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Du-Moxibustion in a Mouse Model of Ankylosing Spondylitis
Published on: October 27, 2023
Cardiovascular risk parameters in men with ankylosing spondylitis in comparison with non-inflammatory control
Hiren Divecha1, Naveed Sattar, Ann Rumley
1Centre for Rheumatic Diseases, Glasgow Royal Infirmary, Scotland, UK.
Insights
Men with ankylosing spondylitis (AS) have increased coronary heart disease (CHD) risk factors, primarily driven by systemic inflammation. Controlling for inflammation significantly reduced observed risk factor differences in AS patients.
Area of Science:
- Rheumatology and Cardiology
- Inflammation and Cardiovascular Disease Research
Background:
- Men with ankylosing spondylitis (AS) face a higher risk of coronary heart disease (CHD).
- Information regarding specific risk factors and the influence of systemic inflammation in AS patients is limited.
Purpose of the Study:
- To compare conventional and novel CHD risk factors in men with AS versus healthy controls.
- To specifically investigate the impact of systemic inflammation on these risk factors in AS.
Main Methods:
- Recruited 27 men with AS and 19 age-matched healthy controls, none on lipid-lowering therapy.
- Measured plasma lipids, inflammatory markers (IL-6, CRP), hemostatic factors (vWF, fibrinogen), and anthropometrics (BMI, blood pressure).
Main Results:
- AS patients showed higher rates of smoking, BMI, IL-6, CRP, fibrinogen, and vWF compared to controls.
- After adjusting for BMI and smoking, elevated IL-6 and CRP were the primary drivers of other risk factor differences.
- Inflammatory markers (IL-6) correlated with fibrinogen and inversely with total cholesterol.
Conclusions:
- Men with AS exhibit multiple CHD risk factor disturbances.
- Systemic inflammation, indicated by IL-6 and CRP, appears to be the principal driver of these risk factors.
- Inflammation-driven atherogenesis likely contributes to the elevated CHD risk observed in AS.
Abstract:
Men with AS (ankylosing spondylitis) are at elevated risk for CHD (coronary heart disease) but information on risk factors is sparse. We compared a range of conventional and novel risk factors in men with AS in comparison with healthy controls and, in particular, determined the influence of systemic inflammation. Twenty-seven men with confirmed AS and 19 controls matched for age were recruited. None of the men was taking lipid-lowering therapy. Risk factors inclusive of plasma lipids, IL-6 (interleukin-6), CRP (C-reactive protein), vWF (von Willebrand factor), fibrin D-dimer, ICAM-1 (intercellular cell-adhesion molecule-1) and fibrinogen were measured, and blood pressure and BMI (body mass index) were determined by standard techniques. A high proportion (70%) of men with AS were smokers compared with 37% of controls (P = 0.024). The AS patients also had a higher BMI. In analyses adjusted for BMI and smoking, men with AS had significantly higher IL-6 and CRP (approx. 9- and 6-fold elevated respectively; P < 0.001), fibrinogen (P = 0.013) and vWF (P = 0.008). Total cholesterol and HDL-C (high-density lipoprotein cholesterol) were lower (P < 0.05 and P = 0.073 respectively) in AS and thus the ratio was not different. Pulse pressure was also significantly higher in AS (P = 0.007). Notably, adjustment for IL-6 and CRP levels rendered all case-control risk factor differences, except pulse pressure, non-significant. In accordance with this finding, IL-6 correlated positively (r = 0.74, P < 0.001) with fibrinogen, but negatively (r = -0.46, P = 0.016) with total cholesterol concentration. In conclusion, men with AS have perturbances in several CHD risk factors, which appear to be driven principally by systemic inflammatory mediators. Inflammation-driven atherogenesis potentially contributes to the excess CHD risk in AS.
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