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Insulin resistant phenotype of polycystic ovary syndrome does not seem to be caused by variation in FTO.
Horm. Metab. Res. 44, 810-813 (2012)
Genetic variation in the FTO gene is associated with increased body weight and reduced insulin sensitivity. We investigated whether genetic variation in FTO is associated with polycystic ovary syndrome (PCOS), a condition also characterized by insulin resistance. Furthermore, we tested whether insulin resistance is specifically associated with genetic variation in FTO in women with PCOS. Sixty-two nondiabetic patients with PCOS defined by the Rotterdam criteria were compared to BMI and age-matched women. Each PCOS case was matched to 2 controls. All participants underwent an oral glucose tolerance test and were genotyped for the single nucleotide polymorphism rs8050136 in the FTO gene. There was no difference in the frequency of FTO genotypes between the PCOS and the non-PCOS groups. In non-PCOS participants, genetic variation in FTO is associated with insulin sensitivity (p = 0.03). This association remained significant after adjustment for age and/or BMI (p < = 0.03). In subjects with PCOS, however, FTO did not associate with insulin sensitivity (p = 0.67). Genetic variation in FTO does not have an impact on insulin sensitivity in women with PCOS and is therefore not involved in the pathogenesis of the insulin resistant phenotype seen in patients with PCOS.
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Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Fto ; Polycystic Ovary Syndrome (pcos) ; Insulin Resistance ; Matched Case-control Study; Body-fat Distribution ; Diagnostic-criteria ; Syndrome Pcos ; Gene ; Women ; Prevalence ; Obesity ; Association ; Variants ; Glucose
Language
english
Publication Year
2012
HGF-reported in Year
2012
ISSN (print) / ISBN
0018-5043
e-ISSN
1439-4286
Journal
Hormone and Metabolic Research
Quellenangaben
Volume: 44,
Issue: 11,
Pages: 810-813
Publisher
Thieme
Reviewing status
Peer reviewed
POF-Topic(s)
90000 - German Center for Diabetes Research
Research field(s)
Helmholtz Diabetes Center
PSP Element(s)
G-502400-001
G-502400-002
G-502400-002
PubMed ID
22847851
WOS ID
WOS:000309654800003
Erfassungsdatum
2012-11-15