Vitamin D, inflammation, and relations to insulin resistance in premenopausal women with morbid obesity

Obesity (Silver Spring). 2015 Aug;23(8):1591-7. doi: 10.1002/oby.21131. Epub 2015 Jul 6.

Abstract

Objective: In this study, the associations between vitamin D, insulin sensitivity, and inflammation and their relationships with adipose tissue expression of vitamin D receptor (VDR) and inflammatory markers in women with morbid obesity were determined.

Methods: An oral glucose tolerance test prior to surgery was completed by healthy premenopausal women (n = 76) seeking bariatric surgery. Abdominal subcutaneous adipose tissue (SAT) and visceral adipose tissue (VAT) were collected during surgery.

Results: Approximately, 70% of our subjects were vitamin D sufficient or optimal, and 80% had normal glucose tolerance. No significant association between serum 25-hydroxyvitamin D [25(OH)D] with circulating inflammatory markers or insulin sensitivity was identified. In subjects with waist circumference of <139 cm (n = 42), log25(OH)D positively predicted VAT logIL-6 mRNA expression (P = 0.003). LogVDR expression was positively correlated with the expression of inflammatory markers in both SAT (logIL-1β mRNA: r = 0.95, P < 0.0001; logTNF mRNA: r = 0.82, P < 0.0001) and VAT (logIL-1β mRNA: r = 0.89, P < 0.0001; logTNF mRNA: r = 0.75, P < 0.0001). VAT logVDR expression positively predicted logHOMA-IR in non-African American subjects (P = 0.05).

Conclusions: The beneficial effects of vitamin D on inflammation and insulin sensitivity were not supported by our findings. VDR does not appear to possess a protective effect in adipose tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Female
  • Glucose Tolerance Test
  • Humans
  • Inflammation / metabolism
  • Insulin Resistance*
  • Intra-Abdominal Fat / metabolism
  • Middle Aged
  • Obesity, Morbid / metabolism*
  • Premenopause
  • Vitamin D / analogs & derivatives*
  • Vitamin D / metabolism

Substances

  • Vitamin D
  • 25-hydroxyvitamin D