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GWAS Study

Genome-wide association study of letrozole plasma concentrations identifies non-exonic variants that may affect CYP2A6 metabolic activity.

Hertz DL, Douglas JA, Kidwell KM et al.

34096894 PubMed ID
GWAS Study Type
228 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HD
Hertz DL
DJ
Douglas JA
KK
Kidwell KM
GC
Gersch CL
DZ
Desta Z
SA
Storniolo AM
SV
Stearns V
ST
Skaar TC
HD
Hayes DF
HN
Henry NL
RJ
Rae JM
Chapter II

Abstract

Summary of the research findings

Objectives: Letrozole is a nonsteroidal aromatase inhibitor used to treat hormone-receptor-positive breast cancer. Variability in letrozole efficacy and toxicity may be partially attributable to variable systemic drug exposure, which may be influenced by germline variants in the enzymes responsible for letrozole metabolism, including cytochrome P450 2A6 (CYP2A6). The objective of this genome-wide association study (GWAS) was to identify polymorphisms associated with steady-state letrozole concentrations.

228 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

228
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S.
Recruitment Country
Chapter IV

AI-Generated Summary

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