Author Identifier

Wei Wang

https://orcid.org/0000-0002-1430-1360

Document Type

Journal Article

Publisher

M D P I AG

Place of Publication

Switzerland

School

School of Medical and Health Sciences

RAS ID

22400

Funders

National Natural Science Foundation of China (81370083, 81273170)

National “12th Five-Year” Plan for Science and Technology Support, China (2012BAI37B03)

Joint Project of the Australian National Health and Medical Research Council and the National Natural Science Foundation of China (NHMRC APP1112767, NSFC 81561128020)

Recovery Medical Science Foundation, China

Beijing Higher Education Young Elite Teacher Project
(YETP1671)

Beijing Nova Program (Z141107001814058)

Grant Number

NHMRC Number : 1112767

Comments

Rao, P., Zhou, Y., Ge, S. Q., Wang, A. X., Yu, X. W., Alzain, M. A., ... & Wang, H. (2016). Validation of Type 2 Diabetes Risk Variants Identified by Genome-Wide Association Studies in Northern Han Chinese. International Journal of Environmental Research and Public Health, 13(9), 863.

https://doi.org/10.3390/ijerph13090863

Abstract

Background:

More than 60 genetic susceptibility loci associated with type 2 diabetes mellitus (T2DM) have been established in populations of Asian and European ancestry. Given ethnic differences and environmental factors, validation of the effects of genetic risk variants with reported associations identified by Genome-Wide Association Studies (GWASs) is essential. The study aims at evaluating the associations of T2DM with 29 single nucleotide polymorphisms (SNPs) from 19 candidate genes derived from GWASs in a northern Han Chinese population.

Method:

In this case-control study, 461 T2DM-diagnosed patients and 434 controls were recruited at the Jidong oil field hospital (Hebei, China) from January 2009 to October 2013. A cumulative genetic risk score (cGRS) was calculated by summation of the number of risk alleles, and a weight GRS (wGRS) was calculated as the sum of risk alleles at each locus multiplied by their effect sizes for T2DM, using the independent variants selected.

Result:

The allelic frequency of the “A” allele at rs17106184 (Fas-associated factor 1, FAF1) was significantly higher in the T2DM patients than that of the healthy controls (11.7% vs. 6.4%, p < 0.001). Individuals in the highestquartile of wGRS had an over three-fold increased risk for developing T2DM compared with those in the lowest quartile (odds ratio = 3.06, 95% CI = 1.92-4.88, p < 0.001) adjusted for age, sex, BMI, total cholesterol (TC), triglycerides (TG), low-density lipoprotein cholesterol (LDL-C), systolic blood pressure (SBP) and diastolic blood pressure (DBP). The results were similar when analyzed with the cGRS.

Conclusions:

We confirmed the association between rs17106184 (FAF1) and T2DM in a northern Han Chinese population. The GRS calculated based on T2DM susceptibility variants may be a useful tool for predicting the T2DM susceptibility.

DOI

10.3390/ijerph13090863

Creative Commons License

Creative Commons Attribution 4.0 License
This work is licensed under a Creative Commons Attribution 4.0 License.

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