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Impact of genetic variation of tumor necrosis factor-α on gestational hypertension

机译:肿瘤坏死因子-α基因变异对妊娠高血压的影响

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Background The mechanisms responsible for the pathogeneses of gestational hypertension and preeclampsia are unclear. Tumor necrosis factor-α (TNF-α) is a pro-inflammatory Th_1-type cytokine. TNFA gene is located in the human leukocyte antigen (HLA) class Ⅲ region of the major histocompatibility complex (MHC) on chromosome 6. The high TNF-α mRNA expression may be associated with the TNF2 (A) allele, which is the polymorphism of TNF-α at position —308 in promoter region. This study assessed whether the TNF2 (A) allele at position —308 plays a role in the alteration of blood pressure (BP) and urinary protein excretion during pregnancy. Methods The original prospective cohort study comprised 1623 pregnant women from January 2000 to October 2001. The G/A polymorphism was done by restriction fragment length polymorphism (RFLP) analysis with Nco Ⅰ enzyme. Results The distributions of the G/A polymorphism of TNF-α in the promoter region at position —308 were wild-type 72.4% and variant 27.6%, respectively. The frequency of TNF2 (A) allele was approximately 0.15 for Caucasian pregnant women in the study. It was not significantly different in the distributions of genotypes and G/A allele frequencies among the three groups of pregnant women with gestational hypertension, preexisting hypertension and normal blood pressure (P > 0.05). The maternal blood pressure in the third trimester was significantly higher in the group of women possessing the TNF2 (A) allele compared to homozygous for the TNF1 (G) allele (systolic BP, P < 0.01 and diastolic BP, P < 0.05). The elevated blood pressure in the TNF2 (A) group was accompanied by higher urinary protein excretion in the third trimester (P < 0.05). The blood pressure and urinary protein excretion did not change apparently between the two groups in the first and second trimesters (P > 0.05). Conclusions Maternal TNF2 (A) allele of TNF-α promoter region at position -308 could play a role in the alteration of blood pressures and/or enhancement of urinary protein excretion during pregnancy, and might play an important role in the development of both gestational hypertension and preeclampsia.
机译:背景引起妊娠高血压和先兆子痫的病因的机制尚不清楚。肿瘤坏死因子-α(TNF-α)是促炎性Th_1型细胞因子。 TNFA基因位于6号染色体上主要组织相容性复合体(MHC)的人类白细胞抗原(HLA)Ⅲ类区域。TNF-αmRNA的高表达可能与TNF2(A)等位基因相关,这是TNFA基因的多态性。 TNF-α在启动子区域的第308位。这项研究评估了—308位的TNF2(A)等位基因是否在怀孕期间血压(BP)和尿蛋白排泄的改变中起作用。方法从2000年1月至2001年10月,对1623例孕妇进行前瞻性队列研究。通过NcoⅠ酶切限制性片段长度多态性(RFLP)分析进行G / A多态性分析。结果TNF-α在/ 308位启动子区的G / A多态性分布分别为野生型72.4%和变异型27.6%。在该研究中,白种人孕妇的TNF2(A)等位基因频率约为0.15。在妊娠高血压,既往高血压和正常血压的三组孕妇中,基因型和G / A等位基因频率的分布没有显着差异(P> 0.05)。与具有TNF1(G)等位基因纯合子的女性相比,拥有TNF2(A)等位基因的妇女在妊娠中期的孕妇血压显着更高(收缩压,P <0.01和舒张压,P <0.05)。 TNF2(A)组的血压升高伴随着妊娠晚期尿蛋白排泄的增加(P <0.05)。两组在孕早期和孕中期的血压和尿蛋白排泄没有明显变化(P> 0.05)。结论-308位TNF-α启动子区域的孕妇TNF2(A)等位基因可能在妊娠期血压的改变和/或尿蛋白排泄的增强中起重要作用,并可能在两种妊娠的发生中起重要作用。高血压和先兆子痫。

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