Unknown

Dataset Information

0

Metoclopramide-Induced Acute Dystonic Reactions May Be Associated With the CYP2D6 Poor Metabolizer Status and Pregnancy-Related Hormonal Changes.


ABSTRACT: We report two cases of metoclopramide-induced acute dystonia in pregnant women and consider the role of genetic variation in the pathogenesis of the adverse effect. By whole-gene sequencing, we found that both women were CYP2D6 poor metabolizers. We theorize that CYP2D6 governs the risk of metoclopramide-related acute dystonia through its role in the synthesis of serotonin, which inhibits the dopamine tone. The effect of CYP2D6 poor metabolism is exaggerated by rises in the estrogen levels during pregnancy, as the hormone augments dopamine sensitivity. Together, the two factors may create a hyper-dopaminergic state that is easily upset by metoclopramide, resulting in acute dystonia.

SUBMITTER: Chua EW 

PROVIDER: S-EPMC6713716 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

altmetric image

Publications

Metoclopramide-Induced Acute Dystonic Reactions May Be Associated With the CYP2D6 Poor Metabolizer Status and Pregnancy-Related Hormonal Changes.

Chua Eng Wee EW   Harger Simon P SP   Kennedy Martin A MA  

Frontiers in pharmacology 20190822


We report two cases of metoclopramide-induced acute dystonia in pregnant women and consider the role of genetic variation in the pathogenesis of the adverse effect. By whole-gene sequencing, we found that both women were CYP2D6 poor metabolizers. We theorize that CYP2D6 governs the risk of metoclopramide-related acute dystonia through its role in the synthesis of serotonin, which inhibits the dopamine tone. The effect of CYP2D6 poor metabolism is exaggerated by rises in the estrogen levels durin  ...[more]

Similar Datasets

| S-EPMC9926081 | biostudies-literature
| S-EPMC7702196 | biostudies-literature
| S-EPMC9321582 | biostudies-literature
| S-EPMC8761935 | biostudies-literature
| S-EPMC8375217 | biostudies-literature
| S-EPMC3818912 | biostudies-literature
| S-EPMC4059401 | biostudies-literature
| S-EPMC8127095 | biostudies-literature
2014-12-04 | GSE50166 | GEO
| S-EPMC6389687 | biostudies-literature