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Psychological consequences of long COVID: comparing trajectories of depressive and anxiety symptoms before and after contracting SARS-CoV-2 between matched long- and short-COVID groups

Published online by Cambridge University Press:  02 December 2022

Daisy Fancourt*
Affiliation:
Department of Behavioural Science and Health, University College London, UK
Andrew Steptoe
Affiliation:
Department of Behavioural Science and Health, University College London, UK
Feifei Bu
Affiliation:
Department of Behavioural Science and Health, University College London, UK
*
Correspondence: Daisy Fancourt. Email: d.fancourt@ucl.ac.uk
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Abstract

Background

There is a growing global awareness of the psychological consequences of long COVID, supported by emerging empirical evidence. However, the emergence and long-term trajectories of psychological symptoms following the infection are still unclear.

Aims

To examine when psychological symptoms first emerge following infection with SARS-CoV-2 and the long-term trajectories of psychological symptoms comparing long- and short-COVID groups.

Method

We analysed longitudinal data from the UCL COVID-19 Social Study (March 2020 to November 2021). We included data from adults living in England who reported contracting SARS-CoV-2 by November 2021 (n = 3115). Of these, 15.9% reported having had long COVID (n = 495). They were matched to participants who had short COVID using propensity score matching on a variety of demographic, socioeconomic and health covariates (n = 962 individuals with 13 325 observations) and data were further analysed using growth curve modelling.

Results

Depressive and anxiety symptoms increased immediately following the onset of infection in both long- and short-COVID groups. But the long-COVID group had substantially greater initial increases in depressive symptoms and heightened levels over 22 months follow-up. Initial increases in anxiety were not significantly different between groups, but only the short-COVID group experienced an improvement in anxiety over follow-up, leading to widening differences between groups.

Conclusions

The findings support work on the psychobiological pathways involved in the development of psychological symptoms relating to long COVID. The results highlight the need for monitoring of mental health and provision of adequate support to be interwoven with diagnosis and treatment of the physical consequences of long COVID.

Type
Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
Copyright © The Author(s), 2022. Published by Cambridge University Press on behalf of the Royal College of Psychiatrists

Background

Long COVID (defined as the continuation of symptoms that develop during or after acute infection with SARS-CoV-2 that cannot be explained by an alternative diagnosisReference Mahase1) is estimated to affect around 10% of people 12 weeks after initial infection, with substantial numbers sustaining symptoms over 6 months.2 Long COVID can involve multiorgan complications including affecting the heart, brain, spleen, liver, blood vessels, gastrointestinal tract, kidneys, pancreas and lungs.Reference Crook, Raza, Nowell, Young and Edison3 These complications involve multiple overlapping disease mechanisms,Reference Xie, Xu and Al-Aly4 and are manifested as a wide range of physiological symptoms (e.g. fatigue, headache, dyspnoea, muscle pain, cardiac abnormalities and anosmia) and neurological symptoms (e.g. sleep disturbances, problems concentrating, cognitive impairment).Reference Crook, Raza, Nowell, Young and Edison3,Reference Aiyegbusi, Hughes, Turner, Rivera, McMullan and Chandan5 However, less well researched are the psychological symptoms associated with long COVID.

Infection with SARS-CoV-2 is, in itself, associated with psychological consequences, including depression, anxiety, stress and adjustment disorders, poorer sleep, increased substance use and increased use of antidepressants and opioids.Reference Xie, Xu and Al-Aly4,Reference Thye, Law, Tan, Pusparajah, Ser and Thurairajasingam6,Reference Fahriani, Ilmawan, Fajar, Maliga, Frediansyah and Masyeni7 Although psychological symptoms generally improve over time, some can linger for substantial periods of time (such as 1 year) without much improvement, or can even worsen over time.Reference Huang, Yao, Gu, Wang, Ren and Wang8,Reference Taquet, Geddes, Husain, Luciano and Harrison9 When focusing specifically on long COVID, a meta-analysis of 39 studies including over 10 000 people found that 19% of people with long COVID reported anxiety and 8% depression as one of their symptoms.Reference Michelen, Manoharan, Elkheir, Cheng, Dagens and Hastie10 But results from individual studies in some countries have reported much higher prevalence (e.g. 42% for anxiety and 41% for low mood in a UK study)2, and anxiety and depression are listed on the UK's official NHS long-COVID symptom list.11

Unanswered questions

Although research is highlighting that psychological symptoms can be a feature of long COVID, a number of questions remain to be answered.

First, when do psychological symptoms of anxiety and depression first emerge in patients with long COVID? Mechanistically, the ability of coronaviruses (including SARS-CoV-2) to directly infect the central nervous system (CNS) and cause neuroinflammation and consequential psychiatric symptoms is well reported.Reference Crook, Raza, Nowell, Young and Edison3,Reference Thye, Law, Tan, Pusparajah, Ser and Thurairajasingam6 Similarly, SARS-CoV-2 has been found to affect the permeability of the blood–brain barrier, facilitating the entry of peripheral inflammatory cytokines to the CNS, further increasing neuroinflammation.Reference Yachou, el Idrissi, Belapasov and Ait Benali12,Reference Troyer, Kohn and Hong13 Systemic inflammation as a result of immune–inflammatory dysregulation as a result of SARS-CoV-2 infection has also been shown to contribute to psychiatric and cognitive symptoms in patients.Reference Penninx14 So it is plausible that heightened anxiety and depression could be experienced soon after SARS-CoV-2 infection. However, increased social isolation because of long-COVID symptoms and anxiety related to persistent symptoms could mean that psychological symptoms in fact emerge and increase during and beyond the acute state of infection among patients with long COVID.Reference Cascella, de Blasio, Cascella and de Blasio15,Reference Burton, Aughterson, Fancourt and Philip16

Second, does the level of psychological symptoms during the acute stage of SARS-CoV-2 infection differ among people who will go on to have short COVID versus long COVID? A relationship between the severity of immune–inflammatory dysregulation in patients with SARS-CoV-2 infection and depressive symptoms 3 months later has been reported,Reference Mazza, de Lorenzo, Conte, Poletti, Vai and Bollettini17 as has a relationship between neuroimmune inflammation and long COVID.Reference Yong18 As such, it is possible that initial psychological experiences around the onset of infection could predict an individual's risk of developing long COVID. But, reciprocally, heightened stress, anxiety and low mood at the onset of illness could itself adversely affect an individual's recovery from SARS-CoV-2 through increasing or prolonging disruption of neuroendocrine and neuroinflammatory processes.Reference Steptoe, Hamer and Chida19 This has been demonstrated both through studies showing bidirectional associations between psychological symptoms and neuro-endo-immune processes as well as genetic studies highlighting pleiotropy between depression and inflammatory processes, suggesting a shared genetic vulnerability that could help explain the relationship between a history of mood disorders and long COVID noted in prior studies.Reference Penninx14

Third, what are the longer-term trajectories of psychological symptoms among people with long COVID beyond the acute stage of infection? To date, much research on this topic has been limited by relatively short-term follow-up (typically of just a few months) and involved limited waves of data collection during that follow-up. Finer-grained data showing trajectories of psychological symptoms over time are still lacking. It is possible that following the acute stage of infection, some of the initial symptoms of psychological distress decline, as can happen for patients with short COVID.Reference Bourmistrova, Solomon, Braude, Strawbridge and Carter20 However, it is also plausible that the reverse is true: the process of dealing with debilitating ongoing symptoms could exacerbate psychological distress.

Aims

This study, therefore, aimed to explore the mental health trajectories of people experiencing long COVID, compared with those with short COVID using data from the University College London (UCL) COVID-19 Social Study. To ensure that any potential differences were not because of imbalances between patients with long and short COVID in relation to sociodemographic factors, histories of mental and physical health prior to infection, or symptoms of COVID-19 during acute infection, we used propensity score matching (PSM) to construct two balanced groups of patients with long versus short COVID. Further, to differentiate experiences post-COVID from usual mental health experiences during the pandemic, we used growth curve models accounting for lockdowns, other social restrictions, and time of the year, tracking individuals in the 10 months prior to their infection with SARS-CoV-2 and for 22 months of follow-up. This study therefore presents one of the largest and longest studies to date of the psychological experiences of patients with long COVID.

Method

Data

Data were derived from the UCL COVID-19 Social Study (CSS); a large panel study of the psychological and social experiences of over 75 000 adults (aged ≥18 years) in the UK during the COVID-19 pandemic. The study commenced on 21 March 2020 and involved weekly and then monthly (August 2020 to November 2021) online data collection during the pandemic. Participants were recruited via convenience sampling and targeted recruitment of underrepresented/vulnerable groups. The study was approved by the UCL Research Ethics Committee (12467/005) and all participants gave written informed consent. Detailed information on the study is available online at https://osf.io/jm8ra/.

This study used data from participants living in England who completed the special module on COVID-19 experience in November 2021 (n = 22 528). Of these, 4938 participants (22%) reported having had COVID-19 by November 2021. We excluded participants (a) with missing data on COVID-19 specific measures (1%), (b) who reported infection with SARS-CoV-2 before 21 March 2020 when the study was launched (see Supplementary Figure 1, available at https://doi.org/10.1192/bjp.2022.155), and (c) who reported having COVID-19 more than once because of the ambiguity in identifying long-COVID dates. This left us with a COVID-19 sample of 3115 participants (see Supplementary Figure 2 for sample selection).

Measures

COVID and long COVID

In November 2021, the CSS included a special module on COVID-19 experience. Participants were asked ‘overall, do you believe you have ever had COVID-19?’ The response options included:

  1. (a) yes, confirmed by a positive COVID-19 test;

  2. (b) yes, confirmed by a positive antibody test;

  3. (c) yes, suspected by a doctor but not tested;

  4. (d) yes, my own suspicions;

  5. (e) no, not that I know of.

As a result of the challenges in diagnosis of COVID-19, (e.g. prior to mass testing being available, due to test shortages and access challenges, and due to testing inaccuracies), definitions of long COVID do not require having had a positive test result, but rather the presence of symptoms that were initially suggestive of COVID-19.Reference Nabavi21 So we considered both patients with positive tests and those with suspected cases as having had COVID-19 (i.e. a–d above).

The information on date of contract was also collected: ‘If you have had COVID-19, when did you first contract it?’ Moreover, participants were asked if they considered themselves to have or have had long COVID, with responses:

  1. (a) yes, a medical professional has formally diagnosed me with long COVID;

  2. (b) yes, I have not been formally diagnosed but consider myself to have long COVID;

  3. (c) no, I do not consider myself to have long COVID;

  4. (d) I am unsure.

Data was recoded into a binary variable (yes/no) with unsure being treated as not having COVID.

Mental health outcomes

Depressive symptoms were measured using the Patient Health Questionnaire (PHQ-9),Reference Löwe, Kroenke, Herzog and Gräfe22 a standardised instrument for screening for depression in primary care. The questionnaire includes nine items with four-point responses with total scores ranging 0–27. Scores of 0–4 suggest minimal depression, 5–9 mild depression, 10–14 moderate depression, 15–19 moderately severe depression, and 20–27 severe depression.Reference Löwe, Kroenke, Herzog and Gräfe22 We used the total score as a continuous measure.

Anxiety symptoms were measured using the Generalized Anxiety Disorder Assessment (GAD-7),Reference Spitzer, Kroenke, Williams and Löwe23 a well-validated tool used to screen for generalised anxiety disorder in clinical practice and research. The GAD-7 comprises seven items with four-point responses with total scores ranging 0–21. Scores of 0–4 are thought to represent minimal anxiety, 5–9 are thought to represent mild anxiety, 10–14 moderate anxiety and ≥15 severe.Reference Spitzer, Kroenke, Williams and Löwe23 Again, the total score was used as a continuous measure.

Time

To examine mental health growth trajectories, a key variable is time. The time variable was constructed as the month since people contracted SARS-CoV-2 (time 0), which took negative values for the period before infection (−21 to 21). It was calculated based on the self-reported contraction date and system-generated survey date (see Supplementary Figure 3 for its distribution). This is relative time as the starting point (and end point) varied across individuals. We controlled for the month (absolute time) in which people contracted SARS-CoV-2 considering an individual's mental health is subject to the impact of time-related contextual factors (e.g. lockdowns and other restrictions). This was used as a series of dummy variables.

Covariates

To construct comparable groups (via PSM), a range of factors were taken into account in our analyses. These included gender (women versus men), ethnicity (White versus ethnic minorities), age groups (age 18–29, 30–45, 46–59, ≥60), education (up to GCSE levels, A-levels or equivalent, university degree or above), income (<£16 000, £16 000–29 000, £30 000–59 000, £60–89 000, ≥£90 000 per annum), employment status (employed non-key worker, employed key worker, other), area of living (city, town, rural), living situation (living alone, living with adults only, living with children), number of close friends (0 to ≥10) and usual social contacts (twice a month or less, once or twice a week, three times a week or more), self-reported diagnosis of any long-term physical health condition or any disability (yes versus no), and self-reported diagnosis of any long-term mental health condition (yes versus no). All above measures were taken from the study baseline when participants joined the study for the first time. Moreover, we included baseline depressive (PHQ-9) and anxiety (GAD-7) symptoms when participants joined the study. Finally, we included a few COVID-19-specific measures, including month when participants had COVID-19 and whether confirmed by a test (COVID-19/antibody test versus doctor's/own suspicion). In addition, we considered self-reported severity of symptoms in the first 1–2 weeks (severe symptoms versus minor/asymptomatic).

Statistical analysis

We employed PSM to construct two comparable groups: short COVID versus long COVID. The propensity score is the probability of being exposed to or having long COVID based on the observed covariates, which is used to pair participants with short COVID and long COVID. The two matched groups should have identical or similar distribution of covariates that are used to estimate the propensity score. We used one-to-one nearest neighbour matching within a calliper (a quarter of one standard deviation of the sample estimated propensity scores) without replacement. PSM was implemented using Stata psmatch2 command.

To compare mental health growth trajectories between the two matched groups, data were analysed using growth curve models. It allowed us to estimate the interindividual heterogeneity in intraindividual changes over time. The model included a quadratic time term to allow for non-linear trajectories (see the Supplement Appendix 1 for mathematic equations). As sensitivity analyses, (a) we reran the analyses using alternative matching methods, namely one-to-many nearest neighbour matching and kernel matching; (b) we excluded anyone who said they were ‘unsure’ if they had long COVID; and (c) we explored further people's understanding of the term ‘long COVID’. If individuals reported believing they had long COVID but subsequently indicated that their symptoms had got better after 2 weeks, they were excluded, as were individuals who reported not having long COVID but who said they had symptoms lasting >4 weeks. The main analysis based on one-to-one matching were unweighted; whereas growth curve models based on one-to-many or kernel matching were weighted using weights of matched controls generated by psmatch2. Analyses were carried out using Stata version 17.

Results

Participant characteristics

Of the 3115 participants considered for matching, 495 (15.9%) reported having had long COVID-19. After matching, 481 participants were successfully matched with a control. There was a considerable reduction of individual covariates imbalance after matching (Supplementary Figure 4 and 5). In total, there were 13 325 observations from 962 participants (13.9 per person).

See Supplementary Table 1 for PSM results. Sample characteristics by the two matched groups are reported in Supplementary Table 2. In total, 78.2% of participants in the long-COVID-19 group were women. Although women were found to be at a higher risk of long COVID-19,Reference Bai, Tomasoni, Falcinella, Barbanotti, Castoldi and Mulè24 it is more than likely that there was an overrepresentation of women in the sample. However, weights were not applied because of a lack of credible information on the demographic characteristics of people who had long COVID in England. Among those with long COVID (n = 481), 23.3% of them were formally diagnosed by a medical professional and 76.7% self-diagnosed (Supplementary Table 3). Both groups experienced a comparable range of symptoms from being asymptomatic to being admitted to hospital (Supplementary Table 3).

Growth trajectories

We initially fitted the growth curve model allowing the long-COVID grouping variable to be associated with the quadratic growth rate. However, there was no evidence supporting this. Therefore, it was removed from the final model.

In the 10 months before contracting COVID-19 there was no evidence that the two COVID groups differed in either the intercept or growth rate of depressive symptoms (Table 1 and Fig. 1). However, at the time of infection, people who went on to develop long COVID had 1.3 points higher depressive symptoms on the PHQ-9 (16% higher) than those with short COVID. This equated to an increase of 35% in depressive symptoms from the month before they contracted SARS-CoV-2 in the long-COVID group versus an increase of 18% in the short-COVID group and was independent of all covariates that were included in the PSM model, including initial symptom severity. Over time, there was no evidence that these two groups differed in the growth rate (‘long COVID × time’ variable, Table 1), but levels of depressive symptoms remained higher in the long-COVID group (‘long COVID’ variable, Table 1) (Supplementary Figure 6(a) additionally shows 95% confidence intervals).

Fig. 1 Predicted growth trajectories of depressive (a) and anxiety (b) symptoms from growth curve models.

Table 1 Results from growth curve model on depressive symptomsa

a. ‘Month of COVID infection’ represents when people contracted SARS-CoV-2 considering an individual's mental health is subject to the impact of time-related contextual factors (e.g. lockdowns and other restrictions). Bold figures are statistically significant. Depressive symptoms were lower on average after the easing of first lockdown compared with at the start of the pandemic.

As for anxiety, in the 10 months before contracting COVID-19 there was no evidence that the two COVID groups differed in either the intercept or growth rate of anxiety symptoms (Table 2 and Fig. 1). At the time of infection, people who went on to develop long COVID were slightly higher in their anxiety levels than those who had short COVID (0.52 points higher anxiety symptoms on the GAD-7; 8.9% higher), but this was not a significant difference (‘long COVID’ variable, Table 2). This equated to an increase of 15% in depressive symptoms from the month before they contracted SARS-CoV-2 in the long-COVID group versus an increase of 13% in the short-COVID group. However, over time, the anxiety symptoms of the long-COVID group were less likely to decrease compared with for those with short COVID, with an increasing discrepancy in anxiety symptoms by 22 months follow-up (35% higher in the long-COVID group) (‘long COVID × time’ variable, Table 2) (Supplementary Figure 6(b) additionally shows 95% confidence intervals).

Table 2 Results from growth curve model on anxiety symptomsa

a. ‘Month of COVID infection’ represents when people contracted SARS-CoV-2 considering an individual's mental health is subject to the impact of time-related contextual factors (e.g. lockdowns and other restrictions). Bold figures are statistically significant. Anxiety symptoms were lower on average after first lockdown was introduced compared with at the start of the pandemic.

Sensitivity analyses

Sensitivity analyses using one-to-many nearest neighbour matching and kernel matching yielded less balanced matches. Further, there was a significant difference in growth factors of depressive and anxiety symptoms between the two matched groups before contracting COVID-19. The results from the one-to-many nearest neighbour matching are presented in Supplementary Figure 7 and 8. Supplementary Figure 9 shows the predicted growth trajectories by COVID group from kernel matching. Good matches were achieved but results were materially unaffected when applying a more rigorous definition of long COVID (Supplementary Figure 10) or when excluding people who were unsure about whether they had long COVID or not (Supplementary Figure 11).

Discussion

Main findings

This study examined the mental health trajectories of people who had long COVID compared with those who had short COVID. Infection with SARS-CoV-2 was associated with significant increases immediately following the onset of infection in depressive and anxiety symptoms in both groups. In the long-COVID group, there was evidence that depressive symptoms rose significantly higher than in the short-COVID group following onset of COVID-19, but anxiety levels were not significantly different between groups. Over time, the long-COVID group maintained heightened levels of depressive symptoms compared with the short-COVID group, and for anxiety the long-COVID group did not experience the improvements in anxiety seen in the short-COVID group, leading to widening differences in mental distress between the two groups.

Interpretation of the findings

This study supports work on the mechanisms at play in the development of long COVID. First, symptoms of depression and anxiety emerge quickly following the onset of SARS-CoV-2 infection, with the peak in both symptoms occurring at the first measurement time point post-infection (i.e. within 1 week of reported infection). This points to immediate psychobiological pathways being implicated in the aetiology of COVID-related mental distress both in long and short COVID. Existing literature proposes that inflammatory mechanisms could be at play,Reference Crook, Raza, Nowell, Young and Edison3,Reference Thye, Law, Tan, Pusparajah, Ser and Thurairajasingam6 but it is also possible that fear related to contracting the virus could also exacerbate mental distress, especially as levels of worries about catching SARS-CoV-2 and potentially becoming seriously ill from it have been associated with heightened anxiety and depression across the pandemic. Although our study included participants who had a range of symptom experiences from hospital admission to symptoms being mild or even asymptomatic, all participants in the study either knew (via testing) or suspected that they had SARS-CoV-2. We were unable to ascertain whether the reported increases in anxiety and depression found here were primarily driven by biological processes or psychological processes (i.e. fear of the virus) as we lacked data on psychological experiences in people with SARS-CoV-2 who were asymptomatic and did not know they had the virus.

Second, even when patients with long and short COVID were matched on physical and psychiatric comorbidities prior to COVID-19 and levels of SARS-CoV-2 symptom severity and even though they displayed similar trajectories of anxiety and depressive symptoms in the 10 months prior to infection, those in the long-COVID group experienced greater increases in depressive symptoms immediately following the onset of SARS-CoV-2 infection. This complements previous work suggesting that the ability of SARS-CoV-2 to raise levels of systemic- and neuro-inflammation may be greater in patients with long COVID and also suggests that whether an individual is likely to experience long COVID is decided early on in their experience of the virus.Reference Mazza, de Lorenzo, Conte, Poletti, Vai and Bollettini17,Reference Yong18 Notably, there was not a significant difference in initial increases in anxiety levels between the two groups, which would support theories that the increase in depressive symptoms among patients with long COVID is biologically driven by the virus rather than a manifestation of a greater predisposition to emotional distress during illness.

However, despite the larger initial increase in depressive symptoms in patients with long COVID, both long-COVID and short-COVID groups experienced parallel decreases in symptoms over time (even within 1 month of contracting SARS-CoV-2, despite patients with long COVID citing their physical symptoms persisting beyond this). This could suggest a process of psychological recovery, even potentially while experiencing ongoing physiological symptoms. However, we did not ask participants about how their symptoms and functioning at follow-up compared with when their virus started. So, some of this improvement in depressive symptoms among patients with long COVID could be illustrative of an improvement in long COVID itself (potentially mirroring reductions in levels of inflammation), while for patients who continued to experience physiological symptoms, this psychological recovery may not have been felt. Further, despite some improvement, levels of depressive symptoms remained higher in the long-COVID group across the entire 22-month follow-up than in the 10 months prior to infection, whereas the short-COVID group returned to baseline or below baseline levels within 4 months. So, any apparent recovery was not complete. Relatedly, levels of anxiety did not improve over time in patients with long COVID over the follow-up, with an increasing discrepancy compared with patients with short COVID.

The evident persistence of mental distress in patients with long COVID mirrors findings from previous studies of patients experiencing other coronaviruses. For example, patients who developed SARS-CoV (‘SARS’) in 2003–2004 reported persistent stress 1 year later without signs of decrease, even if physical symptoms had improved.Reference Lee, Wong, McAlonan, Cheung, Cheung and Sham25 But it may not simply be a case of initial anxiety symptoms experienced during acute infection (whether initially biologically or psychologically driven) persisting, but also a consequence of new psychological challenges relating to the realisation that one's initial infection is becoming long COVID and the associated psychological, social and behavioural consequences of ongoing illness (e.g. challenges accessing treatments, threat's to one's identity and uncertainty about the future).Reference Cascella, de Blasio, Cascella and de Blasio15,Reference Burton, Aughterson, Fancourt and Philip16 Notably, although there was a slight increase in depressive symptoms in both groups towards the end of the follow-up, the confidence intervals widened across the follow-up period as numbers of people who had contracted SARS-CoV-2 early enough in the pandemic to be followed-up 22 months later decreased. So, this increase is likely a feature of the sample rather than a common pattern among both groups over time.

Recommendations

Our findings highlight that for patients with long COVID, psychological symptoms could persist for as long as 2 years post-infection, with clear consequences for the treatment of patients with long COVID. Barriers to diagnosis with long COVID and subsequent challenges navigating and accessing treatments can in itself exacerbate long-COVID symptoms.Reference Burton, Aughterson, Fancourt and Philip16 Given the well-established interconnection between psychological and inflammatory processes, these additional treatment-related stressors could contribute to the prolonging of long-COVID symptoms. So, it is important that patients feel listened to, validated and supported in their diagnosis and treatment.Reference Burton, Aughterson, Fancourt and Philip16 There has been a call for the long-COVID public health response to include personalised treatment and rehabilitation and multidisciplinary care.Reference Alwan26 Our findings support this call, and further suggest that:

  1. (a) clinicians should be aware of the possibility for depression, anxiety and other psychiatric symptoms in patients with long COVID and recognise that such symptoms may not just be a consequence of ongoing physical symptoms but may have been primary outcomes from the initial SARS-CoV-2 infection;

  2. (b) neuropsychological evaluations for patients who are experiencing long COVID could be valuable to determine whether specialised mental health support is also required, and such evaluations should not assume a resolution of psychological symptoms in the absence of treatment; and

  3. (c) psychological support should be provided as part of multidisciplinary care and, given the early onset of psychological symptoms, early provision of such for patients suspected of having long COVID should be recommended.Reference Thye, Law, Tan, Pusparajah, Ser and Thurairajasingam6

In some countries such as the UK, it has been recommended that mental health problems alongside or as a result of long COVID can be managed by following existing relevant guidelines.Reference Crook, Raza, Nowell, Young and Edison3 However, we recommend that any mental health support needs to be provided alongside (rather than as a substitute for) broader medical investigation and support for long COVID, given diagnosis of psychiatric symptoms without adequate attention to other symptoms has been found to be detrimental to mental health in patients with long COVID.Reference Kingstone, Taylor, O'Donnell, Atherton, Blane and Chew-Graham27 Also, informal mental health support for patients experiencing long COVID such as peer support groups and community social and cultural activities via schemes such as social prescribing should be encouraged as evidence is already suggesting that the broader support and validation of experiences from others can assist in recovery.Reference Burton, Aughterson, Fancourt and Philip16

Strengths and limitations

A main strength of this study lies in repeated weekly or monthly follow-ups of the same participant over 22 months since March 2020, allowing the longest and most detailed follow-up to date on psychological experiences of patients with long COVID. By using PSM, we were able to reduce the observed differences between long- and short-COVID groups to render them comparable. We achieved a good-quality match, which resulted in equivalent mental health scores in the months prior to infection, improving the comparability of post-infection mental health changes between people with short and long COVID. However, we cannot rule out the possibility of potential biases because of unobserved covariates that are associated with the risk of having long COVID-19 (despite the wide range of covariates included in our models). Moreover, although our sample showed good heterogeneity in initial severity of SARS-CoV-2 symptoms and subsequent long-COVID experiences, our sample may not be representative of the population who had (long) COVID, especially as those with more severe ongoing long-COVID symptoms may have been more likely to drop out of the study. We followed current best practice in epidemiological research in how we defined long COVID. But some of our patients lacked formal diagnoses, so it is possible that some participants’ symptoms were caused by alternative illnesses. Additionally, our sample was relatively heterogeneous in terms of long-COVID experiences, with a range of different patterns of symptoms reported, from persistent acute symptoms for months, to relapsing–remitting symptoms, to low-level persistent symptoms. Although this heterogeneity is typical in the diagnosis category of ‘long COVID’, future research could consider whether there are differential psychological experiences depending on pattern of long-COVID symptoms. Finally, our sample relied on participants’ self-report of the date they contracted SARS-CoV-2. This could have been affected by recall bias. So although we found an increase in psychological symptoms immediately following reported onset of infection, this increase may have lagged by a few days. Nonetheless, this relatively short lag time does not undermine the conclusions or proposed mechanisms.

Conclusions

Overall, this study presents the longest and most detailed data on psychological experiences of patients with long COVID to date, answering crucial questions. Psychological symptoms of anxiety and depression emerge quickly following onset of SARS-CoV-2 in patients with long COVID, with levels of depression rising significantly above levels in patients who go on to experience short COVID. Over the following 2 years, although there is some decrease in depressive symptoms, they remain above pre-infection levels, whereas anxiety levels show little signs of improvement. This presents a contrast to patients with short COVID where levels return to below-infection levels within 4 months of infection. The findings shed light on the psychobiological pathways involved in the development of psychological symptoms relating to long COVID as well as suggesting that initial psychological experiences during SARS-CoV-2 infection could be explored further as potential predictors of subsequent risk of developing long COVID. The results also show that we cannot assume a gradual organic recovery from the psychological effects of long COVID, highlighting the need for monitoring of mental health and provision of adequate support to be interwoven with diagnosis and treatment of the physical consequences of long COVID.

Supplementary material

To view supplementary material for this article, please visit http://doi.org/10.1192/bjp.2022.155

Data availability

Anonymous data are publicly available via the UK Data service.

Acknowledgements

The researchers are grateful for the support of a number of organisations with their recruitment efforts including: the UKRI Mental Health Networks, Find Out Now, UCL BioResource, SEO Works, FieldworkHub and Optimal Workshop. The study was also supported by HealthWise Wales, the Health and Care Research Wales initiative, which is led by Cardiff University in collaboration with SAIL, Swansea University. We would like to thank the reviewers for their time and valuable suggestions and comments, which helped us in improving the quality of the paper.

Author contributions

D.F. and A.S. developed the study idea. F.B. analysed the data. D.F. and F.B. wrote the first draft. All authors had accessed and verified the underlying data. All authors provided critical revisions, read and approved the submitted manuscript.

Funding

This COVID-19 Social Study was funded by the Nuffield Foundation [WEL/FR-000022583], but the views expressed are those of the authors and not necessarily the Foundation. The study was also supported by the MARCH Mental Health Network funded by the Cross-Disciplinary Mental Health Network Plus initiative supported by UK Research and Innovation [ES/S002588/1], and by the Wellcome Trust [221400/Z/20/Z]. D.F. was funded by the Wellcome Trust [205407/Z/16/Z].

Declaration of interest

None.

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Figure 0

Fig. 1 Predicted growth trajectories of depressive (a) and anxiety (b) symptoms from growth curve models.

Figure 1

Table 1 Results from growth curve model on depressive symptomsa

Figure 2

Table 2 Results from growth curve model on anxiety symptomsa

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