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GWAS Study

Genetic modifiers of cystic fibrosis-related diabetes have extensive overlap with type 2 diabetes and related traits.

Aksit MA, Pace RG, Vecchio-Pagán B et al.

31697830 PubMed ID
GWAS Study Type
6331 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AM
Aksit MA
PR
Pace RG
VB
Vecchio-Pagán B
LH
Ling H
RJ
Rommens JM
BP
Boelle PY
GL
Guillot L
RK
Raraigh KS
PE
Pugh E
ZP
Zhang P
SL
Strug LJ
DM
Drumm ML
KM
Knowles MR
CG
Cutting GR
CH
Corvol H
BS
Blackman SM
Chapter II

Abstract

Summary of the research findings

Context: Individuals with cystic fibrosis (CF) develop a distinct form of diabetes characterized by β-cell dysfunction and islet amyloid accumulation similar to type 2 diabetes (T2D), but generally have normal insulin sensitivity. CF-related diabetes (CFRD) risk is determined by both CFTR, the gene responsible for CF, and other genetic variants.

1,341 European and unknown ancestry cases, 4,399 European and unknown ancestry controls

Chapter III

Study Statistics

Key metrics and study information

6331
Total Participants
GWAS
Study Type
Yes
Replicated
204 European and unknown ancestry cases, 387 European and unknown ancestry controls
Replication Participants
NR, European, European, NR
Ancestry
Canada, U.S., France
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

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Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

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