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DOI 10.1016/j.clinbiochem.2013.05.048

Медицинская библиотека · Clinical biochemistry · 2013

Plasma osteoprotegerin levels increase with the severity of cerebral artery atherosclerosis.

Kim Jinkwon, Song Tae-Jin, Yang Seung-Hee, Lee Ok-Hee, Nam Hyo Suk, Kim Young Dae, Kim Eun Hee, Lee Hye Sun, Nam Chung Mo, Heo Ji Hoe

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVES

Osteoprotegerin (OPG) is a member of the tumor necrosis factor receptor superfamily and suggested as a marker of atherosclerosis. We investigated whether plasma OPG levels were associated with the presence and severity of cerebral atherosclerosis.

DESIGN AND

METHODS

We used an enzyme-linked immunosorbent assay to measure the plasma OPG levels of 107 patients with acute cerebral infarction. We compared the plasma OPG levels according to the presence and number of arteries with cerebral atherosclerosis (≥ 50% stenosis).

RESULTS

Of 107 patients, 73 (68.2%) had cerebral atherosclerosis. OPG levels were increased in patients with cerebral atherosclerosis (374.69 ± 206.48 vs 261.17 ± 166.91 pg/mL, p=0.006). OPG levels showed positive correlation with the number of cerebral arteries with atherosclerosis (Spearman's rho=0.342, p<0.001). After adjustment for vascular risk factors, OPG>229.9 pg/mL was independently associated with the presence [OR 4.61, 95% CI 1.57-13.55, p=0.005, binary logistic regression] of cerebral atherosclerosis and number [OR 3.20, 95% CI 1.26-8.12, p=0.014, ordinal logistic regression] of arteries with cerebral atherosclerosis.

CONCLUSIONS

Plasma OPG levels were significantly associated with the presence and severity of cerebral atherosclerosis. This finding suggests that plasma OPG might have a role in cerebral atherosclerosis.

Для цитирования: Kim Jinkwon, Song Tae-Jin, Yang Seung-Hee, Lee Ok-Hee, Nam Hyo Suk, Kim Young Dae, Kim Eun Hee, Lee Hye Sun, Nam Chung Mo, Heo Ji Hoe. Plasma osteoprotegerin levels increase with the severity of cerebral artery atherosclerosis.. Clinical biochemistry. 2013. DOI: 10.1016/j.clinbiochem.2013.05.048.

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