Literature DB >> 32052165

Prognostic role of slow vital capacity in amyotrophic lateral sclerosis.

Andrea Calvo1, Rosario Vasta2, Cristina Moglia2, Enrico Matteoni2, Antonio Canosa2, Alessio Mattei3, Claudio La Mancusa2, Luana Focaraccio4, Letizia Mazzini5, Adriano Chiò2, Fabrizio D'Ovidio2, Umberto Manera2.   

Abstract

OBJECTIVES: To compare the prognostic role of FVC and SVC at diagnosis in amyotrophic lateral sclerosis (ALS) patients.
METHODS: We included all patients from the Piemonte and Valle D'Aosta ALS register (PARALS) who had been diagnosed with ALS between 1995 and 2015 and underwent spirometry at diagnosis. Survival was considered as time to death/tracheostomy; to assess the prognostic value in typical trial timeframes, survival at 12 and 18 months was calculated too. Cox proportional hazard regression models adjusted by sex, age at diagnosis, diagnostic delay, onset site, and ALSFRS-R total score at the moment of diagnosis were used to assess the prognostic role of FVC and SVC.
RESULTS: A total of 795 ALS patients underwent spirometry at diagnosis during the study period. Four hundred and sixteen (52.3%) performed both FVC and SVC, whereas the others performed FVC only. FVC and SVC values were highly correlated (r = 0.92, p < 0.001) in the overall population and slightly less correlated in patients with bulbar onset (r = 0.86, p < 0.001). Both FVC and SVC proved to have a prognostic role with comparable hazard ratios (HRs) (HR 1.83, 95% CI 1.48-2.27 and 1.88, 95% CI 1.51-2.33, respectively). When considering typical trial timeframes, HRs remained similar and were inversely proportional to FVC and SVC values. DISCUSSION: FVC and SVC at diagnosis can be used interchangeably as independent predictors of survival in both clinical and research settings.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; Cohort studies; Epidemiology; Slow vital capacity

Year:  2020        PMID: 32052165     DOI: 10.1007/s00415-020-09751-1

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


  21 in total

1.  Assessment of respiratory functions by spirometry and phrenic nerve studies in patients of amyotrophic lateral sclerosis.

Authors:  Dilip Singh; Rajesh Verma; Ravindra Kumar Garg; Maneesh Kumar Singh; Rakesh Shukla; S K Verma
Journal:  J Neurol Sci       Date:  2011-04-14       Impact factor: 3.181

2.  Use of respiratory function tests to predict survival in amyotrophic lateral sclerosis.

Authors:  Fusun Baumann; Robert D Henderson; Stephen C Morrison; Michael Brown; N Hutchinson; James A Douglas; Peter J Robinson; Pamela A McCombe
Journal:  Amyotroph Lateral Scler       Date:  2010

Review 3.  Amyotrophic lateral sclerosis.

Authors:  Michael A van Es; Orla Hardiman; Adriano Chio; Ammar Al-Chalabi; R Jeroen Pasterkamp; Jan H Veldink; Leonard H van den Berg
Journal:  Lancet       Date:  2017-05-25       Impact factor: 79.321

4.  A phase II-III trial of olesoxime in subjects with amyotrophic lateral sclerosis.

Authors:  T Lenglet; L Lacomblez; J L Abitbol; A Ludolph; J S Mora; W Robberecht; P J Shaw; R M Pruss; V Cuvier; V Meininger
Journal:  Eur J Neurol       Date:  2014-01-21       Impact factor: 6.089

5.  Secular Trends of Amyotrophic Lateral Sclerosis: The Piemonte and Valle d'Aosta Register.

Authors:  Adriano Chiò; Gabriele Mora; Cristina Moglia; Umberto Manera; Antonio Canosa; Stefania Cammarosano; Antonio Ilardi; Davide Bertuzzo; Enrica Bersano; Paolo Cugnasco; Maurizio Grassano; Fabrizio Pisano; Letizia Mazzini; Andrea Calvo
Journal:  JAMA Neurol       Date:  2017-09-01       Impact factor: 18.302

6.  Disease progression in amyotrophic lateral sclerosis: predictors of survival.

Authors:  T Magnus; M Beck; R Giess; I Puls; M Naumann; K V Toyka
Journal:  Muscle Nerve       Date:  2002-05       Impact factor: 3.217

7.  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

8.  Forced vital capacity (FVC) as an indicator of survival and disease progression in an ALS clinic population.

Authors:  A Czaplinski; A A Yen; S H Appel
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-03       Impact factor: 10.154

9.  The predictive value of respiratory function tests for non-invasive ventilation in amyotrophic lateral sclerosis.

Authors:  T B M Tilanus; J T Groothuis; J M C TenBroek-Pastoor; T B Feuth; Y F Heijdra; J P L Slenders; J Doorduin; B G Van Engelen; M J Kampelmacher; J Raaphorst
Journal:  Respir Res       Date:  2017-07-25

10.  SVC Is a Marker of Respiratory Decline Function, Similar to FVC, in Patients With ALS.

Authors:  Susana Pinto; Mamede de Carvalho
Journal:  Front Neurol       Date:  2019-02-28       Impact factor: 4.003

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  3 in total

Review 1.  Considerations for Amyotrophic Lateral Sclerosis (ALS) Clinical Trial Design.

Authors:  Christina N Fournier
Journal:  Neurotherapeutics       Date:  2022-07-11       Impact factor: 6.088

2.  Using patient-reported symptoms of dyspnea for screening reduced respiratory function in patients with motor neuron diseases.

Authors:  Jochem Helleman; Esther T Kruitwagen-van Reenen; J Bakers; Willeke J Kruithof; Annerieke C van Groenestijn; Rineke J H Jaspers Focks; Arthur de Grund; Leonard H van den Berg; Johanna M A Visser-Meily; Anita Beelen
Journal:  J Neurol       Date:  2020-06-23       Impact factor: 4.849

3.  Comparison of Slow and Forced Vital Capacity on Ability to Evaluate Respiratory Function in Bulbar-Involved Amyotrophic Lateral Sclerosis.

Authors:  Xin Huang; Chenfang Du; Qiong Yang; Dongsheng Fan
Journal:  Front Neurol       Date:  2022-06-28       Impact factor: 4.086

  3 in total

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