Literature DB >> 29438119

Liver disease in patients with cystic fibrosis.

Natasha Kamal1, Pallavi Surana2, Christopher Koh2.   

Abstract

PURPOSE OF REVIEW: The aim of this study was to provide an overview of the current understanding of the pathophysiology, diagnosis and management of cystic fibrosis-liver disease (CFLD). RECENT
FINDINGS: CFLD has a variety of manifestations. Previously, it was thought that patients progressed from mild cholestatic disease to cirrhosis to decompensated cirrhosis with portal hypertension. Newer evidence suggests that some patients may develop cirrhosis while others develop noncirrhotic portal hypertension. Advances in our understanding of the pathophysiology of disease necessitate modifications to the current diagnostic criteria. Both fibroscan and noninvasive biomarkers can be used to identify patients with cirrhosis and portal hypertension. Ursodeoxycholic acid remains the mainstay of therapy despite a paucity of rigorous studies supporting its use. Novel therapeutic agents such as CF transmembrane conductance regulator (CFTR) modulators and potentiators are encouraging but need to be evaluated specifically in CFLD.
SUMMARY: A better understanding of the pathophysiology of disease is critical to developing more disease-specific diagnostics and therapeutics.

Entities:  

Mesh:

Year:  2018        PMID: 29438119      PMCID: PMC7232742          DOI: 10.1097/MOG.0000000000000432

Source DB:  PubMed          Journal:  Curr Opin Gastroenterol        ISSN: 0267-1379            Impact factor:   3.287


  33 in total

1.  Liver disease in cystic fibrosis presents as non-cirrhotic portal hypertension.

Authors:  Peter Witters; Louis Libbrecht; Tania Roskams; Kris De Boeck; Lieven Dupont; Marijke Proesmans; François Vermeulen; Geert Maleux; Diethard Monbaliu; Jacques Pirenne; David Cassiman
Journal:  J Cyst Fibros       Date:  2017-03-25       Impact factor: 5.482

2.  Liver transplantation in adult cystic fibrosis: Clinical, imaging, and pathological evidence of obliterative portal venopathy.

Authors:  Sophie Hillaire; Dominique Cazals-Hatem; Onorina Bruno; Sandra de Miranda; Dominique Grenet; Nicolas Poté; Olivier Soubrane; Serge Erlinger; Florence Lacaille; Francois Mellot; Valerie Vilgrain; Valerie Paradis
Journal:  Liver Transpl       Date:  2017-10       Impact factor: 5.799

Review 3.  Effects of new and emerging therapies on gastrointestinal outcomes in cystic fibrosis.

Authors:  Roderick H J Houwen; Wendy L van der Woerd; Mordechai Slae; Michael Wilschanski
Journal:  Curr Opin Pulm Med       Date:  2017-11       Impact factor: 3.155

4.  Natural history of liver disease in cystic fibrosis.

Authors:  A Lindblad; H Glaumann; B Strandvik
Journal:  Hepatology       Date:  1999-11       Impact factor: 17.425

5.  Aspartate aminotransferase to platelet ratio and fibrosis-4 as biomarkers in biopsy-validated pediatric cystic fibrosis liver disease.

Authors:  Daniel H Leung; Mahjabeen Khan; Charles G Minard; Danielle Guffey; Louise E Ramm; Andrew D Clouston; Gregory Miller; Peter J Lewindon; Ross W Shepherd; Grant A Ramm
Journal:  Hepatology       Date:  2015-09-28       Impact factor: 17.425

6.  Features of Severe Liver Disease With Portal Hypertension in Patients With Cystic Fibrosis.

Authors:  Jaclyn R Stonebraker; Chee Y Ooi; Rhonda G Pace; Harriet Corvol; Michael R Knowles; Peter R Durie; Simon C Ling
Journal:  Clin Gastroenterol Hepatol       Date:  2016-04-05       Impact factor: 11.382

7.  Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report.

Authors:  Philip M Farrell; Beryl J Rosenstein; Terry B White; Frank J Accurso; Carlo Castellani; Garry R Cutting; Peter R Durie; Vicky A Legrys; John Massie; Richard B Parad; Michael J Rock; Preston W Campbell
Journal:  J Pediatr       Date:  2008-08       Impact factor: 4.406

Review 8.  Cirrhosis and other liver disease in cystic fibrosis.

Authors:  Thomas Flass; Michael R Narkewicz
Journal:  J Cyst Fibros       Date:  2012-12-20       Impact factor: 5.482

9.  Cystic Fibrosis Associated with Worse Survival After Liver Transplantation.

Authors:  Sylvester M Black; Frederick W Woodley; Dmitry Tumin; Khalid Mumtaz; Bryan A Whitson; Joseph D Tobias; Don Hayes
Journal:  Dig Dis Sci       Date:  2015-11-24       Impact factor: 3.199

10.  Intestinal lesions are associated with altered intestinal microbiome and are more frequent in children and young adults with cystic fibrosis and cirrhosis.

Authors:  Thomas Flass; Suhong Tong; Daniel N Frank; Brandie D Wagner; Charles E Robertson; Cassandra Vogel Kotter; Ronald J Sokol; Edith Zemanick; Frank Accurso; Edward J Hoffenberg; Michael R Narkewicz
Journal:  PLoS One       Date:  2015-02-06       Impact factor: 3.240

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  19 in total

Review 1.  Hyperinflammation and airway surface liquid dehydration in cystic fibrosis: purinergic system as therapeutic target.

Authors:  Thiago Inácio Teixeira do Carmo; Victor Emanuel Miranda Soares; Jonatha Wruck; Fernanda Dos Anjos; Débora Tavares de Resende E Silva; Sarah Franco Vieira de Oliveira Maciel; Margarete Dulce Bagatini
Journal:  Inflamm Res       Date:  2021-04-27       Impact factor: 4.575

Review 2.  Hepatic Manifestations of Cystic Fibrosis.

Authors:  Sasan Sakiani; David E Kleiner; Theo Heller; Christopher Koh
Journal:  Clin Liver Dis       Date:  2019-02-21       Impact factor: 6.126

3.  [Clinical characteristics and gene variants of patients with infantile intrahepatic cholestasis].

Authors:  Mei-Juan Wang; Xue-Mei Zhong; Xin Ma; Hui-Juan Ning; Dan Zhu; You-Zhe Gong; Meng Jin
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2021-01

Review 4.  Increasing life expectancy in cystic fibrosis: Advances and challenges.

Authors:  Kimberly A McBennett; Pamela B Davis; Michael W Konstan
Journal:  Pediatr Pulmonol       Date:  2021-11-11

Review 5.  Neutrophil dysfunction in the pathogenesis of cystic fibrosis.

Authors:  Guoshun Wang; William M Nauseef
Journal:  Blood       Date:  2022-04-28       Impact factor: 25.476

6.  Characteristics and Outcomes of Children With Cystic Fibrosis Hospitalized With Cirrhosis in the United States.

Authors:  Christina Thornton; Ranjani Somayaji; Michael Parkins; Mark G Swain; Kathleen J Ramos; Christopher H Goss; Abdel A Shaheen
Journal:  Am J Gastroenterol       Date:  2021-08-01       Impact factor: 12.045

Review 7.  Pathophysiology of Cystic Fibrosis Liver Disease: A Channelopathy Leading to Alterations in Innate Immunity and in Microbiota.

Authors:  Romina Fiorotto; Mario Strazzabosco
Journal:  Cell Mol Gastroenterol Hepatol       Date:  2019-05-07

Review 8.  A new era for people with cystic fibrosis.

Authors:  Marlou C Bierlaagh; Danya Muilwijk; Jeffrey M Beekman; Cornelis K van der Ent
Journal:  Eur J Pediatr       Date:  2021-07-02       Impact factor: 3.183

Review 9.  Recent advances in understanding liver fibrosis: bridging basic science and individualized treatment concepts.

Authors:  Ralf Weiskirchen; Sabine Weiskirchen; Frank Tacke
Journal:  F1000Res       Date:  2018-06-27

Review 10.  Gut-Liver Axis and Inflammasome Activation in Cholangiocyte Pathophysiology.

Authors:  Luca Maroni; Elisabetta Ninfole; Claudio Pinto; Antonio Benedetti; Marco Marzioni
Journal:  Cells       Date:  2020-03-17       Impact factor: 6.600

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