Literature DB >> 35217526

Volume Progression and Imaging Classification of Polycystic Liver in Early Autosomal Dominant Polycystic Kidney Disease.

Kyongtae T Bae1, Cheng Tao2, Robert Feldman3, Alan S L Yu4,5, Vicente E Torres6, Ronald D Perrone7, Arlene B Chapman8, Godela Brosnahan9, Theodore I Steinman10, William E Braun11, Michal Mrug12,13, William M Bennett14, Peter C Harris6, Avantika Srivastava15, Douglas P Landsittel15, Kaleab Z Abebe3.   

Abstract

BACKGROUND AND OBJECTIVES: The progression of polycystic liver disease is not well understood. The purpose of the study is to evaluate the associations of polycystic liver progression with other disease progression variables and classify liver progression on the basis of patient's age, height-adjusted liver cystic volume, and height-adjusted liver volume. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Prospective longitudinal magnetic resonance images from 670 patients with early autosomal dominant polycystic kidney disease for up to 14 years of follow-up were evaluated to measure height-adjusted liver cystic volume and height-adjusted liver volume. Among them, 245 patients with liver cyst volume >50 ml at baseline were included in the longitudinal analysis. Linear mixed models on log-transformed height-adjusted liver cystic volume and height-adjusted liver volume were fitted to approximate mean annual rate of change for each outcome. The association of sex, body mass index, genotype, baseline height-adjusted total kidney volume, and Mayo imaging class was assessed. We calculated height-adjusted liver cystic volume ranges for each specific age and divided them into five classes on the basis of annual percentage increase in height-adjusted liver cystic volume.
RESULTS: The mean annual growth rate of height-adjusted liver cystic volume was 12% (95% confidence interval, 11.1% to 13.1%; P<0.001), whereas that for height-adjusted liver volume was 2% (95% confidence interval, 1.9% to 2.6%; P<0.001). Women had higher baseline height-adjusted liver cystic volume than men, but men had higher height-adjusted liver cystic volume growth rate than women by 2% (95% confidence interval, 0.4% to 4.5%; P=0.02). Whereas the height-adjusted liver cystic volume growth rate decreased in women after menopause, no decrease was observed in men at any age. Body mass index, genotype, and baseline height-adjusted total kidney volume were not associated with the growth rate of height-adjusted liver cystic volume or height-adjusted liver volume. According to the height-adjusted liver cystic volume growth rate, patients were classified into five classes (number of women, men in each class): A (24, six); B (44, 13); C (43, 48); D (28, 17); and E (13, nine).
CONCLUSIONS: Compared with height-adjusted liver volume, the use of height-adjusted liver cystic volume showed greater separations in volumetric progression of polycystic liver disease. Similar to the Mayo imaging classification for the kidney, the progression of polycystic liver disease may be categorized on the basis of patient's age and height-adjusted liver cystic volume.
Copyright © 2022 by the American Society of Nephrology.

Entities:  

Keywords:  ADPKD; diagnostic imaging; disease progression; genetic renal disease; kidney volume; liver; liver cysts; polycystic kidney disease

Mesh:

Year:  2022        PMID: 35217526      PMCID: PMC8975034          DOI: 10.2215/CJN.08660621

Source DB:  PubMed          Journal:  Clin J Am Soc Nephrol        ISSN: 1555-9041            Impact factor:   10.614


  35 in total

Review 1.  Medical and surgical treatment options for polycystic liver disease.

Authors:  Joost P H Drenth; Melissa Chrispijn; David M Nagorney; Patrick S Kamath; Vicente E Torres
Journal:  Hepatology       Date:  2010-12       Impact factor: 17.425

2.  Liver transplantation for adult polycystic liver disease.

Authors:  W K Washburn; L B Johnson; W D Lewis; R L Jenkins
Journal:  Liver Transpl Surg       Date:  1996-01

3.  Liver involvement in early autosomal-dominant polycystic kidney disease.

Authors:  Marie C Hogan; Kaleab Abebe; Vicente E Torres; Arlene B Chapman; Kyongtae T Bae; Cheng Tao; Hongliang Sun; Ronald D Perrone; Theodore I Steinman; William Braun; Franz T Winklhofer; Dana C Miskulin; Frederic Rahbari-Oskoui; Godela Brosnahan; Amirali Masoumi; Irina O Karpov; Susan Spillane; Michael Flessner; Charity G Moore; Robert W Schrier
Journal:  Clin Gastroenterol Hepatol       Date:  2014-08-09       Impact factor: 11.382

4.  Portal hypertension due to extensive hepatic cysts in autosomal dominant polycystic kidney disease.

Authors:  A Misra; P Loyalka; F Alva
Journal:  South Med J       Date:  1999-06       Impact factor: 0.954

5.  Polycystic Liver Disease: The Benefits of Targeting cAMP.

Authors:  Nicholas F Larusso; Tatyana V Masyuk; Marie C Hogan
Journal:  Clin Gastroenterol Hepatol       Date:  2016-03-10       Impact factor: 11.382

Review 6.  Liver transplantation for adult polycystic liver disease.

Authors:  K Swenson; P Seu; M Kinkhabwala; M Maggard; P Martin; J Goss; R Busuttil
Journal:  Hepatology       Date:  1998-08       Impact factor: 17.425

Review 7.  Polycystic liver disease: a clinical review.

Authors:  Natasha Chandok
Journal:  Ann Hepatol       Date:  2012 Nov-Dec       Impact factor: 2.400

8.  Expanded Imaging Classification of Autosomal Dominant Polycystic Kidney Disease.

Authors:  Kyongtae T Bae; Tiange Shi; Cheng Tao; Alan S L Yu; Vicente E Torres; Ronald D Perrone; Arlene B Chapman; Godela Brosnahan; Theodore I Steinman; William E Braun; Avantika Srivastava; Maria V Irazabal; Kaleab Z Abebe; Peter C Harris; Douglas P Landsittel
Journal:  J Am Soc Nephrol       Date:  2020-06-02       Impact factor: 10.121

9.  Young women with polycystic liver disease respond best to somatostatin analogues: a pooled analysis of individual patient data.

Authors:  Tom J G Gevers; Joanna Inthout; Anna Caroli; Piero Ruggenenti; Marie C Hogan; Vicente E Torres; Frederik Nevens; Joost P H Drenth
Journal:  Gastroenterology       Date:  2013-05-07       Impact factor: 22.682

10.  Total kidney volume: the most valuable predictor of autosomal dominant polycystic kidney disease progression.

Authors:  Cheng Xue; Chenchen Zhou; Changlin Mei
Journal:  Kidney Int       Date:  2018-03       Impact factor: 10.612

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