Pathways of association between maternal haemoglobin and stillbirth: path-analysis of maternity data from two hospitals in England.
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ABSTRACT: OBJECTIVE:To investigate the mechanisms that link maternal haemoglobin concentration with stillbirth. DESIGN:A retrospective cohort analysis using anonymised maternity data from two hospitals in England. SETTING:The Royal Wolverhampton NHS Trust and Guy's and St Thomas' NHS Foundation Trust. STUDY POPULATION:12?636 women with singleton pregnancies ?24 weeks of gestation giving birth in the two hospitals during 2013-2015. METHOD:A conceptual framework of hypothesised pathways through birth weight-for-gestational age and maternal infection including potential confounders and other risk factors was developed and examined using path-analysis. Path-analysis was performed by fitting a set of regression equations using weighted least squares adjusted for mean and variance. Goodness-of-fit indices were estimated. MAIN OUTCOME MEASURES:Coefficient of association (?) for relationship between each parameter, and direct, indirect and total effects via the postulated pathways. RESULTS:The path-model showed a significant adjusted indirect negative effect of maternal haemoglobin on stillbirth mediated via birth weight-for-gestational age (standardised estimate (SE)=-0.01; 95%?CI=-0.01?to -0.001; P=0.028). The effect through maternal infection was not significant at P<0.05 (SE=0.001; 95%?CI=-0.004?to 0.01; P=0.610). There was a residual direct negative effect of maternal haemoglobin on stillbirth (SE=-0.12; 95%?CI -0.23 to -0.02; P=0.020) after accounting for the two pathways. Total indirect SE=-0.004; 95%?CI -0.01 to 0.003; P=0.267; total direct and indirect SE=-0.13; 95%?CI -0.23 to -0.02; P=0.016. The goodness-of-fit indices showed a good fit between the model and the data. CONCLUSION:While some of the influence on risk of stillbirth acts through low birth weight-for-gestational age, the majority does not. Several new mechanisms have been suggested for how haemoglobin may be exerting its influence on the risk of stillbirth possibly involving genetic, epigenetic and/or alternative obstetric and nutritional pathologies, but much more research is needed.
SUBMITTER: Nair M
PROVIDER: S-EPMC5892753 | biostudies-literature | 2018 Apr
REPOSITORIES: biostudies-literature
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