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Intersections between pneumonia, lowered oxygen saturation percentage and immune activation mediate depression, anxiety, and chronic fatigue syndrome-like symptoms due to COVID-19: A nomothetic network approach.
Al-Jassas, Hawraa Kadhem; Al-Hakeim, Hussein Kadhem; Maes, Michael.
  • Al-Jassas HK; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Kufa, Iraq.
  • Al-Hakeim HK; Department of Chemistry, College of Science, University of Kufa, Iraq.
  • Maes M; School of Medicine, IMPACT-the Institute for Mental and Physical Health and Clinical Translation, Deakin University, Barwon Health, Geelong, Australia; Department of Psychiatry, Medical University of Plovdiv, Plovdiv, Bulgaria; Department of Psychiatry, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand. Electronic address: dr.michaelmaes@hotmail.com.
J Affect Disord ; 297: 233-245, 2022 01 15.
Article in English | MEDLINE | ID: covidwho-1720180
ABSTRACT

BACKGROUND:

COVID-19 is associated with neuropsychiatric symptoms including increased depressive, anxiety and chronic fatigue-syndrome (CFS)-like and physiosomatic symptoms.

AIMS:

To delineate the associations between affective and CFS-like symptoms in COVID-19 and chest computed tomography scan anomalies (CCTAs), oxygen saturation (SpO2), interleukin (IL)-6, IL-10, C-Reactive Protein (CRP), albumin, calcium, magnesium, soluble angiotensin converting enzyme (ACE2) and soluble advanced glycation products (sRAGEs).

METHOD:

The above biomarkers were assessed in 60 COVID-19 patients and 30 healthy controls who had measurements of the Hamilton Depression (HDRS) and Anxiety (HAM-A) and the Fibromyalgia and Chronic Fatigue (FF) Rating Scales.

RESULTS:

Partial Least Squares-SEM analysis showed that reliable latent vectors could be extracted from a) key depressive and anxiety and physiosomatic symptoms (the physio-affective or PA-core), b) IL-6, IL-10, CRP, albumin, calcium, and sRAGEs (the immune response core); and c) different CCTAs (including ground glass opacities, consolidation, and crazy paving) and lowered SpO2% (lung lesions). PLS showed that 70.0% of the variance in the PA-core was explained by the regression on the immune response and lung lesions latent vectors. One common "infection-immune-inflammatory (III) core" underpins pneumonia-associated CCTAs, lowered SpO2 and immune activation, and this III core explains 70% of the variance in the PA core, and a relevant part of the variance in melancholia, insomnia, and neurocognitive symptoms.

DISCUSSION:

Acute SARS-CoV-2 infection is accompanied by lung lesions and lowered SpO2 which may cause activated immune-inflammatory pathways, which mediate the effects of the former on the PA-core and other neuropsychiatric symptoms due to SARS-CoV-2 infection.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Fatigue Syndrome, Chronic / COVID-19 Limits: Humans Language: English Journal: J Affect Disord Year: 2022 Document Type: Article Affiliation country: J.jad.2021.10.039

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Fatigue Syndrome, Chronic / COVID-19 Limits: Humans Language: English Journal: J Affect Disord Year: 2022 Document Type: Article Affiliation country: J.jad.2021.10.039