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肾病型胱氨酸病患者长期服用缓释半胱胺的依从性:来自前瞻性CrYSTobs队列研究的数据

Adherence to delayed-release cysteamine in nephropathic cystinosis over time: data from the prospective CrYSTobs cohort study.

作者信息

Grosyeux Chloé, Gaillard Ségolène, Morin Denis, Hogan Julien, Acquaviva-Bourdain Cécile, Bacchetta Justine, Bertholet-Thomas Aurélia

机构信息

Department of Pediatric Nephrology, Rheumatology and Dermatology, University Children's Hospital, Lyon, France.

Néphrologie-Dialyse-Transplantation Pédiatrique, Centre Hospitalier Universitaire de Nancy, Rue du Morvan, 54511, Vandoeuvre-Lès-Nancy Cedex, France.

出版信息

Pediatr Nephrol. 2025 Feb 4. doi: 10.1007/s00467-025-06699-0.

Abstract

BACKGROUND

Adherence to cysteamine in nephropathic cystinosis (NC) remains challenging. A better adherence with delayed-release (DR) compared to immediate-release (IR) cysteamine at 1 year was previously shown. This study aimed to evaluate adherence to DR cysteamine at 2 years.

METHODS

Treatment adherence was assessed using a medication event monitoring system; adherence ranged from 0 (poor) to 2 (good). Leukocyte cystine level was measured at each 3-month visit. Long-term follow-up data (7 years after the end of the study) on self-reported adherence and quality of life was also obtained in a sub-group of patients.

RESULTS

Seventeen patients with NC under DR cysteamine from three French centers were included at a median age of 13.9 (5.4-33.0) years. The median adherence score was 1.62 (0.03-1.98) over the 2-year follow-up, with 65% of patients having good adherence and 75% having partial or good adherence. No significant difference in leukocyte cystine level between baseline and 2 years was found (0.8 nmol vs. 0.4 nmol, respectively; difference in median of - 1.0 nmol; 95% CI - 0.7, 0.4; P = 0.64). Long-term follow-up data highlighted that no patient wished to switch back to IR cysteamine, as taking the medication twice rather than four times a day was easier.

CONCLUSIONS

This study found a fairly good adherence to DR cysteamine over time. Decreasing the number of intakes per day may improve adherence and limit the side effects of the drug, representing an additional argument in favor of its use in patients with cystinosis.

摘要

背景

在肾病型胱氨酸病(NC)中,坚持服用半胱胺仍然具有挑战性。先前研究表明,与速释型(IR)半胱胺相比,缓释型(DR)半胱胺在1年时的依从性更好。本研究旨在评估2年时对DR半胱胺的依从性。

方法

使用药物事件监测系统评估治疗依从性;依从性范围为0(差)至2(好)。每3个月就诊时测量白细胞胱氨酸水平。还在一组患者中获得了关于自我报告的依从性和生活质量的长期随访数据(研究结束后7年)。

结果

来自法国三个中心的17例接受DR半胱胺治疗的NC患者被纳入研究,中位年龄为13.9(5.4 - 33.0)岁。在2年的随访中,中位依从性评分为1.62(0.03 - 1.98),65%的患者依从性良好,75%的患者部分或完全依从。未发现基线和2年时白细胞胱氨酸水平有显著差异(分别为0.8 nmol和0.4 nmol;中位数差异为 - 1.0 nmol;95%CI - 0.7,0.4;P = 0.64)。长期随访数据表明,没有患者希望换回IR半胱胺,因为每天服药两次比四次更容易。

结论

本研究发现随着时间推移,对DR半胱胺的依从性相当好。减少每日服药次数可能会提高依从性并限制药物的副作用,这是支持其用于胱氨酸病患者的又一论据。

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