Introduction: Forearm QSWEAT recordings are occasionally absent in females, likely due to high skin resistance.
Methods: We identified consecutive subjects with no sudomotor abnormalities but absent/markedly reduced QSWEAT forearm volume, and repeated QSWEAT at the same site after gentle abrasion.
Results: QSWEAT volumes were absent for 4 subjects and markedly reduced for the other 4 (median 0.01, IQR 0-0.03). After gentle skin abrasion, repeat volumes were significantly higher for all subjects and became normal in 7 of 8 subjects.
Discussion: Skin abrasion restores QSWEAT volumes in previously absent/markedly reduced site suggesting that skin preparation using abrasion is more effective.
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http://dx.doi.org/10.1016/j.autneu.2019.102589 | DOI Listing |
Auton Neurosci
December 2019
Department of Neurology, Mayo Clinic, Rochester, MN, USA. Electronic address:
Introduction: Forearm QSWEAT recordings are occasionally absent in females, likely due to high skin resistance.
Methods: We identified consecutive subjects with no sudomotor abnormalities but absent/markedly reduced QSWEAT forearm volume, and repeated QSWEAT at the same site after gentle abrasion.
Results: QSWEAT volumes were absent for 4 subjects and markedly reduced for the other 4 (median 0.
Auton Neurosci
December 2017
Department of Neurology, Stanford University Medical Center, 213 Quarry Road, M/C 5992, Palo Alto, CA 94304, United States.
Introduction: It is not clear if patients with postural tachycardia syndrome (POTS) and Ehlers-Danlos syndrome (hEDS) differ from patients with POTS due to other etiologies. We compared the results of autonomic testing and healthcare utilization in POTS patients with and without hEDS.
Methods: Patients with POTS+hEDS (n=20) and POTS controls without hypermobility (n=20) were included in the study.
BMC Neurosci
June 2012
Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Background: Q-Sweat is a model used for evaluating the post-ganglionic sudomotor function by assessing sweat response. This study aimed to establish the normative database of Q-Sweat test among Chinese individuals since this type of information is currently lacking.
Results: One hundred and fifty (150) healthy volunteers, 76 men and 74 women with age range of 22-76 years were included.
BMC Neurol
May 2011
Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Background: Cerebrotendinous xanthomatosis (CTX) is a rare lipid-storage disease. Neuromuscular abnormality and autonomic system (ANS) dysfuction in CTX are rarely examined in large-scale studies in the literature. We studied the peripheral nervous system, myopathology, and autonomic system of four CTX patients and performed a literature review of the reported CTX patients with peripheral neuropathy.
View Article and Find Full Text PDFMuscle Nerve
February 2010
Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Q-Sweat, a commercial quantitative sweat measurement system, is modeled on quantitative sudomotor axon reflex testing (QSART). This study investigated the sweat response using Q-Sweat and Mayo-QSART recordings under identical conditions in healthy normal controls. Ninety-four participants were recruited for this study.
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