Literature DB >> 27374006

Gastrointestinal Manifestations of Autosomal-Dominant Polycystic Kidney Disease.

Adam E Mikolajczyk1, Helen S Te2, Arlene B Chapman3.   

Abstract

Autosomal-dominant polycystic kidney disease (ADPKD) is the most commonly inherited kidney disease, and the fourth most common cause of end-stage renal disease. ADPKD is a systemic disorder, associated with numerous extrarenal manifestations, including polycystic liver disease, the most common gastrointestinal manifestation, and diverticular disease, inguinal, and ventral hernias, pancreatic cysts, and large bile duct abnormalities. All of these gastrointestinal manifestations play a significant role in disease burden in ADPKD, particularly in the later decades of life. Thus, as ADPKD becomes more recognized, it is important for gastroenterologists to be knowledgeable of this monogenic disorder's effects on the digestive system.
Copyright © 2017 AGA Institute. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ADPKD; Cysts; Diverticulosis; Hernia

Mesh:

Year:  2016        PMID: 27374006     DOI: 10.1016/j.cgh.2016.06.017

Source DB:  PubMed          Journal:  Clin Gastroenterol Hepatol        ISSN: 1542-3565            Impact factor:   11.382


  14 in total

Review 1.  A Practical Approach to Polycystic Liver Disease.

Authors:  Armani Patel; Arlene B Chapman; Adam E Mikolajczyk
Journal:  Clin Liver Dis (Hoboken)       Date:  2019-12-20

2.  Waitlisted Candidates With Polycystic Liver Disease Are More Likely to be Transplanted Than Those With Chronic Liver Failure.

Authors:  Sahil D Doshi; Therese Bittermann; Thomas D Schiano; David Seth Goldberg
Journal:  Transplantation       Date:  2017-08       Impact factor: 4.939

3.  Biliary Tract and Liver Complications in Polycystic Kidney Disease.

Authors:  Parminder K Judge; Charlie H S Harper; Benjamin C Storey; Richard Haynes; Martin J Wilcock; Natalie Staplin; Raph Goldacre; Colin Baigent; Jane Collier; Michael Goldacre; Martin J Landray; Christopher G Winearls; William G Herrington
Journal:  J Am Soc Nephrol       Date:  2017-05-02       Impact factor: 10.121

Review 4.  Regenerative Medicine and the Biliary Tree.

Authors:  Thiago M De Assuncao; Nidhi Jalan-Sakrikar; Robert C Huebert
Journal:  Semin Liver Dis       Date:  2017-02-15       Impact factor: 6.115

Review 5.  Polycystic Liver Disease: Advances in Understanding and Treatment.

Authors:  Tatyana V Masyuk; Anatoliy I Masyuk; Nicholas F LaRusso
Journal:  Annu Rev Pathol       Date:  2021-11-01       Impact factor: 23.472

6.  Autophagy promotes hepatic cystogenesis in polycystic liver disease by depletion of cholangiocyte ciliogenic proteins.

Authors:  Anatoliy I Masyuk; Tatyana V Masyuk; Christy E Trussoni; Nicholas E Pirius; Nicholas F LaRusso
Journal:  Hepatology       Date:  2022-02-08       Impact factor: 17.298

7.  Colonoscopy as Part of Pre-Transplant Work-Up in Successful Kidney Transplant Candidates: Single-Center Experience and Review of Literature.

Authors:  Jarek Kobiela; Małgorzata Dobrzycka; Roman Danielewicz; Justyna Jończyk; Andrzej J Łachiński; Zbigniew Śledziński; Alicja Dębska-Ślizień
Journal:  Ann Transplant       Date:  2018-11-09       Impact factor: 1.530

8.  Kidney and cystic volume imaging for disease presentation and progression in the cat autosomal dominant polycystic kidney disease large animal model.

Authors:  Yoshihiko Yu; Kate L Shumway; Jodi S Matheson; Marie E Edwards; Timothy L Kline; Leslie A Lyons
Journal:  BMC Nephrol       Date:  2019-07-12       Impact factor: 2.388

9.  ADPedKD: A Global Online Platform on the Management of Children With ADPKD.

Authors:  Stéphanie De Rechter; Detlef Bockenhauer; Lisa M Guay-Woodford; Isaac Liu; Andrew J Mallett; Neveen A Soliman; Lucimary C Sylvestre; Franz Schaefer; Max C Liebau; Djalila Mekahli
Journal:  Kidney Int Rep       Date:  2019-05-29

10.  Hepatointestinal complications in polycystic kidney disease.

Authors:  Shih-Ting Huang; Ya-Wen Chuang; Tung-Min Yu; Cheng-Li Lin; Long-Bin Jeng
Journal:  Oncotarget       Date:  2017-09-15
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