Age and subtle cognitive impairment are associated with long‐term olfactory dysfunction after <scp>COVID</scp> ‐19 infection
Bibliographic record
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus responsible for the coronavirus disease 2019 (COVID-19) pandemic, has been widely associated with extra-pulmonary manifestations, including a broad range of neurological symptoms.1 Olfactory and taste disorders have been consistently reported as common nonrespiratory symptoms of SARS-CoV-2 infection, although the persistence of neurosensory dysfunctions is still a theme of debate.2 Age and premorbid health status might play a major role in modulating the vulnerability to long-term olfactory recovery after SARS-CoV-2 infection. Indeed, the prevalence of olfactory dysfunction increases in normal aging but has also been associated with several age-related neurodegenerative conditions.3 In this study, we thus evaluated the prevalence and predictors of olfactory dysfunction in a consecutive series of patients hospitalized for COVID-19 and its potential association with features or symptoms suggestive for long-term neurological involvement. A total of 168 patients hospitalized for mild to moderate COVID-19 were evaluated at 6 months after discharge. Of these, 106 patients were assessed in presence through a standardized assessment. Five patients (5.7%) were excluded from the study for allergic rhinitis, resulting in a final dataset of 101 patients. The Sniffin' Sticks test4 identified 50 patients with an abnormal score ≤ 8, including 11 patients with severe (score < 4) hyposmia (4/11 of them reported subjective olfactory dysfunction) (Table 1). Patients with subjective hyposmia exhibited lower Sniffin' Sticks total score (5.3 ± 3.5 vs. 8.1 ± 2.4, p = 0.012) but three of them exhibited normal scores. Conversely, patients with long-term subjective hypogeusia exhibited similar Sniffin' Sticks total scores compared to subjects without complaints (7.8 ± 2.5 vs. 7.8 ± 2.8, respectively, p = 0.70). Hyposmia and hypogeusia reported during hospitalization did not predict long-term objective hyposmia (odds ratio [OR] 1.1; 95% confidence interval [CI] 0.75–1.7) or subjective hyposmia (OR 1.03; 95% CI 0.70–1.5, p = 0.52). Compared to patients with normal olfactory function, those with objective hyposmia were older (68.2 ± 11.3 vs. 58.2 ± 12.1 years, p = <0.001) but exhibited similar comorbidity score at admission and during hospitalization and did not differ for duration of hospitalization, oxygen therapy, and severity of COVID-19 (OR 1.5; 95% CI 0.83–2.7, p = 0.10). Age was confirmed as the only predictor of long-term objective hyposmia in logistic regression analyses (Wald 6.4, exp[B] = 0.09, p = 0.01); subjects older than 65 years exhibited a 1.86 increased risk of hyposmia (95% CI 1.19–2.9) and subjects older than 75 years of 2.67 (95% CI 1.10–6.5). No difference of either self-reported neurological symptoms at the neuro-checklist or objective neurological signs was documented between patients with normal olfactory function and hyposmia (Table S1). Patients with hyposmia exhibited lower MoCA (Montreal Cognitive Assessment) total score (23.2 ± 3.4 vs. 25.7 ± 2.5) compared to subjects with normal olfactory function in logistic regression analyses adjusted for age, sex, and educational levels (Wald 5.8, exp[B] = 1.2, p = 0.01). The prevalence of objective hyposmia in our cohort of hospitalized patients was 50%, definitively higher compared to prevalence of hyposmia in the general population in the sixth decade of age.5 This prevalence fits well with recent reports adopting sniffing sticks in independent cohorts of SARS-CoV-2 patients.6 Older age was the most important factor associated with long-term hyposmia as patients older than 75 years of age were at three-fold risk of long-term hyposmia compared to younger subjects. Conversely, we failed to find an association between olfactory dysfunction and the severity of COVID-19, thus supporting the claim that hyposmia is independent from the degree of respiratory involvement.7 Our study went also further, by showing an association between long-term hyposmia and cognitive impairment, after controlling for age, gender, and education. These findings corroborate the well-known association between subtle cognitive deficits and olfactory dysfunction in the older subjects.8 Although the mechanisms underlying long-term central nervous system impact of SARS-CoV-2 are still unclear,9, 10 these preliminary results seem to suggest that older subjects with subtle cognitive deficits are a “vulnerable” population with a higher risk of long-term olfactory dysfunction. We acknowledge that this study entails different limitations. First, we limited the observation to patients presenting with mild to moderate COVD-19; second, patients were evaluated only for orthonasal olfaction, whereas taste disorders were not assessed. Furthermore, no data about preexisting objective hyposmia or cognitive deficits were available, although we accurately excluded subjects with premorbid cognitive impairment or subjective hyposmia from the analyses. Despite these limitations, the study underlined the high prevalence of objective hyposmia 6 months after COVID and identified age and subtle cognitive deficits as factors strongly associated with long-term olfactory dysfunction. Further studies evaluating the nature and progression of cognitive changes and olfactory function would be necessary over time. We thank all the patients for their active participation. All authors have no conflict of interest regarding the research related to the manuscript. Conception and design of the study: Viviana Cristillo, Andrea Pilotto, and Alessandro Padovani. Acquisition and analysis of data: Viviana Cristillo, Andrea Pilotto, Stefano Cotti Piccinelli, Nicola Zoppi, Giulio Bonzi, Stefano Gipponi, Davide Sattin, Silvia Schiavolin, Alberto Raggi, Michela Bezzi, Matilde Leonardi, and Alessandro Padovani. Drafting the manuscript and figures: Viviana Cristillo, Andrea Pilotto, and Alessandro Padovani. The study was not financially supported. Table S1. Neurological sign and symptoms in COVID-19 patients at 6 months follow-up. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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How this classification was reachedexpand
Full frame distilled prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.
Codex and Gemma teacher scores by category
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.002 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.001 | 0.001 |
| Bibliometrics | 0.000 | 0.001 |
| Science and technology studies | 0.001 | 0.001 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.003 |
| Insufficient payload (model declined to judge) | 0.000 | 0.000 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one teacher head, not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".