Emphysema and extrapulmonary tissue loss in COPD: a multi-organ loss of tissue phenotype

被引:61
作者
Celli, Bartolome R. [1 ,2 ]
Locantore, Nicholas [3 ]
Tal-Singer, Ruth [3 ]
Riley, John [4 ]
Miller, Bruce [3 ]
Vestbo, Jorgen [5 ,6 ,7 ]
Yates, Julie C. [8 ]
Silverman, Edwin K. [1 ,2 ]
Owen, Caroline A. [1 ,2 ]
Divo, Miguel [1 ,2 ]
Pinto-Plata, Victor [9 ]
Wouters, Emiel F. M. [10 ]
Faner, Rosa [11 ]
Agusti, Alvar [11 ,12 ]
机构
[1] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA USA
[3] GSK Res & Dev, King Of Prussia, PA USA
[4] GSK Res & Dev, Stevenage, Herts, England
[5] Odense Univ Hosp, Dept Resp Med, Odense, Denmark
[6] Univ Southern Denmark, Inst Clin, Odense, Denmark
[7] Univ Hosp South Manchester NHS Fdn Trust, Manchester Acad Hlth Sci Ctr, Translat Med, Manchester, Lancs, England
[8] GSK Res & Dev, Res Triangle Pk, NC USA
[9] Baystate Med Ctr, Pulm & Crit Care Med Div, Springfield, MA USA
[10] Maastricht Univ, Dept Resp Med, Med Ctr, Maastricht, Netherlands
[11] CIBER Enfermedades Resp CIBERES, Madrid, Spain
[12] Univ Barcelona, Resp Inst, Hosp Clin, IDIBAPS, Barcelona, Spain
关键词
OBSTRUCTIVE PULMONARY-DISEASE; LUNG-DISEASE; COMORBIDITIES; PROGRESSION; BIOMARKER; NETWORK; ECLIPSE; PROTEIN; COHORT; CT;
D O I
10.1183/13993003.02146-2017
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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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页数:10
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