Clinical Laboratory, the Affiliated Hospital of Qingdao University, Qingdao, China.
Obstetrics Department, Qingdao Women and Children's Hospital, Qingdao, China.
Biosci Rep. 2020 Feb 28;40(2). doi: 10.1042/BSR20194307.
Preeclampsia (PE) is an excessive systemic inflammation response with dysfunction of endothelial. As a stress protein, heat shock protein 70 (HSP70) plays a pivotal role in protecting cells against apoptosis, oxidative damage and genetic damage. In humans, three genes encode members of the HSP70 class: HSPA1A, HSPA1B and HSPA1L. Our study was to investigate the association between genetic variations of HSPA1L and the susceptibility for PE in Chinese Han population. The polymorphisms of rs2227956, rs1043618 and rs1061581 in HSPA1L were genotyped by TaqMan allelic discrimination real time polymerase chain reaction (PCR) in 929 PE patients and 1024 healthy pregnant women. Statistic difference of the genotypic and allelic frequencies were found in HSPA1L rs1061581 between PE patients and controls (χ2 = 29.863, P < 0.001 by genotype; χ2 = 27.298, P < 0.001, OR = 1.874, 95%CI 1.476-2.379 by allele) and HSPA1L rs1061581 A alleles occurred more frequently in PE patients compared with healthy controls (PE vs. controls 10.28% vs. 5.76%). Furthermore, we divided the PE cases into early-onset/late-onset PE and mild/severe PE subgroups and found statistical differences in genotypic and allelic frequencies of the HSPA1L rs1061581 between early-onset PE, late-onset PE, mild PE, severe PE and controls, respectively. Moreover, HSPA1L rs1061581 A alleles were more frequent in early-onset PE, late-onset PE, mild PE and severe PE than controls respectively. Therefore, we concluded that HSPA1L rs1061581 polymorphism is associated with the risk of PE in Han Chinese women and A alleles may play a role in the susceptibility for PE.
子痫前期 (PE) 是一种过度的全身炎症反应,伴有内皮功能障碍。热休克蛋白 70 (HSP70) 作为一种应激蛋白,在保护细胞免受细胞凋亡、氧化损伤和遗传损伤方面发挥着关键作用。在人类中,有三个基因编码 HSP70 类的成员:HSPA1A、HSPA1B 和 HSPA1L。我们的研究旨在探讨中国汉族人群中 HSPA1L 基因多态性与子痫前期易感性的关系。采用 TaqMan 等位基因鉴别实时聚合酶链反应 (PCR) 对 HSPA1L 中的 rs2227956、rs1043618 和 rs1061581 多态性进行基因分型,共纳入 929 例 PE 患者和 1024 例健康孕妇。在 PE 患者和对照组中,HSPA1L rs1061581 的基因型和等位基因频率存在统计学差异 (基因型:χ2 = 29.863,P < 0.001;等位基因:χ2 = 27.298,P < 0.001,OR = 1.874,95%CI 1.476-2.379),且 HSPA1L rs1061581 A 等位基因在 PE 患者中的频率高于健康对照组 (PE 患者 vs. 对照组:10.28% vs. 5.76%)。此外,我们将 PE 病例分为早发型/晚发型 PE 和轻度/重度 PE 亚组,发现 HSPA1L rs1061581 的基因型和等位基因频率在早发型 PE、晚发型 PE、轻度 PE、重度 PE 与对照组之间存在统计学差异。此外,HSPA1L rs1061581 A 等位基因在早发型 PE、晚发型 PE、轻度 PE 和重度 PE 患者中的频率均高于对照组。因此,我们得出结论,HSPA1L rs1061581 多态性与汉族妇女子痫前期的发病风险相关,A 等位基因可能与子痫前期的易感性有关。