母亲血红蛋白水平和不良妊娠结局:来自2个前瞻性英国妊娠队列的个体患者数据分析

IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS
Christy A. Burden , Gordon C. Smith , Ulla Sovio , Gemma L. Clayton , Abigail Fraser
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引用次数: 2

摘要

背景血红蛋白(Hb)是妊娠不良结局的一个可改变的危险因素。研究报告称,孕妇Hb水平与不良妊娠结局之间存在冲突,包括早产(PTB)、低出生体重(LBW)和围产期死亡率。目的在这项研究中,我们旨在估计高收入环境中妊娠早期(妊娠7-12周)和晚期(妊娠27-32周)母体Hb水平与妊娠结局之间的关系形式和程度。方法我们使用了来自英国两个基于人群的妊娠队列的数据:雅芳亲子纵向研究(ALSPAC)和妊娠结局预测研究(POPS)。我们使用多变量逻辑回归模型来检验Hb与妊娠结局之间的关系,并对母亲年龄、种族、BMI、吸烟状况和产次进行了调整。主要转归指标为PTB、LBW、小于胎龄(SGA)、先兆子痫(PET)和妊娠期糖尿病(GDM)。在汇总分析中,没有证据表明妊娠早期(妊娠7-12周)较高的Hb与PTB(每1g/dL Hb的OR:1.09;95%CI:0.97,1.22)、LBW(1.12:0.99,1.26)和SGA(1.06;0.97,1.15)之间存在关联。妊娠晚期(妊娠27-32周)较高Hb与PT B(1.45:1.30,1.62)、,和SGA(1.45:1.33,1.58)。妊娠早期和晚期较高的Hb分别与ALSPAC的PET相关(1.36:1.12,1.64)和(1.53:1.29,1.82),但与POPS无关(1.17:0.99,1.37)和(1.03:0.86,1.23)。妊娠初期和晚期ALSPAC的较高Hb和GDM均相关[分别为(1.51:1.08,2.11)和(1.35:1.01,1.79)],但在POPS中没有[(0.98:0.81.19)和(0.83:0.68,1.02)]。结论较高的母体Hb可能确定不良妊娠结局的风险。需要进一步的研究来调查这种关联是否是因果关系,并确定潜在的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Maternal hemoglobin levels and adverse pregnancy outcomes: individual patient data analysis from 2 prospective UK pregnancy cohorts

Background

Hemoglobin (Hb) is a modifiable risk factor for adverse pregnancy outcomes. Studies have reported conflicting associations between maternal Hb levels and adverse pregnancy outcomes, including preterm birth (PTB), low birth weight (LBW), and perinatal mortality.

Objective

In this study, we aimed to estimate the shape and magnitude of associations between maternal Hb levels in early (7–12 wk gestation) and late pregnancy (27–32 wk gestation) and pregnancy outcomes in a high-income setting.

Methods

We used data from 2 UK population-based pregnancy cohorts: the Avon Longitudinal Study of Parents and Children (ALSPAC) and Pregnancy Outcome Prediction Study (POPS). We used multivariable logistic regression models to examine the relationship between Hb and pregnancy outcomes, adjusting for maternal age, ethnicity, BMI, smoking status, and parity. Main outcome measures were PTB, LBW, small for gestational age (SGA), pre-eclampsia (PET), and gestational diabetes mellitus (GDM).

Results

Mean Hb in ALSPAC were 12.5 g/dL (SD = 0.90) and 11.2 g/dL (SD = 0.92) in early and late pregnancy, respectively, and 12.7 g/dL (SD = 0.82) and 11.4 g/dL (SD = 0.82) in POPS. In the pooled analysis, there was no evidence of associations between a higher Hb in early pregnancy (7–12 wk gestation) and PTB (OR per 1 g/dL of Hb: 1.09; 95% CI: 0.97, 1.22), LBW (1.12: 0.99, 1.26), and SGA (1.06; 0.97, 1.15). Higher Hb in late pregnancy (27–32 wk gestation) was associated with PTB (1.45: 1.30, 1.62), LBW (1.77: 1.57, 2.01), and SGA (1.45: 1.33, 1.58). Higher Hb in early and late pregnancy was associated with PET in ALSPAC (1.36: 1.12, 1.64) and (1.53: 1.29, 1.82), respectively, but not in POPS (1.17:0.99, 1.37) and (1.03: 0.86, 1.23). There was an association with a higher Hb and GDM in ALSPAC in both early and late pregnancy [(1.51: 1.08, 2.11) and (1.35: 1.01, 1.79), respectively], but not in POPS [(0.98: 0.81, 1.19) and (0.83: 0.68, 1.02)].

Conclusions

Higher maternal Hb may identify the risk of adverse pregnancy outcomes. Further research is required to investigate if this association is causal and to identify the underlying mechanisms.

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来源期刊
CiteScore
12.40
自引率
4.20%
发文量
332
审稿时长
38 days
期刊介绍: American Journal of Clinical Nutrition is recognized as the most highly rated peer-reviewed, primary research journal in nutrition and dietetics.It focuses on publishing the latest research on various topics in nutrition, including but not limited to obesity, vitamins and minerals, nutrition and disease, and energy metabolism. Purpose: The purpose of AJCN is to: Publish original research studies relevant to human and clinical nutrition. Consider well-controlled clinical studies describing scientific mechanisms, efficacy, and safety of dietary interventions in the context of disease prevention or health benefits. Encourage public health and epidemiologic studies relevant to human nutrition. Promote innovative investigations of nutritional questions employing epigenetic, genomic, proteomic, and metabolomic approaches. Include solicited editorials, book reviews, solicited or unsolicited review articles, invited controversy position papers, and letters to the Editor related to prior AJCN articles. Peer Review Process: All submitted material with scientific content undergoes peer review by the Editors or their designees before acceptance for publication.
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