Identifying genetic variants associated with ritodrine-induced pulmonary edema.

Abstract

INTRODUCTION:

Ritodrine is one of the most commonly used tocolytics in preterm labor, acting as a ß2-adrenergic agonist that reduces intracellular calcium levels and prevents myometrial activation. Ritodrine infusion can result in serious maternal complications, and pulmonary edema is a particular concern among these. The cause of pulmonary edema following ritodrine treatment is multifactorial; however, the contributing genetic factors remain poorly understood. This study investigates the genetic variants associated with ritodrine-induced pulmonary edema.

METHODS:

In this case-control study, 16 patients who developed pulmonary edema during ritodrine infusion [case], and 16 pregnant women who were treated with ritodrine and did not develop pulmonary edema [control] were included. The control pregnant women were selected after matching for plurality and gestational age at the time of tocolytic use. Maternal blood was collected during admission for tocolytic treatment, and whole exome sequencing was performed with the stored blood samples.

RESULTS:

Gene-wise variant burden (GVB) analysis resulted in a total of 71 candidate genes by comparing the cumulative effects of multiple coding variants for 19729 protein-coding genes between the patients with pulmonary edema and the matched controls. Subsequent data analysis selected only the statistically significant and deleterious variants compatible with ritodrine-induced pulmonary edema. Two final candidate variants in CPT2 and ADRA1A were confirmed by Sanger sequencing.

CONCLUSIONS:

We identified new potential variants in genes that play a role in cyclic adenosine monophosphate (cAMP)/protein kinase A (PKA) regulation, which supports their putative involvement in the predisposition to ritodrine-induced pulmonary edema in pregnant women.

• Authors: Seung Mi Lee, Yoomi Park, Young Ju Kim, Han-Sung Hwang, Heewon Seo, Byung-Joo Min, Kye Hwa Lee, So Yeon Kim, Young Mi Jung, Suehyun Lee, Chan-Wook Park, Ju Han Kim, Joong Shin Park
• Journal: PloS one (PLoS One) Vol. 15 Issue 11 Pg. e0241215 ( 2020) ISSN: 1932-6203 [Electronic] United States
• PMID: 33166306 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Tocolytic Agents
• Ritodrine

Topics

• Adult
• Case-Control Studies
• Female
• Genetic Variation (genetics)
• Humans
• Myometrium (drug effects)
• Obstetric Labor, Premature (drug therapy, genetics)
• Pregnancy
• Pulmonary Edema (chemically induced, genetics)
• Ritodrine (adverse effects)
• Tocolytic Agents (adverse effects)