Observational studyPediatric nephrology (Berlin, Germany)2026
Single relapse at ≥ 0.5 mg/kg alternate-day prednisone predicts course of childhood nephrotic syndrome.
Observational study in Pediatric nephrology (Berlin, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundAround half of children with steroid-sensitive nephrotic syndrome are eventually diagnosed with frequently relapsing or steroid-dependent disease. To minimize steroid toxicity, guidelines usually recommend switching these patients to steroid-sparing agents. Unfortunately, morbidity from steroids can be irreversible, and patients may suffer even after steroid discontinuation.
methodsThis is a multicenter observational study of children with steroid-sensitive nephrotic syndrome. We compared patients that were eventually diagnosed with frequently relapsing/steroid-dependent nephrotic syndrome with those with non/infrequently relapsing nephrotic syndrome. Additionally, we compared the risk of being diagnosed with frequently relapsing/steroid-dependent nephrotic syndrome, between patients with relapse on a prednisone dose equivalent of ≥ 0.5 mg/kg/every other day versus patients with no relapses above this cutoff.
resultsPatients who relapsed during induction were more likely to develop frequently relapsing/steroid-dependent nephrotic syndrome. Patients with ≥ 1 relapse on prednisone equivalent of ≥ 0.5 mg/kg/every other day were 33 times more likely to develop frequently relapsing/steroid-dependent nephrotic syndrome (p value < 0.001).
conclusionsPatients with one relapse on prednisone equivalent of ≥ 0.5 mg/kg/every other day are at high risk of an eventual diagnosis of frequently relapsing/steroid-dependent nephrotic syndrome. Further studies are needed to determine whether a single relapse above this cutoff is reliable enough to enable clinicians to switch patients to steroid-sparing agents before meeting formal criteria for frequently relapsing/steroid-dependent disease.
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