Department of Biostatistics, Epidemiology & Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Department of Obstetrics and Gynecology, University of Texas Medical Branch, Galveston, TX, USA.
BMC Pregnancy Childbirth. 2024 Jan 24;24(1):82. doi: 10.1186/s12884-024-06266-9.
An incomplete understanding of preterm birth is especially concerning for low-middle income countries, where preterm birth has poorer prognoses. While systemic proinflammatory processes are a reportedly normal component of gestation, excessive inflammation has been demonstrated as a risk factor for preterm birth. There is minimal research on the impact of excessive maternal inflammation in the first trimester on the risk of preterm birth in low-middle income countries specifically.
Pregnant women were enrolled at the rural Bangladesh site of the National Institute of Child Health Global Network Maternal Newborn Health Registry. Serum samples were collected to measure concentrations of the inflammatory markers C-reactive protein (CRP) and Alpha-1-acid glycoprotein (AGP), and stool samples were collected and analyzed for enteropathogens. We examined associations of maternal markers in the first-trimester with preterm birth using logistic regression models. CRP and AGP were primarily modeled with a composite inflammation predictor.
Out of 376 singleton births analyzed, 12.5% were preterm. First trimester inflammation was observed in 58.8% of all births, and was significantly associated with increased odds of preterm birth (adjusted odds ratio [aOR] = 2.23; 95% confidence interval [CI]: 1.03, 5.16), independent of anemia. Maternal vitamin B12 insufficiency (aOR = 3.33; 95% CI: 1.29, 8.21) and maternal anemia (aOR = 2.56; 95% CI: 1.26, 5.17) were also associated with higher odds of preterm birth. Atypical enteropathogenic E. coli detection showed a significant association with elevated AGP levels and was significantly associated with preterm birth (odds ratio [OR] = 2.36; 95% CI: 1.21, 4.57), but not associated with CRP.
Inflammation, anemia, and vitamin B12 insufficiency in the first trimester were significantly associated with preterm birth in our cohort from rural Bangladesh. Inflammation and anemia were independent predictors of premature birth in this low-middle income setting where inflammation during gestation was widespread. Further research is needed to identify if infections such as enteropathogenic E. coli are a cause of inflammation in the first trimester, and if intervention for infection would decrease preterm birth.
对中低收入国家来说,对早产的认识不完整尤其令人担忧,因为早产的预后较差。虽然系统性促炎过程是妊娠的正常组成部分,但过度炎症已被证明是早产的一个危险因素。在中低收入国家,关于妊娠早期母体过度炎症对早产风险的影响的研究很少。
孕妇在孟加拉国农村的国家儿童健康研究所全球母婴健康登记处参加研究。采集血清样本测量炎症标志物 C 反应蛋白(CRP)和α-1-酸性糖蛋白(AGP)的浓度,并采集粪便样本进行肠道病原体分析。我们使用逻辑回归模型检查了孕早期母体标志物与早产之间的关联。CRP 和 AGP 主要通过复合炎症预测因子进行建模。
在分析的 376 例单胎分娩中,12.5%为早产。所有分娩中,58.8%的孕妇在孕早期出现炎症,与早产的几率增加显著相关(调整后的优势比[aOR] = 2.23;95%置信区间[CI]:1.03,5.16),独立于贫血。母体维生素 B12 不足(aOR = 3.33;95%CI:1.29,8.21)和母体贫血(aOR = 2.56;95%CI:1.26,5.17)也与早产几率增加显著相关。非典型肠道病原体 E. coli 的检测与 AGP 水平升高显著相关,与早产显著相关(比值比[OR] = 2.36;95%CI:1.21,4.57),但与 CRP 无关。
在我们来自孟加拉国农村的队列中,妊娠早期的炎症、贫血和维生素 B12 不足与早产显著相关。在这个中低收入环境中,炎症和贫血是早产的独立预测因素,妊娠期间炎症很普遍。需要进一步研究以确定肠道病原体 E. coli 等感染是否是妊娠早期炎症的原因,以及是否对感染进行干预可以降低早产率。