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Parveen, S.;  Alhazmi, Y.A. Intermittent Fasting on Metabolic Syndrome and Periodontal Disease. Encyclopedia. Available online: https://encyclopedia.pub/entry/34930 (accessed on 20 June 2024).
Parveen S,  Alhazmi YA. Intermittent Fasting on Metabolic Syndrome and Periodontal Disease. Encyclopedia. Available at: https://encyclopedia.pub/entry/34930. Accessed June 20, 2024.
Parveen, Sameena, Yaser Ali Alhazmi. "Intermittent Fasting on Metabolic Syndrome and Periodontal Disease" Encyclopedia, https://encyclopedia.pub/entry/34930 (accessed June 20, 2024).
Parveen, S., & Alhazmi, Y.A. (2022, November 16). Intermittent Fasting on Metabolic Syndrome and Periodontal Disease. In Encyclopedia. https://encyclopedia.pub/entry/34930
Parveen, Sameena and Yaser Ali Alhazmi. "Intermittent Fasting on Metabolic Syndrome and Periodontal Disease." Encyclopedia. Web. 16 November, 2022.
Intermittent Fasting on Metabolic Syndrome and Periodontal Disease
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Metabolic syndrome (MetS) prevalence continues to climb significantly worldwide in today’s ad libitum society. MetS have tremendous societal and economic ramifications, making it imperative to develop effective strategies for preventing and controlling it to alleviate this growing burden. Periodontal disease and MetS are associated with several risk factors. Studies in the past have demonstrated that obesity, cardiovascular illness, and type 2 diabetes mellitus have a negative effect on the severity of periodontal disease. Patients with metabolic syndrome have elevated serum levels of proinflammatory mediators such as tumour necrosis factor-alpha interleukin-6 and C-reactive protein. Remarkably, Intermittent fasting is underpinned by scientific evidence, claiming to be the most effective non-pharmacological, potential therapeutic alternative for combating a wide range of metabolic, inflammatory, and lifestyle-related diseases.

intermittent fasting metabolic syndrome calorie restriction periodontal diseases

1. Introduction

MetS is characterized as three of the five interconnected risk factors of diabetes and cardiovascular disease, namely high blood pressure (BP), elevated glucose levels, obesity (especially central adiposity), and low levels of high-density lipoprotein(HDL), or elevated triglyceride levels (TGS) [1]. Globally, the toll of all MetS components is skyrocketing because of increased incidence and prevalence [2]. One of the most important pathophysiological components of MetS is obesity, particularly central obesity, which is the root cause of all other metabolic abnormalities [3]. According to the Global Nutrition Report released in 2020, one out of every nine individuals worldwide suffers from hunger or malnutrition, and one out of every three is overweight or obese [4]. Patients with MetS have elevated serum levels of proinflammatory mediators such as tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), and C-reactive protein (CRP) [5]. Similar inflammatory mediators, such as IL-6, TNF- α, and CRP, are increased in patients with severe periodontal disease (PD). Glycemic management decreases the risk of PD in patients with type 2 diabetes [6], and CRP levels can be lowered when PD is successfully treated [7]. Previous studies confirm that obesity, CVD, and type 2 diabetes mellitus negatively influence PD severity and extent. Thus, cross-sectional findings demonstrated that sustaining a healthy body weight achieved through a well-balanced diet and regular physical activity dramatically reduces gingival inflammation and PD [8][9][10][11]. Several mechanisms have been proposed to relate MetS, obesity, and PD [8][12][13]. PD shares multiple genetic risk factors with CVS, in addition to being an independent risk factor [14][15][16]. MetS-associated inflammation has been linked to endothelial dysfunction, elevating the risk of cardiovascular disease and type 2 diabetes, although the underlying mechanisms driving this systemic response are not yet understood [13][17][18].
Intermittent fasting (IF) is an eating pattern that alternates between periods of fasting and periods of normal eating on a regular schedule [19][20][21]. IF incurs a net reduction in caloric intake, falling below the calories expended. It also leads to a negative energy balance that causes weight loss [22]. IF triggers neuroendocrine activation, adaptive cellular reactions, enhanced cellular repair mechanisms, increasing glycemic management, activation of the adenosine monophosphate protein kinase (AMPK) pathway, and sirtuins [20][23][24]. In addition, IF causes a reduction of mitochondrial oxidative stress, free-radical production, and signaling of insulin and mammalian target of rapamycin (mTOR), thus lowering inflammation [25]. Restriction of calories lessens the inflammatory response and decreases circulating proinflammatory mediators such as TNF-α, IL-6, matrix metalloproteinase-8 (MMP-8), matrix metalloproteinase-9 (MMP-9), and IL-1-beta in gingival crevicular fluid (GCF). To date, pre-clinical investigations have consistently shown that IF has a robust ability to alter chronic illnesses such as cancer, type 2 diabetes, overweight, heart ailments, and neurodegenerative brain disease [19][26][27][28][29].
Chronic metabolic illnesses have significant societal and economic repercussions, making it vital to find ways to avoid and regulate them. Since MetS and obesity are frequently associated with CVD and type 2 diabetes, there is an increasing need for exemplary low-cost, effective therapeutic solutions to alleviate this growing burden. The disease’s entire cost, including health treatment and reduced economic growth, surpasses trillions [2][4]. This motivates the need for an alternative novel approach that is practical and useful for resolving the problem. Modifications to one’s way of life and diet are at the forefront of the therapy of MetS. Remarkably, IF is underpinned by scientific evidence, claiming to be the most effective non-pharmacological, potential therapeutic alternative for preventing and treating chronic inflammation and disorders associated with a sedentary lifestyle [25]. Nonetheless, an insufficient investigation has been performed to determine whether intermittent fasting has therapeutic benefits on periodontal inflammation and disease. It is quite remarkable that this unique area of research has been largely untapped and neglected in the literature. A very negligible amount of information is available about the beneficial effects of fasting on periodontal health and disease at the moment. This clearly warrants the need for further exploration to know the systemic effects of IF on periodontal inflammation and components of MetS.

2. Impact of IF on PD and Mets

2.1. Periodontal Diseases

PD is a chronic inflammatory condition that causes inflammation of the periodontal soft tissues and progressive loss of periodontal ligament and alveolar bone, destroying the tooth-supporting apparatus and potentially resulting in tooth loss [30]. Inflammation is the underlying cause of periodontal diseases, and it plays a critical role in their progression. The presence of a considerable number of bacteria might indirectly result in tissue degeneration by activating host defense cells, which produce and release chemical mediators that promote connective tissue breakdown effectors. Microbial plaque components have the ability to cause an initial infiltrate of inflammatory cells such as lymphocytes, macrophages, and polymorphonuclear leukocytes (PMNs). Microbial components, particularly lipopolysaccharide (LPS), stimulate macrophages to produce and secrete a wide range of proinflammatory molecules, including the cytokines, interleukin-1 IL-1, IL-4, IL-10, IFN, TGF and TNF-alpha; prostaglandins, particularly prostaglandin E2 (PGE2); and hydrolytic enzymes. These cytokines have strong proinflammatory and catabolic properties, and they play an important role in the degradation of periodontal tissue through the action of collagenolytic enzymes such as MMPs [31]. ROS in the inflammatory environment activates these latent collagenolytic enzymes [32]. While it is possible that inflammatory processes originating in one organ induce disorders in another, communication between distant sections of the body and their inflammatory states are accomplished by cells or soluble chemical mediators [30]. Significant evidence has been gathered to support comorbidity between PD and other chronic illnesses such as diabetes mellitus, CVS, preterm birth, rheumatoid arthritis, respiratory diseases, chronic kidney diseases, and Alzheimer’s. Figure 1 demonstrates proposed connections between PD and several systemic diseases using schematic representation [13][30][33][34][35][36].
Figure 1. The relationship between periodontal disease and other systemic disorders.
The periodontium responds to the dental plaque by the release of bacterial lipopolysaccharides (endotoxins), chemotactic peptides, and protein toxins. These molecules stimulate the host to produce a variety of responses with the production of inflammatory mediators IL-6 IL-1β, IL-6, IL-8, IL-12, TNF-α, MMP-8 & 9, PGE2 and fibrinogen. This type of bacteremia causes the liver to initiate an inflammatory and immunological response, resulting in higher blood levels of c-reactive protein and the production of serum amyloid A and fibrinogen. These and other host products' responses may influence a variety of essential disease pathways and are capable of initiation and development of chronic systemic diseases in target organs. COPD—Chronic obstructive pulmonary disease, NAFLD—Non-alcoholic fatty liver disease, MI—Myocardial infarction, PGE2- Prostaglandins, MMP—Matrix metalloproteinase, IL—Interleukin, TNF-α—tumor necrosis factor-alpha, CRP—C-reactive protein.

2.2. Activation and Regulation of Periodontal Inflammation by AMPK Pathway and Role of Sirtuins

Oxidative stress is a critical regulator of the systemic pathophysiological effects of PD. SIRT1’s anti-oxidative stress effects in PD have been elucidated. The activation of SIRT1 phosphorylates and activates AMPK, thereby reducing periodontal inflammation-induced oxidative stress. Significantly decreased alveolar tissue damage, enhanced cell viability, and decreased release of proinflammatory cytokines such as IL-1, IL-6, and TNF were found. SIRT 2 was also found to be positively related with nicotinamide phosphorribosyl transferase (NAMPT) activities in human gingival fibroblasts, which were greatly elevated during PD and involved in osteoclast recruitment by promoting the production of cyclooxygenase-2, matrix metalloproteinase (MMP)-1 and MMP-3 [37]. In a study involving mice, Chen et al. show that SIRT3 inhibits oxidative stress through controlling PGC-1 and mitochondrial function [38]. SIRT6 is also implicated in the regulation of periodontium homeostasis in PD. Huang et al. demonstrated that elevated SIRT6 inhibits cementoblast development and mineralization via inhibiting glucose transporter 1 (GLUT1), a glucose transporter required for cementogenesis, and by activating the AMPK pathway. SIRT6 overexpression improves osteogenic differentiation and reduces LPS-induced inflammatory response through inhibiting the NF-B pathway [39].
Researchers predicted that fasting may halt the course of PD and lessen systemic oxidative stress through the activation of mitochondrial sirtuins and the AMPK pathway. By reducing oxidative stress, fasting may help prevent alveolar bone loss and inflammatory reactions in the periodontium. The exact roles played by IF at the molecular level to inhibit initiation and progression of PD still require further investigation. However, defining the function and mechanism of fasting in the context of PD may be very helpful for the development of novel therapeutic approaches.

2.3. Impact of Intermittent Fasting and Calorie Restriction on Periodontal Inflammation Diseases

Numerous dietary suggestions that improve periodontal health are vitamin C and vitamin D3 dietary supplements, omega-3 complex supplementation, fiber supplements, antioxidant supplementation, and carbohydrate restriction [40]. Regardless of whether persistent plaque is present, anti-inflammatory regimes have been shown to considerably reduce inflammation of gingival tissue [11]. Recent cross-sectional research reveals that healthy body weight, nutritious food, and adequate physical exercise reduce the severity and extent of PD [41]. However, in humans, the effect of IF and calorie restriction on periodontal inflammation and infection is scarce. The long-term, irregular, and unpredictable nature of the periodontal disease progression makes disease evaluations extremely difficult. The inflammatory, immunological, kinetic, and disease progression characteristics of active periodontal destruction were studied in different animal studies [42].
A recent study [43] used an experimental mouse model to assess the positive benefits of IF regimens for periodontal tissues. The authors discovered that fasting regimens resulted in a decreased loss of bone than non-fasting regimens at the ligature-induced PD site and on the contralateral maxillary side. Quantitative computed tomography and calcein-labeled histomorphometric examinations on peripheral bone revealed that the fasted sample subjects had a more excellent capability for regenerating bone than the non-fasted sample group. Additionally, the bone marrow cells of the fasted groups formed more incredible mineralized modules than those of the non-fasted groups [43].
Nonhuman primates are ideal animal models for periodontics research owing to their anatomical and biological similarities. The National Institute on Aging on a Rhesus monkey cohort (Macaca mulatta) conducted a longitudinal to ascertain the influence of calorie restriction on the clinical microbiological and immunological aspects of PD. Monkeys were fed twice daily at 6:30 a.m. and 1 p.m. (16 h fasting period and 8 h eating window, 16:8 ratio). For 13–17 years, monkeys were subjected to a 30% drop in dietary consumption of calories compared with a control ad libitum diet group [44][45][46]. The results proved that long-term exposure to CR and time-restricted eating significantly reduced the degree of naturally occurring chronic periodontitis. The CR diet reduced the ligature-induced gingival index (GI), probing pocket depth (PPD), bleeding on probing (BOP), and clinical attachment level (CAL) by a significant amount [44].
Another study [46] found that the male CR group had significantly decreased depth of the periodontal pocket, substantially lower levels of IgG antibody response, and considerably decreased IL-8 and -glucuronidase levels in GCF in comparison to a control group that received ad libitum meals. However, the male CR group showed a non-significant drop in the IL-1 levels. In the GCF, the female calorie-restricted group had reduced IgG levels of antibodies than the ad libitum group, but both groups had equal levels of markers of inflammation, suggesting that calorie restriction may be beneficial. However, the periodontal microbiota of male and female monkeys was unaffected by a calorie restriction diet [46]. In another study conducted to know the antibody responses and also the acute serum host response in rhesus monkeys, it was demonstrated that gender variations in calorie restrictions have an impact on systemic effects. Samples of male monkey serum had higher quantities of haptoglobin and a1-acid glycoprotein than the sample of female monkey serum, according to the findings. Serum IgG antibody responses to Pophyromonas gingivalis, Campylobacter rectus, and Actinomycetemcomitans were significantly increased in the sample of female rhesus monkeys. Antibodies against Fusobacterium nucleatum, however, demonstrated a substantial impact in females on a calorie-restricted regime [45]. Recent findings from the first human trial indicated that a specified therapeutically supervised periodic fasting regimen had beneficial effects on inflammation of periodontal tissues in female MetS patients.
Bodyweight, waist circumference (WS), body mass index (BMI), BP, fasting plasma glucose (FPG), total cholesterol, CRP, and HDL were all reduced as a result of clinically supervised fasting. At the same time, BOP and GCF levels were also reduced as a result of the fasting [47]. As a result, fasting may be recommended as an additional strategy in addition to routine periodontal therapy in obese and overweight individuals who have been diagnosed with periodontitis. Therefore, it will be imperative to conduct many randomized clinical trials in persons who have MetS and periodontal disease in the future. Figure 1 presents a schematic representation of the impact of IF on CVS, metabolic, and the periodontal health

2.4. Inflammation and Immune Mediation between PD and MetS

Inflammation contributes a significant part in the initiation of the MetS [48]. Numerous studies established correlations between inflammation and obesity. Increased levels of CRP, TNF, IL-6, fibrinogen, and other acute-phase reactants have been documented in obese people [49][50][51][52][53][54][55]. Several diseases, such as hyperlipidemia [56], PD [57][58], and type 2 diabetes mellitus [59], are correlated with elevated cytokine production. Increased IL-1 levels in GCF [60] were observed in patients with insulin depended diabetes and hyperlipidemia, thus, a vicious cycle may develop. Inflammation caused by PD and MetS may further aggravate and exacerbate PD and metabolic sickness [61][62][63][64], resulting in impaired metabolic regulation and type 2 diabetes-related problems. [61] Furthermore, TNF, a cytokine that causes insulin resistance [65][66][67][68][69][70], is dose-dependent and linked with the severity of PD in adult individuals with insulin-dependent diabetes [71]. Thus, the hyper inflammatory state syndrome can amplify the local and systemic inflammatory responses to microbes. The response of the host to the microbial assaults caused by cytokine dysregulation is associated with prolonged TNF expression [72][73].
According to multiple animal and human studies, diabetes may accelerate alveolar bone disintegration via hyperglycemia-mediated modulation of the receptor activator of nuclear factor-kappa B ligand to osteoprotegerin ratio in periodontal tissues [74][75][76]. The rate of osseous regeneration following bone resorption may be reduced as a result of the death of bone-lining cells and the increased number of fibroblasts [77][78][79]. As a result, all of these factors may have a role in the uncoupling of bone breakdown and healing in periodontal diseases, which are commonly noticed in patients with type 2 diabetes. Increased blood glucose levels result in the formation of advanced glycation end products, which bind to the periodontal receptor for advanced glycation end products (RAGE) and initiate an inflammatory response [80]. Blocking the RAGE receptor in diabetic mice reduced the inflammatory response and the subsequent loss of alveolar bone [81]. Insulin resistance in PD patients may be associated with the host’s inflammatory response to lipid alterations, obesity, and periodontal diseases [82]. Reduced amounts of leptin, an anti-obesity adipocytokine in the gingiva, and GCF can aggravate PD [83][84][85]. However, serum leptin levels, on the other hand, tend to rise as periodontal disease progresses [85]. Despite the fact that an in vitro study revealed that adiponectin might have an anti-osteoclastic effect on PD [86], evidence for its anti-inflammatory effect between PD and MetS is limited and conflicting [87][88][89]. Resistin is an adipocytokine that is associated with proinflammatory properties [90] and is linked to insulin resistance [91]. Additionally, when individuals with PD were compared with people who were healthy, there was a link between bleeding on probing and higher levels of serum resistin [88][89].

2.5. Impact of Intermittent Fasting on MetS

As previously stated, short- and long-term IF greatly reduces inflammatory mediator CRP and cytokines such as IL-6 [92]. As a result, it is hypothesized that fasting improves the characteristics of MetS via modulating inflammatory responses. Ramadan fasting can decrease TNF- and IL-6 expression in healthy volunteers as it leads to weight loss and decreases body fat percentage [93]. In addition, it is hypothesized that TNF- and IL-6 limit lipoprotein lipase (LPL) action, resulting in TNF- and IL-6 down-regulation in fasting individuals, increasing LPL activity and decreasing the fat mass of the body [94].
A substantial body of scientific evidence using animal models suggests that IF enhances insulin sensitivity. When fasting or exercising for an extended period of time, the hepatic, cardiac, and skeletal system shift their metabolism to fatty acid oxidation and catabolism of amino acids. However, an energy-dense condition, on the other hand, favors glucose absorption and oxidation [95]. IF induces the gene expression that involves lipid storage (PPAR 2 and Fsp27) and fat oxidation (MCPT1), thereby increasing lipogenesis during the IF unrestricted phase and boosting metabolic flexibility and fat oxidation during the fasting period [96].
Insulin is critical for glucose homeostasis because it promotes glucose storage. Several explanations have been proposed to elucidate how insulin resistance develops. Prevalent hypotheses suggest that obesity is associated with chronic inflammation, leading to insulin resistance in tissues [97]. Growing evidence suggests that obesity is associated with chronic inflammation, which leads to insulin resistance in tissues [96]. So, through CR and metabolic reprogramming, IF helps to lower obesity and insulin resistance. Furthermore, various studies have proven that IF results in decreasing levels of leptin and increasing adiponectin, thereby improving insulin resistance [98].
Therefore, CR helps individuals to lose weight and improve metabolic health [99]. Numerous studies have revealed that humans face difficulties in maintaining daily CR for prolonged periods [100]. However, IF has a higher compliance rate and is effective in weight loss and the reduction of obesity-related risk factors for metabolic disease [21][101][102]. Because of the positive effects of fasting, the body uses fatty acids and ketones as fuel. As shown by research, altering one’s metabolic process to one that utilizes fatty acids for energy rather than glucose preserves muscle mass and function while increasing one’s ability to perform daily activities [101]. Finally, IF has been shown to reduce adipose tissue mass, notably visceral and abdominal fat, due to its mild energy deficits [103][104]. This effect has the additional effect of improving the cardiovascular risk profile by lowering BMI and blood pressure, decreasing resting heart rate, decreasing ischemic injury, decreasing lipid peroxidation, and enhancing cardiovascular stress adaptation and resistance to a cardiac muscle injury in myocardial infarction animal models. CVS risk factors are intimately related to MetS components, and intermittent fasting may play a crucial role in the prevention and management of CVD and MetS [25][101][104]. Figure 2 represents the beneficial effects of IF on CVS, metabolic and periodontal health.
Figure 2. Schematic representation of the effect of intermittent fasting on CVS, Metabolic and Periodontal health. CRP—C-reactive protein, HDL—High-density lipoprotein, LDL—low-density lipoprotein, IL-6 Interleukin-6, Hb1Ac—Hemoglobin A1c, BOP—bleeding on probing, PPD—probing pocket depth, GI—Gingival index, CAL—clinical attachment loss, IgG—Immunoglobulin, BW—body weight, BMI—body mass index, WC—waist circumference, FGLU—fasting glucose, TRG—triglycerides.

References

  1. Alberti, K.G.M.M.; Eckel, R.H.; Grundy, S.M.; Zimmet, P.Z.; Cleeman, J.I.; Donato, K.A.; Fruchart, J.-C.; James, W.P.T.; Loria, C.M.; Smith, S.C.; et al. Harmonizing the Metabolic Syndrome: A Joint Interim Statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity. Circulation 2009, 120, 1640–1645.
  2. Saklayen, M.G. The Global Epidemic of the Metabolic Syndrome. Curr. Hypertens. Rep. 2018, 20, 12.
  3. Bovolini, A.; Garcia, J.; Andrade, M.A.; Duarte, J.A. Metabolic Syndrome Pathophysiology and Predisposing Factors. Int. J. Sports Med. 2021, 42, 199–214.
  4. Global Nutrition Report. 2020. Available online: https://globalnutritionreport.org/reports/2020-global-nutrition-report/ (accessed on 17 July 2020).
  5. Bulló, M.; García-Lorda, P.; Megias, I.; Salas-Salvadó, J. Systemic Inflammation, Adipose Tissue Tumor Necrosis Factor, and Leptin Expression. Obes. Res. 2003, 11, 525–531.
  6. Taylor, G.W. Periodontal Treatment and Its Effects on Glycemic Control: A Review of the Evidence. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endodontol. 1999, 87, 311–316.
  7. Emrich, L.J.; Shlossman, M.; Genco, R.J. Periodontal Disease in Non-Insulin-Dependent Diabetes Mellitus. J. Periodontol. 1991, 62, 123–131.
  8. Pischon, N.; Heng, N.; Bernimoulin, J.-P.; Kleber, B.-M.; Willich, S.N.; Pischon, T. Obesity, Inflammation, and Periodontal Disease. J. Dent. Res. 2007, 86, 400–409.
  9. Baumgartner, S.; Imfeld, T.; Schicht, O.; Rath, C.; Persson, R.; Persson, G.R. The Impact of the Stone Age Diet on Gingival Conditions in the Absence of Oral Hygiene. J. Periodontol. 2009, 80, 759–768.
  10. El Makaky, Y.; Beltagy, T.; El Makakey, A. The Effects of an Anti-Inflammatory Diet on Gingival Health in Children (Randomized Controlled Trial). Egypt. Dent. J. 2019, 65, 1995–2002.
  11. Woelber, J.P.; Bremer, K.; Vach, K.; König, D.; Hellwig, E.; Ratka-Krüger, P.; Al-Ahmad, A.; Tennert, C. An Oral Health Optimized Diet Can Reduce Gingival and Periodontal Inflammation in Humans—A Randomized Controlled Pilot Study. BMC Oral Health 2017, 17, 28.
  12. Iacopino, A.M.; Cutler, C.W. Pathophysiological Relationships between Periodontitis and Systemic Disease: Recent Concepts Involving Serum Lipids. J. Periodontol. 2000, 71, 1375–1384.
  13. Kim, J.; Amar, S. Periodontal Disease and Systemic Conditions: A Bidirectional Relationship. Odontology 2006, 94, 10–21.
  14. Yu, Y.-H.; Chasman, D.I.; Buring, J.E.; Rose, L.; Ridker, P.M. Cardiovascular Risks Associated with Incident and Prevalent Periodontal Disease. J. Clin. Periodontol. 2015, 42, 21–28.
  15. Makkar, H.; Reynolds, M.A.; Wadhawan, A.; Dagdag, A.; Merchant, A.T.; Postolache, T.T. Periodontal, Metabolic, and Cardiovascular Disease: Exploring the Role of Inflammation and Mental Health. Pteridines 2018, 29, 124–163.
  16. Desvarieux, M.; Demmer, R.T.; Jacobs, D.R.; Rundek, T.; Boden-Albala, B.; Sacco, R.L.; Papapanou, P.N. Periodontal Bacteria and Hypertension: The Oral Infections and Vascular Disease Epidemiology Study (INVEST). J. Hypertens. 2010, 28, 1413–1421.
  17. Arcaro, G.; Cretti, A.; Balzano, S.; Lechi, A.; Muggeo, M.; Bonora, E.; Bonadonna, R.C. Insulin Causes Endothelial Dysfunction in Humans: Sites and Mechanisms. Circulation 2002, 105, 576–582.
  18. Kim, J.; Montagnani, M.; Koh, K.K.; Quon, M.J. Reciprocal Relationships between Insulin Resistance and Endothelial Dysfunction: Molecular and Pathophysiological Mechanisms. Circulation 2006, 113, 1888–1904.
  19. Longo, V.D.; Mattson, M.P. Fasting: Molecular Mechanisms and Clinical Applications. Cell Metab. 2014, 19, 181–192.
  20. Grajower, M.M.; Horne, B.D. Clinical Management of Intermittent Fasting in Patients with Diabetes Mellitus. Nutrients 2019, 11, 873.
  21. Varady, K.A.; Bhutani, S.; Church, E.C.; Klempel, M.C. Short-Term Modified Alternate-Day Fasting: A Novel Dietary Strategy for Weight Loss and Cardioprotection in Obese Adults. Am. J. Clin. Nutr. 2009, 90, 1138–1143.
  22. Templeman, I.; Thompson, D.; Gonzalez, J.; Walhin, J.-P.; Reeves, S.; Rogers, P.J.; Brunstrom, J.M.; Karagounis, L.G.; Tsintzas, K.; Betts, J.A. Intermittent Fasting, Energy Balance and Associated Health Outcomes in Adults: Study Protocol for a Randomised Controlled Trial. Trials 2018, 19, 86.
  23. Herzig, S.; Shaw, R.J. AMPK: Guardian of Metabolism and Mitochondrial Homeostasis. Nat. Rev. Mol. Cell Biol. 2018, 19, 121–135.
  24. Kane, A.E.; Sinclair, D.A. Sirtuins and NAD+ in the Development and Treatment of Metabolic and Cardiovascular Diseases. Circ. Res. 2018, 123, 868–885.
  25. De Cabo, R.; Mattson, M.P. Effects of Intermittent Fasting on Health, Aging, and Disease. N. Engl. J. Med. 2019, 381, 2541–2551.
  26. DOGAN, S.; ROGOZINA, O.P.; LOKSHIN, A.E.; GRANDE, J.P.; CLEARY, M.P. Effects of Chronic vs. Intermittent Calorie Restriction on Mammary Tumor Incidence and Serum Adiponectin and Leptin Levels in MMTV-TGF-α Mice at Different Ages. Oncol. Lett. 2010, 1, 167–176.
  27. Di Francesco, A.; Di Germanio, C.; Bernier, M.; de Cabo, R. A Time to Fast. Science 2018, 362, 770–775.
  28. Mattson, M.P.; Moehl, K.; Ghena, N.; Schmaedick, M.; Cheng, A. Intermittent Metabolic Switching, Neuroplasticity and Brain Health. Nat. Rev. Neurosci. 2018, 19, 63–80.
  29. Panda, S. Circadian Physiology of Metabolism. Science 2016, 354, 1008–1015.
  30. Hasturk, H.; Kantarci, A. Activation and Resolution of Periodontal Inflammation and Its Systemic Impact. Periodontol. 2000 2015, 69, 255–273.
  31. Sorsa, T.; Ingman, T.; Suomalainen, K.; Haapasalo, M.; Konttinen, Y.T.; Lindy, O.; Saari, H.; Uitto, V.J. Identification of Proteases from Periodontopathogenic Bacteria as Activators of Latent Human Neutrophil and Fibroblast-Type Interstitial Collagenases. Infect. Immun. 1992, 60, 4491–4495.
  32. Chapple, I.L.C.; Matthews, J.B. The Role of Reactive Oxygen and Antioxidant Species in Periodontal Tissue Destruction. Periodontol. 2000 2007, 43, 160–232.
  33. Nagpal, R.; Yamashiro, Y.; Izumi, Y. The Two-Way Association of Periodontal Infection with Systemic Disorders: An Overview. Mediat. Inflamm. 2015, 2015, 793898.
  34. Konkel, J.E.; O’Boyle, C.; Krishnan, S. Distal Consequences of Oral Inflammation. Front. Immunol. 2019, 10, 1403.
  35. Kaur, S.; White, S.; Bartold, M. Periodontal Disease as a Risk Factor for Rheumatoid Arthritis: A Systematic Review. JBI Libr. Syst. Rev. 2012, 10, 1–12.
  36. Pitiphat, W.; Joshipura, K.J.; Gillman, M.W.; Williams, P.L.; Douglass, C.W.; Rich-Edwards, J.W. Maternal Periodontitis and Adverse Pregnancy Outcomes. Commun. Dent. Oral Epidemiol. 2008, 36, 3–11.
  37. Pan, Z.; Dong, H.; Huang, N.; Fang, J. Oxidative Stress and Inflammation Regulation of Sirtuins: New Insights into Common Oral Diseases. Front. Physiol. 2022, 13, 953078.
  38. Chen, J.; Zhang, Y.; Gao, J.; Li, T.; Gan, X.; Yu, H. Sirtuin 3 Deficiency Exacerbates Age-Related Periodontal Disease. J. Periodontal Res. 2021, 56, 1163–1173.
  39. Huang, L.; Sun, H.; Song, F.; Cao, Z.; Jiang, X.; Zhang, L.; Li, Z.; Huang, C. SIRT6 Overexpression Inhibits Cementogenesis by Suppressing Glucose Transporter 1. J. Cell. Physiol. 2019, 234, 4005–4014.
  40. der Velden, U.V.; Kuzmanova, D.; Chapple, I.L.C. Micronutritional Approaches to Periodontal Therapy. J. Clin. Periodontol. 2011, 38, 142–158.
  41. Al-Zahrani, M.S.; Borawski, E.A.; Bissada, N.F. Periodontitis and Three Health-Enhancing Behaviors: Maintaining Normal Weight, Engaging in Recommended Level of Exercise, and Consuming a High-Quality Diet. J. Periodontol. 2005, 76, 1362–1366.
  42. Parveen, S. Impact of Calorie Restriction and Intermittent Fasting on Periodontal Health. Periodontol. 2000 2021, 87, 315–324.
  43. Wulansari, L.; Kaboosaya, B.; Khan, M.; Takahashi, M.; Nakata, H.; Kuroda, S.; Aoki, K.; Kasugai, S. Beneficial Effects of Fasting Regimens on Periodontal Tissues in Experimental Periodontitis Mice Model. J. Int. Dent. Med. Res. 2018, 11, 362–369.
  44. Branch-Mays, G.L.; Dawson, D.R.; Gunsolley, J.C.; Reynolds, M.A.; Ebersole, J.L.; Novak, K.F.; Mattison, J.A.; Ingram, D.K.; Novak, M.J. The Effects of a Calorie-Reduced Diet on Periodontal Inflammation and Disease in a Non-Human Primate Model. J. Periodontol. 2008, 79, 1184–1191.
  45. Ebersole, J.L.; Steffen, M.J.; Reynolds, M.A.; Branch-Mays, G.L.; Dawson, D.R.; Novak, K.F.; Gunsolley, J.C.; Mattison, J.A.; Ingram, D.K.; Novak, M.J. Differential Gender Effects of a Reduced Calorie Diet on Systemic Inflammatory and Immune Parameters in Nonhuman Primates. J. Periodontal Res. 2008, 43, 500–507.
  46. Reynolds, M.A.; Dawson, D.R.; Novak, K.F.; Ebersole, J.L.; Gunsolley, J.C.; Branch-Mays, G.L.; Holt, S.C.; Mattison, J.A.; Ingram, D.K.; Novak, M.J. Effects of Caloric Restriction on Inflammatory Periodontal Disease. Nutrition 2009, 25, 88–97.
  47. Pappe, C.L.; Steckhan, N.; Hoedke, D.; Jepsen, S.; Rauch, G.; Keller, T.; Michalsen, A.; Dommisch, H. Prolonged Multimodal Fasting Modulates Periodontal Inflammation in Female Patients with Metabolic Syndrome: A Prospective Cohort Study. J. Clin. Periodontol. 2021, 48, 492–502.
  48. Monteiro, R.; Azevedo, I. Chronic Inflammation in Obesity and the Metabolic Syndrome. Mediat. Inflamm. 2010, 2010, 289645.
  49. Pradhan, A.D.; Manson, J.E.; Rifai, N.; Buring, J.E.; Ridker, P.M. C-Reactive Protein, Interleukin 6, and Risk of Developing Type 2 Diabetes Mellitus. JAMA 2001, 286, 327–334.
  50. Vozarova, B.; Weyer, C.; Hanson, K.; Tataranni, P.A.; Bogardus, C.; Pratley, R.E. Circulating Interleukin-6 in Relation to Adiposity, Insulin Action, and Insulin Secretion. Obes. Res. 2001, 9, 414–417.
  51. Dandona, P.; Weinstock, R.; Thusu, K.; Abdel-Rahman, E.; Aljada, A.; Wadden, T. Tumor Necrosis Factor-Alpha in Sera of Obese Patients: Fall with Weight Loss. J. Clin. Endocrinol. Metab. 1998, 83, 2907–2910.
  52. Kern, P.A.; Ranganathan, S.; Li, C.; Wood, L.; Ranganathan, G. Adipose Tissue Tumor Necrosis Factor and Interleukin-6 Expression in Human Obesity and Insulin Resistance. Am. J. Physiol. Endocrinol. Metab. 2001, 280, E745–E751.
  53. Dandona, P.; Aljada, A.; Bandyopadhyay, A. Inflammation: The Link between Insulin Resistance, Obesity and Diabetes. Trends Immunol. 2004, 25, 4–7.
  54. Grace, C.S.; Goldrick, R.B. Fibrinolysis and Body Bulid. Interrelationships between Blood Fibrinolysis, Body Composition and Parameters of Lipid and Carbohydrate Metabolism. J. Atheroscler. Res. 1968, 8, 705–719.
  55. Blood Fibrinolytic Activity in Diabetes Mellitus and Its Bearing on Ischaemic Heart Disease and Obesity. Available online: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2122789/ (accessed on 26 July 2021).
  56. Eggesbø, J.B.; Hjermann, I.; Høstmark, A.T.; Kierulf, P. LPS Induced Release of IL-1 Beta, IL-6, IL-8 and TNF-Alpha in EDTA or Heparin Anticoagulated Whole Blood from Persons with High or Low Levels of Serum HDL. Cytokine 1996, 8, 152–160.
  57. Salvi, G.E.; Yalda, B.; Collins, J.G.; Jones, B.H.; Smith, F.W.; Arnold, R.R.; Offenbacher, S. Inflammatory Mediator Response as a Potential Risk Marker for Periodontal Diseases in Insulin-Dependent Diabetes Mellitus Patients. J. Periodontol. 1997, 68, 127–135.
  58. Stashenko, P.; Fujiyoshi, P.; Obernesser, M.S.; Prostak, L.; Haffajee, A.D.; Socransky, S.S. Levels of Interleukin 1 Beta in Tissue from Sites of Active Periodontal Disease. J. Clin. Periodontol. 1991, 18, 548–554.
  59. Ciampolillo, A.; Guastamacchia, E.; Caragiulo, L.; Lollino, G.; De Robertis, O.; Lattanzi, V.; Giorgino, R. In Vitro Secretion of Interleukin-1 Beta and Interferon-Gamma by Peripheral Blood Lymphomononuclear Cells in Diabetic Patients. Diabetes Res. Clin. Pract. 1993, 21, 87–93.
  60. Lalla, E.; Papapanou, P.N. Diabetes Mellitus and Periodontitis: A Tale of Two Common Interrelated Diseases. Nat. Rev. Endocrinol. 2011, 7, 738–748.
  61. Kebschull, M.; Demmer, R.T.; Papapanou, P.N. “Gum Bug, Leave My Heart Alone!”—Epidemiologic and Mechanistic Evidence Linking Periodontal Infections and Atherosclerosis. J. Dent. Res. 2010, 89, 879–902.
  62. Loos, B.G. Systemic Markers of Inflammation in Periodontitis. J. Periodontol. 2005, 76, 2106–2115.
  63. Paraskevas, S.; Huizinga, J.D.; Loos, B.G. A Systematic Review and Meta-Analyses on C-Reactive Protein in Relation to Periodontitis. J. Clin. Periodontol. 2008, 35, 277–290.
  64. Hotamisligil, G.S.; Budavari, A.; Murray, D.; Spiegelman, B.M. Reduced Tyrosine Kinase Activity of the Insulin Receptor in Obesity-Diabetes. Central Role of Tumor Necrosis Factor-Alpha. J. Clin. Investig. 1994, 94, 1543–1549.
  65. 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.
  66. Pickup, J.C. Inflammation and Activated Innate Immunity in the Pathogenesis of Type 2 Diabetes. Diabetes Care 2004, 27, 813–823.
  67. Shoelson, S.E.; Lee, J.; Goldfine, A.B. Inflammation and Insulin Resistance. J. Clin. Investig. 2006, 116, 1793–1801.
  68. King, G.L. The Role of Inflammatory Cytokines in Diabetes and Its Complications. J. Periodontol. 2008, 79, 1527–1534.
  69. Abbatecola, A.M.; Ferrucci, L.; Grella, R.; Bandinelli, S.; Bonafè, M.; Barbieri, M.; Corsi, A.M.; Lauretani, F.; Franceschi, C.; Paolisso, G. Diverse Effect of Inflammatory Markers on Insulin Resistance and Insulin-Resistance Syndrome in the Elderly. J. Am. Geriatr. Soc. 2004, 52, 399–404.
  70. Serum Levels of Soluble Tumor Necrosis Factor-Alpha Receptor 2 Are Linked to Insulin Resistance and Glucose Intolerance in Children—PubMed. Available online: https://pubmed.ncbi.nlm.nih.gov/15679072/ (accessed on 26 July 2021).
  71. Engebretson, S.; Chertog, R.; Nichols, A.; Hey-Hadavi, J.; Celenti, R.; Grbic, J. Plasma Levels of Tumour Necrosis Factor-Alpha in Patients with Chronic Periodontitis and Type 2 Diabetes. J. Clin. Periodontol. 2007, 34, 18–24.
  72. Naguib, G.; Al-Mashat, H.; Desta, T.; Graves, D.T. Diabetes Prolongs the Inflammatory Response to a Bacterial Stimulus through Cytokine Dysregulation. J. Investig. Dermatol. 2004, 123, 87–92.
  73. Takano, M.; Nishihara, R.; Sugano, N.; Matsumoto, K.; Yamada, Y.; Takane, M.; Fujisaki, Y.; Ito, K. The Effect of Systemic Anti-Tumor Necrosis Factor-Alpha Treatment on Porphyromonas Gingivalis Infection in Type 2 Diabetic Mice. Arch. Oral Biol. 2010, 55, 379–384.
  74. Santos, V.R.; Lima, J.A.; Gonçalves, T.E.D.; Bastos, M.F.; Figueiredo, L.C.; Shibli, J.A.; Duarte, P.M. Receptor Activator of Nuclear Factor-Kappa B Ligand/Osteoprotegerin Ratio in Sites of Chronic Periodontitis of Subjects with Poorly and Well-Controlled Type 2 Diabetes. J. Periodontol. 2010, 81, 1455–1465.
  75. Duarte, P.M.; Neto, J.B.C.; Casati, M.Z.; Sallum, E.A.; Nociti, F.H. Diabetes Modulates Gene Expression in the Gingival Tissues of Patients with Chronic Periodontitis. Oral Dis. 2007, 13, 594–599.
  76. Mahamed, D.A.; Marleau, A.; Alnaeeli, M.; Singh, B.; Zhang, X.; Penninger, J.M.; Teng, Y.-T.A. G(−) Anaerobes–Reactive CD4+ T-Cells Trigger RANKL-Mediated Enhanced Alveolar Bone Loss in Diabetic NOD Mice. Diabetes 2005, 54, 1477–1486.
  77. He, H.; Liu, R.; Desta, T.; Leone, C.; Gerstenfeld, L.C.; Graves, D.T. Diabetes Causes Decreased Osteoclastogenesis, Reduced Bone Formation, and Enhanced Apoptosis of Osteoblastic Cells in Bacteria Stimulated Bone Loss. Endocrinology 2004, 145, 447–452.
  78. Liu, R.; Bal, H.S.; Desta, T.; Krothapalli, N.; Alyassi, M.; Luan, Q.; Graves, D.T. Diabetes Enhances Periodontal Bone Loss through Enhanced Resorption and Diminished Bone Formation. J. Dent. Res. 2006, 85, 510–514.
  79. Liu, R.; Desta, T.; He, H.; Graves, D.T. Diabetes Alters the Response to Bacteria by Enhancing Fibroblast Apoptosis. Endocrinology 2004, 145, 2997–3003.
  80. Lalla, E.; Lamster, I.B.; Schmidt, A.M. Enhanced Interaction of Advanced Glycation End Products with Their Cellular Receptor RAGE: Implications for the Pathogenesis of Accelerated Periodontal Disease in Diabetes. Ann. Periodontol. 1998, 3, 13–19.
  81. Lalla, E.; Lamster, I.B.; Feit, M.; Huang, L.; Spessot, A.; Qu, W.; Kislinger, T.; Lu, Y.; Stern, D.M.; Schmidt, A.M. Blockade of RAGE Suppresses Periodontitis-Associated Bone Loss in Diabetic Mice. J. Clin. Investig. 2000, 105, 1117–1124.
  82. Genco, R.J.; Grossi, S.G.; Ho, A.; Nishimura, F.; Murayama, Y. A Proposed Model Linking Inflammation to Obesity, Diabetes, and Periodontal Infections. J. Periodontol. 2005, 76, 2075–2084.
  83. Johnson, R.B.; Serio, F.G. Leptin within Healthy and Diseased Human Gingiva. J. Periodontol. 2001, 72, 1254–1257.
  84. Karthikeyan, B.V.; Pradeep, A.R. Leptin Levels in Gingival Crevicular Fluid in Periodontal Health and Disease. J. Periodontal Res. 2007, 42, 300–304.
  85. Karthikeyan, B.V.; Pradeep, A.R. Gingival Crevicular Fluid and Serum Leptin: Their Relationship to Periodontal Health and Disease. J. Clin. Periodontol. 2007, 34, 467–472.
  86. Yamaguchi, N.; Kukita, T.; Li, Y.-J.; Martinez Argueta, J.G.; Saito, T.; Hanazawa, S.; Yamashita, Y. Adiponectin Inhibits Osteoclast Formation Stimulated by Lipopolysaccharide from Actinobacillus Actinomycetemcomitans. FEMS Immunol. Med. Microbiol. 2007, 49, 28–34.
  87. Iwamoto, Y.; Nishimura, F.; Soga, Y.; Takeuchi, K.; Kurihara, M.; Takashiba, S.; Murayama, Y. Antimicrobial Periodontal Treatment Decreases Serum C-Reactive Protein, Tumor Necrosis Factor-Alpha, but Not Adiponectin Levels in Patients with Chronic Periodontitis. J. Periodontol. 2003, 74, 1231–1236.
  88. Furugen, R.; Hayashida, H.; Yamaguchi, N.; Yoshihara, A.; Ogawa, H.; Miyazaki, H.; Saito, T. The Relationship between Periodontal Condition and Serum Levels of Resistin and Adiponectin in Elderly Japanese. J. Periodontal Res. 2008, 43, 556–562.
  89. Saito, T.; Yamaguchi, N.; Shimazaki, Y.; Hayashida, H.; Yonemoto, K.; Doi, Y.; Kiyohara, Y.; Iida, M.; Yamashita, Y. Serum Levels of Resistin and Adiponectin in Women with Periodontitis: The Hisayama Study. J. Dent. Res. 2008, 87, 319–322.
  90. Bokarewa, M.; Nagaev, I.; Dahlberg, L.; Smith, U.; Tarkowski, A. Resistin, an Adipokine with Potent Proinflammatory Properties. J. Immunol. 2005, 174, 5789–5795.
  91. Steppan, C.M.; Bailey, S.T.; Bhat, S.; Brown, E.J.; Banerjee, R.R.; Wright, C.M.; Patel, H.R.; Ahima, R.S.; Lazar, M.A. The Hormone Resistin Links Obesity to Diabetes. Nature 2001, 409, 307–312.
  92. Aksungar, F.B.; Topkaya, A.E.; Akyildiz, M. Interleukin-6, C-Reactive Protein and Biochemical Parameters during Prolonged Intermittent Fasting. Ann. Nutr. Metab. 2007, 51, 88–95.
  93. Faris, M.A.-I.E.; Kacimi, S.; Al-Kurd, R.A.; Fararjeh, M.A.; Bustanji, Y.K.; Mohammad, M.K.; Salem, M.L. Intermittent Fasting during Ramadan Attenuates Proinflammatory Cytokines and Immune Cells in Healthy Subjects. Nutr. Res. 2012, 32, 947–955.
  94. Coppack, S.W. Pro-Inflammatory Cytokines and Adipose Tissue. Proc. Nutr. Soc. 2001, 60, 349–356.
  95. Abd El-Kader, S.M.; Saiem Al-Dahr, M.H. Impact of Weight Loss on Oxidative Stress and Inflammatory Cytokines in Obese Type 2 Diabetic Patients. Afr. Health Sci. 2016, 16, 725–733.
  96. Montagner, A.; Polizzi, A.; Fouché, E.; Ducheix, S.; Lippi, Y.; Lasserre, F.; Barquissau, V.; Régnier, M.; Lukowicz, C.; Benhamed, F.; et al. Liver PPARα Is Crucial for Whole-Body Fatty Acid Homeostasis and Is Protective against NAFLD. Gut 2016, 65, 1202–1214.
  97. Petersen, M.C.; Shulman, G.I. Mechanisms of Insulin Action and Insulin Resistance. Physiol. Rev. 2018, 98, 2133–2223.
  98. Cho, Y.; Hong, N.; Kim, K.-W.; Cho, S.J.; Lee, M.; Lee, Y.-H.; Lee, Y.-H.; Kang, E.S.; Cha, B.-S.; Lee, B.-W. The Effectiveness of Intermittent Fasting to Reduce Body Mass Index and Glucose Metabolism: A Systematic Review and Meta-Analysis. J. Clin. Med. 2019, 8, 1645.
  99. Most, J.; Tosti, V.; Redman, L.M.; Fontana, L. Calorie Restriction in Humans: An Update. Aging Res. Rev. 2017, 39, 36–45.
  100. Zubrzycki, A.; Cierpka-Kmiec, K.; Kmiec, Z.; Wronska, A. The Role of Low-Calorie Diets and Intermittent Fasting in the Treatment of Obesity and Type-2 Diabetes. J. Physiol. Pharmacol. 2018, 69, 663–683.
  101. Anton, S.D.; Moehl, K.; Donahoo, W.T.; Marosi, K.; Lee, S.; Mainous, A.G.; Leeuwenburgh, C.; Mattson, M.P. Flipping the Metabolic Switch: Understanding and Applying Health Benefits of Fasting. Obesity 2018, 26, 254–268.
  102. Harvie, M.; Wright, C.; Pegington, M.; McMullan, D.; Mitchell, E.; Martin, B.; Cutler, R.G.; Evans, G.; Whiteside, S.; Maudsley, S.; et al. The Effect of Intermittent Energy and Carbohydrate Restriction v. Daily Energy Restriction on Weight Loss and Metabolic Disease Risk Markers in Overweight Women. Br. J. Nutr. 2013, 110, 1534–1547.
  103. Catenacci, V.A.; Pan, Z.; Ostendorf, D.; Brannon, S.; Gozansky, W.S.; Mattson, M.P.; Martin, B.; MacLean, P.S.; Melanson, E.L.; Troy Donahoo, W. A Randomized Pilot Study Comparing Zero-Calorie Alternate-Day Fasting to Daily Caloric Restriction in Adults with Obesity. Obesity 2016, 24, 1874–1883.
  104. Hoddy, K.K.; Kroeger, C.M.; Trepanowski, J.F.; Barnosky, A.; Bhutani, S.; Varady, K.A. Meal Timing during Alternate Day Fasting: Impact on Body Weight and Cardiovascular Disease Risk in Obese Adults. Obesity 2014, 22, 2524–2531.
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