Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19

Abstract Background Male androgenetic alopecia (AGA) has been implicated as a putative risk factor in severe COVID‐19 based on high incidences of advanced AGA in male hospitalized COVID‐19 patients. Research further suggests that androgen signalling, which plays a central role in AGA aetiology, prom...

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Autores principales: S. K. Henne, L. M. Hochfeld, C. Maj, M. M. Nöthen, S. Heilmann‐Heimbach
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Lenguaje:EN
Publicado: Wiley 2021
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Acceso en línea:https://doaj.org/article/9ba309e23df34bfd82ab692ff2e7e251
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spelling oai:doaj.org-article:9ba309e23df34bfd82ab692ff2e7e2512021-12-02T11:13:08ZSystematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐192690-442X10.1002/ski2.72https://doaj.org/article/9ba309e23df34bfd82ab692ff2e7e2512021-12-01T00:00:00Zhttps://doi.org/10.1002/ski2.72https://doaj.org/toc/2690-442XAbstract Background Male androgenetic alopecia (AGA) has been implicated as a putative risk factor in severe COVID‐19 based on high incidences of advanced AGA in male hospitalized COVID‐19 patients. Research further suggests that androgen signalling, which plays a central role in AGA aetiology, promotes SARS‐CoV‐2 infection and is associated with severe COVID‐19 symptoms in men. Objectives We aimed to systematically investigate a potential association between AGA and COVID‐19 both on an epidemiological and a genetic level in a large single‐population cohort. Methods We performed regression, genetic correlation and polygenic risk score (PRS) analyses using data from the UK Biobank and published GWAS data on AGA and COVID‐19. Results Our analyses did not reveal any significant epidemiological or genome‐wide genetic association between AGA and severe COVID‐19. Pathway‐based PRS analyses however revealed a significant association in specific pathways, namely vitamin metabolism, natural killer cell‐mediated cytotoxicity, WNT signalling and aryl hydrocarbon receptor signalling. Limitations We restricted our analyses to the white British population and used self‐reported AGA status. Sample size may be a limitation in our regression and PRS analyses. Conclusions Our data yield no evidence for an epidemiological association between AGA and COVID‐19 but suggest that a shared genetic basis for both traits exists in specific pathways.S. K. HenneL. M. HochfeldC. MajM. M. NöthenS. Heilmann‐HeimbachWileyarticleDermatologyRL1-803ENSkin Health and Disease, Vol 1, Iss 4, Pp n/a-n/a (2021)
institution DOAJ
collection DOAJ
language EN
topic Dermatology
RL1-803
spellingShingle Dermatology
RL1-803
S. K. Henne
L. M. Hochfeld
C. Maj
M. M. Nöthen
S. Heilmann‐Heimbach
Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
description Abstract Background Male androgenetic alopecia (AGA) has been implicated as a putative risk factor in severe COVID‐19 based on high incidences of advanced AGA in male hospitalized COVID‐19 patients. Research further suggests that androgen signalling, which plays a central role in AGA aetiology, promotes SARS‐CoV‐2 infection and is associated with severe COVID‐19 symptoms in men. Objectives We aimed to systematically investigate a potential association between AGA and COVID‐19 both on an epidemiological and a genetic level in a large single‐population cohort. Methods We performed regression, genetic correlation and polygenic risk score (PRS) analyses using data from the UK Biobank and published GWAS data on AGA and COVID‐19. Results Our analyses did not reveal any significant epidemiological or genome‐wide genetic association between AGA and severe COVID‐19. Pathway‐based PRS analyses however revealed a significant association in specific pathways, namely vitamin metabolism, natural killer cell‐mediated cytotoxicity, WNT signalling and aryl hydrocarbon receptor signalling. Limitations We restricted our analyses to the white British population and used self‐reported AGA status. Sample size may be a limitation in our regression and PRS analyses. Conclusions Our data yield no evidence for an epidemiological association between AGA and COVID‐19 but suggest that a shared genetic basis for both traits exists in specific pathways.
format article
author S. K. Henne
L. M. Hochfeld
C. Maj
M. M. Nöthen
S. Heilmann‐Heimbach
author_facet S. K. Henne
L. M. Hochfeld
C. Maj
M. M. Nöthen
S. Heilmann‐Heimbach
author_sort S. K. Henne
title Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
title_short Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
title_full Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
title_fullStr Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
title_full_unstemmed Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
title_sort systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and covid‐19
publisher Wiley
publishDate 2021
url https://doaj.org/article/9ba309e23df34bfd82ab692ff2e7e251
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