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原发性震颤患者血液中哈尔满(1-甲基-9H-吡啶并[3,4-b]吲哚)浓度升高。

Elevated blood harmane (1-methyl-9H-pyrido[3,4-b]indole) concentrations in essential tremor.

作者信息

Louis Elan D, Jiang Wendy, Pellegrino Kathryn M, Rios Eileen, Factor-Litvak Pam, Henchcliffe Claire, Zheng Wei

机构信息

GH Sergievsky Center, College of Physicians and Surgeons, Columbia University, New York, NY, USA.

出版信息

Neurotoxicology. 2008 Mar;29(2):294-300. doi: 10.1016/j.neuro.2007.12.001. Epub 2007 Dec 27.

Abstract

Essential tremor (ET) is a widespread late-life neurological disease. Genetic and environmental factors likely play an etiological role. Harmane (1-methyl-9H-pyrido[3,4-b]indole) is a potent tremor-producing neurotoxin. In 2002, we demonstrated elevated blood harmane concentrations in an initial sample of 100 ET cases compared to 100 controls. Between 2002 and 2007, we assembled a new and larger sample of ET cases and controls. We now attempt to replicate our previous findings. Cases and controls were frequency-matched on age, gender, and race. Blood harmane concentrations were quantified by high-performance liquid chromatography. Subjects comprised 150 ET cases and 135 controls (mean age 65.3+/-15.5 vs. 65.5+/-14.2 years, p=0.94). Mean log blood harmane concentration was approximately 50% higher in cases than controls (0.50+/-0.54g(-10)/ml vs. 0.35+/-0.62g(-10)/ml, p=0.038). In a logistic regression analysis, log blood harmane concentration was associated with ET (OR(adjusted) 1.56, 95% CI 1.01-2.42, p=0.04), and odds of ET was 1.90 (95% CI 1.07-3.39, p=0.029) in the highest versus lowest log blood harmane tertile. Log blood harmane was highest in ET cases with familial ET (0.53+/-0.57g(-10)/ml), intermediate in cases with sporadic ET (0.43+/-0.45g(-10)/ml) and lowest in controls (0.35+/-0.62g(-10)/ml) (test for trend, p=0.026). Blood harmane appears to be elevated in ET. The higher concentrations in familial ET suggests that the mechanism may involve genetic factors.

摘要

特发性震颤(ET)是一种常见的老年神经系统疾病。遗传和环境因素可能在其病因中起作用。哈尔满(1-甲基-9H-吡啶并[3,4-b]吲哚)是一种强效的致震颤神经毒素。2002年,我们发现,与100名对照相比,在100例ET患者的初始样本中,血液哈尔满浓度升高。在2002年至2007年期间,我们收集了一个新的、更大的ET病例和对照样本。我们现在试图重复我们之前的发现。病例和对照在年龄、性别和种族上进行了频率匹配。通过高效液相色谱法定量血液哈尔满浓度。受试者包括150例ET病例和135名对照(平均年龄65.3±15.5岁 vs. 65.5±14.2岁,p = 0.94)。病例组的平均血液哈尔满对数浓度比对照组高约50%(0.50±0.54g⁻¹⁰/ml vs. 0.35±0.62g⁻¹⁰/ml,p = 0.038)。在逻辑回归分析中,血液哈尔满对数浓度与ET相关(OR(调整后) 1.56,95% CI 1.01 - 2.42,p = 0.04),在血液哈尔满对数浓度最高三分位数与最低三分位数相比,ET的比值比为1.90(95% CI 1.07 - 3.39,p = 0.029)。血液哈尔满对数在家族性ET的ET病例中最高(0.53±0.57g⁻¹⁰/ml),在散发性ET病例中居中(0.43±0.45g⁻¹⁰/ml),在对照组中最低(0.35±0.62g⁻¹⁰/ml)(趋势检验,p = 0.026)。ET患者的血液哈尔满似乎升高。家族性ET中较高的浓度表明其机制可能涉及遗传因素。

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