Evidence map›Paper›PMID 37260991›Full record

ArticleClinical kidney journal2023

Autosomal dominant polycystic kidney disease in young adults.

Víctor Martínez, Mónica Furlano, Laia Sans, Lissett Pulido, Rebeca García, María Vanessa Pérez-Gómez, Jinny Sánchez-Rodríguez, Miquel Blasco, Cristina Castro-Alonso, Gema Fernández-Fresnedo and 15 more

Open access · goldAbstract read
In one paragraph

Article in Clinical kidney journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

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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

25 authors at 20 institutions in 1 country.

Víctor MartínezNephrology Department, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain.ORCID https://orcid.org/0000-0003-0627-3512
Mónica FurlanoInherited Kidney Diseases, Nephrology Department, Fundació Puigvert, Institut d'Investigació Biomèdica Sant Pau (IIB-SANT PAU ).ORCID https://orcid.org/0000-0003-1025-3901
Laia SansNephrology Department, Hospital del Mar, Barcelona, Spain.ORCID https://orcid.org/0000-0002-3628-9489
Lissett PulidoNephrology Department, Hospital Universitario Joan XXIII, Tarragona, Spain.
Rebeca GarcíaNephrology Department, Hospital La Mancha-Centro, Alcázar de San Juan, Spain.ORCID https://orcid.org/0000-0003-0649-2766
María Vanessa Pérez-GómezNephrology Department, IIS-Fundación Jiménez Diaz, Universidad Autónoma de Madrid, IRSIN, RICORS40, Madrid, Spain.ORCID https://orcid.org/0000-0003-4558-5236
Jinny Sánchez-RodríguezNephrology Department, IIS-Fundación Jiménez Diaz, Universidad Autónoma de Madrid, IRSIN, RICORS40, Madrid, Spain.
Miquel BlascoNephrology and Kidney Transplantation Department, Hospital Clínic, Institute of Biomedical Research August Pi i Sunyer (IDIPABS), University of Barcelona, Barcelona, Spain.ORCID https://orcid.org/0000-0003-0789-7992
Cristina Castro-AlonsoNephrology Department, Hospital Universitario Doctor Peset, Valencia, Spain.
Gema Fernández-FresnedoNephrology Department, Hospital Universitario Marqués de Valdecilla, Santander, Spain.
Nicolás Roberto RoblesNephrology Department, Hospital Universitario de Badajoz, Badajoz, Spain.ORCID https://orcid.org/0000-0003-4984-6691
María Pau ValenzuelaNephrology Department, Hospital Universitari Parc Taulí, Sabadell, Spain.
Javier NaranjoNephrology Department, Hospital Universitario Puerta del Mar, Cádiz, Spain.ORCID https://orcid.org/0000-0002-7004-6122
Nadia MartínNephrology Department, Hospital Universitari de Girona Dr Josep Trueta, Gerona, Spain.ORCID https://orcid.org/0000-0002-4370-7562
Melissa PilcoNephrology Department, Hospital Universitari de Girona Dr Josep Trueta, Gerona, Spain.ORCID https://orcid.org/0000-0002-1311-0896
Irene Agraz-PamplonaNephrology Department, Hospital Valle de Hebrón, Barcelona, Spain.ORCID https://orcid.org/0000-0002-4223-6834
Juan David González-RodríguezPediatric Nephrology Department, Hospital Universitario Santa Lucía, Cartagena, Spain.ORCID https://orcid.org/0000-0002-8863-2007
Nayara PanizoNephrology Department, Hospital Universitari i Politècnic la Fe, Valencia, Spain.
Gloria FragaPediatric Nephrology Department, Hospital Santa Creu i Sant Pau, Barcelona, Spain.
Loreto FernándezNephrology Department, Hospital Príncipe de Asturias, Alcalá de Henares, Spain.
María Teresa LópezNephrology Department, Hospital Rey Juan Carlos, Móstoles, Spain.
Cecilia Dall'AneseNephrology Department, Hospital San Pedro, Logroño, Spain.
Alberto OrtizNephrology Department, IIS-Fundación Jiménez Diaz, Universidad Autónoma de Madrid, IRSIN, RICORS40, Madrid, Spain.ORCID https://orcid.org/0000-0002-9805-9523
Roser TorraInherited Kidney Diseases, Nephrology Department, Fundació Puigvert, Institut d'Investigació Biomèdica Sant Pau (IIB-SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain.ORCID https://orcid.org/0000-0001-8714-2332
participants in the REPQRAD
Hospital Universitario Príncipe de Asturias · ESUniversidad Autónoma de Madrid · ESHospital Clínico Universitario de Valencia · ESHospital de Poniente · ESHospital General De Segovia · ESHospital Universitari de Girona Doctor Josep Trueta · ESHospital Universitari Joan XXIII de Tarragona · ESHospital Universitario de Getafe · ESHospital Universitario Doctor Peset · ESHospital Universitario San Agustín · ESCentro de Implantología Cirugía Oral y Maxilofacial · ESDeleted InstitutionFundación Hospital Provincial de Castellón · ESHospital Arnau de Vilanova · ESHospital Del Mar · ESHospital de Palamós · ESHospital de Sagunto · ESHospital de Sant Pau · ESHospital San Pedro · ESHospital Universitari i Politècnic La Fe · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The clinical manifestations of autosomal dominant polycystic kidney disease (ADPKD) usually appear in adulthood, however pediatric series report a high morbidity. The objective of the study was to analyze the clinical characteristics of ADPKD in young adults. Methods: Family history, hypertension, albuminuria, estimated glomerular filtration rate (eGFR) and imaging tests were examined in 346 young adults (18-30 years old) out of 2521 patients in the Spanish ADPKD registry (REPQRAD). A literature review searched for reports on hypertension in series with more than 50 young (age <30 years) ADPKD patients. Results: The mean age of this young adult cohort was 25.24 (SD 3.72) years. The mean age at diagnosis of hypertension was 21.15 (SD 4.62) years, while in the overall REPQRAD population was aged 37.6 years. The prevalence of hypertension was 28.03% and increased with age (18-24 years, 16.8%; 25-30 years, 36.8%). Although prevalence was lower in women than in men, the age at onset of hypertension (21 years) was similar in both sexes. Mean eGFR was 108 (SD 21) mL/min/1.73 m Conclusions: Young adults present non-negligible ADPKD-related morbidity. This supports the need for a thorough assessment of young adults at risk of ADPKD that allows early diagnosis and treatment of hypertension.

Indexed as

ADKPDchildrenglomerular filtration ratehypertensionyoung adults

Identifiers

PMID37260991
PMCPMC10229292
OpenAlexW4310984725

What OpenQuestion holds

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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.