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Cardiomyopathy among first- and second-generation immigrants in Sweden: a nationwide total population study

Abstract

Purpose

We aimed to analyze the risk of cardiomyopathies (CMPs) among first-generation and second-generation immigrants.

Methods

All individuals aged 18 years of age and older, n = 6,123,661 in the first-generation study, and n = 4,587,764 in the second-generation study were analyzed. CMP was defined as at least one registered diagnosis in the National Patient Register between January 1, 1998 and December 31, 2018. Cox regression analysis was used to estimate the relative risk (hazard ratios (HR) with 99% confidence intervals (CI)) of incident CMP with adjustments made for age, cancer, other comorbidities, and sociodemographic factors.

Results

In the first-generation study, a total of 33,321 CMP cases were registered, 20,780 men and 12,541 women, where the fully adjusted models showed HRs (99% CI) for all foreign-born men of 0.92 (0.86–0.98) and for women of 0.90 (0.83–0.98). For dilated CMP, the risk was higher for men from Nordic countries, more specifically men from Finland, and lower for men and women from Asia. For hypertrophic CMP, the risk was higher for men from Africa and Asia. For other types of CMPs, the risk was lower in men and women from Asia. In the second-generation study, a total of 26,559 cases were registered (17,620 men and 8939 women), with no significant differences overall or among specific groups, when Swedish-born with foreign-born parents were compared to Swedish-born with Swedish-born parents.

Conclusions

We observed a generally lower risk of CMPs among foreign-born individuals, but with a higher risk especially for hypertrophic CMPs for men from Africa and Asia, and a higher risk of dilated CMP for men from Nordic countries.

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Introduction

Cardiomyopathies (CMPs) are important as causes of congestive heart failure (CHF) and are crucial to identify in order to treat properly. Globally, as regards background factors for CHF, CMPs are most common in high-income Asian Pacific countries, Sub-Saharan Africa, Latin America and the Caribbean, while lower in other regions of the world [1].

CMPs can be classified in different ways, with the proposal from the European Society of Cardiology (ESC) dividing them into hypertrophic CMP (HCM), dilated CMP (DCM), arrhythmogenic right ventricular CMP (ARVC), restrictive CMP (RCM) and unclassified [2]. There are familial (genetic) dilated types [3], hypertrophic types [4], and non-familial types. Hypertrophic CMP is the most common inherited heart disease [5].

Valvular heart diseases were historically caused by rheumatic heart diseases as a consequence of infections, often by streptococci. However, acute rheumatic fever has decreased during recent decades in industrialized or developed countries, while it is still more common in other parts of the world [6].

CMP is associated with different diseases [7]. Substance abuse is associated with cardiac toxicity, mostly alcohol CMP, which has been described as one of the main causes of non-ischemic dilated CMP [8].

There are several other types of CMPs, including familial Mediterranean fever, which is an autoinflammatory disorder [9], atrial arrhythmogenic right ventricular CMP [10], or Takotsubo CMP [11], thus making it important to study first and second-generation immigrants. Furthermore, many other diseases are associated with CMPs, such as different types of metabolic diseases like amyloidosis, sarcoidosis [12], hemochromatosis, connective tissue disorders, and endocrinological diseases such as diabetes [13, 14] or thyroid disorders as well as cancer.

As there is a paucity of studies on CMP in immigrants in Sweden and other Western countries, this study will fill a knowledge gap. Enhanced knowledge of the risk of CMPs is important both for healthcare and other parts of society in Sweden as well as for other Western countries. Accordingly, our study aimed to estimate the risk of CMPs in general among foreign-born individuals in Sweden compared to Swedes and also sub-categorized as dilated, hypertrophic and other types of CMPs. We also aimed to study CMPs in second-generation immigrants and compare Swedish-born individuals with Swedish-born parents, to obtain more knowledge of the potential genetic and environmental origin of clinically observed CMPs.

Methods

We used national Swedish registers, i.e. the Swedish National Patient Register (NPR), and the Swedish Total Population Register. The NPR includes diagnoses from all Swedish hospitals, i.e. for in-patients since 1987 and for out-patients from 2001 onwards. The Total Population Register includes data on country of origin and sociodemographic factors on all persons in Sweden with a residence permit. Our study was conducted using pseudonymized data. All methods were performed in accordance with the relevant ethical guidelines and regulations in Sweden.

Study population

We included individuals 18 years of age and older and excluded individuals with a diagnosis of CMP before 1998, in total 5037 individuals. A total of 6,123,661 individuals were included in the first-generation study, 2,971,780 men and 3,151,881 women. In the second-generation study, a total of 4,587,764 individuals were included, 2,345,774 men and 2,241,990 women.

Outcomes

We included the following diagnoses (with ICD-10 codes): 1. Dilated CMP (I42.0); 2. Hypertrophic CMP (I42.1–I42.2); and 3. All other types of CMPs (I42.3–I42.9, I43). We also sub-categorized patients into these three main groups. There is no national policy on response to identifying an index case of cardiomyopathy.

Sociodemographic variables

The population was stratified by sex.

Age was used as a continuous variable in the analysis.

Educational attainment was categorized as ≤ 9 years (partial or complete compulsory schooling), 10–12 years (partial or complete secondary schooling) and > 12 years (attendance at college and/or university).

Geographic region of residence was included to adjust for possible regional differences in hospital admissions and was categorized as the following: (1) large cities, (2) southern Sweden and (3) northern Sweden. Large cities were defined as municipalities with a population of > 200,000 and comprised the three largest cities in Sweden: Stockholm, Gothenburg, and Malmö.

Neighborhood socioeconomic levels were derived from Small Area Market Statistics (SAMS). The average population in each SAMS neighborhood is approximately 2000 people for Stockholm and 1000 people for the rest of Sweden. A summary index was calculated to characterize neighborhood-level deprivation. The index was categorized into three groups: more than one standard deviation (SD) below the mean (high SES or low deprivation level), more than one SD above the mean (low SES or high deprivation level), and within one SD of the mean (middle SES or middle deprivation level) [15], with neighborhood status classified as high, middle, or low SES, corresponding to the categories low, middle, and high deprivation in the index [16].

Comorbidities

We included the following comorbidities (with ICD-10 codes): hypertension (I10–I19), coronary heart disease (CHD I20–I25), chronic rheumatic heart disease (I05–I09), non-rheumatic valvular heart diseases (I34–I39), atrial fibrillation (AF I48), congestive heart disease (CHF I50, I11.0), stroke (I60–I69), diabetes mellitus (E10–E14), thyroid disorders (hypothyroidism E02–E03 and hyperthyroidism E05), chronic obstructive pulmonary disease (COPD J40–J47), alcoholism and related disorders (F10, K70), systemic connective tissue disorders (M30–M36), amyloidosis (E85), sarcoidosis (D86), hemochromatosis (E83.1), cancers (C00–C97) and Chagas disease (B57). All types of cancers (C00–C97) were also included as they represent a major cause of death in both Sweden and most other countries.

Statistical analysis

The number of cases of CMP in the first-generation study was presented for all groups and across baseline subject characteristics. We used Cox regression analysis with Hazard Ratios (HRs) and 99% Confidence Intervals (99% CI) to estimate the risk of incident CMPs in different immigrant groups compared to the Swedish-born population, and in second-generation immigrants compared to Swedish-born individuals with Swedish-born parents. All analyzes were stratified by sex. Three models were used: Model 1 was adjusted for age and region of residence in Sweden; Model 2 was adjusted for age, region of residence in Sweden, educational level, marital status, and neighborhood SES; Model 3 was constructed as Model 2 with the inclusion of comorbidities. Analyzes were performed firstly with all CMPs included, secondly by categorizing by age ≤ 54 years of age and > 54 years, and thirdly by categorizing into dilated CMP, hypertrophic CMP, and all other types. We also added a sensitivity analysis that was adjusted for age and cancers.

In addition, we studied second-generation individuals in the same way as first-generation immigrants.

Results

In total 6,123,661 individuals were included in the first-generation study, 2,971,780 men and 3,151,881 women, with 524,226 foreign-born men and 510,760 foreign-born women (Table 1, Additional file 1: Tables 1a and b). A total of 33,321 CMP cases were registered, 20,780 men and 12,541 women, with 2566 CMP cases among foreign-born men and 1499 among foreign-born women.

Table 1 The population in the first-generation study and number of cardiomyopathy (CMP) cases categorized by sex

The relative risk of CMP among foreign-born men and women is shown in Table 2 and Fig. 1. A lower risk of CMP was seen in the fully adjusted models for all foreign-born men, HR 0.92 (99% CI 0.86–0.98), and women, HR 0.90 (99% CI 0.83–0.98). A higher risk was seen in men from Africa, and a lower risk in both men and women from Asia.

Table 2 The relative risk of cardiomyopathy in first-generation immigrants vs Swedish-born individuals expressed as hazard ratios (HR) with 99% confidence intervals (99% CI)
Fig. 1
figure 1

The relative risk of cardiomyopathy in first-generation immigrants vs Swedish-born individuals expressed as hazard ratios (HR) with 99% confidence intervals (99% CI) in men (A) and women (B)

The risk of CMP in individuals ≤ 54 years of age and > 54 years is shown in Table 3. The risk among foreign-born men was lower for both age groups, with fully adjusted HRs of 0.89 (99% CI 0.82–0.97) and of 0.87 (99% CI 0.79–0.96), respectively, and among foreign-born women ≤ 54 years of age, with a HR of 0.84 (99% CI 0.75–0.94). For specific immigrant groups, the risk was higher among men ≤ 54 years of age from Africa, lower among men ≤ 54 years of age from Asia, and men > 54 years from Southern Europe. For foreign-born women, the risk was lower among women ≤ 54 years of age from Nordic countries.

Table 3 The relative risk of cardiomyopathy in first-generation immigrants vs. Swedish-born individuals expressed as hazard ratios (HR) with 99% confidence intervals (99% CI) in younger and older individuals

For the different categories of CMPs among men (Table 4), the risk of dilated CMP was higher in men from Nordic countries, more specifically among men from Finland (n = 287, HR 1.42, 99% CI 1.21–1.66), and lower among men from Asia. The risk of hypertrophic CMPs was higher for all foreign-born men, HR 1.22 (99% CI 1.04–1.43), and among men from Africa, and men from Asia; and the risk of other types of CMPs was lower in all foreign-born men, HR 0.89 (99% CI 0.81–0.98), and in men from Asia. For the different categories of CMPs among women (Table 4), the risk of dilated CMP was lower in all foreign-born women, HR 0.77 (99% CI 0.64–0.93), and in women from Asia; and the risk of all other types of CMPs was lower in all foreign-born women, HR 0.89 (99% CI 0.80–0.99), and among women from Asia.

Table 4 The relative risk of cardiomyopathy in male first-generation immigrants vs male Swedish-born individuals expressed as hazard ratios (HR) with 99% confidence intervals (99% CI) by type of cardiomyopathy (CMP)

In the second-generation immigrant study, a total of 4,587,764 individuals were included, 2,345,774 men and 2,241,990 women, including 275,105 men and 257,922 women with foreign-born parents (Additional file 1: Table S5). In total, 26,559 cases of CMP were registered, 17,620 among men and 8939 among women, including 1500 immigrant men and 730 immigrant women. No statistically significant results were found (Additional file 1: Tables S2–S4), where the fully models adjusted showed HRs (99% CI) for all CMPs among men 0.96 (0.89–1.04) and women 0.97 (0.86–1.08); in men and women combined for ≤ 54 years of age 0.97 (0.90–1.04) and for > 54 years 0.98 (0.83–1.16); and in men and women combined for dilated CMPs HR 0.97 (0.86–1.10), hypertrophic CMPs 0.94 (0.79–1.12), and all other types 1.00 (0.91–1.09).

In the sensitivity analyses, we analyzed the effect of cancer specifically on the risk of cardiomyopathy (Additional file 1: Tables S6 and S7). In the first-generation study, the HRs adjusted for age and all cancers were lower for foreign-born men in general, HR 0.79 (99% CI 0.75–0.84), and among men from Southern Europe, Eastern Europe, Northern America, Latin America, and Asia; and for foreign-born women in general, HR 0.71 (995 CI 0.75–0.87), and among women from Eastern Europe, Africa, Latin America, and Asia (Additional file 1: Table S6). In the second-generation study, the corresponding HRs were lower for all men with foreign-born parents, HR 0.73 (99% CI 0.68–0.79); for men with parents from all European regions except Baltic countries; for men with parents from Latin America and Asia; for all women with foreign-born parents, HR 0.73 (99% CI 0.65–0.82), and women with parents from the Nordic countries, Eastern Europe, and Asia (Additional file 1: Table S7).

Discussion

Our main findings were that when including all CMPs, the risk was, in general, lower in both foreign-born men and women. A lower risk was found among men and women from Asia, while a higher risk was seen among men from Africa. Regarding age patterns, a lower risk of overall CMP was found among men both for those ≤ 54 years of age, and > 54 years. However, for women it was statistically significant only in the younger age group. There were no significant differences between second-generation immigrants compared to native Swedes.

Studies on other diseases in immigrants in Sweden have found a higher risk in many immigrant groups as regards CHD [17], a higher risk of CHF [18], and also of AF among individuals younger than 45 years of age [19], especially in immigrants from some Middle Eastern countries. Furthermore, the risk of type 2 diabetes is higher in immigrants, particularly those from the Middle East region [17].

The lower risk in general for CMPs could be due to the so-called “healthy migrant effect” [20], i.e. that migrating individuals are healthier than their compatriots in the country of origin and that, in this case, individuals with CMPs, to a higher extent, stayed in their home countries. Thus, groups with increased risks could be more important to identify. Hypertrophic CMPs remain the most common inherited heart disease thus making them of special interest to study among immigrants [5], as there are genetic differences between immigrant groups. The risk was higher in men from African and Asian countries, while not among women, perhaps owing to too low case numbers. Dilated CMPs could also be of familial type [3], but we only found an increased risk among men from the Nordic countries, which was driven by an increased risk among men from Finland, perhaps because of differences in risk factors between population groups.

The correlation of CMPs to CHF is of clinical importance. We found a presence of CHF in the first-generation study of 74% among men and 57% among women, with corresponding rates in the second-generation study of 75% and 56%, respectively. In an earlier Swedish immigrant study conducted among individuals aged 45 years and older, the population attributable fraction (PAF) of CMPs for incident CHF was 4.6% for Swedish-born men and 5.7% for foreign-born men, and it was 2.1% for Swedish-born women and 2.4% for foreign-born women [18].

The correlation between CMPs and atrial fibrillation (AF) is also of clinical importance. We found that the rate of AF in the first-generation study among men was 45% and among women the figure was 29%, and that the corresponding rates in the second-generation study were 43% for men and 23% for women. The risk of AF among most first- and second-generation men and women in Sweden has been found to be lower both in those aged 45 years of age and older [21] and in those < 45 years of age [19]. For the younger individuals, i.e. younger than 45 years of age, the PAFs for CMPs regarding incident AF were 2.9% for Swedish-born men and 4.1% for foreign-born men, 3.1% for Swedish-born women and 1.4% for foreign-born women [19].

Not surprisingly, the rates of CHD, hypertension and, to some extent, also of diabetes, COPD, stroke, and non-rheumatic valvular heart disease, were also high, as was the rate of cancer. When only adjusted for age and cancers, the HRs were lower in general, and also for many of the studied groups.

There are certain limitations of this study. We used three large groups, thus not being able to follow the proposal from the ESC [2]. Dilated and hypertrophic CMPs are the most important and prevalent types of CMPs. However, we included them separately and the other types are less prevalent, hence why we merged them into one group for practical and analytical reasons in order to obtain more statistical power. We used diagnoses from the NPR, based on clinical diagnoses from patient records, with no possibility to check diagnostic criteria. However, the diagnoses were obtained from hospital diagnoses, where most patients are seen by specialists at least once. As most individuals with CMPs are examined in hospitals, the coverage of patients with these diagnoses could be expected to be high, even if some cases may be undiagnosed. We did not include ischemic cardiomyopathy (I25.5), and we cannot rule out that some diagnoses are misclassified, but we have no possibility to check for this in the nationwide data that we used. In total, 7191 men and 1943 women were registered with a diagnosis of ischemic cardiomyopathy, and of these 1042 men (14.5%) and 195 women (10.0%) also were registered with another CMP diagnosis. In addition, diagnoses from primary care were not included and most patients with comorbidities, such as hypertension and diabetes, are treated in primary care.

Our study also has several strengths. In Sweden, personal identity numbers allow linkage between different national Swedish registers [22] thus enabling adjustments for many potential confounding factors. Furthermore, many Swedish registers have been shown to have good quality [23, 24].

In conclusion, we found a generally lower risk of CMPs among foreign-born men and women in Sweden, possibly owing to the “healthy migrant effect”, but a higher risk in some specific groups, i.e. for dilated CMP among men from Finland, and for hypertrophic CMP among men from Africa and Asian countries. Hereditary forms of CMPs seem to be of little importance on a population level, as there were no significant findings when we studied second-generation immigrants.

Availability of data and materials

The datasets generated and/or analyzed during the current study are not publicly available due to restraints in the ethical approvals but we are willing to collaborate upon request to the corresponding author.

References

  1. Khatibzadeh S, Farzadfar F, Oliver J, Ezzati M, Moran A. Worldwide risk factors for heart failure: a systematic review and pooled analysis. Int J Cardiol. 2013;168(2):1186–94.

    Article  Google Scholar 

  2. Elliott P, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P, et al. Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur Heart J. 2008;29(2):270–6.

    Article  Google Scholar 

  3. Paldino A, De Angelis G, Merlo M, Gigli M, Dal Ferro M, Severini GM, et al. Genetics of dilated cardiomyopathy: clinical implications. Curr Cardiol Rep. 2018;20(10):83.

    Article  CAS  Google Scholar 

  4. Marques MA, de Oliveira GA. Cardiac troponin and tropomyosin: structural and cellular perspectives to unveil the hypertrophic cardiomyopathy phenotype. Front Physiol. 2016;7:429.

    Article  Google Scholar 

  5. Kuusisto J, Sipola P, Jaaskelainen P, Naukkarinen A. Current perspectives in hypertrophic cardiomyopathy with the focus on patients in the Finnish population: a review. Ann Med. 2016;48(7):496–508.

    Article  CAS  Google Scholar 

  6. Kadir IS, Barker TA, Clarke B, Denley H, Grotte GJ. Recurrent acute rheumatic fever: a forgotten diagnosis? Ann Thorac Surg. 2004;78(2):699–701.

    Article  Google Scholar 

  7. Hantson P. Mechanisms of toxic cardiomyopathy. Clin Toxicol (Philadelphia). 2019;57(1):1–9.

    Article  CAS  Google Scholar 

  8. Mirijello A, Tarli C, Vassallo GA, Sestito L, Antonelli M, d’Angelo C, et al. Alcoholic cardiomyopathy: what is known and what is not known. Eur J Intern Med. 2017;43:1–5.

    Article  Google Scholar 

  9. Alsarah A, Alsara O, Laird-Fick HS. Cardiac manifestations of Familial Mediterranean fever. Avicenna J Med. 2017;7(4):158–63.

    Article  Google Scholar 

  10. Rujirachun P, Wattanachayakul P, Charoenngam N, Winijkul A, Ungprasert P. Prevalence of atrial arrhythmia in patients with arrhythmogenic right ventricular cardiomyopathy: a systematic review and meta-analysis. J Cardiovasc Med (Hagerstown). 2020;21(5):368–76.

    Google Scholar 

  11. Ahmadjee A, Herzallah K, Saleh Y, Abela GS. Takotsubo Cardiomyopathy presenting with different morphological patterns in the same patient: a case report and review of the literature. Cardiovasc Pathol. 2020;47:107204.

    Article  Google Scholar 

  12. Birnie DH, Nery PB, Ha AC, Beanlands RS. Cardiac sarcoidosis. J Am Coll Cardiol. 2016;68(4):411–21.

    Article  Google Scholar 

  13. De Rosa S, Arcidiacono B, Chiefari E, Brunetti A, Indolfi C, Foti DP. Type 2 diabetes mellitus and cardiovascular disease: genetic and epigenetic links. Front Endocrinol (Lausanne). 2018;9:2.

    Article  Google Scholar 

  14. Mizamtsidi M, Paschou SA, Grapsa J, Vryonidou A. Diabetic cardiomyopathy: a clinical entity or a cluster of molecular heart changes? Eur J Clin Invest. 2016;46(11):947–53.

    Article  Google Scholar 

  15. Winkleby M, Sundquist K, Cubbin C. Inequities in CHD incidence and case fatality by neighborhood deprivation. Am J Prev Med. 2007;32(2):97–106.

    Article  Google Scholar 

  16. Zoller B, Li X, Sundquist J, Sundquist K. Neighbourhood deprivation and hospitalization for atrial fibrillation in Sweden. Europace. 2013;15(8):1119–27.

    Article  Google Scholar 

  17. Wandell PE. Population groups in dietary transition. Food Nutr Res. 2013;57.

  18. Wandell P, Carlsson AC, Li X, Gasevic D, Arnlov J, Holzmann MJ, et al. Heart failure in immigrant groups: a cohort study of adults aged 45 years and over in Sweden. Scand Cardiovasc J. 2018;52(6):292–300.

    Article  Google Scholar 

  19. Wandell P, Carlsson AC, Li XJ, Gasevic D, Arnlov J, Holzmann MJ, et al. Atrial fibrillation in immigrants under the age of 45 y in Sweden. Int Health. 2019;11(3):193–202.

    Article  Google Scholar 

  20. Kennedy S, Kidd MP, McDonald JT, Biddle N. The healthy immigrant effect: patterns and evidence from four countries. Int Migration Integration. 2015;16:317–32.

    Article  Google Scholar 

  21. Wandell P, Carlsson AC, Li X, Gasevic D, Arnlov J, Holzmann MJ, et al. Atrial fibrillation in immigrant groups: a cohort study of all adults 45 years of age and older in Sweden. Eur J Epidemiol. 2017;32(9):785–96.

    Article  Google Scholar 

  22. Ludvigsson JF, Otterblad-Olausson P, Pettersson BU, Ekbom A. The Swedish personal identity number: possibilities and pitfalls in healthcare and medical research. Eur J Epidemiol. 2009;24(11):659–67.

    Article  Google Scholar 

  23. Ludvigsson JF, Almqvist C, Bonamy AK, Ljung R, Michaelsson K, Neovius M, et al. Registers of the Swedish total population and their use in medical research. Eur J Epidemiol. 2016;31(2):125–36.

    Article  Google Scholar 

  24. Ludvigsson JF, Andersson E, Ekbom A, Feychting M, Kim JL, Reuterwall C, et al. External review and validation of the Swedish national inpatient register. BMC Public Health. 2011;11:450.

    Article  Google Scholar 

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Acknowledgements

We thank Patrick O’Reilly for language editing.

Funding

Open access funding provided by Karolinska Institute. This work was supported by ALF funding awarded to Kristina Sundquist and by grants from the Swedish Research Council.

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Authors

Contributions

PW: concept, manuscript drafting, revisions. XL: statistical analysis, constructive review of manuscript. ACC: concept, manuscript drafting and review. JS: concept, acquisition of data, constructive review of manuscript. KS: concept, acquisition of data, constructive review of manuscript, funding. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Axel C. Carlsson.

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Ethical approval and consent to participate

Consent to participate was not applicable and deemed unnecessary according to national legislation, as the study was based on pseudonymized data from registers [23, 24]. No additional administrative permissions and/or licenses were required to access the clinical/personal patient data used in the research. The study was approved by the ethics committee named “Regional Ethical Review Board in Lund” (ref nr 2012/795, with later amendments).

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Additional file 1

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Wändell, P., Li, X., Carlsson, A.C. et al. Cardiomyopathy among first- and second-generation immigrants in Sweden: a nationwide total population study. BMC Cardiovasc Disord 22, 524 (2022). https://doi.org/10.1186/s12872-022-02968-0

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Keywords

  • Cardiomyopathy
  • Immigrants
  • Neighborhood
  • Sex
  • Socioeconomic status