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GWAS Study

A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome.

Skuladottir AT, Bjornsdottir G, Ferkingstad E et al.

35332129 PubMed ID
GWAS Study Type
1239680 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SA
Skuladottir AT
BG
Bjornsdottir G
FE
Ferkingstad E
EG
Einarsson G
SL
Stefansdottir L
NM
Nawaz MS
OA
Oddsson A
OT
Olafsdottir TA
SS
Saevarsdottir S
WG
Walters GB
MS
Magnusson SH
BA
Bjornsdottir A
SO
Sveinsson OA
VA
Vikingsson A
HT
Hansen TF
JR
Jacobsen RL
EC
Erikstrup C
SM
Schwinn M
BS
Brunak S
BK
Banasik K
OS
Ostrowski SR
TA
Troelsen A
HC
Henkel C
PO
Pedersen OB
JI
Jonsdottir I
GD
Gudbjartsson DF
SP
Sulem P
TT
Thorgeirsson TE
SH
Stefansson H
SK
Stefansson K
Chapter II

Abstract

Summary of the research findings

Carpal tunnel syndrome (CTS) is the most common entrapment neuropathy and has a largely unknown underlying biology. In a genome-wide association study of CTS (48,843 cases and 1,190,837 controls), we found 53 sequence variants at 50 loci associated with the syndrome. The most significant association is with a missense variant (p.Glu366Lys) in SERPINA1 that protects against CTS (P = 2.9 × 10-24, OR = 0.76). Through various functional analyses, we conclude that at least 22 genes mediate CTS risk and highlight the role of 19 CTS variants in the biology of the extracellular matrix. We show that the genetic component to the risk is higher in bilateral/recurrent/persistent cases than nonrecurrent/nonpersistent cases. Anthropometric traits including height and BMI are genetically correlated with CTS, in addition to early hormonal-replacement therapy, osteoarthritis, and restlessness. Our findings suggest that the components of the extracellular matrix play a key role in the pathogenesis of CTS.

48,843 European ancestry cases, 1,190,837 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1239680
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Finland, Denmark, U.K., Iceland
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.