Bartzokis G, Goldstein I B, Hance D B, Beckson M, Shapiro D, Lu P H, Edwards N, Mintz J, Bridge P
Mental Health Service Line, Central Arkansas Veterans Healthcare System, Little Rock 72114, USA.
AJNR Am J Neuroradiol. 1999 Oct;20(9):1628-35.
Cocaine and its metabolites can produce vasospasm, and cocaine-dependent patients are at increased risk for stroke. Based on previous case reports, we hypothesized that the incidence of hyperintense brain lesions observed on T2-weighted MR images would also be increased in asymptomatic cocaine-dependent individuals.
Sixty-two male "crack" (smoked) cocaine-dependent participants ranging in age from 25 to 66 years were compared with 116 normal male control participants ranging in age from 25 to 80 years. Those with histories of neurologic symptoms or illnesses were excluded. The severity of hyperintense lesions was rated on a 0- to 3-point scale, and ratings of 3 were used in the data analysis as an indicator of a probable pathologic process. Three regions were separately rated: the cerebral white matter, insular subcortex white matter, and subcortical gray matter (basal ganglia and thalamus region).
Significantly increased risk of severe lesions was observed in the two white matter regions of the cocaine-dependent group (odds ratio of 16.7 and 20.3) but not in the subcortial gray matter region (odds ratio of 1.4). In the insula subcortex white matter, the risk of lesions increased with age in the cocaine-dependant sample, but remained essentially absent among normal controls through the age of 80 years. In the cerebral white matter, the relationship of age and risk of lesion among normal participants was similar in shape to that in cocaine-dependent participants, but equivalent risk was seen 20 years earlier among cocaine-dependent participants.
Cocaine-dependent participants had a significantly increased age-related risk of white matter damage. The possible clinical implications of this damage are discussed.
可卡因及其代谢产物可导致血管痉挛,可卡因依赖患者发生中风的风险增加。基于既往病例报告,我们推测在无症状的可卡因依赖个体中,T2加权磁共振成像上观察到的脑内高强度病变的发生率也会增加。
将62名年龄在25至66岁之间的男性“快克”(吸食)可卡因依赖参与者与116名年龄在25至80岁之间的正常男性对照参与者进行比较。排除有神经症状或疾病史的参与者。高强度病变的严重程度按0至3分进行评分,在数据分析中,评分为3分被用作可能存在病理过程的指标。对三个区域分别进行评分:脑白质、岛叶皮质下白质和皮质下灰质(基底神经节和丘脑区域)。
在可卡因依赖组的两个白质区域观察到严重病变的风险显著增加(优势比分别为16.7和20.3),但在皮质下灰质区域未观察到增加(优势比为1.4)。在岛叶皮质下白质中,可卡因依赖样本中病变的风险随年龄增加,而在80岁之前的正常对照组中基本不存在这种情况。在脑白质中,正常参与者中年龄与病变风险的关系与可卡因依赖参与者相似,但在可卡因依赖参与者中,同等风险在早20年时出现。
可卡因依赖参与者与年龄相关的白质损伤风险显著增加。讨论了这种损伤可能的临床意义。