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Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Systemic sclerosis is an independent risk factor for ischemic heart disease, especially in patients carrying certain
Abdulla Watad1, Dennis McGonagle2, Nicola L Bragazzi3
1Department of Medicine 'B', The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel-Hashomer, Israel; Rheumatology Unit, Sheba Medical Center, Tel-Hashomer, Israel; Sackler Faculty of Medicine, Tel-Aviv University, Israel; Section of Musculoskeletal Disease, Leeds Institute of Molecular Medicine, University of Leeds, NIHR Leeds Musculoskeletal Biomedical Research Unit, Chapel Allerton Hospital, Leeds, UK.
Insights
Systemic sclerosis (SSc) patients face a higher risk of ischemic heart disease (IHD). Certain autoantibodies, like anti-cardiolipin (aCL) and anti-beta2GPI, further elevate this risk, impacting SSc patient mortality.
Area of Science:
- Cardiovascular Medicine
- Rheumatology
- Immunology
Background:
- Systemic sclerosis (SSc) is associated with an increased prevalence of ischemic heart disease (IHD).
- The role of SSc-related and antiphospholipid autoantibodies in IHD risk among SSc patients remains controversial.
- This study investigates the association between SSc and IHD, its impact on mortality, and the influence of specific autoantibodies.
Purpose of the Study:
- To determine the prevalence of IHD in patients with SSc compared to controls.
- To assess the independent predictive value of SSc for IHD.
- To evaluate the impact of IHD on SSc mortality.
- To examine the role of SSc-related and antiphospholipid autoantibodies in IHD among SSc patients.
Main Methods:
- A large cohort study utilized the Clalit-Health-Service (CHS) database.
- 2431 SSc patients were compared with 12,710 age- and sex-matched controls.
- Prevalence of IHD, SSc-associated mortality, and the impact of autoantibodies (anti-beta2GPI, aCL) were assessed.
Main Results:
- IHD prevalence was significantly higher in SSc patients (20.4%) versus controls (15.0%).
- SSc was an independent predictor of IHD (OR 1.91).
- IHD in SSc patients was associated with higher mortality (HR 2.67).
- Positivity for anti-beta2GPI (IgM) or aCL (IgA) increased IHD risk in SSc patients (OR 1.89 and 3.72, respectively).
Conclusions:
- SSc patients exhibit an elevated risk of developing IHD.
- Specific autoantibodies, namely anti-cardiolipin (aCL) and anti-beta2GPI, are identified as risk factors for IHD in SSc.
- Routine monitoring and pre-emptive screening for IHD in SSc patients, particularly those with positive autoantibodies, are recommended.
Background:
A higher prevalence of ischemic heart disease (IHD) in patients with systemic sclerosis (SSc) was reported. However, contrasting findings were published concerning the role of SSc-related autoantibodies in IHD risk which remains controversial. The current study explored the link between SSc and IHD, impact of putative links on SSc mortality and the role of SSc-related and antiphospholipid autoantibodies in disease associated IHD.
Methods:
A large cohort study utilising the Clalit-Health-Service (CHS) database was conducted on 2431 SSc patients and 12,710 age- and sex matched controls. The proportion of IHD was compared between patients diagnosed with SSc and age- and gender-matched controls. The role of SSc-linked and antiphospholipid autoantibodies in disease associated IHD was assessed.
Results:
The prevalence rate of IHD was significantly higher in SSc than controls (20.4% vs 15.0%, p <0.001). At the multivariate analysis, SSc was an independent predictor of IHD with an OR of 1.91 (95%CI 1.57-2.31, p < 0.0001). SSc patients with IHD had a higher mortality rate with an HR of 2.67 (95%CI 2.03-3.53, p < 0.0001) than those without IHD. In SSc patients positivity for anti-beta2GPI (IgM-isotype) or anti-cardiolipin (aCL) (IgA-isotype) represented a risk factor for IHD with an OR 1.89 (95% 1.04-3.45, p = 0.0369) and OR of 3.72 (95% 1.25-11.11, p = 0.0184), respectively.
Conclusions:
Patients with SSc are at higher risk for developing IHD with an additional risk for the latter in those positive for aCL or anti-beta2GPI. A high degree of suspicion is needed during routine patient follow-up and pre-emptive screening should be considered.
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