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Vitamin D deficiency and depressive symptoms in pregnancy are associated with adverse perinatal outcomes
Authors:Eynav Elgavish Accortt  Amy Lamb  James Mirocha  Calvin J. Hobel
Affiliation:1.Department of Obstetrics and Gynecology,Cedars-Sinai Medical Center,Los Angeles,USA;2.Cedars-Sinai Biostatistics Core, Research Institute, Clinical and Translational Science Institute (CTSI),Clinical and Translational Research Center (CTRC),Los Angeles,USA
Abstract:
Prenatal vitamin D deficiency and prenatal depression are both separately associated with adverse perinatal outcomes; however, to our knowledge no studies have investigated the effects of having both risk factors. Our objective was to determine to what extent vitamin D deficiency predicts adverse perinatal outcomes and whether elevated depressive symptoms in pregnancy places women at additional increased risk. This study was a secondary data analysis of prospective data collected from a cohort of pregnant women (N?=?101) in an obstetric clinic of a large medical center. Maternal vitamin D deficiency (serum 25(OH)D?≤?20 ng/ml) and depressive symptoms (Edinburgh Postnatal Depression Scale, EPDS) were assessed in early pregnancy. A composite of four adverse perinatal outcomes (low birth weight, preterm birth, small-for-gestational age, and preeclampsia) were abstracted from medical charts. Nineteen of the 101 women had one or more adverse perinatal outcome and 84% with an adverse outcome (16/19) were not White. Both prenatal and time of delivery vitamin D deficiency were associated with developing an adverse outcome compared to those vitamin D sufficient (prenatal relative risk 3.43; 95% CI 1.60–7.34, p?=?0.004; delivery time relative risk 5.14, 95% CI 2.68–9.86, p?=?0.004). These both remained significant after adjusting for BMI. A higher rate of adverse outcome was found when women had both prenatal vitamin D deficiency and elevated depressive symptoms (EPDS?≥?10). Sixty percent with both risk factors had an adverse perinatal outcome versus 17% with only one or neither risk factor (relative risk 3.60; 95% CI 1.55–8.38, p?=?0.045), worthy of investigation with larger samples. Together, prenatal vitamin D deficiency and elevated depressive symptoms in pregnancy may increase risk for adverse perinatal outcomes, especially in racial minorities. Obstetric providers should consider routine prenatal depression screening. The impact of vitamin D supplementation to reduce risk for adverse perinatal outcomes should be studied in prospective trials. Our results suggest that supplementation early in pregnancy might be especially beneficial for depressed women.
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