Evidence map›Paper›PMID 41426049›Full record

ReviewKidney international reports2025

Defining Disease Modification in IgA Nephropathy: Toward a Paradigm Shift in Management.

Jonathan Barratt, Laura H Mariani, Jai Radhakrishnan, Dana V Rizk, James A Tumlin, Richard A Lafayette

Abstract readReview
In one paragraph

Review in Kidney international reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jonathan BarrattDepartment of Cardiovascular Sciences, University of Leicester, Leicester, UK.
Laura H MarianiDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Jai RadhakrishnanDepartment of Medicine, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, USA.
Dana V RizkDivision of Nephrology, Department of Medicine, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
James A TumlinDepartment of Medicine, Division of Renal Medicine, Emory University, Atlanta, Georgia, USA.
Richard A LafayetteDivision of Nephrology, Department of Medicine, Stanford University, Stanford, California, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IgA nephropathy (IgAN) is a rare, chronic, immune-mediated kidney disease characterized by a slow, progressive decline in kidney function. As a disease without an existing cure and a leading cause of chronic kidney disease (CKD) and kidney failure, IgAN requires effective interventions for disease modification. However, identifying interventions as "disease modifying" is challenging in IgAN because of a lack of consensus on the term and uncertainty about suitable markers by which "disease modification" should be defined. This review discusses how "disease modification" could be defined in IgAN, based on the simple premise of the need to preserve nephrons and avoid progression to kidney failure within the patient's lifetime. In addition, how disease modification can be meaningfully assessed (e.g., the impact of an intervention on mortality and kidney failure, estimated glomerular filtration rate [eGFR], urinary protein or albumin, nonvisible [microscopic] hematuria, and markers of underlying IgAN pathology) is examined. Further, the concept of a multifaceted approach to IgAN management is discussed, targeting both the IgAN-specific processes leading to nephron loss and the generic maladaptive responses to IgAN-induced nephron loss.

Indexed as

disease modificationglomerular filtration rateIgA nephropathykidney failureproteinuriasurrogate end point

Identifiers

PMID41426049
PMCPMC12712461

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.