Abstract

BackgroundHyperhomocysteinemia may be a risk factor for endothelial dysfunction. Folate and vitamin B12 regulate the homocysteine metabolic process. This study aimed to evaluate the associations between subsequent events of adverse pregnancy outcome and early variables of homocysteine, folate, and vitamin B12 in pregnant women.MethodsThis multicenter, retrospective, case–control study involved 563 pregnant women with adverse pregnancy outcome and 600 controls. Adverse pregnancy outcomes included one or more of the following events: preeclampsia, preterm birth, low birth weight, and stillbirth. The associations between subsequent events of adverse pregnancy outcome and early variables of homocysteine, folate, and vitamin B12; metabolic parameters; inflammatory markers; anthropometrics; and lifestyle habits at 11–12 weeks of gestation were analyzed using the logistic regression model.ResultsCompared to the lower quartile homocysteine concentrations, the upper quartile homocysteine concentrations were associated with preeclampsia, preterm birth and low birth weight. On the contrary, the lower quartile folate concentrations were associated with preeclampsia, preterm birth and low birth weight compared with the upper quartile folate concentrations. The incidence of adverse pregnancy outcome increased progressively from the first to fourth homocysteine quartiles but decreased progressively from the first to fourth folate quartiles. After adjusting for confounding factors, multivariate logistic regression analysis showed that besides systolic blood pressure, diastolic blood pressure, body mass index and age, homocysteine (IV vs I quartile, aOR 5.89, 95% CI 4.08–8.51, P < 0.001), folate (IV vs I quartile, aOR 0.35, 95% CI 0.25–0.50, P < 0.001), folate supplementation (yes vs no, aOR 0.55, 95% CI 0.35–0.86, P = 0.010) during early pregnancy were independently associated with subsequent events of adverse pregnancy outcome, and vitamin B12 was rejected. Of these, the homocysteine revealed the highest odds ratio in all risk variables, and folate showed the lowest odds ratio in all protective variables.ConclusionsHigher homocysteine concentration and lower folate level during early pregnancy were associated with adverse pregnancy outcome. However, no association was found between vitamin B12 and adverse pregnancy outcome. Supplementation with folate in early pregnancy may reduce adverse pregnancy outcome.

Highlights

  • Hyperhomocysteinemia may be a risk factor for endothelial dysfunction

  • Comparison of principal characteristics between pregnant women with Adverse pregnancy outcome (APO) and controls in early pregnancy Compared with controls, pregnant women with APO were characterized by increased serum concentrations of Hcy, total cholesterol (TC), TG, Low-density lipoprotein cholesterol (LDL-C), and fasting plasma glucose (FPG); higher value of Systolic blood pressure (SBP), diastolic blood pressure (DBP), and body mass index (BMI); older age; and decreased serum levels of folate, vitamin B12 (VB12), and high-density lipoprotein cholesterol (HDL-C) (P < 0.05)

  • Independent associations of subsequent events of APO with each of the early variables in pregnant women as detected by multivariate logistic regression analysis After adjusting for confounding factors, the multivariate logistic regression analysis showed that Hcy, folate, SBP, DBP, BMI, age, and folate supplementation during early pregnancy were independently associated with subsequent events of APO (P < 0.05); VB12 was rejected

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Summary

Introduction

Hyperhomocysteinemia may be a risk factor for endothelial dysfunction. Folate and vitamin B12 regulate the homocysteine metabolic process. This study aimed to evaluate the associations between subsequent events of adverse pregnancy outcome and early variables of homocysteine, folate, and vitamin B12 in pregnant women. Preeclampsia is a serious, pregnancy-specific syndrome that affects multiple organs. It continues to afflict 5–8% of pregnancies worldwide and is one of the leading causes of morbidity and mortality among pregnant women and fetuses [3]. The burden of APO is substantial in both developed and developing countries It is the primary cause of infant morbidity and mortality and the critical determinant of child survival, disabilities, stunting, and long-term adverse consequences [5, 6]

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