Your browser doesn't support javascript.
loading
Serum bilirubin concentration is modified by UGT1A1 haplotypes and influences risk of type-2 diabetes in the Norfolk Island genetic isolate.
Benton, M C; Lea, R A; Macartney-Coxson, D; Bellis, C; Carless, M A; Curran, J E; Hanna, M; Eccles, D; Chambers, G K; Blangero, J; Griffiths, L R.
Afiliação
  • Benton MC; Genomics Research Centre, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, QLD, 4059, Australia. m.benton@qut.edu.au.
  • Lea RA; Genomics Research Centre, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, QLD, 4059, Australia. rodney.lea@qut.edu.au.
  • Macartney-Coxson D; Kenepuru Science Centre, Institute of Environmental Science and Research, Wellington, 5240, New Zealand. Donia.Macartney@esr.cri.nz.
  • Bellis C; Genomics Research Centre, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, QLD, 4059, Australia. c.bellis@qut.edu.au.
  • Carless MA; Texas Biomedical Research Institute, San Antonio, TX, 78227-5301, USA. c.bellis@qut.edu.au.
  • Curran JE; Texas Biomedical Research Institute, San Antonio, TX, 78227-5301, USA. mcarless@txbiomed.org.
  • Hanna M; Texas Biomedical Research Institute, San Antonio, TX, 78227-5301, USA. jcurran@txbiomedgenetics.org.
  • Eccles D; Genomics Research Centre, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, QLD, 4059, Australia. michelle.hanna@qut.edu.au.
  • Chambers GK; Genomics Research Centre, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, QLD, 4059, Australia. bioinformatics@gringene.org.
  • Blangero J; School of Biological Sciences, Victoria University of Wellington, Wellington, 6140, New Zealand. Geoff.Chambers@vuw.ac.nz.
  • Griffiths LR; South Texas Diabetes and Obesity Institute, University of Texas, Rio Grande Valley School of Medicine, Brownsville, TX, 78520, USA. Blangero@uthscsa.edu.
BMC Genet ; 16: 136, 2015 Dec 02.
Article em En | MEDLINE | ID: mdl-26628212
ABSTRACT

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 × 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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bilirrubina / Haplótipos / Glucuronosiltransferase / Predisposição Genética para Doença / Diabetes Mellitus Tipo 2 Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bilirrubina / Haplótipos / Glucuronosiltransferase / Predisposição Genética para Doença / Diabetes Mellitus Tipo 2 Idioma: En Ano de publicação: 2015 Tipo de documento: Article