[Treatment of familial ALS with the drug tofersen].

IF 0.4 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Bjorn Logi Thorarinsson, Karen Eva Halldorsdottir, Agust Hilmarsson, Olafur Arni Sveinsson
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引用次数: 0

Abstract

Amyotrophic lateral sclerosis (ALS) is a severe and progressive neurodegenerative disorder. We describe four cases of familial ALS based on SOD1 mutations who received intrathecal treatment with the antisense oligonucleotide tofersen at Landspítali University Hospital Iceland. Since initiation of treatment, there has not been any significant deterioration, and three patients have shown signs of cinical improvement. The cerebrospinal fluid concentration of neurofilament light chain (Nf-L), a biomarker of neuronal axonal damage, has decreased to the reference range of healthy individuals. No serious side effects have been observed.

【用托佛生治疗家族性ALS】。
肌萎缩侧索硬化症(ALS)是一种严重的进行性神经退行性疾病。我们描述了4例基于SOD1突变的家族性ALS患者,他们在Landspítali冰岛大学医院接受了鞘内反义寡核苷酸tofersen治疗。自开始治疗以来,没有任何明显的恶化,有三名患者表现出临床改善的迹象。神经纤维轻链(Nf-L)是神经轴突损伤的生物标志物,脑脊液浓度已降至健康个体的参考范围。没有观察到严重的副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Laeknabladid
Laeknabladid MEDICINE, GENERAL & INTERNAL-
CiteScore
0.50
自引率
25.00%
发文量
63
审稿时长
>12 weeks
期刊介绍: Læknablaðið er fræðirit sem birtir vísinda og yfirlitsgreinar og annað efni sem byggir á rannsóknum innan læknisfræði eða skyldra greina. Læknablaðið er gefið út af Læknafélagi Íslands. Blaðið er sent til allra félagsmanna. Það var fyrst gefið út árið 1904 en hefur komið samfellt út frá árinu 1915. Blaðið kemur út 11 sinnum á ári og er prentað í 2000 eintökum. Allt efni Læknablaðsins frá árinu 2000 er aðgengilegt á heimasíðu blaðsins á laeknabladid.is og er aðgangur endurgjaldslaus og öllum opinn.
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