key: cord-0882359-p5273oai
authors: Kyzar, Evan J.; Purpura, Lawrence J.; Shah, Jayesh; Cantos, Anyelina; Nordvig, Anna S.; Yin, Michael T.
title: Anxiety, depression, insomnia, and trauma-related symptoms following COVID-19 infection at long-term follow-up
date: 2021-07-30
journal: Brain Behav Immun Health
DOI: 10.1016/j.bbih.2021.100315
sha: d89adf7b162ca9f6de81779057c728fe6eb7c562
doc_id: 882359
cord_uid: p5273oai

A developing finding from the novel coronavirus 2019 (COVID-19) pandemic is the burden of neuropsychiatric symptoms seen in COVID-19 survivors. While studies have shown clinically significant rates of depression, anxiety, insomnia, and trauma-related symptoms such as post-traumatic stress disorder (PTSD) after COVID-19, little is known about how these symptoms evolve over time. Here, we report findings from a cohort study of 52 participants recruited from the greater New York City area following acute COVID-19 infection. Participants completed the Patient Health Questionnaire-9 (PHQ-9) for depressive symptoms, the Generalized Anxiety Disorder-7 (GAD-7) for anxiety-related symptoms, the Insomnia Severity Scale (ISS) from sleep-related symptoms, and the PTSD Checklist-Civilian version (PCL-C) for trauma-related symptoms both at baseline and at long-term (24 to 60 weeks post-infection) follow-up. We found a high degree of correlation between psychiatric symptom scales within participants. More participants met established cutoffs for clinically significant insomnia and post-traumatic stress at follow-up compared to baseline. Symptom scales for depression, insomnia, and PTSD were increased at long-term follow-up, with only increased PCL-C scores surviving correction for multiple comparisons (Z=2.92, W=434, p=0.004). Our results present evidence from a small cohort that neuropsychiatric symptoms, particularly those related to PTSD, may worsen over time in COVID-19 survivors. Future studies should continue to investigate these questions in broader populations, while additionally exploring the potential biological and sociological mechanisms that may contribute to neuropsychiatric pathology after COVID-19 infection.

The novel coronavirus 2019 pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has infected over 150 million persons worldwide and caused over 3 million deaths as of this writing (Dong et al., 2020) . While the pandemic continues to occasion unprecedented stress on global healthcare systems, numerous outstanding questions remain regarding the long-term consequences of SARS-CoV-2 infection. Principal among these questions is the longterm impact on mental and physical health in survivors of COVID-19 (Del Rio et al., 2020; Nalbandian et al., 2021 ).

An emerging finding from the COVID-19 pandemic is the burden of neuropsychiatric symptoms in survivors (Huang et al., 2021; Taquet et al., 2021a ). An analysis of electronic health records showed increased odds of receiving a diagnosis of depression, anxiety, and insomnia in COVID-19 survivors compared to other respiratory infections (Taquet et al., 2021a ). Short-term follow-up studies of COVID-19 survivors show that symptoms of anxiety, depression, fatigue, and insomnia are prominent in the month following discharge (Mazza et al., 2020; Townsend et al., 2020) . Patients recovering from COVID-19 demonstrated elevated Patient Health Questionnaire-9 (PHQ-9) scores, used to explore symptoms of depression, at 2-to-3-month follow-up after discharge (Raman et al., 2021) . Additionally, 23% of participants reported symptoms of anxiety and/or depression and 26% reported sleep difficulties in a large quality-of-life survey at 6-month follow-up (Huang et al., 2021) . These findings from COVID-19 are similar to the long-term neuropsychiatric symptoms observed after the original SARS outbreak (Lam et al., 2009) . Interestingly, the majority of these studies J o u r n a l P r e -p r o o f have found little to no correlation with initial illness severity and inflammatory markers during acute illness on lasting psychiatric symptoms.

An outstanding question in this emerging research domain is whether post-COVID neuropsychiatric symptoms evolve over time within individual survivors. In order to address this key point, we recruited participants who had recovered from confirmed COVID-19 infection and followed them for at least 24 weeks with measures in multiple neuropsychiatric domains. We hypothesized that COVID-19 survivors would demonstrate a high burden of psychiatric symptoms, and that these symptoms might worsen over time given ongoing psychosocial stressors secondary to the pandemic.

Here, we report longitudinal findings from an observational cohort study of recovered COVID-19 participants with baseline and follow-up measures of depression, anxiety, insomnia, and post-traumatic stress.

Participants recovered from COVID-19 infection were recruited by community advertisement and referral from other ongoing COVID-19 studies from April 15 th , 2020

to February 23 rd , 2021 from the greater New York City area. Inclusion criteria were age > 7 years and confirmation of previous COVID-19 infection. Enrolled participants were offered an online survey with medical and psychiatric questionnaires, as well as inperson visits for laboratory monitoring and physical examinations. In order to establish bona fide COVID-19 infection status, serum antibody testing was performed and participants who were antibody-negative without proof of acute COVID-19 infection (e.g., positive PCR test during acute infection) were excluded from our analysis.

Participants were instructed to fill out follow-up surveys at visits from 24 and 60 weeks following initial enrollment. A total of 52 participants filled out both the baseline and at least one follow-up survey consisting of the PHQ-9 for depressive symptoms, the Generalized Anxiety Disorder-7 (GAD-7) for anxiety-related symptoms, the Insomnia Severity Scale (ISS) from sleep-related and insomnia symptoms, and the PTSD Checklist-Civilian version (PCL-C) for trauma-related symptoms. All investigations were approved by local Institutional Review Board (IRB) at Columbia University Irving Medical Center.

PHQ-9, GAD-7, ISS, and PCL-C scores were examined with regard to established cutoff scores. A cutoff of 10 for PHQ-9 and GAD-7 are commonly used both clinically and in research studies, while we used a cutoff of 10 for the ISS based on a previous analysis (Morin et al., 2011) . A cutoff of 35 was selected for the PCL-C to maximize sensitivity in a population with an identifiable stressor (McDonald and Calhoun, 2010; Walker et al., 2002) . Scores were averaged for participants who filled out surveys at multiple follow-up visits. We analyzed the effects of age, sex, self-defined racial and Hispanic identity, smoking status, weight, hospital admission, and time from symptom onset to study enrollment on PHQ-9, GAD-7, ISS, and PCL-C scores at baseline and follow-up were analyzed with multivariate generalized linear modeling analysis. PHQ-9, GAD-7, ISS, and PCL-C scores were analyzed for within-subject correlation with Pearson's test. Baseline and follow-up values were compared with Wilcoxon signed rank test or t-test depending on data distribution. Initial significance J o u r n a l P r e -p r o o f was set at p<0.05, and a Bonferroni correction was utilized for multiple comparisons.

Exact p-values are reported up to p<0.001.

Basic demographic for our cohort (n=52) and mean PHQ-9, GAD-7, ISS, or PCL-C scores at baseline and follow-up are reported in Table 1 . Multivariate analysis was performed to determine the effects of age, sex, self-defined racial and Hispanic identity, smoking status, weight, hospital admission, or time from symptom onset to study enrollment on PHQ-9, GAD-7, ISS, and PCL-C scores at baseline and at follow-up.

Regression equations meeting initial significance values (α=0.05) were noted for GAD-7 scores at baseline (F(8,41)=2.62, R 2 =0.34, p=0.02) and follow-up (F(8,41)=2.67, R 2 =0.34, p=0.02) and for PCL-C scores at baseline (F(8,40)=4.16, R 2 =0.45, p=0.001) and follow-up (F(8,40)=4.24, R 2 =0.46, p<0.001), but not for PHQ-9 scores or ISS scores. Regression equations for PCL-C scores were significant after Bonferroni correction for multiple comparisons, with subject weight (β=0.07, p=0.004) most likely to predict PCL-C scores at baseline and weight (β=0.07, p=0.003), self-identified racial identity (β=-2.76, p=0.005) and self-identified Hispanic identity (β=7.92, p=0.009) most likely to predict PCL-C scores at long-term follow-up.

We next examined the relationship and independence of the psychometric tests used in our analysis. Pearson correlation confirmed that PHQ-9, GAD-7, ISS, and PCL-C scores were correlated both at baseline and at long-term follow-up, with all tested J o u r n a l P r e -p r o o f correlations meeting criteria for significance after correction for multiple comparisons ( Figure 1 ).

Overall, more participants met the defined cut-off values for insomnia by ISS score and trauma-related symptoms by PCL-C score at follow-up compared to baseline (Table 2 ). PHQ-9 (Z=2.02, W=257, n=52, p=0.044), ISS (t(51)=-2.04, n=52, p=0.047),

and PCL-C scores (Z=2.92, W=434, n=50, p=0.004) met initial criteria for a significant increase at long-term follow-up compared to baseline values ( Figure 2) . However, only PCL-C scores survived correction for multiple comparisons. GAD-7 scores were not significantly altered at follow-up compared to baseline.

Here, we report longitudinal symptoms across multiple neuropsychiatric domains including depression, anxiety, insomnia, and trauma-related symptoms in a cohort of participants recovering from COVID-19. We observed a high degree of correlation between symptom domains within individual participants in our study (Figure 1 ).

Previous studies have shown substantial comorbidity between depression, anxiety, insomnia, and PTSD specifically in trauma-exposed populations (Muller et al., 2014) , and a latent class analysis of trauma-exposed soldiers demonstrated specific subclasses of individuals with extensive symptom burden and comorbidity across psychiatric domains (Contractor et al., 2015) .

Interestingly, symptoms of PTSD appeared to worsen at long-term (24 to 60

week) follow-up in COVID-19 survivors in our cohort (Figure 2) . A previous report found J o u r n a l P r e -p r o o f that greater than 30% of subjects who had recovered from COVID-19 met criteria for PTSD (Janiri et al., 2021) . Another group reported a lower prevalence of PTSD (~10%), but interestingly found that obesity increased risk for PTSD diagnosis (Tarsitani et al., 2021 ) similar to our findings that weight was a predictive factor for PCL-C scores by multivariate analysis. A recent large-scale analysis of electronic medical records showed an increased risk of worsening PHQ-9 scores over time in COVID-19 survivors (Perlis et al., 2021) . Our cohort demonstrated some potential worsening of PHQ-9 and ISS scores, although this did not meet criteria for significance after comparison for multiple comparisons. d Future studies should explore whether biological effects such as ongoing immune activation or sequelae from possible neuroinflammatory insults may underlie any potential worsening of neuropsychiatric outcomes over time. For example, direct central nervous system (CNS) action of COVID-19 (Meinhardt et al., 2021; Rhea et al., 2021 ) may result in long-term sequelae such as microglial activation. Indeed, widespread microglial activation has been noted in postmortem brain tissue after COVID-19 infection, although this did not correlate with the presence of viral RNA (Thakur et al., 2021) . Severe COVID-19 infection leads to a diverse production of autoantibodies, which the CNS being the most common target tissue affected . Alternatively, peripheral effects of COVID-19 on vasculature and other organ systems may perturb central feedback loops and result in somatic symptoms that contribute to neuropsychiatric symptomatology, similar to reports of increased cardiovascular event risk in subjects with high perceived stress (Tawakol et al., 2017) . A recent transcriptomic study found evidence of widespread gene expression changes in J o u r n a l P r e -p r o o f the brain by single nucleus RNA-sequencing (snRNA-seq) but no evidence of direct CNS neuroinvasion, which may indicate that peripheral inflammation is sufficient to grossly impact brain function during and after COVID-19 infection (Yang et al., 2021) .

Further research is needed to more fully understand the effects of this virus on the brain.

Another possibility is that sociocultural factors including lockdowns may contribute to the observed worsening of select psychiatric symptoms. A large population study consisting mostly of participants without COVID-19 infection showed that PHQ-9 and GAD-7 scores decreased over time during the pandemic (Fancourt et al., 2021) .

Additionally, a population-based study from early 2020 in China showed a diminished psychological impact of COVID-19 stress as measured by the Impact of Event Scale (IEG) at 4 weeks compared to a baseline measure, along with unchanged scores on the Depression, Anxiety, and Stress Scale (DASS) (Wang et al., 2020) . The impact of sociocultural stress from COVID-19 may also impact survivors differently from unaffected members of the general population. A latent class analysis of populationlevel data from the UK showed that those with worsening mental health outcomes were more likely to have had COVID-19 and to identify as non-white (Pierce et al., 2021) , which is interesting given our findings that self-identified racial and Hispanic identity are predictive of PCL-C scores.

Our study was limited by a number of important factors including self-selection bias, lack of a control group, and lack of information on socioeconomic factors such as income level that may contribute to mental health outcomes. While our cohort was notable for a low burden of self-reported psychiatric symptoms prior to J o u r n a l P r e -p r o o f infection (Table 1) , we lacked detailed clinical information on pre-COVID psychiatric diagnoses which have been associated with post-COVID sequelae (Taquet et al., 2021b) . While our limited sample size allowed us to collect more nuanced longitudinal information on psychiatric symptoms in our participants, our findings necessitate replication in larger samples in order to more fully understand the clinical consequences of potentially worsening mental health outcomes in patients recovering from COVID-19.

Long-term anxiety, depression, insomnia, PTSD, and other neuropsychiatric symptoms following COVID-19 warrant further detailed investigation. J o u r n a l P r e -p r o o f Abbreviations: PHQ-9 -Patient Health Questionnaire-9; GAD-7 -Generalized Anxiety

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