Liver Ultrasound Patterns in Children With Cystic Fibrosis Correlate With Noninvasive Tests of Liver Disease.


Journal

Journal of pediatric gastroenterology and nutrition
ISSN: 1536-4801
Titre abrégé: J Pediatr Gastroenterol Nutr
Pays: United States
ID NLM: 8211545

Informations de publication

Date de publication:
09 2019
Historique:
entrez: 23 8 2019
pubmed: 23 8 2019
medline: 22 9 2020
Statut: ppublish

Résumé

Early identification of children with cystic fibrosis (CF) at risk for severe liver disease (CFLD) would enable targeted study of preventative therapies. There is no gold standard test for CFLD. Ultrasonography (US) is used to identify CFLD, but with concerns for its diagnostic accuracy. We aim to determine if differences in standard blood tests, imaging variables and noninvasive liver fibrosis indices correlate with liver US patterns, and thus provide supportive evidence that a heterogeneous US liver pattern reflects clinically relevant liver disease. We studied baseline research abdominal US and bloodwork from 244 children with pancreatic insufficient CF, ages 3 to 12 years, enrolled in a prospective study of the ability of US to predict CF cirrhosis (PUSH study). Children with a heterogeneous (HTG) liver pattern on US (n = 62) were matched 1 : 2 in design with children with normal US (NL, n = 122). Analyses included children with nodular (NOD, n = 22) and homogeneous hyperechoic (HMG, n = 38) livers. Univariate analysis showed significant differences between US groups for standard blood tests, spleen size, and noninvasive liver fibrosis indices. Multivariable models discriminated NOD versus NL with excellent accuracy (AUROC 0.96). Models also distinguish HTG versus NL (AUROC 0.76), NOD versus HTG (0.78), and HMG versus NL (0.79). Liver US patterns in children with CF correlate with platelet count, spleen size and indices of liver fibrosis. Multivariable models of these biomarkers have excellent discriminating ability for NL versus NOD, and good ability to distinguish other US patterns, suggesting that US patterns correlate with clinically relevant liver disease.

Identifiants

pubmed: 31436672
doi: 10.1097/MPG.0000000000002413
pii: 00005176-201909000-00019
pmc: PMC6713487
mid: NIHMS1530450
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

351-357

Subventions

Organisme : NIDDK NIH HHS
ID : U01 DK062456
Pays : United States

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Auteurs

Simon C Ling (SC)

The Hospital for Sick Children and Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.

Wen Ye (W)

University of Michigan, Ann Arbor, MI.

Daniel H Leung (DH)

Baylor College of Medicine, Texas Children's Hospital, Houston, TX.

Oscar M Navarro (OM)

Department of Diagnostic Imaging, The Hospital for Sick Children and Department of Medical Imaging, University of Toronto, Toronto, Ontario, Canada.

Alexander Weymann (A)

Washington University School of Medicine, St Louis, MO.

Wikrom Karnsakul (W)

Johns Hopkins University School of Medicine, Baltimore, MD.

A Jay Freeman (AJ)

Emory University School of Medicine, Children's Healthcare of Atlanta, Atlanta, GA.

John C Magee (JC)

University of Michigan Medical School, Ann Arbor, MI.

Michael R Narkewicz (MR)

Digestive Health Institute, Children's Hospital Colorado & University of Colorado School of Medicine, Aurora, CO.

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