Francesco Morra, Matteo Minerva, Silvia Valeggia, Giovanni Librizzi, Elena Tramarin, Caterina Scalpelli, Anna Bordin, Giancarlo Ottaviano, Piergiorgio Gaudioso, Alessandra Bertoldo, Manuela Moretto, Alessandro Miola, Eleonora Lupia, Riccardo Ceccato, Carla Mucignat, Angelo Antonini, Renzo Manara
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Eighty-three subjects (mean-age 43±14 years; 54 females; time-interval infection/MRI: 129±68 days) affected by asymptomatic to mild COVID19 in 2020 and 25 healthy controls (mean-age 40±13 years; 9 females) underwent 3T-MRI and olfactory function evaluation through anamnestic questionnaire and Sniffin' Sticks. Exclusion criteria were intensive care treatment or neurological involvement other than olfaction. Maximal OB area was measured blindly on high-resolution coronal T2w images by two observers. Patients were subdivided into: i) persistently hypo/anosmic, ii) recovered normosmic and iii) never complaining smell dysfunction with proven normal olfactory function. No significant differences were observed among patients' subgroups (p=0.76). Intra-observer and inter-observer reliability were high.(r=0.96 and 0.86). Former COVID19 patients had decreased mean maximal OB area than controls (6.52±1.11mm2 vs 7.26±1.17mm2, p=0.008) even when considering persistently hypo-anosmic (6.46±0.90, p=0.006) or normosmic patients at MRI (6.57±1.25, p=0.04). SARS-CoV-2 infection is associated with mid/late-term morphological changes on the olfactory bulbs, regardless of presence or persistence of olfactory dysfunction. 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引用次数: 0
摘要
一过性或持续性嗅觉减退在 SARS-CoV-2 感染中很常见,但嗅觉通路的晚期形态变化仍在研究中。我们评估了无神经系统症状的 COVID-19 患者的后期嗅球(OB)成像变化及其与嗅觉功能的相关性。2020年,83名无症状至轻度COVID-19患者(平均年龄43±14岁;54名女性;感染/MRI时间间隔:129±68天)和25名健康对照者(平均年龄40±13岁;9名女性)接受了3T-MRI检查,并通过肛门问卷和嗅棒进行了嗅觉功能评估。排除标准是接受过重症监护治疗或患有嗅觉以外的神经系统疾病。由两名观察者在高分辨率冠状 T2w 图像上盲测最大 OB 面积。患者被细分为:i) 持续嗅觉减退/缺失;ii) 已恢复正常嗅觉;iii) 从未抱怨嗅觉功能障碍且经证实嗅觉功能正常。各组患者之间无明显差异(P=0.76)。观察者内部和观察者之间的可靠性很高(r=0.96 和 0.86)。与对照组相比,COVID19 前患者的平均最大 OB 面积较小(6.52±1.11mm2 vs 7.26±1.17mm2,p=0.008),即使考虑到 MRI 时持续低血钾(6.46±0.90,p=0.006)或正常血钾患者(6.57±1.25,p=0.04)。无论嗅觉功能障碍是否存在或持续存在,SARS-CoV-2 感染都与嗅球中期/晚期形态学变化有关。对嗅觉衰老的长期影响需要进一步研究,包括与神经退行性疾病的可能联系。
Transient or persistent hypo-anosmia is common in SARS‑CoV‑2 infection but olfactory pathway late-term morphometric changes are still under investigation. We evaluated late olfactory bulb (OB) imaging changes and their correlates with the olfactory function in otherwise neurologically asymptomatic COVID-19 patients. Eighty-three subjects (mean-age 43±14 years; 54 females; time-interval infection/MRI: 129±68 days) affected by asymptomatic to mild COVID19 in 2020 and 25 healthy controls (mean-age 40±13 years; 9 females) underwent 3T-MRI and olfactory function evaluation through anamnestic questionnaire and Sniffin' Sticks. Exclusion criteria were intensive care treatment or neurological involvement other than olfaction. Maximal OB area was measured blindly on high-resolution coronal T2w images by two observers. Patients were subdivided into: i) persistently hypo/anosmic, ii) recovered normosmic and iii) never complaining smell dysfunction with proven normal olfactory function. No significant differences were observed among patients' subgroups (p=0.76). Intra-observer and inter-observer reliability were high.(r=0.96 and 0.86). Former COVID19 patients had decreased mean maximal OB area than controls (6.52±1.11mm2 vs 7.26±1.17mm2, p=0.008) even when considering persistently hypo-anosmic (6.46±0.90, p=0.006) or normosmic patients at MRI (6.57±1.25, p=0.04). SARS-CoV-2 infection is associated with mid/late-term morphological changes on the olfactory bulbs, regardless of presence or persistence of olfactory dysfunction. The long-term consequences on olfactory aging need to be further investigated including possible links with neurodegenerative disorders.
期刊介绍:
Chemical Senses publishes original research and review papers on all aspects of chemoreception in both humans and animals. An important part of the journal''s coverage is devoted to techniques and the development and application of new methods for investigating chemoreception and chemosensory structures.