Impact of offspring endothelial function from de novo hypertensive disorders during pregnancy: An evidence-based review

被引:2
作者
Sukor, Aslah Nabilah Abdull [1 ]
Ankasha, Sheril June [1 ]
Ugusman, Azizah [1 ]
Aminuddin, Amilia [1 ]
Mokhtar, Norfilza Mohd [1 ]
Abidin, Shahidee Zainal [2 ]
Ahmad, Mohd Faizal [3 ]
Hamid, Adila A. [1 ]
机构
[1] Univ Kebangsaan Malaysia, Fac Med, Dept Physiol, Kuala Lumpur, Malaysia
[2] Univ Malaysia Terengganu, Fac Sci & Marine Environm, Kuala Nerus, Malaysia
[3] Univ Kebangsaan Malaysia, Fac Med, Dept Obstet & Gynaecol, Kuala Lumpur, Malaysia
关键词
hypertensive disorders of pregnancy; preeclampsia; endothelial function; offspring; cardiovascular disease; INTIMA-MEDIA THICKNESS; NECROSIS-FACTOR-ALPHA; CARDIOVASCULAR RISK; UTERINE PERFUSION; CAROTID-ARTERY; BLOOD-PRESSURE; NEONATES BORN; CORD BLOOD; PREECLAMPSIA; DYSFUNCTION;
D O I
10.3389/fsurg.2022.967785
中图分类号
R61 [外科手术学];
学科分类号
摘要
De novo hypertensive disorders of pregnancy (HDP) which consist of gestational hypertension and preeclampsia affect maternal and offspring morbidity and mortality, and potentially increase the risk of cardiovascular disease in the offspring. It is well known that de novo HDP causes various maternal complications, including cardiovascular diseases, placental abruption and liver and kidney failure. However, there are studies suggesting that offspring of pregnancies complicated by de novo HDP have an increased risk of long-term cardiovascular disease. The endothelium is an important regulator of vascular function, and its dysfunction is highly associated with the development of cardiovascular diseases. Hence, this review aimed to systematically identify articles related to the effect of de novo HDP on the endothelial function of the offspring. A computerized database search was conducted on PubMed, Scopus, and Medline from 1976 until 2022. A total of 685 articles were obtained. We identified another three additional articles through review articles and Google Scholar. Altogether, we used 13 articles for data extraction. All studies reported that endothelial function was impaired in the offspring of de novo HDP. This is most likely attributed to impaired vasodilation, subclinical atherosclerosis formation, inflammation, and dysregulated epigenetic regulation of endothelial functions.
引用
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页数:13
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