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Abnormal tactile discrimination and somatosensory plasticity in familial primary hyperhidrosis.

机译:家族性原发性多汗症的触觉辨别异常和体感可塑性。

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摘要

Abnormal sensory processing seems to be involved in hyperhidrosis. To test this hypothesis, we investigated tactile acuity and cortical plastic changes in patients with primary hyperhidrosis (PH) and their asymptomatic relatives. We studied thirteen subjects belonging to two families with PH and thirteen age-matched healthy controls using Johnson-Van Boven-Phillips domes before and after 45min of transient visual deafferentation. Spatial discrimination thresholds (SDTs) were lower in controls than in the familial group (1.08+/-0.25 vs 1.59+/-0.71; p=0.0032). After 45min of light deprivation and blindfolding, SDTs decreased significantly in controls (0.83+/-0.3; p=0.003), but not in patients (1.4+/-0.62; p=0.108). Interestingly, two subjects without clinical complaints of hyperhidrosis had abnormal SDTs behavior after short term visual deprivation. This study demonstrates that sensory processing is abnormal in PH, with a lack of plastic cortical somatosensory changes regardless of clinical condition. These modulatory abnormalities would affect gating processes in the somatosensory cortex which may play a role in maintaining hyperhidrosis.
机译:多汗症似乎与异常的感觉处理有关。为了检验该假设,我们调查了原发性多汗症(PH)及其无症状亲属的触觉敏锐度和皮质可塑性变化。我们研究了短暂性视觉脱盲前后45分钟内使用Johnson-Van Boven-Phillips穹顶对属于PH的两个家族的13位受试者和13位年龄匹配的健康对照组的研究。对照组的空间歧视阈值(SDT)低于家族组(1.08 +/- 0.25对1.59 +/- 0.71; p = 0.0032)。剥夺光明和蒙住眼睛45分钟后,对照组的SDT显着降低(0.83 +/- 0.3; p = 0.003),但患者没有降低(1.4 +/- 0.62; p = 0.108)。有趣的是,在短期视觉剥夺后,没有临床多汗症临床症状的两名受试者的SDTs行为异常。这项研究表明,无论临床情况如何,PH的感觉处理都是异常的,缺乏可塑的皮层体感变化。这些调节异常将影响体感皮层的门控过程,这可能在维持多汗症中起作用。

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