Evidence map›Paper›PMID 40828351›Full record

SynthesisAdvances in therapy2025

Association Between Surrogate Endpoints and Clinical Outcomes in Immunoglobulin A Nephropathy: A Systematic Literature Review.

Maria Lorenzi, Sarah N Ali, Sarah Cadarette, Stephen Ebohon, Vakaramoko Diaby, Mohit Mathur, Ancilla W Fernandes

Abstract readSystematic Review
In one paragraph

Synthesis in Advances in therapy, 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

7 authors.

Maria LorenziCencora, 1 West First Avenue, Conshohocken, PA, 19428, USA. maria.lorenzi@cencora.com.
Sarah N AliOtsuka Pharmaceutical Development and Commercialization, Inc., 508 Carnegie Center Drive, Princeton, NJ, 08540, USA.
Sarah CadaretteCencora, 1 West First Avenue, Conshohocken, PA, 19428, USA.
Stephen EbohonCencora, 5th Floor, Bush House, North West Wing, London, WC2B 4PJ, UK.
Vakaramoko DiabyOtsuka Pharmaceutical Development and Commercialization, Inc., 508 Carnegie Center Drive, Princeton, NJ, 08540, USA.
Mohit MathurVisterra, Inc., 275 Second Avenue, Fourth Floor, Waltham, MA, 02451, USA.
Ancilla W FernandesOtsuka Pharmaceutical Development and Commercialization, Inc., 508 Carnegie Center Drive, Princeton, NJ, 08540, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAt least 50% of patients with immunoglobulin A nephropathy (IgAN) reach kidney failure within 12 years of diagnosis. Delayed progression to kidney failure remains the gold standard treatment endpoint in IgAN, but the prolonged time course limits feasibility as a primary endpoint in clinical trials. Earlier measurable endpoints may serve as surrogate endpoints for clinically important long-term kidney outcomes. Regulatory bodies recognize surrogate endpoints like proteinuria reduction. However, other stakeholders, like payers, health technology assessment agencies, and policymakers, may require additional evidence. This literature review assessed data on associations between surrogate endpoints, including proteinuria and estimated glomerular filtration rate (eGFR), and long-term kidney outcomes in IgAN.

methodsA systematic search of IgAN studies conducted in any country was performed in MEDLINE, Embase, and CENTRAL via Ovid (January 1, 2006-September 1, 2023), supplemented by conference abstracts (2019-2023) and relevant literature reviews and meta-analyses. Eligible studies evaluated the association of surrogate endpoints of kidney disease progression with long-term outcomes in IgAN.

resultsAmong 1833 unique citations screened, 23 publications met inclusion criteria. Proteinuria was associated with progression to kidney failure (p < 0.001-0.021; n = 5 studies), reaching a composite kidney event (p < 0.001-0.02; n = 6), doubling of serum creatinine (p = 0.009; n = 1), and long-term eGFR decline (p < 0.001-0.910; n = 5); absolute eGFR at months 3 and 6 was associated with composite kidney events (p ≤ 0.001-0.03; n = 2); and eGFR slope was associated with kidney failure (p < 0.001; n = 1) and doubling of serum creatinine (p < 0.001-0.007; n = 1).

conclusionThe literature supports associations of proteinuria and eGFR with long-term clinical outcomes in IgAN across multiple studies and geographic regions. Despite regional variability in standard of care, which introduces heterogeneity in the strength of associations, the consistency of findings across regions supports the utility of proteinuria and eGFR as surrogate endpoints for clinically important long-term kidney outcomes.

Indexed as

Glomerulonephritis, IGAProteinuriaBiomarkersDisease ProgressionGlomerular Filtration RateHumansBiomarkersIgANKidney eventKidney failureSurrogate endpointSystematic literature review

Identifiers

PMID40828351
PMCPMC12474693

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Registered trials

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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.