COVID-19-related Genes in Sputum Cells in Asthma. Relationship to Demographic Features and Corticosteroids
Rationale: Coronavirus disease (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). ACE2 (angiotensin-converting enzyme 2), and TMPRSS2 (transmembrane protease serine 2) mediate viral infection of host cells. We reasoned that differences in ACE2 or TMPRSS2 gene expression in sputum cells among patients with asthma may identify subgroups at risk for COVID-19 morbidity.Objectives: To determine the relationship between demographic features and sputum ACE2 and TMPRSS2 gene expression in asthma.Methods: We analyzed gene expression for ACE2 and TMPRSS2, and for ICAM-1 (intercellular adhesion molecule 1) (rhinovirus receptor as a comparator) in sputum cells from 330 participants in SARP-3 (Severe Asthma Research Program-3) and 79 healthy control subjects.Measurements and Main Results: Gene expression of ACE2 was lower than TMPRSS2, and expression levels of both genes were similar in asthma and health. Among patients with asthma, male sex, African American race, and history of diabetes mellitus were associated with higher expression of ACE2 and TMPRSS2. Use of inhaled corticosteroids (ICS) was associated with lower expression of ACE2 and TMPRSS2, but treatment with triamcinolone acetonide did not decrease expression of either gene. These findings differed from those for ICAM-1, where gene expression was increased in asthma and less consistent differences were observed related to sex, race, and use of ICS.Conclusions: Higher expression of ACE2 and TMPRSS2 in males, African Americans, and patients with diabetes mellitus provides rationale for monitoring these asthma subgroups for poor COVID-19 outcomes. The lower expression of ACE2 and TMPRSS2 with ICS use warrants prospective study of ICS use as a predictor of decreased susceptibility to SARS-CoV-2 infection and decreased COVID-19 morbidity.
Errataetall: |
CommentIn: Am J Respir Crit Care Med. 2020 Jul 1;202(1):8-10. - PMID 32437628 |
---|---|
Medienart: |
E-Artikel |
Erscheinungsjahr: |
2020 |
---|---|
Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:202 |
---|---|
Enthalten in: |
American journal of respiratory and critical care medicine - 202(2020), 1 vom: 01. Juli, Seite 83-90 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Peters, Michael C [VerfasserIn] |
---|
Links: |
---|
Themen: |
ACE2 |
---|
Anmerkungen: |
Date Completed 08.07.2020 Date Revised 14.02.2024 published: Print CommentIn: Am J Respir Crit Care Med. 2020 Jul 1;202(1):8-10. - PMID 32437628 Citation Status MEDLINE |
---|
doi: |
10.1164/rccm.202003-0821OC |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM309325250 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM309325250 | ||
003 | DE-627 | ||
005 | 20240214232212.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2020 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1164/rccm.202003-0821OC |2 doi | |
028 | 5 | 2 | |a pubmed24n1292.xml |
035 | |a (DE-627)NLM309325250 | ||
035 | |a (NLM)32348692 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Peters, Michael C |e verfasserin |4 aut | |
245 | 1 | 0 | |a COVID-19-related Genes in Sputum Cells in Asthma. Relationship to Demographic Features and Corticosteroids |
264 | 1 | |c 2020 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 08.07.2020 | ||
500 | |a Date Revised 14.02.2024 | ||
500 | |a published: Print | ||
500 | |a CommentIn: Am J Respir Crit Care Med. 2020 Jul 1;202(1):8-10. - PMID 32437628 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Rationale: Coronavirus disease (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). ACE2 (angiotensin-converting enzyme 2), and TMPRSS2 (transmembrane protease serine 2) mediate viral infection of host cells. We reasoned that differences in ACE2 or TMPRSS2 gene expression in sputum cells among patients with asthma may identify subgroups at risk for COVID-19 morbidity.Objectives: To determine the relationship between demographic features and sputum ACE2 and TMPRSS2 gene expression in asthma.Methods: We analyzed gene expression for ACE2 and TMPRSS2, and for ICAM-1 (intercellular adhesion molecule 1) (rhinovirus receptor as a comparator) in sputum cells from 330 participants in SARP-3 (Severe Asthma Research Program-3) and 79 healthy control subjects.Measurements and Main Results: Gene expression of ACE2 was lower than TMPRSS2, and expression levels of both genes were similar in asthma and health. Among patients with asthma, male sex, African American race, and history of diabetes mellitus were associated with higher expression of ACE2 and TMPRSS2. Use of inhaled corticosteroids (ICS) was associated with lower expression of ACE2 and TMPRSS2, but treatment with triamcinolone acetonide did not decrease expression of either gene. These findings differed from those for ICAM-1, where gene expression was increased in asthma and less consistent differences were observed related to sex, race, and use of ICS.Conclusions: Higher expression of ACE2 and TMPRSS2 in males, African Americans, and patients with diabetes mellitus provides rationale for monitoring these asthma subgroups for poor COVID-19 outcomes. The lower expression of ACE2 and TMPRSS2 with ICS use warrants prospective study of ICS use as a predictor of decreased susceptibility to SARS-CoV-2 infection and decreased COVID-19 morbidity | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 4 | |a ACE2 | |
650 | 4 | |a COVID-19 | |
650 | 4 | |a SARS-CoV-2 | |
650 | 4 | |a TMPRSS2 | |
650 | 4 | |a asthma | |
650 | 7 | |a Adrenal Cortex Hormones |2 NLM | |
700 | 1 | |a Sajuthi, Satria |e verfasserin |4 aut | |
700 | 1 | |a Deford, Peter |e verfasserin |4 aut | |
700 | 1 | |a Christenson, Stephanie |e verfasserin |4 aut | |
700 | 1 | |a Rios, Cydney L |e verfasserin |4 aut | |
700 | 1 | |a Montgomery, Michael T |e verfasserin |4 aut | |
700 | 1 | |a Woodruff, Prescott G |e verfasserin |4 aut | |
700 | 1 | |a Mauger, David T |e verfasserin |4 aut | |
700 | 1 | |a Erzurum, Serpil C |e verfasserin |4 aut | |
700 | 1 | |a Johansson, Mats W |e verfasserin |4 aut | |
700 | 1 | |a Denlinger, Loren C |e verfasserin |4 aut | |
700 | 1 | |a Jarjour, Nizar N |e verfasserin |4 aut | |
700 | 1 | |a Castro, Mario |e verfasserin |4 aut | |
700 | 1 | |a Hastie, Annette T |e verfasserin |4 aut | |
700 | 1 | |a Moore, Wendy |e verfasserin |4 aut | |
700 | 1 | |a Ortega, Victor E |e verfasserin |4 aut | |
700 | 1 | |a Bleecker, Eugene R |e verfasserin |4 aut | |
700 | 1 | |a Wenzel, Sally E |e verfasserin |4 aut | |
700 | 1 | |a Israel, Elliot |e verfasserin |4 aut | |
700 | 1 | |a Levy, Bruce D |e verfasserin |4 aut | |
700 | 1 | |a Seibold, Max A |e verfasserin |4 aut | |
700 | 1 | |a Fahy, John V |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t American journal of respiratory and critical care medicine |d 1994 |g 202(2020), 1 vom: 01. Juli, Seite 83-90 |w (DE-627)NLM074657305 |x 1535-4970 |7 nnns |
773 | 1 | 8 | |g volume:202 |g year:2020 |g number:1 |g day:01 |g month:07 |g pages:83-90 |
856 | 4 | 0 | |u http://dx.doi.org/10.1164/rccm.202003-0821OC |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 202 |j 2020 |e 1 |b 01 |c 07 |h 83-90 |