COVID-19 anosmia and gustatory symptoms as a prognosis factor: a subanalysis of the HOPE COVID-19 (Health Outcome Predictive Evaluation for COVID-19) registry.
Anosmia
COVID-19
Hospital
Pathophysiology
Prognosis
SARS-COV-2
Journal
Infection
ISSN: 1439-0973
Titre abrégé: Infection
Pays: Germany
ID NLM: 0365307
Informations de publication
Date de publication:
Aug 2021
Aug 2021
Historique:
received:
30
11
2020
accepted:
08
02
2021
pubmed:
2
3
2021
medline:
19
8
2021
entrez:
1
3
2021
Statut:
ppublish
Résumé
Olfactory and gustatory dysfunctions (OGD) are a frequent symptom of coronavirus disease 2019 (COVID-19). It has been proposed that the neuroinvasive potential of the novel SARS-CoV-2 could be due to olfactory bulb invasion, conversely studies suggest it could be a good prognostic factor. The aim of the current study was to investigate the prognosis value of OGD in COVID-19. These symptoms were recorded on admission from a cohort study of 5868 patients with confirmed or highly suspected COVID-19 infection included in the multicenter international HOPE Registry (NCT04334291). There was statistical relation in multivariate analysis for OGD in gender, more frequent in female 12.41% vs 8.67% in male, related to age, more frequent under 65 years, presence of hypertension, dyslipidemia, diabetes, smoke, renal insufficiency, lung, heart, cancer and neurological disease. We did not find statistical differences in pregnant (p = 0.505), patient suffering cognitive (p = 0.484), liver (p = 0.1) or immune disease (p = 0.32). There was inverse relation (protective) between OGD and prone positioning (0.005) and death (< 0.0001), but no with ICU (0.165) or mechanical ventilation (0.292). On univariable logistic regression, OGD was found to be inversely related to death in COVID-19 patients. The odds ratio was 0.26 (0.15-0.44) (p < 0.001) and Z was - 5.05. The presence of anosmia is fundamental in the diagnosis of SARS.CoV-2 infection, but also could be important in classifying patients and in therapeutic decisions. Even more knowing that it is an early symptom of the disease. Knowing that other situations as being Afro-American or Latino-American, hypertension, renal insufficiency, or increase of C-reactive protein (CRP) imply a worse prognosis we can make a clinical score to estimate the vital prognosis of the patient. The exact pathogenesis of SARS-CoV-2 that causes olfactory and gustative disorders remains unknown but seems related to the prognosis. This point is fundamental, insomuch as could be a plausible way to find a treatment.
Identifiants
pubmed: 33646505
doi: 10.1007/s15010-021-01587-9
pii: 10.1007/s15010-021-01587-9
pmc: PMC7917537
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
677-684Informations de copyright
© 2021. Springer-Verlag GmbH, DE part of Springer Nature.
Références
Margallo LN, Diaz M, Lim PP. 2019 Novel coronavirus pandemic: what do we know? Medicine. 2020;73:262–4.
Morrison AR, Johnson JM, Griebe KM, et al. Clinical characteristics and predictors of survival in adults with coronavirus disease 2019 receiving tocilizumab. J Autoimmun. 2020. https://doi.org/10.1016/j.jaut.2020.102512 .
doi: 10.1016/j.jaut.2020.102512
pubmed: 32646770
pmcid: 7332925
Beltrán-Corbellini Á, Chico-García JL, Martínez-Poles J, et al. Acute-onset smell and taste disorders in the context of COVID-19: a pilot multicentre polymerase chain reaction based case-control study. Eur J Neurol. 2020. https://doi.org/10.1111/ene.14273 .
doi: 10.1111/ene.14273
pubmed: 32449247
pmcid: 7283814
Gómez-Iglesias P, Porta-Etessam J, Montalvo T, et al. An online observational study of patients with olfactory and gustory alterations secondary to SARS-CoV-2 infection. Front Public Health. 2020;8:243. https://doi.org/10.3389/fpubh.2020.00243 .
doi: 10.3389/fpubh.2020.00243
pubmed: 32574308
pmcid: 7273853
Kanwar D, Baig AM, Wasay M. Neurological manifestations of COVID-19. J Pak Med Assoc. 2020;70:S101–3. https://doi.org/10.5455/JPMA.20 .
doi: 10.5455/JPMA.20
pubmed: 32515379
Cataldi M, Pignataro G, Taglialatela M. Neurobiology of coronaviruses: Potential relevance for COVID-19. Neurobiol Dis. 2020. https://doi.org/10.1016/j.nbd.2020.105007 .
doi: 10.1016/j.nbd.2020.105007
pubmed: 32622086
pmcid: 7329662
Aragão MFVV, Leal MC, Cartaxo Filho OQ, Fonseca TM, Valença MM. Anosmia in COVID-19 associated with injury to the olfactory bulbs evident on MRI. AJNR Am J Neuroradiol. 2020. https://doi.org/10.3174/ajnr.A6675.10.3174/ajnr.A6675 .
doi: 10.3174/ajnr.A6675.10.3174/ajnr.A6675
pubmed: 33272952
Paniz-Mondolfi A, Bryce C, Grimes Z, et al. Central nervous system involvement by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). J Med Virol. 2020;92:699–702. https://doi.org/10.1002/jmv.25915 .
doi: 10.1002/jmv.25915
pubmed: 32314810
Yan CH, Faraji F, Prajapati DP, Ostrander BT, DeConde AS. Self-reported olfactory loss associates with outpatient clinical course in COVID-19. Int Forum Allergy Rhinol. 2020;10:821–31. https://doi.org/10.1002/alr.22592 .
doi: 10.1002/alr.22592
pubmed: 32329222
Lechien JR, Chiesa-Estomba CM, De Siati DR, Horoi M, Le Bon SD, Rodriguez A, et al. Olfactory and gustatory dysfunctions as a clinical present2ation of mild-to-moderate forms of the coronavirus disease (COVID-19): a multicenter European study. Eur Arch Otorhinolaryngol. 2020. https://doi.org/10.1007/s00405-020-05965-1 .
doi: 10.1007/s00405-020-05965-1
pubmed: 33237476
pmcid: 7527148
Klopfenstein T, Kadiane-Oussou NJ, Toko L, Royer PY, Lepiller Q, Gendrin V, Zayet S. Features of anosmia in COVID-19. Med Mal Infect. 2020. https://doi.org/10.1016/j.medmal.2020.04.006 .
doi: 10.1016/j.medmal.2020.04.006
pubmed: 32387320
pmcid: 7442065
Menni C, Valdes AM, Freidin MB, et al. Real-time tracking of self-reported symptoms to predict potential COVID-19. Nat Med. 2020;26:1037–40. https://doi.org/10.1038/s41591-020-0916-2 .
doi: 10.1038/s41591-020-0916-2
pubmed: 32393804
pmcid: 7751267
Mao L, Jin H, Wang M, et al. Neurologic manifestations of hospitalized patients with coronavirus disease 2019 in Wuhan, China. JAMA Neurol. 2020;77:683–90. https://doi.org/10.1001/jamaneurol.2020.1127 .
doi: 10.1001/jamaneurol.2020.1127
pubmed: 32275288
pmcid: 32275288
Imamura F, Hasegawa-Ishii S. Environmental toxicants-induced immune responses in the olfactory mucosa. Front Immunol. 2016;7:475. https://doi.org/10.3389/fimmu.2016.00475 .
doi: 10.3389/fimmu.2016.00475
pubmed: 27867383
pmcid: 5095454
Islam Z, Harkema JR, Pestka JJ. Satratoxin G from the black mold Stachybotrys chartarum evokes olfactory sensory neuron loss and inflammation in the murine nose and brain. Environ Health Perspect. 2006;114:1099–107. https://doi.org/10.1289/ehp.8854 .
doi: 10.1289/ehp.8854
pubmed: 16835065
pmcid: 1513335
Kanaya K, Kondo K, Suzukawa K, Sakamoto T, Kikuta S, Okada K, et al. Innate immune responses and neuroepithelial degeneration and regeneration in the mouse olfactory mucosa induced by intranasal administration of Poly(I:C). Cell Tissue Res. 2014;357:279–99. https://doi.org/10.1007/s00441-014-1848-2 .
doi: 10.1007/s00441-014-1848-2
pubmed: 24744264
pmcid: 4077259
Sultan B, May LA, Lane AP. The role of TNF-alpha in inflammatory olfactory loss. Laryngoscope. 2011;121:2481–6. https://doi.org/10.1002/lary.22190 .
doi: 10.1002/lary.22190
pubmed: 21882204
pmcid: 3540407
Brann JH, Firestein SJ. A lifetime of neurogenesis in the olfactory system. Front Neurosci. 2014;26:182. https://doi.org/10.3389/fnins.2014.00182.PMID:25018692;PMCID:PMC4071289 .
doi: 10.3389/fnins.2014.00182.PMID:25018692;PMCID:PMC4071289
Graziadei GA, Graziadei PP. Neurogenesis and neuron regeneration in the olfactory system of mammals. II. Degeneration and reconstitution of the olfactory sensory neurons after axotomy. J Neurocytol. 1979;8:197–213. https://doi.org/10.1007/BF01175561 .
doi: 10.1007/BF01175561
pubmed: 469573
Matías-Guiu J, Gomez-Pinedo U, Montero-Escribano P, Gomez-Iglesias P, Porta-Etessam J, Matias-Guiu JA. Should we expect neurological symptoms in the SARS-CoV-2 epidemic? Es esperable que haya cuadros neurológicos por la pandemia por SARS-CoV-2? Neurologia. 2020;35:170–5. https://doi.org/10.1016/j.nrl.2020.03.001 .
doi: 10.1016/j.nrl.2020.03.001
pubmed: 32299636
pmcid: 7136883
Li YC, Bai WZ, Hashikawa T. The neuroinvasive potential of SARS-CoV2 may play a role in the respiratory failure of COVID-19 patients. J Med Virol. 2020;92:552–5. https://doi.org/10.1002/jmv.25728 .
doi: 10.1002/jmv.25728
pubmed: 32104915
Kalinke U, Bechmann I, Detje CN. Host strategies against virus entry via the olfactory system. Virulence. 2011;2:367–70. https://doi.org/10.4161/viru.2.4.16138 .
doi: 10.4161/viru.2.4.16138
pubmed: 21758005
Majde JA. Neuroinflammation resulting from covert brain invasion by common viruses—a potential role in local and global neurodegeneration. Med Hypotheses. 2010;75:204–13. https://doi.org/10.1016/j.mehy.2010.02.023 .
doi: 10.1016/j.mehy.2010.02.023
pubmed: 20236772
pmcid: 2897933
Tesoriero C, Codita A, Zhang MD, et al. H1N1 influenza virus induces narcolepsy-like sleep disruption and targets sleep-wake regulatory neurons in mice. Proc Natl Acad Sci U S A. 2016;113:E368–77. https://doi.org/10.1073/pnas.1521463112 .
doi: 10.1073/pnas.1521463112
pubmed: 26668381
Wheeler DL, Athmer J, Meyerholz DK, Perlman S. Murine olfactory bulb interneurons survive infection with a neurotropic coronavirus. J Virol. 2017;91:e01099-e1117. https://doi.org/10.1128/JVI.01099-17 .
doi: 10.1128/JVI.01099-17
pubmed: 28835503
pmcid: 5660484
Youngentob SL, Schwob JE, Saha S, Manglapus G, Jubelt B. Functional consequences following infection of the olfactory system by intranasal infusion of the olfactory bulb line variant (OBLV) of mouse hepatitis strain JHM. Chem Senses. 2001;26:953–63. https://doi.org/10.1093/chemse/26.8.953 .
doi: 10.1093/chemse/26.8.953
pubmed: 11595672
Paterson RW, Brown RL, Benjamin L, et al. The emerging spectrum of COVID-19 neurology: clinical, radiological and laboratory findings. Brain. 2020. https://doi.org/10.1093/brain/awaa240 .
doi: 10.1093/brain/awaa240
pubmed: 33324968
pmcid: 7454352
Brann DH, Tsukahara T, Weinreb C, Logan DW, Datta SR. Non-neural expression of SARS-CoV-2 entry genes in the olfactory epithelium suggests mechanisms underlying anosmia in COVID-19 patients. BioRxiv. 2020. https://doi.org/10.1101/2020.03.25.009084 .
doi: 10.1101/2020.03.25.009084
Cantuti-Castelvetri L, Ojha R, Pedro LD, Djannatian M, Franz J, Kuivanen S, van der Meer F, Kallio K, Kaya T, Anastasina M, Smura T, Levanov L, Szirovicza L, Tobi A, Kallio-Kokko H, Österlund P, Joensuu M, Meunier FA, Butcher SJ, Winkler MS, Mollenhauer B, Helenius A, Gokce O, Teesalu T, Hepojoki J, Vapalahti O, Stadelmann C, Balistreri G, Simons M. Neuropilin-1 facilitates SARS-CoV-2 cell entry and infectivity. Science. 2020;370:856–60. https://doi.org/10.1126/science.abd2985 .
doi: 10.1126/science.abd2985
pubmed: 33082293
pmcid: 33082293
Chen M, Shen W, Rowan NR, Kulaga H, Hillel A, Ramanathan M, Lane AP. Elevated ACE2 expression in the olfactory neuroepithelium: implications for anosmia and upper respiratory SARS-CoV-2 entry and replication. BioRxiv. 2020. https://doi.org/10.1101/2020.05.08.084996 .
doi: 10.1101/2020.05.08.084996
pubmed: 33442690
pmcid: 7781307
Galougahi MK, Ghorbani J, Bakhshayeshkaram M, Naeini AS, Haseli S. Olfactory bulb magnetic resonance imaging in SARS-CoV-2-induced anosmia: the first report. Acad Radiol. 2020;27:892–3. https://doi.org/10.1016/j.acra.2020.04.002 .
doi: 10.1016/j.acra.2020.04.002
pubmed: 32295727
pmcid: 7151240
Eliezer M, Hautefort C, Hamel AL, et al. Sudden and complete olfactory loss function as a possible symptom of COVID-19. JAMA Otolaryngol Head Neck Surg. 2020. https://doi.org/10.1001/jamaoto.2020.0832 .
doi: 10.1001/jamaoto.2020.0832
pubmed: 32672801
Lin R, Mamane Y, Hiscott J. Multiple regulatory domains control IRF-7 activity in response to virus infection. J Biol Chem. 2000;275:34320–7. https://doi.org/10.1074/jbc.M002814200 .
doi: 10.1074/jbc.M002814200
pubmed: 10893229
Tay MZ, Poh CM, Rénia L, MacAry PA, Ng LFP. The trinity of COVID-19: immunity, inflammation and intervention. Nat Rev Immunol. 2020;20:363–74. https://doi.org/10.1038/s41577-020-0311-8 .
doi: 10.1038/s41577-020-0311-8