PMAT variant rs3889348 is associated with metformin-induced gastrointestinal among Chinese type 2 diabetes patients.

Ziqing Liu,Xiao Jia,Peng Wu, Benrui Wu,Ying Pan,Shao Zhong, Luhua Xiao, Yuehong Song,Jinbo Hu,Kaixin Zhou

Pharmacogenomics(2023)

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摘要
This study examined intronic gene variants for their association with metformin intolerance in a Chinese population, focusing on the plasma monoamine transporter () cis-protein expression quantitative trait loci (cis-eQTL) variant rs3889348. We recruited type 2 diabetes patients from two hospitals and identified 111 metformin-intolerant patients using a questionnaire, and selected 206 metformin-tolerant patients from 2180 type 2 diabetes mellitus patients. Genetic testing revealed an association between adverse gastrointestinal effects and and . The single-nucleotide polymorphism rs3889348 is associated with metformin-induced adverse gastrointestinal effects. Each additional copy of the G allele increases the score by 5.23 (95% CI: 1.82-8.64; p = 0.003). Patients taking more transporter inhibitors were more likely to respond to metformin-induced GI intolerance (p = 0.042). cis-eQTL rs3889348 was significantly associated with metformin-induced adverse gastrointestinal effects.
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关键词
gastrointestinal, metformin, PMAT, rs3889348, Type 2 diabetes
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