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Long-COVID cognitive impairments and reproductive hormone deficits in men may stem from GnRH neuronal deathResearch in context

Authors :
Florent Sauve
Sreekala Nampoothiri
Sophie A. Clarke
Daniela Fernandois
Caio Fernando Ferreira Coêlho
Julie Dewisme
Edouard G. Mills
Gaetan Ternier
Ludovica Cotellessa
Cristina Iglesias-Garcia
Helge Mueller-Fielitz
Thibaud Lebouvier
Romain Perbet
Vincent Florent
Marc Baroncini
Ariane Sharif
June Ereño-Orbea
Maria Mercado-Gómez
Asis Palazon
Virginie Mattot
Florence Pasquier
Sophie Catteau-Jonard
Maria Martinez-Chantar
Erik Hrabovszky
Mercé Jourdain
Dominique Deplanque
Annamaria Morelli
Giulia Guarnieri
Laurent Storme
Cyril Robil
François Trottein
Ruben Nogueiras
Markus Schwaninger
Pascal Pigny
Julien Poissy
Konstantina Chachlaki
Claude-Alain Maurage
Paolo Giacobini
Waljit Dhillo
S. Rasika
Vincent Prevot
Source :
EBioMedicine, Vol 96, Iss , Pp 104784- (2023)
Publication Year :
2023
Publisher :
Elsevier, 2023.

Abstract

Summary: Background: We have recently demonstrated a causal link between loss of gonadotropin-releasing hormone (GnRH), the master molecule regulating reproduction, and cognitive deficits during pathological aging, including Down syndrome and Alzheimer's disease. Olfactory and cognitive alterations, which persist in some COVID-19 patients, and long-term hypotestosteronaemia in SARS-CoV-2-infected men are also reminiscent of the consequences of deficient GnRH, suggesting that GnRH system neuroinvasion could underlie certain post-COVID symptoms and thus lead to accelerated or exacerbated cognitive decline. Methods: We explored the hormonal profile of COVID-19 patients and targets of SARS-CoV-2 infection in post-mortem patient brains and human fetal tissue. Findings: We found that persistent hypotestosteronaemia in some men could indeed be of hypothalamic origin, favouring post-COVID cognitive or neurological symptoms, and that changes in testosterone levels and body weight over time were inversely correlated. Infection of olfactory sensory neurons and multifunctional hypothalamic glia called tanycytes highlighted at least two viable neuroinvasion routes. Furthermore, GnRH neurons themselves were dying in all patient brains studied, dramatically reducing GnRH expression. Human fetal olfactory and vomeronasal epithelia, from which GnRH neurons arise, and fetal GnRH neurons also appeared susceptible to infection. Interpretation: Putative GnRH neuron and tanycyte dysfunction following SARS-CoV-2 neuroinvasion could be responsible for serious reproductive, metabolic, and mental health consequences in long-COVID and lead to an increased risk of neurodevelopmental and neurodegenerative pathologies over time in all age groups. Funding: European Research Council (ERC) grant agreements No 810331, No 725149, No 804236, the European Union Horizon 2020 research and innovation program No 847941, the Fondation pour la Recherche Médicale (FRM) and the Agence Nationale de la Recherche en Santé (ANRS) No ECTZ200878 Long Covid 2021 ANRS0167 SIGNAL, Agence Nationale de la recherche (ANR) grant agreements No ANR-19-CE16-0021-02, No ANR-11-LABEX-0009, No. ANR-10-LABEX-0046, No. ANR-16-IDEX-0004, Inserm Cross-Cutting Scientific Program HuDeCA, the CHU Lille Bonus H, the UK Medical Research Council (MRC) and National Institute of Health and care Research (NIHR).

Details

Language :
English
ISSN :
23523964
Volume :
96
Issue :
104784-
Database :
Directory of Open Access Journals
Journal :
EBioMedicine
Publication Type :
Academic Journal
Accession number :
edsdoj.805ae189cc654b398588ba98e00a06f8
Document Type :
article
Full Text :
https://doi.org/10.1016/j.ebiom.2023.104784