Department of Medicine, University of Otago, Christchurch, New Zealand.
Department of Obstetrics and Gynaecology, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
BJOG. 2015 Aug;122(9):1236-43. doi: 10.1111/1471-0528.13397. Epub 2015 Apr 5.
To determine changes in plasma C-type natriuretic peptide (CNP), a paracrine product of the vascular endothelium, in pregnancies with vascular disorders, and relate these to time of presentation and severity.
Retrospective nested cases and controls.
Community study, Auckland New Zealand.
Screening for Pregnancy Endpoints (SCOPE) data and bio-bank of maternal plasma.
Maternal plasma amino terminal proCNP (NTproCNP) was measured by radioimmunoassay in early (14-16 weeks of gestation, and again at 19-21 weeks of gestation) and late (34-36 weeks of gestation) pregnancy in three groups of women (20 per group): pre-eclampsia (pre-eclampsia); gestational hypertension (GHT) with small for gestational age (SGA); and uncomplicated pregnancy.
Change in NTproCNP and associations with concurrent blood pressure, time of case presentation, severity, and infant birthweight.
Plasma NTproCNP in early pregnancy in women with vascular disorders did not differ from those found in controls. In late pregnancy, levels in pre-eclampsia (28.8 ± 2.3 pM) and in GHT with SGA (28.6 ± 4.8 pM) were significantly increased (P = 0.01 and 0.027, respectively) compared with controls (21.3 ± 1 pM). In pre-eclampsia, levels were significantly higher (P < 0.03) at 14-16 weeks of gestation in women diagnosed prior to 34 weeks of gestation. Combining all three groups, associations of NTproCNP with concurrent diastolic and mean arterial pressure were found at 34-36 weeks of gestation (r = 0.46). No significant associations were identified with birthweight.
CNP secretion during gestation is responsive to vascular stress. Plasma NTproCNP measurements may have clinical application in late pregnancy in defining the different phenotypes associated with pre-eclampsia.
确定血管病变孕妇血浆 C 型利钠肽(CNP),一种血管内皮的旁分泌产物,的变化,并将其与出现时间和严重程度相关联。
回顾性巢式病例对照研究。
新西兰奥克兰的社区研究。
妊娠终点筛查(SCOPE)数据和母血浆生物库。
采用放射免疫分析法测定三组孕妇(每组 20 例)早孕期(妊娠 14-16 周,再次在妊娠 19-21 周)和晚孕期(妊娠 34-36 周)的母体血浆氨基末端前 CNP(NTproCNP):子痫前期(子痫前期);伴有小于胎龄儿的妊娠期高血压(GHT);以及无并发症的妊娠。
NTproCNP 的变化及其与同期血压、发病时间、严重程度和婴儿出生体重的关系。
血管疾病孕妇的早期妊娠血浆 NTproCNP 与对照组无差异。在妊娠晚期,子痫前期(28.8 ± 2.3 pM)和伴有 SGA 的 GHT(28.6 ± 4.8 pM)的水平明显升高(P = 0.01 和 0.027)与对照组(21.3 ± 1 pM)相比。在子痫前期中,在妊娠 34 周前诊断为子痫前期的孕妇中,14-16 周时的水平明显升高(P < 0.03)。将三组合并后,在妊娠 34-36 周时发现 NTproCNP 与同期舒张压和平均动脉压存在相关性(r = 0.46)。未发现与出生体重有显著相关性。
妊娠期间 CNP 的分泌对血管应激有反应。血浆 NTproCNP 测量可能在妊娠晚期具有临床应用价值,可用于定义与子痫前期相关的不同表型。