Abstract
Objective
This study aimed to define the clinical course of anosmia in relation to other clinical symptoms.
Methods
135 patients with COVID-19 were reached by phone and subsequently included in the study. Olfactory functions were evaluated using a questionnaire for assessment of self-reported olfactory function. Patients were divided into four subgroups according to the presence of olfactory symptoms and temporal relationship with the other symptoms: group1 had only olfactory complaints (isolated, sudden-onset loss of smell); group2 had sudden-onset loss of smell, followed by COVID-19 related complaints; group3 initially had COVID-19 related complaints, then gradually developed olfactory complaints; and group4 had no olfactory complaints.
Results
In total, 59.3% of the patients interviewed had olfactory complaints during the disease course. The olfactory dysfunction severity during COVID-19 infection was significantly higher in group1 compared to groups 2 and 3. In groups1–3, the odor scores after recovery from COVID-19 disease were significantly lower compared to the status prior to disease onset. The residual olfactory dysfunction was similar between groups1 and 2, but was more evident than group3. Mean duration for loss of smell was 7.8 ± 3.1 (2–15) days. Duration of loss of smell was longer in groups1 and 2 than in group3. Odor scores completely returned back to the pre-disease values in 41 (51.2%) patients with olfactory dysfunction. Rate of complete olfactory dysfunction recovery was higher in group3 compared to groups1 and 2.
Conclusion
In isolated anosmia cases, anosmia is more severe, and complete recovery rates are lower compared to the patients who have other clinical symptoms.
Level of evidence
Level 4.
Keywords: COVID-19, Anosmia, Sudden, Recoverable, Olfactory dysfunction
Introduction
Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has resulted in a worldwide pandemic [1]. Through the course of this pandemic, in addition to the initially described symptoms like fever, cough, and shortness of breath, other symptoms that were not initially recognized like olfactory and gustatory dysfunctions have been started to be reported [2, 3]. Increased recognition of these olfactory/gustatory symptoms is extremely important not just for patient management, but also for timely initiation of isolation precautions to curb the spread of this pandemic. Additionally, earlier detection of the disease may increase the overall prognosis of the patient by earlier utilization of diagnostic procedures and timely initiation of treatment [4].
There is increased recognition of loss of smell and taste complaints in patients with confirmed COVID-19 infection [5–7]. However, pathogenesis of anosmia related to SARS-CoV-2 has not been clearly defined [5]. Olfactory dysfunction may be isolated and with sudden onset followed by usual progression to anosmia over time. While incidence of loss of smell has been reported in up to > 80% of COVID-19 patients in some series, 11.8–35.5% of patients may exhibit olfactory dysfunction without any other symptoms [6, 7]. Majority of patients do not have nasal obstruction or rhinorrhea symptoms, and olfactory dysfunction usually occurs without sinonasal disease, which renders COVID-19 related olfactory dysfunction distinct from the rest of post-viral olfactory dysfunction [5, 6].
Details of olfactory dysfunction in COVID-19 patients are still vague and more research to define its relation to other clinical findings, course over time, and potential pathogenesis would help to better characterize and understand the disease.
This study aimed to determine the clinical features of olfactory dysfunction observed in patients with COVID-19 and describe its temporal evolution through the disease course and relation to other clinical symptoms.
Materials and methods
Participants
In this study, we aimed to evaluate the temporal evolution of odor disorder in a cohort of COVID-19 patients admitted to our hospital. We retrospectively reviewed the hospital database for COVID-19 patients presenting to a single institution. COVID-19 infection was confirmed either by polymerase chain reaction (PCR) on a swab test and/or findings of pneumonia consistent with COVID-19 pneumonia on chest computed tomography (CT). We identified a total of 217 patients discharged prior to end of March 2020. Detailed medical histories of the patients were obtained from hospital records. Patients with previous head trauma, chronic sinonasal disease, neurological disease, metabolic disease, pregnancy, and age < 18 years were excluded.
The patients were then contacted via phone calls and a survey using structured questionnaires focusing on general clinical findings and sense of smell was performed. Information on the presence of olfactory dysfunction, its onset, overall course and accompanying findings was obtained. Patients’ complaints related to COVID-19 were listed in a chronological order. This study was approved by the Institutional Ethical Committee (KAEK No: 315) and was performed in accordance with the Declaration of Helsinki.
Based on olfactory dysfunction status, general symptoms, ENT symptoms, and the clinical course of these symptoms, the patients were divided into four groups: Group 1 included patients with isolated, sudden-onset loss of smell and no other complaints during disease course or follow-up, but hospitalized for chest CT findings; group 2 included patients with initial sudden-onset loss of smell, followed by COVID-19 related symptoms like fever, cough, shortness of breath, sore throat, and diarrhea; group 3 included patients with initial COVID-19 related complaints and gradual development of olfactory dysfunction; and group 4 included patients with COVID-19 related complaints without any olfactory dysfunction during the disease.
Evaluation of olfactory function
Olfactory functions were evaluated using the questionnaire by phone for the assessment of self-reported olfactory function and olfaction-related quality of life, which tests the subjective olfactory capability (SOC) [8]. Due to COVID-19 measures, these patients were not further evaluated with objective olfaction tests such as Sniffin’ Sticks test to minimize disease spread and contamination risk. SOC of the patients before the disease, during the disease, and during the recovery period was assessed. In order to assess the olfactory discrimation, patients were asked to rate odor identification from common household supplies including spice (tangerine, mint, clove, ginger), drink (Turkish coffee or Turkish raki), a cleaning supply (Clorox or soap) and lemon cologne (widely available across households due to traditional usage, and frequently used as a disinfectant during the pandemic). Self-scoring was used to assess the olfactory function. All the patients were asked to rate their ability to smell on a scale of 1–10 (0, unable to smell; 10, best possible sense of smell) [8]. This form was specifically integrated with questions regarding the olfactory function during the disease in order to assess the subclinical course of olfactory dysfunction in patients with COVID-19.
Differences in the self-rating scores prior to and during the disease among groups 1, 2, and 3 were used as an indicator of the severity of olfactory dysfunction. When calculating the olfactory dysfunction recovery rate, the difference between the odor score at the end of the first month and the odor score prior to disease was expressed as percentile.
Statistical analysis
Statistical analyses were performed using SPSS for Windows, version 21 (SPSS, Chicago, IL, USA). Shapiro–Wilk test was used to check the normal distribution of the variables. Continuous variables were presented as mean ± standard deviation (SD), and categorical variables as frequency (n) and percentage (%). Kruskal–Wallis test, Mann–Whitney U test, and Wilcoxon signed-rank test were used to compare the scores prior to disease, during the disease and recovery period. A two-sided p value ≤ 0.05 was considered statistically significant.
Results
Out of a total of 217 patients presented with COVID-19 during March 2020, 38 patients could not be reached subsequently, two patients succumbed to the disease, three patients had chronic olfactory issues, 10 patients did not accept the survey, and 29 patients could not provide clear information about the symptoms. Thus, a total of 135 patients (61 females and 74 males) aged 39.8 ± 11.3 (18–66) years were interviewed. Average duration between the onset of olfactory dysfunction and survey was 31.9 ± 2.8 (21–40) days.
Group 1 comprised 14 patients (10.4%), group 2 of 42 patients (31.1%), group 3 of 24 patients (17.8%), and group 4 of 55 patients (40.7%). In total, 59.3% of the patients had olfactory complaints. Further information on demographic data and clinical characteristics of the groups are provided in Table 1.
Table 1.
Demographics and clinical characteristics of the groups
| Groups | Age (years) | Gender (F/M) n (%) | Comorbidities (%) | Smoking |
|---|---|---|---|---|
| Group 1 n = 14 | 35.4 ± 9.5 (25–54) | 12 (85.7%)/2 (14.3%) | Bronchitis 14.3% | 2 (14.3%) |
| Group 2 n = 42 | 37.6 ± 11 (22–65) | 26 (61.9%)/16 (38.1%) |
Hypertension 7.1% Bronchitis 7.1% Cardiac disease 2.4% |
4 (9.5%) |
| Group 3 n = 24 | 37.2 ± 10.6 (23–61) | 9 (37.5%)/15 (62.5%) |
Hypertension 4.2% Bronchitis 4.2% |
9 (37.5%) |
| Group 4 n = 55 | 43.7 ± 11.3 (18–66) | 14 (25.5%)/41 (74.5%) |
Cardiac disease 5.5% Hypertension 5.5% Diabetes 3.6% Bronchitis 3.6% |
11 (20%) |
Values are presented as mean ± standard deviation (SD), F Female, M Male
Cases with olfactory dysfunction (groupss I–III) were significantly younger with female predominance (mean age 37.1 ± 10.6 (22–65) years; 58.8% females) compared to patients without olfactory dysfunction (group 4; mean age 43.7 ± 11.3 (18–66) years; 25.5% females) (p = 0.001 and p < 0.001, respectively). There was no significant difference in age distribution among the subgroups with olfactory dysfunction.
Self-rating olfactory scores prior to disease were higher in group 1 (9.4 ± 0.5 (9–10)) than in group 2 [8.8 ± 1 (6–10)] and 3 [8.8 ± 1.3 (6–10)] (p = 0.005 and p = 0.03, respectively) (Fig. 1), (Table 2). The olfactory dysfunction severity during COVID-19 infection was significantly higher in group 1 (8.4 ± 1.9 (3–10)), compared to group 2 [7.6 ± 2 (3–10)] and 3 [6.2 ± 2.6 (1–10)], (Fig. 1), (Table 2). Similarly, olfactory dysfunction severity in group 2 was significantly higher than group 3 (Table 2) Total loss of smell (self-rating score: 0) was reported in a total of 64.3%, 59.5%, and 29.2% of patients in groups 1, 2, and 3, respectively (Fig. 2).
Fig. 1.
Self-rating olfactory scores
Table 2.
Olfactory function features of groups
| Group 1 | Group 2 | Group 3 | P1 | P2 | P3 | |
|---|---|---|---|---|---|---|
| Before olfactory scores (self-rating) | 9.4 ± 0.5 (9–10) | 8.8 ± 1 (6–10) | 8.8 ± 1.3 (6–10) | 0.005* | 0.03* | 0.911 |
| OD severity | 8.4 ± 1.9 (3–10) | 7.6 ± 2 (3–10) | 6.2 ± 2.6 (1–10) | 0.040* | 0.003* | 0.048* |
| Duration (days) | 8.3 ± 2.9 (5–14) | (8.5 ± 3.6 (2–15) | 6.3 ± 1.5 (4–10) | 0.909 | 0.036* | 0.032* |
Values are presented as mean ± standard deviation (SD); OD Olfactory dysfunction; P1 Group 1 vs. Group 2; P2 Group 1 vs. Group 3; P3 Group 2 vs. Group 3
*Mann-Whitney U test
Fig. 2.
The flowchart summarizing percentages of total loss of smell and complete recovery rates by groups
In these three groups, the odor scores after recovery from COVID-19 infection were significantly lower compared to scores prior to disease onset. The residual olfactory dysfunction was similar between groups 1 and 2, but was more evident than group 3 (p = 0.01).
Olfactory scores completely returned back to the pre-disease scores in 51.2% of patients (41 patients) with olfactory dysfunction, with a mean duration of olfactory dysfunction of 7.8 ± 3.1 (2–15) days. Sense of smell recovered by 75–100% in 75% of patients with a mean duration of olfactory dysfunction in 8.4 ± 3.4 days. Rate of complete olfactory dysfunction recovery was higher in group 3 compared to groups 1 and 2 (28.6% in group 1, 50% in group 2, and 66.7% in group 3; p = 0.023 and p = 0.189, respectively) (Fig. 2). Similarly, recovery of olfactory dysfunction by 75–100% was more prevalent in group 3 compared to groups 1 and 2 (57.1% in group 1, 66.7% in group 2, and 100% in group 3, p = 0.01 and p < 0.001, respectively). Duration of loss of smell was longer in groups 1 (8.3 ± 2.9 (5–14) days) and 2 [8.5 ± 3.6 (2–15) days] than in group 3 (6.3 ± 1.5 (4–10) days] (p = 0.036 and p = 0.032, respectively; Table 2).
Cases who developed other COVID-19 related symptoms after initial olfactory dysfunction, interval between olfactory dysfunction and other COVID-19 related findings was 1.6 ± 2.6 (0–15). Fever (59.1%), cough (53%), and diarrhea (45.5%) were the most common findings in patients with olfactory dysfunction. Olfactory dysfunction and co-existing typical COVID-19 symptoms are presented further in Table 3. Nasal congestion symptoms was more prevalent in cases with olfactory dysfunction [12 cases (18.2%)] compared to patients without olfactory dysfunction [3 cases (5.5%)] (p = 0.034).
Table 3.
Olfactory dysfunction and coexisting COVID-19 related symptoms
| Symptoms | Patients with OD (Groups 2–3) n (%) | Patients without OD (Group 4) n (%) | p |
|---|---|---|---|
| Fever | 39 (59.1%) | 30 (54.5%) | 0.615 |
| Cough | 35 (53%) | 21 (38.2%) | 0.103 |
| Diarrhea | 30 (45.5%) | 6 (10.9%) | 0.000* |
| Muscle ache | 14 (21.2%) | 7 (12.7%) | 0.220 |
| Dispnea | 8 (12.1%) | 4 (7.3%) | 0.374 |
| Nasal congestion | 12 (18.2%) | 3 (5.5%) | 0.034* |
| Headache | 5 (7.6%) | 6 (10.9%) | 0.525 |
| Throat pain | 3 (4.5%) | 8 (14.5%) | 0.057 |
| Fatigue | 14 (21.2%) | 18 (32.7%) | 0.153 |
| Appetite loss | 5 (7.6%) | 3 (5.5%) | 0.640 |
OD Olfactory dysfunction
*Mann-Whitney U test
Discussion
Olfactory dysfunction has been reported at a high rate in COVID-19 patients in more recent studies, with suggestions to include sudden-onset anosmia as a screening criterion for COVID-19 [8, 9]. Initial experience regarding the differences in clinical presentations/disease course of these patients has been published in large-case series; however, no subgroup analysis to better delineate the study populations has been performed [6, 7, 9]. The distinguishing feature of the current study is segregation of COVID-19 related olfactory dysfunction into different patterns to better characterize the clinical course of COVID-19 related olfactory dysfunction. In this study, we observed three different patterns of olfactory dysfunction in COVID-19 disease as (1) isolated, sudden-onset loss of smell and no other complaints during disease course or follow-up; (2) initial sudden-onset loss of smell, followed by other COVID-19 symptoms; (3) initial COVID-19 complaints and gradual development of olfactory dysfunction.
Various hormonal and genetic factors may account for the gender differences in the clinical course of viral infections [10]. COVID-19 is more common, has more severe course, and is associated with higher mortality rates in males [11] While COVID-19-associated loss of smell is associated with a milder clinical course and more common in female [6, 12]. In our study, COVID-19 related olfactory dysfunction was more prevalent in females, and patients with olfactory dysfunction were younger compared to those without hyposmia/anosmia. This might be related to better sense of smell in women than men and increased sensitivity of females to any change in olfactory function as they use their sense of smell more frequently in daily life.
Pathogenesis of COVID-19 anosmia
Several theories have been proposed to explain the pathogenesis of COVID-19 related anosmia. One plausible mechanism is high viral load in nasal mucosa with secondary inflammation which may result in direct injury to olfactory epithelium [13]. Another plausible mechanism involves angiotensin converting enzyme 2 (ACE2) receptors [14]. The olfactory epithelium has been found to express ACE2 and TMPRSS2, which may enable SARS-CoV-2 to invade the olfactory mucosa and olfactory bulb, and result in subsequent dysfunction [14–16]. However, ACE2 expression is mainly seen in non-neuronal cell types like sustentacular, Bowman’s gland, and microvillar cell, favoring indirect mechanisms of injury [17].
An interesting observation in this study was the more severe and longer olfactory dysfunction in patients with isolated, sudden-onset loss of smell compared to patients who gradually developed olfactory dysfunction. This suggests that initial loss of the olfaction due to immune response at nasal cavity may help alleviate the systemic effects of COVID-19. This is also supported by the observations that COVID-19 patients with olfactory dysfunction have milder disease course and better prognosis compared to COVID-19 cases without anosmia. Whether this mechanism helps prevent both central neuroinvasion and viremia should be further studied.
In our study, similar to the previous literature, younger patients with COVID-19 had more frequent and severe olfactory dysfunction. However, Brann et al. reported that juvenile mice had lower expression of ACE2 and TMPRSS2 in the olfactory epithelium and subsequently had lower olfactory dysfunction [17]. This discrepancy suggests that mechanisms other than ACE2 and TMPRSS2 pathway might be involved in COVID-19 related anosmia.
Olfactory cleft width is an important parameter affecting olfaction [18]. Our research group has previously showed olfactory cleft width as a risk factor for COVID-19 related anosmia [19, 20]. As olfactory cleft width and volume increases, there is increase in mucosal surface area which may lead to higher viral load and resultant neuronal and sustentacular cell damage. Anosmia might be related to inflammation localized to olfactory cleft and seen in patients with nasal reaction due to viral load.
Clinical features of COVID-19 anosmia
A distinctive feature of COVID-19-associated anosmia is its transient course, with its sudden onset independent of other features, with gradual improvement over a short course (about 2 weeks) [6].
Nasal obstruction-related loss of smell is very common in viral infections; however, anosmia associated with COVID-19 is not commonly accompanied by nasal obstruction/congestion [6, 14, 21]. Similarly, in our study, the association of olfactory dysfunction with nasal congestion was found to be low with a ratio of 18.2%. Kaye et al. reported that in cases with COVID-19 anosmia 25% had nasal congestion and 18% had rhinorrhea [22]. This supports the hypothesis that mechanisms other than obstruction are involved in COVID-19 anosmia. Olfactory scores completely returned back to the pre-disease scores in 51.2% of patients after a mean duration of 7.8 ± 3.1 (2–15) days. The rates of complete and partial recovery of olfactory dysfunction in Kaye et al.’s study were 13% and 14%, respectively [22]. Our study had significantly higher olfactory function recovery rate. Available literature supports spontaneous improvement with a mean duration of 2–3 weeks [23, 24]. However, cases with symptoms lasting more than 1 month, so called persistent anosmia, have also been reported [25–27]. Considering the fact that olfactory epithelium undergoes regeneration over 6–8 weeks, SARS-COV2 may result in anosmia longer than 2–3 weeks due to the epithelia damage caused [28]. Kandemirli et al. and Klein et al. reported cases with persistent anosmia at 4-month and 6-month period, respectively, suggesting that there might be other potential mechanisms beyond epithelial damage that lead to permanent anosmia. Further data on this permanent anosmia are important to highlight the pathogenesis of COVID-19 anosmia.
The difference of our study from similar studies in the literature is as follows: we evaluated the severity and duration of anosmia, and total recovery rates in isolated anosmia cases compared to the patients who have anosmia accompanying other clinical symptoms. We found that that patients with isolated, sudden-onset loss of smell had more severe olfactory dysfunction, which seemed to correlate with the longer recovery times in these patients.
Temporal relationship to other clinical symptoms
The most common presenting symptoms of COVID-19 including fever, cough, and headache can be seen in other nonspecific viral upper respiratory tract infections [2, 29, 30]. In our study, fever (59.1%), cough (53%), and diarrhea (45.5%) were the most common symptoms encountered in patients with olfactory dysfunction. Olfactory dysfunction may start before, after, or simultaneously with these clinical symptoms, or it may be the only symptom. Kaye et al. reported that olfactory dysfunction preceded COVID-19 diagnosis in 73% of cases and 27% of cases had anosmia as an isolated symptom [22]. In our study, with lower rates, olfactory dysfunction preceded COVID-19 diagnosis in 41.5% of cases, and in 10.4% of cases, anosmia was the sole symptom.
Different studies across the world assessed the olfactory function based on questionnaires to limit contamination and spread. For the same reason, we used a similar questionnaire-based approach instead of objective psychophysical olfactory test. This constitutes the main limitation of our study [5–7, 31]. Additionally, survey was performed after hospital discharge with a relatively long-interval questioned during the disease course introducing an element of recall bias. Another limiting factor is the single-center nature of the study with relatively limited number of total cases.
Conclusion
The fact that more than 50% patients with COVID-19 develop sudden-onset anosmia prior to respiratory symptoms makes it an important ancillary sign for the disease. Detailed evaluation of the characteristics of olfactory dysfunction and early identification and isolation of symptomatic and asymptomatic carriers are important both for patient management and contact isolation.
Our study described the different temporal evolution of COVID-19-related anosmia with other clinical symptoms to further characterize this symptom. In isolated anosmia cases, anosmia was more severe and complete recovery rates were lower compared to the patients who have other clinical symptoms. Further studies on the pathogenesis of COVID-19-related olfactory dysfunction will contribute not only to the pathogenesis of post-viral olfactory loss (PVOL), but also to the immune response in COVID-19 infection.
Acknowledgements
This study was designed in line with the opinions and suggestions of Professor Thomas Hummel, one of the world’s best-known scientists and clinicians on anosmia. We owe him thanks.
Funding
The authors received no financial support for the research, authorship, and/or publication of this article.
Compliance with ethical standards
Conflict of interest
The authors declare that there is no conflict of interest regarding the publication of this article.
Ethical approval
Ethical approval for this study was obtained from the local ethics committee (2020-05/28).
Informed consent
Informed consent was obtained from all individual participants included in the study.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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