Evidence map›Paper›PMID 35357684›Full record

ArticleJournal of nephrology2022

Estimated GFR in autosomal dominant polycystic kidney disease: errors of an unpredictable method.

Rosa Miquel Rodríguez, Sergio Luis-Lima, Juan Manuel Fernandez, María Vanesa Pérez Gómez, Beatriz González Toledo, Marian Cobo, Patricia Delgado-Mallén, Beatriz Escamilla, Cristina Oramas Marco, Sara Estupiñán and 14 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 6 institutions in 1 country.

Rosa Miquel Rodríguez *Nephrology Department, Hospital Universitario de Canarias, Tenerife, Spain.
Sergio Luis-Lima *Department of Nephrology and Hypertension, IIS-Fundación Jimenez Díaz, UAM, Madrid, Spain.
Juan Manuel Fernandez *Nephrology Department, Hospital Universitario Dr Negrín, Las Palmas, Spain.
María Vanesa Pérez GómezDepartment of Nephrology and Hypertension, IIS-Fundación Jimenez Díaz, UAM, Madrid, Spain.
Beatriz González ToledoDepartment of Nephrology and Hypertension, IIS-Fundación Jimenez Díaz, UAM, Madrid, Spain.
Marian CoboNephrology Department, Hospital Universitario de Canarias, Tenerife, Spain.
Patricia Delgado-MallénNephrology Department, Hospital Universitario de Canarias, Tenerife, Spain.
Beatriz EscamillaNephrology Department, Hospital Universitario de Canarias, Tenerife, Spain.
Cristina Oramas MarcoLaboratory of Renal Function, Faculty of Medicine, University of La Laguna, La Laguna, Spain.
Sara EstupiñánNephrology Department, Hospital Universitario de Canarias, Tenerife, Spain.
Coriolano Cruz PereraResearch Unit, Hospital Universitario de Canarias, Calle Ofra s/n 38023 La Laguna, Tenerife, Spain.
Natalia Negrín MenaResearch Unit, Hospital Universitario de Canarias, Calle Ofra s/n 38023 La Laguna, Tenerife, Spain.
Laura Díaz MartínLaboratory of Renal Function, Faculty of Medicine, University of La Laguna, La Laguna, Spain.
Sergio Pitti ReyesRadiology Unit, Hospital Universitario de Canarias, Tenerife, Spain.
Ibrahim Hernández GonzálezRadiology Unit, Hospital Universitario de Canarias, Tenerife, Spain.
Federico González-RinneResearch Unit, Hospital Universitario de Canarias, Calle Ofra s/n 38023 La Laguna, Tenerife, Spain.
Alejandra González-DelgadoCentral Laboratory, Hospital Universitario de Canarias, Tenerife, Spain.
Carmen Ferrer-MoureCentral Laboratory, Hospital Universitario de Canarias, Tenerife, Spain.
Begoña López-Botet ZuluetaDepartment of Nephrology and Hypertension, IIS-Fundación Jimenez Díaz, UAM, Madrid, Spain.
Armando TorresNephrology Department, Hospital Universitario de Canarias, Tenerife, Spain.
Jose Carlos Rodriguez PérezNephrology Department, Hospital Universitario Dr Negrín, Las Palmas, Spain.
Flavio GaspariLaboratory of Renal Function, Faculty of Medicine, University of La Laguna, La Laguna, Spain.
Alberto OrtizDepartment of Nephrology and Hypertension, IIS-Fundación Jimenez Díaz, UAM, Madrid, Spain.
Esteban PorriniResearch Unit, Hospital Universitario de Canarias, Calle Ofra s/n 38023 La Laguna, Tenerife, Spain. esteban.l.porrini@gmail.com.
Hospital Universitario de Canarias · ESUniversidad de La Laguna · ESHospital Universitario de Gran Canaria Doctor Negrín · ESHospital Universitario Fundación Jiménez Díaz · ESUniversidad Autónoma de Madrid · ESFundación Renal · ES

Funding

Instituto de Salud Carlos III PI19/01220
6 · The paper itself

Abstract

backgroundAutosomal dominant polycystic kidney disease (ADPKD) causes about 10% of cases of end stage renal disease. Disease progression rate is heterogeneous. Tolvaptan is presently the only specific therapeutic option to slow kidney function decline in adults at risk of rapidly progressing ADPKD with chronic kidney disease (CKD) stages 1-4. Thus, a reliable evaluation of kidney function in patients with ADPKD is needed.

methodsWe evaluated the agreement between measured (mGFR) and estimated glomerular filtration rate (eGFR) by 61 formulas based on creatinine and/or cystatin-C (eGFR) in 226 ADPKD patients with diverse GFR values, from predialysis to glomerular hyperfiltration. Also, we evaluated whether incorrect categorization of CKD using eGFR may interfere with the indication and/or reimbursement of Tolvaptan treatment.

resultsNo formula showed acceptable agreement with mGFR. Total Deviation Index averaged about 50% for eGFR based on creatinine and/or cystatin-C, indicating that 90% of the estimations of GFR showed bounds of error of 50% when compared with mGFR. In 1 out of 4 cases with mGFR < 30 ml/min, eGFR provided estimations above this threshold. Also, in half of the cases with mGFR between 30 and 40 ml/min, formulas estimated values < 30 ml/min.

conclusionsThe evaluation of renal function with formulas in ADPKD patients is unreliable. Extreme deviation from real renal function is quite frequent. The consequences of this error deserve attention, especially in rapid progressors who may benefit from starting treatment with tolvaptan and in whom specific GFR thresholds are needed for the indication or reimbursement. Whenever possible, mGFR is recommended.

Indexed as

Polycystic Kidney, Autosomal DominantRenal Insufficiency, ChronicAdultCreatinineGlomerular Filtration RateHumansTolvaptanCreatinineTolvaptanADPKDChronic kidney diseaseGlomerular filtration rate

Identifiers

PMID35357684
PMCPMC9584992
OpenAlexW4220938736

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.