Serum bilirubin concentration is modified by UGT1A1 Haplotypes and influences risk of Type-2 diabetes in the Norfolk Island genetic isolate

被引:21
作者
Benton, M. C. [1 ]
Lea, R. A. [1 ]
Macartney-Coxson, D. [2 ]
Bellis, C. [1 ,3 ]
Carless, M. A. [3 ]
Curran, J. E. [3 ]
Hanna, M. [1 ]
Eccles, D. [1 ]
Chambers, G. K. [4 ]
Blangero, J. [5 ]
Griffiths, L. R. [1 ]
机构
[1] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Genom Res Ctr, Kelvin Grove, Qld 4059, Australia
[2] Inst Environm Sci & Res, Kenepuru Sci Ctr, Wellington 5240, New Zealand
[3] Texas Biomed Res Inst, San Antonio, TX 78227 USA
[4] Victoria Univ Wellington, Sch Biol Sci, Wellington 6140, New Zealand
[5] Univ Texas Brownsville, Rio Grande Valley Sch Med, South Texas Diabet & Obes Inst, Brownsville, TX 78520 USA
基金
英国医学研究理事会;
关键词
Norfolk Island; GWAS; Bilirubin; type-2; diabetes; UGT1A1; GENOME-WIDE ASSOCIATION; CORONARY-ARTERY-DISEASE; GILBERTS-SYNDROME; UDP-GLUCURONOSYLTRANSFERASE; METABOLIC SYNDROME; CRIGLER-NAJJAR; MENDELIAN RANDOMIZATION; CARDIOVASCULAR-DISEASE; POPULATION; LINKAGE;
D O I
10.1186/s12863-015-0291-z
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Background: Located in the Pacific Ocean between Australia and New Zealand, the unique population isolate of Norfolk Island has been shown to exhibit increased prevalence of metabolic disorders (type-2 diabetes, cardiovascular disease) compared to mainland Australia. We investigated this well-established genetic isolate, utilising its unique genomic structure to increase the ability to detect related genetic markers. A pedigree-based genome-wide association study of 16 routinely collected blood-based clinical traits in 382 Norfolk Island individuals was performed. Results: A striking association peak was located at chromosome 2q37.1 for both total bilirubin and direct bilirubin, with 29 SNPs reaching statistical significance (P < 1.84 x 10(-7)). Strong linkage disequilibrium was observed across a 200 kb region spanning the UDP-glucuronosyltransferase family, including UGT1A1, an enzyme known to metabolise bilirubin. Given the epidemiological literature suggesting negative association between CVD-risk and serum bilirubin we further explored potential associations using stepwise multivariate regression, revealing significant association between direct bilirubin concentration and type-2 diabetes risk. In the Norfolk Island cohort increased direct bilirubin was associated with a 28 % reduction in type-2 diabetes risk (OR: 0.72, 95 % CI: 0.57-0.91, P = 0.005). When adjusted for genotypic effects the overall model was validated, with the adjusted model predicting a 30 % reduction in type-2 diabetes risk with increasing direct bilirubin concentrations (OR: 0.70, 95 % CI: 0.53-0.89, P = 0.0001). Conclusions: In summary, a pedigree-based GWAS of blood-based clinical traits in the Norfolk Island population has identified variants within the UDPGT family directly associated with serum bilirubin levels, which is in turn implicated with reduced risk of developing type-2 diabetes within this population.
引用
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页数:15
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