4.5 Article

Effects of hydroxychloroquine on proteinuria in membranous nephropathy

Journal

JOURNAL OF NEPHROLOGY
Volume 35, Issue 4, Pages 1145-1157

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s40620-021-01182-z

Keywords

Membranous nephropathy; Hydroxychloroquine; Proteinuria; Anti-PLA2R antibody

Funding

  1. Natural Science Foundation of China [81870486, 82070732, 82090021]

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This study suggests that hydroxychloroquine as an adjunctive treatment in patients with primary membranous nephropathy can effectively reduce proteinuria and have a positive impact on antibody reduction. In the long term, the hydroxychloroquine group showed a higher clinical remission rate, and no serious adverse events were observed.
Background Many patients with primary membranous nephropathy have severe proteinuria unresponsive to optimized renin-angiotensin-aldosterone system inhibitors (RAASi). We evaluated the efficacy and safety of hydroxychloroquine as an adjunctive agent in membranous nephropathy (MN) treatments. Methods We prospectively recruited 126 patients with biopsy-proven primary membranous nephropathy and urinary protein 1-8 g/day while receiving optimized RAASi treatment for >= 3 months and well-controlled blood pressure. Forty-three patients received hydroxychloroquine and RAASi (hydroxychloroquine-RAASi group), and 83 patients received RAASi alone (RAASi group). Treatment responses, including proteinuria reduction, complete and partial remission rates, and autoantibody against phospholipase A2 receptor (anti-PLA2R) levels, were compared between the two groups at 6 months and over the long term. Results At 6 months, the effective response rate (proteinuria reduction > 30%) (57.5% vs. 28.9%, P = 0.002), clinical remission rate (35.0% vs. 15.7%, P = 0.015), and percentage change in proteinuria (- 51.7% vs. - 21.9%, P < 0.001) were higher, and the rate of switching to immunosuppressants (25.0% vs. 45.8%, P = 0.027) was lower in the hydroxychloroquine-RAASi group than in the RAASi group. Hydroxychloroquine administration was an independent protective factor with an effective response (OR 0.37, P = 0.021). In the long term, the clinical remission rate was higher in the HCQ-RAASi group (62.5% vs. 38.6%, P = 0.013). Hydroxychloroquine therapy was associated with a higher rate of anti-PLA2R reduction (< 20 U/ml) (HR 0.28, P = 0.031). We observed no serious adverse events associated with hydroxychloroquine. Conclusions Hydroxychloroquine could be an option for patients with membranous nephropathy seeking to achieve proteinuria reduction and anti-PLA2R antibody reduction in addition to optimized RAASi. Randomized controlled trials are needed to confirm these findings.

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