An uncoupling protein 2 gene variant is associated with a raised body mass index but not Type II diabetes

• Published in: Diabetologia Vol. 42; no. 6; pp. 688 - 692
• Main Authors: CASSELL, P. G, NEVEROVA, M, EASLICK, J, RAMACHANDRAN, A, SNEHALATHA, C, PECQUEUR, C, RICQUIER, D, WARDEN, C, HITMAN, G. A, JANMOHAMED, S, UWAKWE, N, QURESHI, A, MCCARTHY, M. I, SAKER, P. J, ALBON, L, KOPELMAN, P, NOONAN, K
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01.06.1999; Springer Nature B.V
• Subjects: Adult; Animals; Biological and medical sciences; Body fat; Body Mass Index; Body Weight; Diabetes Mellitus, Type 2 - epidemiology; Diabetes Mellitus, Type 2 - genetics; Electrophoresis, Agar Gel; Exons; Female; Genetic Predisposition to Disease; Humans; India - ethnology; Ion Channels; Male; Medical sciences; Membrane Transport Proteins; Metabolic diseases; Mice; Middle Aged; Mitochondrial Proteins; Obesity; Proteins - genetics; Protons; Risk Factors; Uncoupling Protein 2; United Kingdom - epidemiology; Urban Health; Asia; India; United Kingdom > UK; Endocrinopathy; Human; Obesity; Metabolic disorder; Association; Uncoupling protein; Gene; Leptin; Body weight; Non insulin dependent diabetes; Polymorphism
• ISSN: 0012-186X; 1432-0428
• DOI: 10.1007/s001250051216

Linkage between markers close to the uncoupling protein 2 and 3 genes (11q13) and resting metabolic rate and a pre-diabetic phenotype have been found. The syntenic region in mouse has been found to be linked to quantitative traits associated with obesity and diabetes. UCP2 and UCP3 could therefore have an important role in body weight regulation and susceptibility to diabetes. We investigated a recently identified variant of the UCP2 gene in exon 8 as a marker for glucose and weight homeostasis. Length variation of the UCP2 exon 8 variant was studied by the polymerase chain reaction and agarose gel electrophoresis. Sequence variants of the UCP3 gene were sought by semi-automated DNA sequencing. In 453 South Indian subjects, we found an association in women between the UCP2 exon variant and body mass index (p = 0.018). These findings were replicated in a separate group of South Indian subjects (n = 143, p < 0.001) irrespective of sex. Although no association was found between the UCP2 exon 8 variant and overt obesity in British subjects, the UCP2 genotype of obese women (n = 83) correlated with fasting serum leptin concentration (p = 0.006) in the presence of extreme obesity. These observations could not be explained by tight linkage disequilibrium with a coding region variant in the region of the UCP3 gene of biological significance. Lastly, no association was found between UCP2 and Type II (non-insulin-dependent) diabetes using either a family based design (85 families) or case control study (normal glucose tolerance n = 335, impaired glucose tolerance n = 42, Type II diabetes n = 76). We have described a UCP2 gene exon 8 variant that may affect susceptibility to weight gain by influencing regulation of leptin.