globotriaosylceramide has been researched along with Coronary-Disease* in 3 studies
3 other study(ies) available for globotriaosylceramide and Coronary-Disease
Article | Year |
---|---|
Cardiac microvascular pathology in Fabry disease: evaluation of endomyocardial biopsies before and after enzyme replacement therapy.
In classic Fabry patients, accelerated coronary atherosclerosis and left ventricular hypertrophy manifest in the fourth decade; however, signs of cardiovascular disease also are observed later in life in "cardiac variant" patients and symptomatic female heterozygotes. These disturbances are caused by globotriaosylceramide (GL-3) accumulation in the heart resulting from lysosomal alpha-galactosidase A deficiency.. We analyzed pretreatment and posttreatment endomyocardial biopsies from 58 Fabry patients enrolled in a 5-month, phase 3, double-blind, randomized, placebo-controlled trial, followed by a 54-month open-label extension study of recombinant human alpha-galactosidase A. Baseline evaluations revealed GL-3 deposits in interstitial capillary endothelial cells and large, laminated inclusions within cardiomyocytes. In this study, we evaluated microvascular GL-3 clearance; no clearance of GL-3 was observed in the cardiomyocytes during this trial. Five months of recombinant human alpha-galactosidase A treatment in the phase 3 trial resulted in complete microvascular clearance of GL-3 from 72% of treated patients compared with only 3% of placebo patients (P<0.001). The placebo group achieved similar results after 6 months of treatment in the open-label trial. In addition, the capillary endothelium remained free of GL-3 for up to 60 months in 6 of 8 patients who consented to an end-of-study biopsy.. The findings suggest that long-term treatment with recombinant human alpha-galactosidase A may halt the progression of vascular pathology and prevent the clinical manifestations of atherosclerotic disease. This histopathological study should be a useful guide for clinicians and pathologists who diagnose and follow Fabry patients. Topics: Adolescent; Adult; alpha-Galactosidase; Biopsy; Capillaries; Clinical Trials, Phase III as Topic; Coronary Artery Disease; Coronary Disease; Double-Blind Method; Endocardium; Endothelium, Vascular; Fabry Disease; Female; Humans; Inclusion Bodies; Lysosomes; Male; Microcirculation; Myocytes, Cardiac; Randomized Controlled Trials as Topic; Recombinant Proteins; Trihexosylceramides; Young Adult | 2009 |
Evaluation of recombinant alpha-galactosidase A therapy for amelioration of the cardiovascular manifestations of Fabry disease: an important role for endomyocardial biopsy.
Topics: alpha-Galactosidase; Biopsy; Capillaries; Clinical Trials, Phase III as Topic; Coronary Disease; Endocardium; Endothelium, Vascular; Fabry Disease; Humans; Inclusion Bodies; Microcirculation; Multicenter Studies as Topic; Myocytes, Cardiac; Recombinant Proteins; Trihexosylceramides | 2009 |
Fabry disease: an unusual cause of severe coronary disease in a young man.
Topics: Adult; Coronary Disease; Coronary Vessels; Fabry Disease; Humans; Male; Trihexosylceramides | 1992 |