Autonomic Dysfunction among Migraineurs with and without Complaints of Orthostatic Intolerance: Evidence for Small Fiber Nerve Damage

M. Stillman
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引用次数: 3

Abstract

Background and Objective: Migraineurs often complain of orthostatic intolerance (OI), and its recognition is vital to appropriate treatment. This study attempts to identify and characterize autonomic dysfunction, comparing a sample of migraineurs with OI with a sample of migraineurs without OI. Methods: In a prospective cohort study, we examined one migraine sample complaining of OI for > 6 months (Group 1) and another group without OI (Group 2), using a 70-degree, 45-minute head-up passive tilt-table (HUT45) test, electrocardiographic R-R interval measurements during deep breathing, blood pressure and heart rate monitoring during Valsalva and release, QSART, and skin biopsy for nerve fiber density. We compared results with standard, 10-minute head-up passive tilt-table (HUT10) results to determine which test promoted greater sensitivity, specificity and diagnostic accuracy. Descriptive statistics were computed for each group, defined by the presence or absence of OI. We conducted several receiver operating characteristic analyses to determine whether certain clinical characteristics were predictive of symptoms of OI. Results: Thirty-nine Group 1 and 22 Group 2 subjects were studied and were similar demographically. Thirty eight of 39 (97.4%) Group 1, versus 15/22 (68.2%) Group 2 subjects, manifested abnormal HUT45 results, a significant difference (p=0.002). The HUT45 showed higher sensitivity (0.59; 95% CI: 0.42-0.74) than the standard 10-minute tilt-table test (HUT10) for all expressions of OI (0.31; 95% CI: 0.17-0.48). No differences in autonomic laboratory or skin biopsy findings distinguished the groups. We detected biopsy-proven small fiber neuropathy in 22/39 (56.4%) Group 1 and 10/22 (45.5%) Group 2 subjects. Discussion and Conclusions: In migraineurs, OI is an expression of autonomic dysfunction. We found evidence for a peripheral autonomic deficit on skin biopsy in 45% or more of both groups of migraineurs. Extending the head-up tilt table test to 45-minutes increases diagnostic sensitivity, spares patients misdiagnosis and unnecessary testing, and satisfies the principle of ecological validity.
有或无直立不耐受主诉的偏头痛患者的自主神经功能障碍:小纤维神经损伤的证据
背景与目的:偏头痛患者常主诉直立性不耐受(OI),对其进行识别对适当治疗至关重要。本研究试图通过比较有成骨不全的偏头痛患者和没有成骨不全的偏头痛患者的样本来识别和表征自主神经功能障碍。方法:在一项前瞻性队列研究中,我们使用70度,45分钟的平视被动倾斜试验(HUT45),深呼吸时的心电图R-R间隔测量,Valsalva和释放期间的血压和心率监测,QSART和神经纤维密度的皮肤活检检查了一名患有成骨不全> 6个月的偏头痛样本(第1组)和另一组无成骨不全(第2组)。我们将结果与标准的10分钟平视被动倾斜台(hutt10)结果进行比较,以确定哪种测试能提高灵敏度、特异性和诊断准确性。对每组进行描述性统计,根据有无成骨不全进行定义。我们进行了几项受试者操作特征分析,以确定某些临床特征是否可预测成骨不全症的症状。结果:第一组39例,第二组22例,人口学特征相似。1组39例患者中38例(97.4%)出现HUT45异常,2组15例(68.2%)出现HUT45异常,差异有统计学意义(p=0.002)。HUT45具有较高的敏感性(0.59;95% CI: 0.42-0.74)比标准的10分钟倾斜表试验(hutt10) (0.31;95% ci: 0.17-0.48)。自主神经实验室或皮肤活检结果无差异。第1组22/39(56.4%)和第2组10/22(45.5%)检测到活检证实的小纤维神经病变。讨论与结论:在偏头痛患者中,成骨不全是自主神经功能障碍的一种表现。我们在两组偏头痛患者的皮肤活检中发现了45%或更多的外周自主神经缺损的证据。将平视倾斜台试验延长至45分钟,可提高诊断敏感性,避免患者误诊和不必要的检测,满足生态效度原则。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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