The prevalence of metabolic dysfunction-associated fatty liver disease and its association on adverse pregnancy outcomes in women with gestational diabetes mellitus.


Journal

Diabetes research and clinical practice
ISSN: 1872-8227
Titre abrégé: Diabetes Res Clin Pract
Pays: Ireland
ID NLM: 8508335

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 11 06 2022
revised: 21 07 2022
accepted: 08 08 2022
pubmed: 16 8 2022
medline: 6 10 2022
entrez: 15 8 2022
Statut: ppublish

Résumé

To determine the prevalence of metabolic dysfunction-associated fatty liver disease (MAFLD) and its association on adverse pregnancy outcomes in women with gestational diabetes mellitus (GDM). 380 women with GDM had a FibroScan® performed between 24 and 32 weeks. A Controlled Attenuation Parameter (CAP) ≥ 233.5 dB/m signified MAFLD. Gestational hypertension, pre-eclampsia and eclampsia contributed to a composite of adverse maternal outcomes. A composite of adverse neonatal outcomes included pre-term birth, hypoglycaemia, small/large-for-gestational age and admission to neonatal high dependency. Multiple logistic regression was used to determine independent associations with MAFLD. 147 (38.7 %) women had MAFLD. Higher pre-pregnancy BMI (median 28.4, IQR 24.7-33.0 kg/m Within this GDM cohort, almost 40% had FibroScan®-detected MAFLD in mid-to-late gestation. MAFLD was not associated with worse pregnancy outcomes.

Identifiants

pubmed: 35970401
pii: S0168-8227(22)00852-X
doi: 10.1016/j.diabres.2022.110038
pii:
doi:

Substances chimiques

Insulin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

110038

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Thora Y Chai (TY)

Department of Diabetes and Endocrinology, Westmead Hospital, Westmead, NSW, Australia; Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia; Reproduction and Perinatal Centre, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia. Electronic address: thora.chai@sydney.edu.au.

Difei Deng (D)

Department of Diabetes and Endocrinology, Westmead Hospital, Westmead, NSW, Australia; Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia. Electronic address: difeideng@hotmail.com.

Karen Byth (K)

Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia; Western Sydney Local Health District Research Education Network, Westmead, NSW, Australia. Electronic address: karen.byth@sydney.edu.au.

Jacob George (J)

Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia; Storr Liver Centre, Westmead Millennium Institute for Medical Research, Westmead, NSW, Australia; Department of Gastroenterology and Hepatology, Westmead Hospital, Westmead, NSW, Australia. Electronic address: jacob.george@sydney.edu.au.

Dharmintra Pasupathy (D)

Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia; Reproduction and Perinatal Centre, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia. Electronic address: dharmintra.pasupathy@sydney.edu.au.

Ngai Wah Cheung (NW)

Department of Diabetes and Endocrinology, Westmead Hospital, Westmead, NSW, Australia; Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia; Reproduction and Perinatal Centre, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia. Electronic address: wah.cheung@sydney.edu.au.

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