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Ultramicronized Palmitoylethanolamide and Luteolin Supplement Combined with Olfactory Training to Treat Post-COVID-19 Olfactory Impairment: A Multi-Center Double-Blinded Randomized Placebo-Controlled Clinical Trial

Articolo
Data di Pubblicazione:
2022
Citazione:
Ultramicronized Palmitoylethanolamide and Luteolin Supplement Combined with Olfactory Training to Treat Post-COVID-19 Olfactory Impairment: A Multi-Center Double-Blinded Randomized Placebo-Controlled Clinical Trial / Di Stadio, A.; D'Ascanio, L.; Vaira, L. A.; Cantone, E.; De Luca, P.; Cingolani, C.; Motta, G.; De Riu, G.; Vitelli, F.; Spriano, G.; De Vincentiis, M.; Camaioni, A.; La Mantia, I.; Ferreli, F.; Brenner, M. J.. - In: CURRENT NEUROPHARMACOLOGY. - ISSN 1570-159X. - 20:10(2022), pp. 2001-2012. [10.2174/1570159X20666220420113513]
Abstract:
Background: Olfactory training is the only evidence-based treatment for post-viral olfactory dysfunction. Smell disorders after SARS-CoV-2 infection have been attributed to neuroinflammatory events within the olfactory bulb and the central nervous system. Therefore, targeting neuroinflammation is one potential strategy for promoting recovery from post-COVID-19 chronic olfactory dysfunction. Palmitoylethanolamide and luteolin (PEA-LUT) are candidate antiinflammatory/ neuroprotective agents. Objective: To investigate recovery of olfactory function in patients treated with PEA-LUT oral supplements plus olfactory training versus olfactory training plus placebo. Methods: Multicenter double-blinded randomized placebo-controlled clinical trial was held. Eligible subjects had prior COVID-19 and persistent olfactory impairment >6 months after follow-up SARS-CoV-2 negative testing, without prior history of olfactory dysfunction or other sinonasal disorders. Participants were randomized to daily oral supplementation with ultramicronized PEA-LUT 770 mg plus olfactory training (intervention group) or olfactory training with placebo (control). Sniffin’ Sticks assessments were used to test the patients at baseline and 90 days. Results: A total of 185 patients, including intervention (130) and control (55) were enrolled. The intervention group showed significantly greater improvement in olfactory threshold, discrimination, and identification scores compared to controls (p=0.0001). Overall, 92% of patients in the intervention group improved versus 42% of controls. Magnitude of recovery was significantly greater in the intervention group versus control (12.8 + 8.2 versus mean 3.2 + 3), with >10-fold higher prevalence of anosmia in control versus intervention groups at the 90-day endpoint. Conclusion: Among individuals with olfactory dysfunction post-COVID-19, combining PEA-LUT with olfactory training resulted in greater recovery of smell than olfactory training alone. Clinical Trial Registration: (Italian; Clinicaltrials.gov number: NCT04853836).
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
anosmia; anti-inflammatory; coronavirus; COVID-19; hyposmia; olfaction; olfactory dysfunction; olfactory training; SARS-CoV-2
Elenco autori:
Di Stadio, A.; D'Ascanio, L.; Vaira, L. A.; Cantone, E.; De Luca, P.; Cingolani, C.; Motta, G.; De Riu, G.; Vitelli, F.; Spriano, G.; De Vincentiis, M.; Camaioni, A.; La Mantia, I.; Ferreli, F.; Brenner, M. J.
Autori di Ateneo:
DE RIU Giacomo
VAIRA Luigi Angelo
Link alla scheda completa:
https://iris.uniss.it/handle/11388/313049
Pubblicato in:
CURRENT NEUROPHARMACOLOGY
Journal
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URL

https://pmc.ncbi.nlm.nih.gov/articles/PMC9886808/
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