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Baseline characteristics from a 3-year longitudinal study to phenotype subjects with COPD: the FOOTPRINTS study.
Crapo, James D; Gupta, Abhya; Lynch, David A; Turner, Alice M; Mroz, Robert M; Janssens, Wim; Ludwig-Sengpiel, Andrea; Koegler, Harald; Eleftheraki, Anastasia; Risse, Frank; Diefenbach, Claudia.
Afiliação
  • Crapo JD; Department of Medicine, National Jewish Health, Denver, CO, USA. crapoj@njhealth.org.
  • Gupta A; TA Inflammation Medicine, Boehringer Ingelheim International GmbH, Biberach an Der Riss, Germany.
  • Lynch DA; Department of Radiology, National Jewish Health, Denver, CO, USA.
  • Turner AM; Institute of Applied Health Research, University of Birmingham, Birmingham, UK.
  • Mroz RM; 2nd Department of Lung Diseases and Tuberculosis, Bialystok Medical University, Bialystok, Poland.
  • Janssens W; Department of Chronic Diseases and Metabolism (CHROMETA), Laboratory of Respiratory Diseases and Thoracic Surgery (BREATH), University Hospital Leuven, Louvain, KU, Belgium.
  • Ludwig-Sengpiel A; KLB Gesundheitsforschung Lübeck GmbH, Lübeck, Germany.
  • Koegler H; TA Inflammation Medicine, Boehringer Ingelheim International GmbH, Ingelheim, Germany.
  • Eleftheraki A; Department of Translational Medicine and Clinical Pharmacology, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an Der Riss, Germany.
  • Risse F; Department of Translational Medicine and Clinical Pharmacology, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an Der Riss, Germany.
  • Diefenbach C; Department of Translational Medicine and Clinical Pharmacology, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an Der Riss, Germany.
Respir Res ; 24(1): 290, 2023 Nov 17.
Article em En | MEDLINE | ID: mdl-37978492
ABSTRACT

BACKGROUND:

FOOTPRINTS® is a prospective, longitudinal, 3-year study assessing the association between biomarkers of inflammation/lung tissue destruction and chronic obstructive pulmonary disease (COPD) severity and progression in ex-smokers with mild-to-severe COPD. Here, we present baseline characteristics and select biomarkers of study subjects.

METHODS:

The methodology of FOOTPRINTS® has been published previously. The study population included ex-smokers with a range of COPD severities (Global Initiative for Chronic Obstructive Lung Disease [GOLD] stages 1-3), ex-smokers with COPD and alpha-1-antitrypsin deficiency (A1ATD) and a control group of ex-smokers without airflow limitation (EwAL). At study entry, data were collected for demographics, disease characteristics, history of comorbidities and COPD exacerbations, symptoms, lung function and volume, exercise capacity, soluble biomarkers, and quantitative and qualitative computed tomography. Baseline data are presented with descriptive statistical comparisons for soluble biomarkers in the individual GOLD and A1ATD groups versus EwAL.

RESULTS:

In total, 463 subjects were enrolled. The per-protocol set comprised 456 subjects, mostly male (64.5%). The mean (standard deviation) age was 60.7 (6.9) years. At baseline, increasing pulmonary symptoms, worse lung function, increased residual volume, reduced diffusing capacity of the lung for carbon monoxide (DLco) and greater prevalence of centrilobular emphysema were observed with increasing disease severity amongst GOLD 1-3 subjects. Subjects with A1ATD (n = 19) had similar lung function parameters to GOLD 2-3 subjects, a high residual volume comparable to GOLD 3 subjects, and similar air trapping to GOLD 2 subjects. Compared with EwAL (n = 61), subjects with A1ATD had worse lung function, increased residual volume, reduced DLco, and a greater prevalence of confluent or advanced destructive emphysema. The soluble inflammatory biomarkers white blood cell count, fibrinogen, high-sensitivity C-reactive protein and plasma surfactant protein were higher in GOLD 1-3 groups than in the EwAL group. Interleukin-6 was expressed less often in EwAL subjects compared with subjects in the GOLD and A1ATD groups. Soluble receptor for advanced glycation end product was lowest in GOLD 3 subjects, indicative of more severe emphysema.

CONCLUSIONS:

These findings provide context for upcoming results from FOOTPRINTS®, which aims to establish correlations between biomarkers and disease progression in a representative COPD population. TRIAL REGISTRATION NUMBER NCT02719184, study start date 13/04/2016.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Enfisema Pulmonar / Deficiência de alfa 1-Antitripsina / Doença Pulmonar Obstrutiva Crônica Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Enfisema Pulmonar / Deficiência de alfa 1-Antitripsina / Doença Pulmonar Obstrutiva Crônica Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article