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ORIGINAL RESEARCH article

Front. Psychol., 27 May 2024

Sec. Neuropsychology

Volume 15 - 2024 | https://doi.org/10.3389/fpsyg.2024.1407887

Understanding the olfactory role in post-COVID cognitive and neuropsychiatric manifestations

  • 1. Neurodegenerative Diseases Group, Biobizkaia Health Research Institute, Barakaldo, Spain

  • 2. Department of Neurology, Cruces University Hospital-OSAKIDETZA, Barakaldo, Spain

  • 3. Department of Neurosciences, University of the Basque Country UPV/EHU, Leioa, Spain

  • 4. Department of Neurology, Donostia University Hospital-OSAKIDETZA, San Sebastián, Spain

  • 5. Department of Neurosciences, Biodonostia Health Research Institute, San Sebastián, Spain

  • 6. Department of Neurosciences, University of the Basque Country UPV-EHU, San Sebastián, Spain

  • 7. CIBERNED-CIBER, Institute Carlos III, Madrid, Spain

  • 8. The Basque Foundation for Science, IKERBASQUE, Bilbao, Spain

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Abstract

Introduction:

Olfactory dysfunction (OD) is frequent after SARS-CoV-2 infection. The aim of this study was to examine if long-term OD is common in post-COVID condition, and the relationship between olfaction, cognition, neuropsychiatric symptoms, and disease duration in these patients.

Methods:

This study included 121 participants with post-COVID condition and 51 healthy controls (HC). A comprehensive neuropsychological and neuropsychiatric assessment was conducted, encompassing various domains, including general cognition, processing speed, verbal fluency, attention, verbal memory, visual memory, visuoconstructive ability, visuospatial ability, abstraction, executive functions, anxious-depressive symptoms, general health perception, fatigue level, sleep quality, and olfaction. Statistical analyses were carried out to understand the relationship of OD with cognition, and its role as moderator variable.

Results:

In total, 25% of the post-covid patients had a reduced smell capacity, while only 9.3% of HC presented OD. Post-COVID patients had statistically significantly worse cognitive performance and clinical status than HC. Verbal fluency (AUC = 0.85, p < 0.001), and attention (AUC = 0.82, p < 0.001) were the variables that best discriminate between groups. OD seemed to be a moderator between fatigue and cognition, and between disease duration and attention (β = −0.04; p = 0.014).

Discussion:

The study highlights marked cognitive and neuropsychiatric sequelae in individuals post-COVID relative to HC. Olfactory impairment exhibits correlations with both cognitive performance and general health. Olfaction emerges as a potential prognostic marker owing to its moderating influence on disease severity indicators.

Introduction

The post-COVID condition is a syndrome marked by persistent fatigue, shortness of breath, and “brain fog,” which can be developed after SARS-CoV-2 infection. This term, proposed by NICE, refers to those patients with symptoms that last at least 2 months and usually begin within 3 months after the infection [ICD-11 (RA02)] (Soriano et al., 2021). Approximately 10–15% of individuals recovering from COVID-19 develop this syndrome (Nalbandian et al., 2023). Autonomic dysfunction, headaches, myalgia, anxiety, and depression are prevalent symptoms among these patients (Nalbandian et al., 2023).

In addition to the mentioned symptoms, several studies have highlighted olfactory dysfunction (OD) in the patients with post-COVID condition. OD is a common manifestation of SARS-CoV-2 infection, affecting approximately 50% of individuals during the acute phase (Saniasiaya et al., 2021). This OD is typically sudden and temporary, indicating primarily peripheral inflammation (Kay, 2022). However, in roughly 10% of patients, OD persists for months (Araújo et al., 2021; Ciofalo et al., 2022), suggesting the loss of olfactory epithelium, a disruption in central olfactory processing networks, or a persistent inflammation in either the olfactory epithelium, the olfactory bulb, or both (Xydakis et al., 2021; Doty, 2022).

Olfactory dysfunction (OD) stands as an independent marker distinct from COVID-19 severity and respiratory involvement (Cristillo et al., 2021). Recent inquiries have associated the acute loss of smell during the initial phase with compromised overall cognition (Llana et al., 2023). Cognitive impairments after the infection, particularly affecting memory and executive functions, are evident in less than one-fifth of individuals with prolonged OD (Muccioli et al., 2023). Previous assessments have explored the correlation between cognition and olfaction in post-COVID condition, revealing a link between prolonged hyposmia and cognitive decline (Cristillo et al., 2021; Azcue et al., 2022). Furthermore, patients experiencing post-COVID conditions report heightened instances of “brain fog,” headaches, and semantic memory deficits correlating with the severity of OD (Di Stadio et al., 2022; Fiorentino et al., 2022). Long-term olfactory dysfunction has been linked with structural alterations in the central nervous system (Yus et al., 2022; Campabadal et al., 2023). Essentially, enduring OD following COVID-19 appears to result in damage to olfactory and limbic brain regions, which are interconnected with adjacent areas implicated in memory and attention (Xydakis et al., 2021; Yus et al., 2022; Muccioli et al., 2023), potentially contributing to observed cognitive deficits. This pattern of damage mirrors neurological degeneration observed in conditions such as Alzheimer’s disease, Parkinson’s disease, and Lewy body dementia (Kay, 2022).

While numerous studies underscore significant cognitive differences between patients with hyposmia/anosmia and those without OD, many lack an objective smell evaluation or fail to compare it with healthy controls (HC).

Therefore, this study aims to ascertain if long-term OD is a frequent sign in post-COVID condition, and its relationship with cognition, neuropsychiatric symptoms, and disease duration in this pathology.

Methods

Participants

This study included 121 participants with post-COVID condition and 51 HC, recruited trough the Neurology Department of the Cruces University Hospital. The sample of patients was completed with people who reported post-covid symptoms, and who met the specific criteria of the study. Sex, years of education, disease duration, and smoking habit were recorded for all participants.

The inclusion criteria included participants between 18 and 85 years old, with a sufficient understanding and communication skills. Patients diagnosed with post-COVID condition met the criteria proposed by the NICE guidelines(Soriano et al., 2021), in which signs and symptoms that develop during or after the infection consistent with COVID-19 continued for more than 12 weeks and were not explained by an alternative diagnosis. For the diagnosis of acute COVID-19, the valid diagnostic methods were a positive nasal PCR, the detection of IgG and/or IgM antibodies against SARS-CoV-2 or a medical report supporting the diagnosis. Exclusion criteria included respiratory disease lasting 12 weeks after the infection, having been admitted to an intensive care unit and/or having had severe bilateral pneumonia or other severe disease manifestations requiring hospitalization, pregnancy or lactation, severe trauma, alcoholism, drug addiction, severe heart disease, radiological diagnosis of brain structural pathology, concomitant diseases that could influence the cognitive assessment or the olfactory sense (except smokers), as well as patients who have received some immunomodulatory treatments were excluded.

The study protocol was approved by the Basque Drug Research Ethics Committee [Comité de Ética de la Investigación con medicamentos de Euskadi (CEIm-E) (PI2020210)]. All participants gave written informed consent prior to their participation in the study, in accordance with the tenets of the Declaration of Helsinki.

Cognitive and neuropsychiatric assessment

A comprehensive neuropsychological assessment was conducted, encompassing various domains such general cognition screening (Montreal Cognitive Assessment [MoCA]), attentional verbal and working memory (Digits from Wechsler Adult Intelligence Scale IV [WAIS-IV]), visual attention (Trail Making Test A [TMT A]), sustained attention (Touluose-Piéron Revised [TP-R]), alternating attention (Trail Making Test B [TMT B]) verbal fluency (animals and words starting with P), processing speed (Symbol Digit Modality Test [SDMT] and Salthouse Perceptual Comparison Test [SPCT]), cognitive flexibility (Modified Wisconsin Card Sorting Test [M-WCST]), verbal memory (Hopkins Verbal Learning Test- Revised [HVLT-R], visual memory (Brief Visuospatial Memory Test-Revised [BVMT-R]), visuoconstructive capacity (Taylor Complex Figure Test [TCF]), visual perception (Benton Judgment Of Line Orientation [JLO]), inhibitory capacity (Stroop Test), and abstraction (similarities from WAIS-IV).

Neuropsychiatric and clinical status were also assessed with questionnaires measuring general health (The 36-Item Short Form Health Survey [SF-36]), impact of fatigue or fatigue levels (Modified Fatigue Impact Scale [MFIS]), depressive symptoms (the Short Form of Geriatric Depression Scale [GDS]), anxiety symptoms (State–Trait Anxiety Inventory [STAI]), suicidal ideation (Columbia Suicide Severity Rating Scale [C-SSRS]), and sleep quality (Pittsburgh Sleep Quality Index [PSQI]).

To evaluate olfaction, the Brief Smell Identification Test (BSIT) validated to Hispanic and non-Hispanic white population was employed, consisting of 12 distinct odors. The results were adjusted for age and sex, yielding four possible categories: normal, deficient, relatively abnormal, and abnormal (Doty, 2001; Menon et al., 2013).

Statistics

Statistical analyses were conducted using IBM SPSS Statistics for Windows, version 26.0 (IBM SPSS, Armonk, NY, United States). Prior to analysis, normality and homogeneity of the variables within each group were assessed. The U Mann–Whitney test was employed to examine differences in age and years of education between groups, while the Chi-square test was used to assess differences in sex and smoking habits.

Normalized z-score values were computed for each test, and these z-scores were utilized to construct composites for each cognitive domain. ANCOVA was employed to investigate differences in cognitive domains and BSIT scores between post-COVID and HC groups, with age, sex, years of education, and smoking habits serving as covariates. Pearson bivariate correlations were calculated to explore the relationship between cognitive domains and BSIT z-scores.

ROC curve analysis was performed to identify variables that most effectively discriminated between patients and HC. Stepwise linear regression analysis was undertaken to identify symptoms and variables that best explained cognitive performance in post-COVID patients. Finally, a simple moderation analysis was executed, utilizing the results of the BSIT as a bicategorical moderator with the PROCESS v4.2 macro for SPSS. The BSIT results were categorized as normal and pathological, with the latter encompassing those with deficient, relatively abnormal, and abnormal outcomes. Statistical significance was established at p < 0.05 (two-tailed).

Results

Participants

Age, sex, years of education, and smoking habits were recorded for all participants, with disease duration additionally documented for patients with post-COVID condition (Table 1).

Table 1

HC (n = 51) M (SD) Post-COVID (n = 121) M (SD) Statistics
Age, years 42.17 (9.93) 46.29 (9.64) U = 2369.50*
Education, years 16.70 (2.75) 16.15 (3.30) U = 3480.50
Female, n (%) 41 (81.4%) 92 (76.0%) χ 2 = 0.39
Smoking habit χ 2 = 14.33**
Non-smoker 30 (58.8%) 80 (66.1%)
Smoker 10 (19.6%) 5 (4.1%)
Former smoker 9 (17.6%) 34 (28.1%)
Disease duration, months 15.75 (8.19)
SF-36 96.80 (9.61) 48.42 (24.17) U = 5854.50***
MFIS 10.47 (11.77) 64.49 (14.73) U = 47.00***
PSQI 5.08 (2.98) 10.89 (4.61) U = 935.50***
STAI-state 11.74 (10.28) 28.07 (14.03) U = 1021.00***
STAI-trait 12.98 (9.39) 16.62 (13.09) U = 2566.50
GDS 1.11 (1.53) 7.23 (3.79) U = 364.00***
C-SSRS 0.00 (0.00) 0.28 (0.70) U = 2269.50***

Clinical and demographic data.

*p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001.C-SSRS, Columbia Suicide Severity Rating Scale; GDS, Geriatric Depression Scale; HC, healthy controls; MFIS, Modified Fatigue Impact Scale; PSQI, Pittsburgh Sleep Quality Index; SF-36, The 36-Item Short Form Health Survey; STAI, State–Trait Anxiety Inventory.

Statistical analyses revealed a significant difference in age between groups (U = 2369.50, p = 0.016), with the HC group being younger. Gender distribution and years of education did not exhibit significant differences between the groups. However, there were notable distinctions in smoking habits (χ2 = 14.33, p = 0.006). In the post-COVID condition group, 66.1% were non-smokers, 4.1% were smokers, and 28.1% were former smokers. Conversely, in the HC group, 58.8% were non-smokers, 19.6% were smokers, and 17.6% were former smokers.

Cognitive and neuropsychiatric status

Significant differences between groups were observed in multiple cognitive domains: general cognition (F1,169 = 35.59, p < 0.001), verbal fluency (F1,169 = 68.77, p < 0.001), processing speed (F1,169 = 48.14, p < 0.001), attention (F1,169 = 27.54 p < 0.001), verbal memory (F1,169 = 30.58, p < 0.001), visual memory (F1,169 = 6.74, p = 0.010), visuoconstructive ability (F1,169 = 7.31, p = 0.001), abstraction (F1,169 = 9.69, p = 0.002), and executive functions (F1,169 = 15.03, p = 0.008). Post-COVID condition patients exhibited significantly poorer performance in all cognitive domains, except for general cognition and visuospatial perception (Figure 1A).

Figure 1

Figure 1

Cognitive performance and neuropsychiatric status in post-COVID condition and HC. (A) Cognitive performance. (B) Neuropsychiatric status. Values are shown in z-scores. A higher z indicates a better cognition or neuropsychiatric status. *p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001. C-SSRS, Columbia Suicide Severity Rating Scale; GDS, Geriatric Depression Scale; HC, healthy controls; MFIS, Modified Fatigue Impact Scale; PSQI, Pittsburgh Sleep Quality Index; SF-36: The 36-Item Short Form Health Survey; STAI, State–Trait Anxiety Inventory.

Similarly, the neuropsychiatric status was examined, with comparisons between groups adjusted for age and sex. Statistically significant differences were found in general health (F1,169 = 314.72, p < 0.001), fatigue levels (F1,169=508.65, p < 0.001), sleep quality (F1,169 = 63.15, p < 0.001), anxiety symptoms (F1,169 = 51.03, p < 0.001), depressive symptomatology (F1,169 = 114.48, p < 0.001), and suicidal ideation (F1,169 = 6.73, p = 0.010). Post-COVID condition patients exhibited a clinically worse status compared to HC. However, no statistically significant differences between groups were observed in anxiety trait (Figure 1B).

ROC curve analysis was conducted to identify the domains that most effectively discriminated between patients and HC (Figure 2). The analysis revealed that verbal fluency (AUC = 0.85, p < 0.001), processing speed (AUC = 0.81, p < 0.001), general cognition (AUC = 0.81 p < 0.001), and attention (AUC = 0.80, p < 0.001), were the variables with the highest discriminatory capacity between patients and HC. Verbal memory (AUC = 0.76, p < 0.001), executive functions (AUC = 0.76, p < 0.001), abstraction (AUC = 0.68, p < 0.001), visuoconstructive ability (AUC = 0.67, p = 0.001), visual memory (AUC = 0.65, p = 0.005), and BSIT (AUC = 0.63, p = 0.011) also displayed discriminatory ability, albeit with lower AUC values. Visuospatial perception was the only cognitive domain that did not show discriminatory power between patients and HC.

Figure 2

Figure 2

ROC curve. AUC, Area Under the Curve. Abstraction (AUC = 0.68, p < 0.001); Attention (AUC = 0.80, p < 0.001); Executive functions (AUC = 0.76, p < 0.001); General cognition (AUC = 0.81 p < 0.001); Olfactory sense (AUC = 0.63, p = 0.011); Processing speed (AUC = 0.81, p < 0.001); Verbal fluency (AUC = 0.85, p < 0.001); Verbal memory (AUC = 0.76, p < 0.001); Visual memory (AUC = 0.65, p = 0.005); Visuoconstructive ability (AUC = 0.67, p = 0.001); —Visuospatial perception (AUC = 0.53, p = 609).

Gender differences in individuals with post-COVID condition were examined, with age, years of education, and disease duration serving as covariates. The analysis revealed statistically significant differences in processing speed (F1,118 = 4.14, p = 0.044) and visuospatial perception (F1,118 = 15.52, p < 0.001), indicating that women exhibited poorer performance in these domains. However, no statistically significant differences were observed in general health, fatigue levels, sleep quality, anxiety-state, anxiety-trait, depressive symptoms, or suicidal ideation between men and women with post-COVID condition.

Regarding HC group, differences between gender were only found in visuospatial ability (F1,49 = 5.39, p = 0.025), with women having a better performance in this task.

Olfaction

Significant differences were identified between patients with post-COVID condition and HC (F1,169 = 4.94, p = 0.028), indicating that post-COVID patients exhibited lower olfactory performance (Figure 3A). Specifically, 25% of the patients displayed a reduced smell capacity (deficient, relatively abnormal or abnormal), whereas only 9.3% of the HC had OD (Figure 3B).

Figure 3

Figure 3

Olfactory assessment. (A) Raw BSIT score. (B) BSIT results by categories. *p ≤ 0.05. BSIT, Brief Smell Identification Test; HC, healthy controls.

Furthermore, there were no statistically significant differences in olfaction between men and women among post-COVID patients. This analysis was adjusted for age, years of education, smoking habits, and disease duration. Additionally, no statistically significant differences in olfactory sense were observed among post-COVID patients based on disease duration.

The correlations between participants’ olfactory sense and their cognitive performance were examined. In post-COVID patients, olfactory sense correlated positively with attention (r = 0.23, p = 0.013), visuospatial perception (r = 0.26, p = 0.005), and abstraction capacity (r = 0.19, p = 0.049). Additionally, the olfaction was correlated with general health (r = 0.19, p = 0.044). These findings indicate that better olfactory sense was associated with improved cognitive performance and better general health in post-COVID patients. However, disease duration did not show a correlation with olfaction.

In HC, olfactory sense did not exhibit correlations with any cognitive domains or neuropsychiatric tests.

A linear regression analysis of cognitive domains, symptomatology, BSIT, disease duration, and years of education was conducted. Fatigue, along with education level, were identified as the variables that best explained cognitive performance in post-COVID patients (4.4–27%). Olfactory ability explained 3.3% of visuospatial perception (Figure 4A). Additionally, when performing separate linear regressions for women and men with post-COVID condition, it was found that fatigue most influenced cognitive performance in women (5.3–16.9%) (Figure 4B), whereas in men, depressive symptoms played a more significant role (17.8–35.2%) (Figure 4C).

Figure 4

Figure 4

Linear regression of cognitive domain. (A) Post-covid patients. (B) Post-covid women. (C) Post-covid men. BSIT: Brief Smell Identification Test; MFIS: Modified Fatigue Impact Scale; PSQI: Pittsburgh Sleep Quality Index; STAI: State–Trait Anxiety Inventory.

Finally, simple moderation analyses were conducted with the olfactory sense (pathological/normal) serving as the moderating variable between neuropsychiatric status, clinical data, and cognitive performance (Figure 5). The results revealed differences in the interaction between disease duration and attention (β = −0.03; p = 0.051) (Figure 5A). Specifically, patients with a pathological olfaction demonstrated worse attention capacity as the duration of the disease increased (β = −0.04; p = 0.014).

Figure 5

Figure 5

Olfaction as a moderating variable in cognitive performance. (A) Attention and disease duration. (B) Attention and general health. (C) Attention and fatigue. (D) Verbal memory and fatigue. (E) Visual memory and fatigue. All graphs are shown in z values. *p ≤ 0.05; **p ≤ 0.001; MFIS: Modified Fatigue Impact Scale; SF-36: The 36-Item Short Form Health Survey; STAI: State–Trait Anxiety Inventory.

Furthermore, general health had a statistically significant influence on attention, being moderated by olfaction capacity (β = −0.95; p = 0.003) (Figure 5B). Fatigue levels, as well, impacted attention (β = 0.72; p = 0.021) (Figure 5C), verbal memory (β = 0.90; p = 0.018) (Figure 5D), and visual memory (β = 0.72; p = 0.051) (Figure 5E), with worse performance the higher the fatigue and the worse olfaction capacity.

Discussion

The objective of this study was to investigate whether long-term OD is a prominent feature of post-COVID condition and to explore the associations between olfaction, cognitive performance, and neuropsychiatric symptoms in these patients. Additionally, we aimed to present the neuropsychologic and neuropsychiatric profile of individuals with post-COVID condition.

Regarding olfaction, post-COVID patients exhibited a poorer sense of smell compared to HC. Our findings align with similar studies examining long-term hyposmia without post-COVID condition (Zhu et al., 2021). Acute-phase OD can result from various factors, including inflammation, while long-term OD may also be attributed to neurological alterations, in addition to persistent inflammation (Xydakis et al., 2021; Doty, 2022). In our sample, 25% of participants experienced long-term OD, a proportion similar to that reported in the general population following SARS-CoV-2 infection (Boscolo-Rizzo et al., 2022), but higher than what has been seen in other long-term studies (Araújo et al., 2021; Ciofalo et al., 2022), probably because of the higher proportion of women in our sample, who report smell dysfunction in approximately 2.5 more times than men (Araújo et al., 2021; Mendes Paranhos et al., 2022). The prevalence of OD in the general population is estimated to range from 3–22%, with upper airway infections, sinonasal diseases, and head trauma being the primary cause (Brämerson et al., 2004; Auinger et al., 2021; Renaud-Charest et al., 2021; Schäfer et al., 2021). In our sample, HC showed abnormal olfaction in 4.7%, and relatively abnormal in 4.7% of the cases.

Post-COVID patients displayed worse performance in various cognitive domains, general health, sleep quality, and reported higher levels of fatigue, anxiety symptoms, depressive symptomatology, and suicidal ideation compared to HC (Altuna et al., 2021; Ceban et al., 2022; Cavaco et al., 2023). Notably, these differences were more pronounced in female patients, consistent with previous studies (Ya’qoub et al., 2021; Sylvester et al., 2022). The prevalence of post-COVID condition also appears to be higher in women than men, and women tend to experience more fatigue and neurological symptoms in the post-COVID phase (Sylvester et al., 2022).

In examining the relationship between olfactory sense and cognitive performance, correlations were found with attention, visuospatial perception, and abstraction capacity in post-COVID patients. OD was also correlated with poorer general health. Importantly, these correlations were not observed in HC. This study reinforces the connection between damage to central nervous system areas related to smell and cognitive performance (Cristillo et al., 2021; Campabadal et al., 2023; Muccioli et al., 2023). While significant differences in olfactory ability were identified between patients and HC, fatigue levels emerged as the primary explanatory variable for cognitive performance in these patients. Specifically, fatigue levels explained a higher percentage of cognitive performance in women, whereas depressive symptoms played a more significant role in cognitive performance in men.

Olfaction emerged as a robust moderator variable, influencing the relationship between fatigue, memory, attention, and disease duration and attention capacity. These findings suggest a more pronounced cognitive decline in individuals with OD as the disease progresses. Although no differences in the proportion of patients with OD were observed between those with and without post-COVID condition, these results underscore the significance of long-term OD as an indicator of cognitive deterioration. This implies the need for comprehensive follow-up for post-COVID patients, indicating similarities between OD in post-COVID condition and other pathologies affecting cognitive performance and olfactory sense, such as Parkinson’s disease or Alzheimer’s disease (Rethinavel et al., 2021; Damiano et al., 2022; Di Stadio et al., 2022; Doty, 2022; Kay, 2022). In contrast, in HC, OD may be attributed to other factors like smoking habits (Vennemann et al., 2008). Some researchers propose that inflammatory stimuli causing OD and affecting the central nervous system could accelerate neurodegenerative processes (Xydakis et al., 2021). Impaired olfactory sense could be a prognostic factor, not only in elderly people, but also in different pathologies such as post-covid condition (Delgado-Lima et al., 2023).

Strengths of this study include the sample size of post-COVID patients, who underwent a thorough neuropsychologic and neuropsychiatric assessment, along with an objective olfaction evaluation. However, limitations include the lack of matching in age, gender, and years of education between the HC and patient groups, although statistical controls were applied to address these variables. The lack of information about the SARS-CoV-2 mutation with which the patients were infected was also a limitation due to its involvement in the olfactory sense.

In conclusion, individuals with post-COVID condition exhibited impaired olfactory ability, cognitive performance, and poorer mental health compared to HC. Interestingly, the proportion of post-COVID patients experiencing OD was comparable to that observed in individuals who had SARS-CoV-2 infection but did not develop post-COVID condition. Notably, OD emerged as a moderator, influencing the relationship between fatigue levels, disease duration, and cognitive performance in post-COVID patients. These findings underscore the multi-faceted impact of post-COVID condition on various aspects of health and highlight the potential role of OD as a significant factor in the cognitive well-being of affected individuals.

Statements

Data availability statement

The datasets presented in this article are not readily available because anonymized data not published within this article will be made available upon reasonable request. Requests to access the datasets should be directed to RP, ; JG-E, .

Ethics statement

The studies involving humans were approved by Basque Drug Research Ethics Committee [Comité de Ética de la Investigación con medicamentos de Euskadi (CEIm-E) (PI2020210)]. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.

Author contributions

NA: Formal analysis, Investigation, Methodology, Writing – original draft, Writing – review & editing. RD: Conceptualization, Formal analysis, Investigation, Supervision, Validation, Writing – original draft, Writing – review & editing, Methodology. OS: Investigation, Writing – original draft, Writing – review & editing, Validation. AO: Investigation, Writing – original draft, Writing – review & editing. MA: Investigation, Writing – original draft, Writing – review & editing. TF-V: Investigation, Writing – original draft, Writing – review & editing. NA-M: Investigation, Writing – original draft, Writing – review & editing. JL: Conceptualization, Writing – original draft, Writing – review & editing. MR-L: Investigation, Writing – original draft, Writing – review & editing. AL: Writing – original draft, Writing – review & editing. IG: Writing – original draft, Writing – review & editing. JG-E: Writing – original draft, Writing – review & editing, Funding acquisition, Investigation, Methodology, Resources, Supervision. BT-M: Funding acquisition, Investigation, Methodology, Resources, Supervision, Writing – original draft, Writing – review & editing.

Funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This study has been funded by Instituto de Salud Carlos III (ISCIII) through the project PI20/01076 and co-funded by the European Union, EITB maratoia (BIOS21/COV/006), and grants for health research projects from the Basque Government (2021111006). The first author received a pre-doctoral research grant from the Basque government (PRE_2023_2_0138).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

  • 1

    Altuna M. Sánchez-Saudinós M. B. Lleó A. (2021). Cognitive symptoms after COVID-19. Neurol. Perspect.1, S16S24. doi: 10.1016/j.neurop.2021.10.005

  • 2

    Araújo L. Arata V. Figueiredo R. G. (2021). Olfactory disorders in post-acute COVID-19 syndrome. Dermatol. Sin.5, 116122. doi: 10.3390/sinusitis5020012

  • 3

    Auinger A. B. Besser G. Liu D. T. Renner B. Mueller C. A. (2021). Long-term impact of olfactory dysfunction on daily life. Wien. Klin. Wochenschr.133, 10041011. doi: 10.1007/s00508-020-01751-5

  • 4

    Azcue N. Gómez-Esteban J. C. Acera M. Tijero B. Fernandez T. Ayo-Mentxakatorre N. et al . (2022). Brain fog of post-COVID-19 condition and chronic fatigue syndrome, same medical disorder?J. Transl. Med.20, 569516. doi: 10.1186/s12967-022-03764-2

  • 5

    Boscolo-Rizzo P. Guida F. Polesel J. Marcuzzo A. V. Antonucci P. Capriotti V. et al . (2022). Self-reported smell and taste recovery in coronavirus disease 2019 patients: a one-year prospective study. Eur. Arch. Otorrinolaringol.279, 515520. doi: 10.1007/s00405-021-06839-w

  • 6

    Brämerson A. Johansson L. Ek L. Nordin S. Bende M. (2004). Prevalence of olfactory dysfunction: the Skövde population-based study. Laryngoscope114, 733737. doi: 10.1097/00005537-200404000-00026

  • 7

    Campabadal A. Oltra J. Junqué C. Guillen N. Botí M. Á. Sala-Llonch R. et al . (2023). Structural brain changes in post-acute COVID-19 patients with persistent olfactory dysfunction. Ann. Clin. Trans. Neurol.10, 195203. doi: 10.1002/acn3.51710

  • 8

    Cavaco S. Sousa G. Gonçalves A. Dias A. Andrade C. Pereira D. et al . (2023). Predictors of cognitive dysfunction one-year post COVID-19. Neuropsychology37, 557567. doi: 10.1037/neu0000876

  • 9

    Ceban F. Ling S. Lui L. M. W. Lee Y. Gill H. Teopiz K. M. et al . (2022). Fatigue and cognitive impairment in post-COVID-19 syndrome: a systematic review and meta-analysis. Brain Behav. Immun.101, 93135. doi: 10.1016/j.bbi.2021.12.020

  • 10

    Ciofalo A. Cavaliere C. Masieri S. Di Chicco A. Fatuzzo I. Lo Re F. et al . (2022). Long-term subjective and objective assessment of smell and taste in COVID-19. Cells11:788. doi: 10.3390/cells11050788

  • 11

    Cristillo V. Pilotto A. Cotti Piccinelli S. Zoppi N. Bonzi G. Gipponi S. et al . (2021). Age and subtle cognitive impairment are associated with long-term olfactory dysfunction after COVID-19 infection. J. Am. Geriatr. Soc.69, 27782780. doi: 10.1111/jgs.17296

  • 12

    Damiano R. F. Guedes B. F. de Rocca C. C. de Pádua Serafim A. Castro L. H. M. Munhoz C. D. et al . (2022). Cognitive decline following acute viral infections: literature review and projections for post-COVID-19. Eur. Arch. Psychiatry Clin. Neurosci.272, 139154. doi: 10.1007/s00406-021-01286-4

  • 13

    Delgado-Lima A. H. Bouhaben J. Martínez-Zujeros S. Pallardo-Rodil B. Gómez-Pavón J. Delgado-Losada M. L. (2023). Could olfactory identification be a prognostic factor in detecting cognitive impairment risk in the elderly?GeroScience45, 20112025. doi: 10.1007/s11357-023-00779-5

  • 14

    Di Stadio A. Brenner M. J. De Luca P. Albanese M. D’ascanio L. Ralli M. et al . (2022). Olfactory dysfunction, headache, and mental clouding in adults with long-COVID-19: what is the link between cognition and olfaction? A cross-sectional study. Brain Sci.12:154. doi: 10.3390/brainsci12020154

  • 15

    Doty R. L. (2001). The brief smell identification test administration manual.

  • 16

    Doty R. L. (2022). Olfactory dysfunction in COVID-19: pathology and long-term implications for brain health. Trends Mol. Med.28, 781794. doi: 10.1016/j.molmed.2022.06.005

  • 17

    Fiorentino J. Payne M. Cancian E. Plonka A. Dumas L. É. Chirio D. et al . (2022). Correlations between persistent olfactory and semantic memory disorders after SARS-CoV-2 infection. Brain Sci.12, 46. doi: 10.3390/brainsci12060714

  • 18

    Kay L. M. (2022). COVID-19 and olfactory dysfunction: a looming wave of dementia?J. Neurophysiol.128, 436444. doi: 10.1152/jn.00255.2022

  • 19

    Llana T. Mendez M. Garces-Arilla S. Hidalgo V. Mendez-Lopez M. Juan M. C. (2023). Association between olfactory dysfunction and mood disturbances with objective and subjective cognitive deficits in long-COVID. Front. Psychol.14, 119. doi: 10.3389/fpsyg.2023.1076743

  • 20

    Mendes Paranhos A. C. Nazareth Dias Á. R. Machado Da Silva L. C. Vieira Hennemann Koury G. De Jesus Sousa E. Cerasi A. J. et al . (2022). Sociodemographic characteristics and comorbidities of patients with long COVID and persistent olfactory dysfunction. JAMA Netw. Open5, 112. doi: 10.1001/jamanetworkopen.2022.30637

  • 21

    Menon C. Westervelt H. J. Jahn D. R. Dressel J. A. O’Bryant S. E. (2013). Normative performance on the brief smell identification test (BSIT) in a multi-ethnic bilingual cohort: a project. Front. Clin. Neuropsychol.27, 946961. doi: 10.1080/13854046.2013.796406

  • 22

    Muccioli L. Sighinolfi G. Mitolo M. Ferri L. Jane Rochat M. Pensato U. et al . (2023). Cognitive and functional connectivity impairment in post-COVID-19 olfactory dysfunction. NeuroImage Clin.38:103410. doi: 10.1016/j.nicl.2023.103410

  • 23

    Nalbandian A. Desai A. D. Wan E. Y. (2023). Post-COVID-19 condition. Annu. Rev. Med.74, 5564. doi: 10.1146/annurev-med-043021-030635

  • 24

    Renaud-Charest O. Lui L. M. W. Eskander S. Ceban F. Ho R. Di Vincenzo J. D. et al . (2021). Onset and frequency of depression in post-COVID-19 syndrome: a systematic review. J. Psychiatr. Res.144, 129137. doi: 10.1016/j.jpsychires.2021.09.054

  • 25

    Rethinavel H. S. Ravichandran S. Radhakrishnan R. K. Kandasamy M. (2021). COVID-19 and Parkinson’s disease: defects in neurogenesis as the potential cause of olfactory system impairments and anosmia. J. Chem. Neuroanat.115:101965. doi: 10.1016/j.jchemneu.2021.101965

  • 26

    Saniasiaya J. Islam M. A. Abdullah B. (2021). Prevalence of olfactory dysfunction in coronavirus disease 2019 (COVID-19): a Meta-analysis of 27,492 patients. Laryngoscope131, 865878. doi: 10.1002/lary.29286

  • 27

    Schäfer L. Schriever V. A. Croy I. (2021). Human olfactory dysfunction: causes and consequences. Cell Tissue Res.383, 569579. doi: 10.1007/s00441-020-03381-9

  • 28

    Soriano J. B. Murthy S. Marshall J. C. Relan P. Diaz J. V. (2021). A clinical case definition of post-COVID-19 condition by a Delphi consensus. Lancet Infect. Dis.22, e102e107. doi: 10.1016/s1473-3099(21)00703-9

  • 29

    Sylvester S. V. Rusu R. Chan B. Bellows M. O’Keefe C. Nicholson S. (2022). Sex differences in sequelae from COVID-19 infection and in long COVID syndrome: a review. Curr. Med. Res. Opin.38, 13911399. doi: 10.1080/03007995.2022.2081454

  • 30

    Vennemann M. M. Hummel T. Berger K. (2008). The association between smoking and smell and taste impairment in the general population. J. Neurol.255, 11211126. doi: 10.1007/s00415-008-0807-9

  • 31

    Xydakis M. S. Albers M. W. Holbrook E. H. Lyon D. M. Shih R. Y. Frasnelli J. A. et al . (2021). Post-viral effects of COVID-19 in the olfactory system and their implications. Lancet Neurol.20, 753761. doi: 10.1016/S1474-4422(21)00182-4

  • 32

    Ya’qoub L. Elgendy I. Y. Pepine C. J. (2021). Sex and gender differences in COVID-19: more to be learned!Am. Heart J. Plus Cardiol. Res. Pract.3:100011. doi: 10.1016/j.ahjo.2021.100011

  • 33

    Yus M. Matias-Guiu J. A. Gil-Martínez L. Gómez-Ruiz N. Polidura C. Jorquera M. et al . (2022). Persistent olfactory dysfunction after COVID-19 is associated with reduced perfusion in the frontal lobe. Acta Neurol. Scand.146, 194198. doi: 10.1111/ane.13627

  • 34

    Zhu Y. Cao M. Zheng P. Shen W. (2021). Residual olfactory dysfunction in coronavirus disease 2019 patients after long term recovery. J. Clin. Neurosci.93, 3135. doi: 10.1016/j.jocn.2021.07.050

Summary

Keywords

cognition, neuropsychiatry, neuropsychology, olfaction, post-covid condition

Citation

Azcue N, Del Pino R, Saenz de Argandoña O, Ortiz de Echevarría A, Acera M, Fernández-Valle T, Ayo-Mentxakatorre N, Lafuente JV, Ruiz-Lopez M, López de Munain A, Gabilondo I, Gómez-Esteban JC and Tijero-Merino B (2024) Understanding the olfactory role in post-COVID cognitive and neuropsychiatric manifestations. Front. Psychol. 15:1407887. doi: 10.3389/fpsyg.2024.1407887

Received

27 March 2024

Accepted

29 April 2024

Published

27 May 2024

Volume

15 - 2024

Edited by

Aleksandra Bala, University of Warsaw, Poland

Reviewed by

Sachiko Koyama, Purdue University Indianapolis, United States

Anna R. Egbert, University of British Columbia, Canada

Updates

Copyright

*Correspondence: Rocio Del Pino, ; Juan Carlos Gómez-Esteban,

†ORCID: N Azcue, https://orcid.org/0000-0002-6376-4951Rocio Del Pino, https://orcid.org/0000-0002-6612-4757Amaia Ortiz de Echevarría, https://orcid.org/0009-0008-4054-7971Marian Acera, https://orcid.org/0000-0002-8333-0659T. Fernández-Valle, https://orcid.org/0000-0001-5666-0022N. Ayo-Mentxakatorre, https://orcid.org/0009-0005-0833-8107Jose Vicente Lafuente, https://orcid.org/0000-0001-7246-0987Marta Ruiz-Lopez, https://orcid.org/0000-0002-7056-3728A. López de Munain, https://orcid.org/0000-0002-9509-4032Inigo Gabilondo, https://orcid.org/0000-0001-6045-2840J. C. Gómez-Esteban, https://orcid.org/0000-0002-4697-3890B. Tijero-Merino, https://orcid.org/0000-0001-9894-5712

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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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