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Relation of respiratory muscle strength, cachexia and survival in severe chronic heart failure
BACKGROUND: Respiratory muscle (RM) function predicts prognosis in non-cachectic patients with chronic heart failure (CHF). We hypothesized that weakness of RM (maximum inspiratory mouth occlusion pressure, Pi(max)) is a function of body mass index, and that outcome is more a function of BMI than of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830005/ https://www.ncbi.nlm.nih.gov/pubmed/23794292 http://dx.doi.org/10.1007/s13539-013-0109-7 |
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author | Habedank, Dirk Meyer, F. Joachim Hetzer, Roland Anker, Stefan D. Ewert, Ralf |
author_facet | Habedank, Dirk Meyer, F. Joachim Hetzer, Roland Anker, Stefan D. Ewert, Ralf |
author_sort | Habedank, Dirk |
collection | PubMed |
description | BACKGROUND: Respiratory muscle (RM) function predicts prognosis in non-cachectic patients with chronic heart failure (CHF). We hypothesized that weakness of RM (maximum inspiratory mouth occlusion pressure, Pi(max)) is a function of body mass index, and that outcome is more a function of BMI than of Pi(max) or ventilatory drive (P0.1). SUBJECTS AND METHODS: We enrolled 249 CHF patients (11.2 % female, median age 54.2 years) at the German Heart Institute Berlin. Patients were in NYHA classes I/II/III/IV by n = 16/90/108/35. All patients underwent tests of pulmonary function, RM (Pi(max), P0.1), cardiopulmonary exercise testing (peakVO2, VE/VCO2-slope), and right heart catheterization. RESULTS: Mean follow-up time was 18 (1–36) months, 47 patients (18.9 %) died or underwent cardiac assist implantation. Pi(max) correlated weakly with BMI (r = 0.19), peakVO2 (r = 0.15), and FEV1 (r = 0.34, all p < 0.02), and was lower in females compared to males (3.9 ± 1.7 vs. 6.6 ± 2.7 kPa; p < 0.001). P0.1 correlated with pulmonary pressure (rho = 0.2; p < 0.01) and peakVO2 (rho = −0.14; p < 0.02). Neither Pi(max) [hazard ratio (HR) 0.98; confidence interval (CI) 0.88–1.08] nor P0.1 (HR 0.52; 0.06–4.6) predicted survival. Multivariate regression analysis revealed gender, BMI, and FEV1 as cofactors of Pi(max), with only BMI (HR 0.87; CI 0.80–0.95) predicting survival independently. The lowest quintile in BMI had the worst outcome (log-rank χ² = 13.5, p = 0.009). SUMMARY: In CHF patients including cachexia and NYHA IV, Pi(max) does not predict survival. Pi(max) depends on gender, BMI, FEV1, and peakVO2, with only BMI and peakVO2 predicting survival. The impaired Pi(max) in CHF might be a result of catabolism and weight loss and is not a predictive factor in itself. |
format | Online Article Text |
id | pubmed-3830005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-38300052013-12-01 Relation of respiratory muscle strength, cachexia and survival in severe chronic heart failure Habedank, Dirk Meyer, F. Joachim Hetzer, Roland Anker, Stefan D. Ewert, Ralf J Cachexia Sarcopenia Muscle Original Article BACKGROUND: Respiratory muscle (RM) function predicts prognosis in non-cachectic patients with chronic heart failure (CHF). We hypothesized that weakness of RM (maximum inspiratory mouth occlusion pressure, Pi(max)) is a function of body mass index, and that outcome is more a function of BMI than of Pi(max) or ventilatory drive (P0.1). SUBJECTS AND METHODS: We enrolled 249 CHF patients (11.2 % female, median age 54.2 years) at the German Heart Institute Berlin. Patients were in NYHA classes I/II/III/IV by n = 16/90/108/35. All patients underwent tests of pulmonary function, RM (Pi(max), P0.1), cardiopulmonary exercise testing (peakVO2, VE/VCO2-slope), and right heart catheterization. RESULTS: Mean follow-up time was 18 (1–36) months, 47 patients (18.9 %) died or underwent cardiac assist implantation. Pi(max) correlated weakly with BMI (r = 0.19), peakVO2 (r = 0.15), and FEV1 (r = 0.34, all p < 0.02), and was lower in females compared to males (3.9 ± 1.7 vs. 6.6 ± 2.7 kPa; p < 0.001). P0.1 correlated with pulmonary pressure (rho = 0.2; p < 0.01) and peakVO2 (rho = −0.14; p < 0.02). Neither Pi(max) [hazard ratio (HR) 0.98; confidence interval (CI) 0.88–1.08] nor P0.1 (HR 0.52; 0.06–4.6) predicted survival. Multivariate regression analysis revealed gender, BMI, and FEV1 as cofactors of Pi(max), with only BMI (HR 0.87; CI 0.80–0.95) predicting survival independently. The lowest quintile in BMI had the worst outcome (log-rank χ² = 13.5, p = 0.009). SUMMARY: In CHF patients including cachexia and NYHA IV, Pi(max) does not predict survival. Pi(max) depends on gender, BMI, FEV1, and peakVO2, with only BMI and peakVO2 predicting survival. The impaired Pi(max) in CHF might be a result of catabolism and weight loss and is not a predictive factor in itself. Springer Berlin Heidelberg 2013-06-21 2013-12 /pmc/articles/PMC3830005/ /pubmed/23794292 http://dx.doi.org/10.1007/s13539-013-0109-7 Text en © Springer-Verlag Berlin Heidelberg 2013 |
spellingShingle | Original Article Habedank, Dirk Meyer, F. Joachim Hetzer, Roland Anker, Stefan D. Ewert, Ralf Relation of respiratory muscle strength, cachexia and survival in severe chronic heart failure |
title | Relation of respiratory muscle strength, cachexia and survival in severe chronic heart failure |
title_full | Relation of respiratory muscle strength, cachexia and survival in severe chronic heart failure |
title_fullStr | Relation of respiratory muscle strength, cachexia and survival in severe chronic heart failure |
title_full_unstemmed | Relation of respiratory muscle strength, cachexia and survival in severe chronic heart failure |
title_short | Relation of respiratory muscle strength, cachexia and survival in severe chronic heart failure |
title_sort | relation of respiratory muscle strength, cachexia and survival in severe chronic heart failure |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830005/ https://www.ncbi.nlm.nih.gov/pubmed/23794292 http://dx.doi.org/10.1007/s13539-013-0109-7 |
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