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A novel unbiased method reveals progressive podocyte globotriaosylceramide accumulation and loss with age in females with Fabry disease.
Najafian, Behzad; Silvestroni, Aurelio; Sokolovskiy, Alexey; Tøndel, Camilla; Svarstad, Einar; Obrisca, Bogdan; Ismail, Gener; Holida, Myrl D; Mauer, Michael.
Afiliação
  • Najafian B; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA. Electronic address: najafian@uw.edu.
  • Silvestroni A; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
  • Sokolovskiy A; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
  • Tøndel C; Department of Pediatrics, Haukeland University Hospital, Bergen, Norway; Department of Clinical Medicine, University of Bergen, Bergen, Norway.
  • Svarstad E; Department of Clinical Medicine, University of Bergen, Bergen, Norway.
  • Obrisca B; Discipline Nephrology-Fundeni Clinical Institute, Department of Nephrology, Urology, Immunology and Immunology of Transplant, Dermatology, Allergology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
  • Ismail G; Discipline Nephrology-Fundeni Clinical Institute, Department of Nephrology, Urology, Immunology and Immunology of Transplant, Dermatology, Allergology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
  • Holida MD; Medical Genetics and Genomics, Stead Family Department of Pediatrics, University of Iowa Health Care, Iowa City, Iowa, USA.
  • Mauer M; Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota, USA; Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Kidney Int ; 102(1): 173-182, 2022 07.
Article em En | MEDLINE | ID: mdl-35483528
ABSTRACT
While females can suffer serious complications of Fabry disease, most studies are limited to males to avoid confounding by mosaicism. Here, we developed a novel unbiased method for quantifying globotriaosylceramide (GL3) inclusion volume in affected podocytes (F+) in females with Fabry disease independent of mosaicism leading to important new observations. All podocytes in male patients with Fabry are F+. The probability of observing random profiles from F+ podocytes without GL3 inclusions (estimation error) was modeled from electron microscopic studies of 99 glomeruli from 40 treatment-naïve males and this model was applied to 28 treatment-naïve females. Also, podocyte structural parameters were compared in 16 age-matched treatment-naïve males and females with classic Fabry disease and 11 normal individuals. A 4th degree polynomial equation best described the relationship between podocyte GL3 volume density and the estimation error (R2 =0.94) and was confirmed by k-fold cross-validation. In females, this model showed that age related directly to F+ podocyte GL3 volume (correlation coefficient (r = 0.54) and podocyte volume (r = 0.48) and inversely to podocyte number density (r = -0.56), (all significant). F+ podocyte GL3 volume was significantly inversely related to podocyte number density (r = -0.79) and directly to proteinuria. There was no difference in F+ podocyte GL3 volume or volume fraction between age-matched males and females. Thus, in females with Fabry disease GL3 accumulation in F+ podocytes progresses with age in association with podocyte loss and proteinuria, and F+ podocyte GL3 accumulation in females with Fabry is similar to males, consistent with insignificant cross-correction between affected and non-affected podocytes. Hence, these findings have important pathophysiological and clinical implications.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Fabry / Podócitos Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Fabry / Podócitos Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article