Evidence map›Paper›PMID 39940890›Full record

ReviewInternational journal of molecular sciences2025

Autosomal Dominant Polycystic Kidney Disease Inflammation Biomarkers in the Tolvaptan Era.

Tânia Lapão, Rui Barata, Cristina Jorge, Carlos Flores, Joaquim Calado

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Tânia LapãoUnidade Local de Saúde São José, Serviço de Patologia Clínica, Centro Clínico Académico de Lisboa, 1150-199 Lisboa, Portugal.
Rui BarataUnidade Local de Saúde São José, Serviço de Nefrologia, Centro Clínico Académico de Lisboa, 1069-166 Lisboa, Portugal.
Cristina JorgeUnidade Local de Saúde São José, Serviço de Nefrologia, Centro Clínico Académico de Lisboa, 1069-166 Lisboa, Portugal.
Carlos FloresUnidade Local de Saúde São José, Serviço de Patologia Clínica, Centro Clínico Académico de Lisboa, 1150-199 Lisboa, Portugal.
Joaquim CaladoToxOmics, NOVA Medical School, Universidade Nova de Lisboa, 1150-082 Lisbon, Portugal.

Funding

Centro Hospitalar de Lisboa Central FFI31/2024
6 · The paper itself

Abstract

With the approval of tolvaptan as the first specific medicine for the treatment of rapidly progressive Autosomal Dominant Polycystic Kidney Disease (ADPKD), biomarker discovery has gained renewed interest as it is widely recognized that these will be crucial in clinical decision-making, serving as either prognostic or predictive tools. Since the marketing authorization was first issued in 2015 for ADPKD, tolvaptan has remained the sole pharmacological compound specifically targeting the disease. For ADPKD patients it is an invaluable medicine for retarding disease progression. Although the field of overall biomarker discovery and validation has been detailed in several publications, the role of inflammation remains largely overlooked in ADPKD. The current work aims to provide the reader with an updated review of inflammation biomarkers research in ADPKD, highlighting the role of urinary MCP-1 (monocyte chemoattractant protein-1) as the most promising tool.

Indexed as

Antidiuretic Hormone Receptor AntagonistsBiomarkersInflammationPolycystic Kidney, Autosomal DominantTolvaptanAnimalsChemokine CCL2HumansAntidiuretic Hormone Receptor AntagonistsBiomarkersCCL2 protein, humanChemokine CCL2TolvaptanADPKDgeneinflammationkidneytolvaptan

Identifiers

PMID39940890
PMCPMC11817632

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.