key: cord-0716903-xygwss7m
authors: Gill, Dipender; Arvanitis, Marios; Carter, Paul; Hernández Cordero, Ana I.; Jo, Brian; Karhunen, Ville; Larsson, Susanna C.; Li, Xuan; Lockhart, Sam M.; Mason, Amy; Pashos, Evanthia; Saha, Ashis; Tan, Vanessa Y.; Zuber, Verena; Bossé, Yohan; Fahle, Sarah; Hao, Ke; Jiang, Tao; Joubert, Philippe; Lunt, Alan C.; Ouwehand, Willem Hendrik; Roberts, David J.; Timens, Wim; van den Berge, Maarten; Watkins, Nicholas A.; Battle, Alexis; Butterworth, Adam S.; Danesh, John; Di Angelantonio, Emanuele; Engelhardt, Barbara E.; Peters, James E.; Sin, Don D.; Burgess, Stephen
title: ACE inhibition and cardiometabolic risk factors, lung ACE2 and TMPRSS2 gene expression, and plasma ACE2 levels: a Mendelian randomization study
date: 2020-11-18
journal: R Soc Open Sci
DOI: 10.1098/rsos.200958
sha: ab89aeb78af4a888bf042a7f716528861aa3a94a
doc_id: 716903
cord_uid: xygwss7m

Angiotensin-converting enzyme 2 (ACE2) and serine protease TMPRSS2 have been implicated in cell entry for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus responsible for coronavirus disease 2019 (COVID-19). The expression of ACE2 and TMPRSS2 in the lung epithelium might have implications for the risk of SARS-CoV-2 infection and severity of COVID-19. We use human genetic variants that proxy angiotensin-converting enzyme (ACE) inhibitor drug effects and cardiovascular risk factors to investigate whether these exposures affect lung ACE2 and TMPRSS2 gene expression and circulating ACE2 levels. We observed no consistent evidence of an association of genetically predicted serum ACE levels with any of our outcomes. There was weak evidence for an association of genetically predicted serum ACE levels with ACE2 gene expression in the Lung eQTL Consortium (p = 0.014), but this finding did not replicate. There was evidence of a positive association of genetic liability to type 2 diabetes mellitus with lung ACE2 gene expression in the Gene-Tissue Expression (GTEx) study (p = 4 × 10(−4)) and with circulating plasma ACE2 levels in the INTERVAL study (p = 0.03), but not with lung ACE2 expression in the Lung eQTL Consortium study (p = 0.68). There were no associations of genetically proxied liability to the other cardiometabolic traits with any outcome. This study does not provide consistent evidence to support an effect of serum ACE levels (as a proxy for ACE inhibitors) or cardiometabolic risk factors on lung ACE2 and TMPRSS2 expression or plasma ACE2 levels.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for the current coronavirus disease 2019 (COVID-19) pandemic [1] . Serine protease TMPRSS2 is involved in priming the SARS-CoV-2 spike protein for cellular entry through the angiotensin-converting enzyme 2 (ACE2) receptor [2] [3] [4] [5] . COVID-19 patients most frequently present with respiratory tract infection symptoms [6] [7] [8] [9] [10] [11] . It follows that the expression of ACE2 and TMPRSS2 in the lung epithelium might have implications for the risk of SARS-CoV-2 infection and severity of COVID-19 [2, 12, 13] .

Emerging evidence suggests that patients with underlying cardiometabolic risk factors and airway disease are more likely to suffer from severe COVID-19 [6] [7] [8] [9] [10] [11] . It has been speculated that the angiotensinconverting enzyme inhibitor (ACEi) and angiotensin receptor blocker (ARB) classes of antihypertensive medication that are more commonly prescribed in patients with cardiometabolic risk factors might affect royalsocietypublishing.org/journal/rsos R. Soc. Open Sci. 7: 200958 the expression of ACE2 and thus affect susceptibility to SARS-CoV-2 infection and severity of consequent COVID-19 [14] [15] [16] [17] [18] [19] [20] . Although ACE and ACE2 are both dipeptidyl carboxydipeptidases, they have distinct physiological effects. ACE cleaves angiotensin I to angiotensin II, which consequently activates the angiotensin II receptor type 1 pathway resulting in vasoconstriction and inflammation. By contrast, ACE2 degrades angiotensin II to angiotensin 1-7 and angiotensin I to angiotensin 1-9. Angiotensin 1-9 activates the Mas receptor to have vasodilatory and anti-inflammatory effects. Animal studies have supported effects of ACEi and ARB drugs on ACE2 expression and activity [21] [22] [23] [24] [25] [26] [27] [28] , with mixed findings for associations of ACEi and ARB drug use with ACE2 activity and levels in human tissues also reported [29] [30] [31] . It is important that any causal effects of these medications and cardiometabolic traits on ACE2 expression be further investigated. Identification of a mechanistic basis by which such exposures affect the risk and severity of COVID-19 could provide useful insight for disease prevention and treatment. This could be used to inform optimal medication use and strategies for shielding vulnerable individuals, as well as improving the evidence base for public health campaigns.

The Mendelian randomization approach uses genetic variants related to exposure as instrumental variables for investigating the effect of that exposure on an outcome [32] . Genetic variants are treated analogously to treatment allocation in a randomized controlled trial. Typically, molecular measurements such as gene expression or circulating protein levels are regarded in Mendelian randomization investigations as exposure variables. Here, following the work of Rao et al. [33] , we treat these molecular measurements as the outcomes in our investigation. The aim of this study was to apply Mendelian randomization to investigate whether ACE2 and TMPRSS2 gene expression in the lung and circulating levels of ACE2 in the plasma are associated with (i) genetic variants in the ACE gene region that can be considered as proxies for the effect of ACEi drugs and (ii) genetic variants related to cardiometabolic risk factors. We also use publicly available data on genetic associations with COVID-19 susceptibility to investigate whether genetically predicted serum ACE levels are associated with risk of hospitalization due to COVID-19.

Two different genetic instruments that proxy ACEi drug effects were considered. First, we selected 17 singlenucleotide polymorphisms (SNPs) in the ACE locus that were associated with serum ACE concentration in the Outcome Reduction with Initial Glargine INtervention (ORIGIN) trial and did not have strong pairwise correlation (r 2 < 0.1) [34] . Accounting for correlation, these variants explain 29.0% of the variance in serum ACE concentration, corresponding to an F statistic of 85.4 (INTERVAL), 17.7 (Lung eQTL Consortium) and 8.8 (GTEx). Second, we selected a single SNP, rs4291, located at the ACE locus that was associated with systolic blood pressure (SBP) at p = 9 × 10 −20 in a study of 757 601 European-ancestry individuals [35, 36] . Each blood pressure-lowering allele of this SNP was associated with a 0.28 mmHg reduction in SBP [35] . This variant explains <0.1% of the variance in blood pressure. There were no other SNPs at this locus that were associated with SBP at a genome-wide level of significance ( p < 5 × 10 −8 ) and did not have strong pairwise correlation (r 2 < 0.1) with the index variant [35] . To assess the validity of the serum ACE variants, we assessed their associations with SBP in the UK Biobank study [37] .

We further considered six cardiometabolic traits as exposure variables: body mass index (BMI), chronic obstructive pulmonary disease (COPD), lifetime smoking index, low-density lipoprotein cholesterol (LDL-C), SBP and type 2 diabetes mellitus (T2DM). These traits were chosen as they have been associated with prognosis of COVID-19 [6] [7] [8] [9] [10] [11] . Genetic association estimates for these exposures were obtained from the publicly available genome-wide association study (GWAS) summary data sources listed in table 1. Genetic variants selected as instruments were SNPs associated with the corresponding trait at a genomewide level of statistical significance ( p < 5 × 10 −8 ) and were uncorrelated (r 2 < 0.001). Clumping of correlated variants was performed using the TwoSampleMR package in R [43] .

Genetic associations with the expression of ACE2 and TMPRSS2 in lung tissue were obtained from two sources: (i) the Gene-Tissue Expression (GTEx) project [44] and (ii) the Lung eQTL (expression quantitative trait loci) Consortium [45] . Genetic associations with risk of hospitalization due to COVID-19 were obtained from release 4 (alpha version) of the COVID-19 Host Genomics Initiative [46] . GTEx genetic association estimates were obtained in 515 individuals of predominantly European (85%) ancestry. RNA sequencing was performed using the Illumina TruSeqTM RNA sample preparation protocol, and gene-level expression quantification was performed using RNA-SeQC for gene-level read counts and transcripts per million values [47] . Whole-genome sequencing was performed by the Broad Institute's Genomics Platform and only common variants (minor allele frequency >0.05) were retained. Genomewide eQTL analysis was performed for the expression of ACE2 and TMPRSS2 in primary tissue samples taken from the lung. Genetic associations with imputed variants across the autosomal chromosomes were adjusted for five principal components from the genotype data, 60 probabilistic estimations of expression residuals factors [48] , sequencing platform (Illumina HiSeq 2000 or HiSeq X), sequencing protocol (polymerase chain reaction-based or free) and sex. For each gene, expression values between samples were normalized using the trimmed means of M-values method in EdgeR [49] . Expression values were normalized across samples using an inverse-normal transformation.

Lung eQTL Consortium genetic association estimates were obtained in 1038 individuals of European ancestry [45] . Tissue samples were obtained at three different institutions: University of British Columbia, Laval University and University of Groningen. Genome-wide eQTL analysis was performed for the expression of ACE2 using a probe set 100134205_TGI_at and two probe sets for TMPRSS2, 100130004_TGI_at and 100157336_TGI_at (subsequently referred to as 1 and 2). Expression profiling was performed using an Affymetrix custom array (see Gene Expression Omnibus platform GPL10379) [45] . The probe sets measure different transcripts, and the specific probes for each probe set are detailed in electronic supplementary material, table S1. Expression levels were much higher for the first probe set, and so these results are more reliable. All participants were genotyped using the Illumina Human 1 M Duo BeadChip and the genotypes were imputed using the Haplotype Reference Consortium reference panel. Expression values were first standardized for age, sex and smoking status using robust linear regression. Genetic associations were estimated in each cohort separately using a linear additive genetic model. The estimates were combined across cohorts using an inverse-variance weighted model with fixed effects.

Genetic association estimates with circulating plasma ACE2 levels were obtained in a subcohort of 4998 blood donors enrolled in the INTERVAL BioResource [50] . Plasma ACE2 levels were measured using a multiplex proximity extension immunoassay (Cardiovascular 2 panel, Olink Bioscience, Uppsala, Sweden). A total of 4947 samples passed quality control. The data were pre-processed using standard Olink workflows including applying median centring normalization across plates, where the median is centred to the overall median for all plates, followed by log 2 transformation to provide normalized protein levels (NPX). NPX values were regressed on age, sex, plate, time from blood draw to processing (in days) and season. The residuals were then rank-inverse normalized. Genotype data were processed as described previously [51] . Genome-wide pQTL analysis was performed by linear regression of the rank-inverse normalized residuals on genotype in SNPTEST [52] , with the first three components of multi-dimensional scaling as covariates to adjust for ancestry. Genetic association estimates with hospitalization due to COVID-19 were obtained from version 4 (release alpha) of the COVID-19 Host Genomics Initiative, which included 6492 cases and 1 012 809 controls from the general population from 17 studies, mostly from participants of European ancestries [46] . Association estimates were obtained within each study with adjustment for age, age-squared, sex, at least 20 principal components and technical covariates, and then meta-analysed across studies.

For the analysis investigating genetically proxied ACEi drug effects using the rs4291 variant, we report the genetic associations with lung ACE2 and TMPRSS2 expression, plasma ACE2 levels and risk of COVID-19 hospitalization per blood pressure-lowering allele.

For all other Mendelian randomization analyses, estimates were obtained from the inverse-variance weighted method under a random-effects model [53] . For the polygenic analyses based on the ACE gene locus, we accounted for the correlation between variants using generalized weighted regression [54] . Heterogeneity between Mendelian randomization estimates from different genetic variants for the same exposure trait was expressed using the I 2 statistic [55] . For any identified associations at p < 0.05, the weighted median [56] , MR-Egger [57] and contamination-mixture methods [58] , which are more robust to the inclusion of pleiotropic variants, were performed as sensitivity analyses.

Mendelian randomization estimates represent the change in the outcome per one standard deviation increase in genetically predicted levels of the exposure for continuous exposure traits and per unit increase in the log e odds of the exposure for binary traits. All outcome measures were rank-based inverse-normal transformed, and so changes in the outcome measures are in standard deviation units, with the exception of COVID-19 hospitalization, for which estimates represent odds ratios.

The data used in this work are obtained from published studies that obtained relevant participant consent and ethical approval. All variants used as instruments and their genetic association estimates were selected from publicly available data sources, and are provided in electronic supplementary material, tables S2-S9. GWAS summary data for all the outcomes considered in this study are publicly available at http://dx.doi. [59] . The study protocol and details were not pre-registered.

Results for the analyses investigating genetically proxied ACEi drug effects are displayed in figure 1 . Genetic associations of the variants with serum ACE levels, SBP and the molecular outcome measures are plotted in electronic supplementary material, figure S1. The variants were associated with SBP in the expected direction: 0.22 mmHg (95% confidence interval 0.06 to 0.37, p = 0.006) increase per one standard deviation increase in ACE. There was evidence of an association with ACE2 expression in the Lung eQTL Consortium for the variants associated with serum ACE: -0.087 standard deviation change (95% confidence interval -0.156 to -0.018, p = 0.014) in ACE2 expression per one standard deviation increase in serum ACE. For the other molecular outcome measures, there was no evidence of associations considering the variants associated with serum ACE (figure 1a), or the variant associated with SBP ( figure 1b) . Results were similar in sensitivity analyses restricted to 12 variants associated with serum ACE at a genome-wide level of significance ( p < 5 × 10 −8 ) and for the lead variant (rs4343) only (electronic supplementary material, figure S2 ). There was no evidence of the association between genetically predicted serum ACE and risk of hospitalization due to COVID-19 for the 17 variants (odds ratio 1.02 per standard deviation increase in ACE; 95% confidence interval 0.94 to 1.10) or for the SBP variant (odds ratio 1.05 per blood pressure decreasing allele; 95% confidence interval 0.99 to 1.12).

The main inverse-variance weighted method Mendelian randomization results for the cardiometabolic risk factors are displayed in figure 2 for lung ACE2 expression and plasma ACE2 concentrations, and in figure 3 for lung TMPRSS2 expression. There was evidence of a positive association of genetic liability to T2DM with lung ACE2 gene expression in GTEx ( p = 4 × 10 −4 ) and royalsocietypublishing.org/journal/rsos R. Soc. Open Sci. 7: 200958 with circulating plasma ACE2 levels in INTERVAL ( p = 0.03) (electronic supplementary material, figure  S3 ). Similar point estimates were obtained when performing the weighted median, MR-Egger and contamination-mixture Mendelian randomization sensitivity analyses that are more robust to the presence of pleiotropic variants, although the confidence intervals were wider (electronic supplementary material, table S10). The MR-Egger method did not identify any evidence of directional pleiotropy biasing the analysis (electronic supplementary material, table S10). There was no evidence of an association of genetic liability to T2DM with lung ACE2 gene expression in the Lung eQTL Consortium ( p = 0.68). There was no evidence of an association between genetically predicted levels of any of the other cardiometabolic traits with ACE2 or TMPRSS2 gene expression in GTEx or the Lung eQTL Consortium, or with circulating plasma ACE2 levels in INTERVAL.

In the current COVID-19 pandemic, there is an urgent need to elucidate mechanisms underlying risk and severity of COVID-19, with a view to informing preventative and therapeutic strategies. In this study, we used human genetic variants that proxy ACEi drug effects and cardiometabolic risk factors to provide insight into how these exposures affect lung ACE2 and TMPRSS2 expression and circulating ACE2 levels. We did not find a consistent association of genetically predicted serum ACE levels with lung ACE2 and TMPRSS2 expression or with circulating plasma levels of ACE2. In one dataset, we found evidence that increased serum ACE may lead to decreased expression of ACE2, meaning that ACE inhibition would increase ACE2 expression. However, this finding did not replicate. Additionally, genetically predicted serum ACE levels were not associated with risk of hospitalization due to COVID-19. Previously identified changes in ACE2 expression in human tissues following ACEi treatment may not be applicable to the lung or circulating plasma levels [29, 30] . Our findings support the stance of professional bodies for supporting the continuation of ACEi and ARB antihypertensive drugs in patients with COVID-19 unless there is a clinical justification for stopping [60, 61] . Indeed, appropriate use of these medications is of proven benefit [62, 63] , and their abrupt interruption can also do considerable harm [64, 65] . While there has also been speculation that ACEi and ARB antihypertensive drugs might reduce the severity of COVID-19 [19, [66] [67] [68] , with clinical trials to explore this currently planned [60] , our findings are also consistent with guidance that patients should not start taking these drug classes unless clinically indicated [60] . Our results identified inconsistent support for an effect of liability to T2DM on lung ACE2 expression and plasma ACE2 levels. An association of genetic liability to T2DM with lung ACE2 expression in the GTEx project has previously been described [33] . However, we identified no association of genetic liability to T2DM with lung ACE2 expression in the Lung eQTL Consortium. This discrepancy may be attributable to the different populations considered in the GTEx project and the Lung eQTL Consortium [44, 45] . While the Lung eQTL Consortium considered lung tissue from patients requiring resectional surgery, all samples in the GTEx project were taken from healthy tissue in deceased donors [44, 45] . Taken together, our results do not provide consistent support for an effect of cardiometabolic traits on lung ACE2 or TMPRSS2 expression or plasma ACE2 levels. While the association between cardiometabolic traits and severity of COVID-19 could be attributable to alternative mechanisms [6] [7] [8] [9] [10] [11] , these risk factors can still be used to stratify patients in terms of their vulnerability. Similarly, while our current findings do not support a causal effect of COPD or smoking on lung ACE2 expression, these factors may still be used to inform risk models for severe .

Since the initial submission of this manuscript, further data have become available on genetic associations with susceptibility to COVID-19 [46, 70] . Mendelian randomization analyses have supported the effect of higher BMI and lifetime smoking on increasing susceptibility to severe COVID-19 [71] . The discrepancy with our current findings, which did not identify an association of genetically predicted BMI or smoking with lung ACE2 and TMPRSS2 expression or with circulating plasma levels of ACE2 may be explained by effects of these risk factors on susceptibility to severe COVID-19 through mechanisms unrelated to lung ACE2 or TMPRSS2 gene expression or plasma ACE2 protein expression.

Our study has a number of strengths. We used genetic variants as instrumental variables for studying the effect of ACEi drugs and cardiometabolic risk factors and were therefore able to investigate their causal effects on ACE2 and TMPRSS2 expression in the lung, and ACE levels in the plasma [32] . For ACEi drugs effects, we used two complementary instrument selection strategies based on associations of variants at the ACE locus with circulating serum ACE levels and SBP, respectively, and the consistent findings with both approaches add strength to our conclusions. Our Mendelian randomization approach is better able to overcome the confounding and reverse causation bias that can limit causal inferences from conventional epidemiological approaches [29, 72] . Considering independent cohorts to assess lung expression of ACE2 and TMPRSS2 [44, 45] , and plasma levels of ACE2 [51] , we were able to explore consistency in our results, and our conclusions are therefore less vulnerable to false-positive findings.

Our study also has limitations. We only investigated ACE2 and TMPRSS2 expression in the lung and circulating levels of ACE2 in the plasma, and it may be that expression in other tissues is more relevant to the risk and severity of COVID-19. Similarly, cellular ACE2 may have very different biological effects to circulating plasma ACE2. The GWAS analyses for lung ACE2 expression and plasma ACE2 levels were all performed according to different protocols [44, 45, 51] and may therefore not be directly comparable. There was no available genetic instrument for the ARB antihypertensive drug class [35] , and so we were not able to investigate this. The precision of our analyses was also limited, most notably for the lifetime smoking index results, which had widest confidence intervals. It may therefore be that our study was not sufficiently powered to exclude a clinically relevant effect for some exposures. The genetic variants that we used as instrumental variables may have pleiotropic effects where they affect the outcome through pathways independent of the exposure that they are proxying, and so bias the consequent Mendelian randomization estimates. While it is not possible to exclude this possibility, the relatively low heterogeneity detected between Mendelian randomization estimates produced by different variants, along with the consistency observed when performing analysis methods that are more robust to pleiotropy, suggests that this is unlikely to be a major source of bias [55] . A further reservation is the sample size available for genetic associations with the outcome measures, leading to limited power to detect a causal effect, particularly for the molecular outcomes. Finally, this study was not able to investigate off-target effects of ACE inhibitors that are unrelated to their intended protein target.

In summary, this Mendelian randomization study does not identify consistent evidence to support that ACEi antihypertensive drugs or cardiometabolic traits affect lung expression of ACE2 and TMPRSS2, or plasma ACE2 levels. These findings therefore do not support a deviation from existing royalsocietypublishing.org/journal/rsos R. Soc. Open Sci. 7: 200958 expert consensus guidelines for the management of hypertension in the face of the current COVID-19 pandemic [60] . Efforts should be made by scientists and the news media to ensure that speculative stories with little evidential support are not propagated [73] . While cardiometabolic risk factors can be used to stratify patients in terms of their vulnerability to COVID-19, our data do not provide consistent support that the expression of ACE2 or TMPRSS2 represents causal mechanisms underlying these associations.

Ethics. The data used in this work are obtained from published studies that obtained relevant participant consent and ethical approval.

Data accessibility. All variants used as instruments and their genetic association estimates were selected from publicly available data sources and are provided in electronic supplementary material, Tables S1-S8. GWAS summary data for all the outcomes considered in this study are publicly available at http://dx.doi.org/10.6084/m9.figshare. 12102681 (GTEx), http://dx.doi.org/10.6084/m9.figshare.12102711 (Lung eQTL Consortium), and http://dx.doi. org/10.6084/m9.figshare.12102777 (INTERVAL). The results from the analyses performed in this work are presented in the main manuscript or its supplementary files.

A novel coronavirus from patients with pneumonia in China

SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor

Structural basis for the recognition of SARS-CoV-2 by full-length human ACE2

Structural basis of receptor recognition by SARS-CoV-2

Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor

Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study

Clinical characteristics of coronavirus disease 2019 in China

Covid-19 in critically ill patients in the Seattle region-case series

Epidemiologic features and clinical course of patients infected with SARS-CoV-2 in Singapore

Prevalence of comorbidities in the novel Wuhan coronavirus (COVID-19) infection: a systematic review and metaanalysis

Clinical predictors of mortality due to COVID-19 based on an analysis of data of 150 patients from Wuhan, China

A crucial role of angiotensin converting enzyme 2 (ACE2) in SARS coronavirus-induced lung injury

Tissue distribution of ACE2 protein, the functional receptor for SARS coronavirus: a first step in understanding SARS pathogenesis

Are patients with hypertension and diabetes mellitus at increased risk for COVID-19 infection?

Rapid response: re: preventing a Covid-19 pandemic: ACE inhibitors as a potential risk factor for fatal Covid-19

COVID-19): do angiotensin-converting enzyme inhibitors/ angiotensin receptor blockers have a biphasic effect?

2020 Can angiotensin receptorblocking drugs perhaps be harmful in the COVID-19 pandemic?

Hypothesis: angiotensinconverting enzyme inhibitors and angiotensin receptor blockers may increase the risk of severe COVID-19

Angiotensin receptor blockers as tentative SARS-CoV-2 therapeutics

SARS-CoV2: should inhibitors of the reninangiotensin system be withdrawn in patients with COVID-19?

Perinatally administered losartan augments renal ACE2 expression but not cardiac or renal Mas receptor in spontaneously hypertensive rats

Effect of angiotensin-converting enzyme inhibition and angiotensin II receptor blockers on cardiac angiotensin-converting enzyme 2

Enalapril attenuates downregulation of angiotensin-converting enzyme 2 in the late phase of ventricular dysfunction in myocardial infarcted rat

Localization of ACE2 in the renal vasculature: amplification by angiotensin II type 1 receptor blockade using telmisartan

Azilsartan ameliorates diabetic cardiomyopathy in young db/db mice through the modulation of ACE-2/ANG 1-7/Mas receptor cascade

Olmesartan medoxomil treatment potently improves cardiac myosin-induced dilated cardiomyopathy via the modulation of ACE-2 and ANG 1-7 mas receptor

Cardioprotective effects of telmisartan against heart failure in rats induced by experimental autoimmune myocarditis through the modulation of angiotensin-converting enzyme-2/angiotensin 1-7/Mas receptor axis

Telmisartan attenuates aortic hypertrophy in hypertensive rats by the modulation of ACE2 and profilin-1 expression. royalsocietypublishing.org/journal

Circulating ACE2 activity is increased in patients with type 1 diabetes and vascular complications

Human intestine luminal ACE2 and amino acid transporter expression increased by ACE-inhibitors

Urinary angiotensinconverting enzyme 2 in hypertensive patients may be increased by olmesartan, an angiotensin II receptor blocker

Use of Mendelian randomisation to assess potential benefit of clinical intervention

Exploring diseases/ traits and blood proteins causally related to expression of ACE2, the putative receptor of 2019-nCov: a Mendelian randomization analysis

2020 ACE and type 2 diabetes risk: a mendelian randomization study

Use of genetic variants related to antihypertensive drugs to inform on efficacy and side effects

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Understanding the consequences of education inequality on cardiovascular disease: Mendelian randomisation study

Meta-analysis of genomewide association studies for body fat distribution in 694 649 individuals of European ancestry

Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations

Evidence for causal effects of lifetime smoking on risk for depression and schizophrenia: a Mendelian randomisation study

Discovery and refinement of loci associated with lipid levels

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

The MR-Base platform supports systematic causal inference across the human phenome

Enhancing GTEx Groups, NIH Common Fund BCSSN, Biospecimen Collection Source Site RPCI et al. 2017 Genetic effects on gene expression across human tissues

Lung eQTLs to help reveal the molecular underpinnings of asthma

The COVID-19 host genetics initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic

The GTEx Consortium atlas of genetic regulatory effects across human tissues

Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses

A scaling normalization method for differential expression analysis of RNA-seq data

Efficiency and safety of varying the frequency of whole blood donation (INTERVAL): a randomised trial of 45 000 donors

Genomic atlas of the human plasma proteome

Genotype imputation for genome-wide association studies

Mendelian randomization analysis with multiple genetic variants using summarized data

Combining information on multiple instrumental variables in Mendelian randomization: comparison of allele score and summarized data methods

Detecting pleiotropy in Mendelian randomisation studies with summary data and a continuous outcome

Consistent estimation in Mendelian randomization with some invalid instruments using a weighted median estimator

Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression

2020 A robust and efficient method for Mendelian randomization with hundreds of genetic variants

STROBE-MR: guidelines for strengthening the reporting of Mendelian randomization studies

COVID-19) infection and renin angiotensin system blockers

Renin-angiotensin-aldosterone system inhibitors in patients with Covid-19

Outcomes in hypertensive patients at high cardiovascular risk treated with regimens based on valsartan or amlodipine: the VALUE randomised trial

Indications for ACE inhibitors in the early treatment of acute myocardial infarction: systematic overview of individual data from 100,000 patients in randomized trials

Withdrawal of pharmacological treatment for heart failure in patients with recovered dilated cardiomyopathy (TRED-HF): an open-label, pilot, randomised trial

Clinical consequences of angiotensin-converting enzyme inhibitor withdrawal in chronic heart failure: a doubleblind, placebo-controlled study of quinapril

2020 Coronavirus disease 2019 (COVID-19) and cardiovascular disease: a viewpoint on the potential influence of angiotensin-converting enzyme inhibitors/ angiotensin receptor blockers on onset and severity of severe acute respiratory syndrome coronavirus 2 infection

Renin-angiotensin system inhibitors improve the clinical outcomes of COVID-19 patients with hypertension

inhibitors usage is associated with improved inflammatory status and clinical outcomes in COVID-19 patients with hypertension

2020 ACE-2 expression in the small airway epithelia of smokers and COPD patients: implications for COVID-19

Genomewide association study of severe Covid-19 with respiratory failure

Cardiometabolic traits, sepsis and severe COVID-19: a Mendelian randomization investigation

2020 ACE2 expression is increased in the lungs of patients with comorbidities associated with severe COVID-19

Negative statin-related news stories decrease statin persistence and increase myocardial infarction and cardiovascular mortality: a nationwide prospective cohort study