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GWAS Study

Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes.

Mansour Aly D, Dwivedi OP, Prasad RB et al.

34737425 PubMed ID
GWAS Study Type
3196 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MA
Mansour Aly D
DO
Dwivedi OP
PR
Prasad RB
KA
Käräjämäki A
HR
Hjort R
TM
Thangam M
ÅM
Åkerlund M
MA
Mahajan A
UM
Udler MS
FJ
Florez JC
MM
McCarthy MI
BJ
Brosnan J
MO
Melander O
CS
Carlsson S
HO
Hansson O
TT
Tuomi T
GL
Groop L
AE
Ahlqvist E
Chapter II

Abstract

Summary of the research findings

Type 2 diabetes has been reproducibly clustered into five subtypes with different disease progression and risk of complications; however, etiological differences are unknown. We used genome-wide association and genetic risk score (GRS) analysis to compare the underlying genetic drivers. Individuals from the Swedish ANDIS (All New Diabetics In Scania) study were compared to individuals without diabetes; the Finnish DIREVA (Diabetes register in Vasa) and Botnia studies were used for replication. We show that subtypes differ with regard to family history of diabetes and association with GRS for diabetes-related traits. The severe insulin-resistant subtype was uniquely associated with GRS for fasting insulin but not with variants in the TCF7L2 locus or GRS reflecting insulin secretion. Further, an SNP (rs10824307) near LRMDA was uniquely associated with mild obesity-related diabetes. Therefore, we conclude that the subtypes have partially distinct genetic backgrounds indicating etiological differences.

452 Scandinavian ancestry cases, 2,744 Scandinavian ancestry controls

Chapter III

Study Statistics

Key metrics and study information

3196
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Sweden
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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