Abstract
Objective: We aimed to systematically investigate the associations between racial discrimination and various health outcomes and to evaluate the certainty of evidence from existing meta-analyses of observational studies. Method: We systemically searched the associations between racial discrimination and health outcomes for PubMed/MEDLINE, Embase, WoS, and Google Scholar up until January 31, 2024. Notably, the included studies were predominantly conducted in the USA and Europe, limiting the generalizability of our findings to a global context. Results: Eight meta-analyses of observational studies involving over 1 million individuals were included, describing 15 potential health outcomes related to racial discrimination. The quality assessment revealed that most included meta-analyses were of low quality. For oncological health outcomes, significant associations were found with the mortality of hepatocellular carcinoma (HCC); black patients had a higher risk, while Asian patients had a lower risk when compared to white patients. In addition, black patients with disparities on the cancer care continuum are a protective factor for early-stage HCC diagnosis. For gastroenterological health outcomes, Hispanic patients with nonalcoholic fatty liver disease and black patients with socioeconomic status/differential access to health care, compared to white patients (reference), showed significant associations. For mental health outcomes, racial discriminations were significantly associated with increased odds of psychotic experiences, suicidal ideation, and suicidal attempts. Numerous significant associations were from weak to suggestive evidence levels, indicating variability in the evidence. Conclusion: Despite the complexity of measuring its impact, racial discrimination shows a profound influence across clinical areas, including an unexpected protective association in early-stage HCC diagnosis among black patients.
This systematic review highlights significant associations between racial discrimination and health outcomes, with elevated oncological and gastroenterological risks among black and Hispanic patients compared to white patients.
Despite the complexity of measuring its impact, racial discrimination shows a profound influence across clinical areas, including an unexpected protective association in early-stage hepatocellular carcinoma diagnosis among black patients.
Introduction
Racism is a complex, multifaceted system of oppression and a fundamental cause of health inequalities across populations [1, 2]. Racism encompasses structural racism (e.g., housing policies and neighborhood racial segregation) [3], institutional racism (e.g., policies and practices in organizations) [4], cultural racism (e.g., exalting Western beauty standards) [5], and interpersonal racism, which refers to prejudice and mistreatment experienced on an individual level [6, 7]. Racial discrimination has been shown to impact health in prospective cohort studies [8, 9], resulting in health disparities among different racial groups [3]. In the USA, ethno-racial minorities are disproportionately exposed to stressors and often lack salutary resources, which, in theory, leads to a higher prevalence of multiple health problems [10].
Previous systematic reviews and meta-analyses have demonstrated that racial discrimination is associated with a wide array of adverse health outcomes, including mental health issues such as depression and anxiety, cardiovascular disease, and poorer self-related health [11]. Such reviews have also highlighted the cumulative impact of racial discrimination over the life course and its role in exacerbating existing health disparities [12, 13]. While such literature explored the associations between racial discrimination and related health outcomes, most have focused on specific health outcomes or subsets of individuals experiencing racial discrimination, such as maternal health, perinatal outcomes, cardiovascular outcomes, and the older adult black population in the USA [10, 14‒22]. Including a summary of these findings would help to conceptualize the current studies within the existing body of the literature. However, it is imperative to continuously synthesize emerging literature regarding the impacts of racism, which evolves and shifts over time. In this umbrella review, we focus on racial discrimination with a broad range of health outcomes across multiple nations, focusing on meta-analyses of observational studies. This involved systematically identifying relevant meta-analyses of observational studies, summarizing their outcomes, and evaluating the certainty of evidence; we aimed to offer a comprehensive assessment of the impacts of racial discrimination on health outcomes.
Methods
Literature Search Strategy and Selection Criteria
We conducted an umbrella review to summarize and evaluate the associations between racial discrimination and health outcomes. This review followed the PRISMA 2020 guidelines, and its protocol was registered with PROSPERO (Registration No. 42024513366) [23, 24]. Two authors, J.L. and J.K., systematically searched online databases (PubMed/MEDLINE, Embase, Web of Science, and Google Scholar) for meta-analyses of observational studies examining the association between racial discrimination and health outcomes until January 31, 2024. Our search strategy included keywords related to racism and meta-analysis as follows: (“racism” OR “discrimination” OR “racial” OR “colorism” OR “perceived skin tone discrimination”) AND (“meta”) and their variants. We also manually searched references of eligible articles and reviewed titles, abstracts, and full texts (J.L. and J.K.); for an included paper in our study, we contacted authors and retrieved additional data unavailable in the manuscript. Our study included only observational study-based meta-analyses as no randomized controlled trials’ meta-analyses met the criteria to be included in eligible studies for our manuscript. Details on these exclusion criteria are available in online supplementary Table 1 (for all online suppl. material, see https://doi.org/10.1159/000542988) as an additional resource. The racial discrimination-related factors eligible for our umbrella review included hepatocellular carcinoma (HCC), colon cancer, out-of-hospital cardiac arrest, peripheral artery disease, acute myocardial infarction, nonalcoholic fatty liver disease (NAFLD), and psychosis experiences (PEs). Meta-analyses reporting odds ratio (OR), hazard ratio (HR), and risk ratio (RR) of the association of racial discrimination and its health outcome were included in this review. We recalculated the pool effect size, and HR and RR were converted to equivalent OR (eOR) in reanalysis [23‒25].
Data Quality Assessment
The methodological quality of studies included in our review was evaluated using the A Measurement Tool Assessment Systemic Reviews 2 (AMSTAR2) checklist. In instances of disagreement regarding the quality assessment, another researcher (Y.S.) was consulted to facilitate reaching a consensus.
Data Extraction
Two researchers (J.K. and J.L.) independently screened titles, abstracts, and selected articles for a comprehensive, full-text review. These two researchers have extracted the following key data from the selected articles: publication year, number of primary studies included, outcomes, country of study, number of cases and participants, study design, effect estimation model (random or fixed effects), heterogeneity, and maximally adjusted effect size with 95% confidence interval (CI). Each meta-analysis was re-analyzed by the Der Simonian and Laird random fixed-effects model [25‒27]. Dose-response meta-analyses were not re-analyzed if they lacked sufficient data. Additional analyses were performed to evaluate specific aspects. I2 statistics was performed to evaluate heterogeneity, and an I2 value exceeding 50% indicates significant heterogeneity. P-curve analysis was used to detect p-hacking [25‒27]. The 95% prediction interval (PI) was examined to assess the uncertainty of the observed estimates and predict the value of new future observations based on Bayesian statistics. To mitigate type 1 errors, the Knapp-Sidik-Jonkman random-effects model was utilized [25‒27]. Publication bias was assessed with Egger’s test, indicating bias at a p value <0.1. eOR for various metrics, including the RR, were calculated following the latest guidelines [28]. These analyses were conducted using the “meta” package of R software (version 4.2.2; R Foundation, Vienna, Austria), with significance determined at a two-sided p value of less than 0.05 [29].
Assessment of Quality of Study and Evidence
In this review, we assessed the class and quality of evidence (CE) for each outcome, using criteria from previous umbrella reviews [25‒27]. Observational study associations were categorized into five levels based on the strength of evidence for potential factors (class I, convincing; class II, highly suggestive; class III, suggestive; class IV, weak; NS, not significant). The credibility of evidence from observational studies was rated considering various factors, including the number of events related to the outcome of interest, the p value of the association, the presence of small study effects, excess of significance bias, PIs, statistical significance in the largest study, and heterogeneity.
According to the criteria of observational study, the credibility of evidence was graded. Class I involved exceeding 1,000 cases (or over 20,000 participants); significant summary associations as per random-effects calculations, with p < 10−6; the absence of indications pointing toward small-study effects; no observed evidence suggesting an excess of significance bias; not including the null value in PIs; the largest study is nominally significant, p < 0.05; a low degree of heterogeneity, specifically, I2 value below 50%, Class II involved exceeding 1,000 cases (or over 20,000 participants); significant summary associations as per random-effects calculations, with p < 10−6; the largest study is nominally significant, p < 0.05. Class III involved exceeding 1,000 cases (or over 20,000 participants); significant summary associations as per random-effects calculations, with p < 10−3. Class IV involved any other associations that present a p value lower than 0.05; no significant evidence was defined when p > 0.05.
Results
Of 1,081 studies screened, 286 full-text studies were assessed after duplicate removal, resulting in 8 meta-analyses that examined 15 unique associations between racial discrimination and overall health outcomes; data from one study were directly obtained from the author (Fig. 1 and Table 1). These meta-analyses spanned from 2007 to 2023, covering 113 articles from the USA and the UK (Table 1). In addition, we present the characteristics of systematic reviews measuring racial discrimination among multiple health outcomes (Table 1) [30‒37].
PRISMA 2020 flow diagram for new systematic reviews which included searches of databases and registers only.
PRISMA 2020 flow diagram for new systematic reviews which included searches of databases and registers only.
Characteristics of systematic reviews measuring racial discrimination
First author, year . | Name(s) and timeframe of database search . | Country . | Number of primary studies . | Total sample (sample sizes in the included primary studies; total or range as reported in respective reviews) . | Characteristics of the study populations . | Key finding . |
---|---|---|---|---|---|---|
Rich et al. [34] (2022) | MEDLINE, Embase, Cochrane Library databases from inception to August 1, 2020/manual search of American Association for the Study of Liver Diseases, Digestive Diseases Week, American Society for Clinical Oncology from 2017 to 2019 | USA | 35 | 563,097 | Non-Hispanic. white (white), non-Hispanic black (black), Hispanic, Asian, and others | Black patients with HCC was found to have worse overall survival compared to white patients (pooled HR, 1.08; 95% CI, 1.05–1.12), while Hispanic and Asian patients had better survival outcomes (pooled HR, 0.92; 95% CI, 0.87–0.97 and pooled HR, 0.81; 95% CI, 0.73–0.88, respectively) |
Du XL et al. [30] (2007) | MEDLINE | USA | 10 | 96,464 | African Americans, and Caucasians | African American patients with colon cancer were associated with a higher risk of all-cause mortality compared to Caucasian patients, with a pooled HR of 1.14 (95% CI, 1.00–1.29). Additionally, for colon cancer-specific mortality, African American patients had an HR of 1.13 (95% CI, 1.01–1.28) |
Larik et al. [37] (2023) | PubMed, Cochrane, Scopus from inception to March 2023 | USA | 13 | 238,680 | Black and white patients | Black OHCA patients were associated with a significant decrease in survival to hospital discharge compared to their white counterparts (OR: 0.81; 95% CI: 0.68, 0.96, p = 0.01) |
Jaiswal V et al. [36] (2023) | PubMed, Embase, Cochrane Library, Scopus from inception to November 2022 | USA | 3 | 136,395 | Black and white patients | Black patients with PAD were found to have a significantly higher likelihood of major amputation within 30 days post-procedure compared to white patients (OR, 0.40; 95% CI: 0.19–0.84, p = 0.02). Additionally, white patients had a significantly higher likelihood of MI compared to black patients (OR, 1.29; 95% CI: 1.05–1.58, p = 0.02) |
Shahid I et al. [35] (2022) | PubMed, Scopus from January 2010 to June 2021 | USA | 4 | 52,932 | Black and white patients | Black patients with AMI were not found to have an increased risk of mortality compared to white patients with AMI (HR: 1.02, 95% CI; 0.97–1.08) |
Rich et al. [31] (2018) | MEDLINE, Embase, Cochrane from August 2016 | USA | 34 | 368,569 | Hispanics, whites, and blacks | Racial and ethnic disparities in NAFLD prevalence, severity, and outcomes were observed in the USA. Black individuals had a significantly higher risk of NAFLD incidence compared to white individuals (pooled RR: 1.30; 95% CI, 1.05–1.63). Additionally, Hispanics had higher odds of developing cirrhosis (OR, 2.7; 95% CI, 1.2–5.8) and HCC (OR, 2.5; 95% CI, 1.1–5.5) compared with white individuals. Furthermore, there were conflicting results regarding all-cause mortality among different racial and ethnic groups, with some studies reporting significantly higher hazards of all-cause mortality among black individuals than white individuals, while others reported no significant differences |
Bardol et al. [32] (2020) | Medline, Web of Science, and PsycINFO from January 1960 to January 2019 | UK | 14 | 33,221 | Black, Hispanic (Latino), Asian, Natives, and mixed-race individuals | Subjects who experienced PED were significantly associated with an increased risk of PSs and PEs (OR, 2.29; 95% CI, 1.35–3.88) compared to those who did not perceive such discrimination |
Coimbra et al. [33] (2022) | PubMed, Embase, PsycINFO, and Scopus from September 25, 2021 | USA | 43 | 88,717 | Black, Hispanic, and Asian individuals | Racial discrimination was found to have a small but statistically significant effect on both SI (r = 0.16, 95% CI: 0.12 to 0.19; p < 0.0001) and SAs (r = 0.13, 95% CI: 0.02 to 0.23; p = 0.018). No evidence of publication bias was detected, and fail-safe tests confirmed the robustness of these results. Additionally, analysis of study characteristics revealed that the time frame used to assess SI was the only factor that moderated the effect of RD on SI, with a correlation of r = 0.07 (95% CI: 0.015 to 0.12; p = 0.01) |
First author, year . | Name(s) and timeframe of database search . | Country . | Number of primary studies . | Total sample (sample sizes in the included primary studies; total or range as reported in respective reviews) . | Characteristics of the study populations . | Key finding . |
---|---|---|---|---|---|---|
Rich et al. [34] (2022) | MEDLINE, Embase, Cochrane Library databases from inception to August 1, 2020/manual search of American Association for the Study of Liver Diseases, Digestive Diseases Week, American Society for Clinical Oncology from 2017 to 2019 | USA | 35 | 563,097 | Non-Hispanic. white (white), non-Hispanic black (black), Hispanic, Asian, and others | Black patients with HCC was found to have worse overall survival compared to white patients (pooled HR, 1.08; 95% CI, 1.05–1.12), while Hispanic and Asian patients had better survival outcomes (pooled HR, 0.92; 95% CI, 0.87–0.97 and pooled HR, 0.81; 95% CI, 0.73–0.88, respectively) |
Du XL et al. [30] (2007) | MEDLINE | USA | 10 | 96,464 | African Americans, and Caucasians | African American patients with colon cancer were associated with a higher risk of all-cause mortality compared to Caucasian patients, with a pooled HR of 1.14 (95% CI, 1.00–1.29). Additionally, for colon cancer-specific mortality, African American patients had an HR of 1.13 (95% CI, 1.01–1.28) |
Larik et al. [37] (2023) | PubMed, Cochrane, Scopus from inception to March 2023 | USA | 13 | 238,680 | Black and white patients | Black OHCA patients were associated with a significant decrease in survival to hospital discharge compared to their white counterparts (OR: 0.81; 95% CI: 0.68, 0.96, p = 0.01) |
Jaiswal V et al. [36] (2023) | PubMed, Embase, Cochrane Library, Scopus from inception to November 2022 | USA | 3 | 136,395 | Black and white patients | Black patients with PAD were found to have a significantly higher likelihood of major amputation within 30 days post-procedure compared to white patients (OR, 0.40; 95% CI: 0.19–0.84, p = 0.02). Additionally, white patients had a significantly higher likelihood of MI compared to black patients (OR, 1.29; 95% CI: 1.05–1.58, p = 0.02) |
Shahid I et al. [35] (2022) | PubMed, Scopus from January 2010 to June 2021 | USA | 4 | 52,932 | Black and white patients | Black patients with AMI were not found to have an increased risk of mortality compared to white patients with AMI (HR: 1.02, 95% CI; 0.97–1.08) |
Rich et al. [31] (2018) | MEDLINE, Embase, Cochrane from August 2016 | USA | 34 | 368,569 | Hispanics, whites, and blacks | Racial and ethnic disparities in NAFLD prevalence, severity, and outcomes were observed in the USA. Black individuals had a significantly higher risk of NAFLD incidence compared to white individuals (pooled RR: 1.30; 95% CI, 1.05–1.63). Additionally, Hispanics had higher odds of developing cirrhosis (OR, 2.7; 95% CI, 1.2–5.8) and HCC (OR, 2.5; 95% CI, 1.1–5.5) compared with white individuals. Furthermore, there were conflicting results regarding all-cause mortality among different racial and ethnic groups, with some studies reporting significantly higher hazards of all-cause mortality among black individuals than white individuals, while others reported no significant differences |
Bardol et al. [32] (2020) | Medline, Web of Science, and PsycINFO from January 1960 to January 2019 | UK | 14 | 33,221 | Black, Hispanic (Latino), Asian, Natives, and mixed-race individuals | Subjects who experienced PED were significantly associated with an increased risk of PSs and PEs (OR, 2.29; 95% CI, 1.35–3.88) compared to those who did not perceive such discrimination |
Coimbra et al. [33] (2022) | PubMed, Embase, PsycINFO, and Scopus from September 25, 2021 | USA | 43 | 88,717 | Black, Hispanic, and Asian individuals | Racial discrimination was found to have a small but statistically significant effect on both SI (r = 0.16, 95% CI: 0.12 to 0.19; p < 0.0001) and SAs (r = 0.13, 95% CI: 0.02 to 0.23; p = 0.018). No evidence of publication bias was detected, and fail-safe tests confirmed the robustness of these results. Additionally, analysis of study characteristics revealed that the time frame used to assess SI was the only factor that moderated the effect of RD on SI, with a correlation of r = 0.07 (95% CI: 0.015 to 0.12; p = 0.01) |
AMI, acute myocardial infarction; CI, confidence interval; HCC, hepatocellular carcinoma; HR, hazard ratio; MI, myocardial infarction; NAFLD; nonalcoholic fatty liver disease; OHCA, out-of-hospital cardiac arrest; OR, odds ratio; PAD, peripheral artery disease; PED, perceived ethnic discrimination; PEs, psychotic experiences; PS, psychotic symptom; SA, suicidal attempt.
Utilizing the AMSTAR2 evaluation method, our study determined the quality of the original meta-analysis; those articles were high quality in two meta-analyses, moderate quality in three meta-analyses, and low quality in two meta-analyses (Table 2 and online suppl. Table 2). In the analysis, three meta-analytical associations (20.00%) showed suggestive evidence, five meta-analytical associations (33.33%) met the criteria for weak evidence, and seven meta-analytical associations (46.67%) were found to have nonsignificant evidence (online suppl. Table 3). Except for the mortality of NAFLD of Hispanics, the shape of the p-curve was highly right-skewed for the binomial metrics (p < 0.25), indicating no evidence of p-hacking. In our re-analysis of the thirteen associations through random effects analyses, 40.00% (6/15) demonstrated significant heterogeneity with an I2 value greater than 75 (I2 > 75). Using Egger’s regression test, we observed statistical evidence of publication bias in none of the studies included. The forest plot, funnel plot, and p curve for each association are shown in online supplementary Figures 1–15.
Description of total meta-analysis to investigate the racial discrimination-associated comorbidity outcome
Outcome . | First author . | Published year . | Included countries . | AMSTAR2 . |
---|---|---|---|---|
1. Oncology | ||||
Mortality of HCCa | Rich NE | 2022 | USA | High |
Mortality of HCCb | Rich NE | 2022 | USA | High |
Mortality of HCCc | Rich NE | 2022 | USA | High |
Early stage of HCCd | Rich NE | 2022 | USA | High |
Early stage of HCCe | Rich NE | 2022 | USA | High |
Early stage of HCCf | Rich NE | 2022 | USA | High |
Mortality of colon cancer-specific | Du XL | 2007 | USA | Moderate |
2. Cardiology | ||||
Mortality of OHCA | Larik MO | 2023 | USA | High |
Mortality of peripheral artery diseasesg | Jaiswal V | 2023 | USA | Low |
Mortality of AMIh | Shahid I | 2022 | USA | Low |
3. Gastroenterology | ||||
NAFLDi | Rich NE | 2018 | USA | High |
NAFLDj | Rich NE | 2018 | USA | High |
4. Mental Health | ||||
PEsk | Bardol O | 2020 | UK | Low |
SIl | Bruno M | 2022 | USA | Moderate |
Suicidal attemptm | Bruno M | 2022 | USA | Moderate |
Outcome . | First author . | Published year . | Included countries . | AMSTAR2 . |
---|---|---|---|---|
1. Oncology | ||||
Mortality of HCCa | Rich NE | 2022 | USA | High |
Mortality of HCCb | Rich NE | 2022 | USA | High |
Mortality of HCCc | Rich NE | 2022 | USA | High |
Early stage of HCCd | Rich NE | 2022 | USA | High |
Early stage of HCCe | Rich NE | 2022 | USA | High |
Early stage of HCCf | Rich NE | 2022 | USA | High |
Mortality of colon cancer-specific | Du XL | 2007 | USA | Moderate |
2. Cardiology | ||||
Mortality of OHCA | Larik MO | 2023 | USA | High |
Mortality of peripheral artery diseasesg | Jaiswal V | 2023 | USA | Low |
Mortality of AMIh | Shahid I | 2022 | USA | Low |
3. Gastroenterology | ||||
NAFLDi | Rich NE | 2018 | USA | High |
NAFLDj | Rich NE | 2018 | USA | High |
4. Mental Health | ||||
PEsk | Bardol O | 2020 | UK | Low |
SIl | Bruno M | 2022 | USA | Moderate |
Suicidal attemptm | Bruno M | 2022 | USA | Moderate |
AMSTAR2, A Measurement Tool Assessment Systemic Reviews 2; AMI, acute myocardial infarction; PE, psychotic experience; OHCA, out-of-hospital cardiac arrest.
aAmong black patients with disparities on the cancer care continuum (compared with white [reference] patients).
bAmong Hispanic patients with disparities on the cancer care continuum (compared with white [reference] patients).
cAmong Asian patients with disparities on the cancer care continuum (compared with white [reference] patients).
dAt diagnosis, among black patients with disparities on the cancer care continuum (compared with white [reference] patients).
eAt diagnosis, among Hispanic patients with disparities on the cancer care continuum (compared with white [reference] patients).
fAt diagnosis, among Asian patients with disparities on the cancer care continuum (compared with white [reference] patients).
gMortality of patients, who have experienced disparities, in treatment within 30 days.
hAmong black patients who have experienced disparities in treatment (compared with white [reference] patients).
iAmong Hispanic patients with socioeconomic status/differential access to health care (compared with white [reference] patients).
jAmong black patients with socioeconomic status/differential access to health care (compared with white [reference] patients).
kPatients with significant variations of differential exposures to socio-environmental risk factors, who do not reach the threshold for clinical disorders, the self-reported delusional or hallucinatory symptoms.
lRacial discrimination and its association with increased SI (compared to white [reference] patients).
mRacial discrimination and its association with increased suicidal attempts (compared to white [reference] patients).
We categorized the outcomes into four domains: oncology, cardiology, gastroenterology, and mental health, within identifying six significant associations with racial discrimination (Table 3 and online suppl. Table 4). The results are consolidated into evidence maps in our umbrella review, providing a structured overview of how racial discrimination impacts diverse health outcomes (Table 4). Eight meta-analysis articles have covered over 1 million individuals with 15 unique health outcomes related to racial discrimination. These outcomes included mortality of HCC over multiple races (black, Hispanic, and Asian) compared to white patients, early-stage diagnosis of HCC over multiple races (black, Hispanic, and Asian) who experience disparities on the cancer care continuum compared to white patients, mortality of out-of-hospital cardiac arrest who had treatment within 30 days, mortality of peripheral artery diseases, mortality of acute myocardial infarction, NAFLD over multiple races (black and Hispanic), psychotic experiences, suicidal ideation (SI), and suicidal attempt. Our reanalyses identified eight statistically significant associations, highlighting the impact of racial discrimination on health outcomes (Table 4).
Finding across meta-analyses of observational studies on health outcomes associated with racial discrimination
Outcome . | Author, year . | Sample size . | Effect size . | CEn . | |
---|---|---|---|---|---|
k . | n . | eOR (95% CI) . | |||
1. Oncology | |||||
Mortality of HCCa | Rich NE, 2022 | 17 | 284,827 | 1.10 (1.06 to 1.13) | IV |
Mortality of HCCb | Rich NE, 2022 | 18 | 302,123 | 0.94 (0.87 to 1.01) | NS |
Mortality of HCCc | Rich NE, 2022 | 11 | 247,412 | 0.83 (0.72 to 0.96) | III |
Early stage of HCCd | Rich NE, 2022 | 14 | 44,141 | 0.77 (0.64 to 0.92) | III |
Early stage of HCCe | Rich NE, 2022 | 13 | 25,386 | 0.87 (0.74 to 1.04) | NS |
Early stage of HCCf | Rich NE, 2022 | 6 | 46,884 | 1.00 (0.86 to 1.16) | NS |
Mortality of colon cancer-specific | Du XL, 2007 | 5 | 35,984 | 1.13 (0.98 to 1.31) | NS |
2. Cardiology | |||||
Mortality of OHCA | Larik MO, 2023 | 4 | 157,981 | 1.19 (0.40 to 3.52) | NS |
Mortality of peripheral artery diseasesg | Jaiswal V, 2023 | 3 | 1,797 | 1.10 (0.51 to 2.39) | NS |
Mortality of AMIh | Shahid I, 2022 | 4 | 52,932 | 1.02 (0.95 to 1.10) | NS |
3. Gastroenterology | |||||
NAFLDi | Rich NE, 2018 | 7 | 39,877 | 1.47 (1.35 to 1.61) | IV |
NAFLDj | Rich NE, 2018 | 5 | 731 | 0.74 (0.69 to 0.80) | IV |
4. Mental Health | |||||
PEsk | Bardol O, 2020 | 14 | 12,923 | 2.40 (1.87 to 3.07) | IV |
SIl | Bruno M, 2022 | 39 | 59,164 | 1.80 (1.63 to 2.00) | III |
Suicidal attemptm | Bruno M, 2022 | 15 | 30,574 | 1.61 (1.25 to 2.07) | IV |
Outcome . | Author, year . | Sample size . | Effect size . | CEn . | |
---|---|---|---|---|---|
k . | n . | eOR (95% CI) . | |||
1. Oncology | |||||
Mortality of HCCa | Rich NE, 2022 | 17 | 284,827 | 1.10 (1.06 to 1.13) | IV |
Mortality of HCCb | Rich NE, 2022 | 18 | 302,123 | 0.94 (0.87 to 1.01) | NS |
Mortality of HCCc | Rich NE, 2022 | 11 | 247,412 | 0.83 (0.72 to 0.96) | III |
Early stage of HCCd | Rich NE, 2022 | 14 | 44,141 | 0.77 (0.64 to 0.92) | III |
Early stage of HCCe | Rich NE, 2022 | 13 | 25,386 | 0.87 (0.74 to 1.04) | NS |
Early stage of HCCf | Rich NE, 2022 | 6 | 46,884 | 1.00 (0.86 to 1.16) | NS |
Mortality of colon cancer-specific | Du XL, 2007 | 5 | 35,984 | 1.13 (0.98 to 1.31) | NS |
2. Cardiology | |||||
Mortality of OHCA | Larik MO, 2023 | 4 | 157,981 | 1.19 (0.40 to 3.52) | NS |
Mortality of peripheral artery diseasesg | Jaiswal V, 2023 | 3 | 1,797 | 1.10 (0.51 to 2.39) | NS |
Mortality of AMIh | Shahid I, 2022 | 4 | 52,932 | 1.02 (0.95 to 1.10) | NS |
3. Gastroenterology | |||||
NAFLDi | Rich NE, 2018 | 7 | 39,877 | 1.47 (1.35 to 1.61) | IV |
NAFLDj | Rich NE, 2018 | 5 | 731 | 0.74 (0.69 to 0.80) | IV |
4. Mental Health | |||||
PEsk | Bardol O, 2020 | 14 | 12,923 | 2.40 (1.87 to 3.07) | IV |
SIl | Bruno M, 2022 | 39 | 59,164 | 1.80 (1.63 to 2.00) | III |
Suicidal attemptm | Bruno M, 2022 | 15 | 30,574 | 1.61 (1.25 to 2.07) | IV |
CE, class and quality of evidence; CI, confidence interval; DL, Der Simonian and Laird; HS, Hartung-Knapp-Sidik-Jonkman; OR, odds ratio; RR, risk ratio; AMI, acute myocardial infarction; PE psychotic experience; OHCA, out-of-hospital cardiac arrest.
The numbers in bold indicate a significant difference (p < 0.05).
aAmong black patients with disparities on the cancer care continuum (compared with white [reference] patients).
bAmong Hispanic patients with disparities on the cancer care continuum (compared with white [reference] patients).
cAmong Asian patients with disparities on the cancer care continuum (compared with white [reference] patients).
dAt diagnosis, among black patients with disparities on the cancer care continuum (compared with white [reference] patients).
eAt diagnosis, among Hispanic patients with disparities on the cancer care continuum (compared with white [reference] patients).
fAt diagnosis, among Asian patients with disparities on the cancer care continuum (compared with white [reference] patients).
gMortality of patients who have experienced disparities in treatment within 30 days.
hAmong black patients who have experienced disparities in treatment (compared with white [reference] patients).
iAmong Hispanic patients with socioeconomic status/differential access to health care (compared with white [reference] patients).
jAmong black patients with socioeconomic status/differential access to health care (compared with white [reference] patients).
kPatients with significant variations of differential exposures to socio-environmental risk factors, who do not reach the threshold for clinical disorders, the self-reported delusional or hallucinatory symptoms.
lRacial discrimination and its association with increased SI (compared to white [reference] patients).
mRacial discrimination and its association with increased suicidal attempts (compared to white [reference] patients).
nClass and quality of evidence: Class I (convincing evidence): >1,000 cases (or >20,000 participants for continuous outcomes); statistical significance at p < 10−6 (random effects); no evidence of small study effects and excess significance bias; 95% prediction interval excluded null value; no large heterogeneity (I2 < 50%). Class II (highly suggestive evidence): >1,000 cases (or >20,000 participants for continuous outcomes); statistical significance at p < 10−6 (random effects); largest study with 95% confidence interval excluding null value. Class III (suggestive evidence): >1,000 cases (or >20,000 participants for continuous outcomes); statistical significance at p < 0.001. Class IV (weak evidence): remaining significant associations with p < 0.05. NS (nonsignificant): p > 0.05.
Evidence maps of umbrella review of associations between racial discrimination and health outcomes
Outcome . | eOR (95% CI) . | CEn . | Direction . |
---|---|---|---|
1. Oncology | |||
Mortality of HCCa | 1.10 (1.06 to 1.13) | IV | Associated |
Mortality of HCCb | 0.94 (0.87 to 1.01) | NS | Not associated |
Mortality of HCCc | 0.83 (0.72 to 0.96) | III | Associated |
Early stage of HCCd | 0.77 (0.64 to 0.92) | III | Associated |
Early stage of HCCe | 0.87 (0.74 to 1.04) | NS | Not associated |
Early stage of HCCf | 1.00 (0.86 to 1.16) | NS | Not associated |
Mortality of colon cancer-specific | 1.13 (0.98 to 1.31) | NS | Not associated |
2. Cardiology | |||
Mortality of OHCA | 1.19 (0.40 to 3.52) | NS | Not associated |
Mortality of peripheral artery diseasesg | 1.10 (0.51 to 2.39) | NS | Not associated |
Mortality of AMIh | 1.02 (0.95 to 1.10) | NS | Not associated |
3. Gastroenterology | |||
NAFLDi | 1.47 (1.35 to 1.61) | IV | Associated |
NAFLDj | 0.74 (0.69 to 0.80) | IV | Associated |
4. Mental Health | |||
PEsk | 2.40 (1.87 to 3.07) | IV | Associated |
SIl | 1.80 (1.63 to 2.00) | III | Associated |
Suicidal attemptm | 1.61 (1.25 to 2.07) | IV | Associated |
Outcome . | eOR (95% CI) . | CEn . | Direction . |
---|---|---|---|
1. Oncology | |||
Mortality of HCCa | 1.10 (1.06 to 1.13) | IV | Associated |
Mortality of HCCb | 0.94 (0.87 to 1.01) | NS | Not associated |
Mortality of HCCc | 0.83 (0.72 to 0.96) | III | Associated |
Early stage of HCCd | 0.77 (0.64 to 0.92) | III | Associated |
Early stage of HCCe | 0.87 (0.74 to 1.04) | NS | Not associated |
Early stage of HCCf | 1.00 (0.86 to 1.16) | NS | Not associated |
Mortality of colon cancer-specific | 1.13 (0.98 to 1.31) | NS | Not associated |
2. Cardiology | |||
Mortality of OHCA | 1.19 (0.40 to 3.52) | NS | Not associated |
Mortality of peripheral artery diseasesg | 1.10 (0.51 to 2.39) | NS | Not associated |
Mortality of AMIh | 1.02 (0.95 to 1.10) | NS | Not associated |
3. Gastroenterology | |||
NAFLDi | 1.47 (1.35 to 1.61) | IV | Associated |
NAFLDj | 0.74 (0.69 to 0.80) | IV | Associated |
4. Mental Health | |||
PEsk | 2.40 (1.87 to 3.07) | IV | Associated |
SIl | 1.80 (1.63 to 2.00) | III | Associated |
Suicidal attemptm | 1.61 (1.25 to 2.07) | IV | Associated |
CI, confidence interval; eOR, equivalent odds ratio; AMI, acute myocardial infarction; PE, psychotic experience; OHCA, out-of-hospital cardiac arrest.
The numbers in bold indicate a significant difference (p < 0.05). The gradient of the heatmap visualizes the levels of reported estimates (eOR), with a continuous scale from light red (low) to dark red (high).
aAmong black patients with disparities on the cancer care continuum (compared with white [reference] patients).
bAmong Hispanic patients with disparities on the cancer care continuum (compared with white [reference] patients).
cAmong Asian patients with disparities on the cancer care continuum (compared with white [reference] patients).
dAt diagnosis, among black patients with disparities on the cancer care continuum (compared with white [reference] patients).
eAt diagnosis, among Hispanic patients with disparities on the cancer care continuum (compared with white [reference] patients).
fAt diagnosis, among Asian patients with disparities on the cancer care continuum (compared with white [reference] patients).
gMortality of patients who have experienced disparities in treatment within 30 days.
hAmong black patients who have experienced disparities in treatment (compared with white [reference] patients).
iAmong Hispanic patients with socioeconomic status/differential access to health care (compared with white [reference] patients).
jAmong black patients with socioeconomic status/differential access to health care (compared with white [reference] patients).
kPatients with significant variations of differential exposures to socio-environmental risk factors, who do not reach the threshold for clinical disorders, the self-reported delusional or hallucinatory symptoms.
lRacial discrimination and its association with increased SI (compared to white [reference] patients).
mRacial discrimination and its association with increased suicidal attempts (compared to white [reference] patients).
nClass and quality of evidence: Class I (convincing evidence): >1,000 cases (or >20,000 participants for continuous outcomes); statistical significance at p < 10−6 (random effects); no evidence of small study effects and excess significance bias; 95% prediction interval excluded null value; no large heterogeneity (I2 < 50%). Class II (highly suggestive evidence): >1,000 cases (or >20,000 participants for continuous outcomes); statistical significance at p < 10−6 (random effects); largest study with 95% confidence interval excluding null value. Class III (suggestive evidence): >1,000 cases (or >20,000 participants for continuous outcomes); statistical significance at p < 0.001. Class IV (weak evidence): remaining significant associations with p < 0.05. NS (nonsignificant): p > 0.05.
Oncology
Racial discrimination was significantly associated with three health outcomes, which are mortality of HCC among black patients compared to white (reference) patients (eOR, 1.10 [95% CI, 1.06 to 1.13], CE = weak), mortality of HCC among Asian patients compared to white patients (eOR, 0.83 [95% CI, 0.72 to 0.96], CE = suggestive), and early stage of HCC diagnosed among black patients with disparities on the cancer care continuum, compared to white patients (eOR, 0.77 [95% CI, 0.64 to 0.92], CE = suggestive).
Cardiology
Among three racial discriminations associated with cardiological health outcomes, all had nonsignificant CE. No health outcomes showed statistically significant associations with racial discrimination.
Gastroenterology
Among two racial discrimination-associated gastroenterological health outcomes, both had weak CE. Racial discrimination was significantly and negatively associated with both clinical outcomes, which are among Hispanic patients with NAFLD (eOR, 1.47 [95% CI, 1.35 to 1.61], CE = weak) and black patients (eOR, 0.74 [95% CI, 0.69 to 0.80], CE = weak) with socioeconomic status/differential access to health care, compared to white patients.
Mental Health
For mental health outcomes, racial discriminations were significantly associated with increased odds of psychotic experiences (2.40 [1.87 to 3.07], CE = weak), SI (1.80 [1.63 to 2.00], CE = suggestive), and suicidal attempt (1.61 [1.25 to 2.07], CE = weak). Numerous significant associations were from weak to suggestive evidence levels, indicating variability in the evidence.
Discussion
Findings and Explanation
To our knowledge, our study is the first umbrella review on the relationship between racial discrimination and health outcomes. While previous reviews have focused on specific domains, such as sole examination of mental health outcomes and biomarkers or analysis only among the USA, and are outdated, our review provides a comprehensive highlight across multiple health disparities impacting ethnic minority groups throughout the globe [12, 38‒40]. Eight meta-analyses covering over 1 million participants identified 15 potential associations between racial discrimination and health outcomes. Of 15 previously reported associations, racial discrimination was associated with eight health outcomes. We found five notable health outcomes that were significantly associated with racial discrimination, which are the mortality rate, NAFLD, PEs, SI, and suicide attempts. Importantly, we also found three health outcomes: HCC-related death among Asian patients compared to white patients, early-stage diagnosis of HCC among black patients compared to white patients, and prevalence of NAFLD among black patients with socioeconomic status/differential access to health care, showed significantly lower risk with suggestive or weak CEs, respectively.
Plausible Underlying Mechanisms
Numerous studies have explored the link between racial discrimination and health outcomes, showing that racial discrimination is associated with poorer health. Numerous models have been proposed to help conceptualize the pathways between racial discrimination and health, which include race-based trauma, minority stress theory, and Hatzenbuehler’s integrative mediation framework [41], among other models. However, the pathways are complex and still emerging [42].
Our study shows a significantly higher risk of mortality from HCC among black patients compared to white patients, part of which is associated with racial discrimination. While multiple factors might affect the prevalence of HCC, it can be specifically attributed to the prevalence of hepatitis B and C. HCC, the third most common cause of cancer-related deaths worldwide, is significantly influenced by the presence of chronic hepatitis B and C [43, 44]. Research indicates that Africans, African Americans, and Sub-Saharan Africans have a high prevalence of hepatitis B virus [45]. Similarly, hepatitis C virus prevalence is notably higher among African Americans, highlighting the association between these viral infections and HCC risk within these populations. This trend can be related to socioeconomic disparities and structural racism, leading to limited health care access, missed opportunities for screening and vaccination, and higher engagement in high-risk behaviors. Furthermore, the increased engagement in high-risk behaviors, such as injection drug use, is associated with a risk of hepatitis B virus and hepatitis C virus infections [46]. Additionally, the chronic stress from perceived racial discrimination, which affects black individuals of all ages, has been linked to higher alcohol consumption, contributing to the observed associations between racial discrimination and health disparities in these populations [47]. The higher prevalence of HCC among black individuals, driven by factors like health disparities and socioeconomic conditions, correlates with increased mortality rates, linking it closely to racial discrimination. Interestingly, the trend inversely appears in early-stage HCC diagnoses among black populations, indicating a complex relationship between racial discrimination and health outcomes in HCC [48, 49]. Among various factors that might contribute to such outcomes, systematic racism can be taken as an example: black patients with hepatitis C virus being diagnosed with HCC at earlier liver disease stages yet facing delayed detection due to less rigorous screening not tailored to their risk profile. For instance, the common Fibrosis Index Based on 4 Factors threshold excludes nearly one-third of black patients from HCC screening, highlighting a health care system gap in adequately addressing early-stage HCC diagnosis disparities among black individuals [50].
NAFLD in the Hispanic population shows a higher risk when individuals experience racial discrimination. This link may be due to factors rooted in institutional and structural racism, including access to healthy foods, health care access, and the allostatic load borne by those in impoverished conditions [51, 52]. While both Hispanic and black populations are minorities, a lower risk exists between NAFLD and the racial discrimination-experienced black population is observed, contrasting with Hispanics. In terms of the risk of NAFLD among the black population compared to the white population, while it is common knowledge that NAFLD disease burden is related to metabolic syndrome components such as obesity, diabetes, and dyslipidemia, a notable finding is that some studies suggest black American populations (who have higher rates of diabetes and vs. white populations) may have significantly lower risk of NAFLD. This suggests an explanation through racial discrimination mixed of structural, cultural, and interpersonal racism; for instance, institutional racism can produce unresponsive services and generate mistrust of the black population [53‒56]. The expansion of managed care and for-profit health care, along with historical unethical medical research [57, 58] may have contributed to the observed negative association between NAFLD and racial discrimination, resulting in less detection of NAFLD as more racial discrimination is presented.
In addition, five ethnic groups (Bangladeshi, black Caribbean, Indian, Irish, and Pakistani) experiencing racial discrimination showed a higher vulnerability to PEs, SI, and suicide attempts, suggesting discrimination is associated with increased PE risk through limiting access to health care and resources, exposure to risk factors, and direct stress effects [38]. It is possible to claim that discrimination is associated with limited access to health care, life-promoting resources, and education, resulting in increased exposure to other risk factors during the early stage of developing PEs [57, 59‒61]. Also, social stressors and perceived ethnic discrimination might cause direct, significant emotional stress, leading individuals experiencing racial discrimination to have negative mental health outcomes; such outcomes could also be associated with functional and structural changes in the central nervous system [62].
Policy Implication
Further research is needed to consider various confounding factors and establish robust causation between health outcomes and racial discrimination. Additionally, the ethical implications of our findings highlight the urgent need for health care policies to address and mitigate the impacts of racial discrimination. Given the observed associations found, governments should address these health disparities with targeted interventions to eliminate racism in all its forms and facets, as well as efforts to provide tailored health services in communities. Possible policies could include implementing mandatory cultural competency training among health care providers, establishing community health worker programs, and developing standardized protocols for identifying and addressing discrimination in health care settings. Such findings would help inform the development of comprehensive anti-racist interventions and health care policies that prioritize equity and inclusivity.
Strengths and Limitations
Our umbrella review, a first of its kind on racial discrimination factors, provides evidence of the association of health outcomes with racial discrimination. However, as an umbrella review, it inherently relies on existing meta-analyses, which may introduce limitations related to the scope and quality of those underlying studies. Yet, our study is limited by its keyword scope, focusing only on “racism” and “racial discrimination,” potentially overlooking variations like “perceived skin tone disparities/discrimination” [63, 64], “perceived ethnic discrimination” [32], and “perceived colorism” [65], limiting our search to specific terms related to racism might have narrowed the scope of our findings. However, our focus on structural, institutional, cultural, and interpersonal racism required a precise approach, excluding broader or related terms to maintain a consistent definition throughout our research. Additionally, the manuscript predominantly includes studies conducted in the USA and the UK, which limits the generalizability of the findings to a global context. As it is well known that structural and cultural dimensions vary among regions and areas, it might diminish the relevance of the findings for non-Western populations; such limitation calls for the need for more nuanced contextualization, which we address in the discussion section by exploring regional variation and their implication. Moreover, the inclusion of papers under “racial discrimination” that discuss both racism-related and genetic-related discrimination led to some ambiguity in the analysis of the meta-analyses, potentially blurring the distinctions between these types of discrimination. Not directly assessing the original quality of texts within included meta-analyses might affect the precision of identified issues – also, methodological variances in evaluating each sample size of the meta-analyses, heterogeneity, and statistical significance. If the mathematical method used in this umbrella review changes, efficacy certification could alter the efficacy conclusions. Although our umbrella review highlights the association between health outcomes and racial discrimination, causation remains to be further investigated, as discussed frequently above. The regional focus on North America and Europe also restricts a comprehensive global understanding of the impact of racial discrimination on health.
Conclusions
Our umbrella review identified patterns between racial discrimination and health outcomes, revealing weak and nonsignificant associations based on various methodological approaches. We also observed eight notable associations between racial discrimination and health outcomes. These findings underscore the complexity of these relationships and highlight the necessity for further research to understand such associations better while acknowledging the limitations of current observational evidence and the need for rigorous study designs to establish potential causal pathways.
Statement of Ethics
This systematic review article does not require Institutional Review Board approval. Our systematic review and meta-analysis protocol was registered with PROSPERO (Registration No. CRD42024513366).
Conflict of Interest Statement
We declare no competing interests.
Funding Sources
This research was supported by grants from the National Research Foundation of Korea (NRF) funded by the Korea government (MSIT; RS–2023–00248157) and the Ministry of Science and ICT (MSIT), Korea, under the Information Technology Research Center (ITRC) support program (IITP-2024-RS-2024–00438239) supervised by the Institute for Information & Communications Technology Planning & Evaluation (IITP). The funders had no role in study design, data collection, data analysis, data interpretation, or writing of the report.
Author Contributions
Dr. Dong Keon Yon had full access to all of the data in the study and took responsibility for the integrity of the data and the accuracy of the data analysis. All the authors approved the final version before submission. Study concept and design; acquisition, analysis, or interpretation of data; drafting of the manuscript; and statistical analysis: Jun Hyuk Lee, Hyeri Lee, Yejun Son, Jiseung Kang, and Dong Keon Yon; critical revision of the manuscript for important intellectual content: all the authors; study supervision: Dong Keon Yon and Jiseung Kang supervised the study and those are the guarantors for this study. Jun Hyuk Lee, Hyeri Lee, and Yejun Son contributed as co-first authors. Dong Keon Yon and Jiseung Kang contributed equally as the corresponding authors. The corresponding authors attest that all listed authors meet authorship criteria and that no others meeting the criteria have been omitted.
Additional Information
Jun Hyuk Lee, Hyeri Lee, and Yejun Son are joint first authors.
Data Availability Statement
The data used in this review were derived from publicly available systematic reviews and meta-analyses.