Risk factors for relapse and aggravation in membranous nephropathy after COVID-19 infection.

Publication date: Feb 11, 2025

Relapse of membranous nephropathy (MN) and other glomerular diseases has been observed after COVID-19 infection. The risk factors contributing to disease progression in MN patients after contracting COVID-19 remain unclear. This retrospective study included 656 consecutive patients with biopsy-proven primary MN who received treatment and were regularly followed up for over six months. Logistic regression analyses were conducted to identify risk factors for disease progression. Among the cohort, 555 patients (84. 6%) contracted COVID-19 from November 11th, 2022, to February 22nd, 2023. Of them, 112 patients (20. 2%) experienced a > 50% increase in proteinuria, including 30 patients (5. 4%) who experienced nephrotic syndrome relapse. Sixteen patients (2. 9%) showed immune aggravation with elevated anti-PLA2R antibody levels, and five patients (0. 9%) had immune relapse characterized by antibody reoccurrence. Kidney dysfunction, defined as an eGFR reduction > 30% from baseline, occurred in 10 patients (1. 8%), with two patients (0. 4%) progressing to ESKD. Four patients (0. 7%) died of respiratory failure. Overall, 132 patients (24. 0%) experienced disease progression after COVID-19 infection. Multivariate logistic regression identified longer fever duration (OR 1. 118, 95% CI 1. 029-1. 356, P = 0. 018), withdrawal of immunosuppressants and/or steroids (OR 2. 571, 95% CI 1. 377-4. 799, P = 0. 003) and extended drug cessation (OR 1. 113, 95% CI 1. 045-1. 186, P = 0. 001) as independent risk factors for MN progression. These findings suggest prompt antiviral treatment and minimizing the duration of immunosuppressant withdrawal to optimize kidney outcomes in MN patients with COVID-19.

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Concepts Keywords
February Adult
Immunosuppressant Aged
Kidney Aggravation
COVID-19
COVID-19
Disease Progression
Female
Glomerulonephritis, Membranous
Humans
Immunosuppressive Agents
Immunosuppressive Agents
Male
Membranous nephropathy
Middle Aged
Receptors, Phospholipase A2
Receptors, Phospholipase A2
Recurrence
Relapse
Retrospective Studies
Risk Factors
Risk factors
SARS-CoV-2

Semantics

Type Source Name
disease MESH relapse
disease MESH membranous nephropathy
disease MESH COVID-19
disease MESH infection
disease MESH disease progression
disease MESH proteinuria
disease MESH nephrotic syndrome
disease MESH respiratory failure
pathway REACTOME Reproduction
disease MESH severe acute respiratory syndrome
disease MESH complications
disease MESH pneumonia
disease MESH syndrome
disease MESH abnormalities
disease MESH acute kidney injury
disease MESH minimal change disease
disease MESH lupus nephritis
drug DRUGBANK Trestolone
disease MESH nephritis
disease MESH hepatitis B
pathway KEGG Hepatitis B
disease MESH virus infection
disease MESH malignancy
disease MESH rheumatoid arthritis
pathway KEGG Rheumatoid arthritis
disease MESH sore throat
disease IDO symptom
drug DRUGBANK Creatinine
drug DRUGBANK Indoleacetic acid
disease MESH death
drug DRUGBANK Proline
drug DRUGBANK Human Serum Albumin
disease MESH Hematuria
drug DRUGBANK Rituximab
drug DRUGBANK Cyclophosphamide
drug DRUGBANK Mycophenolate mofetil
drug DRUGBANK Coenzyme M
disease IDO virulence
disease IDO intervention
disease IDO immunosuppression
drug DRUGBANK Ciclosporin
drug DRUGBANK Tacrolimus
disease MESH Kidney Disease
disease MESH myocardial infarction
drug DRUGBANK Hexachlorophene
disease IDO protein

Original Article

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