Quantitative Assessment of the Evolution of Cerebellar Signs in Spinocerebellar Ataxias

被引:23
作者
Chan, Ellis [1 ,2 ]
Charles, Perrine [3 ]
Ribai, Pascale [3 ,4 ,5 ,6 ]
Goizet, Cyril [7 ,8 ]
Marelli, Cecilia [3 ,4 ,5 ,6 ]
Vincitorio, Carlo-Maria [3 ]
Le Bayon, Alice [9 ]
Guyant-Marechal, Lucie [10 ,11 ]
Vandenberghe, Nadia [12 ]
Anheim, Mathieu [3 ]
Devos, David [13 ]
Freeman, Leorah [3 ]
Le Ber, Isabelle [4 ,5 ,6 ]
N'Guyen, Karine [14 ]
Tchikviladze, Maya [3 ,4 ]
Labauge, Pierre [9 ]
Hannequin, Didier [10 ,11 ]
Brice, Alexis [3 ,4 ,5 ,6 ]
Durr, Alexandra [3 ,4 ,5 ,6 ]
du Montcel, Sophie Tezenas [1 ,2 ,15 ]
机构
[1] AP HP, Dept Biostat & Med Informat, Paris, France
[2] AP HP, Pitie Salpetriere Charles Foix Clin Res Unit, Paris, France
[3] Hop La Pitie Salpetriere, AP HP, Dept Genet & Cytogenet, F-75013 Paris, France
[4] Univ Paris 06, Ctr Rech, Inst Cerveau & Moelle Epiniere, UMR S975, Paris, France
[5] INSERM, U975, Paris, France
[6] CNRS, UMR 7225, Paris, France
[7] Dept Med Genet, Bordeaux, France
[8] Univ Bordeaux 2, Bordeaux CHU Hosp, Pellegrin Hosp, Lab Human Genet, F-33076 Bordeaux, France
[9] Caremeau Hosp, CHU Nimes, Serv Neurol, Nimes, France
[10] Rouen Univ Hosp, Dept Neurol, Dept Genet, F-76031 Rouen, France
[11] Rouen Univ Hosp, INSERM, U614, F-76031 Rouen, France
[12] Pierre Wertheimer Neurol Hosp, Lyon Hosp, Serv Neurol C, Lyon, France
[13] Univ Lille Nord France, Fac Lille 2, CHU Lille,Dept Neurol, CNRS FRE3291,IMPRT IFR114, Lille, France
[14] La Timone Hosp, Marseille Hosp, Dept Genet, Marseille, France
[15] Univ Paris 06, ER4, Paris, France
关键词
outcome research; gait disorder/ataxia; responsiveness; clinical neurology examination; spinocerebellar ataxia; RESPONSIVENESS; PHENOTYPE; GENOTYPE; SCALE;
D O I
10.1002/mds.23531
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Responsive ataxia rating scales are essential for determining outcome measures in clinical trials. Methods: We evaluated the responsiveness over time of the composite cerebellar functional severity score, a quantitative score measuring cerebellar ataxia in 133 patients with autosomal dominant cerebellar ataxias (ADCA), which were prospectively evaluated at inclusion and after one-year of follow-up. A more responsive tool was developed, the Cerebellar Functional Severity score writing, incorporating the writing test at dominant hand to the Cerebellar Functional Severity score. Results: Within the one-year follow-up period, the Cerebellar Functional Severity score and its writing version increased significantly and the Scale for the Assessment and Rating of Ataxia decreased significantly reflecting increased severity of the cerebellar symptoms. The Cerebellar Functional Severity score writing responsiveness was best in genotypes SCA1, 2, and 3 compared with the other genotypes (effect size = 0.196, standardized response mean (SRM) = 0.624 versus effect size = -0.051, SRM = -0.150). The Cerebellar Functional Severity score writing used as an outcome measure would require only 163 SCA1, 2, or 3 patients per group in a two-arm interventional trial for a 50% reduction in progression and 80% of power. Discussion: Our study demonstrates that the Cerebellar Functional Severity score and Cerebellar Functional Severity score writing are responsive quantitative scores for evaluating sensitivity to change in ADCA patients and can be used as outcome measures in clinical trials, especially when targeting genotypes SCA1, 2 and 3. (C) 2011 Movement Disorder Society
引用
收藏
页码:534 / 538
页数:5
相关论文
共 18 条
  • [1] ASHWORTH B, 1964, PRACTITIONER, V192, P540
  • [2] Cohen J., 1988, Statistical power analysis for the behavioral sciences, VSecond
  • [3] Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)
    David, G
    Dürr, A
    Stevanin, G
    Cancel, G
    Abbas, N
    Benomar, A
    Belal, S
    Lebre, AS
    Abada-Bendib, M
    Grid, D
    Holmberg, M
    Yahyaoui, M
    Hentati, F
    Chkili, T
    Agid, Y
    Brice, A
    [J]. HUMAN MOLECULAR GENETICS, 1998, 7 (02) : 165 - 170
  • [4] Composite cerebellar functional severity score:: validation of a quantitative score of cerebellar impairment
    Du Montcel, Sophie Tezenas
    Charles, Perrine
    Ribai, Pascale
    Goizet, Cyril
    Le Bayon, Alice
    Labauge, Pierre
    Guyant-Marechal, Lucie
    Forlani, Sylvie
    Jauffret, Celine
    Vandenberghe, Nadia
    N'Guyen, Karine
    Le Ber, Isabelle
    Devos, David
    Vincitorio, Carlo-Maria
    Manto, Mario-Ubaldo
    Tison, Francois
    Hannequin, Didier
    Ruberg, Merle
    Brice, Alexis
    Durr, Alexandra
    [J]. BRAIN, 2008, 131 : 1352 - 1361
  • [5] How is disease progress in Friedreich's ataxia best measured? A study of four rating scales
    Fahey, M. C.
    Corben, L.
    Collins, V.
    Churchyard, A. J.
    Delatycki, M. B.
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2007, 78 (04) : 411 - 413
  • [6] Spinocerebellar ataxia type 6 - Frequency of the mutation and genotype-phenotype correlations
    Geschwind, DH
    Perlman, S
    Figueroa, KP
    Karrim, J
    Baloh, RW
    Pulst, SM
    [J]. NEUROLOGY, 1997, 49 (05) : 1247 - 1251
  • [7] KAMATH C, 2008, WILEY ENCY CLIN TRIA, P306
  • [8] EFFECT SIZES FOR INTERPRETING CHANGES IN HEALTH-STATUS
    KAZIS, LE
    ANDERSON, JJ
    MEENAN, RF
    [J]. MEDICAL CARE, 1989, 27 (03) : S178 - S189
  • [9] The natural history of degenerative ataxia:: a retrospective study in 466 patients
    Klockgether, T
    Lüdtke, R
    Kramer, B
    Bürk, K
    Schöls, L
    Riess, O
    Laccone, F
    Boesch, S
    Lopes-Cendes, I
    Brice, A
    Inzelberg, R
    Zilber, N
    Dichgans, J
    [J]. BRAIN, 1998, 121 : 589 - 600
  • [10] Interpretation of changes in health-related quality of life - The remarkable universality of half a standard deviation
    Norman, GR
    Sloan, JA
    Wyrwich, KW
    [J]. MEDICAL CARE, 2003, 41 (05) : 582 - 592