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Factors associated with high cardiovascular risk in psoriatic arthritis and non-psoriatic spondyloarthritis
Chengappa Kavadichanda1, K C Shanoj2, Sachit Ganapathy3
1Department of Clinical Immunology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, 605005, India. doc.chengappa@gmail.com.
Insights
Sarcopenia and traditional cardiovascular comorbidities significantly increase high cardiovascular risk (HCVR) in psoriatic arthritis (PsA) patients. Psoriatic arthritis patients face a higher CV risk, with sarcopenia being a key determinant.
Area of Science:
- Rheumatology and Cardiology
- Metabolic and Cardiovascular Health
Background:
- Psoriatic arthritis (PsA) and non-psoriatic spondyloarthritis (nPsA-SpA) share inflammatory pathways but differ in cardiovascular risk profiles.
- Understanding factors contributing to high cardiovascular risk (HCVR) in these conditions is crucial for targeted prevention.
Purpose of the Study:
- To investigate associations between traditional cardiovascular risk factors, disease-related factors, body composition, and adipokines with HCVR in PsA and nPsA-SpA.
- To identify predictors of HCVR in patients with spondyloarthritis.
Main Methods:
- A cross-sectional study compared age- and BMI-matched adults with PsA (n=56) and nPsA-SpA (n=58).
- Methods included dual-energy X-ray absorptiometry for body composition, adipokine measurement, disease characteristic assessment, QRISK3 cardiovascular risk scoring, and carotid intimal medial thickness (CIMT) measurement.
- HCVR was defined as QRISK3 ≥10% or CIMT ≥75th percentile.
Main Results:
- HCVR was present in 34.2% of patients.
- Sarcopenia (adjusted odds ratio [aOR] 15.83) and any traditional cardiovascular comorbidity (aOR 18.97) were significantly associated with HCVR.
- Patients with nPsA-SpA had a 97% lower chance of HCVR compared to PsA patients.
- Adipokine levels correlated with body composition but not HCVR.
Conclusions:
- Sarcopenia is a critical determinant of HCVR in spondyloarthritis, potentially linked to ectopic fat deposition in muscles.
- PsA is associated with a higher cardiovascular risk, necessitating further research into underlying mechanisms.
- Interventions focusing on preventing sarcopenia, managing cardiovascular risk factors, and controlling disease activity may mitigate atherosclerosis in SpA.
Abstract:
To identify the association between traditional cardiovascular risk factors, diseases related factors, body composition and adipokines with high cardiovascular risk (HCVR) in psoriatic arthritis and non-psoriatic spondyloarthritis. This was a cross-sectional study involving age and BMI matched adults with psoriatic arthritis (PsA) (n = 56) and non-psoriatic spondyloarthritis (nPsA-SpA) (n = 58). Body composition using whole-body dual energy X-ray absorptiometry, adipokines and disease characteristics along with cardiovascular risk scoring QRISK3 and carotid intimal medial thickness (CIMT) was collected. Individuals with a QRISK3 ≥ 10% or CIMT of ≥ 75 percentile of the general population were categorised as HCVR. Predictors of HCVR were determined by logistic regression. HCVR was detected in 39 (34.2%) of the patients. After adjusting for all the factors, sarcopenia (aOR-15.83; 95% CI 1.16-215.48; p = 0.038) and presence of any traditional CV comorbidity (aOR: 18.97; 95% CI 1.63-221.29; p = 0.019) were associated with HCVR. nPsA-SpA had a 97% lesser chance of having HCVR as compared to PsA. The ROC curve analysis for the multiple logistic regression model which estimated the AUC as 0.787 (95% CI 0.701-0.874) and a P value < 0.001. Adipokine levels correlated well with body composition, but not with HCVR. PsA has a higher CV risk and the mechanisms for the same are poorly understood. Sarcopenia is an important determinant of HCVR and may be due to ectopic adipose tissue deposition in skeletal muscles. Focused physical therapy to prevent sarcopenia, optimum treatment of traditional CV risk factors and adequate disease control may help in preventing atherosclerosis in SpA.
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