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International Journal of Circumpolar Health logoLink to International Journal of Circumpolar Health
. 2015 Jan 12;74:10.3402/ijch.v74.24424. doi: 10.3402/ijch.v74.24424

Prevalence of self-reported myocardial infarction in Sami and non-Sami populations: the SAMINOR study

Bent-Martin Eliassen 1,*, Sidsel Graff-Iversen 2,3, Tonje Braaten 3, Marita Melhus 1, Ann R Broderstad 1,4
PMCID: PMC4289678  PMID: 25579653

Abstract

Objective

Measure the prevalence of self-reported myocardial infarction (SMI) in Sami and non-Sami populations in rural areas of Norway, and explore whether possible ethnic differences could be explained by established cardiovascular risk factors.

Design

Cross-sectional population-based study.

Methods

A health survey was conducted in 2003–2004 in areas with Sami and non-Sami populations (SAMINOR). The response rate was 60.9%. Information concerning lifestyle was collected by 2 self-administrated questionnaires, and clinical examinations provided anthropometric measurements, and data on blood pressure and lipid levels.

Results

The total number for the subsequent analysis was 15,206 men and women aged 36–79 years (born 1925–1968). Sex-specific analyses revealed no ethnic difference in SMI. In terms of the most important risk factors such as smoking, blood pressure, and lipid levels, no or only trivial ethnic differences were found in both women and men.

Conclusion

In this study, we found no difference in SMI between Sami and non-Sami in rural areas in Norway. The similar risk profile is the most plausible explanation; similar living conditions and close interaction between the ethnic groups may explain this.

Keywords: cardiovascular disease, indigenous, Norway


The Sami are an indigenous people whose settlement area (Sápmi) covers the northern parts of Norway, Sweden and Finland, and Russia's Kola Peninsula. The traditional Sami settlement area in Norway stretches from Finnmark in the north to Engerdal in Hedmark County in the south.

In the latter half of the 20th century, Sami and non-Sami populations in Norway underwent lifestyle changes resulting in more sedentary lifestyles and dietary changes (1,2). The knowledge concerning the burden of myocardial infarction among the Sami is limited, and we do not know whether the prevalence of this disease differs between Sami and non-Sami populations in Norway. Some studies have, however, been carried out; for example, the first Finnmark study was initiated in 1974–1975, wherein Sami/Finnish men aged 35–49 years had on average a 40% higher cardiovascular risk score compared with Norwegians (3). The score was based on sex, serum total cholesterol, systolic blood pressure and current cigarette smoking (ibid.). Despite this risk profile, the prevalence of self-reported myocardial infarction (SMI) was considerable lower in the Sami compared with the Norwegian population (ibid.). Since then, prevalence and follow-up data have shown no or only minor differences in risk factors and risk of ischaemic heart disease (IHD) (2,410). In terms of mortality from cardiovascular disease, conflicting results have been presented (11,12). Various definitions of Sami ethnicity have been used in these studies.

The primary objective of this study was to measure the prevalence of SMI in Sami and non-Sami populations, and to explore whether possible differences could be explained by established cardiovascular risk factors.

Methods

As part of the Norwegian Institute of Public Health's (NIPH) health survey in Finnmark, the Centre for Sami Health Research conducted in 2003–2004 a population-based survey in areas with Sami and non-Sami populations (SAMINOR) (13), also including areas outside Finnmark. The age cohorts included in SAMINOR were 30 and 36–79 year-olds. All eligible residents in the selected municipalities registered in the National Population Register were invited regardless of ethnic background (N=27,987). Of these, 16,865 (60.3%) participated and gave consent to medical research. The response rate in the age group 36–79 (n=16,538) was 60.9%. The population was almost exclusively rural. The Regional Committee for Medical Research Ethics approved the study and the participants gave written informed consent.

Questionnaires

Information on ethnicity and lifestyle was collected by using 2 questionnaires, that is, the initial and main questionnaires (13). Ethnicity was measured by the following: What language(s) do/did you, your parents and your grandparents use at home? The response categories were “Norwegian,” “Sami,” “Kven” or “other.” Kvens are descendants of Finnish settlers who immigrated to northern Norway in the 1700s and 1800s (14). Providing the same response options, we also asked: What is your, your father's and your mother's ethnic background? The respondents also reported whether they considered themselves to be Norwegian, Sami, Kven or other (self-perceived ethnicity). On all these questions multiple answers were allowed. These variables are described in detail by Lund et al. (13). Based on these variables we generated 2 ethnic categories: Sami and non-Sami. The Sami category included respondents reporting at least one Sami identity mark (Sami language spoken by the respondent or at least one parent or grandparent, or Sami ethnic background or self-perceived Sami ethnicity). Those not reporting a Sami identity mark were included in the non-Sami group.

Myocardial infarction was measured by the following question: Do you have, or have you ever had: A heart attack? (Yes/No). Missing values (n=640) were considered negative responses; for such variables, this is a conventional ad-hoc imputation method (15).

The following question measured family history of myocardial infarction: Tick off relatives who have, or have ever had, any of the following conditions, and report the age of when they got the illness: “Heart attack before the age of 60 years” and “Heart attack after the age of 60 years.” The possible response categories were “Mother,” “Father,” “Sister,” “Brother,” “Children” and “No one.” The variables were combined to create a variable of total family history of myocardial infarction. Observations providing a negative response but reporting the age for when their relative(s) got the illness were given a positive response (n=9).

Data on smoking were collected by asking: Are you currently, or were you previously, a daily smoker? “Yes, currently,” “Yes, previously,” “Never.” Never smokers (n=37), current smokers (n=86) and observations with missing data on smoking status (n=14) reporting the number of years since they stopped smoking were coded as previous smokers.

Education was measured by asking: How many years of schooling/education have you completed (including all the years you attended school or have been studying)?

Use of cholesterol-lowering drugs during the last 4 weeks was registered by the following item: State the name of the medicine and your reason for taking/having taken them (disease, symptoms): Tick one box for each line. Relevant ATC reference codes were used.

Medical examination

A trained group of experienced fieldworkers from the NIPH performed the medical examinations, which took place in 2 buses traveling between the municipalities. Invitations with the time and date for the medical examination were sent in the mail together with the questionnaires. Waist circumference was measured at the umbilicus to the nearest centimetre at the end of exhalation with the individual standing and breathing normally. The methods used and procedures followed for the measurement of blood pressure, total cholesterol, high-density lipoprotein (HDL) cholesterol and glucose are described in detail elsewhere (9). All blood samples in the SAMINOR study were non-fasting. We used self-reported diabetes and information about anti-diabetic medication to define diabetes. Additionally, a non-fasting blood glucose level ≥11.1 was defined as having diabetes (16).

Statistical analysis

Means in Tables I and II were tested by 2-sample t-tests; rates were tested by Pearson's chi-square tests or 2-sample Wilcoxon rank-sum (Mann–Whitney) tests. The distributions of HDL cholesterol and glucose were skewed and thus log-transformed; the displayed means are geometric. The direct method was used to age-standardize the prevalence of total SMI (Table III) to the European standard population of 1976 (17). Logistic regression was then used to evaluate the effects of the explanatory variables on the relationship between ethnicity and SMI (Table IV). Systolic blood pressure, HDL cholesterol and total cholesterol were included in the regression models as categorical variables, as displayed in Tables I and II. Appropriate goodness-of-fit tests were performed to optimize the regression models. Alcohol consumption, leisure-time physical activity, and intensity and duration of smoking (pack-years in current smokers and time since smoking cessation in previous smokers (18) were also included in the regression models to assess any additional confounding effects. We also performed the regression analysis with and without the ad-hoc imputation to assess if the imputations of negative SMI cases influenced estimates and results in Table IV.

Table I.

Characteristics of the female study group by ethnicity. Values are meansa or percentagesb (95% CI); p-values for differences between ethnic groups (SAMINOR study 2003–2004, n=15,206c)

Non-Sami Sami


Variables n = 5,273 n = 2,611 p
Age (years) 54.5 (54.2–54.8) 54.2 (53.7–54.6) 0.21
Systolic blood pressure (mmHg) 130.4 (129.8–131.0) 129.7 (128.8–130.5) 0.13
 Minimum–119 35.7 (34.4–37.0) 36.5 (34.7–38.3) 0.17
 120–129 17.6 (16.6–18.7) 19.5 (18.0–21.0)
 130–139 16.9 (15.9–17.9) 15.8 (14.4–17.2)
 140–149 12.2 (11.3–13.1) 11.3 (10.1–12.5)
 150–159 8.4 (7.7–9.2) 7.6 (6.6–8.6)
 160 + 9.2 (8.4–10.0) 9.5 (8.4–10.7)
Total cholesterol (mmol/l) 5.99 (5.96–6.02) 5.98 (5.93–6.02) 0.62
 Minimum–4.09 3.2 (2.7–3.7) 3.5 (2.9–4.3) 0.87
 4.10–5.19 23.3 (22.1–24.4) 22.3 (20.7–23.9)
 5.20–6.29 36.7 (35.4–38.0) 36.3 (34.5–38.2)
 6.30–7.29 22.9 (21.7–24.0) 25.7 (24.0–27.4)
 7.3 + 14.0 (13.1–15.0) 12.2 (11.0–13.5)
HDL cholesterol (mmol/l)d 1.44 (1.43–1.45) 1.40 (1.39–1.42) <0.001
 1.61 + 34.2 (33.0–35.5) 29.4 (27.7–31.2) <0.001
 1.30–1.60 33.1 (31.8–34.4) 33.5 (31.7–35.3)
 1.20–1.29 10.3 (9.6–11.2) 10.0 (8.9–11.2)
 0.90–1.19 19.2 (18.1–20.3) 23.3 (21.8–25.0)
 Minimum–0.89 3.2 (2.7–3.7) 3.8 (3.1–4.6)
Type 2 diabetes (yes) 4.3 (3.8–4.8) 5.0 (4.3–5.9) 0.12
Glucose (mmol/l)d 5.44 (5.41–5.47) 5.50 (5.46–5.55) <0.05
Statin use (yes) 11.3 (10.4–12.2) 11.9 (10.7–13.2) 0.43
Family history of MI (yes) 47.1 (45.7–48.4) 51.2 (49.3–53.2) <0.001
Education (≥13 years) (yes) 34.2 (32.9–35.5) 33.5 (31.6–35.4) 0.56
Smoking 0.18
 Never 37.6 (36.3–38.9) 36.4 (34.5–38.2)
 Previous 31.3 (30.1–32.6) 31.0 (29.3–32.8)
 Current 31.1 (29.9–32.4) 32.6 (30.8–34.4)
a

Tested by 2-sample t-test with equal variances.

b

Tested by Pearson's chi-square test or 2-sample Wilcoxon rank-sum (Mann–Whitney) test.

c

Some estimates are based on a smaller n due to missing values.

d

Geometric mean.

Table II.

Characteristics of the male study group by ethnicity. Values are meansa or percentagesb (95% CI), p-values for differences between ethnic groups (SAMINOR study 2003–2004, n=15,206c)

Non-Sami Sami


Variables n=4,746 n=2,576 p
Age (years) 54.8 (54.5–55.1) 55.0 (54.6–55.4) 0.50
Systolic blood pressure (mmHg) 134.2 (133.7–134.7) 134.9 (134.2–135.7) 0.13
 Minimum–119 21.5 (20.3–22.7) 22.1 (20.5–23.7) 0.56
 120–129 21.3 (20.1–22.5) 21.0 (19.4–22.6)
 130–139 23.8 (22.6–25.0) 22.2 (20.6–23.9)
 140–149 15.6 (14.6–16.6) 14.9 (13.6–16.3)
 150–159 8.8 (8.0–9.6) 9.5 (8.4–10.7)
 160 + 9.2 (8.4–10.0) 10.4 (9.3–11.6)
Total cholesterol (mmol/l) 5.89 (5.86–5.92) 5.98 (5.93–6.02) <0.01
 Minimum–4.09 4.2 (3.6–4.8) 4.7 (4.0–5.6) <0.001
 4.10–5.19 22.8 (21.6–24.0) 21.8 (20.3–23.5)
 5.20–6.29 39.7 (38.3–41.1) 34.5 (32.7–36.4)
 6.30–7.29 23.4 (22.3–24.7) 26.3 (24.6–28.0)
 7.3 + 9.9 (9.1–10.8) 12.6 (11.4–14.0)
HDL cholesterol (mmol/l)d 1.21 (1.20–1.22) 1.23 (1.21–1.24 0.12
 1.61 + 13.8 (12.9–14.8) 15.0 (13.7–16.5) 0.32
 1.30–1.60 24.6 (23.4–25.9) 24.9 (23.3–26.6)
 1.20–1.29 13.0 (12.1–14.0) 11.3 (10.1–12.5)
 0.90–1.19 37.6 (36.3–39.0) 38.6 (36.8–40.5)
 Minimum–0.89 11.0 (10.1–11.9) 10.1 (9.0–11.4)
Type 2 diabetes (yes) 4.5 (4.0–5.2) 5.3 (4.5–6.2) 0.14
Glucose (mmol/l)d 5.61 (5.57–5.64) 5.63 (5.58–5.68) 0.50
Statin use (yes) 14.6 (13.6–15.6) 14.9 (13.6–16.3) 0.71
Family history of MI (yes) 45.8 (44.4–47.2) 49.4 (47.5–51.4) <0.01
Education (≥13 years) (yes) 31.4 (30.0–32.7) 26.6 (24.9–28.4) <0.001
Smoking <0.05
 Never 28.4 (27.1–29.7) 25.5 (23.9–27.3)
 Previous 41.5 (40.1–42.9) 42.5 (40.6–44.4)
 Current 30.2 (28.9–31.5) 32.0 (30.2–33.8)
a

Tested by 2-sample t-test with equal variances.

b

Tested by Pearson's chi-square test or 2-sample Wilcoxon rank-sum (Mann–Whitney) test.

c

Some estimates are based on a smaller n due to missing values.

d

Geometric mean.

Table III.

Age-specific, and total crude and age-standardized, prevalence rates of self-reported myocardial infarction by sex and ethnicity (SAMINOR study 2003–2004, n=15,206)

Non-Sami Sami


Age Sample n % Sample n %
Women
 36–49 1,947 4 0.2 1,009 2 0.2
 50–59 1,557 13 0.8 795 12 1.5
 60–69 1,110 36 3.2 496 13 2.6
 70–79 659 39 5.9 311 29 9.3
 Total crude 5,273 92 1.7 2,611 56 2.1
 Total age-adjusteda (95% CI) 5,273 81 1.5 (1.2–1.9) 2,611 51 2.0 (1.5–2.5)
Men
 36–49 1,657 14 0.8 875 5 0.6
 50–59 1,487 72 4.8 850 43 5.1
 60–69 1,041 120 11.5 536 53 9.9
 70–79 561 103 18.4 315 54 17.1
 Total crude 4,746 309 6.5 2,576 155 6.0
 Total age-adjusteda (95% CI) 4,746 273 5.8 (5.2–6.4) 2,576 136 5.3 (4.5–6.1)
a

Direct standardization using the European standard population as reference (18).

Table IV.

Odds ratios (OR) and 95% confidence intervals (CIs) for the differences in self-reported myocardial infarction between non-Sami and Sami by sex (SAMINOR study 2003–2004, n=15,206)

Model 1a Model 2b


OR p 95% CI OR p 95% CI
Women n=7,884 n=7,261c
 Non-Sami Ref Ref
 Sami 1.29 0.14 0.92–1.81 1.25 0.26 0.85–1.85
Men n=7,322 n=6,919c
 Non-Sami Ref Ref
 Sami 0.91 0.36 0.74–1.12 0.88 0.30 0.68–1.13

Controlling for:

a

Age.

b

Age and education, previous and current smoking, systolic blood pressure, HDL cholesterol, type 2 diabetes, family history of myocardial infarction, total cholesterol and use of statins.

c

Lower sample size due to missing values.

An alternative categorization of Sami ethnicity was assessed by dichotomizing Sami ethnicity into Sami I (Sami language is used as the home language by all grandparents and parents and by the participant) and Sami II (at least one Sami identity mark, i.e. Sami language spoken by the respondent or at least one parent or grandparent, or Sami ethnic background or self-perceived Sami ethnicity).

All statistical analyses were performed using STATA version 13.0 (StataCorp, College Station, TX).

Results

The total number for the subsequent analysis was 15,206 men and women aged 36–79 years (born 1925–1968); those aged 30 years (n=327) (low response rate and few disease events) and those who did not respond to the initial (n=207) and main (n=785) questionnaires were excluded from the analysis. Also excluded were recent immigrants (n=257), those with missing information on ethnicity (n=52) and participants who did not turn up for the medical examination (n=31). Recent immigrants were responders who were born abroad and answered “other” to the first 2 questions on ethnicity (see questionnaires).

Tables I and II display the levels of selected risk factors by ethnicity in women and men, respectively. In women, statistically significant (p<0.05) but small differences between non-Sami and Sami were found for HDL cholesterol, glucose and family history of myocardial infarction.

In men, statistically significant (p<0.05) differences were found for total cholesterol, family history of myocardial infarction, years of education and smoking. These differences were also small. In both sexes, the Sami had higher levels of hereditary myocardial infarction.

Nonetheless, in terms of the most important risk factors such as smoking, blood pressure and lipid levels, no or only trivial ethnic differences were found in both women and men.

Table III displays age-specific, and total crude and age-standardized, prevalence rates of SMI by sex and ethnic groups. Similar rates and overlapping confidence intervals were seen when comparing Sami and non-Sami women and men. In women, the total age-standardized rates for non-Sami and Sami were 1.5% (95% CI: 1.2–1.9) and 2.0% (95% CI: 1.5–2.5), respectively. The total age-standardized rates for non-Sami and Sami men were 5.8% (95% CI: 5.2–6.4) and 5.3% (95% CI: 4.5–6.1), respectively.

Odds ratios (ORs) for SMI in Sami compared with non-Sami are presented in Table IV. In both women and men, univariable and multivariable regression analyses revealed no significant ethnic difference in odds of SMI.

No confounding due to alcohol consumption, leisure-time physical activity, and intensity and duration of smoking was observed (data not shown). The ad-hoc imputation of negative cases of SMI did not affect the end result (data not shown). Furthermore, the alternative categorization of ethnicity (see methods) did not affect the results in the univariable and multivariable regression analyses (data not shown).

Discussion

In this study, we found no difference in SMI between Sami and non-Sami in selected rural areas in Norway; the similar risk profile is the most plausible explanation. An alternative categorization of ethnicity (see methods) did not affect the end result (data not shown).

The similar risk profile and burden of SMI in Sami and non-Sami in rural areas of northern Norway are in line with those found in earlier studies (2,410). In Sweden, a few follow-up studies have shown little or no difference between Sami and non-Sami with regard to cardiovascular risk factors (19,20), and a somewhat higher Sami mortality rate due to IHD in women (21,22). A lower incidence rate of acute myocardial infarction has also been documented in Sami reindeer-herding women compared with Swedish women (22). Other Arctic indigenous peoples such as the Greenlandic Inuit present similar IHD morbidity rates compared to American and European populations (23).

Having used the same data as in this study, previous SAMINOR publications have already presented small ethnic differences in risk factors for CVD (2,9,10). The similar living conditions and close interaction between the ethnic groups may explain this; it is likely that the mentioned lifestyle changes have occurred in all parts of the rural population in northern Norway independent of ethnicity (9). However, in a recent publication based on the same data used in this study, Eliassen et al. (24) found an excess of self-reported angina pectoris in Sami compared with non-Sami, which was surprising given the strikingly similar risk profile. This may suggest that our grasp of IHD aetiology in the Sami population may be missing key factors; unknown genetic or environmental factors may influence the occurrence of IHD in this population.

Limitations

Sensitivity has been found to be quite high for SMI in other populations (80–97.7%), whereas positive predictive values have been reported lower (43–87%) (25). A recent study, using the Spanish cohort of the EPIC study, found self-reported information on myocardial infarction to be a valid instrument when compared with medical records (ibid.). Previous population studies in northern Norway support agreement between SMI and medical records (26,27). This may provide some support to the validity of the self-reported data. However, at present we do not know the validity of SMI in this population and in the 2 ethnic groups; the fact that Eliassen et al. (24) found an excess burden of angina pectoris among Sami in the same sample may suggest a potential bias in this study. Body, health, and disease are cultural phenomena; there is no universal connection between a medical condition and the way it is experienced (28); and standardized questions in a self-administrated questionnaire may convey different meanings to different peoples (29). This might thus have produced differential misclassification of disease status by ethnicity.

This study had a cross-sectional design; we were unable to assess potential causal relationships. We have limited information about non-responders other than that they tended to be younger, single and male (2); potential selection bias is thus difficult to assess. We do not know the response rate by ethnicity; we are therefore unable to assess whether differences in participation have influenced the observed disease burden in the ethnic groups.

An additional limitation is that the data are approximately 10 years old; the results may therefore have reduced applicability today.

Strengths

A relatively high overall response rate (61%) and a large population-based sample have enabled an in-depth comparative analysis of SMI in Sami and non-Sami populations. Generalizability in SAMINOR refers to whether the general population in the defined SAMINOR area systematically differs from the rural population in general in northern Norway, and whether those who participated in the study systematically differ from those not included (9). We believe that our results can be generalized to the Sami and non-Sami living in the rural areas of northern Norway. However, they may be less valid for the population in Nordland due to the low response rate in this region (9,13).

Conclusions

In this study, we found no difference in SMI between Sami and non-Sami in rural areas in Norway. The similar risk profile is the most plausible explanation; similar living conditions and close interaction between the ethnic groups may explain this.

Acknowledgements

The Centre for Sami Health Research at UiT The Arctic University of Norway conducted the survey in collaboration with the Norwegian Institute of Public Health.

Conflict of interest and funding

The authors declare that they have no conflict of interest. Funding was provided by the Norwegian Ministry of Health and Care Services.

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