Sivaraj Nagarjuna, K Vijaya Rachel, Suvvari Tarun Kumar, Prasad Shilaja, Sri Harsha Boppana, Majji Vineetha, Vegi Pradeep Kumar, Bunga Papa Kusuma
Research and Development, Great Eastern Medical School and Hospital, Srikakulam, IND.
Biochemistry and Bioinformatics, Gandhi Institute of Technology and Management (Deemed To Be University), Visakhapatnam, IND.
Cureus. 2022 May 6;14(5):e24788. doi: 10.7759/cureus.24788. eCollection 2022 May.
Introduction Many studies have gone into single nucleotide polymorphisms (SNPs) in inflammatory-associated genes and preeclampsia risk; still, the findings are inconclusive. The current study aims to evaluate the association of SNP rs2229238 in the interleukin 6 receptor alpha (IL6RA) gene with the risk of preeclampsia. Methodology An observational case-control study was conducted and 216 patients were included in this study. Of the patients, 104 were normotensive subjects and 112 were subjects with preeclampsia. Genotyping for SNP rs2229238 was performed by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Results The genotype allocation of the SNP 2229238 C/A polymorphism was not different in preeclampsia subjects (CC: 42%; CA: 42%; AA: 16%) and normotensive pregnant women (CC: 37%; CA: 48%; AA: 15%) (p-value = 0.73). The frequency of the A allele was 34% in preeclampsia subjects and 31% in normotensive pregnancies. There was no significant variation seen in the allele frequencies among cases and the control population. Conclusion Our study reported that there is no significant relation between preeclampsia and IL6RA SNP rs2229238. Also, there is no significance in the allele frequencies among both cases and control groups.
引言 许多研究已探讨炎症相关基因中的单核苷酸多态性(SNP)与子痫前期风险的关系;然而,研究结果尚无定论。本研究旨在评估白细胞介素6受体α(IL6RA)基因中的SNP rs2229238与子痫前期风险的关联。
方法 进行了一项观察性病例对照研究,本研究纳入了216例患者。其中,104例为血压正常的受试者,112例为子痫前期患者。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对SNP rs2229238进行基因分型。
结果 SNP 2229238 C/A多态性的基因型分布在子痫前期患者(CC:42%;CA:42%;AA:16%)和血压正常的孕妇(CC:37%;CA:48%;AA:15%)中无差异(p值 = 0.73)。子痫前期患者中A等位基因的频率为34%,血压正常妊娠者中为31%。病例组和对照组人群的等位基因频率未见显著差异。
结论 我们的研究报告称,子痫前期与IL6RA SNP rs2229238之间无显著关联。此外,病例组和对照组的等位基因频率也无显著性差异。