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Multiorgan phenotypes of offspring born following hypertensive disorders of pregnancy: a systematic review

Abstract:

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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Files:
Publisher copy:
10.1161/JAHA.123.033617

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
RDM Cardiovascular Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
RDM Cardiovascular Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
RDM Cardiovascular Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
RDM Cardiovascular Medicine
Role:
Author


More from this funder
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:
2047-9980


Language:
English
Keywords:
Pubs id:
2031424
Local pid:
pubs:2031424
Deposit date:
2024-09-21

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