key: cord-0943396-y9mc9duc
authors: De, Auley; Tiwari, Aparna; Dash, Manoswini; Sinha, Abhinav
title: ACE2 mutation might explain lower COVID-19 burden in malaria endemic areas
date: 2021-01-25
journal: Hum Cell
DOI: 10.1007/s13577-021-00489-0
sha: 3a154e40068b633fdd4f44d119131de298d40877
doc_id: 943396
cord_uid: y9mc9duc

nan

SNPs studied for cardiovascular and related diseases in different ethnicities with a minor allele frequency of > 1%, only one ACE2 SNP (T-allele of rs2106809) has been shown to be negatively associated with severe malaria [4] and positively associated with hypertension through lowered plasma Ang (1-7) level. As Ang (1-7) is mostly derived from Ang II through ACE2, collectively, this indirectly implies that the T-allele of rs2106809 down-regulates the expression of ACE2 [5, 6] . As per the malaria-hypertension hypothesis, the T-allele of rs2106809 might be positively selected in populations that are chronically exposed to malaria and hence increase the likelihood of Ang II-mediated hypertension via downregulating ACE2 [7] . Besides, there are other rs2106809-tagged SNPs, that are under strong linkage disequilibrium with rs2106809 and could have functional significance [5] . Interestingly, ACE2 rs2285666 is one such tagged-SNP that is found to be associated with lower plasma ACE2 level [5] .

We, therefore, rationally speculate that the malariaexposed populations may have a preponderance of compensatory genetic variants (T-allele of rs2106809 and its tagged-SNPs), that protect from severe malaria in childhood, but eventually aggravate the risk of hypertension in adulthood through increased circulating Ang II level [3, 4] . This epidemiological interplay is thought to become even more complex during exposure to the SARS-CoV-2, wherein ACE2 downregulation tends to protect such population from SARS-CoV-2 infection (decreased prevalence of infection), but compensatory Ang II upregulation tends to increase the severity in the infected population (increased proportions of severe infection). The net effect may be compounded/ masked in the presence of other ACE2-upregulating conditions such as smoking, higher age, and comorbidities, thus leading to a mixed epidemiological and clinical profile, as is currently apparent. Thus, the epidemiology and pathogenesis of COVID-19 in populations living in malaria-endemic countries is hypothesised to be dependent on the relative interplay of the specific host genetic epidemiology and other related factors (Fig. 2 ). As per our best knowledge, no published study has analysed the aforesaid association apart from the two indirect published evidence. A case-control study that investigated the association of rs2106809-tag SNP rs2285666 (and different exonic ACE2 variants) with COVID-19 (and its severity) could not find a statistically significant association possibly due to factors related to the study design and sample size [8] . Another study that supports our hypothesis was done on Chinese population that tested rs2106809 (among others including rs2285666) for increased SARS susceptibility and worse outcomes suggested a protective effect of rs2106809 T-allele on SARS susceptibility (OR = 0.9; statistically insignificant) [9] . However, it has to be noted that rs2106809 may not act independently as a genetic determinant of SARS-CoV-2 infection/severity [10] .

A brief analysis of the available data on the distribution of COVID-19 prevalence (cases per million population) and severity (in terms of case fatality rate per 1000 population) in malaria endemic countries with information on The system balances the levels of Angiotensin II (light blue bar) through relative concentrations of Angiotensin-Converting Enzyme (ACE; orange rectangle) which converts Angiotensin I to Angiotensin II and Angiotensin-Converting Enzyme 2 (ACE2; grey rectangle) which converts Angiotensin II to Angiotensin (1-7). The catalytic site of ACE2 is shown to bind Angiotensin II. The SARS-CoV-2 (red spiked solid circle) is shown to use the same catalytic site of ACE2 for its entry into an ACE2 expressing cell (yellow shaded oval). Various relevant factors that disturb the crucial Angiotensin II balance is shown (bottom panel). Angiotensin II levels are increased by ACE2 downregulators (ACE2 rs2106809) and SARS-CoV-2 infection itself. Resulting low ACE2 offers protection from severe malaria (through high Angiotensin II) and from SARS-CoV-2 infection (through decreased ACE2 receptors). Concurrently, ACE2 downregulators tend to increase the risk of hypertension and COVID-19 pathologies due to increased Angiotensin II. On the other hand, ACE2 upregulators may increase the risk of SARS-CoV-2 infection (through increased receptors) and related pathology (through high viral load due to increased receptors). The final COVID-19 pathogenesis depends on the relative balance between ACE2 down-and up-regulators (DM Diabetes Mellitus; HTN Hypertension) the population having the T-allele of rs2106809 currently does not support the proposed hypothesis (data not shown here) due to many factors. Principal among them include those related to ACE2 T-allele (available data lacks internal/ external validities, lack of individual-centric data on both ACE2 SNP and COVID-19), malaria (endemicity is highly Fig. 2 Proposed hypothesis explains that the malaria exposed population (right) has a relatively higher prevalence of naturally selected ACE2 rs2106806 TT/T genotype (pink) as compared to the population not exposed to malaria (left). The T allele is known to be associated with decreased ACE2 expression and hence lesser receptors for SARS-CoV-2, therefore, reducing the chances of viral entry into the cells. The reduced ACE2 also restricts the conversion of Ang II to Ang (1-7) , thereby elevating the level of circulating Ang II which precipitates COVID-19 severity due to lung injury and other negative effects via the Angiotensin Type 1 Receptor (AT 1 R). The pathogenesis of COVID-19 thus differs in the two populations: lesser prevalence of SARS-CoV-2 infections but a higher proportion of severe COVID-19 in malaria exposed population as compared to population not exposed to malaria variable even within an "endemic" country/state), COVID-19 (severity outcome is not available, evolving nature of the pandemic) and health systems (variations in case definitions, diagnostic methods, surveillance strategies). However, if the available data on COVID-19 prevalence and mortality be standardized for some or more of the non-genetic determinants, the role of rs2106809 could be better evaluated. In addition, the attributable fractions of each of these genetic and non-genetic determinants are not currently available which makes it difficult to add a corresponding weightage to each of them. This becomes more valid if the population under consideration has more than two determinants, so that the weighted protective effect of one may be compromised by the weighted aggravating effect/s of other/s and vice versa.

These factors preclude powerful analyses of the available data needed for validating the proposed hypothesis and hence reinforce the need to perform powerful and targeted studies with specific objectives. Amidst all possible uncertainties in the proposed conjecture, the hypothesis certainly warrants confirmation in the immediate future as a testable body of science. We propose that the hypothesis linking malaria-hypertension-COVID-19 stands logical enough to be best tested through powerful case-control studies in the population that has developed a COVID-19-related outcome and evaluate the association with their ACE2 variants. Simultaneously, the mechanism through which the intronic mutations (rs2106809 and rs2285666) affect the expression and regulation of ACE2 needs to be elucidated. It would be fascinating to study the ACE2 expression profile in differentially affected COVID-19 and non-affected population, particularly under different malaria endemicity zones, under different genetic (rs2106809 and tag-SNPs) and non-genetic non-modifiable (age and gender) and modifiable (e.g., smoking) conditions and also in presence of comorbidities and the treatment thereof.

Global spread of coronavirus disease 2019 and malaria: an epidemiological paradox in the early stage of a pandemic

The two faces of ACE2: the role of ACE2 receptor and its polymorphisms in hypertension and COVID-19

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Gene polymorphisms in angiotensin I converting enzyme (ACE I/D) and angiotensin II converting enzyme (ACE2 C → T) protect against cerebral malaria in Indian adults

Relationship between genetic variants of ACE2 gene and circulating levels of ACE2 and its metabolites

Association between circulating levels of ACE2-Ang-(1-7)-MAS axis and ACE2 gene polymorphisms in hypertensive patients

The high blood pressure-malaria protection hypothesis

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