| Title: | Emphysema and extrapulmonary tissue loss in COPD: a multi-organ loss of tissue phenotype |
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| Authors: | ID Celli, Bartolome R. (Author)
ID Locantore, Nicholas (Author)
ID Tal-Singer, Ruth (Author)
ID Riley, John (Author)
ID Vestbo, Jørgen (Author)
ID Yates, Julie C. (Author)
ID Miller, Bruce E. (Author)
ID Silverman, Edwin K (Author)
ID Owen, Caroline A. (Author)
ID Divo, Miguel (Author)
ID Košnik, Mitja (Associated name)
ID Košnik, Mitja (Research coworker) |
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| Files: |  URL - Source URL, visit http://erj.ersjournals.com/content/51/2/1702146
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| Language: | English |
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| Typology: | 1.01 - Original Scientific Article |
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| Organization: |  UKPBAG - University Clinic of Respiratory and Allergic Diseases Golnik
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| Abstract: | We tested whether emphysema progression accompanies enhanced tissue loss in other body compartments in 1817 patients from the ECLIPSE chronic obstructive pulmonary disease (COPD) cohort. Clinical and selected systemic biomarker measurements were compared in subjects grouped by quantitative tomography scan emphysema quartiles using the percentage of low attenuation area (LAA%). Lowest and highest quartile patients had amino-acid metabolomic profiles. We related LAA% to 3 years decline in lung function (forced expiratory volume in 1 s (FEV1)), body mass index (BMI), fat-free mass index (FFMI) and exacerbations, hospitalisations and mortality rates. Participants with more baseline emphysema had lower FEV1, BMI and FFMI, worse functional capacity, and less cardiovascular disease but more osteoporosis. Systemic C-reactive protein and interleukin-6 levels were similar among groups, but club cell protein 16 was higher and interleukin-8, surfactant protein D and soluble receptor for advanced glycation end product were lower with more emphysema. Metabolomics differed between extreme emphysema quartiles. Patients with more emphysema had accelerated FEV1, BMI and FFMI decline and more exacerbations, hospitalisations and mortality. COPD patients with more emphysema undergo excessive loss of pulmonary and extrapulmonary tissue, which is probably related to abnormal tissue maintenance. Because of worse clinical outcomes, we propose this subgroup be named the multi-organ loss of tissue (MOLT) COPD phenotype. |
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| Keywords: | COPD, chronic obstructive pulmonary disease, emphysema |
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| Publication status: | Published |
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| Publication version: | Version of Record |
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| Place of publishing: | Velika Britanija |
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| Publisher: | European Respiratory Society |
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| Year of publishing: | 2018 |
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| Number of pages: | str. 1-10 |
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| Numbering: | Vol. 51, iss. 2 |
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| PID: | 20.500.12556/DiRROS-12903  |
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| UDC: | 616.2 |
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| ISSN on article: | 1399-3003 |
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| DOI: | 10.1183/13993003.02146-2017 |
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| COBISS.SI-ID: | 2048254321 |
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| Copyright: | ©ERS 2018 |
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| Note: | Soavtorji: Nicholas Locantore, Ruth Tal-Singer, John Riley, Bruce Miller, Jørgen Vestbo, Julie C. Yates, Edwin K. Silverman, Caroline A. Owen, Miguel Divo, Victor Pinto-Plata, Emiel F. M. Wouters, Rosa Faner and Alvar Agusti, on behalf of the ECLIPSE Study Investigators;
Nasl. z nasl. zaslona;
Opis vira z dne 7. 3. 2018;
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| Publication date in DiRROS: | 14.12.2020 |
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| Views: | 1664 |
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| Downloads: | 476 |
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