Literature DB >> 30347391

Autosomal Dominant Polycystic Kidney Disease: Clinical Assessment of Rapid Progression.

Mónica Furlano1, Irene Loscos2, Teresa Martí3, Gemma Bullich4, Nadia Ayasreh1, Asunción Rius1,5, Lourdes Roca1,6, José Ballarín7, Elisabet Ars4, Roser Torra1.   

Abstract

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) causes the development of renal cysts and leads to a decline in renal function. Limited guidance exists in clinical practice on the use of tolvaptan. A decision algorithm from the European Renal Association-European Dialysis and Transplant Association (ERA-EDTA) Working Groups of Inherited Kidney Disorders and European Renal Best Practice (WGIKD/ERBP) has been proposed to identify candidates for tolvaptan treatment; however, this algorithm has not been assessed in clinical practice.
METHODS: Eighteen-month cross-sectional, unicenter, observational study assessing 305 consecutive ADPKD patients. The ERA-EDTA WGIKD/ERBP algorithm with a stepwise approach was used to assess rapid progression (RP). Subsequently, expanded criteria based on the REPRISE trial were applied to evaluate the -impact of extended age (≤55 years) and estimated glomerular filtration rate (eGFR; ≥25 mL/min/1.73 m2).
RESULTS: Historical eGFR decline, indicative of RP, was fulfilled in 26% of 73 patients who were candidates for RP assessment, mostly aged 31-55 years. Further tests including ultrasound and MRI measurements of kidney volume plus genetic testing enabled the evaluation of the remaining patients. Overall, 15.7% of patients met the criteria for rapid or likely RP using the algorithm, and the percentage increased to 27% when extending age and eGFR.
CONCLUSIONS: The ERA-EDTA WGIKD/ERBP algorithm provides a valuable means of identifying in routine clinical practice patients who may be eligible for treatment with tolvaptan. The impact of a new threshold for age and eGFR may increase the percentage of patients to be treated.
© 2018 S. Karger AG, Basel.

Entities:  

Keywords:  Autosomal dominant polycystic kidney disease; Chronic kidney disease; Gene; Magnetic resonance imaging; Prediction; Rapid progression; Total kidney volume; Ultrasound

Mesh:

Substances:

Year:  2018        PMID: 30347391     DOI: 10.1159/000493325

Source DB:  PubMed          Journal:  Am J Nephrol        ISSN: 0250-8095            Impact factor:   3.754


  5 in total

Review 1.  Recent advances in the clinical management of autosomal dominant polycystic kidney disease.

Authors:  Roser Torra
Journal:  F1000Res       Date:  2019-01-29

2.  An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the European Rare Kidney Disease Reference Network and Polycystic Kidney Disease International.

Authors:  Roman-Ulrich Müller; A Lianne Messchendorp; Henrik Birn; Giovambattista Capasso; Emilie Cornec-Le Gall; Olivier Devuyst; Albertien van Eerde; Patrick Guirchoun; Tess Harris; Ewout J Hoorn; Nine V A M Knoers; Uwe Korst; Djalila Mekahli; Yannick Le Meur; Tom Nijenhuis; Albert C M Ong; John A Sayer; Franz Schaefer; Aude Servais; Vladimir Tesar; Roser Torra; Stephen B Walsh; Ron T Gansevoort
Journal:  Nephrol Dial Transplant       Date:  2022-04-25       Impact factor: 7.186

3.  Comparative analysis of tools to predict rapid progression in autosomal dominant polycystic kidney disease.

Authors:  Javier Naranjo; Mónica Furlano; Ferran Torres; Jonathan Hernandez; Marc Pybus; Laia Ejarque; Christian Cordoba; Lluis Guirado; Elisabet Ars; Roser Torra
Journal:  Clin Kidney J       Date:  2021-12-28

Review 4.  Prediction models used in the progression of chronic kidney disease: A scoping review.

Authors:  David K E Lim; James H Boyd; Elizabeth Thomas; Aron Chakera; Sawitchaya Tippaya; Ashley Irish; Justin Manuel; Kim Betts; Suzanne Robinson
Journal:  PLoS One       Date:  2022-07-26       Impact factor: 3.752

5.  A Systematic Review of Reported Outcomes in ADPKD Studies.

Authors:  Sara S Jdiaa; Nedaa M Husainat; Razan Mansour; Mohamad A Kalot; Kerri McGreal; Fouad T Chebib; Ronald D Perrone; Alan Yu; Reem A Mustafa
Journal:  Kidney Int Rep       Date:  2022-07-05
  5 in total

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