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A DOUBLE-MASKED CONTROLLED RANDOMIZED CLINICAL TRIAL OF TOPICAL CYSTEAMINE

A DOUBLE-MASKED CONTROLLED RANDOMIZED CLINICAL TRIAL OF TOPICAL CYSTEAMINE
外用半胱胺的双重对照随机临床试验
批准号:
3856038
负责人:
M I KAISER-KUPFER
金额:
$0.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至

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中文摘要
翻译
肾病型胱氨酸病是一种常染色体隐性遗传贮藏
英文摘要
Nephropathic cystinosis is an autosomal, recessively inherited storage disease in which nonprotein cystine accumulates within cellular lysosomes due to a defect in lysosomal cystine transport. Ocular manifestations include photophobia, crystal deposits in the cornea, conjunctiva, and iris, and depigmentation of the retina. Systemic complications include the Fanconi syndrome and renal failure. Nine years ago cysteamine, a free thiol that depletes cystine from cells, was introduced in the therapy of cystinotic patients. Although patients had improved growth and stabilized renal function, there was no noticeable effect on the accumulation of corneal crystals. Recent studies showed that corneal cells in tissue culture are readily depleted of cystine by the introduction of cysteamine, making feasible the use of topical ophthalmic cysteamine to circumvent the humoral route. After appropriate animal studies to test for complications revealed none, we began a double-masked clinical trial to test the efficacy of topical cysteamine (0.1%) in humans. Fourteen patients of ages less than 3 years were enrolled and randomized to 0.1% cysteamine. Five patients showed a significant decrease in crystals in the cysteamine-treated eyes. In order to test the effects of increasing the concentration of cysteamine eye drops in humans, a toxicity study was performed in rabbits. The study showed no adverse reactions. The results permitted an increase in the concentration to 0.5% for human use, and all patients receiving 0.1% cysteamine were switched to 0.5%. An additional five young patients showed a significant decrease in treated eyes. Thus, of 20 young patients, 12 successfully had the code broken; of the remaining 8, 2 died, 3 discontinued medication, 2 are still in the trial, and 1 has been receiving treatment too short a time to tell. Due to the success in the younger patients, this study was expanded to include older patients, 3 to 31 years old. The findings have been most exciting: Fourteen patients have shown a significant decrease in crystals in treated eyes as well as improvements in comfort, ie, relief of pain and photophobia. This study has resulted in significantly improved quality of life for the successfully treated patients.
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VISUAL FUNCTION AND OCULAR PIGMENTATION IN ALBINISM
  • 批准号:
    6106808
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    --
  • 负责人:
    M I KAISER-KUPFER
  • 依托单位:
IRIDO-CORNEAL-ENDOTHELIAL (ICE) SYNDROME
  • 批准号:
    4693321
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    --
  • 负责人:
    M I KAISER-KUPFER
  • 依托单位:
VISUAL FUNCTION AND OCULAR PIGMENTATION IN ALBINISM
  • 批准号:
    4693320
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    --
  • 负责人:
    M I KAISER-KUPFER
  • 依托单位:
NIH INTERINSTITUTE MEDICAL GENETICS PROGRAM--THE GENETICS CLINIC
  • 批准号:
    6162350
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    --
  • 负责人:
    M I KAISER-KUPFER
  • 依托单位:
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