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Homocysteine levels in Takayasu arteritis -- a risk factor for arterial ischemic events
Alexandre Wagner Silva De Souza1, Carla Serrano De Lima, Ana Cecilia Diniz Oliveira
1Rheumatology Division, Universidade Federal de São Paulo/Escola Paulista de Medicina (Unifesp/EPM), São Paulo, Brazil. alexandre_wagner@uol.com.br
Insights
Patients with Takayasu arteritis (TA) have elevated homocysteine levels compared to healthy individuals. Higher homocysteine is linked to an increased risk of arterial ischemic events in TA patients.
Area of Science:
- Cardiovascular Medicine
- Rheumatology
- Clinical Chemistry
Background:
- Takayasu arteritis (TA) is a rare, chronic inflammatory disease affecting large arteries.
- Elevated homocysteine levels are a known risk factor for cardiovascular diseases.
- The role of homocysteine in TA pathogenesis and its association with clinical outcomes require further investigation.
Purpose of the Study:
- To compare homocysteine levels between patients with Takayasu arteritis and healthy controls.
- To investigate the relationship between homocysteine levels and paraoxonase 1 activity, cysteine levels, methotrexate use, disease activity, arterial involvement, and ischemic events in TA patients.
Main Methods:
- A cross-sectional study involving 29 TA patients and 30 controls.
- Clinical evaluation and fasting blood sample collection were performed.
- Homocysteine, cysteine, and paraoxonase 1 (PON1) activity were measured.
Main Results:
- Patients with TA exhibited significantly higher homocysteine levels than controls (10.9 μmol/l vs 6.9 μmol/l, p < 0.001).
- Homocysteine levels were positively correlated with cysteine levels (ρ = 0.676, p < 0.0001) but not with PON1 activity.
- Higher homocysteine levels were associated with a history of ischemic events in TA patients (OR 1.31, p = 0.041).
- TA patients with active disease had lower homocysteine levels than those in remission (p = 0.034).
Conclusions:
- Elevated homocysteine levels are a characteristic finding in patients with Takayasu arteritis.
- Homocysteine is associated with an increased risk of arterial ischemic events in TA.
- Further research is warranted to explore the therapeutic potential of homocysteine-lowering strategies in TA.
Objective:
To evaluate homocysteine levels in patients with Takayasu arteritis (TA) and in controls, and to analyze associations between homocysteine levels and paraoxonase 1 (PON1) activity, cysteine levels, methotrexate use, disease activity, extent of arterial involvement, and ischemic events in patients with TA.
Methods:
A cross-sectional study was performed with 29 patients with TA and 30 controls who underwent clinical evaluation and blood sample collection in the fasting state.
Results:
Among patients with TA, active disease was observed in 9 (31.0%) and previous arterial ischemic events in 10 (34.5%). Therapy with methotrexate was prescribed to 9 (31.0%) patients and it was associated with folic acid in 8 cases. Median homocysteine level was higher in patients with TA [10.9 μmol/l, interquartile range (IQR) 9.6-14.8] than in controls (6.9 μmol/l, IQR 5.1-11.9; p < 0.001). No difference was found regarding mean homocysteine levels between those using methotrexate and those under other therapies (12.8 ± 5.3 μmol/l vs 12.1 ± 3.2 μmol/l, respectively; p = 0.662). TA patients with active disease presented lower homocysteine levels (10.4 ± 2.1 μmol/l) compared to TA patients in remission (13.1 ± 4.2 μmol/l) (p = 0.034). A significant correlation was found between cysteine and homocysteine levels in patients with TA (ρ = 0.676, p < 0.0001), while there was no correlation between homocysteine and PON1 activity (ρ = 0.214, p = 0.265). Median homocysteine levels were higher in patients with ischemic events (13.2 μmol/l, IQR 10.9-17.5) compared to patients with no ischemic events (9.8 μmol/l, IQR 8.7-14.7; p = 0.027) and were associated with arterial ischemia in patients with TA (OR 1.31, 95% CI 1.01-1.71, p = 0.041).
Conclusion:
Patients with TA presented higher homocysteine levels than controls and homocysteine was associated with an increased risk of arterial ischemic events in TA.
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