Intrathecal cyclodextrin in the treatment of Niemann-Pick disease type C

被引:3
|
作者
Roch Santed, Maria [1 ]
Cabanas Poy, Maria Josep [1 ]
Del Toro Riera, Mireia [2 ]
Canete Ramirez, Carme [1 ]
Fernandez Polo, Aurora [1 ]
Clemente Bautista, Susana [1 ]
机构
[1] Hosp Vall dHebron Barcelona, Pharm Dept, Barcelona 08035, Spain
[2] Hosp Vall dHebron Barcelona, Pediat Neurol Dept, Barcelona, Spain
关键词
2-HYDROXYPROPYL-BETA-CYCLODEXTRIN; PATIENT;
D O I
10.1136/ejhpharm-2016-001067
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Case A child with Niemann-Pick disease type C was started on miglustat therapy at the age of 2 years. Intrathecal administration of hydroxypropyl-beta-cyclodextrin was added 5 months later. The initial dose of 175 mg was gradually increased over the first 6 months to reach 325 mg. The drug was administered every 15 days, and the patient received 43 doses. A slight delay in progression of the disease was seen during the first year of intrathecal hydroxypropyl-beta-cyclodextrin. However, additional symptoms have emerged since that time, suggesting a lack of effectiveness of the drug. Our patient has shown no drug-related adverse events. Conclusions Intrathecal hydroxypropyl-beta-cyclodextrin therapy is safe, but its efficacy seems questionable in a patient with the severe infantile form of Niemann-Pick disease type C.
引用
收藏
页码:185 / 188
页数:4
相关论文
共 50 条
  • [41] Treatment of Niemann-Pick Type C Disease by Histone Deacetylase Inhibitors
    Helquist, Paul
    Maxfield, Frederick R.
    Wiech, Norbert L.
    Wiest, Olaf
    NEUROTHERAPEUTICS, 2013, 10 (04) : 688 - 697
  • [42] VTS-270 for the treatment of Niemann-Pick disease type C
    Machielse, Bernardus N.
    Porter, Forbes D.
    Yergey, Alfred L.
    Berry-Kravis, Elizabeth M.
    Darling, Allan
    Rao, Ravi
    MOLECULAR GENETICS AND METABOLISM, 2017, 120 (1-2) : S89 - S90
  • [43] Neurodegeneration in Niemann-Pick type C disease mice
    Wei-Yi Ong
    Ujendra Kumar
    Robert C. Switzer
    Anita Sidhu
    Geetha Suresh
    Chang-Yong Hu
    Shutish C. Patel
    Experimental Brain Research, 2001, 141 : 218 - 231
  • [44] Cholesterol Homeostasis in Niemann-Pick type C disease
    Karten, Barbara
    Hayashi, Hideki
    Francis, Gordon
    Campenot, Robert B.
    Vance, Dennis E.
    Vance, Jean E.
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2007, 33 (01) : 143 - 143
  • [45] Niemann-Pick disease type C: a diagnostic challenge
    Al Menabawy, Nihal M.
    Mahmoud, Iman G.
    EL Khateeb, Nour M.
    Sobhy, Ahmed M.
    Zaki, Maha S.
    Gleeson, Joseph
    Rolfs, Arndt
    Selim, Laila A.
    MOLECULAR GENETICS AND METABOLISM, 2017, 120 (1-2) : S19 - S19
  • [46] Dysphagia in Adults with Niemann-Pick Disease Type C
    Lewis, C.
    Walterfang, M.
    Vogel, A.
    MOVEMENT DISORDERS, 2019, 34 : S213 - S214
  • [47] Linkage of Niemann-Pick disease type D to the same region of human chromosome 18 as Niemann-Pick disease type C
    Greer, WL
    Riddell, DC
    Byers, DM
    Welch, JP
    Girouard, GS
    Sparrow, SM
    Gillan, TL
    Neumann, PE
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (01) : 139 - 142
  • [48] THEORETICAL APPROACH TO THE NIEMANN-PICK TYPE C DISEASE
    Pardo Echeverria, Liz Carolina
    CULTURA CIENTIFICA, 2016, (14): : 82 - 90
  • [49] Altered neurosteroidogenesis in Niemann-Pick type C disease
    Griffin, LD
    Compagnone, N
    Mellon, S
    ANNALS OF NEUROLOGY, 1998, 44 (03) : 471 - 471
  • [50] Neurodegeneration in Niemann-Pick type C disease mice
    Ong, WY
    Kumar, U
    Switzer, RC
    Sidhu, A
    Suresh, G
    Hu, CY
    Patel, SC
    EXPERIMENTAL BRAIN RESEARCH, 2001, 141 (02) : 218 - 231