PD-L1 gene variants as predictors of recurrent pregnancy loss: A case-control study among Kazakh women in Central and West Kazakhstan

• Published in: Journal of reproductive immunology Vol. 169; p. 104524
• Main Authors: Almawi, Wassim Y., Aimagambetova, Gulzhanat, Tursunov, Abay, Turesheva, Akbayan, Marat, Aizada, Ilmaliyeva, Aktoty, Atageldiyeva, Kuralay
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 01.06.2025
• Subjects: Abortion, Habitual - epidemiology; Abortion, Habitual - genetics; Adult; B7-H1 Antigen - genetics; Case-Control Studies; Female; Genetic association; Genetic Predisposition to Disease; Genotype; Humans; Kazakhstan; Obstetrics and Gynecology; PD-L1; Polymorphism, Single Nucleotide; Pregnancy; Recurrent pregnancy loss; Single nucleotide polymorphism; Kazakhstan; PD-L1; Single nucleotide polymorphism; Genetic association; Kazakhstan; Recurrent pregnancy loss
• ISSN: 0165-0378; 1872-7603; 1872-7603
• DOI: 10.1016/j.jri.2025.104524

Emerging evidence implicates immune dysfunction in maintaining maternal-fetal tolerance, particularly the programmed death-ligand 1 (PD-L1) pathway. The association between PD-L1 gene variants and recurrent pregnancy loss (RPL) in women from Central and West Kazakhstan was investigated, and correlations between PD-L1 genotypes and demographic or clinical features were explored. This case-control study included 197 women with RPL and 198 controls of ethnically Kazakh women. Genotyping of rs2297136, rs2297137, rs4143815, rs822336, and rs822337 PD-L1 variants was performed by real-time PCR. Demographic and clinical characteristics did not differ significantly between RPL cases and controls from Central and West Kazakhstan. Significant associations were found in the West Kazakhstan cohort for rs822336 (p = 0.02) and rs822337 (p = 0.004). The G/C genotype of rs822336 (OR = 2.33, 95 % CI = 1.04–5.26) and rs822337 (OR = 308, 95 % CI = 1.34–7.04) was associated with an increased risk of RPL in West Kazakhstan cohort. Haplotype analysis revealed a significant association of the GTGAG haplotype with RPL in West Kazakhstan (p = 0.018) but not in Central Kazakhstan subjects. Correlation analysis showed that rs822336 was positively correlated with age and BMI (p < 0.05) in Central Kazakhstan, while rs822337 was negatively correlated with live births in West Kazakhstan (p < 0.05). The findings underscore population-specific genetic influences on RPL risk, with notable significant associations between RPL and PD-L1 SNPs and GTGAG haplotype in the West Kazakhstan cohort but not in the Central Kazakhstan cohort. This highlights the contribution of genetic factors to RPL pathogenesis in different populations. •PD-L1 gene SNPs rs822336 and rs822337 were associated with RPL in the West but not Central Kazakhstan.•PD-L1 gene SNPs rs822336 and rs822337 G/C genotypes were associated with increased RPL risk in the West Kazakhstan cohort.•PD-L1 gene GTGAG haplotype was associated with RPL in West but not in Central Kazakhstan subjects.•PD-L1 gene SNP rs822336 was positively correlated with age and BMI in Central Kazakhstan•PD-L1 gene SNP rs822337 was negatively correlated with live births in West Kazakhstan