Testosterone in males with COVID-19: A 7-month cohort study.


Journal

Andrology
ISSN: 2047-2927
Titre abrégé: Andrology
Pays: England
ID NLM: 101585129

Informations de publication

Date de publication:
01 2022
Historique:
revised: 03 08 2021
received: 21 06 2021
accepted: 04 08 2021
pubmed: 20 8 2021
medline: 7 1 2022
entrez: 19 8 2021
Statut: ppublish

Résumé

Circulating testosterone levels have been found to be reduced in men with severe acute respiratory syndrome coronavirus 2 infection, COVID-19, with lower levels being associated with more severe clinical outcomes. We aimed to assess total testosterone levels and the prevalence of total testosterone still suggesting for hypogonadism at 7-month follow-up in a cohort of 121 men who recovered from laboratory-confirmed COVID-19. Demographic, clinical, and hormonal values were collected for all patients. Hypogonadism was defined as total testosterone ≤9.2 nmol/L. The Charlson Comorbidity Index was used to score health-significant comorbidities. Descriptive statistics and multivariable linear and logistic regression models tested the association between clinical and laboratory variables and total testosterone levels at follow-up assessment. Circulating total testosterone levels increased at 7-month follow-up compared to hospital admittance (p < 0.0001), while luteinizing hormone and 17β-estradiol levels significantly decreased (all p ≤ 0.02). Overall, total testosterone levels increased in 106 (87.6%) patients, but further decreased in 12 (9.9%) patients at follow-up, where a total testosterone level suggestive for hypogonadism was still observed in 66 (55%) patients. Baseline Charlson Comorbidity Index score (OR 0.36; p = 0.03 [0.14, 0.89]) was independently associated with total testosterone levels at 7-month follow-up, after adjusting for age, BMI, and IL-6 at hospital admittance. Although total testosterone levels increased over time after COVID-19, more than 50% of men who recovered from the disease still had circulating testosterone levels suggestive for a condition of hypogonadism at 7-month follow-up. In as many as 10% of cases, testosterone levels even further decreased. Of clinical relevance, the higher the burden of comorbid conditions at presentation, the lower the probability of testosterone levels recovery over time.

Sections du résumé

BACKGROUND
Circulating testosterone levels have been found to be reduced in men with severe acute respiratory syndrome coronavirus 2 infection, COVID-19, with lower levels being associated with more severe clinical outcomes.
OBJECTIVES
We aimed to assess total testosterone levels and the prevalence of total testosterone still suggesting for hypogonadism at 7-month follow-up in a cohort of 121 men who recovered from laboratory-confirmed COVID-19.
MATERIALS AND METHODS
Demographic, clinical, and hormonal values were collected for all patients. Hypogonadism was defined as total testosterone ≤9.2 nmol/L. The Charlson Comorbidity Index was used to score health-significant comorbidities. Descriptive statistics and multivariable linear and logistic regression models tested the association between clinical and laboratory variables and total testosterone levels at follow-up assessment.
RESULTS
Circulating total testosterone levels increased at 7-month follow-up compared to hospital admittance (p < 0.0001), while luteinizing hormone and 17β-estradiol levels significantly decreased (all p ≤ 0.02). Overall, total testosterone levels increased in 106 (87.6%) patients, but further decreased in 12 (9.9%) patients at follow-up, where a total testosterone level suggestive for hypogonadism was still observed in 66 (55%) patients. Baseline Charlson Comorbidity Index score (OR 0.36; p = 0.03 [0.14, 0.89]) was independently associated with total testosterone levels at 7-month follow-up, after adjusting for age, BMI, and IL-6 at hospital admittance.
CONCLUSIONS
Although total testosterone levels increased over time after COVID-19, more than 50% of men who recovered from the disease still had circulating testosterone levels suggestive for a condition of hypogonadism at 7-month follow-up. In as many as 10% of cases, testosterone levels even further decreased. Of clinical relevance, the higher the burden of comorbid conditions at presentation, the lower the probability of testosterone levels recovery over time.

Identifiants

pubmed: 34409772
doi: 10.1111/andr.13097
pmc: PMC8444879
doi:

Substances chimiques

Testosterone 3XMK78S47O

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

34-41

Subventions

Organisme : Gruppo Prada
Organisme : DiaSorin SpA

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 American Society of Andrology and European Academy of Andrology.

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Auteurs

Andrea Salonia (A)

Division of Experimental Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.
University Vita-Salute San Raffaele, Milan, Italy.

Marina Pontillo (M)

Laboratory Medicine Service, IRCCS Ospedale San Raffaele, Milan, Italy.

Paolo Capogrosso (P)

Division of Experimental Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.
Department of Urology and Andrology, Ospedale di Circolo and Macchi Foundation, Varese, Italy.

Silvia Gregori (S)

San Raffaele Telethon Institute for Gene Therapy (SR-TIGET), IRCCS Ospedale San Raffaele, Milan, Italy.

Cristina Carenzi (C)

Division of Experimental Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.

Anna Maria Ferrara (AM)

Division of Experimental Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.

Isaline Rowe (I)

Division of Experimental Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.

Luca Boeri (L)

Division of Experimental Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.
IRCCS Foundation Ca' Granda, Maggiore Policlinico Hospital, Department of Urology, University of Milan, Milan, Italy.

Alessandro Larcher (A)

Division of Experimental Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.

Giuseppe A Ramirez (GA)

University Vita-Salute San Raffaele, Milan, Italy.
Immunology, Rheumatology, Allergology and Rare Diseases Unit, IRCCS Ospedale San Raffaele, Milan, Italy.

Cristina Tresoldi (C)

Molecular Hematology Unit, IRCCS Ospedale San Raffaele, Milan, Italy.

Massimo Locatelli (M)

Laboratory Medicine Service, IRCCS Ospedale San Raffaele, Milan, Italy.

Giulio Cavalli (G)

University Vita-Salute San Raffaele, Milan, Italy.
Immunology, Rheumatology, Allergology and Rare Diseases Unit, IRCCS Ospedale San Raffaele, Milan, Italy.

Lorenzo Dagna (L)

University Vita-Salute San Raffaele, Milan, Italy.
Immunology, Rheumatology, Allergology and Rare Diseases Unit, IRCCS Ospedale San Raffaele, Milan, Italy.

Antonella Castagna (A)

University Vita-Salute San Raffaele, Milan, Italy.
Department of Infectious Diseases, IRCCS Ospedale San Raffaele, Milan, Italy.

Alberto Zangrillo (A)

University Vita-Salute San Raffaele, Milan, Italy.
Anesthesia and Intensive Care Department, IRCCS Ospedale San Raffaele, Milan, Italy.

Moreno Tresoldi (M)

General Medicine and Advanced Care Unit, IRCCS Ospedale San Raffaele, Milan, Italy.

Giovanni Landoni (G)

University Vita-Salute San Raffaele, Milan, Italy.
Anesthesia and Intensive Care Department, IRCCS Ospedale San Raffaele, Milan, Italy.

Patrizia Rovere-Querini (P)

University Vita-Salute San Raffaele, Milan, Italy.
Internal Medicine, Diabetes, and Endocrinology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Fabio Ciceri (F)

University Vita-Salute San Raffaele, Milan, Italy.
Hematology and Bone Marrow Transplant Unit, IRCCS Ospedale San Raffaele, Milan, Italy.

Francesco Montorsi (F)

Division of Experimental Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.
University Vita-Salute San Raffaele, Milan, Italy.

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