Volume 112, Issue 2, Pages 250–257.e1
Linlin Wang, M.Sc., Longfei Li, Ph.D., Chunyu Huang, M.Sc., Lianghui Diao, Ph.D., Ruochun Lian, M.Sc., Yuye Li, Ph.D., Shan Xiao, M.Sc., Xiuyu Hu, M.Sc., Meilan Mo, M.Sc., Yong Zeng, M.D.
To evaluate whether maternal chronic hepatitis B virus (HBV) infection affects pregnancy outcomes in infertile patients undergoing their first in vitro fertilization (IVF) treatment.
A retrospective case control study.
Female patients, comprising 8,550 infertile women including 180 HBsAg+HBeAg+, 714 HBsAg+HBeAg−, and 7,656 HBsAg seronegative controls undergoing their first IVF treatments.
Clinical characteristics, pregnancy and neonatal outcomes were analyzed by Kruskal-Wallis test, analysis of variance, or chi-square test. Logistic regression was employed to verify the contribution of maternal HBV to clinical pregnancy, live birth, and miscarriage.
Main Outcome Measure(s)
Primary outcome: live-birth rate; secondary outcomes: implantation, clinical pregnancy, and miscarriage rates.
An increased duration of infertility and more secondary infertility and ovulatory disorders were observed in the HBV patients. The implantation rate was statistically significantly lower in the HBsAg+HBeAg− group compared with the controls. However, the clinical pregnancy rate, miscarriage rate, live-birth rate, neonatal outcomes, and pregnancy complications showed no statistically significant differences among the groups. The logistic regression analysis showed that HBV infection status did not affect the clinical pregnancy, miscarriage, or live-birth rates, unlike maternal age, endometrial thickness, and use of high-quality embryos.
Hepatitis B virus infection is not an independent contributor to pregnancy outcomes, although it is associated with prolonged infertility duration, a high frequency of secondary infertility and ovulatory disorders, and a reduced implantation rate.