MDM2 309 polymorphism is associated with missed abortion

35Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Background: In this study, we assessed whether the single nucleotide polymorphism in the murine double minute 2 (MDM2) promoter (SNP309) was associated with the occurrence of missed abortion. Methods: Genotyping of MDM2 SNP309 polymorphism was conducted by polymerase chain reaction-restriction fragment length polymorphism with blood and villous samples from 95 women diagnosed as having 1st trimester missed abortion. Results: The MDM2 SNP309 G/G genotype was associated with a higher risk of missed abortion compared with the T/T+ T/G genotype in blood (P = 0.010; odds ratio (OR): 2.164; 95 confidence interval (CI): 1.207-3.878) and villous samples (P = 0.043; OR: 2.767; 95 CI: 1.092-7.011). Conclusions: The MDM2 SNP309 G/G genotype may be a genetic risk factor for missed abortion.

Cite

CITATION STYLE

APA

Fang, Y., Kong, B., Yang, Q., Ma, D., & Qu, X. (2009). MDM2 309 polymorphism is associated with missed abortion. Human Reproduction, 24(6), 1346–1349. https://doi.org/10.1093/humrep/dep044

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free