TO THE EDITOR—The recent article by Zhang et al [1] described the genetic association of interferon-induced transmembrane protein 3 (IFITM3) with severe coronavirus disease 2019 (COVID-19). Eighty Chinese subjects infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) were recruited and genotyped for the IFITM3 rs12252 gene polymorphism. The authors revealed an age-dependent association of severe COVID-19 in the studied Chinese cohort. Furthermore, subjects harboring the CC genotype had a 6.37-fold higher risk of severe pathogenesis when infected with SARS-CoV-2. These observations encouraged us to investigate the association of the IFITM3 rs12252 polymorphism with susceptibility to SARS-CoV-2 infection and mortality in the worldwide population.
For COVID-19–related worldwide data, we explored the Worldometer website (https://www.worldometers.info/coronavirus/) and extracted data such as country name, number of cases per million, and the number of deaths per million population due to SARS-CoV-2 infections (accessed 10 August 2020). The prevalence of IFITM3 rs12252 genotypes or alleles in different countries was searched through the PubMed database. All relevant publications were inspected, and authors’ details, country name, IFITM3 genotypes, and allele number or frequency of healthy controls were obtained. Reports containing genotype distributions not following Hardy–Weinberg equilibrium (HWE) were excluded from the present study.
The data search on 10 August 2020 revealed the presence of SARS-CoV-2 infection in 215 countries comprising 20 million cases and >0.7 million deaths worldwide. Out of 215 countries, IFITM3 rs12252 polymorphism data were available for 23 countries. The mutant allele (C) ranges from 3.27% to 63.48%.
As the distribution of IFITM3 rs12252 genotypes deviated from HWE in 4 studies from Chinese populations and 1 study each from Vietnam and Iran, these were excluded from the present study. A total of 21 countries were considered for the present analysis (Table 1). Spearman rank correlation analysis revealed an inverse correlation between the SARS-CoV-2 infection rate per million population and the IFITM3 rs12252 minor allele (C) (r = –0.632; P = .002; n = 21) (Table 1). A good healthcare system is believed to minimize the death rate due to SARS-CoV-2 infection. Thus, for analysis of the possible correlation between mortality rate and IFITM3 rs12252 polymorphism, data of 3 countries (Bangladesh, Pakistan, and Sri Lanka) were excluded as those countries spend <3% of their gross domestic product in the health sector. Interestingly, the C allele of IFITM3 rs12252 polymorphism was negatively correlated with the SARS-CoV-2 mortality rate per million (r = –0.715; P = .0008; n = 18) (Table 1).
Table 1.
Country | SARS-CoV-2–Infected Cases per Million Population | SARS-CoV-2–Related Deaths per Million Population | No. of Reports Considered for Prevalence of Genotype Investigation | Total No. of Healthy Controls | C/C Genotype, No. | C/T Genotype, No. | T/T Genotype, No. | C Allele, No. | T Allele, No. | Frequency of Allele C, % | References | No. of Doctors/10 000 Population | No. of Nurses/10 000 Population | Expenditure of % of GDP on Health Sector | Spearman Rank Correlation |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Nigeria | 48 | 3 | 3 | 266 | 18 | 89 | 159 | 125 | 407 | 23.49 | Jiménez et al 2017; Kim et al 2017 | 3.81 | 11.79 | 3.7 | Allele C frequency (%) vs SARS-CoV-2 cases/million (r = –0.632, P = .002, n = 21); Allele C frequency (%) vs deaths/million (r = –0.715, P = .0008, n = 18) |
Kenya | 491 | 8 | 1 | 99 | 8 | 43 | 48 | 59 | 139 | 29.79 | Jiménez et al 2017 | 1.57 | 11.66 | 5.7 | |
The Gambia | 510 | 9 | 1 | 113 | 8 | 33 | 72 | 49 | 177 | 21.68 | Jiménez et al 2017 | 1.02 | 15.45 | 7.3 | |
Sierra Leone | 240 | 9 | 1 | 85 | 5 | 32 | 48 | 42 | 128 | 24.70 | Jiménez et al 2017 | .25 | 2.24 | 11.1 | |
China | 59 | 3 | 9 | 1383 | 351 | 687 | 345 | 1389 | 1377 | 50.21 | Wang et al 2013; Zhang et al 2013; Lee et al 2017; Zhang et al 2013; Lee et al 2017; Pan et al 2017; Zhang et al 2013; Zhang et al 2015 | 19.8 | 26.62 | 5.5 | |
India | 1603 | 32 | 2 | 205 | 5 | 45 | 155 | 55 | 355 | 13.41 | Jiménez et al 2017 | 8.57 | 17.27 | 4.7 | |
South Korea | 285 | 6 | 2 | 858 | 294 | 434 | 130 | 1022 | 694 | 59.55 | Kim et al 2017; Seo et al 2010 | 23.61 | 73.01 | 7.4 | |
Japan | 370 | 8 | 1 | 89 | 39 | 35 | 15 | 113 | 65 | 63.48 | Kim et al 2017 | 24.12 | 121.5 | 10.2 | |
Spain | 7730 | 610 | 3 | 599 | 0 | 41 | 558 | 41 | 1157 | 3.42 | Rodríguez et al 2016; Jiménez et al 2017 | 38.72 | 57.3 | 9 | |
Finland | 1369 | 60 | 1 | 99 | 0 | 16 | 83 | 16 | 182 | 8.08 | Jiménez et al 2017 | 38.12 | 147.4 | 9.7 | |
Italy | 4145 | 582 | 1 | 107 | 0 | 7 | 100 | 7 | 207 | 3.27 | Jiménez et al 2017 | 39.77 | 57.4 | 9.2 | |
Portugal | 5167 | 172 | 3 | 1086 | 2 | 132 | 952 | 136 | 2036 | 6.26 | Gaio et al 2016; David et al 2017 | 51.24 | 69.75 | 9.5 | |
UK | 4576 | 686 | 3 | 3072 | 5 | 228 | 2839 | 238 | 5906 | 3.87 | Mills et al 2013; Everitt et al 2013; Kim et al 2017 | 28.12 | 81.72 | 9.1 | |
Mexico | 3721 | 405 | 5 | 820 | 24 | 248 | 548 | 296 | 1344 | 18.04 | Jiménez et al 2017 | 23.83 | 23.96 | 6.3 | |
US | 15 698 | 500 | 5 | 10 642 | 10 | 701 | 9931 | 721 | 20 563 | 3.38 | Carter et al 2017; Randolph et al 2017; Jiménez et al 2017 | 26.12 | 145.5 | 17.1 | |
Barbados | 249 | 24 | 1 | 96 | 4 | 35 | 57 | 43 | 149 | 22.39 | Jiménez et al 2017 | 24.84 | 30.6 | 7.5 | |
Colombia | 7607 | 252 | 1 | 94 | 0 | 14 | 80 | 14 | 174 | 7.44 | Jiménez et al 2017 | 21.85 | 13.31 | 7.2 | |
Peru | 14 477 | 638 | 1 | 85 | 9 | 40 | 36 | 58 | 112 | 34.11 | Jiménez et al 2017 | 24.4 | 13.05 | 5.5 | |
Bangladesh | 1562 | 21 | 1 | 86 | 3 | 22 | 61 | 28 | 144 | 16.27 | Jiménez et al 2017 | 5.81 | 4.12 | 2.8 | |
Pakistan | 1286 | 28 | 1 | 96 | 5 | 24 | 67 | 34 | 158 | 17.70 | Jiménez et al 2017 | 9.8 | 6.68 | 2.68 | |
Sri Lanka | 133 | .5 | 1 | 102 | 2 | 23 | 77 | 27 | 177 | 13.23 | Jiménez et al 2017 | 10.04 | 21.8 | 3.5 |
Data on SARS-CoV-2–infected cases, related death, and recovery rate were obtained from https://www.worldometers.info/coronavirus/ (accessed 10 August 2020). Correlation analysis was performed by Spearman rank correlation coefficient in GraphPad Prism 8.3.0 software.
Abbreviations: GDP, gross domestic product; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; UK, United Kingdom; US, United States.
Zhang et al [1] have demonstrated a significant association of the rs12252-CC genotype with severe COVID-19, most frequently in Chinese patients who died from SARS-CoV-2 infection. In contrast, we observed a beneficial effect of allele C against SARS-CoV-2 infection and related mortality in worldwide populations. Similar to our observation, a recent preprint report in different ethnic groups of England’s population described a positive correlation of the rs12252 dominant allele with SARS-CoV-2–related death [2]. The reasons for these discrepancies are not known. It is believed that the rs12252-CC genotype produces a truncated variant of 21 amino acids at the N-terminal region of the protein, which leads to loss of antiviral activity. Earlier reports in the Chinese population have demonstrated a significant association of the rs12252-C allele with severity of influenza infection but failed to exhibit such a link in Korean, American, African American, European, and Brazilian cohorts [3]. Furthermore, some reports also failed to detect the presence of truncated IFITM3 isoform in RNAseq data of subjects carrying the rs12252-CC genotype [4, 5]. These observations indicate the possibility of other functional variants in the IFITM3 gene on the determination of the clinical phenotype of viral infections.
A single-nucleotide polymorphism in the 5′ untranslated region of the IFITM3 gene rs34481144 (G > A) has been shown to alter IFITM3 levels in peripheral blood mononuclear cells [6]. Diminished production of IFITM3 messenger RNA is linked with the minor allele A by decreased IRF3 and increased CTCF binding capability [6]. As the number of reports on the prevalence of rs34481144 polymorphism is limited worldwide, we were unable to investigate the possible association of rs34481144 with COVID-19. Distribution of rs12252 and rs3448114 polymorphisms always follows opposite trends: A population with a higher rs12252-C incidence has a lower prevalence of rs3448114-G, and vice-versa. Furthermore, the recessive genotype of both polymorphisms was never inherited together. Based on the results of the present study and other observations, it can be presumed that the minor allele of rs3448114 polymorphism could be positively linked with SARS-CoV-2 susceptibility and mortality. However, further case-control studies in different ethnic groups, including larger sample sizes, are required to validate our observations and to obtain an accurate inference on the role of the IFITM3 gene in the pathogenesis of COVID-19.
Notes
Potential conflicts of interest. All authors: No reported conflicts of interest.
All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
References
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