» Articles » PMID: 21160462

Progressive Podocyte Injury and Globotriaosylceramide (GL-3) Accumulation in Young Patients with Fabry Disease

Overview
Journal Kidney Int
Publisher Elsevier
Specialty Nephrology
Date 2010 Dec 17
PMID 21160462
Citations 80
Authors
Affiliations
Soon will be listed here.
Abstract

Progressive renal failure often complicates Fabry disease, the pathogenesis of which is not well understood. To further explore this we applied unbiased stereological quantitative methods to electron microscopic changes of Fabry nephropathy and the relationship between parameters of glomerular structure and renal function in 14 young Fabry patients (median age 12 years). Renal biopsies were obtained shortly before enzyme replacement therapy from these patients and from nine normal living kidney donors as controls. Podocyte globotriaosylceramide (GL-3) inclusion volume density increased progressively with age; however, there were no significant relationships between age and endothelial or mesangial inclusion volume densities. Foot process width, greater in male Fabry patients, also progressively increased with age compared with the controls, and correlated directly with proteinuria. In comparison to the biopsies of the controls, endothelial fenestration was reduced in Fabry patients. Thus, our study found relationships between quantitative parameters of glomerular structure in Fabry nephropathy and age, as well as urinary protein excretion. Hence, podocyte injury may play a pivotal role in the development and progression of Fabry nephropathy.

Citing Articles

Anderson-Fabry Disease: Focus on Ophthalmological Implications.

Giovannetti F, DAndrea M, Bracci F, Frustaci A, Chimenti C, Mangiantini P Life (Basel). 2025; 14(12.

PMID: 39768240 PMC: 11676308. DOI: 10.3390/life14121531.


Targeted nanoliposomes to improve enzyme replacement therapy of Fabry disease.

Tomsen-Melero J, Molto-Abad M, Merlo-Mas J, Diaz-Riascos Z, Cristobal-Lecina E, Soldevila A Sci Adv. 2024; 10(50):eadq4738.

PMID: 39671483 PMC: 11801267. DOI: 10.1126/sciadv.adq4738.


No differences in native T1 of the renal cortex between Fabry disease patients and healthy subjects in cardiac-dedicated native T1 maps.

Damlin A, Kjellberg F, Themudo R, Chow K, Engblom H, Oscarson M J Cardiovasc Magn Reson. 2024; 26(2):101104.

PMID: 39332708 PMC: 11647495. DOI: 10.1016/j.jocmr.2024.101104.


Reduction in kidney function decline and risk of severe clinical events in agalsidase beta-treated Fabry disease patients: a matched analysis from the Fabry Registry.

Batista J, Hariri A, Maski M, Richards S, Gudivada B, Raynor L Clin Kidney J. 2024; 17(8):sfae194.

PMID: 39139182 PMC: 11320591. DOI: 10.1093/ckj/sfae194.


The role of podocyte injury in the pathogenesis of Fabry disease nephropathy.

Monte Neto J, Mastroianni Kirsztajn G J Bras Nefrol. 2024; 46(3):e20240035.

PMID: 39058283 PMC: 11287863. DOI: 10.1590/2175-8239-JBN-2024-0035en.


References
1.
Meikle P, Ranieri E, Ravenscroft E, Hua C, Brooks D, Hopwood J . Newborn screening for lysosomal storage disorders. Southeast Asian J Trop Med Public Health. 2001; 30 Suppl 2:104-10. View

2.
Macdermot K, Holmes A, Miners A . Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females. J Med Genet. 2001; 38(11):769-75. PMC: 1734754. DOI: 10.1136/jmg.38.11.769. View

3.
Elleder M, Poupetova H, Kozich V . [Fetal pathology in Fabry's disease and mucopolysaccharidosis type I]. Cesk Patol. 1998; 34(1):7-12. View

4.
Shu L, Park J, Byun J, Pennathur S, Kollmeyer J, Shayman J . Decreased nitric oxide bioavailability in a mouse model of Fabry disease. J Am Soc Nephrol. 2009; 20(9):1975-85. PMC: 2736776. DOI: 10.1681/ASN.2008111190. View

5.
Desbois J, Maziere J, Gubler M, Allaneau C, Verhaeghe M, HERRAULT A . [Fabry's disease in children. Clinical and biological study of one family. Structure and ultrastructure of the kidney in a hemizygote and a heterozygote]. Ann Pediatr (Paris). 1977; 24(8-9):575-86. View