Leptomeningeal collaterals are associated with modifiable metabolic risk factors.
Leptomeningeal collaterals are associated with modifiable metabolic risk factors.
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DOI:
10.1002/ana.23906
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发表时间:
2013-08
影响因子:
11.2
通讯作者:
Sohn, Sung Il
中科院分区:
文献类型:
--
作者:
Menon, Bijoy K.;Smith, Eric E.;Coutts, Shelagh B.;Welsh, Donald G.;Faber, James E.;Goyal, Mayank;Hill, Michael D.;Demchuk, Andrew M.;Damani, Zaheed;Cho, Kyung-Hee;Chang, Hyuk-Won;Hong, Jeong-Ho;Sohn, Sung Il
We seek to identify potentially modifiable determinants associated with variability in leptomeningeal collateral status in patients with acute ischemic stroke. Data are from the Keimyung Stroke Registry. Consecutive patients with M1 segment middle cerebral artery (MCA) ± intracranial internal carotid artery (ICA) occlusions on baseline CT-angiography (CTA) from May 2004 to July 2009 were included. Baseline and follow-up imaging was analyzed blinded to all clinical information. Two raters assessed leptomeningeal collaterals on baseline CTA by consensus, using a previously validated regional leptomeningeal score (rLMC). Baseline characteristics (n=206) were: mean age 66.9±11.6 years, median baseline NIHSS 14 (IQR 11-20), and median stroke symptom onset to CTA 166 minutes (IQR 96-262), Poor collateral status at baseline (rLMC score 0-10) was seen in 73/206 (35.4%). On univariate analyses, patients with poor collateral status at baseline were older, hypertensive, had higher white blood cell count, blood glucose, D-dimer, serum uric acid levels, and were more likely to have metabolic syndrome. Multivariable modeling identified metabolic syndrome (OR 3.22 95% CI 1.69-6.15, p<0.001), hyperuricemia (per 1 mg/dl OR 1.35 95% CI 1.12-1.62, p<0.01) and older age (per 10 years, OR 1.34 95% CI 1.02-1.77, p=0.03) as independent predictors of poor leptomeningeal collateral status at baseline. Metabolic syndrome, hyperuricemia and age are associated with poor leptomeningeal collateral status in patients with acute ischemic stroke.
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影响因子:
19.6
作者:
Khosla, UM;Zharikov, S;Johnson, RJ
通讯作者:
Johnson, RJ
影响因子:
4.2
作者:
Omura-Matsuoka, Emi;Yagita, Yoshiki;Kitagawa, Kazuo
通讯作者:
Kitagawa, Kazuo
影响因子:
8.3
作者:
ONEILL, PA;DAVIES, I;BENNETT, D
通讯作者:
BENNETT, D
影响因子:
11.2
作者:
Parsons, MW;Barber, PA;Davis, SM
通讯作者:
Davis, SM
影响因子:
8.3
作者:
Liebeskind, DS
通讯作者:
Liebeskind, DS