Arterial structure and function in children with inflammatory bowel disease.

cardiovascular diseases child heart disease risk factors inflammatory bowel diseases

Journal

JGH open : an open access journal of gastroenterology and hepatology
ISSN: 2397-9070
Titre abrégé: JGH Open
Pays: Australia
ID NLM: 101730833

Informations de publication

Date de publication:
Jun 2024
Historique:
received: 13 02 2024
revised: 12 05 2024
accepted: 18 05 2024
medline: 4 6 2024
pubmed: 4 6 2024
entrez: 4 6 2024
Statut: epublish

Résumé

People with inflammatory bowel disease (IBD) have an increased risk of cardiovascular disease, including in younger adulthood. This may arise in part from chronic, systemic low-grade inflammation. The process of atherosclerosis may begin in childhood. We sought to determine whether pediatric IBD is associated with adverse changes in arterial structure and function as a marker of early increased cardiovascular risk. We performed a case-control study comparing children with IBD for a median disease duration of 2.49 (interquartile range 1.23, 4.38) years with healthy children. In a single visit, we collected baseline clinical and anthropometric data, and measured blood pressure, pulse wave velocity, carotid artery distensibility, and aortic and carotid intima-media thickness. High-sensitivity C-reactive protein and fasting lipids were measured. We enrolled 81 children with IBD (40 with Crohn's disease, 40 with ulcerative colitis, and 1 with unspecified IBD) and 82 control participants. After adjusting for age, sex, body mass index We did not show any differences in arterial structure and function in children with a history of IBD for less than 5 years compared with healthy controls. IBD diagnosed in childhood may provide a window of opportunity to actively reduce standard cardiovascular risk factors and improve future cardiovascular outcomes.

Sections du résumé

Background and Aim UNASSIGNED
People with inflammatory bowel disease (IBD) have an increased risk of cardiovascular disease, including in younger adulthood. This may arise in part from chronic, systemic low-grade inflammation. The process of atherosclerosis may begin in childhood. We sought to determine whether pediatric IBD is associated with adverse changes in arterial structure and function as a marker of early increased cardiovascular risk.
Methods UNASSIGNED
We performed a case-control study comparing children with IBD for a median disease duration of 2.49 (interquartile range 1.23, 4.38) years with healthy children. In a single visit, we collected baseline clinical and anthropometric data, and measured blood pressure, pulse wave velocity, carotid artery distensibility, and aortic and carotid intima-media thickness. High-sensitivity C-reactive protein and fasting lipids were measured.
Results UNASSIGNED
We enrolled 81 children with IBD (40 with Crohn's disease, 40 with ulcerative colitis, and 1 with unspecified IBD) and 82 control participants. After adjusting for age, sex, body mass index
Conclusion UNASSIGNED
We did not show any differences in arterial structure and function in children with a history of IBD for less than 5 years compared with healthy controls. IBD diagnosed in childhood may provide a window of opportunity to actively reduce standard cardiovascular risk factors and improve future cardiovascular outcomes.

Identifiants

pubmed: 38832138
doi: 10.1002/jgh3.13100
pii: JGH313100
pmc: PMC11145743
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e13100

Informations de copyright

© 2024 The Author(s). JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.

Auteurs

Asha Jois (A)

Department of Gastroenterology and Clinical Nutrition The Royal Children's Hospital Melbourne Parkville Victoria Australia.

Diana Zannino (D)

Clinical Epidemiology and Biostatistics Unit Murdoch Children's Research Institute Parkville Victoria Australia.

Anthony G Catto-Smith (AG)

Department of Gastroenterology and Clinical Nutrition The Royal Children's Hospital Melbourne Parkville Victoria Australia.
Department of Paediatrics University of Melbourne Parkville Victoria Australia.
School of Humanities, Arts and Social Sciences, University of New England Armidale New South Wales Australia.

Meg Kaegi (M)

Inflammatory Origins Group, Infection, Immunity and Global Health Theme Murdoch Children's Research Institute Parkville Victoria Australia.

Jonathan P Mynard (JP)

Department of Paediatrics University of Melbourne Parkville Victoria Australia.
Heart Research Group Murdoch Children's Research Institute Parkville Victoria Australia.
Biomedical Engineering, University of Melbourne Faculty of Engineering and Information Technology Parkville Victoria Australia.

Jeremy Rosenbaum (J)

Department of Gastroenterology and Clinical Nutrition The Royal Children's Hospital Melbourne Parkville Victoria Australia.

Mark Oliver (M)

Department of Gastroenterology and Clinical Nutrition The Royal Children's Hospital Melbourne Parkville Victoria Australia.
Department of Paediatrics University of Melbourne Parkville Victoria Australia.

Winita Hardikar (W)

Department of Gastroenterology and Clinical Nutrition The Royal Children's Hospital Melbourne Parkville Victoria Australia.
Department of Paediatrics University of Melbourne Parkville Victoria Australia.

George Alex (G)

Department of Gastroenterology and Clinical Nutrition The Royal Children's Hospital Melbourne Parkville Victoria Australia.
Department of Paediatrics University of Melbourne Parkville Victoria Australia.

David Burgner (D)

Department of Paediatrics University of Melbourne Parkville Victoria Australia.
Inflammatory Origins Group, Infection, Immunity and Global Health Theme Murdoch Children's Research Institute Parkville Victoria Australia.
Infectious Diseases Unit, Department of General Medicine The Royal Children's Hospital Melbourne Parkville Victoria Australia.

Classifications MeSH