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Mexican American and South Asian population-based cohorts reveal high prevalence of type 2 diabetes and crucial differences in metabolic phenotypes.

Gordon P Watt ,
Susan P Fisher-Hoch ,
Mohammad H Rahbar ,
Joseph B McCormick ,
Miryoung Lee ,
Audrey C Choh ,
Sadagopan Thanikachalam ,
Mohan Thanikachalam

Abstract

RESEARCH DESIGN AND METHODS

The Cameron County Hispanic Cohort (CCHC; n=3023) served as the MA sample, and the Population Study of Urban, Rural, and Semi-Urban Regions for the Detection of Endovascular Disease (PURSE; n=8080) served as the SI sample. Using design-based methods, we calculated the prevalence of DM and metabolic comorbidities in each cohort. We determined the association of DM with metabolic phenotypes to evaluate the relative contributions of obesity and metabolic health to the prevalence of DM.

CONCLUSION

Our study provides robust, population-based data to estimate the prevalence of DM and its associations with metabolic health. Our results demonstrate differences in metabolic phenotypes in DM, which should inform DM prevention guidelines in non-European populations.

RESULTS

In the CCHC (overall DM prevalence 26.2%), good metabolic health was associated with lower prevalence of DM, across age groups, regardless of obesity. In PURSE (overall prevalence 27.6%), probability of DM was not strongly associated with metabolic phenotypes, although DM prevalence was high in older age groups irrespective of metabolic health.

OBJECTIVE

Prevalence of type 2 diabetes varies by region and ancestry. However, most guidelines for the prevention of diabetes mellitus (DM) are based on European or non-Hispanic white populations. Two ethnic minority populations-Mexican Americans (MAs) in Texas, USA, and South Indians (SIs) in Tamil Nadu, India-have an increasing prevalence of DM. We aimed to understand the metabolic correlates of DM in these populations to improve risk stratification and DM prevention.

More about this publication

BMJ open diabetes research & care

Volume 6
Issue nr. 1
Pages e000436
Publication date 03-04-2018

Full text links

Publisher website (DOI) 10.1136/bmjdrc-2017-000436
Europe PubMed Central 29607048
Pubmed 29607048

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