Literature DB >> 29306517

Patterns of Kidney Function Decline in Autosomal Dominant Polycystic Kidney Disease: A Post Hoc Analysis From the HALT-PKD Trials.

Godela M Brosnahan1, Kaleab Z Abebe2, Charity G Moore2, Frederic F Rahbari-Oskoui3, Kyongtae T Bae2, Jared J Grantham4, Robert W Schrier5, William E Braun6, Arlene B Chapman7, Michael F Flessner8, Peter C Harris9, Marie C Hogan9, Ronald D Perrone10, Dana C Miskulin10, Theodore I Steinman11, Vicente E Torres9.   

Abstract

BACKGROUND: Previous clinical studies of autosomal dominant polycystic kidney disease (ADPKD) reported that loss of kidney function usually follows a steep and relentless course. A detailed examination of individual patterns of decline in estimated glomerular filtration rate (eGFR) has not been performed. STUDY
DESIGN: Longitudinal post hoc analysis of data collected during the Halt Progression of Polycystic Kidney Disease (HALT-PKD) trials. SETTING & PARTICIPANTS: 494 HALT-PKD Study A participants (younger; preserved eGFR) and 435 Study B participants (older; reduced eGFR) who had more than 3 years of follow-up and 7 or more eGFR assessments. MEASUREMENTS: Longitudinal eGFR assessments using the CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration) creatinine equation. PREDICTORS: Demographic, clinical, laboratory, and imaging features of participants. OUTCOMES: Probability of linear and nonlinear decline patterns or of stable eGFR calculated for each participant from a Bayesian model of individual eGFR trajectories.
RESULTS: Most (62.5% in Study A and 81% in Study B) participants had a linear decline in eGFR during up to 8 years of follow-up. A proportion (22% in Study A and 13% in Study B) of progressors had a nonlinear pattern. 15.5% of participants in Study A and 6% in Study B had a prolonged (≥4.5 years) period of stable eGFRs. These individuals (Study A) had significantly smaller total kidney volumes, higher renal blood flows, lower urinary albumin excretion, and lower body mass index at baseline and study end. In Study B, participants with reduced but stable eGFRs were older than the progressors. Two-thirds of nonprogressors in both studies had PKD1 mutations, with enrichment for weak nontruncating mutations. LIMITATIONS: Relatively short follow-up of a clinical trial population.
CONCLUSIONS: Although many individuals with ADPKD have a linear decline in eGFR, prolonged intervals of stable GFRs occur in a substantial fraction. Lower body mass index was associated with more stable kidney function in early ADPKD.
Copyright © 2017 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Autosomal dominant polycystic kidney disease (ADPKD); Bayesian models; eGFR slope; eGFR trajectory; end-stage renal disease (ESRD); estimated glomerular filtration rate (eGFR); kidney disease progression; mutation analysis; total kidney volume

Mesh:

Year:  2018        PMID: 29306517      PMCID: PMC5916329          DOI: 10.1053/j.ajkd.2017.10.023

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  37 in total

1.  Trajectories of kidney function decline in the 2 years before initiation of long-term dialysis.

Authors:  Ann M O'Hare; Adam Batten; Nilka Ríos Burrows; Meda E Pavkov; Leslie Taylor; Indra Gupta; Jeff Todd-Stenberg; Charles Maynard; Rudolph A Rodriguez; Fliss E M Murtagh; Eric B Larson; Desmond E Williams
Journal:  Am J Kidney Dis       Date:  2012-02-04       Impact factor: 8.860

Review 2.  Autosomal dominant polycystic kidney disease.

Authors:  Vicente E Torres; Peter C Harris; Yves Pirson
Journal:  Lancet       Date:  2007-04-14       Impact factor: 79.321

3.  Type of PKD1 mutation influences renal outcome in ADPKD.

Authors:  Emilie Cornec-Le Gall; Marie-Pierre Audrézet; Jian-Min Chen; Maryvonne Hourmant; Marie-Pascale Morin; Régine Perrichot; Christophe Charasse; Bassem Whebe; Eric Renaudineau; Philippe Jousset; Marie-Paule Guillodo; Anne Grall-Jezequel; Philippe Saliou; Claude Férec; Yannick Le Meur
Journal:  J Am Soc Nephrol       Date:  2013-02-21       Impact factor: 10.121

Review 4.  Glomerular filtration rate decline as a surrogate end point in kidney disease progression trials.

Authors:  Sunil V Badve; Suetonia C Palmer; Carmel M Hawley; Elaine M Pascoe; Giovanni F M Strippoli; David W Johnson
Journal:  Nephrol Dial Transplant       Date:  2015-07-11       Impact factor: 5.992

5.  Nonlinear trajectory of GFR in children before RRT.

Authors:  Yichen Zhong; Alvaro Muñoz; George J Schwartz; Bradley A Warady; Susan L Furth; Alison G Abraham
Journal:  J Am Soc Nephrol       Date:  2014-01-02       Impact factor: 10.121

6.  The HALT polycystic kidney disease trials: design and implementation.

Authors:  Arlene B Chapman; Vicente E Torres; Ronald D Perrone; Theodore I Steinman; Kyongtae T Bae; J Philip Miller; Dana C Miskulin; Frederic Rahbari Oskoui; Amirali Masoumi; Marie C Hogan; Franz T Winklhofer; William Braun; Paul A Thompson; Catherine M Meyers; Cass Kelleher; Robert W Schrier
Journal:  Clin J Am Soc Nephrol       Date:  2010-01       Impact factor: 8.237

7.  Magnetic resonance measurements of renal blood flow and disease progression in autosomal dominant polycystic kidney disease.

Authors:  Vicente E Torres; Bernard F King; Arlene B Chapman; Marijn E Brummer; Kyongtae T Bae; James F Glockner; Kraisthith Arya; Dana Risk; Joel P Felmlee; Jared J Grantham; Lisa M Guay-Woodford; William M Bennett; Saulo Klahr; Catherine M Meyers; Xiaoling Zhang; Paul A Thompson; J Philip Miller
Journal:  Clin J Am Soc Nephrol       Date:  2006-11-02       Impact factor: 8.237

8.  Rate of functional deterioration in polycystic kidney disease.

Authors:  K A Franz; F C Reubi
Journal:  Kidney Int       Date:  1983-03       Impact factor: 10.612

9.  Predicted Mutation Strength of Nontruncating PKD1 Mutations Aids Genotype-Phenotype Correlations in Autosomal Dominant Polycystic Kidney Disease.

Authors:  Christina M Heyer; Jamie L Sundsbak; Kaleab Z Abebe; Arlene B Chapman; Vicente E Torres; Jared J Grantham; Kyongtae T Bae; Robert W Schrier; Ronald D Perrone; William E Braun; Theodore I Steinman; Michal Mrug; Alan S L Yu; Godela Brosnahan; Katharina Hopp; Maria V Irazabal; William M Bennett; Michael F Flessner; Charity G Moore; Douglas Landsittel; Peter C Harris
Journal:  J Am Soc Nephrol       Date:  2016-01-28       Impact factor: 10.121

10.  Defective glucose metabolism in polycystic kidney disease identifies a new therapeutic strategy.

Authors:  Isaline Rowe; Marco Chiaravalli; Valeria Mannella; Valeria Ulisse; Giacomo Quilici; Monika Pema; Xuewen W Song; Hangxue Xu; Silvia Mari; Feng Qian; York Pei; Giovanna Musco; Alessandra Boletta
Journal:  Nat Med       Date:  2013-03-24       Impact factor: 53.440

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  15 in total

1.  The value of genotypic and imaging information to predict functional and structural outcomes in ADPKD.

Authors:  Sravanthi Lavu; Lisa E Vaughan; Sarah R Senum; Timothy L Kline; Arlene B Chapman; Ronald D Perrone; Michal Mrug; William E Braun; Theodore I Steinman; Frederic F Rahbari-Oskoui; Godela M Brosnahan; Kyongtae T Bae; Douglas Landsittel; Fouad T Chebib; Alan Sl Yu; Vicente E Torres; Peter C Harris
Journal:  JCI Insight       Date:  2020-08-06

2.  Long-term trajectory of kidney function in autosomal-dominant polycystic kidney disease.

Authors:  Alan S L Yu; Chengli Shen; Douglas P Landsittel; Jared J Grantham; Larry T Cook; Vicente E Torres; Arlene B Chapman; Kyongtae Ty Bae; Michal Mrug; Peter C Harris; Frederic F Rahbari-Oskoui; Tiange Shi; William M Bennett
Journal:  Kidney Int       Date:  2019-03-04       Impact factor: 10.612

3.  Examining the Role of Novel CKD Therapies for the ADPKD Patient.

Authors:  Dipal M Patel; Neera K Dahl
Journal:  Kidney360       Date:  2021-03-24

4.  Perspectives on Drug Development in Early ADPKD.

Authors:  Djalila Mekahli; Hayley Womack; Neera K Dahl
Journal:  Clin J Am Soc Nephrol       Date:  2022-08-23       Impact factor: 10.614

5.  Quest for the Cure: Testing the Old and New to Prevent Progression of Autosomal Dominant Polycystic Kidney Disease.

Authors:  Godela Brosnahan
Journal:  Kidney Med       Date:  2019-10-31

6.  Use of the Urine-to-Plasma Urea Ratio to Predict ADPKD Progression.

Authors:  Judith E Heida; Ron T Gansevoort; A Lianne Messchendorp; Esther Meijer; Niek F Casteleijn; Wendy E Boertien; Debbie Zittema
Journal:  Clin J Am Soc Nephrol       Date:  2021-01-27       Impact factor: 8.237

Review 7.  Is serum copeptin a modifiable biomarker in autosomal dominant polycystic kidney disease?

Authors:  Moomal Tasneem; Carly Mannix; Annette Wong; Jennifer Zhang; Gopala Rangan
Journal:  World J Nephrol       Date:  2018-03-06

8.  Modelling the long-term benefits of tolvaptan therapy on renal function decline in autosomal dominant polycystic kidney disease: an exploratory analysis using the ADPKD outcomes model.

Authors:  Hayley Bennett; Phil McEwan; Karina Hamilton; Karl O'Reilly
Journal:  BMC Nephrol       Date:  2019-04-23       Impact factor: 2.388

9.  Smoking accelerates renal cystic disease and worsens cardiac phenotype in Pkd1-deficient mice.

Authors:  Marciana V Sousa; Andressa G Amaral; Jessica A Freitas; Gilson M Murata; Elieser H Watanabe; Bruno E Balbo; Marcelo D Tavares; Renato A Hortegal; Camila Rocon; Leandro E Souza; Maria C Irigoyen; Vera M Salemi; Luiz F Onuchic
Journal:  Sci Rep       Date:  2021-07-14       Impact factor: 4.379

10.  Safety and efficacy of Tolvaptan in real-world patients with autosomal dominant polycystic kidney disease- interim results of SLOW-PKD surveillance.

Authors:  Toshio Mochizuki; Satoru Muto; Masateru Miyake; Toshiki Tanaka; Wenchyi Wang
Journal:  Clin Exp Nephrol       Date:  2021-07-06       Impact factor: 2.801

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