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Biomark Res. 2015 Oct 13;3:22. doi: 10.1186/s40364-015-0047-y. eCollection 2015.

Circulating micrornas associated with glycemic impairment and progression in Asian Indians.

Author information

1
Department of Physiological Nursing, School of Nursing, University of California, 2 Koret Way #N605L, CA 94143 San Francisco, USA.
2
Division of General Internal Medicine, University of California, San Francisco, USA.
3
Department of Physiological Nursing, School of Nursing, University of California, 2 Koret Way #N605L, CA 94143 San Francisco, USA ; Institute for Human Genetics, University of California, San Francisco, USA.
4
Division of General Internal Medicine, University of California, San Francisco, USA ; Department of Epidemiology and Biostatistics, University of California, San Francisco, USA.

Abstract

AIMS/HYPOTHESIS:

Asian Indians have a high incidence of type 2 diabetes, but factors associated with glycemic progression in this population are not understood. MicroRNAs are emerging as important mediators of glucose homeostasis and have not been previously studied in Asian Indians. We examined microRNA (miR) expression associated with glycemic impairment and progression in Asian Indians from the San Francisco Bay Area. We studied 128 Asian Indians age 45-84 years without known cardiovascular disease and not taking diabetes medications. Oral glucose tolerance tests were performed at baseline and after 2.5 years. We quantified circulating miRs from plasma collected during the enrollment visit using a flow cytometry-based assay.

RESULTS:

Glycemic impairment was present in 57 % (n = 73) at baseline. MiR-191 was positively associated with glycemic impairment (odds ratio (OR) 1.7 (95 % CI 1.2, 2.4), p < 0.01). The prevalence of glycemic progression after 2.5 years was 24 % (n = 23). Six miRs were negatively associated with glycemic progression: miR-122 (OR 0.5 (0.2, 0.8), p < 0.01), miR-15a (OR 0.6 (0.4, 0.9), p < 0.01), miR-197 (OR 0.6 (0.4, 0.9), p < 0.01), miR-320a (OR 0.6 (0.4, 0.9), p < 0.01), miR-423 (OR 0.6 (0.4, 0.9), p < 0.01), and miR-486 (OR 0.5 (0.3, 0.8), p < 0.01). Further multivariate adjustment did not attenuate these results.

CONCLUSIONS/INTERPRETATION:

This is the first study to investigate circulating miRs associated with glycemic status among this high-risk ethnic group. Individual miRs were significantly associated with both glycemic impairment and glycemic progression. Further studies are needed to determine whether miR (s) might be useful clinical biomarkers for incident T2D in the Asian Indian population.

KEYWORDS:

Asian Indians; Biomarkers; Glycemic impairment; MicroRNA; Type 2 diabetes

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