Cargando…
Baseline low ALT activity is associated with increased long-term mortality after COPD exacerbations
BACKGROUND: COPD exacerbations have negative impact on patients’ survival. Several risk factors for grave outcomes of such exacerbations have been descried. Muscle dysfunction and mass loss were shown to impact negatively on prognosis and survival. Low activity of the enzyme ALT (Alanine amino-trans...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216624/ https://www.ncbi.nlm.nih.gov/pubmed/32393221 http://dx.doi.org/10.1186/s12890-020-1169-z |
_version_ | 1783532450104737792 |
---|---|
author | Lasman, N. Shalom, M. Turpashvili, N. Goldhaber, G. Lifshitz, Y. Leibowitz, E. Berger, G. Saltzman-Shenhav, G. Brom, A. Cohen, D. Avaky, C. Segal, G. |
author_facet | Lasman, N. Shalom, M. Turpashvili, N. Goldhaber, G. Lifshitz, Y. Leibowitz, E. Berger, G. Saltzman-Shenhav, G. Brom, A. Cohen, D. Avaky, C. Segal, G. |
author_sort | Lasman, N. |
collection | PubMed |
description | BACKGROUND: COPD exacerbations have negative impact on patients’ survival. Several risk factors for grave outcomes of such exacerbations have been descried. Muscle dysfunction and mass loss were shown to impact negatively on prognosis and survival. Low activity of the enzyme ALT (Alanine amino-transferase) in the blood is a known indicator for sarcopenia and frailty, however, no previous studies addressed the association of low ALT amongst patients hospitalized due to COPD exacerbation and long-term survival. METHODS: This is a historic prospective cohort study of patients hospitalized due to acute COPD exacerbation. RESULTS: Included were 232 consecutive COPD exacerbation patients. The median time of follow-up was 34.9 months (IQR 23.13–41.73 months). During this period 104 (44.8%) patients died. All patients were grouped to quartiles according to blood ALT levels (after exclusion of cases considered to have hepatic tissue damage (ALT > 40 IU)). The risk of long-term mortality increased, in a statistically significant manner, amongst patients with low ALT values: the median survival of patients with ALT < 11 IU was 18.5 months only while the median survival for the rest of the study group was not reached. For ALT < 11 IU; 12-16 IU; 17-20 IU and > 21 IU the mortality rates were 69%; 40.9%; 36.3 and 25% respectively (p < 0.001 for comparison of lower quartile with upper three quartiles). The crude hazard ratio for mortality amongst patients with ALT levels lower than 11 IU was 2.37 (95% CI; 1.6–3.5). This increased risk of mortality remained significant after adjustment for age, weight, creatinine, albumin concentration and cardiovascular diseases (HR = 1.83; 95% CI 1.08–3.1, p < 0.05). CONCLUSIONS: Low ALT values, a biomarker of sarcopenia and frailty, are associated with poor long-term survival amongst patients hospitalized due to COPD exacerbation. |
format | Online Article Text |
id | pubmed-7216624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72166242020-05-18 Baseline low ALT activity is associated with increased long-term mortality after COPD exacerbations Lasman, N. Shalom, M. Turpashvili, N. Goldhaber, G. Lifshitz, Y. Leibowitz, E. Berger, G. Saltzman-Shenhav, G. Brom, A. Cohen, D. Avaky, C. Segal, G. BMC Pulm Med Research Article BACKGROUND: COPD exacerbations have negative impact on patients’ survival. Several risk factors for grave outcomes of such exacerbations have been descried. Muscle dysfunction and mass loss were shown to impact negatively on prognosis and survival. Low activity of the enzyme ALT (Alanine amino-transferase) in the blood is a known indicator for sarcopenia and frailty, however, no previous studies addressed the association of low ALT amongst patients hospitalized due to COPD exacerbation and long-term survival. METHODS: This is a historic prospective cohort study of patients hospitalized due to acute COPD exacerbation. RESULTS: Included were 232 consecutive COPD exacerbation patients. The median time of follow-up was 34.9 months (IQR 23.13–41.73 months). During this period 104 (44.8%) patients died. All patients were grouped to quartiles according to blood ALT levels (after exclusion of cases considered to have hepatic tissue damage (ALT > 40 IU)). The risk of long-term mortality increased, in a statistically significant manner, amongst patients with low ALT values: the median survival of patients with ALT < 11 IU was 18.5 months only while the median survival for the rest of the study group was not reached. For ALT < 11 IU; 12-16 IU; 17-20 IU and > 21 IU the mortality rates were 69%; 40.9%; 36.3 and 25% respectively (p < 0.001 for comparison of lower quartile with upper three quartiles). The crude hazard ratio for mortality amongst patients with ALT levels lower than 11 IU was 2.37 (95% CI; 1.6–3.5). This increased risk of mortality remained significant after adjustment for age, weight, creatinine, albumin concentration and cardiovascular diseases (HR = 1.83; 95% CI 1.08–3.1, p < 0.05). CONCLUSIONS: Low ALT values, a biomarker of sarcopenia and frailty, are associated with poor long-term survival amongst patients hospitalized due to COPD exacerbation. BioMed Central 2020-05-11 /pmc/articles/PMC7216624/ /pubmed/32393221 http://dx.doi.org/10.1186/s12890-020-1169-z Text en © The Author(s). 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Lasman, N. Shalom, M. Turpashvili, N. Goldhaber, G. Lifshitz, Y. Leibowitz, E. Berger, G. Saltzman-Shenhav, G. Brom, A. Cohen, D. Avaky, C. Segal, G. Baseline low ALT activity is associated with increased long-term mortality after COPD exacerbations |
title | Baseline low ALT activity is associated with increased long-term mortality after COPD exacerbations |
title_full | Baseline low ALT activity is associated with increased long-term mortality after COPD exacerbations |
title_fullStr | Baseline low ALT activity is associated with increased long-term mortality after COPD exacerbations |
title_full_unstemmed | Baseline low ALT activity is associated with increased long-term mortality after COPD exacerbations |
title_short | Baseline low ALT activity is associated with increased long-term mortality after COPD exacerbations |
title_sort | baseline low alt activity is associated with increased long-term mortality after copd exacerbations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216624/ https://www.ncbi.nlm.nih.gov/pubmed/32393221 http://dx.doi.org/10.1186/s12890-020-1169-z |
work_keys_str_mv | AT lasmann baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations AT shalomm baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations AT turpashvilin baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations AT goldhaberg baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations AT lifshitzy baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations AT leibowitze baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations AT bergerg baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations AT saltzmanshenhavg baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations AT broma baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations AT cohend baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations AT avakyc baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations AT segalg baselinelowaltactivityisassociatedwithincreasedlongtermmortalityaftercopdexacerbations |