首页> 外文期刊>JAMA: the Journal of the American Medical Association >Cocaine-induced cerebral vasoconstriction detected in humans with magnetic resonance angiography.
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Cocaine-induced cerebral vasoconstriction detected in humans with magnetic resonance angiography.

机译:可卡因诱发的脑血管收缩在磁共振血管造影中检测到。

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CONTEXT: Clinical observations and case reports suggest that there are important cerebrovascular complications of cocaine use, but no studies have documented a direct link. OBJECTIVE: To determine whether low-dose cocaine administration induces cerebral vasoconstriction in healthy cocaine users. DESIGN: Randomized controlled trial. SUBJECTS: Twenty-four healthy and neurologically normal men (mean age, 29 years) reporting median cocaine use of 8 lifetime exposures (range, 3 to >40). INTERVENTION: Double-blind intravenous administration of cocaine (0.4 or 0.2 mg/kg) or placebo, with cerebral magnetic resonance angiography performed at baseline and 20 minutes following infusion. MAIN OUTCOME MEASURE: Cocaine-induced angiographic change indicative of vasoconstriction, as independently and concordantly rated by 2 reviewers blind to treatment condition. RESULTS: Cocaine-induced cerebral vasoconstriction in a dose-related fashion (P=.03), with angiograms indicative of vasoconstriction found in 5 of 8 and 3 of 9 subjects receiving 0.4- and 0.2-mg/kg cocaine, respectively, compared with 1 of 7 subjects administered placebo. Outcome stratification by frequency of self-reported lifetime cocaine use (3-10 times, 11-40 times, or >40 times) revealed a statistically stronger dose-related effect (P<.001), suggesting that greater lifetime cocaine use was associated with a greater likelihood of vasoconstriction. CONCLUSIONS: Cocaine administration induced dose-related cerebral vasoconstriction on magnetic resonance angiograms. These changes occurred at low cocaine doses and in the absence of other risk factors, including polydrug abuse, hypertension, or cerebrovascular disease. Outcome stratification by prior cocaine use statistically strengthened the relationship between cocaine administration and vasoconstriction, suggesting that cocaine may have a cumulative residual effect in promoting cerebrovascular dysfunction.
机译:背景:临床观察和病例报告表明,使用可卡因存在重要的脑血管并发症,但尚无研究记录直接联系。目的:确定低剂量可卡因的使用是否可诱发健康可卡因使用者的脑血管收缩。设计:随机对照试验。研究对象:二十四名健康和神经系统正常的男性(平均年龄,29岁)报告中位数可卡因使用了8次终生暴露(范围从3到> 40)。干预:可卡因(0.4或0.2 mg / kg)或安慰剂的双盲静脉内给药,在基线和输注后20分钟进行脑磁共振血管造影。主要观察指标:可卡因引起的血管造影改变提示血管收缩,由2位对治疗状况不了解的评价者独立和一致地评价。结果:可卡因诱导的脑血管收缩呈剂量相关性(P = .03),与之相比,分别有0.4和0.2 mg / kg可卡因的9名受试者中有5名和3名中有5名发现血管造影指示血管收缩。 7名受试者中有1名服用了安慰剂。自我报告终生可卡因使用频率的结果分层(3-10次,11-40次或> 40次)显示出统计学上更强的剂量相关效应(P <.001),表明与终生可卡因使用量更大相关血管收缩的可能性更大。结论:可卡因给药在磁共振血管造影上可引起剂量相关的脑血管收缩。这些变化发生在可卡因剂量低和没有其他危险因素(包括滥用多种药物,高血压或脑血管疾病)的情况下。先前使用可卡因的结果分层统计学上加强了可卡因给药与血管收缩之间的关系,这表明可卡因可能在促进脑血管功能障碍方面具有累积性残留作用。

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