Journal article
Multiorgan phenotypes of offspring born following hypertensive disorders of pregnancy: a systematic review
- Abstract:
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Background: Hypertensive pregnancies are associated with an increased risk of cardiovascular and neurological diseases in the offspring during later life. However, less is known about the potential impact on multiorgan phenotypes in offspring before disease symptoms occur. The objective of this systematic review was to determine the associations of fetal exposure to maternal hypertensive pregnancy with multiorgan phenotypes across developmental stages.
Methods and Results: Ovid MEDLINE, EMBASE, CENTRAL, Scopus, WoS, CINAHL, and ClinicalTrials.gov were systematically searched until February 2024. Records were independently screened by two authors. Studies reporting on the structure or function of the heart, blood vessels, brain, liver, and kidneys in offspring of hypertensive pregnancies compared to a normotensive control population were included. Risk of bias was assessed using the NewcastleOttawa Scale. Extracted data were presented using harvest plots. Seventy-three studies including 7,091 offspring of hypertensive pregnancies and 42,164 controls were identified that met the inclusion criteria. Thirty-two studies were investigations in fetuses, 24 in neonates and infants, 12 in children, two in adolescents, and three in adults. Offspring of hypertensive pregnancies had structural and functional changes in the heart compared to controls in some studies across developmental stages. Offspring of hypertensive pregnancies also had smaller occipital and parietal vessels, higher aortic intima-media thickness, and lower retinal arteriolar-to-venular ratio. Some conflicting evidence existed for other phenotypical alterations.
Conclusions: There is still inconsistent evidence of multiorgan structural and functional differences in offspring of hypertensive pregnancies. The evidence base could therefore be further strengthened through well-designed and conducted prospective studies.
Registration: URL: https://www.crd.york.ac.uk/; Unique identifier: CRD42023387550
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 3.4MB, Terms of use)
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- Publisher copy:
- 10.1161/JAHA.123.033617
Authors
- Funder identifier:
- https://ror.org/02wdwnk04
- Grant:
- FS/18/3/33292
- Publisher:
- Wiley
- Journal:
- Journal of the American Heart Association More from this journal
- Volume:
- 13
- Issue:
- 21
- Article number:
- e033617
- Publication date:
- 2024-10-25
- Acceptance date:
- 2024-09-13
- DOI:
- EISSN:
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2047-9980
- Language:
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English
- Keywords:
- Pubs id:
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2031424
- Local pid:
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pubs:2031424
- Deposit date:
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2024-09-21
Terms of use
- Copyright holder:
- Sattwika et al
- Copyright date:
- 2024
- Rights statement:
- © 2024 The Author(s). Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
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