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International Cardiovascular Research Journal logoLink to International Cardiovascular Research Journal
. 2013 Jun 1;7(2):46–50.

Premature Coronary Heart Disease and Traditional Risk Factors-Can We Do Better?

Roxana Sadeghi 1,*, Nadia Adnani 2, Azam Erfanifar 2, Latif Gachkar 3, Zohre Maghsoomi 2
PMCID: PMC3987428  PMID: 24757620

Abstract

Background

Traditional cardiovascular risk factors are strong predictors of an increased likelihood for premature CHD. Considering the benefits of risk factors᾿ management, it is imperative to find and treat them before looking for more unknown and weak risk factors.

Objectives

Limited information is available about the demographic and historical characteristics of the patients with premature Coronary Heart Disease (CHD) in IR Iran. The main objective of this study was to determine the prevalence of the traditional risk factors in these patients. Also, the researchers hypothesized that there are insufficient risk assessment and preventive intervention methods for the asymptomatic adult population.

Methods

This study was conducted on 125 patients with premature CHD (age<50 years) who were admitted in two academic hospitals with acute coronary syndromes. The patients were accepted since they had a definite CHD on the basis of acute myocardial infarction (elevated cardiac enzymes) or documented CAD in coronary angiography.

Results

The mean age of the study population was 42.50±5.65 (26 to 49 years). Among the patients,92 (73.6%) were male, 113 (90.4%) were married, 58 (46.4%) were smokers,19 (15.2%) were opium users, 97 (77.6%) had dyslipidemia, 44 (35.2%) had hypertension, and 33 (26.4%) had diabetes mellitus. In addition, family history was presented in 54 patients (43.2%).

Among the study population, 120 patients (96%) had at least one of the traditional risk factors, including dyslipidemia, hypertension, diabetes mellitus, cigarette smoking, and family history of CHD. However, none of the dyslipidemic patients had controlled total cholesterol, LDL, HDL, and triglyceride. Also, none of the diabetic patients had hemoglobin A1C<7%. Among the 44 hypertensive patients, blood pressure of 15 ones (34%) was within the normal range. Besides, only 3 patients (2.4%) had regular physical activity (at least 30 minutes, three times a week).

Conclusions

Premature Coronary Heart Disease is a public health problem. However, there is lack of effective and intensive treatments of well-defined traditional risk factors and prevention methods for the majority of the patients experiencing premature CHD. In sum, there is still plenty of room for improvement of risk management in IR Iran.

Keywords: Atherosclerosis, Risk Factors, Coronary Heart Disease, Coronary Artery Disease

1. Background

The incidence of premature Coronary Heart Disease (CHD) is quite high in IR Iran as well as many other countries (1,2). It is necessary to know the true magnitude of this problem for improving risk stratification as well as the prevention methods in order to provide optimal care for those with or at risk of developing CHD. Multiple clinical trials have proven that appropriate detection and treatment of the risk factors can slow the progression of atherosclerosis and reduce the occurrence of cardiovascular events.

In multiple studies, traditional risk factors, such as family history of premature CHD (3-5), dyslipidemia (6), hypertension, diabetes mellitus, and cigarette smoking, have been shown to be significantly associated with early CHD.

Despite this fact, the application of primary prevention is not optimal for well-known risk factors and further risk stratification and aggressive treatment is needed. Non-traditional risk factors and inflammatory biomarkers would also be the second treatment goal; however, they are only applicable after optimal treatment of the traditional risk factors.

2. Objectives

The aim of this study is to show the prevalence and management of traditional risk factors in a population with premature CHD.

3. Patients and Methods

Among all the patients with acute coronary syndromes who had been admitted in the cardiovascular centers in two academic hospitals between January 2011 and March 2012,125 ones with definite premature CHD were selected. Coronary Artery Disease (CAD) before the age of 50 was determined as premature. The patients were identified as having definite CHD on the basis of acute myocardial infarction (elevated cardiac enzymes) or documented CAD in coronary angiography. Information about age, gender, family history of CAD (male first degree relatives<55 years old and female first degree relatives<65 years old), dyslipidemia (high LDL-cholestrol based on ATP III or HDL-cholestrol<40 mg/dL or triglycerides>150 mg/dL) (7), diabetes mellitus (fasting blood glucose≥126 mg/dL, 2 hours postprandial glucose≥200 mg/dL, or use of hypoglycemic agents or insulin), hypertension (positive past history of hypertension or use of antihypertensive drugs), smoking, and opium consumption were collected. The clinical presentations, electrocardiographic and echocardiographic results, and coronary angiographic findings were gathered and recorded, as well. A diameter stenosis>50% in each epicardial coronary artery was defined as significant CAD and a narrowing<50% was considered as mild CAD. It should be noted that written informed consents were obtained from all the study patients.

3.1. Statistical Analysis

Continuous variables were expressed as mean±standard deviation and dichotomous variables as frequencies. All the statistical analyses were performed using the SPSS statistical software (version 16).

4. Results

The mean age of the study population was 42.50±5.65 years (26 to 49 years) and 92 patients (73.6 %) were male. In addition, 58 patients (46.4%) were smokers and 19 ones (15.2%) were opium users. However, none of the study subjects used amphetamine or alcohol. Moreover, 97 (77.6%), 44 (35.2%), 33 (26.4%), and 1 (0.8%) patients had dyslipidemia, hypertension, diabetes mellitus, and renal insufficiency, respectively, while none had chronic lung disease. Besides, none of the patients presented with peripheral vascular disease, cerebrovascular disease, and prior congestive heart failure. Yet, prior CAD, prior percutaneous coronary intervention, and prior coronary artery bypass graft were detected in 4 (3.2%), 3 (2.4%), and 1 (0.8%) patients, respectively. The mean of total cholesterol, LDL, HDL, and triglyceride were 193.0±46.0 (98 to 403 mg/ dL), 113.4±41.1 (22 to 279 mg/ dL), 41.8±13.0 (20 to 100 mg/ dL), and 182.1±96.6 (35.3 to 523 mg/ dL), respectively. Likewise, the mean of non-HDL cholesterol was 151.3±46.9.

Among the study population, 116 patients (92.8%) had at least one of the traditional risk factors, including dyslipidemia, hypertension, diabetes mellitus, and cigarette smoking. Besides, 120 ones (96%) had dyslipidemia, hypertension, diabetes mellitus, cigarette smoking, or family history of CHD. Nonetheless, none of the dyslipidemic patients had controlled total cholesterol, LDL, HDL, and triglyceride. Also, none of the diabetic patients had hemoglobin A1C<7%. Among the 44 hypertensive patients, only 15 ones (34%) reached the normal blood pressure. Furthermore, regular physical activity (at least 30 minutes, three times a week) was restricted to 3 study patients (2.4%). Demographic and historical characteristics of the study patients are summarized in Table 1.

Table 1. Demographic and Historical Characteristics of the Patients with Premature Coronary Heart Disease .

Characteristics Number (%) or mean± SD
Age, years 42.50±5.65
Male gender 92(73.6)
Marriage 113(90.4)
Family history of CAD 54(43.2)
Smoker 58(46.4)
Opium user 19(15.2)
Alcohol 0(0)
Hypertension 44(35.2)
Dyslipidemia 97(77.6)
Elevated Cholestrol (>200mg/dL) 47(37.6)
Total Cholestrol (mg/dL) 193.0±46.0
Elevated LDL 38(30.4)
LDL (mg/dL) 113.4±41.1
Non HDL cholesterol (mg/dL) 151.3±46.9
Low HDL (<40mg/dL) 63(50.4)
HDL (mg/dL) 41.8±13.0
Elevated Triglyceride (>150mg/dL) 71(56.8)
Triglyceride (mg/dL) 182.1±96.6
Diabetes mellitus 33(26.4)
FBS (mg/dL) 110.1±39.3
Renal insufficiency 1(0.8)
Serum Cr (mg/L) 1.10±0.52
WBC (cells/µL) 8242.3±2677.2
Hemoglobin (g/dL) 14.6±9.9
Platelet (106/L) 246760±225975
Chronic lung disease 0(0)
Peripheral vascular disease 0(0)
Prior cerebrovascular disease 0(0)
Prior coronary artery disease 4(3.2)
Prior congestive heart failure 0(0)
Prior CoronaryArtery Bypass Graft 1(0.8)
Prior Percutaneous Coronary Intervention 3(2.4)
Regular physical activity (at least 30 min, 3 times per week) 3(2.4)

Values are presented as n (%) unless otherwise expressed.

The clinical presentation was unstable angina, non ST elevation Myocardial Infarction (MI), or ST elevation MI in 60.8%, 7.2%, and 32% of the patients, respectively. The first electrocardiogram showed normal findings in 35.2% of the cases and left ventricular ejection fraction was more than 50% in 72% of the patients. Moreover, minimal coronary artery disease, one-vessel disease, two-vessel disease, three-vessel disease, and left main involvement in coronary angiography were observed in 18.4%, 44%, 16%, 16%, and 0% of the subjects, respectively. Also, 5.6% of the patients had no coronary artery stenosis.Clinical and Para clinical characteristics of the enrolled patients with premature CHD are shown in Table 2.

Table 2. Clinical and Para Clinical Characteristics of the Patients with Premature Coronary Heart Disease .

Characteristics Number (%)
Electrocardiogram
Available 125(100)
Normal 44(35.2)
Clinical Presentation
Unstable Angina 76(60.8)
Non ST elevation Myocardial Infarction 9(7.2)
ST elevation Myocardial Infarction 40(32)
LV Ejection Fraction
Available 124(99.2)
LV Ejection Fraction≥50% 90(72)
Coronary Artery Angiogram
Available 125(100)
Normal 7(5.6)
Minimal Coronary Artery Disease 23(18.4)
One Vessel Disease 55(44)
Two Vessel Disease 20(16)
Three Vessel Disease 20(16)
Proximal LAD 23(18.4)
Left Main Coronary Disease 0(0)

Abbreviations: LAD, Left Anterior Descending; LCX, Left Circumflex; RCA, Right Coronary Artery

5. Discussion

The mean age and gender distribution of the patients with premature CHD in this study was similar to those of the previous reports (1). In general, family history of premature CHD is a known risk factor for cardiovascular events. Evidence supports a higher incidence of subclinical atherosclerosis in the individuals with positive familial history of premature CHD (8). Even a positive family history which is not premature should be considered important (9). Of course, the causes of this familial clustering have not been established, yet. The prevalence of a positive family history in the patients with early CAD was up to 75% in some studies; however, it was 43.2% in this study (10). Thus, familial history provides an opportunity for these asymptomatic individuals who may benefit from vascular disease screening (11).

Dyslipidemia management as emerged as a key therapeutic strategy to reduce both primary and secondary cardiovascular events. In the last European guideline, the optimal LDL-C level for the asymptomatic patients was stated as less than 100 mg/dL (12).Yet, some studies have demonstrated that less than 30% of the patients have achieved the recommended level (13). In addition, the patients with low HDL-C and/or elevated triglycerides remained at an elevated residual risk even at the recommended LDL-C targets. Hypertriglyceridemia is a significant independent predictor of CHD, but its association is not as strong as that of LDL (14). Low level of HDL cholesterol is an independent and important risk factor for coronary artery disease . The combination of moderately elevated triglycerides and low concentration of HDL cholesterol is very common in diabetic patients (15). In comparison to LDL, non-HDL cholesterol is more strongly associated with CAD risk. It is particularly more reliable than LDL calculated through the formula in the patients with hypertriglyceridemia (16). In this study, none of the dyslipidemic patients had controlled total cholesterol, LDL, HDL, and triglyceride. Thus, dyslipidemia can be another important therapeutic target for health providers.

Hypertension is one of the leading preventable causes of premature CHD and thereby death (17). Hypertensive patients more commonly have other atherosclerotic risk factors which may interact with high blood pressure. Thus, hypertensive patients are at increased risk despite the mild or moderate elevation in blood pressure. Therapeutic lifestyle changes and pharmacologic interventions are mandatory for controlling hypertension. However, only 34% of the hypertensive patients achieved controlled blood pressure in this study.

Furthermore, diabetic patients have a two- to four- fold increased risk for development of CAD and death (18). In diabetic patients, intensive management of hyperglycemia reduces the percentage of microvascular complications and, to a lower degree, the percentage of macrovascular complications. Overall, the target HbA1C in diabetic patients is<7% after the treatment; however, none of the diabetic patients had hemoglobin A1C<7% in this study.

Smoking is the most important risk factor for vascular disease worldwide. Some studies have shown that 40% of all heart diseases are related to smoking (19). Also, evidence has demonstrated that smoking cessation is associated with significant reduction in the risk of CHD, cerebrovascular diseases, and cancers. The relative risk of heart attack in the smokers below 50 years old is five folds higher than that of the non-smokers, while this risk is only doubled in the smokers above 60 years old (20).

Passive smoking also increases the risk of CAD more than it might be expected (21). Therefore, behavioral skills and pharmacologic treatments are recommended to facilitate smoking cessation (22). In the current study, 46.4% of the patients with premature CHD were smokers and none of them had successful smoking cessation.

Among the study subjects, 120 ones (96%) had at least one of the risk factors, including dyslipidemia, hypertension, diabetes mellitus, cigarette smoking, and family history of CHD. In other studies also, 90% of the patients with CHD had one atherosclerotic risk factor (23).

Regular physical activity reduces the risk of fatal and non-fatal coronary events in not only the healthy individuals, but also the patients suffering from atherosclerotic risk factors (24). Hence, guidelines have recommended physical activity as a very effective non-pharmacological tool in primary prevention (12). In the present study, regular physical activities were restricted to 2.4% of the patients.

CHD with its long asymptomatic latent period provides an opportunity for early effective preventions (25).

Atherosclerotic cardiovascular disease, especially CHD, is the leading cause of death worldwide; however, the mortality rate can be significantly reduced (more than 50%) with good primary prevention of CHD (12).

6. Conclusion

Traditional risk factors, such as dyslipidemia, hypertension, diabetes, and smoking, are significantly related to premature CHD. However, the researchers assume that full treatment of known and well-defined risk factors was not accomplished in this study.

Study limitations

The present study had some limitations. First, the data regarding weight, height, and body mass index were incomplete. Furthermore, physical activity as a part of the occupational work of the patients was not taken into consideration. Second, self-reported family histories might be potentially impacted by recall bias. In the previous studies, the positive predictive value for self-reports of premature CHD was low, while the negative predictive value was high (26). Finally, further studies are needed to be conducted on a larger number of patients in order to arrive at more reliable findings.

Acknowledgments

This study was approved and supported by Shahid Beheshti University of Medical Sciences, Tehran,IR Iran.

Footnotes

Implication for health policy/practice/research/medical education:

Premature Coronary Heart Disease is a public health problem. Traditional cardiovascular risk factors are strong predictors of an increased likelihood for premature CHD. However, there is lack of intensive treatments of well-defined risk factors and prevention methods for the majority of the patients experiencing premature CHD. The main objective of this study was to determine the prevalence and management of these risk factors in patients with early CHD. The findings can be useful in better and more aggressive treatment of risk factors in patients without CAD.

Please cite this paper as:

Sadeghi R, Adnani N, Erfanifar A, Gachkar L, Maghsoomi Z. Premature Coronary Heart Disease and Traditional Risk Factors-Can We Do Better? Int Cardiovasc Res J.2013;7(2):46-50.11408

Financial Disclosure:

None declared.

Funding/Support:

None declared.

References

  • 1.Akosah KO, Gower E, Groon L, Rooney BL, Schaper A. Mild hypercholesterolemia and premature heart disease: do the national criteria underestimate disease risk? J Am Coll Cardiol. 2000;35(5):1178–84. doi: 10.1016/s0735-1097(00)00556-8. [DOI] [PubMed] [Google Scholar]
  • 2.Hosseini SK, Soleimani A, Salarifar M, Pourhoseini H, Nematipoor E, Abbasi SH, et al. Demographics and Angiographic Findings in Patients under 35 Years of Age with Acute ST Elevation Myocardial Infarction. J Tehran Heart Cent. 2011;6(2):62–7. [PMC free article] [PubMed] [Google Scholar]
  • 3.Murabito JM, Pencina MJ, Nam BH, D'Agostino RB, Sr., Wang TJ, Lloyd-Jones D, et al. Sibling cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults. JAMA. 2005;294(24):3117–23. doi: 10.1001/jama.294.24.3117. [DOI] [PubMed] [Google Scholar]
  • 4.Nasir K, Budoff MJ, Wong ND, Scheuner M, Herrington D, Arnett DK, et al. Family history of premature coronary heart disease and coronary artery calcification: Multi-Ethnic Study of Atherosclerosis (MESA). Circulation. 2007;116(6):619–26. doi: 10.1161/CIRCULATIONAHA.107.688739. [DOI] [PubMed] [Google Scholar]
  • 5.Lloyd-Jones DM, Nam BH, D'Agostino RB, Sr., Levy D, Murabito JM, Wang TJ, et al. Parental cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults: a prospective study of parents and offspring. JAMA. 2004;291(18):2204–11. doi: 10.1001/jama.291.18.2204. [DOI] [PubMed] [Google Scholar]
  • 6.Pletcher MJ, Lazar L, Bibbins-Domingo K, Moran A, Rodondi N, Coxson P, et al. Comparing impact and cost-effectiveness of primary prevention strategies for lipid-lowering. Ann Intern Med. 2009;150(4):243–54. doi: 10.7326/0003-4819-150-4-200902170-00005. [DOI] [PubMed] [Google Scholar]
  • 7.Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report. Circulation. 2002;106(25):3143–421. [PubMed] [Google Scholar]
  • 8.Bensen JT, Li R, Hutchinson RG, Province MA, Tyroler HA. Family history of coronary heart disease and pre-clinical carotid artery atherosclerosis in African-Americans and whites: the ARIC study: Atherosclerosis Risk in Communities. Genet Epidemiol. 1999;16(2):165–78. doi: 10.1002/(SICI)1098-2272(1999)16:2&#x0003c;165::AID-GEPI4&#x0003e;3.0.CO;2-H. [DOI] [PubMed] [Google Scholar]
  • 9.Sesso HD, Lee IM, Gaziano JM, Rexrode KM, Glynn RJ, Buring JE. Maternal and paternal history of myocardial infarction and risk of cardiovascular disease in men and women. Circulation. 2001;104(4):393–8. doi: 10.1161/hc2901.093115. [DOI] [PubMed] [Google Scholar]
  • 10.Hawe E, Talmud PJ, Miller GJ, Humphries SE. Family history is a coronary heart disease risk factor in the Second Northwick Park Heart Study. Ann Hum Genet. 2003;67(Pt 2):97–106. doi: 10.1046/j.1469-1809.2003.00017.x. [DOI] [PubMed] [Google Scholar]
  • 11.Greenland P, Smith SC,, Jr., Grundy SM. Improving coronary heart disease risk assessment in asymptomatic people: role of traditional risk factors and noninvasive cardiovascular tests. Circulation. 2001;104(15):1863–7. doi: 10.1161/hc4201.097189. [DOI] [PubMed] [Google Scholar]
  • 12.Perk J, De Backer G, Gohlke H, Graham I, Reiner Z, Verschuren M, et al. European Guidelines on cardiovascular disease prevention in clinical practice (version 2012). The Fifth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of nine societies and by invited experts). Eur Heart J. 2012;33(13):1635–701. doi: 10.1093/eurheartj/ehs092. [DOI] [PubMed] [Google Scholar]
  • 13.Ghandehari H, Kamal-Bahl S, Wong ND. Prevalence and extent of dyslipidemia and recommended lipid levels in US adults with and without cardiovascular comorbidities: the National Health and Nutrition Examination Survey 2003-2004. Am Heart J. 2008;156(1):112–9. doi: 10.1016/j.ahj.2008.03.005. [DOI] [PubMed] [Google Scholar]
  • 14.Sarwar N, Danesh J, Eiriksdottir G, Sigurdsson G, Wareham N, Bingham S, et al. Triglycerides and the risk of coronary heart disease: 10,158 incident cases among 262,525 participants in 29 Western prospective studies. Circulation. 2007;115(4):450–8. doi: 10.1161/CIRCULATIONAHA.106.637793. [DOI] [PubMed] [Google Scholar]
  • 15.Chapman MJ, Ginsberg HN, Amarenco P, Andreotti F, Boren J, Catapano AL, et al. Triglyceride-rich lipoproteins and high-density lipoprotein cholesterol in patients at high risk of cardiovascular disease: evidence and guidance for management. Eur Heart J. 2011;32(11):1345–61. doi: 10.1093/eurheartj/ehr112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Robinson JG, Wang S, Smith BJ, Jacobson TA. Meta-analysis of the relationship between non-high-density lipoprotein cholesterol reduction and coronary heart disease risk. J Am Coll Cardiol. 2009;53(4):316–22. doi: 10.1016/j.jacc.2008.10.024. [DOI] [PubMed] [Google Scholar]
  • 17.Kearney PM, Whelton M, Reynolds K, Muntner P, Whelton PK, He J. Global burden of hypertension: analysis of worldwide data. Lancet. 2005;365(9455):217–23. doi: 10.1016/S0140-6736(05)17741-1. [DOI] [PubMed] [Google Scholar]
  • 18.Preis SR, Hwang SJ, Coady S, Pencina MJ, D'Agostino RB, Sr., Savage PJ, et al. Trends in all-cause and cardiovascular disease mortality among women and men with and without diabetes mellitus in the Framingham Heart Study, 1950 to 2005. Circulation. 2009;119(13):1728–35. doi: 10.1161/CIRCULATIONAHA.108.829176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Teo KK, Ounpuu S, Hawken S, Pandey MR, Valentin V, Hunt D, et al. Tobacco use and risk of myocardial infarction in 52 countries in the INTERHEART study: a case-control study. Lancet. 2006;368(9536):647–58. doi: 10.1016/S0140-6736(06)69249-0. [DOI] [PubMed] [Google Scholar]
  • 20.Edwards R. The problem of tobacco smoking. BMJ. 2004;328(7433):217–9. doi: 10.1136/bmj.328.7433.217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Raupach T, Schafer K, Konstantinides S, Andreas S. Secondhand smoke as an acute threat for the cardiovascular system: a change in paradigm. Eur Heart J. 2006;27(4):386–92. doi: 10.1093/eurheartj/ehi601. [DOI] [PubMed] [Google Scholar]
  • 22.Bairey Merz CN, Alberts MJ, Balady GJ, Ballantyne CM, Berra K, Black HR, et al. ACCF/AHA/ACP 2009 competence and training statement: a curriculum on prevention of cardiovascular disease: a report of the American College of Cardiology Foundation/American Heart Association/American College of Physicians Task Force on Competence and Training (Writing Committee to Develop a Competence and Training Statement on Prevention of Cardiovascular Disease): developed in collaboration with the American Academy of Neurology; American Association of Cardiovascular and Pulmonary Rehabilitation; American College of Preventive Medicine; American College of Sports Medicine; American Diabetes Association; American Society of Hypertension; Association of Black Cardiologists; Centers for Disease Control and Prevention; National Heart, Lung, and Blood Institute; National Lipid Association; and Preventive Cardiovascular Nurses Association. J Am Coll Cardiol. 2009;54(14):1336–63. doi: 10.1016/j.jacc.2009.05.019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Greenland P, Knoll MD, Stamler J, Neaton JD, Dyer AR, Garside DB, et al. Major risk factors as antecedents of fatal and nonfatal coronary heart disease events. JAMA. 2003;290(7):891–7. doi: 10.1001/jama.290.7.891. [DOI] [PubMed] [Google Scholar]
  • 24.Lollgen H, Bockenhoff A, Knapp G. Physical activity and all-cause mortality: an updated meta-analysis with different intensity categories. Int J Sports Med. 2009;30(3):213–24. doi: 10.1055/s-0028-1128150. [DOI] [PubMed] [Google Scholar]
  • 25.Greenland P, Alpert JS, Beller GA, Benjamin EJ, Budoff MJ, Fayad ZA, et al. 2010 ACCF/AHA guideline for assessment of cardiovascular risk in asymptomatic adults: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Circulation. 2010;122(25):e584–636. doi: 10.1161/CIR.0b013e3182051b4c. [DOI] [PubMed] [Google Scholar]
  • 26.Murabito JM, Nam BH, D'Agostino RB, Sr., Lloyd-Jones DM, O'Donnell CJ, Wilson PW. Accuracy of offspring reports of parental cardiovascular disease history: the Framingham Offspring Study. Ann Intern Med. 2004;140(6):434–40. doi: 10.7326/0003-4819-140-6-200403160-00010. [DOI] [PubMed] [Google Scholar]

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