ReviewKidney international reports2025
Defining Disease Modification in IgA Nephropathy: Toward a Paradigm Shift in Management.
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.
What it found
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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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
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.
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Registered trials
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