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Identification of novel high-impact recessively inherited type 2 diabetes risk variants in the Greenlandic population.
Grarup, Niels; Moltke, Ida; Andersen, Mette K; Bjerregaard, Peter; Larsen, Christina V L; Dahl-Petersen, Inger K; Jørsboe, Emil; Tiwari, Hemant K; Hopkins, Scarlett E; Wiener, Howard W; Boyer, Bert B; Linneberg, Allan; Pedersen, Oluf; Jørgensen, Marit E; Albrechtsen, Anders; Hansen, Torben.
Affiliation
  • Grarup N; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, 2200, Copenhagen, Denmark.
  • Moltke I; The Bioinformatics Centre, Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, 2200, Copenhagen, Denmark.
  • Andersen MK; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, 2200, Copenhagen, Denmark.
  • Bjerregaard P; National Institute of Public Health, University of Southern Denmark, Copenhagen, Denmark.
  • Larsen CVL; Greenland Centre for Health Research, University of Greenland, Nuuk, Greenland.
  • Dahl-Petersen IK; National Institute of Public Health, University of Southern Denmark, Copenhagen, Denmark.
  • Jørsboe E; Greenland Centre for Health Research, University of Greenland, Nuuk, Greenland.
  • Tiwari HK; National Institute of Public Health, University of Southern Denmark, Copenhagen, Denmark.
  • Hopkins SE; The Bioinformatics Centre, Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, 2200, Copenhagen, Denmark.
  • Wiener HW; Department of Biostatistics, School of Public Health, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Boyer BB; Center for Alaska Native Health Research, University of Alaska Fairbanks, Fairbanks, AK, USA.
  • Linneberg A; Department of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Pedersen O; Center for Alaska Native Health Research, University of Alaska Fairbanks, Fairbanks, AK, USA.
  • Jørgensen ME; Center for Clinical Research and Prevention, Bispebjerg and Frederiksberg Hospital, The Capital Region, Copenhagen, Denmark.
  • Albrechtsen A; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Hansen T; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, 2200, Copenhagen, Denmark.
Diabetologia ; 61(9): 2005-2015, 2018 09.
Article in En | MEDLINE | ID: mdl-29926116
ABSTRACT
AIMS/

HYPOTHESIS:

In a recent study using a standard additive genetic model, we identified a TBC1D4 loss-of-function variant with a large recessive impact on risk of type 2 diabetes in Greenlanders. The aim of the current study was to identify additional genetic variation underlying type 2 diabetes using a recessive genetic model, thereby increasing the power to detect variants with recessive effects.

METHODS:

We investigated three cohorts of Greenlanders (B99, n = 1401; IHIT, n = 3115; and BBH, n = 547), which were genotyped using Illumina MetaboChip. Of the 4674 genotyped individuals passing quality control, 4648 had phenotype data available, and type 2 diabetes association analyses were performed for 317 individuals with type 2 diabetes and 2631 participants with normal glucose tolerance. Statistical association analyses were performed using a linear mixed model.

RESULTS:

Using a recessive genetic model, we identified two novel loci associated with type 2 diabetes in Greenlanders, namely rs870992 in ITGA1 on chromosome 5 (OR 2.79, p = 1.8 × 10-8), and rs16993330 upstream of LARGE1 on chromosome 22 (OR 3.52, p = 1.3 × 10-7). The LARGE1 variant did not reach the conventional threshold for genome-wide significance (p < 5 × 10-8) but did withstand a study-wide Bonferroni-corrected significance threshold. Both variants were common in Greenlanders, with minor allele frequencies of 23% and 16%, respectively, and were estimated to have large recessive effects on risk of type 2 diabetes in Greenlanders, compared with additively inherited variants previously observed in European populations. CONCLUSIONS/

INTERPRETATION:

We demonstrate the value of using a recessive genetic model in a historically small and isolated population to identify genetic risk variants. Our findings give new insights into the genetic architecture of type 2 diabetes, and further support the existence of high-effect genetic risk factors of potential clinical relevance, particularly in isolated populations. DATA

AVAILABILITY:

The Greenlandic MetaboChip-genotype data are available at European Genome-Phenome Archive (EGA; https//ega-archive.org/ ) under the accession EGAS00001002641.
Subject(s)
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Full text: 1 Database: MEDLINE Main subject: Diabetes Mellitus, Type 2 Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Country/Region as subject: America do norte / Europa Language: En Journal: Diabetologia Year: 2018 Type: Article Affiliation country: Denmark

Full text: 1 Database: MEDLINE Main subject: Diabetes Mellitus, Type 2 Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Country/Region as subject: America do norte / Europa Language: En Journal: Diabetologia Year: 2018 Type: Article Affiliation country: Denmark