4.3 Article

Common variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/2), adiponectin concentrations, and diabetes incidence in the Diabetes Prevention Program

期刊

DIABETIC MEDICINE
卷 29, 期 12, 页码 1579-1588

出版社

WILEY
DOI: 10.1111/j.1464-5491.2012.03662.x

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资金

  1. Swedish Research Council
  2. Swedish Heart-Lung Foundation
  3. Pahlssons Foundation
  4. Swedish Diabetes Association
  5. Novo Nordisk
  6. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) of the National Institutes of Health
  7. NIDDK
  8. Indian Health Service
  9. Office of Research on Minority Health
  10. National Institute of Child Health and Human Development
  11. National Institute on Aging
  12. Centers for Disease Control and Prevention
  13. Office of Research on Women's Health
  14. American Diabetes Association
  15. Henry M. Jackson Foundation
  16. [DK072041]
  17. Novo Nordisk Fonden [NNF11OC1014855] Funding Source: researchfish

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Diabet. Med. 29, 15791588 (2012) Abstract Aims Baseline adiponectin concentrations predict incident Type 2 diabetes mellitus in the Diabetes Prevention Program. We tested the hypothesis that common variants in the genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1, ADIPOR2) would associate with circulating adiponectin concentrations and/or with diabetes incidence in the Diabetes Prevention Program population. Methods Seventy-seven tagging single-nucleotide polymorphisms (SNPs) in ADIPOQ (24), ADIPOR1 (22) and ADIPOR2 (31) were genotyped. Associations of SNPs with baseline adiponectin concentrations were evaluated using linear modelling. Associations of SNPs with diabetes incidence were evaluated using Cox proportional hazards modelling. Results Thirteen of 24 ADIPOQ SNPs were significantly associated with baseline adiponectin concentrations. Multivariable analysis including these 13 SNPs revealed strong independent contributions of rs17366568, rs1648707, rs17373414 and rs1403696 with adiponectin concentrations. However, no ADIPOQ SNPs were directly associated with diabetes incidence. Two ADIPOR1 SNPs (rs1342387 and rs12733285) were associated with similar to 18% increased diabetes incidence for carriers of the minor allele without differences across treatment groups, and without any relationship with adiponectin concentrations. Conclusions ADIPOQ SNPs are significantly associated with adiponectin concentrations in the Diabetes Prevention Program cohort. This observation extends prior observations from unselected populations of European descent into a broader multi-ethnic population, and confirms the relevance of these variants in an obese/dysglycaemic population. Despite the robust relationship between adiponectin concentrations and diabetes risk in this cohort, variants in ADIPOQ that relate to adiponectin concentrations do not relate to diabetes risk in this population. ADIPOR1 variants exerted significant effects on diabetes risk distinct from any effect of adiponectin concentrations.

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