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Urinary mulberry bodies as a potential biomarker for early diagnosis and efficacy assessment of enzyme replacement therapy in Fabry nephropathy.
Yonishi, Hiroaki; Namba-Hamano, Tomoko; Hamano, Takayuki; Hotta, Masaki; Nakamura, Jun; Sakai, Shinsuke; Minami, Satoshi; Yamamoto, Takeshi; Takahashi, Atsushi; Kobayashi, Wataru; Maeda, Ikuhiro; Hidaka, Yoh; Takabatake, Yoshitsugu; Sakai, Norio; Isaka, Yoshitaka.
Afiliação
  • Yonishi H; Department of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Namba-Hamano T; Department of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Hamano T; Department of Nephrology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Hotta M; Laboratory for Clinical Investigation, Osaka University Hospital, Osaka, Japan.
  • Nakamura J; Department of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Sakai S; Department of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Minami S; Department of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Yamamoto T; Department of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Takahashi A; Department of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Kobayashi W; Laboratory for Clinical Investigation, Osaka University Hospital, Osaka, Japan.
  • Maeda I; Laboratory for Clinical Investigation, Osaka University Hospital, Osaka, Japan.
  • Hidaka Y; Department of Medical Technology, Osaka University Hospital, Osaka, Japan.
  • Takabatake Y; Department of Laboratory Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Sakai N; Department of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Isaka Y; Division of Health Sciences, Child Healthcare and Genetic Science Laboratory, Osaka University Graduate School of Medicine, Osaka, Japan.
Nephrol Dial Transplant ; 37(1): 53-62, 2021 12 31.
Article em En | MEDLINE | ID: mdl-33367839
ABSTRACT

BACKGROUND:

The inability of enzyme replacement therapy (ERT) to prevent progression of Fabry nephropathy (FN) in the presence of >1 g/day proteinuria underscores the necessity of identifying effective biomarkers for early diagnosis of FN preceding proteinuria. Here we attempted to identify biomarkers for early detection of FN.

METHODS:

Fifty-one Fabry disease (FD) patients were enrolled. Urinary mulberry bodies (uMBs) were immunostained for globotriaosylceramide (Gb3) and renal cell markers to determine their origin. The association between semiquantitative uMB excretion and the histological severity of podocyte vacuolation was investigated in seven patients using the vacuolated podocyteglomerular average area ratio. The association between the semiquantitative estimate of uMB excretion and duration of ERT was analyzed. A longitudinal study was conducted to assess the effect of ERT on uMB excretion.

RESULTS:

Thirty-two patients (63%) had uMBs, while only 31% showed proteinuria. The uMBs were positive for Gb3, lysosomal-associated membrane protein 1 and podocalyxin, suggesting they were derived from lysosomes with Gb3 accumulation in podocytes. We observed more severe podocyte vacuolation with increased uMB excretion (P = 0.03 for trend); however, the same was not observed with increased proteinuria. The percentage of patients with substantial uMB excretion increased with shorter ERT duration (P = 0.018). Eighteen-month-long ERT reduced uMB excretion (P = 0.03) without affecting proteinuria.

CONCLUSIONS:

uMB excretion, implying ongoing podocyte injury, preceded proteinuria in most patients. Semiquantitative uMB estimates can serve as novel biomarkers for early FN diagnosis and for monitoring the efficacy of FD-specific therapies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Fabry Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Revista: Nephrol Dial Transplant Assunto da revista: NEFROLOGIA / TRANSPLANTE Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Fabry Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Revista: Nephrol Dial Transplant Assunto da revista: NEFROLOGIA / TRANSPLANTE Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão