Independent and opposite associations of trunk and leg fat depots with adipokines, inflammatory markers, and metabolic syndrome in middle-aged and older Chinese men and women

Hongyu Wu, Qibin Qi, Zhijie Yu, Qi Sun, Jing Wang, Oscar H. Franco, Liang Sun, Huaixing Li, Yong Liu, Frank B. Hu, Xu Lin

Résultat de recherche: Articleexamen par les pairs

46 Citations (Scopus)

Résumé

Objective: The objective was to investigate associations of regional fat depots with adipokines, inflammatory markers, and risk of metabolic syndrome (MetS) in a Chinese population. Design and Methods: Trunk and leg fat mass were determined in a population-based sample of 1150 Chinese (479 men and 671 women) aged 50-70 yr by using whole-body dual-energy x-ray absorptiometry scan. Plasma adiponectin, plasminogen activator inhibitor-1 (PAI-1), retinol-binding protein 4 (RBP4), resistin, C-reactive protein, and IL-6 were measured. The updated National Cholesterol Education Program Adult Treatment Panel III criterion for Asian Americans was used to define MetS. Results: Larger body-size adjusted trunk fat mass was significantly associated with lower adiponectin and higher PAI-1, RBP4, C-reactive protein, and IL-6 levels in both genders (P < 0.05). Larger body-size adjusted leg fat mass was significantly associated with higher adiponectin levels in both genders but lower RBP4 and PAI-1 concentrations in men (P < 0.05). Comparing with the lowest body-size adjusted leg fat mass tertile, the odds ratio (95% confidence interval) of MetS in the highest tertile was 0.33 (0.18-0.62; P for trend <0.001) for men and 0.43 (0.28-0.65; P for trend <0.001) for women. The association was attenuated with further controlling adipokines and inflammatory markers (P = 0.09 for men and P = 0.004 for women). Conclusion: In contrast to trunk fat, large leg fat appears to have favorable effects on adipokines, inflammatory markers, and MetS risk among Chinese. The opposite associations between regional fat depots and MetS risk may partially mediated by adipokines and inflammatory status.

Langue d'origineEnglish
Pages (de-à)4389-4398
Nombre de pages10
JournalJournal of Clinical Endocrinology and Metabolism
Volume95
Numéro de publication9
DOI
Statut de publicationPublished - sept. 2010
Publié à l'externeOui

Note bibliographique

Funding Information:
This work was supported by the following: Chief Scientist Program of Shanghai Institutes for Biological Sciences ; Chinese Academy of Sciences Grant SIBS2008006 ; the Ministry of Science and Technology of China 973 Program, Grant 2006CB503900 and 863 Program, Grant 2007AA02Z332 ; Shanghai Municipal Science and Technology Commission , Grant 08dj1400601 ; International Collaboration Program Grant 2008DFA31960 , and the Chinese Academy of Sciences under the Knowledge Innovation Program Grant KSCX1-YW-02 .

ASJC Scopus Subject Areas

  • Endocrinology, Diabetes and Metabolism
  • Biochemistry
  • Endocrinology
  • Clinical Biochemistry
  • Biochemistry, medical

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