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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

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  • معلومة اضافية
    • Contributors:
      Di Stadio, Arianna; D'Ascanio, Luca; Vaira, Luigi Angelo; Cantone, Elena; De Luca, Pietro; Cingolani, Cristina; Motta, Gaetano; De Riu, Giacomo; Vitelli, Federica; Spriano, Giuseppe; De Vincentiis, Marco; Camaioni, Angelo; La Mantia, Ignazio; Ferreli, Fabio; Brenner, Michael J
    • بيانات النشر:
      Bentham Science Publishers Ltd.
      Sharjah, Emirati Arabi Uniti
    • الموضوع:
      2022
    • Collection:
      Sapienza Università di Roma: CINECA IRIS
    • نبذة مختصرة :
      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.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/35450527; info:eu-repo/semantics/altIdentifier/wos/WOS:000858546800019; volume:20; issue:10; firstpage:2001; lastpage:2012; numberofpages:12; journal:CURRENT NEUROPHARMACOLOGY; https://hdl.handle.net/11573/1693520; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85130994694
    • الرقم المعرف:
      10.2174/1570159X20666220420113513
    • Rights:
      info:eu-repo/semantics/openAccess
    • الرقم المعرف:
      edsbas.3F8D4DCB