Evidence map›Paper›PMID 40095037›Full record

ReviewPediatric nephrology (Berlin, Germany)2025

Cystic fibrosis-related kidney disease-emerging morbidity and disease modifier.

Merrill Hart, Manish Kumar, Himanshu Ballav Goswami, William Tom Harris, Sladjana Skopelja-Gardner, Agnieszka Swiatecka-Urban

Abstract readReview
In one paragraph

Review in Pediatric nephrology (Berlin, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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

6 authors.

Merrill HartUniversity of Virginia, Charlottesville, VA, 22903, USA.
Manish KumarDepartment of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, 35233, USA.
Himanshu Ballav GoswamiDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, 03756, USA.
William Tom HarrisDepartment of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, 35233, USA.
Sladjana Skopelja-GardnerDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, 03756, USA.
Agnieszka Swiatecka-UrbanDepartment of Pediatrics, University of Virginia School of Medicine, Charlottesville, VA, 22903, USA. as6xx@virginia.edu.

Funding

Zhao - Proj 2P20GM130454 · NIGMS · DARTMOUTH COLLEGE · PI MICHAEL L WHITFIELD · 2019 to 2026
$27.2M
Translational Research CoreP30DK117469 · NIDDK · DARTMOUTH COLLEGE · PI DEBORAH A HOGAN · 2018 to 2026
$13.9M
Single-Cell Epigenomics, Transcriptomics, and Bioinformatics CoreP50DK096373 · NIDDK · UNIVERSITY OF VIRGINIA · PI ROBERTO Ariel GOMEZ · 2012 to 2026
$13.8M
Correcting Pathogenic TGF beta Activity in the AirwayR01HL144539 · NHLBI · UNIVERSITY OF VIRGINIA · PI SWIATECKA-URBAN, AGNIESZKA · 2019 to 2022
$1.7M
Cystic Fibrosis Foundation HARRIS24A0-MPICystic Fibrosis Foundation SKOPEL24A0-MPICystic Fibrosis Foundation SWIATE24A0-MPINHLBI Division of Intramural Research R01HL144539NHLBI NIH HHS R01 HL144539NIDDK NIH HHS P20GM130454-04NIDDK NIH HHS P30 DK117469NIDDK NIH HHS P30DK117469NIDDK NIH HHS P50 DK096373NIDDK NIH HHS P50DK096373-11NIGMS NIH HHS P20 GM130454NIH HHS P50DK096373-11
6 · The paper itself

Abstract

Cystic fibrosis (CF) is a life-shortening multisystem disease resulting from mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, causing the most devastating phenotypes in the airway and pancreas. Significant advances in treatment for CF lung disease, including the expanded use of high-efficiency modulator therapies (HEMT) such as Trikafta, have dramatically increased both quality of life and life expectancy for people with CF (PwCF). With these advances, long-term extrapulmonary manifestations are more frequently recognized. Pseudo-Barter syndrome, acute kidney injury (AKI) induced by medications or dehydration, amyloidosis, nephrolithiasis, and IgA and diabetic nephropathies have been previously reported in PwCF. Newer data suggest that chronic kidney disease (CKD) is a new morbidity in the aging CF population, affecting 19% of people over age 55. CKD carries a high risk of premature death from cardiovascular complications. Studies suggest that CFTR dysfunction increases kidneys' vulnerability to injury caused by the downstream effects of CF. Improving the mutant CFTR function by HEMT may help to tease apart the kidney responses resulting from extrinsic factors and those intrinsically related to the CFTR gene mutations. Additionally, given the novelty of HEMT approaches, the potential off-target effects of their long-term use are currently unknown. We review the evolving kidney complications in PwCF and propose the term CF-related kidney disease. We hope this review will increase awareness about the changing phenotype of kidney dysfunction in PwCF and help prevent morbidity related to this condition.

Indexed as

Cystic FibrosisRenal Insufficiency, ChronicCystic Fibrosis Transmembrane Conductance RegulatorHumansMutationCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorAKICFKDCFTRCKDCystic fibrosisHigh-efficiency modulator therapyKidney

Identifiers

PMID40095037
PMCPMC12549735

What Socratic holds

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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 Socratic graph.