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Inflamm-aging: Why older men are the most susceptible to SARS-CoV-2 complicated outcomes.
Bonafè, Massimiliano; Prattichizzo, Francesco; Giuliani, Angelica; Storci, Gianluca; Sabbatinelli, Jacopo; Olivieri, Fabiola.
  • Bonafè M; Department of Experimental, Diagnostic and Specialty Medicine, AlmaMater Studiorum, Università di Bologna, Bologna, Italy.
  • Prattichizzo F; IRCCS MultiMedica, Milano, Italy. Electronic address: francesco.prattichizzo@multimedica.it.
  • Giuliani A; Department of Clinical and Molecular Sciences, DISCLIMO, Università Politecnica delle Marche, Ancona, Italy. Electronic address: angelica.giuliani@staff.univpm.it.
  • Storci G; Department of Experimental, Diagnostic and Specialty Medicine, AlmaMater Studiorum, Università di Bologna, Bologna, Italy.
  • Sabbatinelli J; Department of Clinical and Molecular Sciences, DISCLIMO, Università Politecnica delle Marche, Ancona, Italy.
  • Olivieri F; Department of Clinical and Molecular Sciences, DISCLIMO, Università Politecnica delle Marche, Ancona, Italy; Center of Clinical Pathology and Innovative Therapy, IRCCS INRCA, Ancona, Italy.
Cytokine Growth Factor Rev ; 53: 33-37, 2020 06.
Article in English | MEDLINE | ID: covidwho-154941
ABSTRACT
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is characterized by a high mortality of elderly men with age-related comorbidities. In most of these patients, uncontrolled local and systemic hyperinflammation induces severe and often lethal outcomes. The aging process is characterized by the gradual development of a chronic subclinical systemic inflammation (inflamm-aging) and by acquired immune system impairment (immune senescence). Here, we advance the hypothesis that four well-recognized features of aging contribute to the disproportionate SARS-CoV-2 mortality suffered by elderly men i. the presence of subclinical systemic inflammation without overt disease, ii. a blunted acquired immune system and type I interferon response due to the chronic inflammation; iii. the downregulation of ACE2 (i.e. the SARS-CoV-2 receptor); and iv. accelerated biological aging. The high mortality rate of SARS-CoV-2 infection suggests that clarification of the mechanisms of inflamm-aging and immune senescence can help combat not only age-related disorders but also SARS-CoV-2 infection.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Aging / Interleukin-6 / Coronavirus Infections / Peptidyl-Dipeptidase A Type of study: Prognostic study Limits: Aged / Female / Humans / Male Language: English Journal: Cytokine Growth Factor Rev Journal subject: Allergy and Immunology / Biochemistry Year: 2020 Document Type: Article Affiliation country: J.cytogfr.2020.04.005

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Aging / Interleukin-6 / Coronavirus Infections / Peptidyl-Dipeptidase A Type of study: Prognostic study Limits: Aged / Female / Humans / Male Language: English Journal: Cytokine Growth Factor Rev Journal subject: Allergy and Immunology / Biochemistry Year: 2020 Document Type: Article Affiliation country: J.cytogfr.2020.04.005