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骨化三醇治疗安全,并能提高弗里德里希共济失调患者的铁调素水平。

Calcitriol Treatment Is Safe and Increases Frataxin Levels in Friedreich Ataxia Patients.

机构信息

Ataxia Unit, Neurology Service, ICS/IAS, Hospital Josep Trueta/Hospital Santa Caterina, Girona/Salt, Spain.

Department of Medical Sciences, University of Girona (UdG), Girona, Spain.

出版信息

Mov Disord. 2024 Jul;39(7):1099-1108. doi: 10.1002/mds.29808. Epub 2024 May 2.

Abstract

BACKGROUND

Calcitriol, the active form of vitamin D (also known as 1,25-dihydroxycholecalciferol), improves the phenotype and increases frataxin levels in cell models of Friedreich ataxia (FRDA).

OBJECTIVES

Based on these results, we aimed measuring the effects of a calcitriol dose of 0.25 mcg/24h in the neurological function and frataxin levels when administered to FRDA patients for a year.

METHODS

20 FRDA patients where recluted and 15 patients completed the treatment for a year. Evaluations of neurological function changes (SARA scale, 9-HPT, 8-MWT, PATA test) and quality of life (Barthel Scale and Short Form (36) Health Survey [SF-36] quality of life questionnaire) were performed. Frataxin amounts were measured in isolated platelets obtained from these FRDA patients, from heterozygous FRDA carriers (relatives of the FA patients) and from non-heterozygous sex and age matched controls.

RESULTS

Although the patients did not experience any observable neurological improvement, there was a statistically significant increase in frataxin levels from initial values, 5.5 to 7.0 pg/μg after 12 months. Differences in frataxin levels referred to total protein levels were observed among sex- and age-matched controls (18.1 pg/μg), relative controls (10.1 pg/μg), and FRDA patients (5.7 pg/μg). The treatment was well tolerated by most patients, and only some of them experienced minor adverse effects at the beginning of the trial.

CONCLUSIONS

Calcitriol dosage used (0.25 mcg/24 h) is safe for FRDA patients, and it increases frataxin levels. We cannot rule out that higher doses administered longer could yield neurological benefits. © 2024 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

摘要

背景

活性维生素 D(也称为 1,25-二羟胆钙化醇)的形式——骨化三醇可改善弗里德里希共济失调(FRDA)的细胞模型中的表型并增加 frataxin 水平。

目的

基于这些结果,我们旨在测量在 FRDA 患者中使用 0.25 mcg/24h 的骨化三醇剂量一年对神经功能和 frataxin 水平的影响。

方法

招募了 20 名 FRDA 患者,其中 15 名患者完成了一年的治疗。进行了神经功能变化的评估(SARA 量表、9-HPT、8-MWT、PATA 测试)和生活质量(巴氏量表和简短形式(36)健康调查 [SF-36] 生活质量问卷)。从这些 FRDA 患者、FRDA 杂合子携带者(FA 患者的亲属)和非杂合子性别和年龄匹配的对照中分离的血小板中测量了 frataxin 量。

结果

尽管患者没有观察到任何明显的神经改善,但 frataxin 水平从初始值 5.5 增加到 12 个月后的 7.0 pg/μg,具有统计学意义。在性别和年龄匹配的对照组(18.1 pg/μg)、相对对照组(10.1 pg/μg)和 FRDA 患者(5.7 pg/μg)中观察到 frataxin 水平与总蛋白水平的差异。该治疗方案被大多数患者耐受良好,只有少数患者在试验开始时出现轻微不良反应。

结论

使用的骨化三醇剂量(0.25 mcg/24 h)对 FRDA 患者是安全的,并且可以增加 frataxin 水平。我们不能排除更长时间给予更高剂量可能会带来神经益处。© 2024 作者。运动障碍由 Wiley 期刊有限责任公司代表国际帕金森病和运动障碍学会出版。

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