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Metabolic and hormonal consequencies of the "obesity risk" MC4R variant (rs12970134) in Czech women
O. Bradnová, D. Vejražková, M. Vaňková, P. Lukášová, J. Včelák, S. Stanická, K. Dvořáková, B. Bendlová
Language English Country Czech Republic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NT13544
MZ0
CEP Register
Digital library NLK
Full text - Article
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NLK
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- MeSH
- Adult MeSH
- Genetic Predisposition to Disease epidemiology genetics MeSH
- Genetic Variation genetics MeSH
- Cohort Studies MeSH
- Middle Aged MeSH
- Humans MeSH
- Obesity blood epidemiology genetics MeSH
- Receptor, Melanocortin, Type 4 genetics MeSH
- Risk Factors MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
Although the mutations in MC4R gene became known as the most common genetic cause of human obesity, the effect of rs12970134 A/G near MC4R gene on insulin resistance has been described. The aim of this study was to determine the effect of rs12970134 on obesity, hormone levels, and glucose metabolism in a cohort of women varying in glucose tolerance: 850 normoglycemic women, 423 diagnosed with polycystic ovary syndrome (PCOS), 402 gestational diabetics (GDM), and 250 type 2 diabetic (T2D) women. We did not confirm the explicit effect of rs12970134 on obesity. However, the influence of the A-allele on body adiposity index was observed in a cohort of women diagnosed with PCOS. In normoglycemic women, the A-allele carriership was associated with lower fasting levels of glucose, insulin, C-peptide, and index of insulin resistance. Furthermore, higher levels of growth hormone, leptin and SHBG, and lower levels of fT3, testosterone, and androstenedione were recorded in normoglycemic A-allele carriers. In conclusion, the study presents the evidence of the impact of rs12970134 on complex hypothalamic regulations.
References provided by Crossref.org
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