirsch, A. Cancer immunotherapy efficacy and patients’ sex: A systematic review and meta-analysis. Lancet Oncol. 2018, 19, 737–746.
  162. Org, E.; Mehrabian, M.; Parks, B.W.; Shipkova, P.; Liu, X.; Drake, T.A.; Lusis, A.J. Sex differences and hormonal effects on gut microbiota composition in mice. Gut. Microbes. 2016, 7, 313–322.
  163. Loeb, L.A.; Ernster, V.L.; Warner, K.; Abbotts, J.; Laszlo, J. Smoking and lung cancer: An overview. Cancer Res. 1984, 44, 5940–5958.
  164. Cornfield, J.; Haenszel, W.; Hammond, E.C.; Lilienfeld, A.M.; Shimkin, M.B.; Wynder, E.L. Smoking and lung cancer: Recent evidence and a discussion of some questions. J. Natl. Cancer Inst. 1959, 22, 173–203.
  165. Correa, P.; Fontham, E.; Pickle, L.W.; Lin, Y.; Haenszel, W. Passive smoking and lung cancer. Lancet 1983, 322, 595–597.
  166. Trichopoulos, D.; Kalandidi, A.; Sparros, L.; Macmahon, B. Lung cancer and passive smoking. Int. J. Cancer 1981, 27, 1–4.
  167. Dare, S.; Mackay, D.F.; Pell, J.P. Relationship between smoking and obesity: A cross-sectional study of 499,504 middle-aged adults in the UK general population. PLoS ONE 2015, 10, e0123579.
  168. Watanabe, T.; Tsujino, I.; Konno, S.; Ito, Y.M.; Takashina, C.; Sato, T.; Isadaa, A.; Ohira, H.; Ohtsuka, Y.; Fukutomi, Y. Association between smoking status and obesity in a nationwide survey of Japanese adults. PLoS ONE 2016, 11, e0148926.
  169. Mineur, Y.S.; Abizaid, A.; Rao, Y.; Salas, R.; DiLeone, R.J.; Gündisch, D.; Diano, S.; De Biasi, M.; Horvath, T.L.; Gao, X.-B.; et al. Nicotine decreases food intake through activation of POMC neurons. Science 2011, 332, 1330–1332.
  170. Jacobs, D.R., Jr.; Gottenborg, S. Smoking and weight: The Minnesota Lipid Research Clinic. Am. J. Public Health 1981, 71, 391–396.
  171. Wannamethee, S.G.; Shaper, A.G.; Walker, M. Weight change, body weight and mortality: The impact of smoking and ill health. Int. J. Epidemiol. 2001, 30, 777–786.
  172. Kaye, S.A.; Folsom, A.R.; Prineas, R.J.; Potter, J.; Gapstur, S.M. The association of body fat distribution with lifestyle and reproductive factors in a population study of postmenopausal women. Int. J. Obes. 1990, 14, 583–591.
  173. Shimokata, H.; Muller, D.C.; Andres, R. Studies in the distribution of body fat: III. Effects of cigarette smoking. Jama 1989, 261, 1169–1173.
  174. Barrett-Connor, E.; Khaw, K.-T. Cigarette smoking and increased central adiposity. Ann. Intern. Med. 1989, 111, 783–787.
  175. Yun, J.E.; Kimm, H.; Choi, Y.J.; Jee, S.H.; Huh, K.B. Smoking is associated with abdominal obesity, not overall obesity, in men with type 2 diabetes. J. Prev. Med. Public Health 2012, 45, 316–322.
  176. Lindholm, A.; Roswall, J.; Alm, B.; Almquist-Tangen, G.; Bremander, A.; Dahlgren, J.; Staland-Nyman, C.; Bergman, S. Body mass index classification misses to identify children with an elevated waist-to-height ratio at 5 years of age. Pediatr. Res. 2019, 85, 30–35.
  177. Christakoudi, S.; Tsilidis, K.K.; Muller, D.C.; Freisling, H.; Weiderpass, E.; Overvad, K.; Soderberg, S.; Haggstrom, C.; Pischon, T.; Dahm, C.C. A Body Shape Index (ABSI) achieves better mortality risk stratification than alternative indices of abdominal obesity: Results from a large European cohort. Sci. Rep. 2020, 10, 14541.
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