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增加半胱氨酸结合巯基药物剂量对胱氨酸尿症患者胱氨酸容量的影响。

Effect of increasing doses of cystine-binding thiol drugs on cystine capacity in patients with cystinuria.

机构信息

Division of Nephrology, Department of Medicine, Hofstra Northwell School of Medicine, Hempstead, NY, USA.

Nephrology Division, NYU Langone Medical Center, New York, NY, USA.

出版信息

Urolithiasis. 2019 Dec;47(6):549-555. doi: 10.1007/s00240-019-01128-y. Epub 2019 Apr 13.

Abstract

Appropriate dosing of cystine-binding thiol drugs in the management of cystinuria has been based on clinical stone activity. When new stones form, the dose is increased. Currently, there is no method of measuring urinary drug levels to guide the titration of therapy. Increasing cystine capacity, a measure of cystine solubility, has been promoted as a method of judging the effects of therapy. In this study, we gave increasing doses of tiopronin or D-penicillamine, depending on the patients' own prescriptions, to ten patients with cystinuria and measured cystine excretion and cystine capacity. The doses were 0, 1, 2, 3 g per day, given in two divided doses, and administered in a random order. Going from 0 to 1 g/day led to an increase in cystine capacity from - 39.1 to 130.4 mg/L (P < 0.009) and decreased 24 h cystine excretion from 1003.9 to 834.8 mg/day (P = 0.039). Increasing the doses from 1 to 2 to 3 g/day had no consistent or significant effect to further increase cystine capacity or decrease cystine excretion. Whether doses higher than 1 g/day have additional clinical benefit is not clear from this study. Limiting doses might be associated with fewer adverse effects without sacrificing the benefit of higher doses if higher doses do not offer clinical importance. However, trials with stone activity as an outcome would be desirable.

摘要

在胱氨酸尿症的管理中,适当的半胱氨酸结合硫醇药物剂量是基于临床结石活动的。当新结石形成时,剂量会增加。目前,没有测量尿液药物水平的方法来指导治疗的滴定。增加胱氨酸容量,即胱氨酸溶解度的衡量标准,已被推广为判断治疗效果的方法。在这项研究中,我们根据患者自己的处方,给 10 名胱氨酸尿症患者递增剂量的硫普罗宁或 D-青霉胺,每天分两次服用,剂量分别为 0、1、2、3g,并以随机顺序给药。从 0 增加到 1g/天,胱氨酸容量从-39.1 增加到 130.4mg/L(P<0.009),24 小时胱氨酸排泄量从 1003.9 减少到 834.8mg/天(P=0.039)。从 1g/天增加到 2g/天再增加到 3g/天,胱氨酸容量或胱氨酸排泄量没有持续或显著的增加。从这项研究中尚不清楚每天 1g 以上的剂量是否有额外的临床获益。限制剂量可能与减少不良反应有关,而不会牺牲高剂量的获益,如果高剂量没有带来临床重要性的话。然而,以结石活动为结果的试验是理想的。

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