Anxiety and depression in COVID-19 survivors: Role of inflammatory and clinical predictors

Mario Gennaro Mazza, Rebecca De Lorenzo, Caterina Conte, Sara Poletti, Benedetta Vai, Irene Bollettini, Elisa Maria Teresa Melloni, Roberto Furlan, Fabio Ciceri, Patrizia Rovere-Querini, COVID-19 BioB Outpatient Clinic Study group, Francesco Benedetti, Mario Gennaro Mazza, Rebecca De Lorenzo, Caterina Conte, Sara Poletti, Benedetta Vai, Irene Bollettini, Elisa Maria Teresa Melloni, Roberto Furlan, Fabio Ciceri, Patrizia Rovere-Querini, COVID-19 BioB Outpatient Clinic Study group, Francesco Benedetti

Abstract

Infection-triggered perturbation of the immune system could induce psychopathology, and psychiatric sequelae were observed after previous coronavirus outbreaks. The spreading of the Severe Acute Respiratory Syndrome Coronavirus (COVID-19) pandemic could be associated with psychiatric implications. We investigated the psychopathological impact of COVID-19 in survivors, also considering the effect of clinical and inflammatory predictors. We screened for psychiatric symptoms 402 adults surviving COVID-19 (265 male, mean age 58), at one month follow-up after hospital treatment. A clinical interview and a battery of self-report questionnaires were used to investigate post-traumatic stress disorder (PTSD), depression, anxiety, insomnia, and obsessive-compulsive (OC) symptomatology. We collected sociodemographic information, clinical data, baseline inflammatory markers and follow-up oxygen saturation levels. A significant proportion of patients self-rated in the psychopathological range: 28% for PTSD, 31% for depression, 42% for anxiety, 20% for OC symptoms, and 40% for insomnia. Overall, 56% scored in the pathological range in at least one clinical dimension. Despite significantly lower levels of baseline inflammatory markers, females suffered more for both anxiety and depression. Patients with a positive previous psychiatric diagnosis showed increased scores on most psychopathological measures, with similar baseline inflammation. Baseline systemic immune-inflammation index (SII), which reflects the immune response and systemic inflammation based on peripheral lymphocyte, neutrophil, and platelet counts, positively associated with scores of depression and anxiety at follow-up. PTSD, major depression, and anxiety, are all high-burden non-communicable conditions associated with years of life lived with disability. Considering the alarming impact of COVID-19 infection on mental health, the current insights on inflammation in psychiatry, and the present observation of worse inflammation leading to worse depression, we recommend to assess psychopathology of COVID-19 survivors and to deepen research on inflammatory biomarkers, in order to diagnose and treat emergent psychiatric conditions.

Keywords: Anxiety; COVID-19; COVID-19 survivors; Depression; Inflammation; Insomnia; Mental health; Obsessive-compulsive disorder; PTSD; Psychopathology.

Copyright © 2020 Elsevier Inc. All rights reserved.

References

    1. Armour C., Contractor A., Shea T. Factor structure of the PTSD checklist for DSM-5: relationships among symptom clusters, anger, and impulsivity. J. Nerv. Ment. Dis. 2016;204:108–115.
    1. Arteaga-Henríquez G., Simon M.S., Burger B. Low-grade inflammation as a predictor of antidepressant and anti-inflammatory therapy response in MDD patients: a systematic review of the literature in combination with an analysis of experimental data collected in the EU-Moodinflame Consortium. Front. Psychiatry. 2019;10
    1. Banerjee D.D. The other side of COVID-19: impact on obsessive compulsive disorder (OCD) and hoarding. Psychiatry Res. 2020;288
    1. Beck A.T., Steer R.A. Internal consistencies of the original and revised Beck Depression Inventory. J. Clin. Psychol. 1984;40:1365–1367.
    1. Benedetti F., Poletti S., Hoogenboezem T.A. Higher baseline proinflammatory cytokines mark poor antidepressant response in bipolar disorder. J. Clin. Psychiatry. 2017;78:e986–e993.
    1. Benedetti F., Aggio V., Pratesi M.L. Neuroinflammation in bipolar depression. Front. Psychiatry. 2020;11:71.
    1. Benedetti F., Aggio V., Pratesi M.L. Neuroinflammation in bipolar depression. Front. Psychiatry. 2020;11:71.
    1. Bohmwald K., Galvez N.M.S., Rios M. Neurologic alterations due to respiratory virus infections. Front. Cell Neurosci. 2018;12:386.
    1. Brooks S.K., Webster R.K., Smith L.E. The psychological impact of quarantine and how to reduce it: rapid review of the evidence. Lancet. 2020;395:912–920.
    1. Cameron M.J., Bermejo-Martin J.F., Danesh A. Human immunopathogenesis of severe acute respiratory syndrome (SARS) Virus Res. 2008;133:13–19.
    1. Capuron L., Miller A.H. Immune system to brain signaling: neuropsychopharmacological implications. Pharmacol. Ther. 2011;130:226–238.
    1. Carvalho P.M.M., Moreira M.M., de Oliveira M.N.A. The psychiatric impact of the novel coronavirus outbreak. Psychiatry Res. 2020;286
    1. Channappanavar R., Perlman S. Pathogenic human coronavirus infections: causes and consequences of cytokine storm and immunopathology. Semin. Immunopathol. 2017;39:529–539.
    1. Cheng S.K., Wong C.W., Tsang J. Psychological distress and negative appraisals in survivors of severe acute respiratory syndrome (SARS) Psychol. Med. 2004;34:1187–1195.
    1. Creamer M., Bell R., Failla S. Psychometric properties of the impact of event scale – revised. Behav. Res. Ther. 2003;41:1489–1496.
    1. Cuijpers P., Vogelzangs N., Twisk J. Is excess mortality in depression generic or specific? A comprehensive meta-analysis of community and patient studies. Am. J. Psychiatry. 2014
    1. Dantzer R. Neuroimmune interactions: from the brain to the immune system and vice versa. Physiol. Rev. 2018;98:477–504.
    1. Desforges M., Le Coupanec A., Dubeau P. Human coronaviruses and other respiratory viruses: underestimated opportunistic pathogens of the central nervous system? Viruses. 2019;12
    1. Dobson A.J. Chapman & Hall; New York: 1990. An Introduction to Generalized Linear Models.
    1. Feng X., Li S., Sun Q. Immune-inflammatory parameters in COVID-19 cases: a systematic review and meta-analysis. Front. Med. (Lausanne) 2020;7:301.
    1. Foa E.B., Huppert J.D., Leiberg S. The obsessive-compulsive inventory: development and validation of a short version. Psychol. Assess. 2002;14:485–496.
    1. Hays R.D., Martin S.A., Sesti A.M. Psychometric properties of the Medical Outcomes Study Sleep measure. Sleep Med. 2005;6:41–44.
    1. Hill, T., Lewicki, P., 2006. Statistics: methods and applications. A comprehensive reference for science, industry, and data mining. General Linear Models, StatSoft, Tulsa (OK); Chapter 18:245-276.
    1. Huang H., Liu Q., Zhu L. Prognostic value of preoperative systemic immune-inflammation index in patients with cervical cancer. Sci. Rep. 2019;9:3284.
    1. Huang C., Wang Y., Li X. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020;395:497–506.
    1. Jones K.A., Thomsen C. The role of the innate immune system in psychiatric disorders. Mol. Cell. Neurosci. 2013;53:52–62.
    1. Kohler C.A., Freitas T.H., Maes M. Peripheral cytokine and chemokine alterations in depression: a meta-analysis of 82 studies. Acta Psychiatr. Scand. 2017;135:373–387.
    1. Lam M.H., Wing Y.K., Yu M.W. Mental morbidities and chronic fatigue in severe acute respiratory syndrome survivors: long-term follow-up. Arch. Intern. Med. 2009;169:2142–2147.
    1. Leigh-Hunt N., Bagguley D., Bash K. An overview of systematic reviews on the public health consequences of social isolation and loneliness. Public Health. 2017;152:157–171.
    1. Levine D.W., Kripke D.F., Kaplan R.M. Reliability and validity of the women's health initiative insomnia rating scale. Psychol. Assess. 2003;15:137–148.
    1. Miller B.J., Buckley P., Seabolt W. Meta-analysis of cytokine alterations in schizophrenia: clinical status and antipsychotic effects. Biol. Psychiatry. 2011;70:663–671.
    1. Miller A.H., Raison C.L. The role of inflammation in depression: from evolutionary imperative to modern treatment target. Nat. Rev. Immunol. 2016;16:22–34.
    1. Najjar S., Pearlman D.M., Alper K. Neuroinflammation and psychiatric illness. J. Neuroinflamm. 2013;10:43.
    1. Netland J., Meyerholz D.K., Moore S. Severe acute respiratory syndrome coronavirus infection causes neuronal death in the absence of encephalitis in mice transgenic for human ACE2. J. Virol. 2008;82:7264–7275.
    1. Okusaga O., Yolken R.H., Langenberg P. Association of seropositivity for influenza and coronaviruses with history of mood disorders and suicide attempts. J. Affect Disord. 2011;130:220–225.
    1. Ozamiz-Etxebarria N., Dosil-Santamaria M., Picaza-Gorrochategui M. Stress, anxiety, and depression levels in the initial stage of the COVID-19 outbreak in a population sample in the northern Spain. Cad Saude Publica. 2020;36
    1. Ozbay F., Johnson D.C., Dimoulas E. Social support and resilience to stress: from neurobiology to clinical practice. Psychiatry (Edgmont) 2007;4:35–40.
    1. Pappa S., Ntella V., Giannakas T. Prevalence of depression, anxiety, and insomnia among healthcare workers during the COVID-19 pandemic: a systematic review and meta-analysis. Brain Behav. Immun. 2020
    1. Peiris J.S., Lai S.T., Poon L.L. Coronavirus as a possible cause of severe acute respiratory syndrome. Lancet. 2003;361:1319–1325.
    1. Poletti S., Leone G., Hoogenboezem T.A. Markers of neuroinflammation influence measures of cortical thickness in bipolar depression. Psychiatry Res. Neuroimag. 2019;285:64–66.
    1. Renna M.E., O'Toole M.S., Spaeth P.E. The association between anxiety, traumatic stress, and obsessive-compulsive disorders and chronic inflammation: a systematic review and meta-analysis. Depress Anxiety. 2018;35:1081–1094.
    1. Rogers J.P., Chesney E., Oliver D. Psychiatric and neuropsychiatric presentations associated with severe coronavirus infections: a systematic review and meta-analysis with comparison to the COVID-19 pandemic. Lancet Psychiatry. 2020
    1. Shafran R., Coughtrey A., Whittal M. Recognising and addressing the impact of COVID-19 on obsessive-compulsive disorder. Lancet Psychiatry. 2020;7:570–572.
    1. Sheng B., Cheng S.K., Lau K.K. The effects of disease severity, use of corticosteroids and social factors on neuropsychiatric complaints in severe acute respiratory syndrome (SARS) patients at acute and convalescent phases. Eur. Psychiatry. 2005;20:236–242.
    1. Teixeira A.L., Rodrigues D.H., Marques A.H. Searching for the immune basis of obsessive-compulsive disorder. NeuroImmunoModulation. 2014;21:152–158.
    1. Troyer E.A., Kohn J.N., Hong S. Are we facing a crashing wave of neuropsychiatric sequelae of COVID-19? Neuropsychiatric symptoms and potential immunologic mechanisms. Brain Behav. Immun. 2020
    1. Vigneau F., Cormier S. The factor structure of the state-trait anxiety inventory: an alternative view. J. Pers. Assess. 2008;90:280–285.
    1. Vindegaard N., Eriksen Benros M. COVID-19 pandemic and mental health consequences: systematic review of the current evidence. Brain Behav. Immun. 2020
    1. Wang C., Pan R., Wan X. A longitudinal study on the mental health of general population during the COVID-19 epidemic in China. Brain Behav. Immun. 2020
    1. Williams L.M. Precision psychiatry: a neural circuit taxonomy for depression and anxiety. Lancet Psychiatry. 2016;3:472–480.
    1. Wu Y., Xu X., Chen Z. Nervous system involvement after infection with COVID-19 and other coronaviruses. Brain Behav. Immun. 2020
    1. Ye Q., Wang B., Mao J. The pathogenesis and treatment of the ‘Cytokine Storm' in COVID-19. J. Infect. 2020;80:607–613.
    1. Zhou L., Ma X., Wang W. Inflammation and coronary heart disease risk in patients with depression in china mainland: a cross-sectional study. Neuropsychiatr. Dis. Treat. 2020;16:81.
    1. Zung W.W. A self-rating depression scale. Arch. Gen. Psychiatry. 1965;12:63–70.

Source: PubMed

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