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A preliminary report on stem cell therapy for neuropathic pain in humans

OBJECTIVE: Mesenchymal stem cells (MSCs) have been shown in animal models to attenuate chronic neuropathic pain. This preliminary study investigated if: i) injections of autologous MSCs can reduce human neuropathic pain and ii) evaluate the safety of the procedure. METHODS: Ten subjects with symptom...

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Autores principales: Vickers, E Russell, Karsten, Elisabeth, Flood, John, Lilischkis, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020887/
https://www.ncbi.nlm.nih.gov/pubmed/24855388
http://dx.doi.org/10.2147/JPR.S63361
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author Vickers, E Russell
Karsten, Elisabeth
Flood, John
Lilischkis, Richard
author_facet Vickers, E Russell
Karsten, Elisabeth
Flood, John
Lilischkis, Richard
author_sort Vickers, E Russell
collection PubMed
description OBJECTIVE: Mesenchymal stem cells (MSCs) have been shown in animal models to attenuate chronic neuropathic pain. This preliminary study investigated if: i) injections of autologous MSCs can reduce human neuropathic pain and ii) evaluate the safety of the procedure. METHODS: Ten subjects with symptoms of neuropathic trigeminal pain underwent liposuction. The lipoaspirate was digested with collagenase and washed with saline three times. Following centrifugation, the stromal vascular fraction was resuspended in saline, and then transferred to syringes for local injections into the pain fields. Outcome measures at 6 months assessed reduction in: i) pain intensity measured by standard numerical rating scale from 0–10 and ii) daily dosage requirements of antineuropathic pain medication. RESULTS: Subjects were all female (mean age 55.3 years ± standard deviation [SD] 14.67; range 27–80 years) with pain symptoms lasting from 4 months to 6 years and 5 months. Lipoaspirate collection ranged from 102–214 g with total cell numbers injected from 33 million to 162 million cells. Cell viability was 62%–91%. There were no systemic or local tissue side effects from the stem cell therapy (n=41 oral and facial injection sites). Clinical pain outcomes showed that at 6 months, 5/9 subjects had reduced both pain intensity scores and use of antineuropathic medication. The mean pain score pre-treatment was 7.5 (SD 1.58) and at 6 months had decreased to 4.3 (SD 3.28), P=0.018, Wilcoxon signed-rank test. Antineuropathic pain medication use showed 5/9 subjects reduced their need for medication (gabapentin, P=0.053, Student’s t-test). CONCLUSION: This preliminary open-labeled study showed autologous administration of stem cells for neuropathic trigeminal pain significantly reduced pain intensity at 6 months and is a safe and well tolerated intervention.
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spelling pubmed-40208872014-05-22 A preliminary report on stem cell therapy for neuropathic pain in humans Vickers, E Russell Karsten, Elisabeth Flood, John Lilischkis, Richard J Pain Res Original Research OBJECTIVE: Mesenchymal stem cells (MSCs) have been shown in animal models to attenuate chronic neuropathic pain. This preliminary study investigated if: i) injections of autologous MSCs can reduce human neuropathic pain and ii) evaluate the safety of the procedure. METHODS: Ten subjects with symptoms of neuropathic trigeminal pain underwent liposuction. The lipoaspirate was digested with collagenase and washed with saline three times. Following centrifugation, the stromal vascular fraction was resuspended in saline, and then transferred to syringes for local injections into the pain fields. Outcome measures at 6 months assessed reduction in: i) pain intensity measured by standard numerical rating scale from 0–10 and ii) daily dosage requirements of antineuropathic pain medication. RESULTS: Subjects were all female (mean age 55.3 years ± standard deviation [SD] 14.67; range 27–80 years) with pain symptoms lasting from 4 months to 6 years and 5 months. Lipoaspirate collection ranged from 102–214 g with total cell numbers injected from 33 million to 162 million cells. Cell viability was 62%–91%. There were no systemic or local tissue side effects from the stem cell therapy (n=41 oral and facial injection sites). Clinical pain outcomes showed that at 6 months, 5/9 subjects had reduced both pain intensity scores and use of antineuropathic medication. The mean pain score pre-treatment was 7.5 (SD 1.58) and at 6 months had decreased to 4.3 (SD 3.28), P=0.018, Wilcoxon signed-rank test. Antineuropathic pain medication use showed 5/9 subjects reduced their need for medication (gabapentin, P=0.053, Student’s t-test). CONCLUSION: This preliminary open-labeled study showed autologous administration of stem cells for neuropathic trigeminal pain significantly reduced pain intensity at 6 months and is a safe and well tolerated intervention. Dove Medical Press 2014-05-08 /pmc/articles/PMC4020887/ /pubmed/24855388 http://dx.doi.org/10.2147/JPR.S63361 Text en © 2014 Vickers et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Vickers, E Russell
Karsten, Elisabeth
Flood, John
Lilischkis, Richard
A preliminary report on stem cell therapy for neuropathic pain in humans
title A preliminary report on stem cell therapy for neuropathic pain in humans
title_full A preliminary report on stem cell therapy for neuropathic pain in humans
title_fullStr A preliminary report on stem cell therapy for neuropathic pain in humans
title_full_unstemmed A preliminary report on stem cell therapy for neuropathic pain in humans
title_short A preliminary report on stem cell therapy for neuropathic pain in humans
title_sort preliminary report on stem cell therapy for neuropathic pain in humans
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020887/
https://www.ncbi.nlm.nih.gov/pubmed/24855388
http://dx.doi.org/10.2147/JPR.S63361
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