Pattern of spread and prognosis in lower limb-onset ALS

被引:54
作者
Turner, Martin R. [1 ]
Brockington, Alice [2 ]
Scaber, Jakub [1 ]
Hollinger, Hannah [2 ]
Marsden, Rachael [1 ]
Shaw, Pamela J. [2 ]
Talbot, Kevin [1 ]
机构
[1] Univ Oxford, Dept Clin Neurol, Oxford, England
[2] Univ Sheffield, Acad Neurol Unit, Dept Neurosci, Sheffield, S Yorkshire, England
来源
AMYOTROPHIC LATERAL SCLEROSIS | 2010年 / 11卷 / 04期
关键词
Epidemiology; prognostic; survival; AMYOTROPHIC-LATERAL-SCLEROSIS; SUPEROXIDE DISMUTASE MUTATION; MOTOR-NEURON DEGENERATION; D90A SOD1 ALS; NATURAL-HISTORY; FLAIL ARM; FOCALITY; SURVIVAL; VARIANT;
D O I
10.3109/17482960903420140
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Our objective was to establish the pattern of spread in lower limb-onset ALS (contra-versus ipsi-lateral) and its contribution to prognosis within a multivariate model. Pattern of spread was established in 109 sporadic ALS patients with lower limb-onset, prospectively recorded in Oxford and Sheffield tertiary clinics from 2001 to 2008. Survival analysis was by univariate Kaplan-Meier log-rank and multivariate Cox proportional hazards. Variables studied were time to next limb progression, site of next progression, age at symptom onset, gender, diagnostic latency and use of riluzole. Initial progression was either to the contralateral leg (76%) or ipsilateral arm (24%). Factors independently affecting survival were time to next limb progression, age at symptom onset, and diagnostic latency. Time to progression as a prognostic factor was independent of initial direction of spread. In a regression analysis of the deceased, overall survival from symptom onset approximated to two years plus the time interval for initial spread. In conclusion, rate of progression in lower limb-onset ALS is not influenced by whether initial spread is to the contralateral limb or ipsilateral arm. The time interval to this initial spread is a powerful factor in predicting overall survival, and could be used to facilitate decision-making and effective care planning.
引用
收藏
页码:369 / 373
页数:5
相关论文
共 21 条
  • [1] Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation - A clinical and genealogical study of 36 patients
    Andersen, PM
    Forsgren, L
    Binzer, M
    Nilsson, P
    AlaHurula, V
    Keranen, ML
    Bergmark, L
    Saarinen, A
    Haltia, T
    Tarvainen, I
    Kinnunen, E
    Udd, B
    Marklund, SL
    [J]. BRAIN, 1996, 119 : 1153 - 1172
  • [2] Brooks BR, 2000, AMYOTROPHIC LATERAL, P31
  • [3] Cappellari A, 2008, Electromyogr Clin Neurophysiol, V48, P75
  • [4] Prognostic factors in ALS: A critical review
    Chio, Adriano
    Logroscino, Giancarlo
    Hardiman, Orla
    Swingler, Robert
    Mitchell, Douglas
    Beghi, Ettore
    Traynor, Bryan G.
    [J]. AMYOTROPHIC LATERAL SCLEROSIS, 2009, 10 (5-6): : 310 - 323
  • [5] The natural history of primary lateral sclerosis
    Gordon, PH
    Cheng, B
    Katz, IB
    Pinto, M
    Hays, AP
    Mitsumoto, H
    Rowland, LP
    [J]. NEUROLOGY, 2006, 66 (05) : 647 - 653
  • [6] GOWERS WR, 1893, DIS NERV SYST, P483
  • [7] NATURAL-HISTORY OF AMYOTROPHIC-LATERAL-SCLEROSIS IN A DATABASE POPULATION - VALIDATION OF A SCORING SYSTEM AND A MODEL FOR SURVIVAL PREDICTION
    HAVERKAMP, LJ
    APPEL, V
    APPEL, SH
    [J]. BRAIN, 1995, 118 : 707 - 719
  • [8] Flail arm syndrome: a distinctive variant of amyotrophic lateral sclerosis
    Hu, MTM
    Ellis, CM
    Al-Chalabi, A
    Leigh, PN
    Shaw, CE
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1998, 65 (06) : 950 - 951
  • [9] Corticospinal tract degeneration in the progressive muscular atrophy variant of ALS
    Ince, PG
    Evans, J
    Knopp, M
    Forster, G
    Hamdalla, HHM
    Wharton, SB
    Shaw, PJ
    [J]. NEUROLOGY, 2003, 60 (08) : 1252 - 1258
  • [10] Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues
    Logroscino, G.
    Traynor, B. J.
    Hardiman, O.
    Chio', A.
    Couratier, P.
    Mitchell, J. D.
    Swingler, R. J.
    Beghi, E.
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2008, 79 (01) : 6 - 11