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ACE2 expression in adipose tissue is associated with COVID-19 cardio-metabolic risk factors and cell type composition.

Authors :
El-Sayed Moustafa JS
Jackson AU
Brotman SM
Guan L
VillicaƱa S
Roberts AL
Zito A
Bonnycastle L
Erdos MR
Narisu N
Stringham HM
Welch R
Yan T
Lakka T
Parker S
Tuomilehto J
Collins FS
Pajukanta P
Boehnke M
Koistinen HA
Laakso M
Falchi M
Bell JT
Scott LJ
Mohlke KL
Small KS
Source :
MedRxiv : the preprint server for health sciences [medRxiv] 2020 Aug 14. Date of Electronic Publication: 2020 Aug 14.
Publication Year :
2020

Abstract

COVID-19 severity has varied widely, with demographic and cardio-metabolic factors increasing risk of severe reactions to SARS-CoV-2 infection, but the underlying mechanisms for this remain uncertain. We investigated phenotypic and genetic factors associated with subcutaneous adipose tissue expression of Angiotensin I Converting Enzyme 2 ( ACE2 ), which has been shown to act as a receptor for SARS-CoV-2 cellular entry. In a meta-analysis of three independent studies including up to 1,471 participants, lower adipose tissue ACE2 expression was associated with adverse cardio-metabolic health indices including type 2 diabetes (T2D) and obesity status, higher serum fasting insulin and BMI, and lower serum HDL levels (P<5.32x10 <superscript>-4</superscript> ). ACE2 expression levels were also associated with estimated proportions of cell types in adipose tissue; lower ACE2 expression was associated with a lower proportion of microvascular endothelial cells (P=4.25x10 <superscript>-4</superscript> ) and higher macrophage proportion (P=2.74x10 <superscript>-5</superscript> ), suggesting a link to inflammation. Despite an estimated heritability of 32%, we did not identify any proximal or distal genetic variants (eQTLs) associated with adipose tissue ACE2 expression. Our results demonstrate that at-risk individuals have lower background ACE2 levels in this highly relevant tissue. Further studies will be required to establish how this may contribute to increased COVID-19 severity.

Details

Language :
English
Database :
MEDLINE
Journal :
MedRxiv : the preprint server for health sciences
Accession number :
32817962
Full Text :
https://doi.org/10.1101/2020.08.11.20171108