首页|p Placental characteristics and risks of maternal mortality 50 years after delivery
p Placental characteristics and risks of maternal mortality 50 years after delivery
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NSTL
Elsevier
Introduction: Adverse pregnancy outcomes such as preterm delivery and preeclampsia are associated with a higher maternal risk for subsequent cardiovascular disease (CVD) and all-cause mortality. While such pregnancy conditions are related to abnormal placentation, little research has investigated whether pathologic placental measures could serve as a risk factor for future CVD mortality in mothers. Methods: Longitudinal study of 33,336 women from the Collaborative Perinatal Project (CPP; 1959-1966) linked to mortality information through December 2016. Pathologists took extensive morphological and histopathological measures. Apart from assessing associations with morphological features, we derived an overall composite score and specific inflammation-related, hemorrhage-related, and hypoxia-related pathologic placenta index scores. Cox regression estimated hazard ratios (HR) and 95% confidence intervals (CI) for mortality adjusting for covariates. Results: Thirty-nine percent of women died with mean (standard deviation, SD) time to death of 39 (12) years. Mean (SD) placental weight and birthweight were 436 g (98) and 3156 g (566), respectively. Placenta-tobirthweight ratio was associated with all-cause mortality (adjusted HR 1.03: 1.01, 1.05 per SD in ratio). In cause-specific analyses, it was significantly associated with respiratory (HR 1.06), dementia (HR: 1.10) and liver (HR 1.04) related deaths. CVD, cancer, diabetes and kidney related deaths also tended to increase, whereas infection related deaths did not (HR 0.94; 0.83, 1.06). Placental measures of thickness, diameters, and histopathological measures grouped by inflammatory, hemorrhagic, or hypoxic etiology were not associated with mortality. Discussion: Placental weight in relation to birthweight was associated with long-term maternal mortality but other histopathologic or morphologic features were not.
Yeung, E. H.、Saha, A.、Zhu, C.、Trinh, M. H.、Hinkle, S. N.、Pollack, A. Z.、Grantz, K. L.、Mills, J. L.、Mumford, S. L.、Zhang, C.、Robinson, S. L.、Gillman, M. W.、Zhang, J.、Mendola, P.、Sundaram, R.