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http://purl.uniprot.org/citations/21747906http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21747906http://www.w3.org/2000/01/rdf-schema#comment"

Background

Recent genome-wide association studies have identified a number of common variants associated with fasting glucose homeostasis and type 2 diabetes in populations of European origin. This is a replication study to examine whether such associations are also observed in Chinese Hans.

Methods

We genotyped nine variants in or near MADD, ADRA2A, CRY2, GLIS3, PROX1, FADS1, C2CD4B, IGF1 and IRS1 in a population-based cohort including 3,210 unrelated Chinese Hans from Beijing and Shanghai.

Results

We confirmed the associations of GLIS3-rs7034200 with fasting glucose (beta = 0.07 mmol/l, P = 0.03), beta cell function (HOMA-B) (beta = -3.03%, P = 0.009), and type 2 diabetes (OR [95%CI]  = 1.27 [1.09-1.49], P = 0.003) after adjustment for age, sex, region and BMI. The association for type 2 diabetes remained significant after adjusting for other diabetes related risk factors including family history of diabetes, lipid profile, medication information, hypertension and life style factors, while further adjustment for HOMA-B abolished the association. The A-allele of CRY2-rs11605924 was moderately associated with increased risk of combined IFG/type 2 diabetes (OR [95%CI]  = 1.15[1.01-1.30], P = 0.04). SNPs in or near MADD, ADRA2A, PROX1, FADS1, C2CD4B, IGF1, and IRS1 did not exhibit significant associations with type 2 diabetes or related glycemic traits (P≥0.10).

Conclusions

In conclusion, our results indicate the associations of GLIS3 locus with type 2 diabetes and impaired fasting glucose in Chinese Hans, partially mediated through impaired beta-cell function. In addition, we also found modest evidence for the association of CRY2-rs11605924 with combined IFG/type 2 diabetes."xsd:string
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http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/author"Li H."xsd:string
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/author"Liu C."xsd:string
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/author"Lin X."xsd:string
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/author"Lu L."xsd:string
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/author"Qi L."xsd:string
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/author"Qi Q."xsd:string
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/author"Gan W."xsd:string
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/author"Loos R.J."xsd:string
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/name"PLoS One"xsd:string
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/pages"e21464"xsd:string
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/title"Variants in GLIS3 and CRY2 are associated with type 2 diabetes and impaired fasting glucose in Chinese Hans."xsd:string
http://purl.uniprot.org/citations/21747906http://purl.uniprot.org/core/volume"6"xsd:string
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