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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004402naa a2200349 4500
001oai:DiVA.org:liu-192334
003SwePub
008230315s2023 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-1923342 URI
024a https://doi.org/10.3390/brainsci130202292 DOI
040 a (SwePub)liu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Rahin, Hedayatu Linköpings universitet,Avdelningen för neurobiologi,Medicinska fakulteten,Region Östergötland, Neurofysiologiska kliniken US4 aut0 (Swepub:liu)hedra98
2451 0a Effect of Transcutaneous Spinal Direct Current Stimulation in Patients with Painful Polyneuropathy and Influence of Possible Predictors of Efficacy including BDNF Polymorphism: A Randomized, Sham-Controlled Crossover Study
264 c 2023-01-30
264 1b MDPI,c 2023
338 a electronic2 rdacarrier
500 a Funding Agencies|ALF Grants [LIO-936176]; Region OEstergotland [SC-2019-00155-33]; Swedish Society of medicine; Medical Council of southeast Sweden [FORSS-940600]; OEstergotland County Council; Neurofonden [F2018-0056]; Linkoeping Society of Medicine; Knut and Alice Wallenberg Foundation [2019.0047]; Wallenberg Center for Molecular Medicine-Linkoeping
520 a Introduction: The neuromodulating effects of transcutaneous-spinal Direct Current Stimulation (tsDCS) have been reported to block pain signaling. For patients with chronic pain, tsDCS could be a potential treatment option. To approach this, we studied the effect of anodal tsDCS on patients with neuropathic pain approaching an optimal paradigm including the investigation of different outcome predictors. Methods: In this randomized, double-blinded, sham-controlled crossover study we recruited twenty patients with neurophysiologically evaluated neuropathic pain due to polyneuropathy (PNP). Variables (VAS; pain and sleep quality) were reported daily, one week prior to, and one week after the stimulation/sham period. Anodal tsDCS (2.5 mA, 20 min) was given once daily for three days during one week. BDNF-polymorphism, pharmacological treatment, and body mass index (BMI) of all the patients were investigated. Results: Comparing the effects of sham and real stimulation at the group level, there was a tendency towards reduced pain, but no significant effects were found. However, for sleep quality a significant improvement was seen. At the individual level, 30 and 35% of the subjects had a clinically significant improvement of pain level and sleep quality, respectively, the first day after the stimulation. Both effects were reduced over the coming week and these changes were negatively correlated. The BDNF polymorphism Val66Met was carried by 35% of the patients and this group was found to have a lower general level of pain but there was no significant difference in the tsDCS response effect. Neither pharmacologic treatment or BMI influenced the treatment effect. Conclusions: Short-term and sparse anodal thoracic tsDCS reduces pain and improves sleep with large inter-individual differences. Roughly 30% will benefit in a clinically meaningful way. The BDNF genotype seems to influence the level of pain that PNP produces. Individualized and intensified tsDCS may be a treatment option for neuropathic pain due to PNP.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Hälsovetenskapx Sjukgymnastik0 (SwePub)303072 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Health Sciencesx Physiotherapy0 (SwePub)303072 hsv//eng
653 a neuromodulation; trans-spinal direct current stimulation; tsDCS; neuropathic pain; BDNF
700a Jackson, Walkeru Linköpings universitet,Avdelningen för neurobiologi,Medicinska fakulteten4 aut0 (Swepub:liu)walja90
700a Thordstein, Magnusu Linköpings universitet,Avdelningen för neurobiologi,Medicinska fakulteten,Region Östergötland, Neurofysiologiska kliniken US4 aut0 (Swepub:liu)magth09
710a Linköpings universitetb Avdelningen för neurobiologi4 org
773t Brain Sciencesd : MDPIg 13:2q 13:2x 2076-3425
856u https://liu.diva-portal.org/smash/get/diva2:1743522/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-192334
8564 8u https://doi.org/10.3390/brainsci13020229

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