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胱氨酸病:接受速释半胱胺治疗患者的治疗依从性和代谢监测

Cystinosis: Therapy adherence and metabolic monitoring in patients treated with immediate-release cysteamine.

作者信息

Linden Simone, Klank Sabrina, Harms Erik, Grüneberg Marianne, Park Julien H, Marquardt Thorsten

机构信息

Department of General Pediatrics, Metabolic Diseases, University Children's Hospital, Albert-Schweitzer-Campus 1, Münster, NRW DE 48149, Germany.

出版信息

Mol Genet Metab Rep. 2020 Jul 13;24:100620. doi: 10.1016/j.ymgmr.2020.100620. eCollection 2020 Sep.

Abstract

BACKGROUND

Cystinosis is a metabolic disease caused by intracellular accumulation of cystine within lysosomes. Development of symptoms can be delayed significantly by a life-long therapy with cysteamine, a drug that enters the lysosome and reacts with cystine thereby enabling its export from the organelle.

METHODS

During a period of 16 years, blood samples of 330 cystinosis patients were analyzed to investigate therapeutic adherence and metabolic control in patients treated with immediate-release cysteamine. The accepted therapeutic goal is to measure intracellular cystine levels in white blood cells every 3 months and to keep them below 0.5 nmol cystine/mg protein (= 1 nmol hemicystine/mg protein).

RESULTS

42% of measurements were within the desired 3-month interval, 38% were done every 3-5 months, 11% every 6-8 months, 5% every 9-12 months and 4% after a 12-month interval only. 64.4% of the measurements were higher than the therapeutic target value. Median cystine levels increased with longer control intervals.

CONCLUSIONS

The majority of the cystinosis patients showed insufficient metabolic adjustment. Intracellular cystine levels were not done as often as recommended and were not within therapeutic range. Poor therapy adherence is likely to be caused by gastrointestinal side effects of immediate-release cysteamine. Incorrect intervals between drug intake and blood sampling could contribute to the results.

摘要

背景

胱氨酸贮积症是一种由溶酶体内胱氨酸细胞内蓄积引起的代谢性疾病。通过使用半胱胺进行终身治疗,症状的发展可得到显著延迟。半胱胺是一种能进入溶酶体并与胱氨酸反应从而使其从细胞器中排出的药物。

方法

在16年的时间里,对330例胱氨酸贮积症患者的血样进行分析,以研究接受速释半胱胺治疗的患者的治疗依从性和代谢控制情况。公认的治疗目标是每3个月测量一次白细胞内的胱氨酸水平,并使其低于0.5 nmol胱氨酸/毫克蛋白质(=1 nmol半胱氨酸/毫克蛋白质)。

结果

42%的测量在期望的3个月间隔内进行,38%每3至5个月进行一次,11%每6至8个月进行一次,5%每9至12个月进行一次,4%仅在12个月间隔后进行。64.4%的测量值高于治疗目标值。随着控制间隔时间延长,胱氨酸水平中位数升高。

结论

大多数胱氨酸贮积症患者的代谢调整不足。细胞内胱氨酸水平的测量未按推荐频率进行,且不在治疗范围内。速释半胱胺的胃肠道副作用可能导致治疗依从性差。药物摄入与血样采集之间的间隔不正确可能影响结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90d5/7358454/3c5b89c049b2/gr1.jpg

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