Untangling the relationship between smoking and systemic sclerosis: an analysis of the EUSTAR cohort.


Journal

RMD open
ISSN: 2056-5933
Titre abrégé: RMD Open
Pays: England
ID NLM: 101662038

Informations de publication

Date de publication:
20 May 2024
Historique:
received: 10 01 2024
accepted: 12 04 2024
medline: 22 5 2024
pubmed: 22 5 2024
entrez: 21 5 2024
Statut: epublish

Résumé

To untangle the association between smoking and systemic sclerosis (SSc). In the European Scleroderma Trials and Research cohort, the autoantibody status was compared between ever-smokers and never-smokers. Time until disease progression was assessed using Kaplan-Meier curves. Cox models were built to investigate the influence of smoking over 15 years of follow-up. All analyses were performed for the total cohort and stratified for sex and for positivity of anti-centromere (ACA) and anti-topoisomerase antibodies (ATA). Overall, 12 314 patients were included in the study. Of these, 10 393 were women (84%), 4637 were ACA-positive (38%), 3919 were ATA-positive (32%) and 4271 (35%) were ever-smokers. In men, but not in women, smoking was associated with mortality (HR 1.63, 95% CI 1.23 to 2.16, p=0.001). Ever-smoking women were at higher risk for skin progression (HR 1.10, 95% CI 1.00 to 1.22, p=0.046) and for 'any organ progression' (HR 1.07, 95% CI 1.00 to 1.13, p=0.036). In women, 34% of never-smokers were ATA-positive compared with 21% of ever-smokers (p<0.001). In the group of ever-smokers, higher exposure rates, reflected by the number of pack-years (OR 0.98, 95% CI 0.97 to 0.99, p<0.001) and by smoking duration (OR 0.96, 95% CI 0.95 to 0.97, p<0.001), were associated with lower frequency of ATA. In ACA-positive patients, the risk of mortality (HR 1.29, 95% CI 1.02 to 1.63, p=0.033), cardiac involvement (HR 1.25, 95% CI 1.03 to 1.43, p=0.001), skin progression (HR 1.21, 95% CI 1.03 to 1.42, p=0.018) and 'any organ progression' (HR 1.14, 95% CI 1.05 to 1.24, p=0.002) was increased among smokers. In ATA-positive smoking patients, mortality (HR 1.40, 95% CI 1.10 to 1.78, p=0.006), skin progression (HR 1.19, 95% CI 1.03 to 1.37, p=0.020) digital ulcers (HR 1.17, 95% CI 1.02 to 1.34, p=0.029) and 'any organ progression' (HR 1.11, 95% CI 1.00 to 1.22, p=0.048) occurred more frequently. Our stratified analysis demonstrates that smoking is associated with an increased risk for mortality in male SSc patients but not in women. Strikingly, smoking is associated with lower prevalence of ATA positivity, in particular in women. In both ATA-positive and ACA-positive patients, smoking is a risk factor for mortality, skin progression and 'any organ progression'.

Identifiants

pubmed: 38772679
pii: rmdopen-2024-004101
doi: 10.1136/rmdopen-2024-004101
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Jacopo Ciaffi (J)

Medicine and Rheumatology Unit, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy jacopo.ciaffi@ior.it.
Department of Biomedical and Neuromotor Sciences (DIBINEM), Alma Mater Studiorum University of Bologna, Bologna, Italy.

Sophie I E Liem (SIE)

Department of Rheumatology, Leiden University Medical Centre (LUMC), Leiden, The Netherlands.

Suzanne Cannegieter (S)

Department of Clinical Epidemiology, Leiden University Medical Center (LUMC), Leiden, The Netherlands.
Department of Internal Medicine, Division of Thrombosis and Haemostasis, Leiden University Medical Center (LUMC), Leiden, The Netherlands.

Saad Ahmed (S)

Department of Rheumatology, Leiden University Medical Centre (LUMC), Leiden, The Netherlands.

Eva M Hoekstra (EM)

Department of Rheumatology, Leiden University Medical Centre (LUMC), Leiden, The Netherlands.

Piotr Wiland (P)

Department of Rheumatology and Internal Medicine, Wroclaw Medical University, Wroclaw, Poland.

Tatsuya Atsumi (T)

Department of Rheumatology, Endocrinology and Nephrology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Gabriella Szücs (G)

Department of Rheumatology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Alexandra Balbir Gurman (A)

Rheumatology Department, Rambam Health Care Campus, Rappaport Faculty of Medicine, Technion, Haifa, Israel.

László Czirják (L)

Department of Rheumatology and Immunology, Medical School, University of Pécs, Pécs, Hungary.

Elisabetta Zanatta (E)

Department of Medicine-DIMED, Unit of Rheumatology, Padova University Hospital, Padova, Italy.

Ina Koetter (I)

Medical Department 4, Rheumatology, Immunology, Nephrology, Asklepios Klinik Altona, Hamburg, Germany.

Joerg C Henes (JC)

Internal Medicine II - Oncology, haematology, clinical immunology and rheumatology, University Hospital and Faculty of Medicine, University of Tübingen, Tubingen, Germany.

Marco Matucci-Cerinic (M)

Unit of Immunology, Rheumatology, Allergy and Rare Diseases (UnIRAR), IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.

Paolo Airò (P)

Rheumatology and Clinical Immunology Service, Spedali Civili di Brescia, Brescia, Italy.

Francesco Ursini (F)

Medicine and Rheumatology Unit, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
Department of Biomedical and Neuromotor Sciences (DIBINEM), Alma Mater Studiorum University of Bologna, Bologna, Italy.

Tom W J Huizinga (TWJ)

Department of Rheumatology, Leiden University Medical Centre (LUMC), Leiden, The Netherlands.

Jeska De Vries-Bouwstra (J)

Department of Rheumatology, Leiden University Medical Centre (LUMC), Leiden, The Netherlands.

Eustar Collaborators (E)

EUropean Scleroderma Trials And Research group, None, UK.

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