Five-year cardiovascular event risk in early rheumatoid arthritis patients who received treat-to-target management: a case-control study

Author:

Lam Tsz On1,Cheng Isaac T1,Lam Steven H1ORCID,Mok Chi Chiu2,Ho Carmen T3,Cheung Tommy T3,Lao Virginia W4,Pang Hin Ting4,To Chi Hung5,Yim Cheuk Wan6,Ng Alexandra7,Kwok Kitty Y8,Lee Ka Lai9,Ying Shirley K10,Wan Man Choi11,Lee Jolly M12,Tam Lai-Shan1ORCID

Affiliation:

1. Department of Medicine and Therapeutics, The Chinese University of Hong Kong , Hong Kong, China

2. Department of Medicine and Geriatrics, Tuen Mun Hospital , Hong Kong, China

3. Department of Medicine, Queen Mary Hospital , Hong Kong, China

4. Department of Medicine and Geriatrics, Kwong Wah Hospital , Hong Kong, China

5. Department of Medicine and Geriatrics, Pok Oi Hospital , Hong Kong, China

6. Department of Medicine, Tseung Kwan O Hospital , Hong Kong, China

7. Department of Medicine and Geriatrics, Caritas Medical Centre , Hong Kong, China

8. Department of Medicine, Queen Elizabeth Hospital , Hong Kong, China

9. Department of Medicine, Pamela Youde Nethersole Eastern Hospital , Hong Kong, China

10. Department of Medicine and Geriatrics, Princess Margaret Hospital , Hong Kong, China

11. Department of Medicine and Geriatrics, Ruttonjee Hospital , Hong Kong, China

12. Department of Medicine and Geriatrics, Tai Po Hospital , Hong Kong, China

Abstract

Abstract Objectives This study explored whether the excess cardiovascular (CV) disease (CVD) risk in RA could be ameliorated by suppression of inflammation using a treat-to-target (T2T) approach. We compared the CV event (CVE) incidence among ERA patients managed by a T2T strategy with a CV risk factor-matched non-RA population and a historical RA cohort (HRA). Methods This was an observational study using the city-wide hospital data and the ERA registry. ERA patients received T2T management while HRA patients received routine care. Each ERA/HRA patient was matched to three non-RA controls according to age, gender and CV risk factors. Patients on antiplatelet/anticoagulant agents, with pre-existing CVD, chronic kidney disease or other autoimmune diseases were excluded. All subjects were followed for up to 5 years. The primary end point was the first occurrence of a CVE. Results The incidence of CVE in the ERA cohort (n = 261) and ERA controls were similar with a hazard ratio of 0.53 (95% CI 0.15, 1.79). In contrast, the incidence of CVE in the HRA cohort (n = 268) was significantly higher than that of the HRA controls with a hazard ratio of 1.9 (95% CI 1.16, 3.13). The incidence of CVE in the ERA cohort was significantly lower than that of the HRA cohort and the difference became insignificant after adjusting for inflammation, the use of methotrexate and traditional CV risk factors. Conclusion ERA patients managed by a T2T strategy did not develop excess CVE compared with CV risk factor-matched controls over 5 years.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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