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Published in: Journal of Neurology 7/2020

01-07-2020 | Amyotrophic Lateral Sclerosis | Original Communication

Diaphragmatic CMAP amplitude from phrenic nerve stimulation predicts functional decline in ALS

Authors: Bruno Miranda, Marta Gromicho, Mariana Pereira, Susana Pinto, Michael Swash, Mamede de Carvalho

Published in: Journal of Neurology | Issue 7/2020

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Abstract

Objective

To evaluate phrenic nerve motor amplitude (PhrenicAmp) as an independent predictor of functional decline in amyotrophic lateral sclerosis (ALS). We also assessed both PhrenicAmp and forced vital capacity (FVC) as predictors of functional loss in patients with bulbar dysfunction.

Methods

We included consecutive ALS patients with PhrenicAmp and FVC at baseline. Participants were evaluated with the revised ALS Functional Rating Scale (ALSFRS-R) at inclusion and at, at least, one subsequent follow-up visit. The outcome measure of functional decline was the percentage reduction in ALSFRS-R from baseline. Bulbar dysfunction was defined by the presence of any relevant symptom on the ALSFRS-R bulbar sub-score. Correlations and mixed-effects regressions were used to study the relationship between functional decline and both PhrenicAmp and FVC baseline evaluations.

Results

A total of 249 ALS patients were included; 64.2% of these had bulbar dysfunction. At inclusion, significant correlations were found between PhrenicAmp and FVC (p < 0.001), as well as between each respiratory measure and ALSFRS-R (all p < 0.001). The functional decline at first (median 3 months) and second (median 6 months) follow-up visits was significantly correlated with baseline values of both respiratory evaluations (all p < 0.01) in the entire ALS population, but only with baseline PhrenicAmp (all p < 0.05) in bulbar dysfunction cases. Regression analysis revealed that PhrenicAmp (all p < 0.05), but not FVC, was a significant independent predictor of functional decline in ALS patients and in those with bulbar dysfunction.

Conclusion

Baseline PhrenicAmp is an independent predictor of functional decline in ALS, whether or not bulbar dysfunction is present.
Literature
1.
go back to reference Kiernan MC, Vucic S, Cheah BC, Turner MR, Eisen A, Hardiman O et al (2011) Amyotrophic lateral sclerosis. Lancet 377:942–955CrossRef Kiernan MC, Vucic S, Cheah BC, Turner MR, Eisen A, Hardiman O et al (2011) Amyotrophic lateral sclerosis. Lancet 377:942–955CrossRef
2.
go back to reference Chiò A, Logroscino G, Hardiman O, Swingler R, Mitchell D, Beghi E et al (2009) Prognostic factors in ALS: a critical review. Amyotroph Lateral Scler 10:310–323CrossRef Chiò A, Logroscino G, Hardiman O, Swingler R, Mitchell D, Beghi E et al (2009) Prognostic factors in ALS: a critical review. Amyotroph Lateral Scler 10:310–323CrossRef
3.
go back to reference Creemers H, Grupstra H, Nollet F, van den Berg LH, Beelen A (2014) Prognostic factors for the course of functional status of patients with ALS: a systematic review. J Neurol 262:1407–1423CrossRef Creemers H, Grupstra H, Nollet F, van den Berg LH, Beelen A (2014) Prognostic factors for the course of functional status of patients with ALS: a systematic review. J Neurol 262:1407–1423CrossRef
4.
go back to reference Bowser R, Turner MR, Shefner J (2011) Biomarkers in amyotrophic lateral sclerosis: opportunities and limitations. Nat Rev Neurol 7:631–638CrossRef Bowser R, Turner MR, Shefner J (2011) Biomarkers in amyotrophic lateral sclerosis: opportunities and limitations. Nat Rev Neurol 7:631–638CrossRef
5.
go back to reference Simon NG, Turner MR, Vucic S, Al-Chalabi A, Shefner J, Lomen-Hoerth C et al (2014) Quantifying disease progression in amyotrophic lateral sclerosis. Ann Neurol 76:643–657CrossRef Simon NG, Turner MR, Vucic S, Al-Chalabi A, Shefner J, Lomen-Hoerth C et al (2014) Quantifying disease progression in amyotrophic lateral sclerosis. Ann Neurol 76:643–657CrossRef
6.
go back to reference Berry JD, Miller R, Moore DH, Cudkowicz ME, van den Berg LH, Kerr DA et al (2013) The combined assessment of function and survival (CAFS): a new endpoint for ALS clinical trials. Amyotroph Lateral Scler Frontotemporal Degener 14:162–168CrossRef Berry JD, Miller R, Moore DH, Cudkowicz ME, van den Berg LH, Kerr DA et al (2013) The combined assessment of function and survival (CAFS): a new endpoint for ALS clinical trials. Amyotroph Lateral Scler Frontotemporal Degener 14:162–168CrossRef
7.
go back to reference Tramacere I, Dalla Bella E, Chio A, Mora G, Filippini G, Lauria G et al (2015) The MITOS system predicts long-term survival in amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry 86:1180–1185CrossRef Tramacere I, Dalla Bella E, Chio A, Mora G, Filippini G, Lauria G et al (2015) The MITOS system predicts long-term survival in amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry 86:1180–1185CrossRef
8.
go back to reference Proudfoot M, Jones A, Talbot K, Al-Chalabi A, Turner MR (2016) The ALSFRS as an outcome measure in therapeutic trials and its relationship to symptom onset. Amyotroph Lateral Scler Frontotemporal Degener 17:414–425CrossRef Proudfoot M, Jones A, Talbot K, Al-Chalabi A, Turner MR (2016) The ALSFRS as an outcome measure in therapeutic trials and its relationship to symptom onset. Amyotroph Lateral Scler Frontotemporal Degener 17:414–425CrossRef
9.
go back to reference van den Berg LH, Sorensen E, Gronseth G et al (2019) Revised Airlie House consensus guidelines for design and implementation of ALS clinical trials. Neurology 92:e1610–e1623CrossRef van den Berg LH, Sorensen E, Gronseth G et al (2019) Revised Airlie House consensus guidelines for design and implementation of ALS clinical trials. Neurology 92:e1610–e1623CrossRef
10.
go back to reference Cedarbaum JM, Stambler N, Malta E, Fuller C, Hilt D, Thurmond B et al (1999) The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III). J Neurol Sci 169:13–21CrossRef Cedarbaum JM, Stambler N, Malta E, Fuller C, Hilt D, Thurmond B et al (1999) The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III). J Neurol Sci 169:13–21CrossRef
11.
go back to reference Magnus T, Beck M, Giess R, Puls I, Naumann M, Toyka KV (2002) Disease progression in amyotrophic lateral sclerosis: predictors of survival. Muscle Nerve 25:709–714CrossRef Magnus T, Beck M, Giess R, Puls I, Naumann M, Toyka KV (2002) Disease progression in amyotrophic lateral sclerosis: predictors of survival. Muscle Nerve 25:709–714CrossRef
12.
go back to reference Kaufmann P, Levy G, Thompson JL, Delbene ML, Battista V, Gordon PH et al (2005) The ALSFRS-R predicts survival time in an ALS clinic population. Neurology 64:38–43CrossRef Kaufmann P, Levy G, Thompson JL, Delbene ML, Battista V, Gordon PH et al (2005) The ALSFRS-R predicts survival time in an ALS clinic population. Neurology 64:38–43CrossRef
13.
go back to reference Kimura F, Fujimura C, Ishida S, Nakajima H, Furutama D, Uehara H et al (2006) Progression rate of ALSFRS-R at time of diagnosis predicts survival time in ALS. Neurology 66:265–267CrossRef Kimura F, Fujimura C, Ishida S, Nakajima H, Furutama D, Uehara H et al (2006) Progression rate of ALSFRS-R at time of diagnosis predicts survival time in ALS. Neurology 66:265–267CrossRef
14.
go back to reference Corcia P, Pradat PF, Salachas F, Bruneteau G, Le Forestier N, Seilhean D et al (2008) Causes of death in a post-mortem series of ALS patients. Amyotroph Lateral Scler 9:59–62CrossRef Corcia P, Pradat PF, Salachas F, Bruneteau G, Le Forestier N, Seilhean D et al (2008) Causes of death in a post-mortem series of ALS patients. Amyotroph Lateral Scler 9:59–62CrossRef
15.
go back to reference Miller RG, Jackson CE, Kasarskis EJ, England JD, Forshew D, Johnston W et al (2009) Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology 73:1218–1226CrossRef Miller RG, Jackson CE, Kasarskis EJ, England JD, Forshew D, Johnston W et al (2009) Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology 73:1218–1226CrossRef
16.
go back to reference EFNS Task Force on Diagnosis and Management of Amyotrophic Lateral Sclerosis, Andersen PM, Abrahams S, Borasio GD, de Carvalho M, Chio A, Van Damme P et al (2012) EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)—revised report of an EFNS task force. Eur J Neurol 19:360–375 EFNS Task Force on Diagnosis and Management of Amyotrophic Lateral Sclerosis, Andersen PM, Abrahams S, Borasio GD, de Carvalho M, Chio A, Van Damme P et al (2012) EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)—revised report of an EFNS task force. Eur J Neurol 19:360–375
17.
go back to reference Fallat RJ, Jewitt B, Bass M, Kamm B, Norris F (1979) Spirometry in amyotrophic lateral sclerosis. Arch Neurol 36:74–80CrossRef Fallat RJ, Jewitt B, Bass M, Kamm B, Norris F (1979) Spirometry in amyotrophic lateral sclerosis. Arch Neurol 36:74–80CrossRef
18.
go back to reference Traynor BJ, Zhang H, Shefner JM, Schoenfeld D, Cudkowicz ME (2004) Functional outcome measures as clinical trial endpoints in ALS. Neurology 63:1933–1935CrossRef Traynor BJ, Zhang H, Shefner JM, Schoenfeld D, Cudkowicz ME (2004) Functional outcome measures as clinical trial endpoints in ALS. Neurology 63:1933–1935CrossRef
19.
go back to reference Baumann F, Henderson RD, Morrison SC, Brown M, Hutchinson N, Douglas JA et al (2010) Use of respiratory function tests to predict survival in amyotrophic lateral sclerosis. Amyotroph Lateral Scler 11:194–202CrossRef Baumann F, Henderson RD, Morrison SC, Brown M, Hutchinson N, Douglas JA et al (2010) Use of respiratory function tests to predict survival in amyotrophic lateral sclerosis. Amyotroph Lateral Scler 11:194–202CrossRef
20.
go back to reference Schiffman PL, Belsh JM (1993) Pulmonary function at diagnosis of amyotrophic lateral sclerosis: rate of deterioration. Chest 103:508–513CrossRef Schiffman PL, Belsh JM (1993) Pulmonary function at diagnosis of amyotrophic lateral sclerosis: rate of deterioration. Chest 103:508–513CrossRef
21.
go back to reference Czaplinski A, Yen AA, Appel SH (2006) Forced vital capacity (FVC) as an indicator of survival and disease progression in an ALS clinic population. J Neurol Neurosurg Psychiatry 77:390–392CrossRef Czaplinski A, Yen AA, Appel SH (2006) Forced vital capacity (FVC) as an indicator of survival and disease progression in an ALS clinic population. J Neurol Neurosurg Psychiatry 77:390–392CrossRef
22.
go back to reference Westeneng HJ, Debray TPA, Visser AE et al (2018) Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model. Lancet Neurol 17:423–433CrossRef Westeneng HJ, Debray TPA, Visser AE et al (2018) Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model. Lancet Neurol 17:423–433CrossRef
23.
go back to reference Pinto S, de Carvalho M (2014) Breathing new life into treatment advances for respiratory failure in amyotrophic lateral sclerosis patients. Neurodegener Dis Manag 4:83–102CrossRef Pinto S, de Carvalho M (2014) Breathing new life into treatment advances for respiratory failure in amyotrophic lateral sclerosis patients. Neurodegener Dis Manag 4:83–102CrossRef
24.
go back to reference Pinto S, Pinto A, Atalaia A, Peralta R, De Carvalho M (2007) Respiratory apraxia in amyotrophic lateral sclerosis. Amyotroph Lateral Scler 8:180–184CrossRef Pinto S, Pinto A, Atalaia A, Peralta R, De Carvalho M (2007) Respiratory apraxia in amyotrophic lateral sclerosis. Amyotroph Lateral Scler 8:180–184CrossRef
25.
go back to reference Evangelista T, de Carvalho M, Pinto A, Sales-Luis ML (1995) Phrenic nerve conduction in amyotrophic lateral sclerosis. J Neurol Sci 129:35–37CrossRef Evangelista T, de Carvalho M, Pinto A, Sales-Luis ML (1995) Phrenic nerve conduction in amyotrophic lateral sclerosis. J Neurol Sci 129:35–37CrossRef
26.
go back to reference de Carvalho M, Pinto S, Swash M (2018) Diaphragm motor responses to phrenic nerve stimulation in ALS: surface and needle recordings. Clin Neurophysiol 129:349–353CrossRef de Carvalho M, Pinto S, Swash M (2018) Diaphragm motor responses to phrenic nerve stimulation in ALS: surface and needle recordings. Clin Neurophysiol 129:349–353CrossRef
27.
go back to reference Pinto S, Geraldes R, Vaz N, Pinto A, de Carvalho M (2009) Changes of the phrenic nerve motor response in amyotrophic lateral sclerosis: longitudinal study. Clin Neurophysiol 120:2082–2085CrossRef Pinto S, Geraldes R, Vaz N, Pinto A, de Carvalho M (2009) Changes of the phrenic nerve motor response in amyotrophic lateral sclerosis: longitudinal study. Clin Neurophysiol 120:2082–2085CrossRef
28.
go back to reference Pinto S, Pinto A, de Carvalho M (2012) Phrenic nerve studies predict survival in amyotrophic lateral sclerosis. Clin Neurophysiol 123:2454–2459CrossRef Pinto S, Pinto A, de Carvalho M (2012) Phrenic nerve studies predict survival in amyotrophic lateral sclerosis. Clin Neurophysiol 123:2454–2459CrossRef
29.
go back to reference Pinto S, Turkman A, Pinto A, Swash M, de Carvalho M (2009) Predicting respiratory insufficiency in amyotrophic lateral sclerosis: the role of phrenic nerve studies. Clin Neurophysiol 120:941–946CrossRef Pinto S, Turkman A, Pinto A, Swash M, de Carvalho M (2009) Predicting respiratory insufficiency in amyotrophic lateral sclerosis: the role of phrenic nerve studies. Clin Neurophysiol 120:941–946CrossRef
30.
go back to reference de Carvalho M, Swash M, Pinto S (2019) Diaphragmatic neurophysiology and respiratory markers in ALS. Front Neurol 10:143CrossRef de Carvalho M, Swash M, Pinto S (2019) Diaphragmatic neurophysiology and respiratory markers in ALS. Front Neurol 10:143CrossRef
31.
go back to reference Brooks BR, Miller RG, Swash M, Munsat TL, World Federation of Neurology Research Group on Motor Neuron Diseases (2000) El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord 1:293–299 Brooks BR, Miller RG, Swash M, Munsat TL, World Federation of Neurology Research Group on Motor Neuron Diseases (2000) El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord 1:293–299
32.
go back to reference de Carvalho M, Dengler R, Eisen A, England JD, Kaji R, Kimura J et al (2008) Electrodiagnostic criteria for diagnosis of ALS. Clin Neurophysiol 119:497–503CrossRef de Carvalho M, Dengler R, Eisen A, England JD, Kaji R, Kimura J et al (2008) Electrodiagnostic criteria for diagnosis of ALS. Clin Neurophysiol 119:497–503CrossRef
33.
go back to reference Pinto S, de Carvalho M (2010) Symmetry of phrenic nerve motor response in amyotrophic lateral sclerosis. Muscle Nerve 42:882–884CrossRef Pinto S, de Carvalho M (2010) Symmetry of phrenic nerve motor response in amyotrophic lateral sclerosis. Muscle Nerve 42:882–884CrossRef
34.
go back to reference Pinto S, de Carvalho M (2017) Comparison of slow and forced vital capacities on ability to predict survival in ALS. Amyotroph Lateral Scler Frontotemporal Degener 18:528–533CrossRef Pinto S, de Carvalho M (2017) Comparison of slow and forced vital capacities on ability to predict survival in ALS. Amyotroph Lateral Scler Frontotemporal Degener 18:528–533CrossRef
35.
go back to reference Abe K, Aoki M, Tsuji S, Itoyama Y, Sobue G, Togo M et al (2017) Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial. Lancet Neurol 16:505–512CrossRef Abe K, Aoki M, Tsuji S, Itoyama Y, Sobue G, Togo M et al (2017) Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial. Lancet Neurol 16:505–512CrossRef
37.
go back to reference Lyall RA, Donaldson N, Polkey MI, Leigh PN, Moxham J (2001) Respiratory muscle strength and ventilatory failure in amyotrophic lateral sclerosis. Brain 124:2000–2013CrossRef Lyall RA, Donaldson N, Polkey MI, Leigh PN, Moxham J (2001) Respiratory muscle strength and ventilatory failure in amyotrophic lateral sclerosis. Brain 124:2000–2013CrossRef
38.
go back to reference Torrieri MC, Miranda B, Gromicho M, Pinto S, de Carvalho M (2020) Reliability of phrenic nerve conduction study: In healthy controls and in patients with primary lateral sclerosis. Clin Neurophysiol 131:994–999CrossRef Torrieri MC, Miranda B, Gromicho M, Pinto S, de Carvalho M (2020) Reliability of phrenic nerve conduction study: In healthy controls and in patients with primary lateral sclerosis. Clin Neurophysiol 131:994–999CrossRef
39.
go back to reference de Carvalho M, Chio A, Dengler R, Hecht M, Weber M, Swash M (2005) Neurophysiological measures in amyotrophic lateral sclerosis: markers of progression in clinical trials. Amyotroph Lateral Scler 6:17–28CrossRef de Carvalho M, Chio A, Dengler R, Hecht M, Weber M, Swash M (2005) Neurophysiological measures in amyotrophic lateral sclerosis: markers of progression in clinical trials. Amyotroph Lateral Scler 6:17–28CrossRef
Metadata
Title
Diaphragmatic CMAP amplitude from phrenic nerve stimulation predicts functional decline in ALS
Authors
Bruno Miranda
Marta Gromicho
Mariana Pereira
Susana Pinto
Michael Swash
Mamede de Carvalho
Publication date
01-07-2020
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 7/2020
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-020-09818-z

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