Fat mass and obesity associated gene variants are associated with increased growth hormone levels and affect glucose and lipid metabolism in lean women
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26680478
DOI
10.33549/physiolres.933088
PII: 933088
Knihovny.cz E-zdroje
- MeSH
- adipozita fyziologie MeSH
- dospělí MeSH
- gen pro FTO MeSH
- genetická variace genetika MeSH
- glukosa metabolismus MeSH
- hubenost krev diagnóza genetika MeSH
- index tělesné hmotnosti MeSH
- kohortové studie MeSH
- lidé MeSH
- lidský růstový hormon krev MeSH
- metabolismus lipidů fyziologie MeSH
- mladý dospělý MeSH
- obezita krev genetika MeSH
- proteiny genetika MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mladý dospělý MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- FTO protein, human MeSH Prohlížeč
- gen pro FTO MeSH
- glukosa MeSH
- lidský růstový hormon MeSH
- proteiny MeSH
First intron variability of the fat mass and obesity associated gene (FTO) has strong impact on adiposity. We focused on lean women carrying the most "obesity-risk" haplotype to study their anthropometric parameters and hormonal and metabolic profile. Genotype-phenotype correlation was performed in a group of 172 lean women (body mass index (BMI) >/=18.5 and 25 kg/m(2); age 26.8+/-7.26 years), 77 of them used hormonal contraceptives. Even in lean women the association of the risk haplotype CAGA with BMI was confirmed but it did not influence the anthropometric indices of body composition. CAGA carriers compared to non-carriers had significantly higher both fasting (p=0.016) and post glucose load (p<0.001) levels of growth hormone (GH), significantly higher glucose, insulin and C-peptide levels in the late phase of oGTT and lower fasting concentration of total cholesterol and LDL-cholesterol. Administration of hormonal contraceptives further increased observed hormonal and metabolic effects in CAGA carriers. We conclude that higher levels of GH in lean women carrying the FTO "obesity risk" haplotype could protect them from the development of obesity. The relation between the FTO gene variability and GH secretion has to be elucidated. This is the first study demonstrating the interaction of FTO genotype with hormonal contraception.
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