The role of uncoupling protein 2 and 3 genes polymorphism and energy expenditure in obese Indonesian children
-
Maria Mexitalia
, Taro Yamauchi
, Agustini Utari , Damayanti R. Sjarif , Hertanto W. Subagio , Agustinus Soemantri and Takafumi Ishida
Abstract
Aim: Uncoupling protein (UCP) genes, which may contribute to energy metabolism in mitochondria, may be involved in the pathogenesis of obesity. We analyzed the differences in energy expenditure between single nucleotide polymorphisms (SNPs) UCP3-55C/T, UCP3 Y210Y, and UCP2 A55V among Indonesian children.
Methods: The study included 76 schoolchildren (36 obese and 40 healthy; mean age, 12.8 years) in Semarang, Indonesia. Body composition was measured by bioelectrical impedance analysis; resting energy expenditure (REE) by indirect calorimetry; physical activity by uniaxial accelerometer; and total energy expenditure (TEE) by the equations extrapolated from REE and physical activity. UCP3-55C/T, UCP3 Y210Y, and UCP2 A55V were examined by restriction length fragment polymorphism analysis.
Results: The TEE of the subjects with the T/T genotype at UCP3-55C/T after adjusting for fat-free mass (63.2±7.2 kcal/kg/day) and T/T at UCP2 A55V (62.8±5.6 kcal/kg/day) was lower than that of the subjects with the C/C and C/T genotypes (p<0.05). The REE of the subjects with these T/T genotypes tended to be lower than that of the subjects with C/C and C/T (p≥0.05). No significant differences in REE or TEE were found between the UCP3 Y210Y genotypes.
Conclusions: The subjects with the T/T genotypes of UCP3-55C/T or UCP2 A55V had lower TEE than those with other genotypes.
References
1. Haslam DW, James WP. Obesity. Lancet 2005;366:1197–209.Search in Google Scholar
2. Koletzko B, Girardet JP, Klish W, Tabacco O. Obesity in children and adolescents worldwide: current views and future directions – working group report of the first World Congress of Pediatric Gastroenterology, Hepatology, and Nutrition. J Pediatr Gastroenterol Nutr 2002;35:S205–12.Search in Google Scholar
3. FAO, Food and Nutrition Technical Report Series. Human energy requirements. Report of a joint FAO/WHO/UNU Expert Consultation. Rome: FAO, 2001:17–24.Search in Google Scholar
4. Goran M. Measurement issues related to studies of childhood obesity: assessment of body composition, body fat distribution, physical activity, and food intake. Pediatrics 1998;101:505–18.Search in Google Scholar
5. Kohl III HW, Hobbs KE. Development of physical activity behaviors among children and adolescents. Pediatrics 1998;101:549–55.Search in Google Scholar
6. Clement K, Ferre P. Genetics and pathophysiology of obesity. Pediatr Res 2003;53:721–5.Search in Google Scholar
7. Rankinen T, Zuberi A, Chagnon YC, Weisnagel SJ, Argyropoulos G, et al. The human obesity gene map: the 2005 update. Obesity 2006;14:529–644.Search in Google Scholar
8. Li S, Loos RJ. Progress in the genetics of common obesity: size matters. Curr Opin Lipidol 2008;19:113–21.Search in Google Scholar
9. Nedergaard J, Cannon B. The novel uncoupling protein UCP2 and UCP3: what do they really do? Pros and cons for suggested functions. Exp Physiol 2003;88:65–84.Search in Google Scholar
10. Nubel T, Ricquier D. Respiration under control of uncoupling proteins: clinical perspective. Horm Res 2006;65:300–10.Search in Google Scholar
11. Sudoyo H. Uncoupling protein (UCP) dan metabolisme energi. In: Tjokroprawiro A, Soegih R, Soegondo S, Wijaya A, Sutardjo B, et al., editors. The 3rd National Obesity Symposium. Jakarta: ISSO, 2004:15–30.Search in Google Scholar
12. Dalgaard LT, Pedersen O. Uncoupling proteins: functional characteristics and role in the pathogenesis of obesity and type II diabetes. Diabetologia 2001;40:946–65.Search in Google Scholar
13. Urhammer SA, Dalgaard LT, Sorensen TI, Tybjaerg-Hansen A, Echwald SM, et al. Organisation of the coding exons and mutational screening of the uncoupling protein 3 gene in subjects with juvenile-onset obesity. Diabetologia 1998;41:241–4.Search in Google Scholar
14. Kovacs P, Ma L, Hanson RL, Franks P, Stumvoll M, et al. Genetic variation in UCP2 (uncoupling protein-2) is associated with energy metabolism in Pima Indians. Diabetologia 2005;48:2292–5.Search in Google Scholar
15. Schrauwen P, Xia J, Bogardus C, Prately RE, Ravussin E. Skeletal muscle uncoupling protein 3 expression is a determinant of energy expenditure in Pima Indians. Diabetes 1999;48:146–9.Search in Google Scholar
16. Bouchard C, Perusse L, Chagnon YC, Warden C, Ricquier D. Linkage between markers in the vicinity of the uncoupling protein 2 gene and resting metabolic rate. Hum Mol Genet 1997;6:1887–9.Search in Google Scholar
17. Walder K, Norman RA, Hanson RL, Schrauwen P, Neverova M, et al. Association between uncoupling protein polymorphisms (UCP2-UCP3) and energy metabolism/obesity in Pima Indians. Human Mol Genet 1998;7:1431–5.Search in Google Scholar
18. Yanovski JA, Diament AL, Sovik KN, Nguyen TT, Li H, et al. Associations between uncoupling protein 2, body composition, and resting energy expenditure in lean and obese African American, Caucasian, and Asian children. Am J Clin Nutr 2000;71:1405–12.Search in Google Scholar
19. Argyropoulos G, Brown AM, Willi SM, Zhu J, He Y, et al. Mutations in the human uncoupling protein 3 gene on the respiratory quotient and fat oxidation in severe obesity and type 2 diabetes. J Clin Invest 1998;102:1345–51.Search in Google Scholar
20. Astrup A, Toubro S, Dalgaard LT, Urhammer SA, Sorensen TI, et al. Impact of the v/v 55 polymorphism of the uncoupling protein 2 gene on 24-h energy expenditure and substrate oxidation. Int J Obes 1999;23:1030–4.Search in Google Scholar
21. Kimm SY, Glynn NW, Aston CE, Damcott CM, Poehlman ET, et al. Racial differences in the relation between uncoupling protein genes and resting energy expenditure. Am J Clin Nutr 2002;75:714–9.Search in Google Scholar
22. Buemann B, Schierning B, Toubro S, Bibby BM, Sorensen T, et al. The association between the val/ala-55 polymorphism of the uncoupling protein 2 gene and exercise efficiency. Int J Obes 2001;25:467–71.Search in Google Scholar
23. Berentzen T, Dalgaard LT, Petersen L, Pedersen O, Sorensen TI. Interaction between physical activity and variants of the genes encoding uncoupling proteins-2 adn-3 in relation to body weight changes during a 10-y follow-up. Int J Obes 2005;29:93–9.Search in Google Scholar
24. Chung WK, Luke A, Cooper RS, Rotini C, Vidal-Puig A, et al. Genetic and physiologic analysis of the role of uncoupling protein 3 in human energy homeostasis. Diabetes 1999;48:1890–5.Search in Google Scholar
25. Jun HS, Kim IK, Lee HJ, Lee HJ, Kang JH, et al. Effects of UCP2 and UCP3 variants on the manifestation of overweight in Korean children. Obesity 2009;17:355–62.Search in Google Scholar
26. Ochoa MC, Santos JL, Azcona C, Moreno-Aliaga MJ, Martınnez-Gonzalez MA, et al. Association between obesity and insulin resistance with UCP2–UCP3 gene variants in Spanish children and adolescents. Mol Genet Metab 2007;92:351–8.Search in Google Scholar
27. Alonso A, Marti A, Corbalan MS, Martinez-Gonzales MA, Forga L, et al. Association of UCP3 gene -55C/T polymorphism and obesity in a Spanish population. Ann Nutr Metab 2005;49:183–8.Search in Google Scholar
28. Hosking J, Metcalf BS, Jeffery AN, Voss LD, Wilkin TJ. Validation of foot-to-foot bioelectrical impedance analysis with dual-energy X-ray absorptiometry in the assessment of body composition in young children: the EarlyBird cohort. Br J Nutr 2006;96:1163–8.Search in Google Scholar
29. L’Abee C, Visser GH, Liem WT, Kok DE, Sauer PJ, et al. Comparison of methods to assess body fat in non-obese six to seven-year-old children. ClinNutr 2010;29:317–22.Search in Google Scholar
30. Yamauchi T, Ohtsuka R. Basal metabolic rate and energy costs at rest and during exercise in rural- and urban-dwelling Papua New Guinea Highlanders. Eur J Clin Nutr 2000;54: 494–9.Search in Google Scholar
31. Yamauchi T, Kim SN, Lu Z, Ichimaru N, Maekawa R, et al. Age and gender differences in the physical activity patterns of urban schoolchildren in Korea and China. J Physiol Anthropol 2007;26:101–7.Search in Google Scholar
32. Kumahara H, Schutz Y, Ayabe M, Yoshioka M, Yoshitake Y, et al. The use of uniaxial accelerometry for the assessment of physical-activity-related energy expenditure: a validation study against whole-body indirect calorimetry. Br J Nutr 2004;91:235–43.Search in Google Scholar
33. Liu YJ, Liu PY, Long J, Lu Y, Elze L, et al. Linkage and association analyses of the UCP3 gene with obesity phenotypes in Caucasian families. Physiol Genomics 2005;22:197–203.Search in Google Scholar
34. Argyropoulos G, Harper ME. Molecular biology of thermoregulation. Invited review: uncoupling proteins and thermoregulation. J Appl Physiol 2002;92:2187–98.Search in Google Scholar
35. Lanouette CM, Giacobino JP, Pérusse L, Lacaille M, Yvon C, et al. Association between uncoupling protein 3 gene and obesity-related phenotypes in the Québec family study. Mol Med 2001;7:433–41.Search in Google Scholar
36. Lanouette CM, Chagnon YC, Rice T, Perusse L, Muzzin P, et al. Uncoupling protein 3 gene is associated with body composition changes with training in Heritage study. J Appl Physiol 2002;92:1111–8.Search in Google Scholar
©2013 by Walter de Gruyter Berlin Boston
Articles in the same Issue
- Masthead
- Masthead
- Editorial
- Success has many fathers, failure is orphan
- Review Article
- Normosmic idiopathic hypogonadotropic hypogonadism: update on the genetic background and future challenges
- Original Articles
- Temporary brittle bone disease: association with intracranial bleeding
- Asymmetric dimethylarginine (ADMA) and L-arginine levels in children with glycogen storage disease type I
- Application of liquid chromatography-tandem mass spectrometry in the diagnosis and follow-up of maple syrup urine disease in a Chinese population
- The role of uncoupling protein 2 and 3 genes polymorphism and energy expenditure in obese Indonesian children
- Thyroid dysfunctions of prematurity and their impacts on neurodevelopmental outcome1)
- Frequency of the E23K polymorphism of the KCNJ11 gene in children born small for gestational age and its influence on auxological and metabolic parameters in the prepubertal period
- Reference intervals for serum thyroid hormones in preterm hospitalized infants1)
- The clinical and biochemical presentation of vitamin D deficiency and insufficiency in children and adolescents
- A risk score for identifying overweight adolescents with dysglycemia in primary care settings1)
- Thyroid function and morphology in overweight and obese children and adolescents in a Chinese population
- Propionic acidaemia: demographic characteristics and complicationsa
- Negative correlation between serum IL-6 level and cardiorespiratory fitness in 10- to 11-year-old boys with increased BMI
- Penile length and genital anomalies in Egyptian male newborns: epidemiology and influence of endocrine disruptors
- Efficacy of vitamin D loading doses on serum 25-hydroxy vitamin D levels in school going adolescents: an open label non-randomized prospective trial
- Characteristics of infants admitted with hypoglycemia to a neonatal unit
- Increasing thyroid-stimulating hormone is associated with impaired glucose metabolism in euthyroid obese children and adolescents
- The role of FTO genotype on eating behavior in obese Sardinian children and adolescents
- Prevalence of multiple forms of autoimmunity in Egyptian patients with Turner syndrome: relation to karyotype
- A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree
- Patient Reports
- Pseudohypoparathyroidism type Ia: a novel GNAS mutation in a Brazilian boy presenting with an early primary hypothyroidism
- Diabetic ketoacidosis with cerebral hemorrhage and alpha coma in an adolescent female
- A novel mutation in thyrotropin (thyroid-stimulating hormone) gene in congenital hypothyroidism
- Citric acid as the last therapeutic approach in an acute life-threatening metabolic decompensation of propionic acidaemia
- A case of autosomal dominant osteopetrosis type II with a novel TCIRG1 gene mutation
- The interpretation of color – an endocrine cause of skin discoloration mimicking cyanosis
- Novel heterozygous thyrotropin receptor mutation presenting with neonatal hyperthyrotropinaemia, mild thyroid hypoplasia and absent uptake on radioisotope scan
- Turner Syndrome and apparent absent uterus: a case report and review of the literature
- 10.1515/jpem-2012-0133
- Vaginal bleeding in a 4-month-old preterm girl: extreme minipuberty mimicking central precocious puberty
- A rare case of isolated Cushing syndrome in a 3-month-old boy
- Letters to the Editors
- Gynecomastia in puberty is usually asymptomatic and regresses spontaneously
- Is endometriosis ultimately the end result of the interplay between interferon-γ (IFN-γ) and the HOXA10 gene network?
- Does treatment with L-selenomethionine reduce thyroid volume in euthyroid children with autoimmune thyroiditis?
- Meetings
- Meetings Calendar
Articles in the same Issue
- Masthead
- Masthead
- Editorial
- Success has many fathers, failure is orphan
- Review Article
- Normosmic idiopathic hypogonadotropic hypogonadism: update on the genetic background and future challenges
- Original Articles
- Temporary brittle bone disease: association with intracranial bleeding
- Asymmetric dimethylarginine (ADMA) and L-arginine levels in children with glycogen storage disease type I
- Application of liquid chromatography-tandem mass spectrometry in the diagnosis and follow-up of maple syrup urine disease in a Chinese population
- The role of uncoupling protein 2 and 3 genes polymorphism and energy expenditure in obese Indonesian children
- Thyroid dysfunctions of prematurity and their impacts on neurodevelopmental outcome1)
- Frequency of the E23K polymorphism of the KCNJ11 gene in children born small for gestational age and its influence on auxological and metabolic parameters in the prepubertal period
- Reference intervals for serum thyroid hormones in preterm hospitalized infants1)
- The clinical and biochemical presentation of vitamin D deficiency and insufficiency in children and adolescents
- A risk score for identifying overweight adolescents with dysglycemia in primary care settings1)
- Thyroid function and morphology in overweight and obese children and adolescents in a Chinese population
- Propionic acidaemia: demographic characteristics and complicationsa
- Negative correlation between serum IL-6 level and cardiorespiratory fitness in 10- to 11-year-old boys with increased BMI
- Penile length and genital anomalies in Egyptian male newborns: epidemiology and influence of endocrine disruptors
- Efficacy of vitamin D loading doses on serum 25-hydroxy vitamin D levels in school going adolescents: an open label non-randomized prospective trial
- Characteristics of infants admitted with hypoglycemia to a neonatal unit
- Increasing thyroid-stimulating hormone is associated with impaired glucose metabolism in euthyroid obese children and adolescents
- The role of FTO genotype on eating behavior in obese Sardinian children and adolescents
- Prevalence of multiple forms of autoimmunity in Egyptian patients with Turner syndrome: relation to karyotype
- A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree
- Patient Reports
- Pseudohypoparathyroidism type Ia: a novel GNAS mutation in a Brazilian boy presenting with an early primary hypothyroidism
- Diabetic ketoacidosis with cerebral hemorrhage and alpha coma in an adolescent female
- A novel mutation in thyrotropin (thyroid-stimulating hormone) gene in congenital hypothyroidism
- Citric acid as the last therapeutic approach in an acute life-threatening metabolic decompensation of propionic acidaemia
- A case of autosomal dominant osteopetrosis type II with a novel TCIRG1 gene mutation
- The interpretation of color – an endocrine cause of skin discoloration mimicking cyanosis
- Novel heterozygous thyrotropin receptor mutation presenting with neonatal hyperthyrotropinaemia, mild thyroid hypoplasia and absent uptake on radioisotope scan
- Turner Syndrome and apparent absent uterus: a case report and review of the literature
- 10.1515/jpem-2012-0133
- Vaginal bleeding in a 4-month-old preterm girl: extreme minipuberty mimicking central precocious puberty
- A rare case of isolated Cushing syndrome in a 3-month-old boy
- Letters to the Editors
- Gynecomastia in puberty is usually asymptomatic and regresses spontaneously
- Is endometriosis ultimately the end result of the interplay between interferon-γ (IFN-γ) and the HOXA10 gene network?
- Does treatment with L-selenomethionine reduce thyroid volume in euthyroid children with autoimmune thyroiditis?
- Meetings
- Meetings Calendar