Department of Medicine, Surgery and Dentistry, University of Salerno, Baronissi, 84081 Salerno, Italy.
Otolaryngology Department, San Giovanni-Addolorata Hospital, 00184 Rome, Italy.
Cells. 2022 Aug 17;11(16):2552. doi: 10.3390/cells11162552.
In this study, we investigated whether treatment with palmitoylethanolamide and luteolin (PEA-LUT) leads to improvement in the quantitative or qualitative measures of olfactory dysfunction or relief from mental clouding in patients affected by long COVID. Patients with long COVID olfactory dysfunction were allocated to different groups based on the presence ("previously treated") or absence ("naïve") of prior exposure to olfactory training. Patients were then randomized to receive PEA-LUT alone or in combination with olfactory training. Olfactory function and memory were assessed at monthly intervals using self-report measures and quantitative thresholds. A total of 69 patients (43 women, 26 men) with an age average of 40.6 + 10.5 were recruited. PEA-LUT therapy was associated with a significant improvement in validated odor identification scores at the baseline versus each subsequent month; assessment at 3 months showed an average improvement of 10.7 + 2.6, CI 95%: 6-14 ( < 0.0001). The overall prevalence of parosmia was 79.7% (55 patients), with a significant improvement from the baseline to 3 months ( < 0.0001), namely in 31 patients from the Naïve 1 group (72%), 15 from the Naïve 2 group (93.7%), and 9 from the remaining group (90%). Overall, mental clouding was detected in 37.7% (26 subjects) of the cases, with a reduction in severity from the baseline to three months ( = 0.02), namely in 15 patients from the Naïve 1 group (34.8%), 7 from the Naïve 2 group (43.7%), and 4 from the remaining group (40%). Conclusions. In patients with long COVID and chronic olfactory loss, a regimen including oral PEA-LUT and olfactory training ameliorated olfactory dysfunction and memory. Further investigations are necessary to discern biomarkers, mechanisms, and long-term outcomes.
在这项研究中,我们调查了棕榈酰乙醇酰胺和叶黄素(PEA-LUT)治疗是否会改善长期 COVID 患者嗅觉功能障碍的定量或定性指标,或减轻他们的精神模糊。根据患者是否接受过嗅觉训练(“先前治疗过”或“未经治疗”),将长期 COVID 嗅觉障碍患者分配到不同的组中。然后,患者被随机分配接受 PEA-LUT 单独治疗或与嗅觉训练联合治疗。使用自我报告措施和定量阈值,每月评估一次嗅觉功能和记忆。共招募了 69 名年龄平均为 40.6+10.5 岁的患者(43 名女性,26 名男性)。PEA-LUT 治疗与基线时相比,在每个后续月的验证气味识别评分上均有显著改善;3 个月时的评估显示,平均改善 10.7+2.6,CI95%:6-14(<0.0001)。总体味觉障碍的患病率为 79.7%(55 名患者),从基线到 3 个月时显著改善(<0.0001),即在未经治疗的 1 组中,有 31 名患者(72%)、未经治疗的 2 组中 15 名患者(93.7%)和其余组中 9 名患者(90%)。总体而言,在 37.7%(26 名)的病例中发现存在精神模糊,从基线到三个月时严重程度降低(=0.02),即在未经治疗的 1 组中,有 15 名患者(34.8%)、未经治疗的 2 组中 7 名患者(43.7%)和其余组中 4 名患者(40%)。结论:在长期 COVID 和慢性嗅觉丧失的患者中,包含口服 PEA-LUT 和嗅觉训练的方案可改善嗅觉功能障碍和记忆力。需要进一步研究以辨别生物标志物、机制和长期结果。