# Real-World Analysis of Patients With C3 Glomerulopathy in the United States

**Authors:** Briana C. Ndife, Carolina Aldworth, Jennifer Nguyen, Irina Pivneva, Marie Louise Edwards, Annika Anderson, James Signorovitch, Pietro A. Canetta

PMC · DOI: 10.1016/j.ekir.2026.103773 · Kidney International Reports · 2026-01-14

## TL;DR

This study examines the characteristics and progression of kidney disease in U.S. patients with C3 glomerulopathy, a rare condition linked to overactivation of the alternative pathway.

## Contribution

The study provides real-world data on C3 glomerulopathy progression in the U.S., emphasizing the need for novel treatments.

## Key findings

- Most patients had advanced kidney disease at diagnosis, with over half having CKD stage ≥3.
- Over half of patients experienced CKD stage progression within 14.9 months on average.
- 26% of patients progressed to CKD stage 5 or kidney failure.

## Abstract

C3 glomerulopathy (C3G) is a rare kidney disease caused by alternative pathway (AP) overactivation. This analysis describes demographic and clinical characteristics of patients with C3G in the United States (US) and evaluates chronic kidney disease (CKD) stage progression.

This retrospective cohort study used electronic health records (EHRs) to identify patients aged ≥ 12 years with a C3G diagnosis (index) and with continuous clinical activity ≥ 12 months before (baseline) and ≥ 6 months after index (follow-up; until death or data end). Patients were stratified by prior kidney transplant status, CKD stage progression during follow-up, and baseline serum C3 level. CKD stage progression was assessed in patients with CKD stages 1 to 4 (at index) and adequate data to assess progression during follow-up.

Overall, 260 patients with C3G were identified: 51.9% were female; mean (SD) age was 47.8 (20.6) years; median follow-up was 2.1 years. Of those assessed, most had CKD stage ≥ 3 (56.6%) and proteinuria (54.4%) at index. Posttransplant recurrent C3G was reported in 27 patients (10.4%). Of those assessed for CKD stage progression, 102 (59.0%) and 45 (26.0%) progressed to a higher CKD stage or CKD stage 5 or kidney failure, respectively. Median time to progression of CKD stage or to stage 5 or kidney failure was 14.9 months and not estimable (NE), respectively.

In a real-world US population of patients with C3G, we identified a population with both advanced kidney disease around the time of diagnosis and high rates of CKD stage progression, highlighting the need to utilize novel treatments to improve patient outcomes.

## Linked entities

- **Diseases:** C3 glomerulopathy (MONDO:0018013), chronic kidney disease (MONDO:0005300), kidney failure (MONDO:0001106)

## Full-text entities

- **Genes:** C3 (complement C3) [NCBI Gene 718] {aka AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1}, RAPGEF1 (Rap guanine nucleotide exchange factor 1) [NCBI Gene 2889] {aka C3G, GRF2}
- **Diseases:** C3 Glomerulopathy (MESH:C562875), inflammation (MESH:D007249), AP abnormalities (MESH:C536589), Hematuria (MESH:D006417), kidney failure (MESH:D051437), CKD (MESH:D051436), complex (MESH:D048090), stroke (MESH:D020521), acute kidney deterioration (MESH:D058186), fatigue (MESH:D005221), Proteinuria (MESH:D011507), CCI (MESH:C566784), glomerulonephritis (MESH:D005921), hypertension (MESH:D006973), death (MESH:D003643), CKD stage 5/kidney failure (MESH:D007676), monoclonal gammopathy (MESH:D010265), dense deposit disease (MESH:D015432), myocardial infarction (MESH:D009203), Cardiovascular conditions (MESH:D002318), infection (MESH:D007239), heart failure (MESH:D006333), Kidney Disease (MESH:D007674), endocarditis (MESH:D004696), C3 glomerulonephritis (MESH:C567033), transient ischemic attack (MESH:D002546)
- **Chemicals:** mycophenolate mofetil (MESH:D009173), eculizumab (MESH:C481642), ACEi (-), pegcetacoplan (MESH:C000716074), creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12914277/full.md

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Source: https://tomesphere.com/paper/PMC12914277