Osteoprotegerin, fibroblast growth factor 23, and vitamin D3 levels in male patients with hypogonadism


MERİÇ C., Sonmez A., Aydogdu A., Tapan S., HAYMANA C., Basaran Y., ...Daha Fazla

Hormone and Metabolic Research, cilt.46, sa.13, ss.955-958, 2014 (SCI-Expanded, Scopus)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 46 Sayı: 13
  • Basım Tarihi: 2014
  • Doi Numarası: 10.1055/s-0034-1387789
  • Dergi Adı: Hormone and Metabolic Research
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.955-958
  • Anahtar Kelimeler: hypogonadism, asymmetric dimethyl arginine, osteoprotegerin, fibroblast growth factor-23, vitamin D3
  • Sağlık Bilimleri Üniversitesi Adresli: Evet

Özet

Cardiometabolic disorders and osteoporosis are prevalent in patients with hypogonadism. Osteoprotegerin (OPG) and fibroblast growth factor-23 (FGF-23), are co-secreted from bones and vascular endothelium, regulating bone mineral metabolism and vascular functions. Vitamin D is another hormone with dual effects on bone and vascular metabolism. The aim of this study was to search for any difference between the serum levels of OPG, FGF-23, and vitamin D in patients with hypogonadism and the healthy controls. We also aimed to search for any relationship between these parameters and endothelial dysfunction or insulin resistance. Forty-nine male patients with congenital hypogonadotropic hypogonadism (CHH) (mean age 20.71±1.75 years) and 43 BMI matched healthy male subjects (mean age 21.37±1.04 years) were enrolled. OPG, FGF-23, vitamin D, and asymmetric dimethylarginine (ADMA) levels were measured from the fasting serum samples. The insulin sensitivity was estimated by homeostatic model assessment-insulin resistance (HOMA-IR) formula. Triglycerides, insulin, HOMA-IR, and ADMA levels in the patient group were significantly higher than the values of the control group (p=0.014, p=0.002, p=0.003, p<0.001, respectively). The OPG, FGF-23, and vitamin D levels of the patients were not significantly different from the healthy controls. In addition, these markers were not correlated to ADMA or HOMA-IR levels. The results show that young and treatment naive subjects with CHH have endothelial dysfunction and insulin resistance when compared to their healthy counterparts. However, the OPG, FGF-23, and vitamin D levels were similar in the 2 groups. In addition, these parameters are not significantly related to the endothelial functions or insulin resistance in these subjects.