Adipose tissue insulin resistance in peripubertal girls with first-degree family history of polycystic ovary syndrome  

Oleh:

Trottier, Andréanne ; Battista, Marie-Claude ; Geller, David H. ; Moreau, Brigitte

Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: Fertility and Sterility (keterangan: ada di ClinicalKey) vol. 98 no. 06 (Dec. 2012), page 1627-1634.
Topik: REPRODUCTIVE ENDOCRINOLOGY; Polycystic ovary syndrome; nonesterified fatty acids; insulin resistance; adipose tissue metabolism; adolescents/children

Ketersediaan

Perpustakaan FK Nomor Panggil: F02.K.2012.03 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

Lihat Detail Induk

Isi artikel

Objective To assess metabolic and endocrine defects in girls genetically predisposed to polycystic ovary syndrome (PCOS). Design Controlled cross-sectional study. Setting University hospital. Patient(s) Nine girls, aged 8–14 years, having a first-degree relative diagnosed with PCOS (PCOSr) and 10 age-matched girls without a family history of PCOS. Intervention(s) None. Main Outcome Measure(s) Insulin sensitivity (ISFSIVGTT) determined by frequently sampled IV glucose tolerance testing (GTT) and insulin-induced nonesterified fatty acid (NEFA) suppression, estimated by the log-linear slope of NEFA levels during the first 20 minutes of GTT. Result(s) In comparison to controls, PCOSr had higher body mass index (BMI) Z-score, waist circumference, and waist-to-height ratio. Levels of the androgen 17a-hydroxyprogesterone (17-OHP) were significantly increased in PCOSr, independent of adiposity, and inversely correlated with ISFSIVGTT. The ISFSIVGTT was decreased and the NEFA suppression was less steep in PCOSr compared with controls, independent of BMI and 17-OHP. The NEFA suppression was more pronounced with increasing ISFSIVGTT, independent of adiposity. Conclusion(s) Girls at high risk of developing PCOS display increased adiposity and 17-OHP levels, but are mainly characterized by global insulin resistance and resistance to insulin-induced suppression of lipolysis that were independent of adiposity and 17-OHP levels. Therefore, genetic predisposition to PCOS may be related to early insulin resistance and adipocyte dysfunction.

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