Chen Yequn, Ou Weichao, Lin Dong, Lin Mengyue, Huang Xiru, Ni Shuhua, Chen Shaoxing, Yong Jian, O'Gara Mary Clare, Tan Xuerui, Liu Ruisheng
First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Shantou University Medical College, Shantou, China.
Front Cardiovasc Med. 2021 Oct 15;8:756140. doi: 10.3389/fcvm.2021.756140. eCollection 2021.
Previous studies have reported that biomarkers of liver injury and renal dysfunction were associated with hypertensive disorders of pregnancy (HDP). However, the associations of these biomarkers in early pregnancy with the risk of HDP and longitudinal blood pressure pattern during pregnancy were rarely investigated in prospective cohort studies. A total of 1,041 pregnant women were enrolled in this prospective cohort study. BP was assessed in four stages throughout pregnancy. The following biomarkers were measured at early pregnancy before 18 weeks gestation: lactate dehydrogenase (LDH), aspartate aminotransferase to alanine aminotransferase ratio (AST/ALT), gamma-glutamyl transpeptidase (GGT), alkaline phosphatase (ALP), uric acid (UA), and estimated glomerular filtration rate (eGFR). Linear mixed-effects and logistic regression models were used to examine the associations of these biomarkers with longitudinal BP pattern during pregnancy and HDP incidence, respectively. In unadjusted models, higher serum UA, GGT, ALP, and LDH levels, as well as lower eGFR and AST/ALT, were associated with higher BP levels during pregnancy and an increased risk of HDP. After adjustment for maternal age, pre-pregnancy BMI and other potential confounders, UA, GGT, ALP, and LDH remained positively associated with both BP and HDP. However, eGFR and AST/ALT were not associated with HDP after adjusting for potential confounders. When including all 6 biomarkers simultaneously in multivariable analyses, increased UA, GGT, and ALP significantly associated with gestational hypertension and preeclampsia. This study suggests that increased UA, GGT, and ALP in early-pregnancy are independent risk factors of gestational hypertension and preeclampsia.
以往研究报道,肝损伤和肾功能不全的生物标志物与妊娠高血压疾病(HDP)有关。然而,在前瞻性队列研究中,很少探讨这些孕早期生物标志物与HDP风险及孕期纵向血压模式之间的关联。本前瞻性队列研究共纳入了1041名孕妇。在孕期的四个阶段评估血压。在妊娠18周前的孕早期测量以下生物标志物:乳酸脱氢酶(LDH)、天冬氨酸转氨酶与丙氨酸转氨酶比值(AST/ALT)、γ-谷氨酰转肽酶(GGT)、碱性磷酸酶(ALP)、尿酸(UA)和估计肾小球滤过率(eGFR)。分别使用线性混合效应模型和逻辑回归模型来检验这些生物标志物与孕期纵向血压模式及HDP发生率之间的关联。在未调整的模型中,较高的血清UA、GGT、ALP和LDH水平,以及较低的eGFR和AST/ALT,与孕期较高的血压水平及HDP风险增加有关。在调整了母亲年龄、孕前BMI和其他潜在混杂因素后,UA、GGT、ALP和LDH仍然与血压和HDP呈正相关。然而,在调整潜在混杂因素后,eGFR和AST/ALT与HDP无关。在多变量分析中同时纳入所有6种生物标志物时,UA、GGT和ALP升高与妊娠期高血压和先兆子痫显著相关。本研究表明,孕早期UA、GGT和ALP升高是妊娠期高血压和先兆子痫的独立危险因素。