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Cannabidiol-enriched cannabis extraction product in Parkinson’s disease: A randomized, double-blind, and placebo-controlled trial in Buriram Hospital

OBJECTIVES: The objective of this study was to assess cannabidiol-enriched cannabis extraction product (CBDEP) efficacy in patients with Parkinson’s disease (PD). MATERIALS AND METHODS: Forty patients with PD were randomly assigned to the sublingual CBDEP (n = 20) or placebo (n = 20) group. All pati...

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Autores principales: Kanjanarangsichai, Auempa, Mitarnun, Witoon, Mitarnun, Wenika, Pangwong, Wilasinee, Laoharattanahirun, Nutchaya, Kajornrith, Warut, Junlaor, Panomporn, Nonghan, Pawarin, Witthayapirote, Wannisa, Sangkarom, Gorawan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894020/
https://www.ncbi.nlm.nih.gov/pubmed/36743777
http://dx.doi.org/10.25259/JNRP-2022-6-19
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author Kanjanarangsichai, Auempa
Mitarnun, Witoon
Mitarnun, Wenika
Pangwong, Wilasinee
Laoharattanahirun, Nutchaya
Kajornrith, Warut
Junlaor, Panomporn
Nonghan, Pawarin
Witthayapirote, Wannisa
Sangkarom, Gorawan
author_facet Kanjanarangsichai, Auempa
Mitarnun, Witoon
Mitarnun, Wenika
Pangwong, Wilasinee
Laoharattanahirun, Nutchaya
Kajornrith, Warut
Junlaor, Panomporn
Nonghan, Pawarin
Witthayapirote, Wannisa
Sangkarom, Gorawan
author_sort Kanjanarangsichai, Auempa
collection PubMed
description OBJECTIVES: The objective of this study was to assess cannabidiol-enriched cannabis extraction product (CBDEP) efficacy in patients with Parkinson’s disease (PD). MATERIALS AND METHODS: Forty patients with PD were randomly assigned to the sublingual CBDEP (n = 20) or placebo (n = 20) group. All patients were prescribed a low initial dose with gradual titration within 2 weeks based on individual response – including side effects – followed by 6 weeks of stable dosing. The primary outcome was the Unified Parkinson’s Disease Rating Scale (UPDRS) score. The secondary outcomes were as follows: Quality of life (QOL) evaluated by the EQ-5D-5L, timed up and go (TUG) test, 5 times sit to stand (FTSTS) test, gait velocity, hospital anxiety and depression scale (HADS), renal and liver function indices, and adverse events. All outcomes were measured at baseline and at 8 weeks. The generalized estimating equation adjusted for baseline scores was used to compare the values at baseline and at 8 weeks, and between the groups. RESULTS: Four patients were lost to follow-up (CBDEP group, n = 1; placebo group, n = 3) and 36 were included in the analysis (CBDEP group, n = 19; placebo group, n = 17). The CBDEP group received mean cannabidiol and tetrahydrocannabinol dosages of 15.59 ± 5.04 mg/day and 0.61 ± 0.19 mg/day, respectively. No significant differences were found between the groups in terms of the UPDRS, TUG test, FTSTS test, gait velocity, HADS-anxiety, and HADS-depression. The placebo group had significantly improved EQ-5D-5L scores for QOL (P = 0.004). The CBDEP group showed significantly improved blood urea nitrogen (BUN), serum albumin, serum globulin levels, and albumin/globulin ratio (P = 0.037, P < 0.001, P = 0.011, and P = 0.002, respectively) compared with the placebo group. Neither group had serious side effects. CONCLUSION: No evidence was found that CBDEP can reduce disease severity or improve functional performance, anxiety, or depression in PD. However, CBDEP is safe and can improve the levels of BUN, serum albumin, serum globulin, and albumin/globulin ratio in patients with PD. TRIAL REGISTRATION: Thai Clinical Trials Registry (registration number: TCTR 20210303005).
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spelling pubmed-98940202023-02-03 Cannabidiol-enriched cannabis extraction product in Parkinson’s disease: A randomized, double-blind, and placebo-controlled trial in Buriram Hospital Kanjanarangsichai, Auempa Mitarnun, Witoon Mitarnun, Wenika Pangwong, Wilasinee Laoharattanahirun, Nutchaya Kajornrith, Warut Junlaor, Panomporn Nonghan, Pawarin Witthayapirote, Wannisa Sangkarom, Gorawan J Neurosci Rural Pract Original Article OBJECTIVES: The objective of this study was to assess cannabidiol-enriched cannabis extraction product (CBDEP) efficacy in patients with Parkinson’s disease (PD). MATERIALS AND METHODS: Forty patients with PD were randomly assigned to the sublingual CBDEP (n = 20) or placebo (n = 20) group. All patients were prescribed a low initial dose with gradual titration within 2 weeks based on individual response – including side effects – followed by 6 weeks of stable dosing. The primary outcome was the Unified Parkinson’s Disease Rating Scale (UPDRS) score. The secondary outcomes were as follows: Quality of life (QOL) evaluated by the EQ-5D-5L, timed up and go (TUG) test, 5 times sit to stand (FTSTS) test, gait velocity, hospital anxiety and depression scale (HADS), renal and liver function indices, and adverse events. All outcomes were measured at baseline and at 8 weeks. The generalized estimating equation adjusted for baseline scores was used to compare the values at baseline and at 8 weeks, and between the groups. RESULTS: Four patients were lost to follow-up (CBDEP group, n = 1; placebo group, n = 3) and 36 were included in the analysis (CBDEP group, n = 19; placebo group, n = 17). The CBDEP group received mean cannabidiol and tetrahydrocannabinol dosages of 15.59 ± 5.04 mg/day and 0.61 ± 0.19 mg/day, respectively. No significant differences were found between the groups in terms of the UPDRS, TUG test, FTSTS test, gait velocity, HADS-anxiety, and HADS-depression. The placebo group had significantly improved EQ-5D-5L scores for QOL (P = 0.004). The CBDEP group showed significantly improved blood urea nitrogen (BUN), serum albumin, serum globulin levels, and albumin/globulin ratio (P = 0.037, P < 0.001, P = 0.011, and P = 0.002, respectively) compared with the placebo group. Neither group had serious side effects. CONCLUSION: No evidence was found that CBDEP can reduce disease severity or improve functional performance, anxiety, or depression in PD. However, CBDEP is safe and can improve the levels of BUN, serum albumin, serum globulin, and albumin/globulin ratio in patients with PD. TRIAL REGISTRATION: Thai Clinical Trials Registry (registration number: TCTR 20210303005). Scientific Scholar 2022-12-16 2022 /pmc/articles/PMC9894020/ /pubmed/36743777 http://dx.doi.org/10.25259/JNRP-2022-6-19 Text en © 2022 Published by Scientific Scholar on behalf of Journal of Neurosciences in Rural Practice https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Kanjanarangsichai, Auempa
Mitarnun, Witoon
Mitarnun, Wenika
Pangwong, Wilasinee
Laoharattanahirun, Nutchaya
Kajornrith, Warut
Junlaor, Panomporn
Nonghan, Pawarin
Witthayapirote, Wannisa
Sangkarom, Gorawan
Cannabidiol-enriched cannabis extraction product in Parkinson’s disease: A randomized, double-blind, and placebo-controlled trial in Buriram Hospital
title Cannabidiol-enriched cannabis extraction product in Parkinson’s disease: A randomized, double-blind, and placebo-controlled trial in Buriram Hospital
title_full Cannabidiol-enriched cannabis extraction product in Parkinson’s disease: A randomized, double-blind, and placebo-controlled trial in Buriram Hospital
title_fullStr Cannabidiol-enriched cannabis extraction product in Parkinson’s disease: A randomized, double-blind, and placebo-controlled trial in Buriram Hospital
title_full_unstemmed Cannabidiol-enriched cannabis extraction product in Parkinson’s disease: A randomized, double-blind, and placebo-controlled trial in Buriram Hospital
title_short Cannabidiol-enriched cannabis extraction product in Parkinson’s disease: A randomized, double-blind, and placebo-controlled trial in Buriram Hospital
title_sort cannabidiol-enriched cannabis extraction product in parkinson’s disease: a randomized, double-blind, and placebo-controlled trial in buriram hospital
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894020/
https://www.ncbi.nlm.nih.gov/pubmed/36743777
http://dx.doi.org/10.25259/JNRP-2022-6-19
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