Association of the MDR1 (ABCB1) gene 3435C> T polymorphism with male infertility

• Published in: Pharmacological reports 2009-07, Vol.61 (4), p.690-696
• Main Authors: Droździk, Marek, Stefankiewicz, Joanna, Kurzawa, Rafał, Górnik, Wanda, Bączkowski, Tomasz, Kurzawski, Mateusz
• Format: Article
• Language: English
• Subjects: Adult; Alleles; ATP Binding Cassette Transporter, Subfamily B; ATP Binding Cassette Transporter, Subfamily B, Member 1 - genetics; Drug Safety and Pharmacovigilance; genetic polymorphism; Genotype; Humans; Infertility, Male - diagnosis; Infertility, Male - genetics; Male; male infertility; MDR1 (ABCB1); Middle Aged; P-glycoprotein; Pharmacotherapy; Pharmacy; Polymorphism, Single Nucleotide - genetics; Semen - physiology; Thymidine - genetics; Young Adult
• ISSN: 1734-1140; 2299-5684
• DOI: 10.1016/S1734-1140(09)70121-5

Infertility is a common problem affecting one in six couples, and in 30% of infertile couples, the male factor is a major cause due to defective sperm quality. P-glycoprotein (P-gp), a product of the MDR1 (ABCB1) gene, may be a link between genetic and environmental factors contributing to the development of male infertility because pesticides (P-gp substrates) are well established factors of male infertility. The aim of the present study was to examine the effect of the MDR1 gene 3435C>T polymorphism on male infertility. In total, 162 male patients undergoing semen analysis due to initial infertility workup were included in the study. The control group consisted of 191 healthy males with proven fertility. MDR1 3435C>T genotyping was performed by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Assessment of MDR1 genotypes among the infertile men showed that 17.9% of subjects were carriers of the CC genotype, 58.0% were CT and 24.1% were TT. Among fertile men, 30.4% of subjects were characterised by the CC genotype, 49.7% were CT and 19.9% were TT. In addition, the frequency of carriers of at least one T allele (i.e., CT and TT genotypes) among infertile and fertile subjects was 82.1% and 69.6%, respectively. The risk of infertility was significantly elevated by two-fold in individuals carrying at least one T allele (CT and TT genotypes: p=0.009, OR=2.00, 95% CI: 1.20–3.32). Furthermore, this elevated risk was still found when considering each of the CT and TT genotypes alone (TT genotype: p=0.027, OR=2.05, 95% CI: 1.09–3.86; CT genotype: p=0.013, OR=1.98, 95% CI: 1.16–3.36). This preliminary report suggests that P-gp may play some role in male infertility, mediating detrimental effects of environmental factors.