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DOI 10.1016/j.clineuro.2009.08.018

Медицинская библиотека · Clinical neurology and neurosurgery · 2009

Plasma level of sICAM-1 is associated with the extent of white matter lesion among asymptomatic elderly subjects.

Han Jing Hao, Wong Ka Sing, Wang Yan Yan, Fu Jian Hui, Ding Ding, Hong Zhen

СтатьяПеревод пока не подготовлен

Аннотация

OBJECTIVE

Inflammatory endothelial activation mediated by intercellular adhesion molecule-1 (ICAM-1) plays a role in the pathogenesis of large- and small-vessel disease. We explored the association between soluble ICAM-1 (sICAM-1) and white matter lesion (WML) as a manifestation of cerebral small-vessel disease.

METHODS

One hundred and seventy-five elderly individuals aged >or= 60 without neurological deficits were studied. Subcortical deep white matter hyperintensity (SDWMH) and periventricular hyperintensity (PVH) were rated separately. Lesions in each category were then divided into three groups (grade 0-I, grade II, grade III) according to the Fazekas scale.

RESULTS

Plasma sICAM-1 levels were positively associated with grades of WML (for SDWMH: 297.4+/-135.6ng/mL in grade 0-I, 391.3+/-145.5ng/mL in grade II, and 450.2+/-232.9ng/mL in grade III, p<0.001; for PVH: 282.5+/-116.5ng/mL in grade 0-I, 402.3+/-160.4ng/mL in grade II, and 428.1+/-227.7ng/mL in grade III, p<0.001). Multivariate analysis showed higher sICAM-1 levels, age and hypertension were the independent risk factors associated with the presence and severity of WML. More than 4-fold increased risk of WML was observed in patients with the highest quartile of sICAM-1 (all WML OR=4.694, 95% CI: 1.805-12.204; moderate WML OR=4.618, 95% CI: 1.543-13.825; severe WML OR=4.893, 95% CI: 1.236-19.368).

CONCLUSION

Increased plasma sICAM-1 suggests inflammatory process may be involved in the pathogenesis of WML.

Для цитирования: Han Jing Hao, Wong Ka Sing, Wang Yan Yan, Fu Jian Hui, Ding Ding, Hong Zhen. Plasma level of sICAM-1 is associated with the extent of white matter lesion among asymptomatic elderly subjects.. Clinical neurology and neurosurgery. 2009. DOI: 10.1016/j.clineuro.2009.08.018.

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