Literature DB >> 25134777

ESRD from autosomal dominant polycystic kidney disease in the United States, 2001-2010.

Scott Reule1, Donal J Sexton1, Craig A Solid2, Shu-Cheng Chen2, Allan J Collins1, Robert N Foley3.   

Abstract

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is amenable to early detection and specialty care. Thus, while important to patients with the condition, end-stage renal disease (ESRD) from ADPKD also may be an indicator of the overall state of nephrology care. STUDY
DESIGN: Retrospective cohort study of temporal trends in ESRD from ADPKD and pre-renal replacement therapy (RRT) nephrologist care, 2001-2010 (n = 23,772). SETTING & PARTICIPANTS: US patients who initiated maintenance RRT from 2001 through 2010 (n = 1,069,343) from US Renal Data System data. PREDICTOR: ESRD from ADPKD versus from other causes for baseline characteristics and clinical outcomes; interval 2001-2005 versus 2006-2010 for comparisons of cohort of patients with ESRD from ADPKD. OUTCOMES: Death, wait-listing for kidney transplant, kidney transplantation. MEASUREMENTS: US census data were used as population denominators. Poisson distribution was used to compute incidence rates (IRs). Incidence ratios were standardized to rates in 2001-2002 for age, sex, and race/ethnicity. Patients with and without ADPKD were matched to compare clinical outcomes. Poisson regression was used to calculate IRs and adjusted HRs for clinical events after inception of RRT.
RESULTS: General population incidence ratios in 2009-2010 were unchanged from 2001-2002 (incidence ratio, 1.02). Of patients with ADPKD, 48.1% received more than 12 months of nephrology care before RRT; preemptive transplantation was the initial RRT in 14.3% and fistula was the initial hemodialysis access in 35.8%. During 4.9 years of follow-up, patients with ADPKD were more likely to be listed for transplantation (IR, 11.7 [95% CI, 11.5-12.0] vs 8.4 [95% CI, 8.2-8.7] per 100 person-years) and to undergo transplantation (IR, 9.8 [95% CI, 9.5-10.0] vs 4.8 [95% CI, 4.7-5.0] per 100 person-years) and less likely to die (IR, 5.6 [95% CI, 5.4-5.7] vs 15.5 [95% CI, 15.3-15.8] per 100 person-years) than matched controls without ADPKD. LIMITATIONS: Retrospective nonexperimental registry-based study of associations; cause-and-effect relationships cannot be determined.
CONCLUSIONS: Although outcomes on dialysis therapy are better for patients with ADPKD than for those without ADPKD, access to predialysis nephrology care and nondeclining ESRD rates may be a cause for concern.
Copyright © 2014 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Dialysis; autosomal dominant polycystic kidney disease (ADPKD); clinical outcome; end-stage renal disease (ESRD); incidence; registry data; renal replacement therapy (RRT); renal transplant

Mesh:

Year:  2014        PMID: 25134777      PMCID: PMC4396817          DOI: 10.1053/j.ajkd.2014.05.020

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


  11 in total

1.  Improved prognosis in patients with autosomal dominant polycystic kidney disease in Denmark.

Authors:  Bjarne Orskov; Vibeke Rømming Sørensen; Bo Feldt-Rasmussen; Svend Strandgaard
Journal:  Clin J Am Soc Nephrol       Date:  2010-07-29       Impact factor: 8.237

2.  US Renal Data System 2012 Annual Data Report.

Authors:  Allan J Collins; Robert N Foley; Charles Herzog; Blanche Chavers; David Gilbertson; Charles Herzog; Areef Ishani; Kirsten Johansen; Bertram Kasiske; Nancy Kutner; Jiannong Liu; Wendy St Peter; Shu Ding; Haifeng Guo; Allyson Kats; Kenneth Lamb; Shuling Li; Suying Li; Tricia Roberts; Melissa Skeans; Jon Snyder; Craig Solid; Bryn Thompson; Eric Weinhandl; Hui Xiong; Akeem Yusuf; David Zaun; Cheryl Arko; Shu-Cheng Chen; Frank Daniels; James Ebben; Eric Frazier; Christopher Hanzlik; Roger Johnson; Daniel Sheets; Xinyue Wang; Beth Forrest; Edward Constantini; Susan Everson; Paul Eggers; Lawrence Agodoa
Journal:  Am J Kidney Dis       Date:  2013-01       Impact factor: 8.860

3.  Tolvaptan in autosomal dominant polycystic kidney disease.

Authors:  François Jouret; Jean-Marie Krzesinski
Journal:  N Engl J Med       Date:  2013-03-28       Impact factor: 91.245

4.  Survival after end-stage renal disease in autosomal dominant polycystic kidney disease: contribution of extrarenal complications to mortality.

Authors:  R D Perrone; R Ruthazer; N C Terrin
Journal:  Am J Kidney Dis       Date:  2001-10       Impact factor: 8.860

5.  Use of antihypertensive medications and mortality of patients with autosomal dominant polycystic kidney disease: a population-based study.

Authors:  Christine Patch; Judith Charlton; Paul J Roderick; Martin C Gulliford
Journal:  Am J Kidney Dis       Date:  2011-04-02       Impact factor: 8.860

6.  Rapamycin for treatment of type I autosomal dominant polycystic kidney disease (RAPYD-study): a randomized, controlled study.

Authors:  Giovanni Stallone; Barbara Infante; Giuseppe Grandaliano; Christos Bristogiannis; Luca Macarini; Daniela Mezzopane; Francesca Bruno; Eustacchio Montemurno; Annalisa Schirinzi; Massimo Sabbatini; Antonio Pisani; Tiziana Tataranni; Francesco Paolo Schena; Loreto Gesualdo
Journal:  Nephrol Dial Transplant       Date:  2012-07-10       Impact factor: 5.992

7.  Trends in the incidence of renal replacement therapy for end-stage renal disease in Europe, 1990-1999.

Authors:  Bénédicte Stengel; Solenne Billon; Paul C W Van Dijk; Kitty J Jager; Friedo W Dekker; Keith Simpson; J Douglas Briggs
Journal:  Nephrol Dial Transplant       Date:  2003-09       Impact factor: 5.992

8.  Trends in incidence of end-stage renal disease in Japan, 1983-2000: age-adjusted and age-specific rates by gender and cause.

Authors:  Kenji Wakai; Shigeru Nakai; Kenjiro Kikuchi; Kunitoshi Iseki; Naoko Miwa; Ikuto Masakane; Atsushi Wada; Takahiro Shinzato; Yuji Nagura; Takashi Akiba
Journal:  Nephrol Dial Transplant       Date:  2004-06-01       Impact factor: 5.992

9.  Epidemiology of adult polycystic kidney disease, Olmsted County, Minnesota: 1935-1980.

Authors:  C G Iglesias; V E Torres; K P Offord; K E Holley; C M Beard; L T Kurland
Journal:  Am J Kidney Dis       Date:  1983-05       Impact factor: 8.860

10.  Polycystic kidney disease re-evaluated: a population-based study.

Authors:  F Davies; G A Coles; P S Harper; A J Williams; C Evans; D Cochlin
Journal:  Q J Med       Date:  1991-06
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  15 in total

1.  Urinary Lithogenic Risk Profile in ADPKD Patients Treated with Tolvaptan.

Authors:  Matteo Bargagli; Nasser A Dhayat; Manuel Anderegg; Mariam Semmo; Uyen Huynh-Do; Bruno Vogt; Pietro Manuel Ferraro; Daniel G Fuster
Journal:  Clin J Am Soc Nephrol       Date:  2020-06-11       Impact factor: 8.237

Review 2.  ADPKD: clinical issues before and after renal transplantation.

Authors:  Piergiorgio Messa; Carlo Maria Alfieri; Emanuele Montanari; Mariano Ferraresso; Roberta Cerutti
Journal:  J Nephrol       Date:  2016-10-20       Impact factor: 3.902

3.  Effect of Statin Therapy on the Progression of Autosomal Dominant Polycystic Kidney Disease. A Secondary Analysis of the HALT PKD Trials.

Authors:  Godela M Brosnahan; Kaleab Z Abebe; Frederic F Rahbari-Oskoui; Charity G Patterson; Kyongtae T Bae; Robert W Schrier; William E Braun; Arlene B Chapman; Michael F Flessner; Peter C Harris; Ronald D Perrone; Theodore I Steinman; Vicente E Torres
Journal:  Curr Hypertens Rev       Date:  2017

4.  Patient characteristics and outcomes by GN subtype in ESRD.

Authors:  Michelle M O'Shaughnessy; Maria E Montez-Rath; Richard A Lafayette; Wolfgang C Winkelmayer
Journal:  Clin J Am Soc Nephrol       Date:  2015-06-19       Impact factor: 8.237

Review 5.  New treatment paradigms for ADPKD: moving towards precision medicine.

Authors:  Matthew B Lanktree; Arlene B Chapman
Journal:  Nat Rev Nephrol       Date:  2017-10-09       Impact factor: 28.314

6.  Analysis of Nationwide Data to Determine the Incidence and Diagnosed Prevalence of Autosomal Dominant Polycystic Kidney Disease in the USA: 2013-2015.

Authors:  Cynthia Willey; Siddhesh Kamat; Robert Stellhorn; Jaime Blais
Journal:  Kidney Dis (Basel)       Date:  2019-01-09

7.  The genetic background significantly impacts the severity of kidney cystic disease in the Pkd1RC/RC mouse model of autosomal dominant polycystic kidney disease.

Authors:  Jennifer Arroyo; Diana Escobar-Zarate; Harrison H Wells; Megan M Constans; Ka Thao; Jessica M Smith; Cynthia J Sieben; Madeline R Martell; Timothy L Kline; Maria V Irazabal; Vicente E Torres; Katharina Hopp; Peter C Harris
Journal:  Kidney Int       Date:  2021-03-09       Impact factor: 18.998

8.  End-Stage Kidney Disease in Patients With Autosomal Dominant Polycystic Kidney Disease: A 12-Year Study Based on the Canadian Organ Replacement Registry.

Authors:  Brandon Budhram; Ayub Akbari; Pierre Brown; Mohan Biyani; Gregory Knoll; Deborah Zimmerman; Cedric Edwards; Brendan McCormick; Ann Bugeja; Manish M Sood
Journal:  Can J Kidney Health Dis       Date:  2018-06-11

9.  Comparative Study of Outcomes among Patients with Polycystic Kidney Disease on Hemodialysis and Peritoneal Dialysis.

Authors:  Ju-Yeh Yang; Likwang Chen; Chia-Ter Chao; Yu-Sen Peng; Chih-Kang Chiang; Tze-Wah Kao; Kuo-Liong Chien; Hon-Yen Wu; Jenq-Wen Huang; Kuan-Yu Hung
Journal:  Sci Rep       Date:  2015-08-06       Impact factor: 4.379

10.  Hypokalemic Hypertension Leading to a Diagnosis of Autosomal Dominant Polycystic Kidney Disease.

Authors:  Wasawat Vutthikraivit; Montira Assanatham; Chutintorn Sriphrapradang
Journal:  Electrolyte Blood Press       Date:  2016-06-30
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