Abnormal urinary protein loss is a marker associated with a diverse range of renal diseases including preeclampsia. Current measures of urine protein used in the diagnostic criteria for the diagnosis of preeclampsia include urine protein:creatinine ratio and 24-hour urine protein. However very little is known about the value of urine albumin:creatinine ratio (uACR) in pregnancy. In this study we examined the prognostic value of microalbuminuria detected antepartum to predict adverse pregnancy outcomes. This is a single-centre retrospective analysis of 84 pregnant women over the age of 16 attending a tertiary ’high-risk’ pregnancy outpatient clinic between July 2010 and June 2013. Utilising medical records, antepartum peak uACR level and pregnancy maternal and fetal outcomes were recorded. To be included in the study, the participant had to have at least one uACR measurement performed during pregnancy (excluding measurements performed at or near to delivery). uACR measurements were obtained at various time points in the pregnancy, from gestational periods 0–19+6 weeks, 20–27+6 weeks, 28–33+6 weeks. As not all participants had uACR measurements at each of these time points, the peak uACR measurement prior to 34 weeks gestation (and prior to delivery date, to ensure that the uACR was not measured at the time of an adverse pregnancy outcome such as preeclampsia) was chosen for the final analysis. Patient characteristics, medications (particularly the use of aspirin and calcium), blood pressure, urinalysis, serum creatinine, fetal and maternal outcomes of the pregnancy were collected from patient medical records and electronic databases. Those patients who did not have at least one uACR performed prior to <34 wks or did not have data on the pregnancy outcomes of interest were excluded from the study. Out of 116 patients attending the renal pregnancy clinic between July 2010 and June 2013, 33 patients were excluded due to absence of at least one uACR performed prior to <34 wks or missing data on the pregnancy outcomes, leaving 83 patients for the final analysis. The women had a mean age of 33.1 (±5.4) years. Mean BMI was 29.4 (±8.1) kg/m2. Almost half the population (47.6%) had a previous history of hypertension, one fifth (20.2%) had a previous history of preeclampsia, and more than a third (36.9%) had chronic kidney disease. Over a third of the population (36.9%) had diabetes mellitus (DM) either in the form of gestational diabetes mellitus (GDM), Type 2 DM or Type 1 DM. The primary outcome was a composite of poor maternal and fetal outcomes including preeclampsia, maternal death, eclampsia, stillbirth, neonatal death, IUGR, premature delivery and placental abruption. As the antepartum peak uACR level (in mg/mmol) increased from normoalbuminuria (uACR <3.5) to microalbuminuria (uACR 3.5–35) to macroalbuminuria (>35), the percentage of women with the primary composite outcome increased in a stepwise fashion (13.8% to 24.1% to 62.1%, respectively, p < 0.001). After adjusting for covariates including history of hypertension, chronic kidney disease and aspirin therapy during pregnancy, micro- and macroalbuminuria remained significant predictors of the primary outcome. We have shown that antepartum peak uACR is a useful simple marker to help predict adverse maternal and fetal outcomes. Further prospective studies are required to assess uACR as a prognostic tool in pregnancy before it can be applied in clinical practice.
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