Barden A E, Herbison C E, Beilin L J, Michael C A, Walters B N, Van Bockxmeer F M
University of Western Australia, Department of Medicine, Royal Perth Hospital, Perth, Australia.
J Hypertens. 2001 Oct;19(10):1775-82. doi: 10.1097/00004872-200110000-00011.
This study examined the frequency of the Lys198Asn polymorphism in the endothelin-1 (ET-1) gene in women with pre-eclampsia and normal pregnancy; and its contribution to levels of plasma ET-1 and blood pressure.
This was a retrospective study examining the frequency of the ET-1 Lys198Asn polymorphism in 72 proteinuric pre-eclamptics and 81 normal pregnant women. Height, weight, blood pressure and plasma ET-1 were measured antenatally and at 6 weeks post-partum. Using specific mutagenic primers, the frequency of the G/G (normal), G/T heterozygote and T/T (mutant) genotypes of the Lys198Asn polymorphism were examined.
The polymorphism was not associated with pre-eclampsia. However, in the combined pregnant groups after correction for BMI and group, a significant effect of the T-allele (T/T,G/T) on systolic blood pressure was found (121 +/- 1.5 mmHg compared with 116 +/- 1.3 mmHg in the G/G homozygotes). A significant interaction was found between the T-allele and pregnancy in determining systolic blood pressure, so that the effect was no longer seen post-partum. Pregnant women with the T/T genotype had significantly elevated plasma ET-1 levels 5.8 pg/ml [confidence interval (CI) 3.7-9.1] compared with 3.1 pg/ml (CI 2.6-3.8) in the G/T heterozygotes and 3.6 pg/ml (CI 3.0-4.1) in the normal G/G homozygotes.
The Lys198Asn polymorphism does not directly contribute to the incidence of pre-eclampsia. However, the association of the T-allele with raised blood pressure and the T/T genotype with increased plasma ET-1 levels suggest that this polymorphism may interact with other genes or environmental factors to sensitize pregnant women to develop pre-eclampsia.
本研究检测了子痫前期妇女和正常妊娠妇女内皮素-1(ET-1)基因中Lys198Asn多态性的频率;并研究了该多态性对血浆ET-1水平和血压的影响。
这是一项回顾性研究,检测了72例蛋白尿性子痫前期患者和81例正常孕妇中ET-1 Lys198Asn多态性的频率。在产前和产后6周测量身高、体重、血压和血浆ET-1。使用特异性诱变引物,检测Lys198Asn多态性的G/G(正常)、G/T杂合子和T/T(突变)基因型的频率。
该多态性与子痫前期无关。然而,在校正BMI和分组后,在合并的孕妇组中,发现T等位基因(T/T、G/T)对收缩压有显著影响(T/T、G/T组收缩压为121±1.5 mmHg,G/G纯合子组为116±1.3 mmHg)。在决定收缩压方面,发现T等位基因与妊娠之间存在显著交互作用,因此产后不再出现这种影响。与G/T杂合子组的3.1 pg/ml(可信区间[CI]2.6 - 3.8)和正常G/G纯合子组的3.6 pg/ml(CI 3.0 - 4.1)相比,T/T基因型的孕妇血浆ET-1水平显著升高,为5.8 pg/ml(CI 3.7 - 9.1)。
Lys198Asn多态性并不直接导致子痫前期的发生。然而,T等位基因与血压升高以及T/T基因型与血浆ET-1水平升高之间的关联表明,这种多态性可能与其他基因或环境因素相互作用,使孕妇更易患子痫前期。