Clinical, regional, and genetic characteristics of Covid-19 patients from UK Biobank

David A. Kolin; Scott Kulm; Paul J. Christos; Olivier Elemento

doi:10.1371/journal.pone.0241264

Abstract

Background

Coronavirus disease 2019 (Covid-19) has rapidly infected millions of people worldwide. Recent studies suggest that racial minorities and patients with comorbidities are at higher risk of Covid-19. In this study, we analyzed the effects of clinical, regional, and genetic factors on Covid-19 positive status.

Methods

The UK Biobank is a longitudinal cohort study that recruited participants from 2006 to 2010 from throughout the United Kingdom. Covid-19 test results were provided to UK Biobank starting on March 16, 2020. The main outcome measure in this study was Covid-19 positive status, determined by the presence of any positive test for a single individual. Clinical risk factors were derived from UK Biobank at baseline, and regional risk factors were imputed using census features local to each participant’s home zone. We used robust adjusted Poisson regression with clustering by testing laboratory to estimate relative risk. Blood types were derived using genetic variants rs8176719 and rs8176746, and genomewide tests of association were conducted using logistic-Firth hybrid regression.

Results

This prospective cohort study included 397,064 UK Biobank participants, of whom 968 tested positive for Covid-19. The unadjusted relative risk of Covid-19 for Black participants was 3.66 (95% CI 2.83–4.74), compared to White participants. Adjusting for Townsend deprivation index alone reduced the relative risk to 2.44 (95% CI 1.86–3.20). Comorbidities that significantly increased Covid-19 risk included chronic obstructive pulmonary disease (adjusted relative risk [ARR] 1.64, 95% CI 1.18–2.27), ischemic heart disease (ARR 1.48, 95% CI 1.16–1.89), and depression (ARR 1.32, 95% CI 1.03–1.70). There was some evidence that angiotensin converting enzyme inhibitors (ARR 1.48, 95% CI 1.13–1.93) were associated with increased risk of Covid-19. Each standard deviation increase in the number of total individuals living in a participant’s locality was associated with increased risk of Covid-19 (ARR 1.14, 95% CI 1.08–1.20). Analyses of genetically inferred blood types confirmed that participants with type A blood had increased odds of Covid-19 compared to participants with type O blood (odds ratio [OR] 1.16, 95% CI 1.01–1.33). A meta-analysis of genomewide association studies across ancestry groups did not reveal any significant loci. Study limitations include confounding by indication, bias due to limited information on early Covid-19 test results, and inability to accurately gauge disease severity.

Conclusions

When assessing the association of Black race with Covid-19, adjusting for deprivation reduced the relative risk of Covid-19 by 33%. In the context of sociological research, these findings suggest that discrimination in the labor market may play a role in the high relative risk of Covid-19 for Black individuals. In this study, we also confirmed the association of blood type A with Covid-19, among other clinical and regional factors.

Citation: Kolin DA, Kulm S, Christos PJ, Elemento O (2020) Clinical, regional, and genetic characteristics of Covid-19 patients from UK Biobank. PLoS ONE 15(11): e0241264. https://doi.org/10.1371/journal.pone.0241264

Editor: Sreeram V. Ramagopalan, University of Oxford, UNITED KINGDOM

Received: August 6, 2020; Accepted: October 12, 2020; Published: November 17, 2020

Copyright: © 2020 Kolin et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability: All data used for this study were obtained from the UK Biobank. Data requests may be sent via https://urldefense.proofpoint.com/v2/url?u=https-3A__www.ukbiobank.ac.uk_principles-2Dof-2Daccess_&d=DwIGaQ&c=lb62iw4YL4RFalcE2hQUQealT9-RXrryqt9KZX2qu2s&r=emeY7OEhMRMUYvaBlIQYiCIjDZ1mhvSZ60GkRC5Srzc&m=cJaZ7BO-L3FOaMbcCRxa9NVCPhPzFwQdIYYHV3RjnZ8&s=EZ8e5hVazSLARKaJF7NIdwBPJcKfRn9SlngrTOU8TKw&e=. The authors of the present study had no special access privileges in accessing these datasets which other interested researchers would not have.

Funding: This research was supported by the National Institutes of Health (Grant Numbers: U24 CA210989, R01 CA194547, P50CA211024, UL1TR002384) and by the Emerson Research Collective. Dr. Paul Christos was partially supported by the following grant: Clinical and Translational Science Center at Weill Cornell Medical College (1-UL1-TR002384-01). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: OE reports grants from the National Institutes of Health and the Emerson Research Collective. The funders had no role in any aspect of study design, analysis, writing, or other aspects related to the submitted work. There are no relationships or activities that have influenced the submitted work. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

Introduction

The coronavirus disease 2019 (Covid-19) pandemic, caused by severe acute respiratory syndrome 2 (SARS-CoV-2), has affected millions of people worldwide. At the onset of the pandemic, it became apparent that Covid-19 was disproportionately afflicting minority populations, and Black individuals were being particularly affected [1–4]. The risk of death from Covid-19 for Black Americans is 92.3 per 100,000 individuals, while for White Americans, risk of death is 45.2 per 100,000 individuals. The association between Black race and Covid-19 is not unique to the United States. In the United Kingdom, the Office for National Statistics found that Black individuals in England and Wales were over fourfold more likely to die from Covid-19 than White individuals [5]. After adjusting for several confounding socioeconomic factors, Black individuals remained at twofold increased risk in that study.

Current evidence indicates that age, male sex, high body-mass index, and comorbidities–including diabetes and hypertension–are also associated with increased risk of Covid-19 [6, 7] For diabetic patients, the combination of increased angiotensin converting enzyme 2 (ACE2), increased furin, impaired T-cell function, and increased interleukin-6 may increase disease severity [8]. For patients with hypertension, differential expression of ACE2 may modulate disease risk [9]. Because coronaviruses use ACE2 to gain entry into cells, at the beginning of the pandemic, concerns arose regarding medications targeting the angiotensin system. However, some evidence suggests that angiotensin converting enzyme inhibitors and angiotensin II receptor blockers do not increase the risk of Covid-19 [10, 11]. Not only do individual characteristics modulate disease risk, but the local environment also affects the likelihood of Covid-19. Regional factors associated with risk of death from Covid-19 include commuting by public transportation, average winter temperatures, and median household income [12].

Recent evidence also suggests that genetics may influence susceptibility to Covid-19. A twins study estimated that total heritability of Covid-19 risk was 50% (95% CI 29–70%) [13]. Analyses of host genomes indicate that ACE2 and OR4C5 gene variants may impact severity of Covid-19 [14, 15]. OR4C5 is a pseudogene in the olfactory receptor loci region that codes for a G-protein-coupled receptor arising from a single-coding exon gene. The Severe Covid-19 GWAS Group recently found an association between the 3p21.31 gene cluster and Covid-19 with respiratory failure [16]. One gene within the cluster, SLC6A20, may increase Covid-19 susceptibility by encoding sodium-imino acid (proline) transporter 1 (SIT1), a protein that interacts with ACE2.

Despite growing knowledge about both the clinical and genetic factors associated with Covid-19 risk, there is a need for additional studies in order to further elucidate the multitude of factors that influence Covid-19 susceptibility [17, 18]. Our study aims to address gaps in current knowledge by analyzing clinical, regional, and genetic risk factors within the UK Biobank, one of the largest, most comprehensive cohorts currently available. In order to assess the association of risk factors with Covid-19, we created adjusted models and conducted genomewide tests of association. The extensive phenotype data contained in the UK Biobank allows for statistical adjustments that are not possible in other cohorts. Our study confirms some previously-observed findings and uncovers several novel associations.

Materials and methods

Study design

The UK Biobank review board approved this study. This is an analysis of a single large prospective cohort study from the United Kingdom. The details of patient recruitment and data collection are publicly available. Data were analyzed anonymously.

This prospective cohort study included a population of 397,064 participants from England between the ages of 40 and 69 recruited from 2006 to 2010. While the UK Biobank does include participants from Scotland and Wales, these participants were excluded because testing laboratories were only located in England. Data on baseline characteristics were obtained during an in-person interview at recruitment, and health outcome data were obtained prospectively from electronic health records.

Recently, Public Health England began providing UK Biobank with information on participants’ Covid-19 test results from March 16, 2020 onwards. Covid-19 data included specimen date, specimen type, processing laboratory, inpatient status, and test results. Most UK testing performed during this period was completed in-hospital. Samples were categorized as inpatient if they were retrieved from an emergency care provider, an inpatient location, or if the sample was related to healthcare associated infection. Samples obtained from patients were kept on a medium salt solution during transfer to a testing facility, where samples were tested for Covid-19 using polymerase chain reaction. Approximately four days elapsed between the time of sample retrieval and the time of data transfer to Public Health England.

Clinical risk factors for each participant were extracted at baseline. Regional risk factors were ascribed to each individual by utilizing each participant’s home location, accurate to one kilometer. Regional information was derived from the national census recorded in 2011, specific to each Lower Layer Super Output Areas for England [19]. Genotypic data was sequenced with the Affymetrix UK Biobank Axiom array, with general imputation completed with IMPUTE2 and HLA-specific imputation completed with HLA*IMP:02 [20, 21]. Quality control of genotypic data excluded individuals who were reported as outliers in heterozygosity, contained sex chromosome aneuploidy, had excess relatives in the cohort, and held a genotyping missing rate above 0.1. The variants analyzed were bi-allelic, with a minor allele frequency above 0.001. Written informed consent was obtained from all study participants.

Study outcome

The main study outcome was any positive test for a single individual. In order to better understand risk factors for inpatient and outpatient Covid-19, we also conducted a nested case-control study within the population of patients that tested positive for Covid-19 on at least one occasion. Patients were categorized as inpatient cases if they had any Covid-19 testing sample marked as inpatient. Any patient without an inpatient sample was considered an outpatient control.

Statistical analyses

We then calculated the association of clinical, regional, and genetic factors with Covid-19 positive status. Frequencies and percentages, along with means and standard deviations, were calculated for clinical factors for each of the three following categories: all participants, participants with only negative tests, and participants with a minimum of one positive test. We used Poisson regression, with robust standard errors and clustering by laboratory, to estimate risk ratios for Covid-19 positive status [22]. Uncertainty of each laboratory’s final date of testing prevented the use of hazard ratios. Adjusted estimates accounted for age, sex, body-mass index, systolic blood pressure, Townsend deprivation index, and race. Sensitivity analyses with quasi-Poisson models, correcting for overdispersion, generated nearly identical results. Risk ratios for age, body-mass index, and systolic blood pressure were calculated by determining the change in risk of Covid-19 positive status for each ten unit increase in the risk factor.

Analyses of regional demographics were conducted by similarly adjusted risk models, where the risk ratio indicated the change in risk of positive Covid-19 status for each standard deviation increase in the regional risk factor. In order to avoid over-adjustment due to collinearity, when analyzing regional factors, we did not adjust for Townsend deprivation index, which utilizes local census features.

For analyses of genetic associations, we first analyzed the association of ABO blood types with Covid-19 positive status. We then conducted genomewide tests of association to identify novel genetic variants associated with Covid-19. ABO blood types were inferred from the variants rs8176719 and rs8176746, as previously described [23]. Odds ratios of positive Covid-19 status for the inferred blood types were calculated using logistic regression, adjusted for age, sex, body-mass index, race, and Townsend deprivation index. Genomewide tests of association for positive Covid-19 status were calculated using logistic Firth hybrid regression adjusted for age, sex, and the first ten genetic principal components. These tests were performed on samples of either European, Asian, or African ancestry. These samples were determined by applying k-means clustering to the top 40 genetic principal components, identifying clusters based on overlap with reported race, and removing outliers (distance to cluster center greater than the 99^th percentile of all distances). The results of the ancestry-specific genomewide association studies were meta-analyzed through weighted Z-scores, as implemented in the PLINK program [24, 25]. For the genomewide analysis, we used the common P value threshold of 5x10^-8 to determine statistical significance. Pre-specified analyses of the HLA region were conducted using Bonferroni-corrected P value thresholds based on the number of alleles analyzed. Odds ratios of inpatient status for clinical, regional, and genetic analyses were recalculated for the nested population of Covid-19 positive participants. Ninety-five percent confidence intervals (95% CI) were calculated for all effect parameters of interest to assess the precision of the obtained estimates. All analyses were performed in R Version 4.0 (R Foundation for Statistical Computing, Vienna, Austria).

Ethical approval

This study was approved by Weill Cornell Medical College and UK Biobank. The UK Biobank is overseen by an independent advisory committee, and the data used within this analysis was accessed through the approved application #47137.

Results

Among 397,064 participants, there were 4,811 (1.2%) tests for Covid-19 in the most recent UK Biobank Covid-19 release (May 18, 2020), of which 1,868 (38.8%) were inpatient (S1 and S2 Figs in S1 Appendix). A total of 1,623 (33.7%) tests were positive, and one participant was tested 20 times. Although, Public Health England notes that duplicate tests may be present in this study due to the arrival of results via several different routes. The majority of tests were upper respiratory tract swabs (31.1%), nasal swabs (16.1%), or nose and throat swabs (12.3%). Of the patients tested, 968 (31.1%) tested positive at least one time. The mean age (± standard deviation) of Covid-19 positive participants was 57.0 ± 9.1 years, 521 (53.8%) were male, and mean body-mass index was 29.1 ± 5.5 kg/m² (S1-S8 Tables in S1 Appendix).

Black participants were disproportionately Covid-19 positive. The unadjusted relative risk of Covid-19 for Black participants was 3.66 (95% CI 2.83–4.74) relative to White participants. After only adjusting for deprivation, the relative risk was 2.44 (95% CI 1.86–3.20). After adjusting for age, sex, body-mass index, systolic blood pressure, and Townsend deprivation index, Black participants remained at over two times increased risk of testing positive for Covid-19 compared to White participants (adjusted relative risk [ARR] 2.53, 95% CI 1.92–3.33) (Fig 1). Amongst the 61 Black participants who tested positive for Covid-19, 7 (11.5%) had diabetes and 3 (4.9%) had ischemic heart disease. In exploratory analyses also adjusting for history of diabetes or ischemic heart disease, Black participants remained at increased risk of Covid-19 (ARR 2.54, 95% CI 1.92–3.34) compared to White participants. Asian participants were also at increased risk of testing positive for Covid-19 compared to White participants (ARR 2.13, 95% CI 1.60–2.85). Analyses of serological markers identified that baseline white blood cell count, lymphocyte count, monocyte, and neutrophil count were positively associated with Covid-19.

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Fig 1. Adjusted risk ratio for Covid-19 positive status with baseline attributes, social habits, comorbidities, and serology.

*Adjusted relative risk represents a ten-unit increase in the risk factor. All other risk ratios for continuous variables are for single unit increases in the risk factor. ¹Risk ratios were adjusted for age, sex, body-mass index, systolic blood pressure, Townsend deprivation index, and race.

https://doi.org/10.1371/journal.pone.0241264.g001

Among the participants reporting at least one positive Covid-19 test, 91 (9.4%) had a history of diabetes, 40 (4.1%) had a history of chronic obstructive pulmonary disease (COPD), and 77 (8.0%) had a history of ischemic heart disease. After adjusting for confounding, we found that patients were at increased risk of Covid-19 if they had a history of COPD (ARR 1.64, 95% CI 1.18–2.27) or ischemic heart disease (ARR 1.48, 95% CI 1.16–1.89). Participants with depression were at 32% increased risk of Covid-19 (ARR 1.32, 95% CI 1.03–1.70).

Next, we investigated the association of common classes of medications with Covid-19 (Fig 2). Participants were at increased risk of Covid-19 if they used angiotensin converting enzyme inhibitors (RR 1.48, 95% CI 1.13–1.93) but not angiotensin II receptor blockers (ARR 1.27, 95% CI 0.93–1.74). Of the 61 Black Covid-19 patients, 11 (18.0%) were using either an angiotensin converting enzyme inhibitor or an angiotensin II receptor blocker. Of all Black participants, 494 (6.6%) were using either of the two medications. Adjusted risk ratios for use of non-steroidal anti-inflammatory drugs and acetaminophen were 1.06 (95% CI, 0.92–1.23) and 1.23 (95% CI, 1.05–1.43), respectively. Analyses of Covid-19 positive inpatients and outpatients in the nested case-control study found that the groups were similar across clinical factors.

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Fig 2. Adjusted risk ratio for Covid-19 positive status with common medications.

¹Risk ratios were adjusted for age, sex, body-mass index, systolic blood pressure, Townsend deprivation index, and race.

https://doi.org/10.1371/journal.pone.0241264.g002

We then analyzed regional factors, using counts of individuals per census zone, to further understand the effects of the local environment on Covid-19 (S9 and S10 Tables in S1 Appendix). After adjusting for covariates, each standard deviation increase in the number of unemployed individuals was associated with a 19% increased risk of Covid-19, and households with a lone parent in the participant’s home zone was associated with an 18% increased risk. Other regional factors associated with increased Covid-19 risk included the total number of individuals per hectare (ARR 1.14, 95% CI 1.08–1.20), the number of individuals with no academic qualifications (ARR 1.14, 95% CI 1.07–1.21), and the number of individuals who rent their residence (ARR 1.18, 95% CI 1.12–1.24).

Lastly, we investigated the genetics of participants with any positive Covid-19 test. ABO blood types of participants were inferred through genetic profiles [23]. Participants with blood type A had increased odds of at least one positive Covid-19 test relative to blood type O participants (odds ratio [OR] 1.16, 95% CI 1.01–1.33) (Fig 3 and S11 Table in S1 Appendix) [26]. Genomewide association analysis of any positive Covid-19 test in the meta-analysis and ancestry specific analyses did not uncover any significant loci (Fig 4). The HLA regional analysis also did not reveal any significant alleles, and analyses of Covid-19 positive inpatients and outpatients identified no significant variants (S3-S9 Figs in S1 Appendix).

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Fig 3. Odds of Covid-19 positive status by blood type.

https://doi.org/10.1371/journal.pone.0241264.g003

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Fig 4. Cross-ancestry genomewide association analysis of Covid-19 positive status.

https://doi.org/10.1371/journal.pone.0241264.g004

Discussion

In this cohort study of participants from the United Kingdom, we found that the unadjusted risk of Covid-19 was over threefold higher for Black participants than for White participants. Adjusting for deprivation alone reduced the relative risk by 33%, and adjusted effect estimates–accounting for a range of comorbidities–did not alter the relative risk of Covid-19 for Black participants considerably. These novel analyses suggest that differences in deprivation amongst racial groups is one of the greatest drivers of Covid-19 for Black individuals. Our analyses also identified that patients with COPD, ischemic heart disease, and depression were more likely to test positive for Covid-19. Participants in impoverished, populous regions, with high unemployment and low home ownership, were at higher risk of Covid-19. Finally, blood type A was associated with Covid-19 positive status.

Overall, data from recent studies suggest that comorbidities play a significant role in Covid-19 disease severity. A study from two New York City hospitals found that about one quarter of all Covid-19 patients were diabetic, and half of all patients had hypertension [27]. A separate study of 5,700 patients found that the most common comorbidities were hypertension (56.6%), obesity (41.7%), and diabetes (33.8%) [28]. The OpenSAFELY study, which analyzed data from over 17,000,000 patients, found significant associations between Covid-19-related-death and comorbidities, including hypertension, obesity, and diabetes [29]. Additionally, the study found that reduced kidney function (eGFR <30), hematological malignancy, organ transplant, and other neurological disease were associated with over threefold increased risk of Covid-19-related-death. To our knowledge, our study is the first study to suggest that depression is a risk factor for Covid-19. It is well-established that the common comorbidities identified in Covid-19 patients are associated with inflammation [30–32]. In our study, novel serological analyses within the UK Biobank cohort further emphasized the importance of inflammation; increased white blood cell, lymphocyte, monocyte, and neutrophil counts were all associated with increased risk of Covid-19. Higher baseline inflammation may result in more severe Covid-19 and subsequent testing.

This study lends some support to the reported hypothesis that upregulation of ACE2 is a risk factor for Covid-19. After adjustment for several confounding factors, there was an association between medications targeting the angiotensin system and Covid-19 [33, 34]. When considering the totality of current evidence, it is unlikely that medications targeting the angiotensin system increase the likelihood of Covid-19. Rather, residual confounding in this study–due to confounding by indication–may have led to the observed association. Residual confounding likely remained, despite our efforts to control for six confounders at baseline.

The regional factors in this study suggest that impoverished neighborhoods have a greater burden of Covid-19. Participants in this cohort were more likely to test positive for Covid-19 if there were more unemployed individuals, more renters, and more individuals without advanced degrees in their locality. One potential explanation for this finding is that less affluent individuals may not be able to quarantine effectively during the pandemic due to financial limitations and the need to ensure job security. According to analyses of data provided by Cuebiq, a company that tracks approximately 15 million cellphone users daily, wealthier individuals began staying home earlier and are moving less than poorer individuals [35]. In light of these findings, additional efforts should be made to safeguard impoverished individuals from infection. In order to reduce viral transmission, employers should provide masks to employees and grant sick leave to employees who are ill (without repercussions) [36].

Recently, a significant association between blood type A and Covid-19 has been identified in multiple different populations, including our own [16, 37]. The GATC haplotype–prevalent in non-O blood type patients–is associated with ACE activity, potentially facilitating SARS-CoV-2 entry into host cells [23]. Although we did not discover any genomewide significant loci in this analysis of the UK Biobank, Ellinghaus et al. reported a single significant locus on 3p21.31, which includes a gene associated with the renin-angiotensin-aldosterone-system (RAAS) pathway. While the association of a RAAS gene with Covid-19 increases causal likelihood, our inability to confirm its significance may underscore its weak effect on Covid-19 susceptibility [38, 39].

Multiple reports both in the United States and the United Kingdom have shown that Covid-19 is disproportionately affecting Black populations [18, 40]. A previous study of the UK Biobank found that participants in the lowest socioeconomic disadvantage quartile were over twice as likely to have a confirmed infection, than those in the highest quartile [41]. In order to understand these effects, we further investigated the effects of adjusting for the Townsend deprivation index alone. When considered as a whole, the findings from this study suggest that racial discrimination may be contributing to the higher likelihood that Black individuals test positive for Covid-19 relative to White individuals [4]. Adjustment only for the Townsend deprivation index–a score that combines household overcrowding, non-home ownership, non-car ownership, and unemployment–led to a relative risk reduction of 33%. Census analyses also found that that unemployment is strongly associated with increased Covid-19 risk.

Numerous randomized sociological studies have confirmed strong associations between race and diminished employment prospects. In the United States, a randomized trial of equivalent job applications with White and Black sounding names led to 50% more callbacks for applicants with White sounding names [42]. Studies in the United Kingdom have led to similar findings [43]. Recently, a randomized controlled trial of nearly 3,200 identical job applications found that, relative to the White British majority, Black British individuals–from Nigeria, Ethiopia, Somalia, and Uganda–had to send twice as many job applications to receive a callback [44]. Differences in response to identical job applications may partially explain why Black participants in this study had greater deprivation, a measure of unemployment, than White participants. Given the strong associations between deprivation, race, and Covid-19 in this study, our findings may be due, in part, to discriminatory hiring practices within the labor market. Finally, any genetic differences amongst races are highly unlikely to explain our results, as multiple studies have shown that genetic variation within racial groups is greater than between racial groups [45–47].

Limitations

This study has several limitations. We primarily used log-link robust Poisson regression to estimate the relative risk of Covid-19 positive status in this longitudinal cohort. While the effect estimates produced by hazard ratios likely would have been superior to those generated by robust Poisson regression, the calculation of hazard ratios in this study was not possible. While testing center sample reporting to UK Biobank began on March 16, 2020, the final date of testing for each individual center could not be reliably established, as data release to UK Biobank is ongoing. Because inclusion of testing results into UK Biobank did not occur until March 16, 2020, participants may have been included as at-risk, despite having had a positive Covid-19 test result that was not included in the dataset. However, the bias caused by inclusion of early Covid-19 positive patients was likely small because, on March 16, there were only 1,391 confirmed Covid-19 cases in the United Kingdom [48]. Additionally, limitations in the availability of testing likely prevented some participants with severe disease, and many participants with mild disease, from testing positive for Covid-19. It is important to note that the primary outcome in this study was Covid-19 positive status, verified by testing. Many individuals in the cohort likely were positive for Covid-19, without ever having a positive test. While inpatient status was used as a proxy for severe disease, other markers of disease severity–such as degree of hypoxemia and length of intensive care unit stay–were not recorded.

Conclusions

In this study, we analyzed a cohort of nearly 400,000 participants, 968 of whom tested positive for Covid-19. We found that participants with comorbidities, including COPD, ischemic heart disease, and depression, were at increased risk of Covid-19. We also confirmed the association of Covid-19 with blood type A. In this study, the relative risk of Covid-19 for Black participants, relative to White participants, was reduced by 33% with adjustment for deprivation alone. When assessing differences in risk of Covid-19 between White and Black participants, adjustment for deprivation had a greater effect on the relative risk than any other risk factor analyzed. The increased risk of Covid-19 for Black participants may be linked to discrimination against Black individuals in the labor market, among other factors.

Supporting information

S1 Appendix.

https://doi.org/10.1371/journal.pone.0241264.s001

(DOCX)

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Figures

Abstract

Background

Methods

Results

Conclusions

Introduction

Materials and methods

Study design

Study outcome

Statistical analyses

Ethical approval

Results

Discussion

Limitations

Conclusions

Supporting information

S1 Appendix.

References