Daher Silvia, Sass Nelson, Oliveira Leandro G, Mattar Rosiane
Obstetrics Department, Universidade Federal de São Paulo, SP, Brazil.
Am J Reprod Immunol. 2006 Feb;55(2):130-5. doi: 10.1111/j.1600-0897.2005.00341.x.
Considering that cytokines are involved in preeclampsia (PE) pathogenesis and that cytokine gene polymorphism may affect cytokine production, our purpose was to investigate the association of PE with tumor necrosis factor (TNF)-alpha (-308), transforming growth factor-beta1 (+10; 25), interleukin (IL)-10 (-1082), IL-6 (-174), and interferon-gamma (+874) polymorphisms.
Genotyping was performed in women with PE (56 White and 95 non-White women) and in women without obstetric pathology (92 White and 97 non-White women). Data were analyzed by the chi-square or Fisher exact test. We performed a meta-analysis encompassing these and results from other laboratories on the association of TNF-alpha polymorphisms and PE.
We observed a lower frequency of the IL-10 -1082-G/G genotype in White women with PE (PE: 5%; Control (C): 15%, P = 0.02) and no association for all other polymorphisms, including meta-analysis of TNF-alpha results.
Our study suggests that PE is associated with IL-10-(1082) polymorphism but not with TNF-(308) polymorphism. On the basis of meta-analysis, we confirm the need for more studies for the evaluation of cytokine genotype in disease.
鉴于细胞因子参与子痫前期(PE)的发病机制,且细胞因子基因多态性可能影响细胞因子的产生,我们的目的是研究PE与肿瘤坏死因子(TNF)-α(-308)、转化生长因子-β1(+10;25)、白细胞介素(IL)-10(-1082)、IL-6(-174)和干扰素-γ(+874)基因多态性之间的关联。
对患有PE的女性(56名白人女性和95名非白人女性)以及无产科病理情况的女性(92名白人女性和97名非白人女性)进行基因分型。通过卡方检验或Fisher精确检验分析数据。我们进行了一项荟萃分析,纳入了这些数据以及其他实验室关于TNF-α基因多态性与PE关联的结果。
我们观察到患有PE的白人女性中IL-10 -1082-G/G基因型的频率较低(PE:5%;对照(C):15%,P = 0.02),而所有其他多态性均无关联,包括TNF-α结果的荟萃分析。
我们的研究表明,PE与IL-10-(1082)多态性相关,但与TNF-(308)多态性无关。基于荟萃分析,我们确认需要更多研究来评估疾病中的细胞因子基因型。