Effects of Body Position on Respiratory Pressure and Muscle Activity in Amyotrophic Lateral Sclerosis and Healthy Subjects.

Background: Amyotrophic lateral sclerosis (ALS) is a fatal heterogeneous neurodegenerative disease characterized by the degeneration of both upper and lower motor neurons and spinal cord. Measurement of respiratory muscle strength has been shown to be an important assessment in the decision-making p...

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Publicado en:Respiratory Care Vol. 71; no. 3; pp. 307 - 315
Autores principales: Maciel, Ana Cristina de Medeiros Garcia, da Silva, Ana Aline Marcelino, Medeiros da Fonseca, Jéssica Danielle, Vieira, Rayane Grayce da Silva, da Silva, Lailane Saturnino, Lima, Thiago Bezerra Wanderley e, Pondofe, Karen de Medeiros, Otto-Yáñez, Matías, Torres-Castro, Rodrigo, Vera-Uribe, Roberto, Vilaró, Jordi, Dourado Junior, Mario Emilio Teixeira, Resqueti, Vanessa Regiane, Fregonezi, Guilherme Augusto de Freitas
Formato: research tables/charts Journal Article
Publicado: Mary Ann Liebert, Inc. Mar2026
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Mar2026
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      pub: Mary Ann Liebert, Inc.
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        atl: Effects of Body Position on Respiratory Pressure and Muscle Activity in Amyotrophic Lateral Sclerosis and Healthy Subjects.
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        au:
          Maciel, Ana Cristina de Medeiros Garcia
          da Silva, Ana Aline Marcelino
          Medeiros da Fonseca, Jéssica Danielle
          Vieira, Rayane Grayce da Silva
          da Silva, Lailane Saturnino
          Lima, Thiago Bezerra Wanderley e
          Pondofe, Karen de Medeiros
          Otto-Yáñez, Matías
          Torres-Castro, Rodrigo
          Vera-Uribe, Roberto
          Vilaró, Jordi
          Dourado Junior, Mario Emilio Teixeira
          Resqueti, Vanessa Regiane
          Fregonezi, Guilherme Augusto de Freitas
        affil: Ms. Maciel, Ms. da Silva, Dr. da Fonseca, Ms. da Silva Vieira, Ms. da Silva, Ms. Lima, Dr. Pondofe, Dr. Resqueti, and Dr. Fregonezi are affiliated with the Pneumocardiovascular Lab/HUOL and the Laboratório de Inovação Tecnológica em Reabilitação, Departamento de Fisioterapia, Universidade Federal do Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
      sug:
        subj:
          Amyotrophic Lateral Sclerosis Physiopathology
          Respiratory Muscles Physiopathology
          Muscle Strength Evaluation
          Body Positions
          Peak Expiratory Flow Rate Methods
          Human
          Case Control Studies
          Spirometry
          Electromyography
          Respiratory Function Tests
          Functional Assessment
          Data Analysis Software
          Descriptive Statistics
          Wilcoxon Rank Sum Test
          Paired T-Tests
          Funding Source
      ab: Background: Amyotrophic lateral sclerosis (ALS) is a fatal heterogeneous neurodegenerative disease characterized by the degeneration of both upper and lower motor neurons and spinal cord. Measurement of respiratory muscle strength has been shown to be an important assessment in the decision-making process and can be assessed by maximum inspiratory (PImax) and expiratory pressures (PEmax), sniff nasal inspiratory (SNIP) and expiratory (SNEP) pressures. Body position appears to have a significant effect on respiratory muscle strength. The aim of this study was to observe the difference in peak values of SNIP and SNEP of the respiratory muscles measured in 2 different positions (seated and supine with 45° elevation) in subjects with ALS and a group of matched healthy subjects. Methods: This is a case–control study of subjects with ALS and healthy subjects. Spirometry and surface electromyography (EMG) of the sternocleidomastoid, scalene, rectus abdominis, and external oblique muscles were assessed during PImax and PEmax maneuvers in the seated position, and SNIP and SNEP in the seated and supine positions at 45° elevation (randomized). Results: SNEP values in the 45° elevation were lower than in the sitting position in ALS (70.3 ± 26.7 vs 57.3 ± 22.8 cm H2O, P =.041). SNIP and SNEP were lower in ALS in the 45° elevation compared with healthy subjects (69.1 ± 27.2 vs 95.5 ± 23.5 cm H2O; 57.3 ± 22.5 vs 92.7 ± 26.4 cm H2O, P =.041). In subjects with ALS, baseline electromyographic activity of the sternocleidomastoid muscle at rest was higher than in healthy subjects in both positions (P =.041). No significant differences in electrical activity were found for other variables and measurements. Conclusions: In ALS, nasal pressure may be affected by reduced diaphragm and abdominal muscle effectiveness in the supine position. The sternocleidomastoid muscle showed increased electrical activity in the supine position with 45° elevation compared with controls, which may indicate muscle weakness.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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