Effect of edaravone therapy in Korean amyotrophic lateral sclerosis (ALS) patients

被引:37
|
作者
Park, Jin-Mo [1 ]
Kim, Sun-Young [2 ]
Park, Donghwi [3 ]
Park, Jin-Sung [4 ]
机构
[1] Dongguk Univ, Coll Med, Dept Neurol, Gyeongju Hosp, Gyeongju, South Korea
[2] Univ Ulsan, Ulsan Univ Hosp, Dept Neurol, Coll Med, Ulsan, South Korea
[3] Daegu Fatima Hosp, Dept Rehabil, Daegu, South Korea
[4] Kyungpook Natl Univ, Chilgok Hosp, Sch Med, Dept Neurol, 807 Hoguk Ro, Daegu 41944, South Korea
基金
新加坡国家研究基金会;
关键词
Amyotrophic lateral sclerosis (ALS); Edaravone; Korean ALS; ALSFS-R; DOUBLE-BLIND; DECLINE; DISEASE;
D O I
10.1007/s10072-019-04055-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Oxidative stress caused by free radicals has been implicated in the pathogenesis of amyotrophic lateral sclerosis (ALS). Edaravone (also known as MCI-186), a free radical scavenger, was approved as an ALS treatment in 2015 in Japan. However, the therapeutic effects of edaravone on patients with ALS outside of Japan are not yet reported. This study aims to investigate effects of edaravone on ALS patients in the Korean population. The study included 22 patients with ALS who were treated with edaravone. Of the 16 patients who finished six cycles of treatment, a mean decline of ALSFRS-R after the treatments was 5.75 +/- 6.07 points and the average change of FVC was - 8.7 +/- 17.0%. Patients experienced only minor adverse events. This study reports on the open-label study of edaravone on patients in Korea for ALS patients, which showed a modest effect of edaravone in this population of ALS patients.
引用
收藏
页码:119 / 123
页数:5
相关论文
共 50 条
  • [21] Telomerase expression in amyotrophic lateral sclerosis (ALS) patients
    De Felice, Bruna
    Annunziata, Anna
    Fiorentino, Giuseppe
    Manfellotto, Francesco
    D'Alessandro, Raffaella
    Marino, Rita
    Borra, Marco
    Biffali, Elio
    JOURNAL OF HUMAN GENETICS, 2014, 59 (10) : 555 - 561
  • [22] Parkinsonian features in patients with amyotrophic lateral sclerosis (ALS)
    Szczudlik, P.
    Ostrowska, M.
    Tomik, B.
    Kwiecinski, H.
    EUROPEAN JOURNAL OF NEUROLOGY, 2008, 15 : 350 - 351
  • [23] Gastrointestinal Dysmotility in Patients with Amyotrophic Lateral Sclerosis (ALS)
    Schaff, Christina Martin
    Heiman-Patterson, Terry
    Deboo, Anahita
    Barr, Christine
    MUSCLE & NERVE, 2022, 66 : S26 - S26
  • [24] PSYCHOLOGICAL CHARACTERISTICS OF PATIENTS WITH AMYOTROPHIC LATERAL SCLEROSIS (ALS)
    HOUPT, JL
    GOULD, BS
    NORRIS, FH
    PSYCHOSOMATIC MEDICINE, 1977, 39 (05): : 299 - 303
  • [25] Telomerase expression in amyotrophic lateral sclerosis (ALS) patients
    Bruna De Felice
    Anna Annunziata
    Giuseppe Fiorentino
    Francesco Manfellotto
    Raffaella D'Alessandro
    Rita Marino
    Marco Borra
    Elio Biffali
    Journal of Human Genetics, 2014, 59 : 555 - 561
  • [26] Home care of patients with amyotrophic lateral sclerosis (ALS)
    Krivickas, LS
    Shockley, L
    Mitsumoto, H
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 152 : S82 - S89
  • [27] Excessive exercising in patients with amyotrophic lateral sclerosis (als)
    Ebel, Leonie
    Kammeyer, Johanna
    Petri, Susanne
    Mueller, Astrid
    De Zwaan, Martina
    JOURNAL OF BEHAVIORAL ADDICTIONS, 2017, 6 : 65 - 65
  • [28] Speech Therapy in Palliative Therapy Settings: Amyotrophic Lateral Sclerosis (ALS)
    Regelmann, Eva-Maria
    Beushausen, Ulla
    SPRACHE-STIMME-GEHOR, 2022, 46 (01): : 41 - 43
  • [29] Long-term effects of edaravone on patients with amyotrophic lateral sclerosis
    Okada, M.
    Ueyamaa, H.
    Ishizaki, M.
    Maeda, Y.
    Yamashita, S.
    Ando, Y.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2017, 381 : 572 - 572
  • [30] Therapy in Amyotrophic Lateral Sclerosis (ALS): an unexpected evolving scenario
    Silani, V
    ARCHIVES ITALIENNES DE BIOLOGIE, 2017, 155 (04): : 228 - 241