Liver stiffness assessment by transient elastography suggests high prevalence of liver involvement in common variable immunodeficiency.


Journal

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
ISSN: 1878-3562
Titre abrégé: Dig Liver Dis
Pays: Netherlands
ID NLM: 100958385

Informations de publication

Date de publication:
11 2019
Historique:
received: 29 01 2019
revised: 06 05 2019
accepted: 09 05 2019
pubmed: 4 6 2019
medline: 5 6 2020
entrez: 4 6 2019
Statut: ppublish

Résumé

Up to 50% of patients with common variable immunodeficiency (CVID) present persistently increased serum levels of liver enzymes and/or mild hepatomegaly. Ultrasound-based transient elastography (TE) is largely used for early detection of the progression of chronic liver diseases, but has never been employed in CVID. We performed a cross-sectional study to evaluate TE values in a cohort of adult CVID-patients. Full blood count, liver function test, liver and spleen sonogram and ultrasound-based TE were performed in 77 adult CVID patients. Demographic and clinical data were retrospectively collected from medical files. 33.8% (26/77) patients presented increased TE values ranging from moderate fibrosis to cirrhosis. TE values were positively correlated with ALP, γGT, spleen longitudinal diameter and peripheral blood counts (no significant correlation with BMI, AST, ALT, total proteins, albumin, bilirubin and hemoglobin). Moreover, liver stiffness was higher in patients with the clinical phenotypes polyclonal lymphoproliferation and enteropathy, and patients with both these complications had an increased risk (OR: 7.14) of presenting pathologic TE values compared with those without anyone of these. Transient elastography is a useful tool to be used alongside clinical and laboratory data to assess liver involvement in CVID.

Sections du résumé

BACKGROUND
Up to 50% of patients with common variable immunodeficiency (CVID) present persistently increased serum levels of liver enzymes and/or mild hepatomegaly. Ultrasound-based transient elastography (TE) is largely used for early detection of the progression of chronic liver diseases, but has never been employed in CVID. We performed a cross-sectional study to evaluate TE values in a cohort of adult CVID-patients.
METHODS
Full blood count, liver function test, liver and spleen sonogram and ultrasound-based TE were performed in 77 adult CVID patients. Demographic and clinical data were retrospectively collected from medical files.
RESULTS
33.8% (26/77) patients presented increased TE values ranging from moderate fibrosis to cirrhosis. TE values were positively correlated with ALP, γGT, spleen longitudinal diameter and peripheral blood counts (no significant correlation with BMI, AST, ALT, total proteins, albumin, bilirubin and hemoglobin). Moreover, liver stiffness was higher in patients with the clinical phenotypes polyclonal lymphoproliferation and enteropathy, and patients with both these complications had an increased risk (OR: 7.14) of presenting pathologic TE values compared with those without anyone of these.
CONCLUSIONS
Transient elastography is a useful tool to be used alongside clinical and laboratory data to assess liver involvement in CVID.

Identifiants

pubmed: 31155490
pii: S1590-8658(19)30595-X
doi: 10.1016/j.dld.2019.05.016
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1599-1603

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Auteurs

Ludovica Crescenzi (L)

Department of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy.

Antonio Pecoraro (A)

Department of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy.

Andrea Fiorentino (A)

Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.

Remo Poto (R)

Department of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy.

Gilda Varricchi (G)

Department of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy.

Antonio Rispo (A)

Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.

Filomena Morisco (F)

Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.

Giuseppe Spadaro (G)

Department of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy. Electronic address: spadaro@unina.it.

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