Literature DB >> 22425799

Chronic kidney disease progression in patients with autosomal dominant polycystic kidney disease.

Nayara Panizo1, Marian Goicoechea, Soledad García de Vinuesa, David Arroyo, Claudia Yuste, Abraham Rincón, Ursula Verdalles, Caridad Ruiz-Caro, Borja Quiroga, José Luño.   

Abstract

OBJECTIVES: The aim of this study was to analyse the factors influencing chronic kidney disease (CKD) progression in patients with autosomal dominant polycystic kidney disease (ADPKD). MATERIAL AND
METHOD: We studied 101 patients (mean age: 43 +/- 17.3 years, 43.56% male) followed during a median (interquartile range) follow-up time of 69 (35-128) months from 1997 to 2010. The primary end point was: time to a 50% decrease of estimated glomerular filtration rate (eGFR) (CKD-EPI) since the first-time visit and/or time to initiation of renal replacement therapy, and the annual mean change of eGFR was also analysed. Clinical and demographic data, blood pressure, concomitant medications, and analytical parameters were collected at each visit. Baseline kidney size was also recorded by ultrasound.
RESULTS: Thirty-one patients achieved the primary end point after a median (IQR) time of 102 (53-131) months. Those patients who achieved the primary end point had higher SBP and DBP (P=0.017 and P=0.001), higher LDL-cholesterol (P=0.011), higher creatinine (P=0.006), higher uricemia (P=0.041), more severe proteinuria (P=0.033) and greater kidney size (P=0.05). The mean annual eGFR change was of -3.52 +/- 7.3ml/min/1.73m2. Forty-nine patients had a rapid decline in renal function: Group A (higher than -3.52ml/min/1.73m2) and 52 patients had a lower renal disease progression: Group B (<-3.2 ml/min/1.73 m2). Adjusted Cox regression analysis showed that higher SBP and younger age at the first visit were independent variables for poorer renal outcome (P=0.026).
CONCLUSIONS: Initial kidney function, proteinuria, renal size, hypercholesterolemia, hyperuricemia, and SBP are the factors that influence CKD progression in ADPKD. SBP and younger age at diagnosis are the only factors that maintain their independent predictive value in a multivariant analysis.

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Year:  2012        PMID: 22425799     DOI: 10.3265/Nefrologia.pre2011.Dec.11177

Source DB:  PubMed          Journal:  Nefrologia        ISSN: 0211-6995            Impact factor:   2.033


  5 in total

1.  Crystal deposition triggers tubule dilation that accelerates cystogenesis in polycystic kidney disease.

Authors:  Jacob A Torres; Mina Rezaei; Caroline Broderick; Louis Lin; Xiaofang Wang; Bernd Hoppe; Benjamin D Cowley; Vincenzo Savica; Vicente E Torres; Saeed Khan; Ross P Holmes; Michal Mrug; Thomas Weimbs
Journal:  J Clin Invest       Date:  2019-07-30       Impact factor: 14.808

Review 2.  A systematic review of the predictors of disease progression in patients with autosomal dominant polycystic kidney disease.

Authors:  Claire Woon; Ashleigh Bielinski-Bradbury; Karl O'Reilly; Paul Robinson
Journal:  BMC Nephrol       Date:  2015-08-15       Impact factor: 2.388

3.  Hyperuricemia and deterioration of renal function in autosomal dominant polycystic kidney disease.

Authors:  Miyeun Han; Hayne Cho Park; Hyunsuk Kim; Hyung Ah Jo; Hyuk Huh; Joon Young Jang; Ah-Young Kang; Seung Hyup Kim; Hae Il Cheong; Duk-Hee Kang; Jaeseok Yang; Kook-Hwan Oh; Young-Hwan Hwang; Curie Ahn
Journal:  BMC Nephrol       Date:  2014-04-16       Impact factor: 2.388

4.  Clinical presentation and outcome of autosomal dominant polycystic kidney disease in Nigeria.

Authors:  Fatiu A Arogundade; Akinwumi A Akinbodewa; Abefe A Sanusi; Oluyomi Okunola; Muzamil O Hassan; Adewale Akinsola
Journal:  Afr Health Sci       Date:  2018-09       Impact factor: 0.927

5.  Clinical burden of autosomal dominant polycystic kidney disease.

Authors:  Peir-Haur Hung; Chien-Hung Lin; Kuan-Yu Hung; Chih-Hsin Muo; Mu-Chi Chung; Chao-Hsiang Chang; Chi-Jung Chung
Journal:  Aging (Albany NY)       Date:  2020-02-24       Impact factor: 5.682

  5 in total

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