Fibrinogen-albumin ratio predicts treatment response in phospholipase A2 receptor-associated membranous nephropathy with nephrotic syndrome

Ren Fail. 2024 Dec;46(1):2359024. doi: 10.1080/0886022X.2024.2359024. Epub 2024 Jun 4.

Abstract

Background: The M-type phospholipase A2 receptor (PLA2R)-associated primary membranous nephropathy (PMN) is an immune-related disease in adults with increasing morbidity and variable treatment response, in which inflammation may contribute to the multifactorial immunopathogenesis. The relationship between fibrinogen-albumin ratio (FAR), serving as a novel inflammatory biomarker, and PMN is still unclear. Therefore, this study aims to clarify the association between FAR and disease activity and therapy response of PMN.

Methods: 110 biopsy-proven phospholipase A2 receptor (PLA2R) -associated PMN participants with nephrotic syndrome from January 2017 to December 2021 were recruited in the First Affiliated Hospital of Nanjing Medical University. The independent risk factors of non-remission (NR) and the predictive ability of FAR were explored by Cox regression and receiver-operating characteristic (ROC) curve analysis. According to the optimal cutoff value, study patients were categorized into the low-FAR group (≤the cutoff value) and the high-FAR group (>the cutoff value). Spearman's correlations were used to examine the associations between FAR and baseline clinicopathological characteristics. Kaplan-Meier method was used to assess the effects of FAR on remission.

Results: In the entire study cohort, 78 (70.9%) patients reached complete or partial remission (CR or PR). The optimal cutoff value of FAR for predicting the remission outcome (CR + PR) was 0.233. The Kaplan-Meier survival analysis demonstrated that the high-FAR group (>0.233) had a significantly lower probability to achieve CR or PR compared to the low-FAR group (≤0.233) (Log Rank test, p = 0.021). Higher levels of FAR were identified as an independent risk factor for NR, and the high-FAR group was associated with a 2.27 times higher likelihood of NR than the low-FAR group (HR 2.27, 95% CI 1.01, 5.13, p = 0.048). These relationships remained robust with further analysis among calcineurin inhibitors (CNIs)-receivers. In the multivariate Cox regression model, the incidence of NR was 4.00 times higher in the high-FAR group than in the low-FAR group (HR 4.00, 95% CI 1.41, 11.31, p = 0.009). Moreover, ROC analysis revealed the predictive value of FAR for CR or PR with a 0.738 area under curve (AUC), and the AUC of anti-PLA2R Ab was 0.675. When combining FAR and anti-PLA2R Ab, the AUC was boosted to 0.766.

Conclusions: FAR was significantly correlated with proteinuria and anti-PLA2R Ab in PMN. As an independent risk factor for NR, FAR might serve as a potential inflammation-based prognostic tool for identifying cases with poor treatment response, and the best predictive cutoff value for outcomes was 0.233.

Keywords: Fibrinogen-albumin ratio; phospholipase A2 receptor; predictor; primary membranous nephropathy; proteinuria.

MeSH terms

  • Adult
  • Biomarkers* / blood
  • Female
  • Fibrinogen* / analysis
  • Fibrinogen* / metabolism
  • Glomerulonephritis, Membranous* / blood
  • Glomerulonephritis, Membranous* / drug therapy
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Kaplan-Meier Estimate
  • Male
  • Middle Aged
  • Nephrotic Syndrome* / blood
  • Nephrotic Syndrome* / complications
  • Nephrotic Syndrome* / drug therapy
  • ROC Curve
  • Receptors, Phospholipase A2* / immunology
  • Remission Induction
  • Retrospective Studies
  • Risk Factors
  • Serum Albumin / analysis
  • Serum Albumin / metabolism
  • Treatment Outcome

Substances

  • Receptors, Phospholipase A2
  • Biomarkers
  • Fibrinogen
  • Immunosuppressive Agents
  • Serum Albumin

Grants and funding

This work was supported by grants from the National Natural Science Foundation of China (82170699, 81870469 to Yanggang Yuan, No. 82100767 to Suyan Duan), the Natural Science Foundation of Jiangsu Province (BK20191075 to Suyan Duan), ‘PRO•Run’ Fund of the Nephrology Group of CEBM (KYJ202206–0003-6 to Yanggang Yuan), the ‘333 Project’ of Jiangsu Province, the Six Talent Peaks Project in Jiangsu Province (WSN-010 to Yanggang Yuan), ‘Yiluqihang·Shenmingyuanyang’ medical development And Scientific Research Fund project on Kidney Diseases (SMYY20220301001 to Yanggang Yuan), Project of clinical capability improvement of the First Affiliated Hospital of Nanjing Medical University (JSPH-MC-2021-14 to Suyan Duan), and the Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institution.