Literature DB >> 370586

Ineffectiveness of ascorbic acid therapy in nephropathic cystinosis.

J A Schneider, J J Schlesselman, S A Mendoza, S Orloff, J G Thoene, W A Kroll, A D Godfrey, J D Schulman.   

Abstract

Because high concentrations of ascorbic acid (0.57 mM) lower the free (nonprotein) cystine content of cultured cystinotic skin fibroblasts by over 50 per cent, we did a double-blind clinical trial to establish whether this drug would benefit cystinotic children. Sixty-four patients were randomized into the study; 32 received ascorbic acid (200 mg per kilogram of body weight per day), and 32 placebo. The study was terminated after approximately two years because there was no indication that vitamin C was beneficial and accumulating evidence that it might be harmful. Of 11 patients who left the study because of death or the requirement for dialysis or renal transplantation, eight were receiving ascorbic acid. The estimated relative risk (treatment vs. control) of an adverse event was R = 2.7, with a 90 per cent confidence interval of (0.8, 11.5). The serum creatinine concentration increased 0.53 mg per deciliter per year in patients receiving vitamin C and 0.24 mg per deciliter per year in patients receiving placebo (P = 0.08).

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Year:  1979        PMID: 370586     DOI: 10.1056/NEJM197904053001403

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  12 in total

1.  Predicted reciprocal serum creatinine at age 10 years as a measure of renal function in children with nephropathic cystinosis treated with oral cysteamine.

Authors:  W A Gahl; J A Schneider; J D Schulman; J G Thoene; G F Reed
Journal:  Pediatr Nephrol       Date:  1990-03       Impact factor: 3.714

2.  Hypercholesterolemia in children with cystinosis.

Authors:  J L Murphy; P C Papathakis
Journal:  Pediatr Nephrol       Date:  1993-04       Impact factor: 3.714

3.  Progression of chronic renal failure in a historical group of patients with nephropathic cystinosis. European Collaborative Study on Cystinosis.

Authors:  F Manz; N Gretz
Journal:  Pediatr Nephrol       Date:  1994-08       Impact factor: 3.714

4.  Long-term management of inherited renal tubular disorders.

Authors:  F Manz; K Schärer
Journal:  Klin Wochenschr       Date:  1982-09-15

5.  Cystinosis in the Federal Republic of Germany. Coordination and analysis of the data.

Authors:  F Manz; N Gretz
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

6.  Cysteamine depletes cystinotic leucocyte granular fractions of cystine by the mechanism of disulphide interchange.

Authors:  W A Gahl; F Tietze; J D Butler; J D Schulman
Journal:  Biochem J       Date:  1985-06-15       Impact factor: 3.857

7.  Association of certain human leukocyte antigens with nephropathic cystinosis in the absence of linkage between these loci.

Authors:  R Steinherz; D Raiford; K K Mittal; J D Schulman
Journal:  Am J Hum Genet       Date:  1981-03       Impact factor: 11.025

8.  Effect of indomethacin on clinical progress and renal function in cystinosis.

Authors:  G B Haycock; J Al-Dahhan; R H Mak; C Chantler
Journal:  Arch Dis Child       Date:  1982-12       Impact factor: 3.791

9.  Management dilemmas in pediatric nephrology: Cystinosis.

Authors:  Martine T P Besouw; Maria Van Dyck; David Cassiman; Kathleen J Claes; Elena N Levtchenko
Journal:  Pediatr Nephrol       Date:  2015-05-09       Impact factor: 3.714

Review 10.  Recent advances in the treatment of cystinosis.

Authors:  J A Schneider; K F Clark; A A Greene; J S Reisch; T C Markello; W A Gahl; J G Thoene; P K Noonan; K A Berry
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

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