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Selective Decrease in Central Nervous System Serotonin Turnover in Children with Dopa-Nonresponsive Dystonia

机译:多巴无反应性肌张力障碍患儿中枢神经系统血清素转换的选择性降低

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Childhood dystonia that does not respond to treatment with levodopa (dopa-nonresponsive dystonia, DND) has an unclear pathogenesis and is notoriously difficult to treat. To test the hypothesis that there may be abnormalities in serotonin turnover in DND we measured cerebrospinal fluid (CSF) concentrations of homovanillic (HVA) and 5-hydroxyindoleacetic (HIAA) acids, metabolites of dopamine and serotonin, respectively, in 18 children with dystonia not responsive to levodopa. These were combined with a reference population of 85 children with neurologic or metabolic disease known not to affect dopamine or serotonin metabolism. Because of the known natural age-related decrement in HVA and HIAA concentrations, the results were analyzed using multiple regression using age and DND as predictors of CSF HIAA and HVA concentrations. DND was a highly significant predictor of CSF HIAA concentration (p p = 0.59). After fitting a regression model, the geometric mean ratio of CSF HIAA in DND compared with the reference range was 0.53 whereas that for CSF HVA was 0.95. We also analyzed CSF HIAA/HVA ratios. After fitting a regression model, we found no dependence on age, and the mean of CSF HIAA/HVA in DND was 0.28 whereas that for the reference range was 0.49 (p Abbreviations: CSF, cerebrospinal fluid; HIAA, 5-hydroxyindoleacetic acid; HVA, homovanillic acid; DND, dopa-nonresponsive dystonia
机译:对左旋多巴治疗无反应的儿童肌张力障碍(多巴无反应性肌张力障碍,DND)的发病机理尚不清楚,而且众所周知难以治疗。为了检验DND中5-羟色胺转换可能存在异常的假设,我们测量了18例没有张力障碍的儿童的脑脊髓液(CSF)的高香草酸(HVA)和5-羟吲哚乙酸(HIAA)酸,多巴胺和5-羟色胺的代谢产物浓度。对左旋多巴有反应。将这些与参照的85名患神经系统疾病或新陈代谢疾病的儿童(不影响多巴胺或5-羟色胺代谢)结合在一起。由于HVA和HIAA浓度与年龄相关的自然下降,因此使用年龄和DND作为CSF HIAA和HVA浓度的预测因子,使用多元回归分析了结果。 DND是脑脊液HIAA浓度的高度重要预测因子(p p = 0.59)。拟合回归模型后,DND中CSF HIAA的几何平均比率与参考范围相比为0.53,而CSF HVA的几何平均比率为0.95。我们还分析了脑脊液HIAA / HVA比率。拟合回归模型后,我们发现没有年龄依赖性,DND中CSF HIAA / HVA的平均值为0.28,而参考范围的平均值为0.49(p缩写:CSF,脑脊液; HIAA,5-羟基吲哚乙酸; HVA ,高香草酸; DND,多巴无反应性肌张力障碍

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