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Genetics of obesity


Authors: I. Aldhoon Hainerová
Authors‘ workplace: Klinika dětí a dorostu 3. lékařské fakulty UK a FN Královské Vinohrady Praha, Centrum pro výzkum diabetu, metabolismu a výživy, přednosta doc. MU Dr. Felix Votava, Ph. D.
Published in: Vnitř Lék 2010; 56(10): 1035-1042
Category: Obesity 2010

Overview

Animal models and family studies led to the identification of cases of rare monogenic forms of human obesity. Rare Mendelian syndromes as Prader‑ Willi syndrome and Bardet‑ Biedl syndrome represent cases of genetically determined obesity. Genome wide linkage and classical candidate gene studies were in general unsuccessful concerning the identification of genes of common obesity. On the other hand, genome‑ wide association studies (GWAS) were found to be effective, as also variants with only a minor effect have been detected. Seventeen polygenic variants influencing body weight regulation were clearly confirmed. It is assumed that more of these variants exist and therefore they might be identified in near future by GWAS. It is possible that the size effect of some variants can be within few grams of body weight. In order to detect variants with small effect there is a need of meta‑analyses based on hundreds of thousands of individuals. Newly identified variants result in an increase of 0.06– 0.33 kg/ m2 of BMI per allele. In an adult of an average height of 170 cm, it corresponds to 173– 954 g per risk allele. It was estimated that subjects carrying 13 or more risk alleles were on average 1.46 body mass index units heavier (representing 3.7– 4.7 kg) than carriers of less than three risk alleles. Further research should be focused on a gene‑ gene interaction. An interaction of gene and environment should be statistically analyzed in adequate proband cohorts. If we are able to identify a large number of risk variants, the predisposition to a certain disease could be predicted. Currently a detailed family history has more predictive power.

Key words:
genetics –  Mendelian syndromes with obesity –  polygenic obesity –  polymorphism –  genome- wide association studies


Sources

1. Prader A, Labhart A, Willi H. Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach Myatonieartigem Zustand im Neugeborenenalter. Schweiz Med Wschr 1956; 86: 1260– 1261.

2. Bouchard C, Tremblay A, Després JP et al. The response to long‑term overfeeding in identical twins. N Engl J Med 1990; 322: 1477– 1482.

3. Stunkard AJ, Sørensen TI, Hanis C et al. An adoption study of human obesity. N Engl J Med 1986; 314: 193– 198.

4. Stunkard AJ, Harris JR, Pedersen NL et al. The body‑mass index of twins who have been reared apart. N Engl J Med 1990; 322: 1483– 1487.

5. Zhang Y, Proenca R, Maffei M et al. Positional cloning of the mouse obese gene and its human homologue. Nature 1994; 372: 425– 432.

6. Taubes G. As obesity rates rise, experts struggle to explain why. Science 1998; 280: 1367– 1368.

7. Neel JV. Diabetes mellitus: “thrifty” genotype rendered detrimental by “progress”? Am J Hum Genet 1962; 14: 353– 362.

8. Reilly JJ, Armstrong J, Dorosty AR et al. Early life risk factors for obesity in childhood: cohort study. Br Med J 2005; 330: 1357.

9. Whitaker RC, Wright JA, Koepsell TD et al. Characteristics of children selecting low‑ fat foods in an elementary school lunch program. Arch Pediatr Adolesc Med 1994; 148: 1085– 1091.

10. Magnusson PK, Rasmussen F. Familial resemblance of body mass index and familial risk of high and low body mass index. A study of young men in Sweden. Int J Obes Relat Metab Disord 2002; 26: 1225– 1231.

11. Stunkard AJ, Sørensen TI, Hanis C et al. An adoption study of human obesity. N Engl J Med 1986; 314: 193– 198.

12. Haworth CM, Carnell S, Meaburn EL et al. Increasing heritability of BMI and stronger associations with the FTO gene over childhood. Obesity (Silver Spring) 2008; 16: 2663– 2668.

13. Pietiläinen KH, Kaprio J, Rissanen A et al. Distribution and heritability of BMI in Finnish adolescents aged 16y and 17y: a study of 4 884 twins and 2 509 singletons. Int J Obes Relat Metab Disord 1999; 23: 107– 115.

14. Hainer V, Stunkard AJ, Kunesová M et al. Intrapair resemblance in very low calorie diet‑induced weight loss in female obese identical twins. Int J Obes Relat Metab Disord 2000; 24: 1051– 1057.

15. Rutherford J, McGuffin P, Katz RJ et al. Genetic influences on eating attitudes in a normal female twin population. Psychol Med 1993; 23: 425– 436.

16. Plomin R, Corley R, Carey G et al. Individual differences in television viewing in early childhood: nature as well as nurture. Psychol Sci 1990; 1: 371– 377.

17. Haemer MA, Huang TT, Daniels SR. The effect of neurohormonal factors, epigenetic factors, and gut microbio­ta on risk of obesity. Prev Chronic Dis 2009; 6: A96.

18. Newnham JP, Pennell CE, Lye SJ et al. Early life origins of obesity. Obstet Gynecol Clin North Am 2009; 36: 227– 244.

19. Hainerová I. Obesity based on mutation of genes involved in energy balance. Čas Lék Česk 2007; 146: 240– 245.

20. Caqueret A, Yang C, Duplan S et al. Looking for trouble: a search for developmental defects of the hypothalamus. Horm Res 2005; 64: 222– 230.

21. Tan TM, Vanderpump M, Khoo B et al. Somatostatin infusion lowers plasma ghrelin without reducing appetite in adults with Prader‑ Willi syndrome. J Clin Endocrinol Metab 2004; 89: 4162– 4165.

22. Rankinen T, Zuberi A, Chagnon YC et al. The human obesity gene map: the 2005 update. Obesity (Silver Spring) 2006; 14: 529– 644.

23. Saunders CL, Chiodini BD, Sham P et al. Meta‑analysis of genome‑ wide linkage studies in BMI and obesity. Obesity (Silver Spring) 2007; 15: 2263– 2275.

24. Frayling TM. Genome‑ wide association studies provide new insights into type 2 diabetes aetiology. Nat Rev Genet 2007; 8: 657– 662.

25. Thorleifsson G, Walters GB, Gudbjartsson DF et al. Genome‑ wide association yields new sequence variants at seven loci that associate with measures of obesity. Nat Genet 2009; 41: 18– 24.

26. Loos RJ, Lindgren CM, Li S et al. Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat Genet 2008; 40: 768– 775.

27. Hinney A, Hebebrand J. Three at one swoop! Obes Facts 2009; 2: 3– 8.

28. Hinney A, Hebebrand J. Polygenic obesity in humans. Obes Facts 2008; 1: 35– 42.

29. Geller F, Reichwald K, Dempfle A et al. Melanocortin‑4 receptor gene variant I103 is negatively associated with obesity. Am J Hum Genet 2004; 74: 572– 581.

30. Stutzmann F, Vatin V, Cauchi S et al. Non‑ synonymous polymorphisms in melanocortin‑4 receptor protect against obesity: the two facets of a Janus obesity gene. Hum Mol Genet 2007; 16: 1837– 1844.

31. Heid IM, Vollmert C, Hinney A et al. Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveys. J Med Genet 2005; 42: e21.

32. Young EH, Wareham NJ, Farooqi S et al. The V103I polymorphism of the MC4R gene and obesity: population based studies and meta‑analysis of 29 563 individuals. Int J Obes (Lond) 2007; 31: 1437– 1441.

33. Wang D, Ma J, Zhang S et al. Association of the MC4R V103I Polymorphism With Obesity: A Chinese case‑ control study and metaanalysis in 55,195 individuals. Obesity (Silver Spring) 2010; 18: 573– 579.

34. Stutzmann F, Vatin V, Cauchi S et al. Non‑ synonymous polymorphisms in melanocortin‑4 receptor protect against obesity: the two facets of a Janus obesity gene. Hum Mol Genet 2007; 16: 1837– 1844.

35. Willer CJ, Speliotes EK, Loos RJ et al. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat Genet 2009; 41: 25– 34.

36. Frayling TM, Timpson NJ, Weedon MN et al. A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science 2007; 316: 889– 894.

37. Scott LJ, Mohlke KL, Bonnycastle LL et al. A genome‑ wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 2007; 316: 1341– 1345.

38. Hakanen M, Raitakari OT, Lehtimäki T et al. FTO genotype is associated with body mass index after the age of seven years but not with energy intake or leisure‑time physical activity. J Clin Endocrinol Metab 2009; 94: 1281– 1287.

39. Speakman JR, Rance KA, Johnstone AM. Polymorphisms of the FTO gene are associated with variation in energy intake, but not energy expenditure. Obesity (Silver Spring) 2008; 16: 1961– 1965.

40. Cecil JE, Tavendale R, Watt P et al. An obesity‑associated FTO gene variant and increased energy intake in children. N Engl J Med 2008; 359: 2558– 2566.

41. Wardle J, Carnell S, Haworth CM et al. Obesity associated genetic variation in FTO is associated with diminished satiety. J Clin Endocrinol Metab 2008; 93: 3640– 3643.

42. Jonsson A, Renström F, Lyssenko Vet al. Assessing the effect of interaction between an FTO variant (rs9939609) and physical activity on obesity in 15,925 Swedish and 2,511 Finnish adults. Diabetologia 2009; 52: 1334– 1348.

43. Tanofsky‑ Kraff M, Han JC, Anandalingam K et al. The FTO gene rs9939609 obesity‑ risk allele and loss of control over eating. Am J Clin Nutr 2009; 90: 1483– 1488.

44. Reinehr T, Hinney A, Toschke AM et al. Aggravating effect of INSIG2 and FTO on overweight reduction in a one‑year lifestyle intervention. Arch Dis Child 2009; 94: 965– 967.

45. Herbert A, Gerry NP, McQueen MB et al. A common genetic variant is associated with adult and childhood obesity. Science 2006; 312: 279– 283.

46. Heid IM, Huth C, Loos RJ et al. Meta‑analysis of the INSIG2 association with obesity including 74, 345 individuals: does heterogeneity of estimates relate to study design? PLoS Genet 2009; 5: e1000694.

47. Sha BY, Yang TL, Zhao LJ et al. Genome‑ wide association study suggested copy number variation may be associated with body mass index in the Chinese population. J Hum Genet 2009; 54: 199– 202.

48. Hainer V, Zamrazilová H, Spálová J et al. Role of hereditary factors in weight loss and its maintenance. Physiol Res 2008; 57 (Suppl 1): S1– S15.

49. Yoon Y, Park BL, Cha MH et al. Effects of genetic polymorphisms of UCP2 and UCP3 on very low calorie diet‑induced body fat reduction in Korean female subjects. Biochem Biophys Res Commun 2007; 359: 451– 456.

50. Soenen S, Mariman EC, Vogels N et al. Relationship between perilipin gene polymorphisms and body weight and body composition during weight loss and weight maintenance. Physiol Behav 2009; 96: 723– 728.

51. Hinney A, Vogel CI, Hebebrand J. From monogenic to polygenic obesity: recent advances. Eur Child Adolesc Psychiatry 2010; 19: 297– 310.

Labels
Diabetology Endocrinology Internal medicine
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