School of Public Health, University College Cork, Cork, Ireland.
Irish Centre for Maternal & Child Health, University College Cork, Cork, Ireland.
JAMA Netw Open. 2020 Feb 5;3(2):e1920964. doi: 10.1001/jamanetworkopen.2019.20964.
Adverse pregnancy outcomes, such as hypertensive disorders of pregnancy, gestational diabetes, and preterm delivery, are associated with increased risk of maternal cardiovascular disease. Little is known about whether adverse pregnancy outcomes are associated with increased risk of maternal chronic kidney disease (CKD) and end-stage kidney disease (ESKD).
To review and synthesize the published literature on adverse pregnancy outcomes (hypertensive disorders of pregnancy, gestational diabetes, and preterm delivery) and subsequent maternal CKD and ESKD.
PubMed, Embase, and Web of Science were searched from inception to July 31, 2019, for cohort and case-control studies of adverse pregnancy outcomes and maternal CKD and ESKD.
Selected studies included the following: a population of pregnant women, exposure to an adverse pregnancy outcome of interest, and at least 1 primary outcome (CKD or ESKD) or secondary outcome (hospitalization or death due to kidney disease). Adverse pregnancy outcomes included exposure to hypertensive disorders of pregnancy (preeclampsia, gestational hypertension, or chronic hypertension), preterm delivery (<37 weeks), and gestational diabetes. Three reviewers were involved in study selection. Of 5656 studies retrieved, 23 were eligible for inclusion.
The Meta-analyses of Observational Studies in Epidemiology (MOOSE) guidelines were followed throughout. Three reviewers extracted data and appraised study quality. Random-effects meta-analyses were used to calculate overall pooled estimates using the generic inverse variance method.
Primary outcomes included CKD and ESKD diagnosis, defined using established clinical criteria (estimated glomerular filtration rate or albuminuria values) or hospital records. The protocol for this systematic review was registered on PROSPERO (CRD42018110891).
Of 23 studies included (5 769 891 participants), 5 studies reported effect estimates for more than 1 adverse pregnancy outcome. Preeclampsia was associated with significantly increased risk of CKD (pooled adjusted risk ratio [aRR], 2.11; 95% CI, 1.72-2.59), ESKD (aRR, 4.90; 95% CI, 3.56-6.74), and kidney-related hospitalization (aRR, 2.65; 95% CI, 1.03-6.77). Gestational hypertension was associated with increased risk of CKD (aRR, 1.49; 95% CI, 1.11-2.01) and ESKD (aRR, 3.64; 95% CI, 2.34-5.66). Preterm preeclampsia was associated with increased risk of ESKD (aRR, 5.66; 95% CI, 3.06-10.48); this association with ESKD persisted for women who had preterm deliveries without preeclampsia (aRR, 2.09; 95% CI, 1.64-2.66). Gestational diabetes was associated with increased risk of CKD among black women (aRR, 1.78; 95% CI, 1.18-2.70), but not white women (aRR, 0.81; 95% CI, 0.58-1.13).
In this meta-analysis, exposure to adverse pregnancy outcomes, including hypertensive disorders of pregnancy, gestational diabetes, and preterm delivery, was associated with higher risk of long-term kidney disease. The risk of ESKD was highest among women who experienced preeclampsia. A systematic approach may be warranted to identify women at increased risk of kidney disease, particularly after hypertensive disorders of pregnancy, and to optimize their long-term follow-up.
妊娠不良结局,如妊娠高血压疾病、妊娠期糖尿病和早产,与增加的母亲心血管疾病风险相关。关于妊娠不良结局是否与增加的母亲慢性肾脏病(CKD)和终末期肾病(ESKD)风险相关,知之甚少。
综述和综合已发表的关于妊娠不良结局(妊娠高血压疾病、妊娠期糖尿病和早产)以及随后的母亲 CKD 和 ESKD 的文献。
从成立到 2019 年 7 月 31 日,在 PubMed、Embase 和 Web of Science 上搜索了队列和病例对照研究,以评估妊娠不良结局和母亲 CKD 和 ESKD 的相关性。
入选研究包括以下内容:孕妇人群、妊娠不良结局(子痫前期、妊娠高血压或慢性高血压)的暴露以及至少 1 个主要结局(CKD 或 ESKD)或次要结局(因肾脏疾病住院或死亡)。妊娠不良结局包括暴露于妊娠高血压疾病(子痫前期、妊娠高血压或慢性高血压)、早产(<37 周)和妊娠期糖尿病。3 位评审员参与了研究选择。在检索到的 5656 篇研究中,有 23 篇符合纳入标准。
在整个研究过程中都遵循了观察性研究的荟萃分析(MOOSE)指南。3 位评审员提取数据并评估研究质量。使用通用倒数方差法计算随机效应荟萃分析的总体汇总估计值。
主要结局包括 CKD 和 ESKD 诊断,使用既定的临床标准(估计肾小球滤过率或白蛋白尿值)或医院记录定义。该系统评价的方案已在 PROSPERO(CRD42018110891)上注册。
在纳入的 23 项研究(5769891 名参与者)中,有 5 项研究报告了超过 1 种妊娠不良结局的效应估计值。子痫前期与 CKD(调整后的风险比[ARR],2.11;95%置信区间[CI],1.72-2.59)、ESKD(ARR,4.90;95%CI,3.56-6.74)和与肾脏相关的住院(ARR,2.65;95%CI,1.03-6.77)风险显著增加相关。妊娠高血压与 CKD(ARR,1.49;95%CI,1.11-2.01)和 ESKD(ARR,3.64;95%CI,2.34-5.66)风险增加相关。早产子痫前期与 ESKD(ARR,5.66;95%CI,3.06-10.48)风险增加相关;这种与 ESKD 的关联在没有子痫前期的早产妇女中仍然存在(ARR,2.09;95%CI,1.64-2.66)。妊娠期糖尿病与黑人妇女的 CKD(ARR,1.78;95%CI,1.18-2.70)风险增加相关,但与白人妇女(ARR,0.81;95%CI,0.58-1.13)无关。
在这项荟萃分析中,妊娠不良结局(包括妊娠高血压疾病、妊娠期糖尿病和早产)的暴露与长期肾脏疾病的风险增加相关。ESKD 的风险在经历子痫前期的妇女中最高。可能需要采取系统方法来识别患有肾脏疾病风险增加的妇女,尤其是在经历妊娠高血压疾病后,并优化其长期随访。