Individual lifetime benefit from low-dose colchicine in patients with chronic coronary artery disease.

Cardiovascular risk prediction Colchicine Coronary artery disease ESC Guidelines Inflammation Secondary prevention

Journal

European journal of preventive cardiology
ISSN: 2047-4881
Titre abrégé: Eur J Prev Cardiol
Pays: England
ID NLM: 101564430

Informations de publication

Date de publication:
06 Jul 2023
Historique:
received: 22 03 2023
revised: 30 05 2023
accepted: 04 07 2023
medline: 6 7 2023
pubmed: 6 7 2023
entrez: 6 7 2023
Statut: aheadofprint

Résumé

Low-dose colchicine reduces cardiovascular risk in patients with coronary artery disease (CAD), but absolute benefits may vary between individuals. This study aimed to assess the range of absolute benefit from low-dose colchicine according to individual patient risk profile. The ESC guideline-recommended SMART-REACH model was combined with the relative treatment effect of low-dose colchicine, and applied to CAD patients from the LoDoCo2 trial and UCC-SMART cohort (n = 10,830). Individual treatment benefit was expressed as 10-year absolute risk reductions (ARRs) for myocardial infarction, stroke, or cardiovascular death (MACE), and MACE-free life-years gained. Predictions were also performed for MACE plus coronary revascularization (MACE+), using a new lifetime model derived in the REACH registry. Colchicine was compared to other ESC guideline-recommended intensified (step 2) prevention strategies, i.e. low density lipoprotein-cholesterol (LDL-c) reduction to 1.4 mmol/L, and systolic blood pressure (SBP) reduction to 130 mmHg. Generalizability to other populations was assessed in CAD patients from REACH North America and Western Europe (n = 25,812). Median 10-year ARR from low-dose colchicine was 4.6% (interquartile range [IQR] 3.6-6.0%) for MACE, and 8.6% (IQR 7.6-9.8%) for MACE + . Lifetime benefit was 2.0 (IQR 1.6-2.5) MACE-free years, and 3.4 (IQR 2.6-4.2) MACE + -free life-years gained. For LDL-c and SBP reduction respectively, median 10-year ARR for MACE was 3.0% (IQR 1.5-5.1%) and 1.7% (IQR 0.0-5.7%), and lifetime benefit was 1.2 (IQR 0.6-2.1) and 0.7 (IQR 0.0-2.3) MACE-free life-years gained. Similar results were obtained for MACE+, and in American and European patients from REACH. The absolute benefits of low-dose colchicine vary between individual patients with chronic CAD. They may be expected to be of at least similar magnitude to those of intensified LDL-c and SBP reduction in a majority of patients already on conventional lipid-lowering and blood pressure-lowering therapy. The long-term benefits of treatment with low-dose colchicine were estimated for 36,642 individuals with coronary heart disease, and compared to those of lipid- and blood pressure-lowering therapy. On average, low-dose colchicine was estimated to lower the risk of cardiovascular disease in the next 10 years from 17.8% to 13.2% (a reduction of 4.6 percentage points), and to afford 2.0 additional years of life without cardiovascular disease.Low-dose colchicine was estimated to be the most effective treatment in 49%, intensive blood pressure-lowering therapy in 28%, and intensive lipid-lowering therapy in 23% of patients.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Low-dose colchicine reduces cardiovascular risk in patients with coronary artery disease (CAD), but absolute benefits may vary between individuals. This study aimed to assess the range of absolute benefit from low-dose colchicine according to individual patient risk profile.
METHODS METHODS
The ESC guideline-recommended SMART-REACH model was combined with the relative treatment effect of low-dose colchicine, and applied to CAD patients from the LoDoCo2 trial and UCC-SMART cohort (n = 10,830). Individual treatment benefit was expressed as 10-year absolute risk reductions (ARRs) for myocardial infarction, stroke, or cardiovascular death (MACE), and MACE-free life-years gained. Predictions were also performed for MACE plus coronary revascularization (MACE+), using a new lifetime model derived in the REACH registry. Colchicine was compared to other ESC guideline-recommended intensified (step 2) prevention strategies, i.e. low density lipoprotein-cholesterol (LDL-c) reduction to 1.4 mmol/L, and systolic blood pressure (SBP) reduction to 130 mmHg. Generalizability to other populations was assessed in CAD patients from REACH North America and Western Europe (n = 25,812).
RESULTS RESULTS
Median 10-year ARR from low-dose colchicine was 4.6% (interquartile range [IQR] 3.6-6.0%) for MACE, and 8.6% (IQR 7.6-9.8%) for MACE + . Lifetime benefit was 2.0 (IQR 1.6-2.5) MACE-free years, and 3.4 (IQR 2.6-4.2) MACE + -free life-years gained. For LDL-c and SBP reduction respectively, median 10-year ARR for MACE was 3.0% (IQR 1.5-5.1%) and 1.7% (IQR 0.0-5.7%), and lifetime benefit was 1.2 (IQR 0.6-2.1) and 0.7 (IQR 0.0-2.3) MACE-free life-years gained. Similar results were obtained for MACE+, and in American and European patients from REACH.
CONCLUSIONS CONCLUSIONS
The absolute benefits of low-dose colchicine vary between individual patients with chronic CAD. They may be expected to be of at least similar magnitude to those of intensified LDL-c and SBP reduction in a majority of patients already on conventional lipid-lowering and blood pressure-lowering therapy.
The long-term benefits of treatment with low-dose colchicine were estimated for 36,642 individuals with coronary heart disease, and compared to those of lipid- and blood pressure-lowering therapy. On average, low-dose colchicine was estimated to lower the risk of cardiovascular disease in the next 10 years from 17.8% to 13.2% (a reduction of 4.6 percentage points), and to afford 2.0 additional years of life without cardiovascular disease.Low-dose colchicine was estimated to be the most effective treatment in 49%, intensive blood pressure-lowering therapy in 28%, and intensive lipid-lowering therapy in 23% of patients.

Autres résumés

Type: plain-language-summary (eng)
The long-term benefits of treatment with low-dose colchicine were estimated for 36,642 individuals with coronary heart disease, and compared to those of lipid- and blood pressure-lowering therapy. On average, low-dose colchicine was estimated to lower the risk of cardiovascular disease in the next 10 years from 17.8% to 13.2% (a reduction of 4.6 percentage points), and to afford 2.0 additional years of life without cardiovascular disease.Low-dose colchicine was estimated to be the most effective treatment in 49%, intensive blood pressure-lowering therapy in 28%, and intensive lipid-lowering therapy in 23% of patients.

Identifiants

pubmed: 37409348
pii: 7220081
doi: 10.1093/eurjpc/zwad221
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Investigateurs

S M Nidorf (SM)
X F Xu (XF)
M A Ireland (MA)
D Latchem (D)
A Whelan (A)
R Hendriks (R)
P Salkani (P)
I W Tan (IW)
A G Thompson (AG)
A M Morton (AM)
B E Hockings (BE)
P L Thompson (PL)
B King (B)
J H Cornel (JH)
H Bakker-Lohmeijer (H)
A Mosterd (A)
P Bunschoten (P)
S H K The (SHK)
S van der Kooi (S)
T Lenderink (T)
R G J L Lardinois (RGJL)
P A M Hoogslag (PAM)
A de Vos (A)
A Jerzewski (A)
S Jansen (S)
P R Nierop (PR)
M van der Knaap (M)
H P Swart (HP)
R Kingma (R)
J Schaap (J)
L B Blom (LB)
A F M Kuijper (AFM)
E Bayraktar-Verver (E)
M W J van Hessen (MWJ)
W C T C Engelen (WCTC)
J W M van Eck (JWM)
N van der Ven-Elzebroek (N)
J M C van Hal (JMC)
I M J Drost (IMJ)
F R den Hartog (FR)
D van Wijk (D)
E van Beek (E)
C van der Horst (C)
L Bartels (L)
M Hendriks (M)
C de Nooijer (C)
C Welten (C)
E Ronner (E)
A Dijkshoorn (A)
F J Prins (FJ)
R N A Rutten (RNA)
D P W Beele (DPW)
I Hendriks (I)
A van der Sluis (A)
E A Badings (EA)
I C D Westendorp (ICD)
A Melein (A)
Tj J Römer (TJ)
P Bruines (P)
R van de Wal (R)
I Leenders-van Lieshout (I)
M E W Hemels (MEW)
K Meinen-Werner (K)
M R de Groot (MR)
G Post (G)
M W C Mulder (MWC)
S Stuij (S)
E van Nes (E)
P Luyten (P)
J Plomp (J)
S V Veldmeijer (SV)
M J Asselman (MJ)
P A Scholtus (PA)
F W Asselbergs (FW)
M J Cramer (MJ)
M G van der Meer (MG)
H M Nathoe (HM)
G J de Borst (GJ)
M L Bots (ML)
M H Emmelot-Vonk (MH)
P A de Jong (PA)
A T Lely (AT)
N P van der Kaaij (NP)
L J Kappelle (LJ)
Y M Ruigrok (YM)
M C Verhaar (MC)
F L J Visseren (FLJ)
J A N Dorresteijn (JAN)
D L Bhatt (DL)
P G Steg (PG)
E M Ohman (EM)
J Röther (J)
P W F Wilson (PWF)
M J Alberts (MJ)
D L Bhatt (DL)
R D'Agostino (R)
K A Eagle (KA)
S Goto (S)
A T Hirsch (AT)
C S Liau (CS)
J L Mas (JL)
E M Ohman (EM)
J Röther (J)
S C Smith (SC)
P G Steg (PG)
P W F Wilson (PWF)

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Pascal M Burger (PM)

University Medical Centre Utrecht, Utrecht, the Netherlands.

Jannick A N Dorresteijn (JAN)

University Medical Centre Utrecht, Utrecht, the Netherlands.

Aernoud T L Fiolet (ATL)

University Medical Centre Utrecht, Utrecht, the Netherlands.
Dutch Cardiovascular Research Network (WCN), Utrecht, the Netherlands.

Stefan Koudstaal (S)

Dutch Cardiovascular Research Network (WCN), Utrecht, the Netherlands.
Green Heart Hospital, Gouda, the Netherlands.

John W Eikelboom (JW)

Department of Medicine, McMaster University, Hamilton, Canada.

Stefan M Nidorf (SM)

GenesisCare Western Australia, Perth, Australia.
Heart Research Institute of Western Australia, Perth, Australia.

Peter L Thompson (PL)

GenesisCare Western Australia, Perth, Australia.
Heart Research Institute of Western Australia, Perth, Australia.

Jan H Cornel (JH)

Dutch Cardiovascular Research Network (WCN), Utrecht, the Netherlands.
Radboud University Medical Centre, Nijmegen, the Netherlands.

Charley A Budgeon (CA)

School of Population and Global Health, University of Western Australia, Perth, Australia.

Iris C D Westendorp (ICD)

Red Cross Hospital, Beverwijk, the Netherlands.

Driek P W Beelen (DPW)

IJsselland Hospital, Capelle aan den IJssel, the Netherlands.

Fabrice M A C Martens (FMAC)

Dutch Cardiovascular Research Network (WCN), Utrecht, the Netherlands.
Deventer Hospital, Deventer, the Netherlands.

P Gabriel Steg (PG)

Assistance Publique-Hôpitaux de Paris, Hôpital Bichat, Université de Paris, Paris, France.

Folkert W Asselbergs (FW)

University Medical Centre Utrecht, Utrecht, the Netherlands.

Maarten J Cramer (MJ)

University Medical Centre Utrecht, Utrecht, the Netherlands.

Martin Teraa (M)

University Medical Centre Utrecht, Utrecht, the Netherlands.

Deepak L Bhatt (DL)

Brigham and Women's Hospital Heart & Vascular Centre and Harvard Medical School, Boston, USA.

Frank L J Visseren (FLJ)

University Medical Centre Utrecht, Utrecht, the Netherlands.

Arend Mosterd (A)

Dutch Cardiovascular Research Network (WCN), Utrecht, the Netherlands.
Meander Medical Centre, Amersfoort, the Netherlands.

Classifications MeSH