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

Author:

El-Sayed Moustafa Julia S.ORCID,Jackson Anne U.,Brotman Sarah M.,Guan Li,Villicaña Sergio,Roberts Amy L.,Zito Antonino,Bonnycastle Lori,Erdos Michael R.,Narisu Narisu,Stringham Heather M.,Welch Ryan,Yan Tingfen,Lakka Timo,Parker Stephen,Tuomilehto Jaakko,Collins Francis S.,Pajukanta Päivi,Boehnke Michael,Koistinen Heikki A.,Laakso Markku,Falchi Mario,Bell Jordana T.,Scott Laura J.,Mohlke Karen L.,Small Kerrin S.

Abstract

AbstractCOVID-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<5.32×10-4). 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=4.25×10-4) and higher macrophage proportion (P=2.74×10-5), 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.

Publisher

Cold Spring Harbor Laboratory

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