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Plasma homocysteine level in patients with Behcet's disease with or without thrombosis
Farhad Shahram1, Alireza Faridar, Mohammad Ghaffari Hamedani
1Behcet's Disease Unit, Rheumatology Research Center, Shariati Hospital, Tehran University of Medical Sciences, Kargar Avenue, Tehran, Iran. shahramf@tums.ac.ir
Insights
Elevated plasma homocysteine levels are linked to vascular thrombosis in Behcet's disease (BD) patients. This study suggests hyperhomocysteinemia may be an independent risk factor for thrombosis in BD.
Area of Science:
- Vascular Medicine
- Rheumatology
- Clinical Biochemistry
Background:
- Behcet's disease (BD) is a multisystem inflammatory disorder associated with a high risk of vascular complications, including thrombosis.
- The role of hyperhomocysteinemia as a potential risk factor for thrombosis in BD remains to be fully elucidated.
Purpose of the Study:
- To investigate the association between plasma homocysteine levels and the occurrence of venous and arterial thrombosis in patients with Behcet's disease.
- To determine if hyperhomocysteinemia is an independent risk factor for vascular thrombosis in BD.
Main Methods:
- A case-control study involving 96 Behcet's disease patients (47 with thrombosis, 49 without) and 49 healthy controls.
- Plasma homocysteine levels were measured using ELISA.
- Statistical analyses included ANOVA, Chi-square tests, and Pearson correlation.
Main Results:
- Plasma homocysteine levels were significantly higher in BD patients compared to healthy controls (P<0.02).
- BD patients with thrombosis exhibited significantly higher homocysteine levels than those without thrombosis and controls (P<0.0001).
- A negative correlation was observed between HLA-B51 positivity and plasma homocysteine levels in BD patients (P<0.05).
Conclusions:
- Hyperhomocysteinemia may serve as an independent risk factor for vascular thrombosis in Behcet's disease.
- This study provides the first evidence of a negative correlation between HLA-B51 and plasma homocysteine levels in BD.
Aim:
To find the possible role of plasma homocysteine level as a contributing factor in venous and arterial thrombosis in patients with Behcet's disease (BD).
Methods:
In a case control study, two groups of BD patients were included: 47 with thrombosis and 49 without thrombosis. All patients fulfilled the International Study Group Criteria for BD and the confirming diagnostic procedures for vascular thrombosis were either Doppler sonography or angiography. Forty-nine controls were selected by consecutive sampling among age and sex matched healthy subjects. Plasma homocysteine level was measured by ELISA in all. The clinical and laboratory characteristics of the disease were compared between the two groups of BD patients. Comparisons were done by ANOVA and Chi square tests; correlations were analyzed with Pearson test.
Results:
The mean plasma homocysteine level was significantly higher in BD patients (14.9±13.9 μMol/L) than in healthy controls (9.9±6.7 μMol/L), P<0.02. The difference was also significant when comparing the three groups by ANOVA: BD patients with thrombosis (24.2±13.2 μMol/L), BD patients without thrombosis (5.9±7.0 μMol/L), and healthy controls (P<0.0001). We found no correlation between plasma homocysteine level and any organ involvement other than thrombosis. The mean plasma homocysteine level was lower in HLA-B51 positive BD patients (11.6±12.1 vs. 21.7±16.3 μMol/L, P<0.05), but the difference was not significant in those with thrombosis (20.9±13.2 vs. 29.5±12.7 μMol/L, P=0.18).
Conclusion:
Hyperhomocysteinaemia may be an independent risk factor for vascular thrombosis in patients with BD. This is the first study showing a negative correlation between HLA-B51 and plasma homocysteine level.
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