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IgA nephropathy in children with minimal proteinuria: to biopsy or not to biopsy?
Cambier, Alexandra; Roy, Jean-Philippe; Dossier, Claire; Patey, Natacha; Rabant, Marion; Boyer, Olivia; Delbet, Jean Daniel; Lapeyraque, Anne-Laure; Hogan, Julien.
Afiliação
  • Cambier A; Division of Nephrology, Centre Hospitalier Universitaire Sainte-Justine, University of Montreal, Montreal, QC, Canada. alexandra.cambier.med@ssss.gouv.qc.ca.
  • Roy JP; Sainte-Justine Hospital Pediatric Research Centre: Centre Hospitalier Universitaire Sainte-Justine Centre de Recherche, Montreal, QC, Canada. alexandra.cambier.med@ssss.gouv.qc.ca.
  • Dossier C; Division of Nephrology, Centre Hospitalier Universitaire Sainte-Justine, University of Montreal, Montreal, QC, Canada.
  • Patey N; Division of Nephrology, Hôpital Robert Debré, Paris, France.
  • Rabant M; Department of Pathology, Centre Hospitalier Universitaire Sainte-Justine, University of Montreal, Montreal, QC, Canada.
  • Boyer O; Division of Pathology, Hôpital Necker, Paris, France.
  • Delbet JD; Néphrologie Pédiatrique, Centre de Référence MARHEA, Hôpital Necker-Enfants Malades, APHP, Centre, Institut Imagine, Inserm U1163, Université Paris Cité, Paris, France.
  • Lapeyraque AL; Division of Nephrology, Hôpital Trousseau, Paris, France.
  • Hogan J; Division of Nephrology, Centre Hospitalier Universitaire Sainte-Justine, University of Montreal, Montreal, QC, Canada.
Pediatr Nephrol ; 39(3): 781-787, 2024 Mar.
Article em En | MEDLINE | ID: mdl-37698655
ABSTRACT

BACKGROUND:

Tubulointerstitial lesions and glomerular inflammation severity have been shown to correlate with proteinuria in children with IgA nephropathy (cIgAN). However, there is a lack of data regarding severity of histopathologic findings in cIgAN in patients with minimal to absent proteinuria since kidney biopsy indications are not well defined in these cases.

METHODS:

Twenty-eight cIgAN patients with kidney biopsy from 4 different centers in Paris (France) and Montreal (Canada) with a urine protein/creatinine ratio (UPCr) ≤ 0.03 g/mmol and a normal estimated glomerular filtration rate (eGFR > 90 ml/min/1.73 m2) on the day of kidney biopsy prior to treatment were included.

RESULTS:

Median age was 11.82 (9.32-13.45) years, and median follow-up was 4 years (2.87-6.53). At time of biopsy, median eGFR was 116 (102.3-139.7) ml/min/1.73 m2, and median UPCr was 0.02 (0.011-0.03) g/mmol. Microscopic or macroscopic hematuria was present in 35.7% and 64.3% of cases, respectively. Kidney biopsy microscopy analysis showed mesangial (M1), endocapillary (E1), or extracapillary (C1) hypercellularity in 53.5%, 32.1%, and 7.1% of patients, respectively. Chronic histological lesions were also present glomerulosclerosis (S1) in 42.8% and tubular atrophy/interstitial fibrosis in 7.1%. Podocytopathic features were detected in 21.4%. An ACE inhibitor or immunosuppressive therapy (IS) was prescribed in 42.8% and 21.4% of these patients respectively. One-third (35.7%) received no treatment. At last follow-up, median eGFR was 111.9 (90.47-136.1) ml/min/1.73 m2, and median UPCr was 0.028 (0.01-0.03) g/mmol.

CONCLUSION:

cIgAN with minimal proteinuria at time of biopsy might be linked with acute and chronic glomerular lesions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glomerulonefrite por IGA Limite: Adolescent / Child / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glomerulonefrite por IGA Limite: Adolescent / Child / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article