Literature DB >> 16773270

Amyotrophic lateral sclerosis: early predictors of prolonged survival.

Adam Czaplinski1, Albert A Yen, Stanley H Appel.   

Abstract

OBJECTIVE: In order to define the predictors of prolonged survival available at the time of first examination we performed a historical cohort study of amyotrophis sclerosis (ALS) patients referred to our ALS Clinic over the last 20 years.
METHODS: In a group of 1034 patients with the diagnosis of definite or probable ALS the effects of individual prognostic factors on tracheostomy-free survival were assessed with the Kaplan-Meier life-table method. The prognostic value of each factor was estimated using univariate and multivariate Cox proportional hazard analyses.
RESULTS: The median survival time was 3.45 years, (95%CI 3.27-3.74). Both the univariate and multivariate Cox models indicated that younger age, limb site of onset, longer diagnostic delay, lower Appel ALS score (AALSS) at first examination, lower AALSS-rate of change between first symptom and first exam (preslope), and higher baseline forced vital capacity (FVC) were associated with longer survival. In addition, four factors: age, diagnostic delay, baseline FVC and AALSS preslope have been identified as independent predictors of survival in our patient population.
CONCLUSIONS: The identification of younger age, limb site of onset and longer diagnostic delay as predictors of prolonged survival in ALS clinic population supports the findings of several, earlier studies that were based on smaller groups of patients. More significantly, several additional variables assessed at the first examination predict longer survival: lower baseline AALSS, lower AALSS- preslope and higher baseline FVC. All of these parameters are of value in patient management and in clinical trial development.

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Year:  2006        PMID: 16773270     DOI: 10.1007/s00415-006-0226-8

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  33 in total

1.  Functional outcome measures as clinical trial endpoints in ALS.

Authors:  B J Traynor; H Zhang; J M Shefner; D Schoenfeld; M E Cudkowicz
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2.  El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial "Clinical limits of amyotrophic lateral sclerosis" workshop contributors.

Authors:  B R Brooks
Journal:  J Neurol Sci       Date:  1994-07       Impact factor: 3.181

3.  ALS in Rochester, Minnesota, 1925-1977.

Authors:  S M Juergens; L T Kurland; H Okazaki; D W Mulder
Journal:  Neurology       Date:  1980-05       Impact factor: 9.910

4.  Selegiline is ineffective in a collaborative double-blind, placebo-controlled trial for treatment of amyotrophic lateral sclerosis.

Authors:  D J Lange; P L Murphy; B Diamond; V Appel; E C Lai; D S Younger; S H Appel
Journal:  Arch Neurol       Date:  1998-01

5.  The ALSFRSr predicts survival time in an ALS clinic population.

Authors:  P Kaufmann; G Levy; J L P Thompson; M L Delbene; V Battista; P H Gordon; L P Rowland; B Levin; H Mitsumoto
Journal:  Neurology       Date:  2005-01-11       Impact factor: 9.910

6.  A randomized, placebo-controlled trial of topiramate in amyotrophic lateral sclerosis.

Authors:  M E Cudkowicz; J M Shefner; D A Schoenfeld; R H Brown; H Johnson; M Qureshi; M Jacobs; J D Rothstein; S H Appel; R M Pascuzzi; T D Heiman-Patterson; P D Donofrio; W S David; J A Russell; R Tandan; E P Pioro; K J Felice; J Rosenfeld; R N Mandler; G M Sachs; W G Bradley; E M Raynor; G D Baquis; J M Belsh; S Novella; J Goldstein; J Hulihan
Journal:  Neurology       Date:  2003-08-26       Impact factor: 9.910

7.  The natural history of amyotrophic lateral sclerosis.

Authors:  S P Ringel; J R Murphy; M K Alderson; W Bryan; J D England; R G Miller; J H Petajan; S A Smith; R I Roelofs; F Ziter
Journal:  Neurology       Date:  1993-07       Impact factor: 9.910

8.  Prognosis of amyotrophic lateral sclerosis and the effect of referral selection.

Authors:  J R Lee; J F Annegers; S H Appel
Journal:  J Neurol Sci       Date:  1995-10       Impact factor: 3.181

9.  Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction.

Authors:  L J Haverkamp; V Appel; S H Appel
Journal:  Brain       Date:  1995-06       Impact factor: 13.501

10.  Duration of amyotrophic lateral sclerosis is age dependent.

Authors:  A Eisen; M Schulzer; M MacNeil; B Pant; E Mak
Journal:  Muscle Nerve       Date:  1993-01       Impact factor: 3.217

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  30 in total

Review 1.  Military service, deployments, and exposures in relation to amyotrophic lateral sclerosis etiology and survival.

Authors:  John D Beard; Freya Kamel
Journal:  Epidemiol Rev       Date:  2014-10-31       Impact factor: 6.222

2.  Decreased brain activation to tongue movements in amyotrophic lateral sclerosis with bulbar involvement but not Kennedy syndrome.

Authors:  Bahram Mohammadi; Katja Kollewe; Amir Samii; Klaus Krampfl; Reinhard Dengler; Thomas F Münte
Journal:  J Neurol       Date:  2009-04-08       Impact factor: 4.849

3.  Motoneuron afterhyperpolarisation duration in amyotrophic lateral sclerosis.

Authors:  Maria Piotrkiewicz; Irena Hausmanowa-Petrusewicz
Journal:  J Physiol       Date:  2011-03-28       Impact factor: 5.182

4.  Stratification of amyotrophic lateral sclerosis patients: a crowdsourcing approach.

Authors:  Robert Kueffner; Neta Zach; Maya Bronfeld; Raquel Norel; Nazem Atassi; Venkat Balagurusamy; Barbara Di Camillo; Adriano Chio; Merit Cudkowicz; Donna Dillenberger; Javier Garcia-Garcia; Orla Hardiman; Bruce Hoff; Joshua Knight; Melanie L Leitner; Guang Li; Lara Mangravite; Thea Norman; Liuxia Wang; Jinfeng Xiao; Wen-Chieh Fang; Jian Peng; Chen Yang; Huan-Jui Chang; Gustavo Stolovitzky
Journal:  Sci Rep       Date:  2019-01-24       Impact factor: 4.379

5.  Factors affecting survival of patients with neurodegenerative disease.

Authors:  Kyle Steenland; Jessica MacNeil; Ryan Seals; Allan Levey
Journal:  Neuroepidemiology       Date:  2010-04-08       Impact factor: 3.282

6.  Requests for euthanasia: origin of suffering in ALS, heart failure, and cancer patients.

Authors:  Maud Maessen; Jan H Veldink; Leonard H van den Berg; Henrike J Schouten; Gerrit van der Wal; Bregje D Onwuteaka-Philipsen
Journal:  J Neurol       Date:  2010-02-11       Impact factor: 4.849

7.  Effects of demographic factors on survival time after a diagnosis of amyotrophic lateral sclerosis.

Authors:  Heather Jordan; Jerald Fagliano; Lindsay Rechtman; Daniel Lefkowitz; Wendy Kaye
Journal:  Neuroepidemiology       Date:  2015-03-17       Impact factor: 3.282

8.  Prognosis and epidemiology of amyotrophic lateral sclerosis: Analysis of a clinic population, 1997-2011.

Authors:  Kim Traxinger; Crystal Kelly; Brent A Johnson; Robert H Lyles; Jonathan D Glass
Journal:  Neurol Clin Pract       Date:  2013-08

Review 9.  Prognostic factors in ALS: A critical review.

Authors:  Adriano Chiò; Giancarlo Logroscino; Orla Hardiman; Robert Swingler; Douglas Mitchell; Ettore Beghi; Bryan G Traynor
Journal:  Amyotroph Lateral Scler       Date:  2009 Oct-Dec

10.  Mortality from neurodegenerative diseases in a cohort of US flight attendants.

Authors:  Lynne E Pinkerton; Misty J Hein; Barbara Grajewski; Freya Kamel
Journal:  Am J Ind Med       Date:  2016-05-17       Impact factor: 2.214

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