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GWAS Study

Association of Genetic Variants in NUDT15 With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease.

Walker GJ, Harrison JW, Heap GA et al.

30806694 PubMed ID
GWAS Study Type
919 Participants
61 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WG
Walker GJ
HJ
Harrison JW
HG
Heap GA
VM
Voskuil MD
AV
Andersen V
AC
Anderson CA
AA
Ananthakrishnan AN
BJ
Barrett JC
BL
Beaugerie L
BC
Bewshea CM
CA
Cole AT
CF
Cummings FR
DM
Daly MJ
EP
Ellul P
FR
Fedorak RN
FE
Festen EAM
FT
Florin TH
GD
Gaya DR
HJ
Halfvarson J
HA
Hart AL
HN
Heerasing NM
HP
Hendy P
IP
Irving PM
JS
Jones SE
KJ
Koskela J
LJ
Lindsay JO
MJ
Mansfield JC
MD
McGovern D
PM
Parkes M
PR
Pollok RCG
RS
Ramakrishnan S
RD
Rampton DS
RM
Rivas MA
RR
Russell RK
SM
Schultz M
SS
Sebastian S
SP
Seksik P
SA
Singh A
SK
So K
SH
Sokol H
SK
Subramaniam K
TA
Todd A
AV
Annese V
WR
Weersma RK
XR
Xavier R
WR
Ward R
WM
Weedon MN
GJ
Goodhand JR
KN
Kennedy NA
AT
Ahmad T
Chapter II

Abstract

Summary of the research findings

Importance: Use of thiopurines may be limited by myelosuppression. TPMT pharmacogenetic testing identifies only 25% of at-risk patients of European ancestry. Among patients of East Asian ancestry, NUDT15 variants are associated with thiopurine-induced myelosuppression (TIM).

311 European ancestry cases, 608 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

919
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

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