Statin Use for Primary Cardiovascular Disease Prevention Is Low in Inflammatory Arthritis.


Journal

The Canadian journal of cardiology
ISSN: 1916-7075
Titre abrégé: Can J Cardiol
Pays: England
ID NLM: 8510280

Informations de publication

Date de publication:
08 2022
Historique:
received: 01 03 2022
revised: 04 04 2022
accepted: 05 04 2022
pubmed: 17 4 2022
medline: 17 8 2022
entrez: 16 4 2022
Statut: ppublish

Résumé

Patients with inflammatory arthritis (IA) are at high risk for atherosclerotic cardiovascular disease (ASCVD), yet management of dyslipidemia is infrequently prioritized. We applied Canadian dyslipidemia guidelines to determine how many patients with IA would be eligible for primary prevention with statins. We conducted a cross-sectional study of patients with IA in a cardio-rheumatology clinic, with no known CVD and without statin therapy at cohort entry. We stratified patients by Framingham Risk Score (FRS) and summarized the proportion meeting guideline statin-indicated criteria. Multivariable logistic regression analyses determined the association of variables with statin indication after adjustment for age, sex, traditional ASCVD risk factors, and arthritis characteristics. Among 302 patients, most had rheumatoid arthritis (59%). Mean age was 58 years, and 71% were female. Overall, 50% of the cohort was eligible for statin therapy. The majority was low FRS risk category (68%), and the most frequent qualifier for statins was elevated apolipoprotein B (ApoB) levels or low-density lipoprotein cholesterol (LDL-c) levels. In the intermediate FRS group, 91% met criteria for statin therapy based on the presence of a coronary artery calcification (CAC) score > 0 or an elevated high-sensitivity C-reactive protein. Male sex, hypertension, elevated ApoB, and a CAC score > 0 were the factors most strongly associated with indication for statin therapy. Statin therapy is suboptimal in IA despite a significant number of patients meeting indication based on lipoprotein thresholds or CAC scores. Understanding the barriers and potential facilitators of implementing and interpreting these CVD screening tools in IA is needed.

Sections du résumé

BACKGROUND
Patients with inflammatory arthritis (IA) are at high risk for atherosclerotic cardiovascular disease (ASCVD), yet management of dyslipidemia is infrequently prioritized. We applied Canadian dyslipidemia guidelines to determine how many patients with IA would be eligible for primary prevention with statins.
METHODS
We conducted a cross-sectional study of patients with IA in a cardio-rheumatology clinic, with no known CVD and without statin therapy at cohort entry. We stratified patients by Framingham Risk Score (FRS) and summarized the proportion meeting guideline statin-indicated criteria. Multivariable logistic regression analyses determined the association of variables with statin indication after adjustment for age, sex, traditional ASCVD risk factors, and arthritis characteristics.
RESULTS
Among 302 patients, most had rheumatoid arthritis (59%). Mean age was 58 years, and 71% were female. Overall, 50% of the cohort was eligible for statin therapy. The majority was low FRS risk category (68%), and the most frequent qualifier for statins was elevated apolipoprotein B (ApoB) levels or low-density lipoprotein cholesterol (LDL-c) levels. In the intermediate FRS group, 91% met criteria for statin therapy based on the presence of a coronary artery calcification (CAC) score > 0 or an elevated high-sensitivity C-reactive protein. Male sex, hypertension, elevated ApoB, and a CAC score > 0 were the factors most strongly associated with indication for statin therapy.
CONCLUSIONS
Statin therapy is suboptimal in IA despite a significant number of patients meeting indication based on lipoprotein thresholds or CAC scores. Understanding the barriers and potential facilitators of implementing and interpreting these CVD screening tools in IA is needed.

Identifiants

pubmed: 35429590
pii: S0828-282X(22)00218-5
doi: 10.1016/j.cjca.2022.04.002
pii:
doi:

Substances chimiques

Apolipoproteins B 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1244-1252

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.

Auteurs

Bindee Kuriya (B)

Division of Rheumatology, Sinai Health System, Toronto, Ontario, Canada; Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Division of Cardiology, Women's College Hospital, Toronto, Ontario, Canada. Electronic address: bindee.kuriya@sinaihealth.ca.

Shadi Akhtari (S)

Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Division of Cardiology, Women's College Hospital, Toronto, Ontario, Canada.

Mohammad Movahedi (M)

Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada; Ontario Best Practices Research Initiative, University Health Network, Toronto, Ontario, Canada.

Jacob A Udell (JA)

Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada; Division of Cardiology, Women's College Hospital, Toronto, Ontario, Canada; Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada.

Patrick R Lawler (PR)

Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada.

Michael E Farkouh (ME)

Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada.

Edward C Keystone (EC)

Division of Rheumatology, Sinai Health System, Toronto, Ontario, Canada.

Kate Hanneman (K)

Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada; Department of Medical Imaging, University Health Network and Women's College Hospital, Toronto, Ontario, Canada.

Elsie Nguyen (E)

Department of Medical Imaging, University Health Network and Women's College Hospital, Toronto, Ontario, Canada.

Paula J Harvey (PJ)

Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Division of Cardiology, Women's College Hospital, Toronto, Ontario, Canada.

Lihi Eder (L)

Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada; Division of Rheumatology, Women's College Hospital, Toronto, Ontario, Canada.

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