Bhatnagar Sonu, Bhattacharjee Jayashree, Vaid Mudit, Madan Taruna, Trivedi Shubha S, Sarma Puranam U
Department of Biochemistry, Lady Hardinge Medical College, New Delhi, India.
Aust N Z J Obstet Gynaecol. 2007 Dec;47(6):477-82. doi: 10.1111/j.1479-828X.2007.00783.x.
Pre-eclampsia is one of the most frequent complications of pregnancy, however, little is known about its aetiology.
The objective of this study was to investigate the association between inducible nitric oxide synthase (iNOS) genotypes and pre-eclampsia. We also measured the concentrations of tumour necrosis factor-alpha (TNF-alpha), nitric oxide (NO) and superoxide dismutase (SOD) in patients with pre-eclampsia to evaluate their relations to the single nucleotide polymorphisms (SNPs) observed.
This cross-sectional study included 30 pregnant women with pre-eclampsia and 30 healthy pregnant women. They were screened at 28th, 36th weeks of gestation and just after delivery (within 48 h), and their blood samples were analysed for NO, SOD, TNF-alpha and iNOS gene polymorphism.
Patients with pre-eclampsia at 36 weeks gestation showed significantly increased serum NO levels (P=0.007), whereas SOD activity was decreased significantly (P=0.004). A doublefold increase was observed in TNF-alpha levels at 36 weeks in patients with pre-eclampsia (P=0.003) which decreased significantly (P=0.001) after delivery. A total of four SNPs were observed, of which two (G300A exon 8 and G274T exon 16) showed statistically significant association with pre-eclampsia. When compared, G274T exon 16 SNP also showed association with TNF-alpha levels and SOD activity in pre-eclamptic patients.
As pre-eclampsia is a disease of multifactorial aetiopathology, NO, TNF-alpha, SOD activity and NOS2A polymorphism might play an intermingled role in its development.
子痫前期是妊娠最常见的并发症之一,但其病因知之甚少。
本研究旨在调查诱导型一氧化氮合酶(iNOS)基因多态性与子痫前期之间的关联。我们还测量了子痫前期患者体内肿瘤坏死因子-α(TNF-α)、一氧化氮(NO)和超氧化物歧化酶(SOD)的浓度,以评估它们与观察到的单核苷酸多态性(SNP)之间的关系。
这项横断面研究纳入了30例子痫前期孕妇和30例健康孕妇。在妊娠第28周、36周及产后(48小时内)对她们进行筛查,并分析她们血液样本中的NO、SOD、TNF-α和iNOS基因多态性。
妊娠36周的子痫前期患者血清NO水平显著升高(P=0.007),而SOD活性显著降低(P=0.004)。子痫前期患者在36周时TNF-α水平增加了一倍(P=0.003),产后显著下降(P=0.001)。共观察到4个SNP,其中2个(第8外显子G300A和第16外显子G274T)与子痫前期存在统计学显著关联。相比之下,第16外显子G274T SNP在子痫前期患者中也与TNF-α水平和SOD活性有关联。
由于子痫前期是一种多因素病因病理的疾病,NO、TNF-α、SOD活性和NOS2A多态性可能在其发展过程中起相互交织的作用。