Evidence map›Paper›PMID 41064343›Full record

ArticleGlomerular diseases

Treatment and Disease Burden in Patients with Complement 3 Glomerulopathy: Multinational Real-World Study Results.

Smeeta Sinha, Jonathan de Courcy, Susanna Libby, Alice Simons, Briana Ndife, Katharina Pannagl, Clare Proudfoot, Raymond Przybysz, Raisa Sidhu, Serge Smeets and 1 more

Abstract read
In one paragraph

Article in Glomerular diseases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

11 authors.

Smeeta SinhaDepartment of Renal Medicine, Salford Royal Hospital, Northern Care Alliance, Manchester, UK.
Jonathan de CourcyRare Diseases Franchise, Adelphi Real World, Bollington, UK.
Susanna LibbyRare Diseases Franchise, Adelphi Real World, Bollington, UK.
Alice SimonsRare Diseases Franchise, Adelphi Real World, Bollington, UK.
Briana NdifeUS Medical Affairs, Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
Katharina PannaglHealth Economics & Outcomes Research, Novartis Pharmaceuticals UK Ltd., London, UK.
Clare ProudfootInternational Value & Access, Novartis Pharma AG, Basel, Switzerland.
Raymond PrzybyszEvidence Generation, Global Medical Affairs, Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
Raisa SidhuInternational Value & Access, Novartis Pharma AG, Basel, Switzerland.
Serge SmeetsGlobal Medical Affairs, Novartis Pharma AG, Basel, Switzerland.
Richard A LafayetteDivision of Nephrology, Stanford Glomerular Disease Center, Stanford University, Stanford, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Patients with complement 3 glomerulopathy (C3G) have poor clinical outcomes, although new targeted therapies have very recently been approved. Here, we describe the burden and management of C3G in global clinical practice. Methods: Retrospective analysis of data obtained from a cross-sectional survey (Adelphi Real World C3G Disease Specific Programme™) of nephrologists actively managing C3G ( Results: Records for 385 patients with C3G were completed by 129 nephrologists. Most patients had moderate to severe disease at the time of diagnosis (85.1%), based on individual nephrologist assessment. At the time of PRF completion, 83.4% of patients were receiving pharmacological treatment, which included angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers (70.4%) and corticosteroids (48.6%). In patients receiving treatment, proteinuria remained the most common nephrologist-reported sign of C3G (66.0%), irrespective of treatment duration; of patients with available data, 68.9% had proteinuria ≥1 g/day. At the time of PRF completion, 8.3% of patients were on dialysis, 41.6% of patients were considered eligible for a kidney transplant, and 6.5% were transplant recipients. Patients experienced anxiety/depression (73.7%), pain/discomfort (65.3%), fatigue (90.7%), and problems doing usual activities (62.7%) at the time of PSCF completion. Conclusion: Despite most patients receiving current guideline-recommended standard of care, the burden of C3G remains high worldwide, demonstrating the need for more effective treatment options. In addition, most patients presented with advanced disease by the time of diagnosis, warranting a need to address significant diagnostic delays to facilitate earlier therapeutic intervention.

Indexed as

Complement 3 glomerulopathyDialysisQuality of lifeTransplantTreatment

Identifiers

PMID41064343
PMCPMC12503786

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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.