Abstract
OBJECTIVE: Uncoupling protein 3 (UCP-3) uncouples oxidative metabolism from ATP synthesis, resulting in the production of heat instead of energy storage. Single nucleotide polymorphisms (SNPs) in UCP-3 might result in a reduced function or expression of UCP-3 and therefore lead to an increased capacity to store energy as fat.
DESIGN: We conducted a population-based, cross-sectional single-center study among 400 Dutch men between 40 and 80 years.
METHODS: Seven SNPs in the UCP-3 gene were genotyped by means of an allele-specific real-time TaqMan PCR. Linear regression analyses were performed to examine the independent effects of these SNPs on obesity phenotypes.
RESULTS: We found a significant association between homozygosity for the minor allele of rs647126, rs1685356, and rs2075577 and an increase in body mass index (BMI; P=0.033, P=0.016, and P=0.019 respectively). Heterozygosity for rs1685354 was associated with a significant decrease in visceral fat mass (P=0.030).
CONCLUSIONS: Our results suggest that genetic variations in the UCP-3 gene are associated with an increase in BMI. A plausible mechanism by which these SNPs lead to an increase in BMI is that due to these SNPs, the UCP-3 activity might be decreased. As a result, uncoupling activity may also decrease, which will lead to an increase in body weight and BMI.
| Original language | English |
|---|---|
| Pages (from-to) | 669-76 |
| Number of pages | 8 |
| Journal | European Journal of Endocrinology |
| Volume | 158 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - 2008 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Adenosine Triphosphate
- Adipose Tissue
- Adult
- Aged
- Aged, 80 and over
- Body Mass Index
- Cross-Sectional Studies
- Genetic Predisposition to Disease
- Genetic Variation
- Genotype
- Humans
- Ion Channels
- Male
- Middle Aged
- Mitochondrial Proteins
- Netherlands
- Obesity
- Phenotype
- Polymorphism, Single Nucleotide
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