Background The lysosomal storage disease cystinosis resultsin renal failure at approximately 10 years of age. Althoughoral cysteamine therapy is recognized to preserve kidney function,the extent of renal benefit has not been determined.
Methods Between 1960 and 1992, we determined 24-hour creatinineclearances in 76 children with cystinosis during 1081 admissionsto the National Institutes of Health. Seventeen children wereconsidered to have received adequate treatment with cysteamine,since they had depletion of cystine from leukocytes and begantherapy before the age of 2 years; treatment lasted a mean of7.1 years. Thirty-two children were considered to have receivedpartial treatment, since they had poor compliance with therapyor began treatment after the age of 2; treatment lasted a meanof 4.5 years. Twenty-seven children were followed in the erabefore cysteamine therapy and thus never received cysteamine.
Results Of the 27 children who never received cysteamine, 16were followed at the National Institutes of Health until renalfailure occurred; their mean (±SD) creatinine clearancewas 8.0 ±4.8 ml per minute per 1.73 m2 of body-surfacearea at a mean age of 8.3 ±1.9 years. Of the 17 childrenwho received adequate treatment, none had renal failure; theirmean creatinine clearance was 57 ±20 ml per minute per1.73 m2 at 8.3 ±3.8 years of age. The mean creatinineclearance of the children who received partial or adequate treatmentwith cysteamine increased with age up to the age of five yearsand then declined linearly with age at a normal rate. For thechildren who received adequate treatment, the mean creatinineclearance was predicted to reach 0 ml per minute per 1.73 m2at the age of 74 years, as compared with 20 years of age forthe children who received partial treatment. With no therapy,the mean creatinine clearance reaches 0 ml per minute per 1.73m2 at 10 years of age.
Conclusions Children with cystinosis who are treated early andadequately with cysteamine have renal function that increasesduring the first five years of life and then declines at a normalrate. Patients with poorer compliance and those who are treatedat an older age do less well.
Source Information
From the Section on Human Biochemical Genetics, Human Genetics Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Md.
Address reprint requests to Dr. Gahl at Bldg. 10, Rm. 9S-242, NICHD, NIH, Bethesda, MD 20892.
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