Li Jin-Xin, Tang Bao-Peng, Sun Hui-Ping, Feng Min, Cheng Zu-Heng, Niu Wen-Quan
Cardiology Department, The First Affiliated Hospital of Xinjiang Medical University, Xinjiang, China.
Cell Stress Chaperones. 2009 Jul;14(4):355-62. doi: 10.1007/s12192-008-0089-2. Epub 2008 Dec 16.
Experimental evidence suggesting that heat shock protein 70 (Hsp70) gene or associated genes are responsible for the pathophysiology of hypertension is accumulating. In this study, we focused on five polymorphisms in three genes (HSPA1A, HSPA1B, and HSPA1L) of Hsp70 family to explore the genetic contribution, alone and in combination, of these polymorphisms to essential hypertension risk in a Uygur population. Genotyping was performed using PCR-RFLP and direct sequencing techniques. Data were analyzed using haplotype and multifactor dimensionality reduction (MDR) methods. Genotype distributions of all the polymorphisms satisfied the Hardy-Weinberg proportions in cases and controls. Statistical significance was only observed in the genotype (P = 0.0028) and (P = 0.0146) allele distributions of -110A/C polymorphism, with the -110C allele conferring a 1.45- and 2.83-fold of relative risk, assuming the additive and recessive models, respectively, and in 1267A/G genotype distribution (P = 0.0106) with the 1267G allele conferring a 44% reduced risk. The interaction information analysis indicated that polymorphisms -110A/C and 1267A/G had a strong synergistic effect, while polymorphisms 2074G/C and 2437T/C had a moderate synergistic effect. Haplotype analyses further strengthened the interaction information. Using the haplotype H(1) as a reference, haplotype H(4) had a 40% reduced risk, while haplotypes H(5) and H(8) had a significantly 5.00- and 3.75-fold increased risk for essential hypertension, respectively. Taken together, our results supported strong genetic interaction of the studied polymorphisms with the risk of having essential hypertension in Uygur ethnicity. Functional studies are warranted to confirm or refute these findings. This is the first study to evaluate the genetic interaction information of the Hsp70 in Uygur ethnicity, which represents one of the major nationalities in China with high homogeneity and unique lifestyles. Moreover, we employed the haplotype and MDR methods to explore the potential interaction of Hsp70 genetic polymorphisms in the pathogenesis of essential hypertension in Uygur.
越来越多的实验证据表明,热休克蛋白70(Hsp70)基因或相关基因与高血压的病理生理学有关。在本研究中,我们聚焦于Hsp70家族三个基因(HSPA1A、HSPA1B和HSPA1L)中的五个多态性位点,以探究这些多态性位点单独及联合作用对维吾尔族人群原发性高血压风险的遗传贡献。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和直接测序技术进行基因分型。使用单倍型和多因素降维(MDR)方法分析数据。所有多态性位点的基因型分布在病例组和对照组中均符合Hardy-Weinberg平衡。仅在-110A/C多态性的基因型(P = 0.0028)和等位基因分布(P = 0.0146)中观察到统计学意义,假设分别为加性模型和隐性模型时,-110C等位基因的相对风险分别为1.45倍和2.83倍;在1267A/G基因型分布(P = 0.0106)中,1267G等位基因的风险降低44%。相互作用信息分析表明,-110A/C和1267A/G多态性具有强协同效应,而2074G/C和2437T/C多态性具有中等协同效应。单倍型分析进一步强化了相互作用信息。以单倍型H(1)作为参照,单倍型H(4)的风险降低40%,而单倍型H(5)和H(8)患原发性高血压的风险分别显著增加5.00倍和3.75倍。综上所述,我们的结果支持所研究的多态性位点与维吾尔族人群原发性高血压风险之间存在强遗传相互作用。需要进行功能研究以证实或反驳这些发现。这是首次评估Hsp70在维吾尔族人群中遗传相互作用信息的研究,维吾尔族是中国主要民族之一,具有高度同质性和独特的生活方式。此外,我们采用单倍型和MDR方法探究了Hsp70基因多态性在维吾尔族原发性高血压发病机制中的潜在相互作用。