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Abdominal fat depots associated with insulin resistance and metabolic syndrome risk factors in black African young adults.


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Authors

De Lucia Rolfe, Emanuella  ORCID logo  https://orcid.org/0000-0003-3542-2767
Ong, Ken K 
Sleigh, Alison 
Dunger, David B 
Norris, Shane A 

Abstract

BACKGROUND: Individuals of black African ethnicity tend to have less visceral adipose tissue (VAT) but more subcutaneous-abdominal adipose tissue (SCAT) than white Caucasians. However, it is unclear whether such distribution of abdominal fat is beneficial for metabolic disease risk in black individuals. Here we compared the associations between these specific abdominal fat depots, insulin sensitivity and metabolic syndrome risk. METHODS: A cross-sectional analysis of 76 black South African young adults (36 men; 40 women) aged 18-19 years participating in the Birth to Twenty Cohort Study had VAT and SCAT measured by MRI. The metabolic syndrome traits (blood pressure, lipid profile, fasting glucose and insulin) were measured and the values were combined into a metabolic syndrome risk score. Fasting glucose and insulin were used to derive the HOMA-index of insulin resistance (HOMA-IR). RESULTS: Compared to men, women had greater VAT (mean: 16.6 vs. 12.5 cm(2)) and SCAT (median 164.0 vs. 59.9 cm(2)). In men, SCAT (r = 0.50) was more strongly correlated to the metabolic syndrome score (MetS) than was VAT (r = 0.23), and was associated with both MetS (P = 0.001) and HOMA-IR (P = 0.001) after adjustment for VAT and total fat mass. In women, both abdominal fat compartments showed comparable positive correlations with MetS (r = 0.26 to 0.31), although these trends were weaker than in men. CONCLUSIONS: In young black South African adults, SCAT appears to be more relevant than VAT to metabolic syndrome traits.

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Keywords

Abdominal Fat, Adult, Black People, Cohort Studies, Cross-Sectional Studies, Female, Humans, Insulin, Insulin Resistance, Lipids, Male, Metabolic Syndrome, Risk Factors, Sex Factors, South Africa, White People, Young Adult

Journal Title

BMC Public Health

Conference Name

Journal ISSN

1471-2458
1471-2458

Volume Title

15

Publisher

Springer Science and Business Media LLC
Sponsorship
Medical Research Council (MC_UU_12015/2)
Medical Research Council (G1001333)
Medical Research Council (MC_U106179472)
The study was supported by the Medical Research Councils of South Africa and UK. Shane Norris is supported by the UK MRC/DfID Africa Research Leader Scheme. Alison Sleigh is supported by core staff funding from the NIHR/Wellcome Trust Cambridge Clinical Research Facility. EDLR and KO are supported by the Medical Research Council (UK) [programme number MC_UU_12015/2].