Birth weight and cardiac function assessed by echocardiography in adolescence: Avon Longitudinal Study of Parents and Children.


Journal

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
ISSN: 1469-0705
Titre abrégé: Ultrasound Obstet Gynecol
Pays: England
ID NLM: 9108340

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 26 03 2018
revised: 09 09 2018
accepted: 20 09 2018
pubmed: 27 9 2018
medline: 8 2 2020
entrez: 26 9 2018
Statut: ppublish

Résumé

Maternal hemodynamics in pregnancy is associated with fetal growth and birth weight, which in turn are associated with offspring cardiovascular disease later in life. The aim of this study was to quantify the extent to which birth weight is associated with cardiac structure and function in adolescence. A subset of offspring (n = 1964; 55% female) of the Avon Longitudinal Study of Parents and Children were examined with echocardiography at a mean age of 17.7 (SD, 0.3) years. The associations of birth-weight Z-score for sex and gestational age with cardiac structure (assessed by relative wall thickness, left ventricular mass index (LVMI) and left atrial diameter index), systolic function (assessed by ejection fraction and left ventricular wall velocity) and diastolic function (assessed by early/late mitral inflow velocity (E/A) and early mitral inflow velocity/mitral annular early diastolic velocity (E/e')) were evaluated. Linear regression models were adjusted for several potential confounders, including maternal prepregnancy body mass index, age, level of education and smoking during pregnancy. Higher birth-weight Z-score was associated with lower E/A (mean difference, -0.024; 95% CI, -0.043 to -0.005) and E/e' (mean difference, -0.05; 95% CI, -0.10 to -0.001) and higher LVMI (mean difference, 0.38 g/m Higher birth weight adjusted for sex and gestational age was associated with differences in measures of diastolic function in adolescence, but the observed associations were small. It remains to be determined the extent to which these associations translate into increased susceptibility to cardiovascular disease later in life. © 2018 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of the International Society of Ultrasound in Obstetrics and Gynecology.

Identifiants

pubmed: 30251286
doi: 10.1002/uog.20128
pmc: PMC6771817
doi:

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

225-231

Subventions

Organisme : Wellcome Trust
ID : 086676/7/08/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : G9815508
Pays : United Kingdom
Organisme : British Heart Foundation
ID : CS/15/6/31468
Pays : United Kingdom
Organisme : British Heart Foundation
ID : CS/13/1/30327
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12013/5
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12019/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 102215/2/13/2
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/M009351/1
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/06/145 & CS/15/6/31468
Pays : United Kingdom

Informations de copyright

© 2018 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of the International Society of Ultrasound in Obstetrics and Gynecology.

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Auteurs

S Timpka (S)

Genetic and Molecular Epidemiology Unit, Lund University Diabetes Centre, Lund University, Malmö, Sweden.
Connors Center for Women's Health and Gender Biology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

A D Hughes (AD)

Institute of Cardiovascular Science, University College London, London, UK.

N Chaturvedi (N)

Institute of Cardiovascular Science, University College London, London, UK.

P W Franks (PW)

Genetic and Molecular Epidemiology Unit, Lund University Diabetes Centre, Lund University, Malmö, Sweden.
Harvard T. H. Chan School of Public Health, Harvard University, Boston, MA, USA.

D A Lawlor (DA)

Department of Population Health Sciences, Medical School, University of Bristol, Bristol, UK.
MRC Integrative Epidemiology Unit at the University of Bristol, University of Bristol, Bristol, UK.
NIHR Biomedical Research Centre at the University Hospitals Bristol NHS Foundation Trust and the University of Bristol, Bristol, UK.

J W Rich-Edwards (JW)

Connors Center for Women's Health and Gender Biology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Harvard T. H. Chan School of Public Health, Harvard University, Boston, MA, USA.

A Fraser (A)

Department of Population Health Sciences, Medical School, University of Bristol, Bristol, UK.
MRC Integrative Epidemiology Unit at the University of Bristol, University of Bristol, Bristol, UK.
NIHR Biomedical Research Centre at the University Hospitals Bristol NHS Foundation Trust and the University of Bristol, Bristol, UK.

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Classifications MeSH