Lipid plaque burden in NSTE-ACS patients with or without COPD: insights from the SCAP Trial.


Journal

Minerva cardiology and angiology
ISSN: 2724-5772
Titre abrégé: Minerva Cardiol Angiol
Pays: Italy
ID NLM: 101776555

Informations de publication

Date de publication:
12 2021
Historique:
pubmed: 2 12 2020
medline: 15 12 2021
entrez: 1 12 2020
Statut: ppublish

Résumé

Chronic obstructive pulmonary disease (COPD) patients have higher recurrence of adverse events and worse prognosis after acute coronary syndrome (ACS). The underlying pathophysiological mechanism is not fully elucidated. In screening for COPD in ACS (SCAP) Trial (NCT02324660), ACS patients with smoking habit underwent a predischarge screening procedure to detect undiagnosed chronic obstructive pulmonary disease (UCOPD) confirmed with spirometry at 60 days. Patients were then categorized as UCOPD or no-COPD. In 65 NSTE-ACS patients, we performed near infrared spectroscopy (NIRS) in the culprit and at least one non-culprit vessel (151 vessels overall), and we calculated the SYNTAX I Score. Primary endpoint was max lipid core burden index (LCBI) 4 mm. Secondary endpoints were SYNTAX Score I and vessel LCBI. Max LCBI 4 mm and vessel LCBI were significantly higher in the UCOPD compared to the no-COPD group (UCOPD 388±122, no-COPD 264±131, P<0.001; UCOPD 118±50, no-COPD 82±42, P<0.001, respectively). UCOPD patients showed higher max LCBI 4 mm and LCBI vessel both in culprit and non-culprit vessels. SYNTAX Score I was comparable between the two groups (UCOPD: 13.5 [5.5-24], no-COPD: 12.5 [5-24.5], P=0.7). NSTE-ACS patients with UCOPD showed a higher LCBI compared to those without COPD, while SYNTAX Score I was comparable between the two groups.

Sections du résumé

BACKGROUND
Chronic obstructive pulmonary disease (COPD) patients have higher recurrence of adverse events and worse prognosis after acute coronary syndrome (ACS). The underlying pathophysiological mechanism is not fully elucidated.
METHODS
In screening for COPD in ACS (SCAP) Trial (NCT02324660), ACS patients with smoking habit underwent a predischarge screening procedure to detect undiagnosed chronic obstructive pulmonary disease (UCOPD) confirmed with spirometry at 60 days. Patients were then categorized as UCOPD or no-COPD. In 65 NSTE-ACS patients, we performed near infrared spectroscopy (NIRS) in the culprit and at least one non-culprit vessel (151 vessels overall), and we calculated the SYNTAX I Score. Primary endpoint was max lipid core burden index (LCBI) 4 mm. Secondary endpoints were SYNTAX Score I and vessel LCBI.
RESULTS
Max LCBI 4 mm and vessel LCBI were significantly higher in the UCOPD compared to the no-COPD group (UCOPD 388±122, no-COPD 264±131, P<0.001; UCOPD 118±50, no-COPD 82±42, P<0.001, respectively). UCOPD patients showed higher max LCBI 4 mm and LCBI vessel both in culprit and non-culprit vessels. SYNTAX Score I was comparable between the two groups (UCOPD: 13.5 [5.5-24], no-COPD: 12.5 [5-24.5], P=0.7).
CONCLUSIONS
NSTE-ACS patients with UCOPD showed a higher LCBI compared to those without COPD, while SYNTAX Score I was comparable between the two groups.

Identifiants

pubmed: 33258568
pii: S0026-4725.20.05424-9
doi: 10.23736/S2724-5683.20.05424-9
doi:

Substances chimiques

Lipids 0

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

738-745

Auteurs

Rossella Ruggiero (R)

Cardiovascular Institute, Sant'Anna Ferrara University Hospital, Cona, Ferrara, Italy.

Alessandra Scoccia (A)

Cardiovascular Institute, Sant'Anna Ferrara University Hospital, Cona, Ferrara, Italy.

Matteo Serenelli (M)

Cardiovascular Institute, Sant'Anna Ferrara University Hospital, Cona, Ferrara, Italy.

Andrea Erriquez (A)

Cardiovascular Institute, Sant'Anna Ferrara University Hospital, Cona, Ferrara, Italy.

Giulia Passarini (G)

Cardiovascular Institute, Sant'Anna Ferrara University Hospital, Cona, Ferrara, Italy.

Matteo Tebaldi (M)

Cardiovascular Institute, Sant'Anna Ferrara University Hospital, Cona, Ferrara, Italy.

Salvatore Brugaletta (S)

Cardiovascular Institute, Hospital Clinic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

Sean Madden (S)

Infraredx, Inc., Burlington, MA, USA.

Davide Bernucci (D)

Cardiovascular Institute, Sant'Anna Ferrara University Hospital, Cona, Ferrara, Italy.

Rita Pavasini (R)

Cardiovascular Institute, Sant'Anna Ferrara University Hospital, Cona, Ferrara, Italy.

Paolo Cimaglia (P)

Maria Cecilia Hospital, GVM Care and Research, Health Science Foundation, Cotignola, Ravenna, Italy.

Elisa Maietti (E)

Center for Clinical Epidemiology, Department of Medical Science, University of Ferrara, Ferrara, Italy.

Gianluca Campo (G)

Cardiovascular Institute, Sant'Anna Ferrara University Hospital, Cona, Ferrara, Italy.

Simone Biscaglia (S)

Cardiovascular Institute, Sant'Anna Ferrara University Hospital, Cona, Ferrara, Italy - bscsmn@unife.it.

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