Journal article
T2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibility
Scientific reports, Vol.4(1), pp.7351-7351
12/08/2014
DOI: 10.1038/srep07351
PMCID: PMC5376673
PMID: 25483131
Abstract
Genome-wide association studies (GWAS) of multiple populations with distinctive genetic and lifestyle backgrounds are crucial to the understanding of Type 2 Diabetes Mellitus (T2DM) pathophysiology. We report a GWAS on the genetic basis of T2DM in a 3,286 Lebanese participants. More than 5,000,000 SNPs were directly genotyped or imputed using the 1000 Genomes Project reference panels. We identify genome-wide significant variants in two loci CDKAL1 and TCF7L2, independent of sex, age and BMI, with leading variants rs7766070 (OR = 1.39, P = 4.77 x 10(-9)) and rs34872471 (OR = 1.35, P = 1.01 x 10(-8)) respectively. The current study is the first GWAS to find genomic regions implicated in T2DM in the Lebanese population. The results support a central role of CDKAL1 and TCF7L2 in T2DM susceptibility in Southwest Asian populations and provide a plausible component for understanding molecular mechanisms involved in the disease.
Details
- Title: Subtitle
- T2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibility
- Creators
- Michella Ghassibe-Sabbagh - Lebanese American UniversityMarc Haber - Lebanese American UniversityAngelique K. Salloum - Lebanese American UniversityYasser Al-Sarraj - Shafallah CenterYasmine Akle - Centre Hospitalier du Nord-CHN, Zgharta, Lebanon.Kamal Hirbli - University Medical Center Rizk HospitalJihane Romanos - Lebanese American UniversityFrancis Mouzaya - Lebanese American UniversityDominique Gauguier - Centre de Recherche des CordeliersDaniel E. Platt - IBM (United States)Hatem El-Shanti - University of IowaPierre A. Zalloua - Lebanese American University
- Resource Type
- Journal article
- Publication Details
- Scientific reports, Vol.4(1), pp.7351-7351
- DOI
- 10.1038/srep07351
- PMID
- 25483131
- PMCID
- PMC5376673
- NLM abbreviation
- Sci Rep
- ISSN
- 2045-2322
- eISSN
- 2045-2322
- Publisher
- Springer Nature
- Number of pages
- 9
- Grant note
- NPRP 09-215-3-049 / Qatar National Research Fund; Qatar National Research Fund (QNRF)
- Language
- English
- Date published
- 12/08/2014
- Academic Unit
- Stead Family Department of Pediatrics; Medical Genetics and Genomics
- Record Identifier
- 9984353936502771
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