Cocaine Use and White Matter Hyperintensities in Homeless and Unstably Housed Women.
Cocaine Use and White Matter Hyperintensities in Homeless and Unstably Housed Women.
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DOI:
10.1016/j.jstrokecerebrovasdis.2021.105675
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发表时间:
2021-05
期刊:
影响因子:
--
通讯作者:
Hess CP
中科院分区:
文献类型:
--
作者:
Riley ED;Chow FC;Josephson SA;Dilworth SE;Lynch KL;Wade AN;Braun C;Hess CP
Cocaine use has been linked to stroke in several studies. However, few studies have considered the influence of cocaine use on stroke mechanisms such as small vessel disease (SVD). We conducted a study to assess associations between the toxicology-confirmed use of multiple drugs, including cocaine, and a marker of SVD, white matter hyperintensities (WMH). We conducted a nested case-control study (n=30) within a larger cohort study (N=245) of homeless and unstably housed women recruited from San Francisco community venues. Participants completed six monthly study visits consisting of an interview, blood draw, vital sign assessment and baseline brain MRI. We examined associations between toxicology-confirmed use of multiple substances, including cocaine, methamphetamine, heroin, alcohol and tobacco, and WMH identified on MRI. Mean study participant age was 53 years, 70% of participants were ethnic minority women and 86% had a history of cocaine use. Brain MRIs indicated the presence of WMH (i.e., Fazekas score>0) in 54% (18/30) of imaged participants. The odds of WMH were significantly higher in women who were toxicology-positive for cocaine (Odd Ratio=7.58, p=0.01), but not in women who were toxicology-positive for other drugs or had several other cerebrovascular risk factors. Over half of homeless and unstably housed women showed evidence of WMH. Cocaine use is highly prevalent and a significant correlate of WMH in this population, while several traditional CVD risk factors are not. Including cocaine use in cerebrovascular risk calculators may improve stroke risk prediction in high-risk populations and warrants further investigation.
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影响因子:
4
作者:
Chong, JY;Sacco, RL
通讯作者:
Sacco, RL
DOI:
10.1136/bmj.c3666
发表时间:
2010-07-26
期刊:
BMJ (Clinical research ed.)
影响因子:
--
作者:
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通讯作者:
Markus HS
影响因子:
37.8
作者:
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通讯作者:
Waters, DD
影响因子:
3.8
作者:
Lee W;Hwang SH;Choi H;Kim H
通讯作者:
Kim H
影响因子:
8.3
作者:
KIYOHARA, Y;KATO, I;FUJISHIMA, M
通讯作者:
FUJISHIMA, M