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ORIGINAL ARTICLE

Sex dimorphisms in inflammatory markers and adiposity in African-American youth

, , , , , & show all
Pages 327-333 | Received 03 Jun 2009, Accepted 25 Oct 2009, Published online: 18 Jan 2010
 

Abstract

Objective. There are demonstrated sex differences in the association between adiposity and inflammation in adults. Our aim was to determine sex differences in inflammatory markers and in the association between adiposity and inflammation in a sample of African-American adolescents. Methods. Adiposity variables including body mass index (BMI), waist circumference, weight, total fat, trunk fat, and inflammatory markers including interleukin-6 (IL-6), leptin, monocyte chemotactic protein 1 (MCP1), C-reactive Protein (CRP), adiponectin were examined in 166 (53% female) African-American adolescents, aged 14–19 years. Total fat and trunk fat were measured using Dual-Energy X-ray Absorptiometry (DXA). Results. Results revealed males had higher weight (p=0.01); females had higher BMI, trunk fat, and total fat (p's <0.01). With inflammation, males had higher MCP1 (p=0.024); females had higher leptin (p<0.001), adiponectin (p=0.006), and IL-6 (p=0.026). Partial correlations in males indicated associations of adiposity variables with leptin, adiponectin (all p's <0.01), and CRP (p<0.05); in females, leptin, CRP, and IL-6 were associated with adiposity variables (all p's <0.05). multiple regression analyses revealed female adiposity variables predicted CRP, (R2=0.254), IL-6 (R2=0.167), and MCP1 (R2=0.220). Adiposity variables in males predicted lower adiponectin (R2=0245). For both, leptin was predicted by adiposity (males R2=0.420 and females R2=0.410). Conclusions. Data indicate clear sex dimorphisms in the associations between inflammatory markers and adiposity in African-American adolescents, suggesting that preventive measures and treatments for adolescent obesity may need to be sex-specific.

Acknowledgements

Harry Davis is acknowledged for statistical consultation. Ying Huang, Kimberly Hawkins Ledbetter, and Nikki S. Wright are acknowledged for data collection, entry and management. This study was supported by grants from the National Heart, Lung, and Blood Institute (HL077230 and HL085817).

Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

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