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范荣华, 闵峰, 陈炜, 张丽, 高幸幸, 李莉, 陈远华. 母体孕期乙型肝炎病毒感染与早产关联队列研究[J]. 中国公共卫生, 2021, 37(1): 70-73. DOI: 10.11847/zgggws1125685
引用本文: 范荣华, 闵峰, 陈炜, 张丽, 高幸幸, 李莉, 陈远华. 母体孕期乙型肝炎病毒感染与早产关联队列研究[J]. 中国公共卫生, 2021, 37(1): 70-73. DOI: 10.11847/zgggws1125685
FAN Rong-hua, MIN Feng, CHEN Wei, . Maternal hepatitis B virus infection and preterm delivery: a retrospective cohort study[J]. Chinese Journal of Public Health, 2021, 37(1): 70-73. DOI: 10.11847/zgggws1125685
Citation: FAN Rong-hua, MIN Feng, CHEN Wei, . Maternal hepatitis B virus infection and preterm delivery: a retrospective cohort study[J]. Chinese Journal of Public Health, 2021, 37(1): 70-73. DOI: 10.11847/zgggws1125685

母体孕期乙型肝炎病毒感染与早产关联队列研究

Maternal hepatitis B virus infection and preterm delivery: a retrospective cohort study

  • 摘要:
      目的  研究母体乙型肝炎病毒(HBV)感染与早产的关联。
      方法  将2011年1月 — 2014年12月期间在安徽医科大学第一附属医院分娩的12 186对母亲 – 单胎配对资料纳入本次研究,回顾性分析母体孕期HBV感染与早产的关联。
      结果  该队列人群包括对照11 550例(94.78 %),HBV感染乙肝e抗原阴性者HBeAg(–)362例(2.97 %)和HBeAg(+)者274例(2.25 %)。母体HBV感染组平均孕周低于对照组,其中HBeAg(+)组平均孕周最低。HBV感染HBeAg(–)组早产儿发生率为17.13 %,与对照组相比差异无统计学意义。HBV感染HBeAg(+)组早产儿发生率为24.09 %,显著高于对照组的14.66 %(调整RR = 1.75,95 % CI = 1.29~2.38)。进一步分析发现,HBV感染HBeAg(–)组早期早产发生率为4.14 %,显著高于对照组的2.60 %(调整RR = 1.93,95 % CI = 1.02~3.65);HBV感染HBeAg(+)组晚期早产发生率为19.35 %,显著高于对照组的11.97 %(调整RR = 1.74,95 % CI = 1.25~2.41),HBV感染HBeAg(+)组早期早产发生率为4.74 %,也显著高于对照组(调整RR = 2.04,95 % CI = 1.17~3.56)。
      结论  HBV感染HBeAg(–)是早期早产危险因素,HBV感染HBeAg(+)不仅增加早期早产而且增加晚期早产发生风险。

     

    Abstract:
      Objective  To investigate the association between maternal hepatitis B virus (HBV) infection and the risk of preterm delivery in a birth cohort study.
      Methods  We collected the data on 12 186 mother-singleton infant pairs registered at First Affiliated Hospital of Anhui Medical University between January 2011 and December 2014 for a retrospective cohort study on the association between maternal HBV infection and preterm delivery. The puerperae of the cohort were grouped into cases (serum HBV surface antigen positive HBsAg+) and controls (HBsAg negative HBsAg–) based on the results of enzyme-linked immunosorbent assay.
      Results  Of all the puerpaerae studied, 94.78% were controls; 2.97% were the cases being HBV e antigen negative (HBeAg–) and 2.25% were cases being HBeAg positive (HBeAg+). The mean gestational age of the cases was lower than that of the controls and the mean gestational age was the lowest in the HBeAg+ cases. The incidence rate of preterm delivery was 17.13% in the HBeAg– cases and was not significantly differ from that of the controls; but in the HBeAg+ cases, the incidence rate was 24.09% and significantly higher than that (14.66%) in the controls, with an adjusted relative risk adj RR of 1.75 (95% confidence interval 95% CI: 1.25 – 2.41). Compared to the controls, the HBeAg– cases had a significantly increased incidence of early preterm delivery (4.14% vs 2.60%, adj RR = 1.93 95% CI: 1.02 – 3.65); in comparison with the controls, the HBeAg+ cases had a significantly higher incidence of late preterm delivery (19.35% vs. 11.97%, adj RR = 1.74 95% CI: 1.36 – 2.59) and also a significantly higher incidence of early preterm delivery (4.74% vs. 2.69%, adj RR = 2.04 95% CI: 1.17 – 3.56).
      Conclusion  Maternal HBV infection with negative serum HBeAg is associated with an increased risk of early preterm delivery; maternal HBV infection with positive serum HBeAg increases both the risk of early and late preterm delivery.

     

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