Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1 -- 2762 2022-07-29 14:45:03 |
2 format correction -3 word(s) 2759 2022-08-01 04:05:18 |

Video Upload Options

We provide professional Video Production Services to translate complex research into visually appealing presentations. Would you like to try it?

Confirm

Are you sure to Delete?
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Martín-Rodríguez, A.;  Bustamante-Sánchez, �.;  Martínez-Guardado, I.;  Navarro-Jiménez, E.;  Plata-Sanjuan, E.;  Tornero-Aguilera, J.F.;  Clemente-Suárez, V.J. Infancy Dietary Patterns, Development, and Health. Encyclopedia. Available online: https://encyclopedia.pub/entry/25668 (accessed on 26 December 2024).
Martín-Rodríguez A,  Bustamante-Sánchez �,  Martínez-Guardado I,  Navarro-Jiménez E,  Plata-Sanjuan E,  Tornero-Aguilera JF, et al. Infancy Dietary Patterns, Development, and Health. Encyclopedia. Available at: https://encyclopedia.pub/entry/25668. Accessed December 26, 2024.
Martín-Rodríguez, Alexandra, Álvaro Bustamante-Sánchez, Ismael Martínez-Guardado, Eduardo Navarro-Jiménez, Erika Plata-Sanjuan, José Francisco Tornero-Aguilera, Vicente Javier Clemente-Suárez. "Infancy Dietary Patterns, Development, and Health" Encyclopedia, https://encyclopedia.pub/entry/25668 (accessed December 26, 2024).
Martín-Rodríguez, A.,  Bustamante-Sánchez, �.,  Martínez-Guardado, I.,  Navarro-Jiménez, E.,  Plata-Sanjuan, E.,  Tornero-Aguilera, J.F., & Clemente-Suárez, V.J. (2022, July 29). Infancy Dietary Patterns, Development, and Health. In Encyclopedia. https://encyclopedia.pub/entry/25668
Martín-Rodríguez, Alexandra, et al. "Infancy Dietary Patterns, Development, and Health." Encyclopedia. Web. 29 July, 2022.
Infancy Dietary Patterns, Development, and Health
Edit

Correct dietary patterns are important for a child’s health from birth to adulthood. Understanding a child’s health as a state of entire physical, mental, and social well-being is essential.

nutrition children infancy dietary patterns

1. Progenitors Culture and Dietary Patterns in Infancy

Culture is an integral component of food habits, affecting what, when, and how we eat [1]. These habits are achieved mostly through transference in parental guidance [2]. Thus, eating behaviors have been investigated over the years to develop healthy habits and command children’s nutrition for preemptive intentions. However, it seems to be a multifactorial context where progenitors’ culture and their domestic life play a role in setting up and promoting practices that will persist throughout the lifespan, not only in infancy [3]. Although preferences can change, children are also under the influence of biological, social, and environmental factors where their eating-related attitudes are built [4]. These attitudes could have crucial implications, such as undernutrition or, contrarily, increased obesity risk [5]. Even though progenitors’ practices should be appropriated to prevent unhealthy eating patterns, unfortunately, it is not always the case.
Regarding food selection, the relationship between nutrition and culture has been demonstrated previously [6]. This relationship is based on people’s beliefs and preferences. It is known that people can do an inadequate food selection and, therefore, have bad eating habits despite the fact all kinds of foods are available in their countries. For this reason, it is not surprising to find differences in food selection between countries, as well as between different locations in the same country. In fact, in the last decades, a phenomenon of nutrition transition has been developed, and it has been defined as the shift from the traditional to a ‘‘Westernized’’ diet. Evidence suggests that food choices are affected by demographic transition [7]. However, regardless of location, a child’s early experience influences food likes later in life [8]. After birth, in some cultures, children are deliberately exposed to strong flavors. For example, Mexican culture uses chili peppers to increase strength in food. Learning to like initially strong tastes may be part of the socialization process [3]. Moreover, in Western cultures, when tofu, or plain, salted, or sweetened foods are given to preschool children repeatedly, they came to prefer the version that had become familiar to them [9], which suggests that repeated exposure to food increases their acquaintance, and it is one of the substantive determinants of their acceptance.
Findings have also revealed that food choices and even new food practices are adopted by migrants when they start a new life in a new country as a part of their inclusion process [10][11]. Though traditional practices are maintained, they include new foods in their diet to generate a connection with the new location [9][12][13][14]. Therefore, due to mobility, urbanization, and every attempt to belong to the new culture, low-income immigrant families spend a lot of time away from home and are unable to establish healthy eating habits; thus, malnutrition and obesity have become major risks [14]. The latter phenomenon is also due, in part, to dietary acculturation, signaled by the adoption of the eating and consumption patterns of the host country. It is now widely recognized that the Western diet is deficient in nutrient-rich foods such as fruits, vegetables, and whole grains, and superfluous in energy sources of solid fats, added sugars, and alcoholic beverages [15].
Food selection and dietary habits are often conditioned by food allergies. Whether a child is more or less likely to suffer from a food allergy can be determined by family culture. It has been demonstrated that children of immigrants (second-generation immigrants) have been suggested to be at high risk of food sensitization. In addition, environmental changes in the microbiome and/or diet due to migration to industrialized and/or Western countries may contribute to atopy presentation [16]. Even migrants and natives living in the same geographical location have differing allergy prevalence that forces them to adjust their dietary habits. Increased populations living in cities, migration, and economic growth have led to an increase in the incidence of food allergies [17]. Studies show that the environment and ethnicity play a part in this [18].
Further research is needed to understand how progenitor culture affects infants´ dietary habits. Considering that societies are currently a mixture of traditional cultures and Western culture, as well as the results presented, as future research lines in this area, the study of the effect of this culture exchange on infant feeding. Knowing these mechanisms, pediatricians could develop effective nutrition programs and create healthy food practices among the child population.

2. Socioeconomic Status of Progenitors and Dietary Patterns in Infancy

An unhealthy diet is a well-known risk factor that can lead to chronic non-communicable diseases such as obesity and hypertension. It should be noted that it is crucial not only to focus on the poor nutrition of children, but also on the poor nutrition of parents. The majority do little to change their lifestyle to prepare for pregnancy, and socioeconomic status plays a part in it. Pre-pregnancy Body Mass Index (BMI) (body weight (kg)/height2 (m)) and preconception supplementation are strongly related to health outcomes. This fact is important for fetal development; however, implementing healthy habits is not accessible to all [19]. Furthermore, both parents’ health is relevant, and some studies demonstrated that dietary zinc deficiency impairs reproduction in males and females [20]. It is estimated that one-third of the world population has a zinc shortage [21]. Particular attention should be also paid to the intake and status of some other micronutrients, especially folate, in women of reproductive age. Studies show strong links between health before pregnancy and maternal and child health outcomes, with consequences that can extend across generations [22]. Concretely, dietary supplementation with iron, vitamin D, vitamin B12, iodine, and others may be indicated in women at risk of poor supply and insufficiency of these micronutrients. Globally, preconception use of folic acid is estimated to be under 50% [23], with particular concern that young women from lower socio-economic backgrounds are the least likely to follow the recommendations [24].
As mentioned above, the economic status (SES) plays an important role in this process, and further research is needed in countries with resource-limited countries. Research in high-income countries partly attributes disparities in obesity and other health conditions to differences in dietary quality [25][26]. In most high-income countries, high-calorie foods are cheaper, whereas healthier foods tend to be more expensive [27][28], so this will be a crucial factor in determining diet quality [29][30]. Due to this, childhood obesity has increased, and it is now recognized as a global public health problem [31]. Several authors have confirmed a high incidence of overweight and obesity among children aged 5–18 years in various parts of the world [32][33][34]. Findings have also reported a prevalence of overweight among children ranging from 11.8% to 16.33%, whereas the prevalence of obesity was moderately lower, ranging from 4.9% to 10.69% [31][32][33][34].
In contrast, undernutrition is a global health issue concerning children in low- and middle-income countries (LMICs). Approximately one in five children worldwide suffers from childhood malnutrition and its complications, including increased susceptibility to inflammation and infectious diseases [35]. Even so, Coetzee et.al found in a 7-year longitudinal study conducted in 181 South African school children (63 Caucasian and 118 black and mixed-race) that BMI increased over the period studied (2010–2016). Children in higher SES groups were more likely to be overweight and obese (compared to lower socio-economic status groups (overweight: 1.09–2.17% and obese: 2.17–4.35%)). The results further indicate that although there was a decrease in obesity in high-SES children, its prevalence was still higher than in low-SES children [36].

3. Mother’s Diet during Pregnancy and Baby’s Health

To point out the factors that determine a correct dietary pattern during childhood, it is necessary to address the gestation process. In this line, it seems that to reduce health problems and the risk of suffering from chronic diseases during the early stages of life, it is very important to control the nutritional and metabolic environment during pregnancy [37].
The development of the child is affected by the diet and exercise habits of the pregnant woman [38][39]. Having a healthy lifestyle may prevent complications during pregnancy, as well as prevent the newborn from developing non-communicable diseases [40]. Due to this evidence, parents’ habits will possibly alter the whole life of their children [41]. Overweight and obesity have been linked to most diseases [42]. Fetal macrosomia and low birth weight have been associated with gestational diabetes in studies with overweight and obese mothers [43][44].
Thus, findings suggest that this maternal overweight or obesity may also lead to a lower life expectancy for the child, as well as miscarriages and premature births [45][46][47][48]. It has been shown that a high-calorie diet is detrimental to both the mother and the child’s health [49][50]. Therefore, during the pre-gestational period, mothers should try to maintain an adequate weight and healthy eating habits, since during the gestational period, their BMI will largely determine many of the consequences later on [51][52]. It has been shown that even a 10% weight loss in obese women can be a crucial factor for the development of the child. Regarding evidence and general recommendations, a balanced diet is required [52]. The increased consumption of vegetables and fruits, as well as wholegrain products, legumes, and fish showed a lower risk of gestational diabetes is needed to prevent diseases. Additionally, it should be noted that nutrient-dense foods are favorable during gestation because more energy is absorbed. In pregnant women, three servings of vegetables and two servings of fruit should be implemented every day [53]. Foods such as cereal products, especially whole grains, and potatoes are rich in vitamins, minerals, and fiber. Protein, calcium, and iodine may be provided by milk and dairy products [54]. Finally, fish is an important source of vitamin B 12, zinc, and iron. All of them are essential components of a balanced diet. Measures to achieve this should be indicated by medical personnel following scientific evidence [55].
A balanced diet, regular exercise, and a healthy lifestyle are very important before and during pregnancy. The time before conception and the first 1000 days of the child’s life provide the opportunity to lay the foundation for the health of the child and the mother-to-be. The revised recommendations presented here provide practical and up-to-date knowledge-based recommendations for pregnancy and also for women/couples wishing to have a child [41].

4. Nutrients Intake in Infancy and Child Development

Early child development is a crucial period for ensuring an individual’s physical and mental health, with nutrition being among the most important risk factors for early child development [56]. The latest estimates suggest that around 250 million children under five in low- and middle-income countries were at risk of not achieving their full development potential due to stunting and extreme poverty [57]. Contrary, in industrialized countries, child obesity is an important public health challenge, with the most recent data indicating that approximately 18.5% of the population from 2–19 years of age are obese in the United States alone, and current trends in the United Kingdom suggest that by 2050, 25% of all children under 20 years of age will be classified as obese [58][59].
Therefore, an optimal balance between micro and macronutrients is necessary for optimal development and to be able to avoid typical Western diseases in the future; thus, nutrition is essential to children’s future. Industrialized countries are more than sufficient to meet physiological requirements among children [60], but it is also easy to exceed it, and a high protein intake in early childhood has been linked to a higher risk of obesity [61]. One study showed high protein intake in early childhood to be associated with a higher fat mass index (FMI), but not with a higher fat-free mass index at school age. This association is stronger from animals than from vegetable protein [62]. An official upper limit of protein intake is yet to be established among children.
Regarding micronutrients (vitamins and minerals), research on the relationship between micronutrient status during early childhood and obesity in later life is urgently needed. Growth (weight and length) during the first 2 years of life shows the nutritional status of infants and young children is the consequence of breastfeeding and complementary feeding [63]. Particularly, a review carried out by Singhal et al. revealed that rapid weight gain in infancy is positively associated with obesity in later life [64]. A slower rate of weight gain and possibly a decreased risk of overweight in childhood and adolescence compared to formula feeding have been related to exclusive breastfeeding [63]. Breastfeeding is associated with ~a 20% reduction in the odds of being overweight, whereas a lack of breastfeeding, low birth weight, and rapid weight gain were associated with obesity [64].

5. Dietary Patterns in Infancy and Cognitive Function

Good cognitive development and brain function during the prenatal period and early years is influenced by nutrition [65]. Findings have suggested that children with a better nutritional status could have improved their cognitive and neuropsychological function [66]. The quality of nutrition during pregnancy and breastfeeding is reported to be relevant for better test scores of cognitive functions [67]. Furthermore, studies have looked at the relationship between early nutrition status and growth in infancy and childhood. Knowing these two aspects and the complex interactions between environmental stimuli and nutritional patterns, this issue should be further explored in future research.
Children´s growth is determined by their early nutrition status. Evidence has established that early nutrition can have a long-term effect on growth, metabolic outcome, and long-term health [68]. This status depends on many factors, including the mother’s diet [69], her socioeconomic status [69], and if her children are breastfed or not. Thus, a balanced maternal diet during pregnancy is essential. The formation of the neural tube depends on these nutrients, and a deficiency can adversely affect brain development, resulting in neural tube defects, spina bifida, and encephalocele [70]. Moreover, iron is necessary for neurogenesis and dopamine production. A deficiency in these nutrients may cause significant cognitive impairment in the offspring [71][72][73]. Concerning breastfeeding, neurological benefits of breastfeeding in infancy were demonstrated previously [70][74]. When the supply of long-chain polyunsaturated fatty acids through the placenta is interrupted, this supplementation depends on the mother´s diet [75]. The evolution of the mother’s body has created mechanisms that adjust the amount of fat in milk to the needs of the child [76]. Knowing that breast milk contains long-chain polyunsaturated fatty acids which form the major 34 structures of 35 neuronal membranes, it is important to highlight that it could play a critical role in human nervous system functioning [77][78]. Firstly, there is considerable evidence linking breastfeeding with better performance in intelligence tests [79]. Studies show that three months of breastfeeding improves intelligence quotients 2.1 times over others [67]. Additionally, improvements in motor skills, as well as language development, have also been found [80]. Even if breastfeeding is extended to 6 months, there seems to be a lower risk of developing attention deficit, hyperactivity, or autism spectrum syndrome [81]. However, other studies have found no difference between the promotion of exclusive breastfeeding and children aged 5–8 years on several measures of children’s cognitive development [82][83]. Although diets have been extensively studied concerning children’s cognitive development, there is less research showing interest in the transition from liquid foods to solids. Therefore, further research is needed to understand how the influence of context and socioeconomic status may influence cognitive functions. However, evidence suggests that the promotion and support of breastfeeding and other healthy feeding practices are especially important for children of low socioeconomic status, who are at increased risk of obesity [84] and cognitive impairment [85].
Regarding the nutritional status, the degree of nutrient deficiency may be modified or even increased during the mother’s and child’s lifespans. Findings suggest that certain types of deficiency, such as iron deficiency, are related to impaired brain development [86]. All the influences surrounding both mother and child have attributed a relevant role in this process. The rapid growth of the brain during the gestational period makes it very vulnerable to an inadequate diet. Comparing both types of countries, developing and industrialized, evidence in Kenya and Mexico showed that where the mother’s energy intake declines gradually throughout pregnancy, not only do mothers gain only half as much as European or North American women, but also, they even lose weight and fat in the last month of pregnancy [87]. In both, iron scantiness occurs commonly, which is known to adversely influence cognition [65][88]. Although maternal nutrient deficiencies could be modified with micronutrient supplementation starting in pregnancy, increasing birth weight, there is a burgeoning importance of maternal health before conception and the key risk factors for unfavorable birth outcomes, such as those related to cognitive development. There is a need to develop programs and policies to enhance nutritional status across the life course and especially during reproductive ages to promote healthy patterns in infancy. Moreover, the importance of health before and after pregnancy and possible actions to take may contribute to this [22].

References

  1. Centrone Stefani, M.; Humphries, D.L. Exploring culture in the world of international nutrition and nutrition sciences. Adv. Nutr. 2013, 4, 536–538.
  2. Monterrosa, E.C.; Frongillo, E.A.; Drewnowski, A.; de Pee, S.; Vandevijvere, S. Sociocultural Influences on Food Choices and Implications for Sustainable Healthy Diets. Food Nutr. Bull. 2020, 41, 59S–73S.
  3. Scaglioni, S.; De Cosmi, V.; Ciappolino, V.; Parazzini, F.; Brambilla, P.; Agostoni, C. Factors Influencing Children’s Eating Behaviours. Nutrients 2018, 10, 706.
  4. Ventura, A.K.; Worobey, J. Early influences on the development of food preferences. Curr. Biol. 2013, 23, R401–R408.
  5. Askie, L.M.; Baur, L.A.; Campbell, K.; Daniels, L.A.; Hesketh, K.; Magarey, A.; Mihrshahi, S.; Rissel, C.; Simes, J.; Taylor, B.; et al. The Early Prevention of Obesity in CHildren (EPOCH) Collaboration—An Individual Patient Data Prospective Meta-Analysis. BMC Public Health 2010, 10, 728.
  6. Rose, C.M.; Birch, L.L.; Savage, J.S. Dietary patterns in infancy are associated with child diet and weight outcomes at 6 years. Int. J. Obes. 2017, 41, 783–788.
  7. Aounallah-Skhiri, H.; Traissac, P.; El Ati, J.; Eymard-Duvernay, S.; Landais, E.; Achour, N.; Delpeuch, F.; Ben Romdhane, H.; Maire, B. Nutrition transition among adolescents of a south-Mediterranean country: Dietary patterns, association with socio-economic factors, overweight and blood pressure. A cross-sectional study in Tunisia. Nutr. J. 2011, 10, 38.
  8. Birch, L.L. Development of food preferences. Annu. Rev. Nutr. 1999, 19, 41–62.
  9. Sullivan, S.A.; Birch, L.L. Pass the sugar, pass the salt: Experience dictates preference. Dev. Psychol. 1990, 26, 546–551.
  10. Hetherington, M.M.; Schwartz, C.; Madrelle, J.; Croden, F.; Nekitsing, C.; Vereijken, C.M.J.L.; Weenen, H. A step-by-step introduction to vegetables at the beginning of complementary feeding. The effects of early and repeated exposure. Appetite 2015, 84, 280–290.
  11. Wilson, A.; Renzaho, A. Intergenerational differences in acculturation experiences, food beliefs and perceived health risks among refugees from the Horn of Africa in Melbourne, Australia. Public Health Nutr. 2015, 18, 176–188.
  12. Sanlier, N.; Ulusoy, H.G.; Kocabaş, S.; Çelik, B.; Göbel, P.; Yilmaz, S. Mediterranean Diet Adherence among Preschoolers and its Association with Parents’ Beliefs, Attitudes, and Practices. Ecol. Food Nutr. 2021, 60, 225–243.
  13. Choo, S. Eating Satay Babi: Sensory perception of transnational movement. J. Intercult. Stud. 2004, 25, 203–213.
  14. Lindsay, A.C.; Wallington, S.F.; Lees, F.D.; Greaney, M.L. Exploring How the Home Environment Influences Eating and Physical Activity Habits of Low-Income, Latino Children of Predominantly Immigrant Families: A Qualitative Study. Int. J. Environ. Res. Public. Health 2018, 15, 978.
  15. Viladrich, A. Curbing the Obesity Epidemic: Understanding Latinos’ Challenges to Healthy Eating in the United States. J. Food Nutr. 2014, 1, 1–2.
  16. Jiang, J.; Dinakar, C.; Fierstein, J.L.; Gupta, O.K.; Gupta, R.S. Food allergy among Asian Indian immigrants in the United States. J. Allergy Clin. Immunol. Pract. 2020, 8, 1740–1742.
  17. Loh, W.; Tang, M.L.K. The Epidemiology of Food Allergy in the Global Context. Int. J. Environ. Res. Public. Health 2018, 15, 2043.
  18. Wegienka, G.; Johnson, C.C.; Zoratti, E.; Havstad, S. Racial Differences in Allergic Sensitization: Recent Findings and Future Directions. Curr Allergy Asthma Rep 2013, 13, 255–261.
  19. Barrett, G.; Shawe, J.; Howden, B.; Patel, D.; Ojukwu, O.; Pandya, P.; Stephenson, J. Why do women invest in pre-pregnancy health and care? A qualitative investigation with women attending maternity services. BMC Pregnancy Childbirth 2015, 15, 236.
  20. Fallah, A.; Mohammad-Hasani, A.; Colagar, A.H. Zinc is an Essential Element for Male Fertility: A Review of Zn Roles in Men’s Health, Germination, Sperm Quality, and Fertilization. J. Reprod. Infertil. 2018, 19, 69–81.
  21. Swain, P.S.; Rao, S.B.N.; Rajendran, D.; Dominic, G.; Selvaraju, S. Nano zinc, an alternative to conventional zinc as animal feed supplement: A review. Anim. Nutr. 2016, 2, 134–141.
  22. Stephenson, J.; Heslehurst, N.; Hall, J.; Schoenaker, D.A.J.M.; Hutchinson, J.; Cade, J.E.; Poston, L.; Barrett, G.; Crozier, S.R.; Barker, M.; et al. Before the beginning: Nutrition and lifestyle in the preconception period and its importance for future health. Lancet 2018, 391, 1830–1841.
  23. Ray, J.G.; Singh, G.; Burrows, R.F. Evidence for suboptimal use of periconceptional folic acid supplements globally. BJOG Int. J. Obstet. Gynaecol. 2004, 111, 399–408.
  24. Stockley, L.; Lund, V. Use of folic acid supplements, particularly by low-income and young women: A series of systematic reviews to inform public health policy in the UK. Public Health Nutr. 2008, 11, 807–821.
  25. Drewnowski, A.; Aggarwal, A.; Cook, A.; Stewart, O.; Moudon, A.V. Geographic disparities in Healthy Eating Index scores (HEI-2005 and 2010) by residential property values: Findings from Seattle Obesity Study (SOS). Prev. Med. 2016, 83, 46–55.
  26. Buszkiewicz, J.; Rose, C.; Gupta, S.; Ko, L.K.; Mou, J.; Moudon, A.V.; Hurvitz, P.M.; Cook, A.; Aggarwal, A.; Drewnowski, A. A cross-sectional analysis of physical activity and weight misreporting in diverse populations: The Seattle Obesity Study III. Obes. Sci. Pract. 2020, 6, 615–627.
  27. Faria, A.P.; Albuquerque, G.; Moreira, P.; Rosário, R.; Araújo, A.; Teixeira, V.; Barros, R.; Lopes, Ó.; Moreira, A.; Padrão, P. Association between energy density and diet cost in children. Porto Biomed. J. 2016, 1, 106–111.
  28. Conklin, A.I.; Monsivais, P.; Khaw, K.-T.; Wareham, N.J.; Forouhi, N.G. Dietary Diversity, Diet Cost, and Incidence of Type 2 Diabetes in the United Kingdom: A Prospective Cohort Study. PLoS Med. 2016, 13, e1002085.
  29. Żukiewicz-Sobczak, W.; Wróblewska, P.; Zwoliński, J.; Chmielewska-Badora, J.; Adamczuk, P.; Krasowska, E.; Zagórski, J.; Oniszczuk, A.; Piątek, J.; Silny, W. Obesity and poverty paradox in developed countries. Ann. Agric. Environ. Med. 2014, 21, 590–594.
  30. Darmon, N.; Drewnowski, A. Does social class predict diet quality? Am. J. Clin. Nutr. 2008, 87, 1107–1117.
  31. Obesidad. Available online: https://www.who.int/es/health-topics/obesity (accessed on 9 April 2022).
  32. Ahrens, W.; Pigeot, I.; Pohlabeln, H.; De Henauw, S.; Lissner, L.; Molnár, D.; Moreno, L.A.; Tornaritis, M.; Veidebaum, T.; Siani, A.; et al. Prevalence of overweight and obesity in European children below the age of 10. Int. J. Obes. 2014, 38 (Suppl. 2), S99–S107.
  33. Zhang, J.; Wang, H.; Wang, Y.; Xue, H.; Wang, Z.; Du, W.; Su, C.; Zhang, J.; Jiang, H.; Zhai, F.; et al. Dietary patterns and their associations with childhood obesity in China. Br. J. Nutr. 2015, 113, 1978–1984.
  34. Zhang, Y.-X.; Wang, S.-R. Changes in skinfold thickness and body composition among children and adolescents in Shandong, China from 1995 to 2010. J. Hum. Nutr. Diet. 2013, 26, 252–258.
  35. Galler, J.R.; Bringas-Vega, M.L.; Tang, Q.; Rabinowitz, A.G.; Musa, K.I.; Chai, W.J.; Omar, H.; Abdul Rahman, M.R.; Abd Hamid, A.I.; Abdullah, J.M.; et al. Neurodevelopmental effects of childhood malnutrition: A neuroimaging perspective. NeuroImage 2021, 231, 117828.
  36. Coetzee, D.; du Plessis, W.; van Staden, D. Longitudinal Effects of Excessive Weight and Obesity on Academic Performance of Primary School Boys in Different Socio-Economic Statuses: The NW-CHILD Study. Int. J. Environ. Res. Public Health 2021, 18, 8891.
  37. Godfrey, K.M.; Gluckman, P.D.; Hanson, M.A. Developmental origins of metabolic disease: Life course and intergenerational perspectives. Trends Endocrinol. Metab. 2010, 21, 199–205.
  38. Labonte-Lemoyne, E.; Curnier, D.; Ellemberg, D. Exercise during pregnancy enhances cerebral maturation in the newborn: A randomized controlled trial. J. Clin. Exp. Neuropsychol. 2017, 39, 347–354.
  39. Polańska, K.; Muszyński, P.; Sobala, W.; Dziewirska, E.; Merecz-Kot, D.; Hanke, W. Maternal lifestyle during pregnancy and child psychomotor development—Polish Mother and Child Cohort study. Early Hum. Dev. 2015, 91, 317–325.
  40. Gaillard, R.; Santos, S.; Duijts, L.; Felix, J.F. Childhood Health Consequences of Maternal Obesity during Pregnancy: A Narrative Review. Ann. Nutr. Metab. 2016, 69, 171–180.
  41. Koletzko, B.; Cremer, M.; Flothkötter, M.; Graf, C.; Hauner, H.; Hellmers, C.; Kersting, M.; Krawinkel, M.; Przyrembel, H.; Röbl-Mathieu, M.; et al. Diet and Lifestyle Before and During Pregnancy—Practical Recommendations of the Germany-wide Healthy Start—Young Family Network. Geburtshilfe Frauenheilkd. 2018, 78, 1262–1282.
  42. Darmon, N.; Drewnowski, A. Contribution of food prices and diet cost to socioeconomic disparities in diet quality and health: A systematic review and analysis. Nutr. Rev. 2015, 73, 643–660.
  43. Gaudet, L.; Ferraro, Z.M.; Wen, S.W.; Walker, M. Maternal obesity and occurrence of fetal macrosomia: A systematic review and meta-analysis. BioMed Res. Int. 2014, 2014, 640291.
  44. Blake-Lamb, T.L.; Locks, L.M.; Perkins, M.E.; Woo Baidal, J.A.; Cheng, E.R.; Taveras, E.M. Interventions for Childhood Obesity in the First 1,000 Days A Systematic Review. Am. J. Prev. Med. 2016, 50, 780–789.
  45. Nicklas, J.M.; Barbour, L.A. Optimizing Weight for Maternal and Infant Health—Tenable, or Too Late? Expert Rev. Endocrinol. Metab. 2015, 10, 227–242.
  46. Hsu, M.-H.; Chen, Y.-C.; Sheen, J.-M.; Huang, L.-T. Maternal Obesity Programs Offspring Development and Resveratrol Potentially Reprograms the Effects of Maternal Obesity. Int. J. Environ. Res. Public Health 2020, 17, 1610.
  47. Pietrobelli, A.; Agosti, M.; MeNu Group. Nutrition in the First 1000 Days: Ten Practices to Minimize Obesity Emerging from Published Science. Int. J. Environ. Res. Public. Health 2017, 14, 1491.
  48. Li, N.; Liu, E.; Guo, J.; Pan, L.; Li, B.; Wang, P.; Liu, J.; Wang, Y.; Liu, G.; Baccarelli, A.A.; et al. Maternal prepregnancy body mass index and gestational weight gain on pregnancy outcomes. PLoS ONE 2013, 8, e82310.
  49. Tielemans, M.J.; Garcia, A.H.; Peralta Santos, A.; Bramer, W.M.; Luksa, N.; Luvizotto, M.J.; Moreira, E.; Topi, G.; de Jonge, E.A.L.; Visser, T.L.; et al. Macronutrient composition and gestational weight gain: A systematic review. Am. J. Clin. Nutr. 2016, 103, 83–99.
  50. Rasmussen, K.M.; Abrams, B.; Bodnar, L.M.; Butte, N.F.; Catalano, P.M.; Maria Siega-Riz, A. Recommendations for weight gain during pregnancy in the context of the obesity epidemic. Obstet. Gynecol. 2010, 116, 1191–1195.
  51. Beyerlein, A.; Lack, N.; von Kries, R. Within-population average ranges compared with Institute of Medicine recommendations for gestational weight gain. Obstet. Gynecol. 2010, 116, 1111–1118.
  52. Marshall, N.E.; Abrams, B.; Barbour, L.A.; Catalano, P.; Christian, P.; Friedman, J.E.; Hay, W.W.; Hernandez, T.L.; Krebs, N.F.; Oken, E.; et al. The importance of nutrition in pregnancy and lactation: Lifelong consequences. Am. J. Obstet. Gynecol. 2021, 226, 607–638.
  53. Woodside, J.V.; Young, I.S.; McKinley, M.C. Fruits and vegetables: Measuring intake and encouraging increased consumption. Proc. Nutr. Soc. 2013, 72, 236–245.
  54. Gernand, A.D.; Schulze, K.J.; Stewart, C.P.; West, K.P.; Christian, P. Micronutrient deficiencies in pregnancy worldwide: Health effects and prevention. Nat. Rev. Endocrinol. 2016, 12, 274–289.
  55. Busetto, L.; Dicker, D.; Azran, C.; Batterham, R.L.; Farpour-Lambert, N.; Fried, M.; Hjelmesæth, J.; Kinzl, J.; Leitner, D.R.; Makaronidis, J.M.; et al. Practical Recommendations of the Obesity Management Task Force of the European Association for the Study of Obesity for the Post-Bariatric Surgery Medical Management. Obes. Facts 2017, 10, 597–632.
  56. Black, M.M.; Walker, S.P.; Fernald, L.C.H.; Andersen, C.T.; DiGirolamo, A.M.; Lu, C.; McCoy, D.C.; Fink, G.; Shawar, Y.R.; Shiffman, J.; et al. Early childhood development coming of age: Science through the life course. Lancet 2017, 389, 77–90.
  57. Lu, C.; Black, M.M.; Richter, L.M. Risk of poor development in young children in low-income and middle-income countries: An estimation and analysis at the global, regional, and country level. Lancet Glob. Health 2016, 4, e916–e922.
  58. Hales, C.M.; Carroll, M.D.; Fryar, C.D.; Ogden, C.L. Prevalence of Obesity among Adults and Youth: United States, 2015–2016. NCHS Data Brief 2017, 288, 1–8.
  59. Kopelman, P.; Jebb, S.A.; Butland, B. Executive summary: Foresight “Tackling Obesities: Future Choices” project. Obes. Rev. 2007, 8 (Suppl. 1), vi–ix.
  60. Hörnell, A.; Lagström, H.; Lande, B.; Thorsdottir, I. Protein intake from 0 to 18 years of age and its relation to health: A systematic literature review for the 5th Nordic Nutrition Recommendations. Food Nutr. Res. 2013, 57, 21083.
  61. Rolland-Cachera, M.F.; Deheeger, M.; Akrout, M.; Bellisle, F. Influence of macronutrients on adiposity development: A follow up study of nutrition and growth from 10 months to 8 years of age. Int. J. Obes. Relat. Metab. Disord. J. Int. Assoc. Study Obes. 1995, 19, 573–578.
  62. Voortman, T.; Braun, K.V.E.; Kiefte-de Jong, J.C.; Jaddoe, V.W.V.; Franco, O.H.; van den Hooven, E.H. Protein intake in early childhood and body composition at the age of 6 years: The Generation R Study. Int. J. Obes. 2016, 40, 1018–1025.
  63. Yang, Z.; Huffman, S.L. Nutrition in pregnancy and early childhood and associations with obesity in developing countries. Matern. Child. Nutr. 2013, 9 (Suppl. 1), 105–119.
  64. Singhal, A. Does early growth affect long-term risk factors for cardiovascular disease? Nestle Nutr. Workshop Ser. Paediatr. Programme 2010, 65, 55–64, discussion 64–69.
  65. Benton, D.; ILSI Europe a.i.s.b.l. The influence of children’s diet on their cognition and behavior. Eur. J. Nutr. 2008, 47 (Suppl. 3), 25–37.
  66. Bellisle, F. Effects of diet on behaviour and cognition in children. Br. J. Nutr. 2004, 92 (Suppl. 2), S227–S232.
  67. Jedrychowski, W.; Perera, F.; Jankowski, J.; Butscher, M.; Mroz, E.; Flak, E.; Kaim, I.; Lisowska-Miszczyk, I.; Skarupa, A.; Sowa, A. Effect of exclusive breastfeeding on the development of children’s cognitive function in the Krakow prospective birth cohort study. Eur. J. Pediatr. 2012, 171, 151–158.
  68. Haschke, F.; Binder, C.; Huber-Dangl, M.; Haiden, N. Early-Life Nutrition, Growth Trajectories, and Long-Term Outcome. Nestle Nutr. Inst. Workshop Ser. 2019, 90, 107–120.
  69. Rahman, M.S.; Howlader, T.; Masud, M.S.; Rahman, M.L. Association of Low-Birth Weight with Malnutrition in Children under Five Years in Bangladesh: Do Mother’s Education, Socio-Economic Status, and Birth Interval Matter? PLoS ONE 2016, 11, e0157814.
  70. Rao, R.; Tkac, I.; Townsend, E.L.; Ennis, K.; Gruetter, R.; Georgieff, M.K. Perinatal iron deficiency predisposes the developing rat hippocampus to greater injury from mild to moderate hypoxia–ischemia. J. Cereb. Blood Flow Metab. Off. J. Int. Soc. Cereb. Blood Flow Metab. 2007, 27, 729–740.
  71. Bernal, J. Thyroid Hormones in Brain Development and Function. In Endotext; Feingold, K.R., Anawalt, B., Boyce, A., Chrousos, G., de Herder, W.W., Dhatariya, K., Dungan, K., Hershman, J.M., Hofland, J., et al., Eds.; MDText.com, Inc.: South Dartmouth, MA, USA, 2000.
  72. Wiesinger, J.A.; Buwen, J.P.; Cifelli, C.J.; Unger, E.L.; Jones, B.C.; Beard, J.L. Down-regulation of dopamine transporter by iron chelation in vitro is mediated by altered trafficking, not synthesis. J. Neurochem. 2007, 100, 167–179.
  73. Lozoff, B.; De Andraca, I.; Castillo, M.; Smith, J.B.; Walter, T.; Pino, P. Behavioral and developmental effects of preventing iron-deficiency anemia in healthy full-term infants. Pediatrics 2003, 112, 846–854.
  74. Kramer, M.S.; Aboud, F.; Mironova, E.; Vanilovich, I.; Platt, R.W.; Matush, L.; Igumnov, S.; Fombonne, E.; Bogdanovich, N.; Ducruet, T.; et al. Breastfeeding and child cognitive development: New evidence from a large randomized trial. Arch. Gen. Psychiatry 2008, 65, 578–584.
  75. Sabel, K.-G.; Lundqvist-Persson, C.; Bona, E.; Petzold, M.; Strandvik, B. Fatty acid patterns early after premature birth, simultaneously analysed in mothers’ food, breast milk and serum phospholipids of mothers and infants. Lipids Health Dis. 2009, 8, 20.
  76. Bobiński, R.; Bobińska, J. Fatty acids of human milk—A review. Int. J. Vitam. Nutr. 2020, 21, 1–12.
  77. Martinat, M.; Rossitto, M.; Di Miceli, M.; Layé, S. Perinatal Dietary Polyunsaturated Fatty Acids in Brain Development, Role in Neurodevelopmental Disorders. Nutrients 2021, 13, 1185.
  78. Brown Belfort, M. The Science of Breastfeeding and Brain Development. Breastfeed. Med. 2017, 12, 459–461.
  79. Horta, B.L.; Loret de Mola, C.; Victora, C.G. Breastfeeding and intelligence: A systematic review and meta-analysis. Acta Paediatr. 2015, 104, 14–19.
  80. Der, G.; Batty, G.D.; Deary, I.J. Effect of breast feeding on intelligence in children: Prospective study, sibling pairs analysis, and meta-analysis. BMJ 2006, 333, 945.
  81. Dee, D.L.; Li, R.; Lee, L.-C.; Grummer-Strawn, L.M. Associations between breastfeeding practices and young children’s language and motor skill development. Pediatrics 2007, 119 (Suppl. 1), S92–S98.
  82. Yang, S.; Martin, R.M.; Oken, E.; Hameza, M.; Doniger, G.; Amit, S.; Patel, R.; Thompson, J.; Rifas-Shiman, S.L.; Vilchuck, K.; et al. Breastfeeding during infancy and neurocognitive function in adolescence: 16-year follow-up of the PROBIT cluster-randomized trial. PLoS Med. 2018, 15, e1002554.
  83. Tumwine, J.K.; Nankabirwa, V.; Diallo, H.A.; Engebretsen, I.M.S.; Ndeezi, G.; Bangirana, P.; Sanou, A.S.; Kashala-Abotnes, E.; Boivin, M.; Giordani, B.; et al. Exclusive breastfeeding promotion and neuropsychological outcomes in 5-8 year old children from Uganda and Burkina Faso: Results from the PROMISE EBF cluster randomized trial. PLoS ONE 2018, 13, e0191001.
  84. Gibbs, B.G.; Forste, R. Socioeconomic status, infant feeding practices and early childhood obesity. Pediatr. Obes. 2014, 9, 135–146.
  85. Roberts, S.B.; Franceschini, M.A.; Silver, R.E.; Taylor, S.F.; de Sa, A.B.; Có, R.; Sonco, A.; Krauss, A.; Taetzsch, A.; Webb, P.; et al. Effects of food supplementation on cognitive function, cerebral blood flow, and nutritional status in young children at risk of undernutrition: Randomized controlled trial. BMJ 2020, 370, m2397.
  86. Prado, E.L.; Dewey, K.G. Nutrition and brain development in early life. Nutr. Rev. 2014, 72, 267–284.
  87. Neumann, C.G.; Harrison, G.G. Onset and evolution of stunting in infants and children. Examples from the Human Nutrition Collaborative Research Support Program. Kenya and Egypt studies. Eur. J. Clin. Nutr. 1994, 48 (Suppl. 1), S90–S102.
  88. Wasantwisut, E. Nutrition and development: Other micronutrients’ effect on growth and cognition. Southeast Asian J. Trop. Med. Public Health 1997, 28 (Suppl. 2), 78–82.
More
Information
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : , , , , , ,
View Times: 746
Entry Collection: Gastrointestinal Disease
Revisions: 2 times (View History)
Update Date: 01 Aug 2022
1000/1000
Video Production Service