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Prepregnancy renal function and risk of preterm birth and related outcomes
Authors:Ziv Harel  Alison L Park  Eric McArthur  Michelle Hladunewich  Jade S Dirk  Ron Wald  Amit X Garg  Joel G Ray
Institution:Division of Nephrology (Harel, Wald) and Department of Medicine (Ray), St. Michael’s Hospital, Toronto, Ont.; ICES (Park, McArthur, Dirk, Garg, Ray), Ontario; Division of Nephrology (Hladunewich), Sunnybrook Health Sciences Centre, Toronto, Ont.; Division of Nephrology (Garg), Western University, London, Ont.
Abstract:BACKGROUND:Prepregnancy kidney dysfunction has been associated with preterm birth, which is the leading cause of neonatal morbidity and mortality; however, the relation is not well understood. We determined the risk of preterm birth in women with prepregnancy kidney dysfunction, defined using pregnancy-specific serum creatinine cut points.METHODS:This population-based cohort study in the province of Ontario, Canada, involved women aged 16 to 50 years who had a singleton birth between 2006 and 2016 and measurement of serum creatinine within 10 weeks preceding their estimated conception date. The exposure was abnormally elevated prepregnancy serum creatinine, defined as greater than the 95th percentile (> 77 μmol/L), a value derived from a population-based sample of women without known kidney disease who became pregnant soon after the measurement was obtained. The main outcome was any preterm birth from 23 to 36 weeks’ gestation. Secondary outcomes included provider-initiated preterm birth before 37 weeks’ gestation and spontaneous preterm birth before 37 weeks.RESULTS:Among 55 946 pregnancies, preterm birth before 37 weeks’ gestation occurred in 3956 women (7.1%). The risk of preterm birth before 37 weeks was higher among women with prepregnancy creatinine above the 95th percentile, relative to those with prepregnancy creatinine at or below the 95th percentile (9.1% v. 7.0%; adjusted relative risk RR] 1.23, 95% confidence interval CI] 1.09 to 1.38). The effect was significant for provider-initiated preterm birth (adjusted RR 1.30, 95% CI 1.11 to 1.52) but not for spontaneous preterm birth (adjusted RR 1.12, 95% CI 0.91 to 1.37).INTERPRETATION:Given that prepregnancy kidney dysfunction conferred an increased risk of preterm birth, measurement of serum creatinine (a relatively inexpensive blood test) may form part of the assessment of risk for preterm birth among those planning pregnancy.

Prepregnancy kidney dysfunction may perturb the normal physiologic adaptations of pregnancy, predisposing a woman and her fetus to adversity, at least partly mediated by placental and endothelial dysfunction.1 Complications such as preeclampsia2 and poor fetal growth3 may necessitate provider-initiated preterm birth. Preterm birth of any form before 37 weeks’ gestation occurs in 6% to 11% of viable pregnancies and is the leading cause of infant death.4Prepregnancy kidney dysfunction has been associated with preterm birth.57 Prior studies of the relation between prepregnancy kidney dysfunction and preterm birth were primarily case series and thus had inadequate statistical power to differentiate between the outcomes of spontaneous versus provider-initiated preterm birth. In addition, arbitrary cut points were used in these studies to define prepregnancy kidney dysfunction, and there was no accounting for important confounders.5,814In an effort to overcome the aforementioned limitations, we completed a large cohort study in a setting where prenatal and obstetric care is covered under a provincial health insurance plan. Using population-derived cut points for prepregnancy serum creatinine to define kidney dysfunction, we examined the risk of preterm birth and other related outcomes.
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