Cross-sectional Associations between Abdominal and Thoracic Adipose Tissue Compartments and Adiponectin and Resistin in the Framingham Heart Study
- Shilpa H. Jain, MD1,
- Joseph M. Massaro, PhD2,
- Udo Hoffmann, MD, MPH3,
- Guido A. Rosito, MD3,4,
- Vasan S. Ramachandran, MD5,
- Annaswamy Raji, MBBS, MMSc1,
- Christopher J. O'Donnell, MD, MPH5,6,
- James B. Meigs, MD, MPH6 and
- Caroline S. Fox, MD, MPH (foxca{at}nhlbi.nih.gov)1,5
- 1Brigham and Women's Hospital, Division of Endocrinology, Diabetes and Hypertension, Boston, MA
- 2Boston University, Department of Mathematics, Boston, MA
- 3Massachusetts General Hospital, Division of Radiology, Boston, MA
- 4Federal Foundation School of Medical Sciences of Porto Alegre, Porto Alegre, Rio Grande de Sul, Brazil
- 5NHLBI's Framingham Heart Study, Framingham, MA
- 6Massachusetts General Hospital, Division of General Internal Medicine, Boston, MA
Abstract
Objective: To test the association of regional fat depots with circulating adiponectin and resistin concentrations, and to assess the potential mediating effect of adipokines on associations between abdominal fat depots and cardiometabolic risk factors.
Research Design and Methods: Participants from the Framingham Heart Study Offspring cohort (n = 916, 55% women; mean age 59 years) free of CVD underwent computed tomography measurement of visceral adipose tissue (VAT), subcutaneous adipose tissue (SAT), pericardial fat, and intra-thoracic fat volumes and assays of circulating adiponectin and resistin.
Results: VAT, SAT, pericardial fat, and intra-thoracic fat were negatively correlated with adiponectin (r = −0.19 to −0.34, p<0.001 [women]; r = −0.15 to −0.26, p<0.01 [men] except SAT) and positively correlated with resistin (r = 0.16 to 0.21, p<0.001 [women]; r = 0.11 to 0.14, p<0.05 [men] except VAT). VAT increased the multivariable model R-squared for adiponectin from 2-4% to 10-13% and for resistin from 3-4% to 3-6%. Adjustment for adipokines did not fully attenuate associations between VAT, SAT, and cardiometabolic risk factors.
Conclusions: Adiponectin and resistin are correlated with fat depots cross-sectionally, but none of the adipokines can serve as surrogates for the fat depots. Relations between VAT, SAT, and cardiometabolic risk factors were not fully explained by adiponectin or resistin concentrations.
Footnotes
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- Received September 28, 2008.
- Accepted February 4, 2009.
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