4.7 Article

Ethnic and Sex Differences in Adiponectin: From Childhood to Adulthood

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 101, Issue 12, Pages 4808-4815

Publisher

ENDOCRINE SOC
DOI: 10.1210/jc.2016-1137

Keywords

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Funding

  1. Adult General Clinical Research Center National Institutes of Health (NIH) [M01-RR00051]
  2. Pediatric Clinical Translational Research Center NIH Grant [5MO1 RR00069]
  3. Colorado Clinical and Translational Science Award from National Center for Advancing Translational Sciences/NIH [UL1 TR001082]
  4. NIH [P30-DK048520, K23 RR020038-05, R56 DK088971]
  5. Pediatric Endocrine Society fellowship
  6. American Heart Association Grant [CRP 13CRP1412001]
  7. Building Interdisciplinary Research Careers in Women's Health Grant [K12-HD057022]
  8. Pediatric Endocrinology Fellowship training grant
  9. National Institute of Diabetes and Digestive and Kidney Diseases Grant [T32 DK063687]
  10. Thrasher Pediatric Research Foundation
  11. Center for Women's Health Research
  12. Endocrine Society Women's Health Fellowship
  13. American Diabetes Association Junior Faculty Award [1-11-JF-23]
  14. NIH/National Institute of Child Health and Human Development Building Interdisciplinary Research Careers in Women's Health Grant [K12 HD057022-04]
  15. Juvenile Diabetes Research Foundation Grant [5-2008-291]
  16. American Diabetes Association Grant [7-11-CD-08]
  17. Clinical and Translational Research Institute Community and Academic Engagement Pilot
  18. American Heart Association Fellowship Award
  19. Thrasher Research Foundation NewScholar Award
  20. Children's Hospital Research Institute Scholar Award

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Context: Insulin resistance (IR) and type 2 diabetes are increasing, particularly in Hispanic (H) vs non-Hispanic White (NHW) populations. Adiponectin has a known role in IR, and therefore, understanding ethnic and sex-specific behavior of adiponectin across the lifespan is of clinical significance. Objective: To compare ethnic and sex differences in adiponectin, independent of body mass index, across the lifespan and relationship to IR. Design: Cross-sectional. Setting: Primary care, referral center. Patients: Atotal of 187NHWand 117Hparticipants (8-57 y) without diabetes. Life stage: pre-/early puberty (Tanner 1/2), midpubertal (Tanner 3/4), late pubertal (Tanner 5, <21 years), and adult (Tanner 5, >= 21). Interventions: None. Main Outcome Measure(s): Fasting adiponectin, insulin, glucose, and revised homeostatic model assessment of insulin resistance. Results: Adiponectin was significantly inversely correlated with revised homeostatic model assessment of insulin resistance. Regarding puberty, adiponectin trended downward in late puberty, but only males were significantly lower in adulthood. By sex, adiponectin was lower in adult males vs females of both ethnicities. Regarding ethnicity, Hadults of both sexes had lower adiponectin than NHW adults. Of note, in NHW females, adiponectin trended highest in adulthood, whereas in H females, adiponectin fell in late puberty and remained lower in adulthood. Conclusions: Adiponectin inversely correlated with IR, trended down in late puberty, and was lowest in adult males. H adults of both sexes had lower adiponectin than NHW adults, and H females followed a more male pattern, lacking the rebound in adiponectin seen in NHW females after puberty. These data suggest that adiponectin, independent of body mass index, may relate to the greater cardiometabolic risk seen in H populations and in particular H females.

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