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Abstract Considering that cardiovascular diseases continue to be the leading cause of mortality in industrialized countries, more effort was required to reduce the burden of these diseases. In this context, lifestyle modifications based on avoiding smoking, taking regular physical exercise, and improving control of hypertension could be the most effective intervention at the population level. Despite the advances in our understanding of nontraditional risk factors/biomarkers for CVD, the clinical utility of nontraditional risk factors/biomarkers for CVD were limited in young age population because of inconsistent associations and lack of replication of findings. With the increasing connection between obesity at young age and CVD, biomarkers produced from adipose tissue and those with roles in inflammation and oxidative stress were increasingly being studied. This knowledge should eventually lead to the development of more directed therapeutic strategies to prevent CVD at an early age. It is likely that nontraditional risk factors/biomarkers could be used as a second layer of screening to follow interventions or efficacy of therapy and in Summary predicting specific patient groups likely to benefit from targeted interventions. The current evidence did not support the routine use of any of the nine risk factors for further risk stratification of intermediate-risk persons. According to the American Heart Association and the Centers for Disease Control and Prevention, we recommend against the use of hs-CRP as a risk marker in the general population and against the use of other inflammatory markers or acute-phase reactants for CHD risk prediction (Class III, Level of Evidence C). The AHA/ACC recommendation stated that ”measurement of hs-CRP is an independent marker of risk and, in those judged at intermediate risk by global risk assessment (10 to 20% risk of CHD per 10 years), at the discretion of the physician, may help direct further evaluation and therapy in the primary prevention of CVD. The benefits of such therapy based on this strategy remain uncertain. (Class IIa, Level of Evidence B).” Homocysteine level, hs-CRP level, carotid IMT, and CAC score on EBCT may be useful in certain circumstances but we do not recommend incorporating any emerging risk Summary factors into risk assessment for all persons receiving primary prevention risk assessment. According to current guidelines provided, we can advise on screening and identifying asymptomatic individuals at risk of developing CVD. The objectives of these guidelines were to reduce the incidence of first or recurrent clinical events due to coronary heart disease, ischemic stroke, and peripheral artery disease. The focus is on prevention of disability and early death. Also we recommend the role of lifestyle changes, the management of major cardiovascular risk factors and the use of different prophylactic drug therapies in the prevention of clinical CVD. On the other hand, we do not have to consider cardiovascular risk functions as diagnostic test because their sensitivity and specificity was low. These risk functions are screening test that help us to rationalize the selection of patients to implement different possible primary prevention strategies and their intensity. |