2017
DOI: 10.1161/circulationaha.116.024600
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Association Between Fetal Congenital Heart Defects and Maternal Risk of Hypertensive Disorders of Pregnancy in the Same Pregnancy and Across Pregnancies

Abstract: Linked pathophysiological mechanisms may be involved in some congenital heart defects and preterm preeclampsia. The strong associations across pregnancies support a predominantly maternal origin of effect.

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Cited by 78 publications
(90 citation statements)
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“…In line with Jansen's hypothesis, we believe that not only a subclinical level of placental dysfunction, but also genetic or epigenetic determinants of abnormal embryological neurodevelopment should be investigated to explain abnormal cranial growth in CHDs [14]. Recent studies [6,27,28] gave a potential insight into the connection between impaired fetal growth and CHD, suggesting a common pathway between cardiovascular (angio)genesis and placental function. Interestingly, a Spanish study [29] explored the gene expression profile of Down syndrome fetal heart tissue and found an antiangiogenic profile that was very similar to that found in the CHD fetal heart tissue gene profile.…”
Section: Discussionsupporting
confidence: 58%
“…In line with Jansen's hypothesis, we believe that not only a subclinical level of placental dysfunction, but also genetic or epigenetic determinants of abnormal embryological neurodevelopment should be investigated to explain abnormal cranial growth in CHDs [14]. Recent studies [6,27,28] gave a potential insight into the connection between impaired fetal growth and CHD, suggesting a common pathway between cardiovascular (angio)genesis and placental function. Interestingly, a Spanish study [29] explored the gene expression profile of Down syndrome fetal heart tissue and found an antiangiogenic profile that was very similar to that found in the CHD fetal heart tissue gene profile.…”
Section: Discussionsupporting
confidence: 58%
“…While speculative, another explanation for our findings, as well as the general overrepresentation of depression and anxiety diagnosis in ACHD patients, might originate from factors involved in prenatal neurodevelopment, rather than the contemporary hemodynamic effects of having a congenital lesion. We can only hypothesize whether the abnormalities we found, are a consequence of, for example, genetic predisposition or angiogenic imbalance during pregnancy, as ASD were strongly associated with early preterm preeclampsia (OR: 12.0 [CI: 8.96‐16.1]), perhaps affecting the neurodevelopment in the fetal period . Additionally, preterm birth might be a contributing factor, as it have been associated with psychiatric disorders …”
Section: Discussionmentioning
confidence: 89%
“…12.0 [CI: 8.96-16.1]), perhaps affecting the neurodevelopment in the fetal period. 29 Additionally, preterm birth might be a contributing factor, as it have been associated with psychiatric disorders. 30 Although life expectancy is improved over the last decades, patients with ASD, even if small and unrepaired, continue to have an increased mortality risk compared to the reference group.…”
Section: Discussionmentioning
confidence: 99%
“…There is coincidence of both CHD and preterm PE in about five per 100 000 pregnancies. The epidemiological studies highlighting the association between fetal CHD and PE reported that the increased risk affected mainly the rate of early PE with delivery at < 34 weeks' gestation [6][7][8] . However, the incidence of such early PE in the general population is very low (0.2-0.3%) 7,8 and, even with a seven-fold increased incidence of cases of fetal CHD 8 , the expected incidence in such cases would be only 1-2%.…”
Section: Main Findings Of Studymentioning
confidence: 99%