Respiratory Muscle and Lung Function in Lung Allograft Recipients

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Respiratory Muscle and Lung Function in Lung Allograft Recipients : Association with Exercise Intolerance. / Spiesshoefer, Jens; Henke, Carolin; Kabitz, Hans Joachim; Nofer, Jerzy Roch; Mohr, Michael; Evers, Georg; Strecker, Jan-Kolia; Brix, Tobias; Randerath, Winfried Johannes; Herkenrath, Simon; Schmidt, Lars Henning; Boentert, Matthias.

In: RESPIRATION, Vol. 99, No. 5, 14.05.2020, p. 398-408.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Spiesshoefer, J, Henke, C, Kabitz, HJ, Nofer, JR, Mohr, M, Evers, G, Strecker, J-K, Brix, T, Randerath, WJ, Herkenrath, S, Schmidt, LH & Boentert, M 2020, 'Respiratory Muscle and Lung Function in Lung Allograft Recipients: Association with Exercise Intolerance', RESPIRATION, vol. 99, no. 5, pp. 398-408. https://doi.org/10.1159/000507264

APA

Spiesshoefer, J., Henke, C., Kabitz, H. J., Nofer, J. R., Mohr, M., Evers, G., Strecker, J-K., Brix, T., Randerath, W. J., Herkenrath, S., Schmidt, L. H., & Boentert, M. (2020). Respiratory Muscle and Lung Function in Lung Allograft Recipients: Association with Exercise Intolerance. RESPIRATION, 99(5), 398-408. https://doi.org/10.1159/000507264

Vancouver

Spiesshoefer J, Henke C, Kabitz HJ, Nofer JR, Mohr M, Evers G et al. Respiratory Muscle and Lung Function in Lung Allograft Recipients: Association with Exercise Intolerance. RESPIRATION. 2020 May 14;99(5):398-408. https://doi.org/10.1159/000507264

Bibtex

@article{5ee8669ec19a4d4ca947782dd4c23b49,
title = "Respiratory Muscle and Lung Function in Lung Allograft Recipients: Association with Exercise Intolerance",
abstract = "BACKGROUND: In lung transplant recipients (LTRs), restrictive ventilation disorder may be present due to respiratory muscle dysfunction that may reduce exercise capacity. This might be mediated by pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6).OBJECTIVE: We investigated lung respiratory muscle function as well as circulating pro-inflammatory cytokines and exercise capacity in LTRs.METHODS: Fifteen LTRs (6 female, age 56 ± 14 years, 63 ± 45 months post-transplantation) and 15 healthy controls matched for age, sex, and body mass index underwent spirometry, measurement of mouth occlusion pressures, diaphragm ultrasound, and recording of twitch transdiaphragmatic (twPdi) and gastric pressures (twPgas) following magnetic stimulation of the phrenic nerves and the lower thoracic nerve roots. Exercise capacity was quantified using the 6-min walking distance (6MWD). Plasma IL-6 and TNF-α were measured using enzyme-linked immunosorbent assays.RESULTS: Compared with controls, patients had lower values for forced vital capacity (FVC; 81 ± 30 vs.109 ± 18% predicted, p = 0.01), maximum expiratory pressure (100 ± 21 vs.127 ± 17 cm H2O, p = 0.04), diaphragm thickening ratio (2.2 ± 0.4 vs. 3.0 ± 1.1, p = 0.01), and twPdi (10.4 ± 3.5 vs. 17.6 ± 6.7 cm H2O, p = 0.01). In LTRs, elevation of TNF-α was related to lung function (13 ± 3 vs. 11 ± 2 pg/mL in patients with FVC ≤80 vs. >80% predicted; p < 0.05), and lung function (forced expiratory volume after 1 s) was closely associated with diaphragm thickening ratio (r = 0.81; p < 0.01) and 6MWD (r = 0.63; p = 0.02).CONCLUSION: There is marked restrictive ventilation disorder and respiratory muscle weakness in LTRs, especially inspiratory muscle weakness with diaphragm dysfunction. Lung function impairment relates to elevated levels of circulating TNF-α and diaphragm dysfunction and is associated with exercise intolerance.",
author = "Jens Spiesshoefer and Carolin Henke and Kabitz, {Hans Joachim} and Nofer, {Jerzy Roch} and Michael Mohr and Georg Evers and Jan-Kolia Strecker and Tobias Brix and Randerath, {Winfried Johannes} and Simon Herkenrath and Schmidt, {Lars Henning} and Matthias Boentert",
note = "{\textcopyright} 2020 S. Karger AG, Basel.",
year = "2020",
month = may,
day = "14",
doi = "10.1159/000507264",
language = "English",
volume = "99",
pages = "398--408",
journal = "RESPIRATION",
issn = "0025-7931",
publisher = "S. Karger AG",
number = "5",

}

RIS

TY - JOUR

T1 - Respiratory Muscle and Lung Function in Lung Allograft Recipients

T2 - Association with Exercise Intolerance

AU - Spiesshoefer, Jens

AU - Henke, Carolin

AU - Kabitz, Hans Joachim

AU - Nofer, Jerzy Roch

AU - Mohr, Michael

AU - Evers, Georg

AU - Strecker, Jan-Kolia

AU - Brix, Tobias

AU - Randerath, Winfried Johannes

AU - Herkenrath, Simon

AU - Schmidt, Lars Henning

AU - Boentert, Matthias

N1 - © 2020 S. Karger AG, Basel.

PY - 2020/5/14

Y1 - 2020/5/14

N2 - BACKGROUND: In lung transplant recipients (LTRs), restrictive ventilation disorder may be present due to respiratory muscle dysfunction that may reduce exercise capacity. This might be mediated by pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6).OBJECTIVE: We investigated lung respiratory muscle function as well as circulating pro-inflammatory cytokines and exercise capacity in LTRs.METHODS: Fifteen LTRs (6 female, age 56 ± 14 years, 63 ± 45 months post-transplantation) and 15 healthy controls matched for age, sex, and body mass index underwent spirometry, measurement of mouth occlusion pressures, diaphragm ultrasound, and recording of twitch transdiaphragmatic (twPdi) and gastric pressures (twPgas) following magnetic stimulation of the phrenic nerves and the lower thoracic nerve roots. Exercise capacity was quantified using the 6-min walking distance (6MWD). Plasma IL-6 and TNF-α were measured using enzyme-linked immunosorbent assays.RESULTS: Compared with controls, patients had lower values for forced vital capacity (FVC; 81 ± 30 vs.109 ± 18% predicted, p = 0.01), maximum expiratory pressure (100 ± 21 vs.127 ± 17 cm H2O, p = 0.04), diaphragm thickening ratio (2.2 ± 0.4 vs. 3.0 ± 1.1, p = 0.01), and twPdi (10.4 ± 3.5 vs. 17.6 ± 6.7 cm H2O, p = 0.01). In LTRs, elevation of TNF-α was related to lung function (13 ± 3 vs. 11 ± 2 pg/mL in patients with FVC ≤80 vs. >80% predicted; p < 0.05), and lung function (forced expiratory volume after 1 s) was closely associated with diaphragm thickening ratio (r = 0.81; p < 0.01) and 6MWD (r = 0.63; p = 0.02).CONCLUSION: There is marked restrictive ventilation disorder and respiratory muscle weakness in LTRs, especially inspiratory muscle weakness with diaphragm dysfunction. Lung function impairment relates to elevated levels of circulating TNF-α and diaphragm dysfunction and is associated with exercise intolerance.

AB - BACKGROUND: In lung transplant recipients (LTRs), restrictive ventilation disorder may be present due to respiratory muscle dysfunction that may reduce exercise capacity. This might be mediated by pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6).OBJECTIVE: We investigated lung respiratory muscle function as well as circulating pro-inflammatory cytokines and exercise capacity in LTRs.METHODS: Fifteen LTRs (6 female, age 56 ± 14 years, 63 ± 45 months post-transplantation) and 15 healthy controls matched for age, sex, and body mass index underwent spirometry, measurement of mouth occlusion pressures, diaphragm ultrasound, and recording of twitch transdiaphragmatic (twPdi) and gastric pressures (twPgas) following magnetic stimulation of the phrenic nerves and the lower thoracic nerve roots. Exercise capacity was quantified using the 6-min walking distance (6MWD). Plasma IL-6 and TNF-α were measured using enzyme-linked immunosorbent assays.RESULTS: Compared with controls, patients had lower values for forced vital capacity (FVC; 81 ± 30 vs.109 ± 18% predicted, p = 0.01), maximum expiratory pressure (100 ± 21 vs.127 ± 17 cm H2O, p = 0.04), diaphragm thickening ratio (2.2 ± 0.4 vs. 3.0 ± 1.1, p = 0.01), and twPdi (10.4 ± 3.5 vs. 17.6 ± 6.7 cm H2O, p = 0.01). In LTRs, elevation of TNF-α was related to lung function (13 ± 3 vs. 11 ± 2 pg/mL in patients with FVC ≤80 vs. >80% predicted; p < 0.05), and lung function (forced expiratory volume after 1 s) was closely associated with diaphragm thickening ratio (r = 0.81; p < 0.01) and 6MWD (r = 0.63; p = 0.02).CONCLUSION: There is marked restrictive ventilation disorder and respiratory muscle weakness in LTRs, especially inspiratory muscle weakness with diaphragm dysfunction. Lung function impairment relates to elevated levels of circulating TNF-α and diaphragm dysfunction and is associated with exercise intolerance.

U2 - 10.1159/000507264

DO - 10.1159/000507264

M3 - SCORING: Journal article

C2 - 32403109

VL - 99

SP - 398

EP - 408

JO - RESPIRATION

JF - RESPIRATION

SN - 0025-7931

IS - 5

ER -