論文

査読有り 国際誌
2009年2月

Relationships between serum adiponectin levels versus bone mineral density, bone metabolic markers, and vertebral fractures in type 2 diabetes mellitus.

European journal of endocrinology
  • Ippei Kanazawa
  • ,
  • Toru Yamaguchi
  • ,
  • Masahiro Yamamoto
  • ,
  • Mika Yamauchi
  • ,
  • Shozo Yano
  • ,
  • Toshitsugu Sugimoto

160
2
開始ページ
265
終了ページ
73
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1530/EJE-08-0642

BACKGROUND: Although, adiponectin might be associated with bone metabolism, the relationships between serum adiponectin and bone mineral density (BMD) as well as vertebral fracture in type 2 diabetes are still unclear. OBJECTIVE AND METHODS: We investigated the relationships between each of serum total and high molecular weight (HMW) adiponectin versus BMD, bone markers, and the presence of vertebral fractures in a total of 231 men and 170 post-menopausal women with type 2 diabetes. RESULTS: Multiple regression analysis adjusted for age, duration of diabetes, BMI, serum creatinine, and HbA(1c) showed that serum total adiponectin was negatively correlated with BMD at the total, lumbar spine, and femoral neck (r=-0.165, P<0.05; r=-0.187, P<0.05; and r=-0.136, P<0.05 respectively) and positively with urinary N-terminal cross-linked telopeptide of type-I collagen in men (r=0.148, P<0.05), and that serum HMW adiponectin was negatively correlated with BMD at the lumbar spine (r=-0.146, P<0.05). Multivariate logistic regression analysis adjusted for the parameters described above showed that total adiponectin was associated with the presence of vertebral fractures in men (odds ratio (OR)=1.396, 95% confidential interval (CI) 1.020-1.911 per s.d. increase, P<0.05), and both total and HMW adiponectin were associated with moderate or severe vertebral fractures (OR=1.709, 95% CI 1.048-2.787 per s.d. increase, P<0.05 and OR=1.810, 95% CI 1.112-2.946 per s.d. increase, P<0.05 respectively), but not in post-menopausal women. CONCLUSIONS: Serum adiponectin could be associated with BMD and turnover and clinically useful for assessing the risk of vertebral fractures in type 2 diabetic men.

リンク情報
DOI
https://doi.org/10.1530/EJE-08-0642
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/18996964
ID情報
  • DOI : 10.1530/EJE-08-0642
  • PubMed ID : 18996964

エクスポート
BibTeX RIS