Cardiovascular disease |
|
Micrograph of a heart with fibrosis (yellow) and amyloidosis (brown). Movat's stain. |
Specialty |
Cardiology |
Usual onset |
Older adults[1] |
Types |
Coronary artery diseases, stroke, heart failure, hypertensive heart disease, rheumatic heart disease, cardiomyopathy[2][3] |
Prevention |
Healthy eating, exercise, avoiding tobacco smoke, limited alcohol intake[2] |
Treatment |
Treating high blood pressure, high blood lipids, diabetes[2] |
Deaths |
17.9 million / 32% (2015)[4] |
Cardiovascular disease (CVD) is a class of diseases that involve the heart or blood vessels.[2] Cardiovascular disease includes coronary artery diseases (CAD) such as angina and myocardial infarction (commonly known as a heart attack).[2] Other CVDs include stroke, heart failure, hypertensive heart disease, rheumatic heart disease, cardiomyopathy, heart arrhythmia, congenital heart disease, valvular heart disease, carditis, aortic aneurysms, peripheral artery disease, thromboembolic disease, and venous thrombosis.[2][3]
The underlying mechanisms vary depending on the disease in question.[2] Coronary artery disease, stroke, and peripheral artery disease involve atherosclerosis.[2] This may be caused by high blood pressure, smoking, diabetes, lack of exercise, obesity, high blood cholesterol, poor diet, and excessive alcohol consumption, among others.[2] High blood pressure results in 13% of CVD deaths, while tobacco results in 9%, diabetes 6%, lack of exercise 6% and obesity 5%.[2] Rheumatic heart disease may follow untreated strep throat.[2]
It is estimated that 90% of CVD is preventable.[5] Prevention of atherosclerosis involves improving risk factors through: healthy eating, exercise, avoidance of tobacco smoke and limiting alcohol intake.[2] Treating risk factors, such as high blood pressure, blood lipids and diabetes is also beneficial.[2] Treating people who have strep throat with antibiotics can decrease the risk of rheumatic heart disease.[6] The effect of the use of aspirin in people who are otherwise healthy is of unclear benefit.[7][8]
Cardiovascular diseases are the leading cause of death globally.[2] This is true in all areas of the world except Africa.[2] Together they resulted in 17.9 million deaths (32.1%) in 2015, up from 12.3 million (25.8%) in 1990.[4][3] Deaths, at a given age, from CVD are more common and have been increasing in much of the developing world, while rates have declined in most of the developed world since the 1970s.[9][10] Coronary artery disease and stroke account for 80% of CVD deaths in males and 75% of CVD deaths in females.[2] Most cardiovascular disease affects older adults. In the United States 11% of people between 20 and 40 have CVD, while 37% between 40 and 60, 71% of people between 60 and 80, and 85% of people over 80 have CVD.[1] The average age of death from coronary artery disease in the developed world is around 80 while it is around 68 in the developing world.[9] Disease onset is typically seven to ten years earlier in men as compared to women.[11]
Contents
- 1 Types
- 2 Risk factors
- 2.1 Genetics
- 2.2 Age
- 2.3 Sex
- 2.4 Tobacco
- 2.5 Physical inactivity
- 2.6 Diet
- 2.7 Celiac disease
- 2.8 Socioeconomic disadvantage
- 2.9 Air pollution
- 2.10 Cardiovascular risk assessment
- 2.11 Occupational exposure
- 2.11.1 Chemical risk factors
- 2.11.2 Non-chemical risk factors
- 2.12 Somatic mutations
- 3 Pathophysiology
- 4 Screening
- 5 Prevention
- 5.1 Diet
- 5.2 Medication
- 5.3 Physical activity
- 5.4 Dietary supplements
- 6 Management
- 7 Epidemiology
- 8 Research
- 9 References
- 10 External links
Types
Disability-adjusted life year for inflammatory heart diseases per 100,000 inhabitants in 2004[12]
no data
less than 70
70–140
140–210
210–280
280–350
350–420
420–490
490–560
560–630
630–700
700–770
more than 770
There are many cardiovascular diseases involving the blood vessels. They are known as vascular diseases.
- Coronary artery disease (also known as coronary heart disease and ischemic heart disease)
- Peripheral arterial disease – disease of blood vessels that supply blood to the arms and legs
- Cerebrovascular disease – disease of blood vessels that supply blood to the brain (includes stroke)
- Renal artery stenosis
- Aortic aneurysm
There are also many cardiovascular diseases that involve the heart.
- Cardiomyopathy – diseases of cardiac muscle
- Hypertensive heart disease – diseases of the heart secondary to high blood pressure or hypertension
- Heart failure - a clinical syndrome caused by the inability of the heart to supply sufficient blood to the tissues to meet their metabolic requirements
- Pulmonary heart disease – a failure at the right side of the heart with respiratory system involvement
- Cardiac dysrhythmias – abnormalities of heart rhythm
- Inflammatory heart disease
- Endocarditis – inflammation of the inner layer of the heart, the endocardium. The structures most commonly involved are the heart valves.
- Inflammatory cardiomegaly
- Myocarditis – inflammation of the myocardium, the muscular part of the heart, caused most often by viral infection and less often by bacterial infections, certain medications, toxins, and autoimmune disorders. It is characterized in part by infiltration of the heart by lymphocyte and monocyte types of white blood cells.
- Eosinophilic myocarditis - inflammation of the myocardium caused by pathologically activated eosinophilic white blood cells. This disorder differs from myocarditis in its causes and treatments.
- Valvular heart disease
- Congenital heart disease – heart structure malformations existing at birth
- Rheumatic heart disease – heart muscles and valves damage due to rheumatic fever caused by Streptococcus pyogenes a group A streptococcal infection.
Risk factors
There are many risk factors for heart diseases: age, gender, tobacco use, physical inactivity, excessive alcohol consumption, unhealthy diet, obesity, genetic predisposition and family history of cardiovascular disease, raised blood pressure (hypertension), raised blood sugar (diabetes mellitus), raised blood cholesterol (hyperlipidemia), undiagnosed celiac disease, psychosocial factors, poverty and low educational status, and air pollution.[13][14][15][16][17] While the individual contribution of each risk factor varies between different communities or ethnic groups the overall contribution of these risk factors is very consistent.[18] Some of these risk factors, such as age, gender or family history/genetic predisposition, are immutable; however, many important cardiovascular risk factors are modifiable by lifestyle change, social change, drug treatment (for example prevention of hypertension, hyperlipidemia, and diabetes).[19] People with obesity are at increased risk of atherosclerosis of the coronary arteries.[20]
Genetics
Genetic factors influence the development of cardiovascular disease in men who are less than 55 years-old and in women who are less than 65 years old.[19] Cardiovascular disease in a person's parents increases their risk by 3 fold.[21] Multiple single nucleotide polymorphisms (SNP) have been found to be associated with cardiovascular disease in genetic association studies,[22][23] but usually their individual influence is small, and genetic contributions to cardiovascular disease are poorly understood.[23]
Age
Calcified heart of an older woman with cardiomegaly
Age is by far the most important risk factor in developing cardiovascular or heart diseases, with approximately a tripling of risk with each decade of life.[24] Coronary fatty streaks can begin to form in adolescence.[25] It is estimated that 82 percent of people who die of coronary heart disease are 65 and older.[26] At the same time, the risk of stroke doubles every decade after age 55.[27]
Multiple explanations have been proposed to explain why age increases the risk of cardiovascular/heart diseases. One of them is related to serum cholesterol level.[28] In most populations, the serum total cholesterol level increases as age increases. In men, this increase levels off around age 45 to 50 years. In women, the increase continues sharply until age 60 to 65 years.[28]
Aging is also associated with changes in the mechanical and structural properties of the vascular wall, which leads to the loss of arterial elasticity and reduced arterial compliance and may subsequently lead to coronary artery disease.[29]
Sex
Men are at greater risk of heart disease than pre-menopausal women.[24][30] Once past menopause, it has been argued that a woman's risk is similar to a man's[30] although more recent data from the WHO and UN disputes this.[24] If a female has diabetes, she is more likely to develop heart disease than a male with diabetes.[31]
Coronary heart diseases are 2 to 5 times more common among middle-aged men than women.[28] In a study done by the World Health Organization, sex contributes to approximately 40% of the variation in sex ratios of coronary heart disease mortality.[32] Another study reports similar results finding that gender differences explains nearly half the risk associated with cardiovascular diseases[28] One of the proposed explanations for gender differences in cardiovascular diseases is hormonal difference.[28] Among women, estrogen is the predominant sex hormone. Estrogen may have protective effects on glucose metabolism and hemostatic system, and may have direct effect in improving endothelial cell function.[28] The production of estrogen decreases after menopause, and this may change the female lipid metabolism toward a more atherogenic form by decreasing the HDL cholesterol level while increasing LDL and total cholesterol levels.[28]
Among men and women, there are notable differences in body weight, height, body fat distribution, heart rate, stroke volume, and arterial compliance.[29] In the very elderly, age-related large artery pulsatility and stiffness is more pronounced among women than men.[29] This may be caused by the women's smaller body size and arterial dimensions which are independent of menopause.[29]
Tobacco
Cigarettes are the major form of smoked tobacco.[2] Risks to health from tobacco use result not only from direct consumption of tobacco, but also from exposure to second-hand smoke.[2] Approximately 10% of cardiovascular disease is attributed to smoking;[2] however, people who quit smoking by age 30 have almost as low a risk of death as never smokers.[33]
Physical inactivity
Insufficient physical activity (defined as less than 5 x 30 minutes of moderate activity per week, or less than 3 x 20 minutes of vigorous activity per week) is currently the fourth leading risk factor for mortality worldwide.[2] In 2008, 31.3% of adults aged 15 or older (28.2% men and 34.4% women) were insufficiently physically active.[2] The risk of ischemic heart disease and diabetes mellitus is reduced by almost a third in adults who participate in 150 minutes of moderate physical activity each week (or equivalent).[34] In addition, physical activity assists weight loss and improves blood glucose control, blood pressure, lipid profile and insulin sensitivity. These effects may, at least in part, explain its cardiovascular benefits.[2]
Diet
High dietary intakes of saturated fat, trans-fats and salt, and low intake of fruits, vegetables and fish are linked to cardiovascular risk, although whether all these associations are a cause is disputed. The World Health Organization attributes approximately 1.7 million deaths worldwide to low fruit and vegetable consumption.[2] The amount of dietary salt consumed is also an important determinant of blood pressure levels and overall cardiovascular risk.[2] Frequent consumption of high-energy foods, such as processed foods that are high in fats and sugars, promotes obesity and may increase cardiovascular risk.[2] A Cochrane review found that replacing saturated fat with polyunsaturated fat (plant based oils) reduced cardiovascular disease risk. Cutting down on saturated fat reduced risk of cardiovascular disease by 17% including heart disease and stroke.[35] High trans-fat intake has adverse effects on blood lipids and circulating inflammatory markers,[36] and elimination of trans-fat from diets has been widely advocated.[37] There is evidence that higher consumption of sugar is associated with higher blood pressure and unfavorable blood lipids,[38] and sugar intake also increases the risk of diabetes mellitus.[39] High consumption of processed meats is associated with an increased risk of cardiovascular disease, possibly in part due to increased dietary salt intake.[40]
The relationship between alcohol consumption and cardiovascular disease is complex, and may depend on the amount of alcohol consumed. There is a direct relationship between high levels of alcohol consumption and risk of cardiovascular disease.[2] Drinking at low levels without episodes of heavy drinking may be associated with a reduced risk of cardiovascular disease.[41] Overall alcohol consumption at the population level is associated with multiple health risks that exceed any potential benefits.[2][42]
Celiac disease
Untreated celiac disease can cause the development of many types of cardiovascular diseases, most of which improve or resolve with a gluten-free diet and intestinal healing. However, delays in recognition and diagnosis of celiac disease can cause irreversible heart damage.[17]
Socioeconomic disadvantage
Cardiovascular disease affects low- and middle-income countries even more than high-income countries.[43] There is relatively little information regarding social patterns of cardiovascular disease within low- and middle-income countries,[43] but within high-income countries low income and low educational status are consistently associated with greater risk of cardiovascular disease.[44] Policies that have resulted in increased socio-economic inequalities have been associated with greater subsequent socio-economic differences in cardiovascular disease[43] implying a cause and effect relationship. Psychosocial factors, environmental exposures, health behaviours, and health-care access and quality contribute to socio-economic differentials in cardiovascular disease. [45] The Commission on Social Determinants of Health recommended that more equal distributions of power, wealth, education, housing, environmental factors, nutrition, and health care were needed to address inequalities in cardiovascular disease and non-communicable diseases.[46]
Air pollution
Particulate matter has been studied for its short- and long-term exposure effects on cardiovascular disease. Currently, PM2.5 is the major focus, in which gradients are used to determine CVD risk. For every 10 μg/m3 of PM2.5 long-term exposure, there was an estimated 8–18% CVD mortality risk.[47] Women had a higher relative risk (RR) (1.42) for PM2.5 induced coronary artery disease than men (0.90) did.[47] Overall, long-term PM exposure increased rate of atherosclerosis and inflammation. In regards to short-term exposure (2 hours), every 25 μg/m3 of PM2.5 resulted in a 48% increase of CVD mortality risk.[48] In addition, after only 5 days of exposure, a rise in systolic (2.8 mmHg) and diastolic (2.7 mmHg) blood pressure occurred for every 10.5 μg/m3 of PM2.5.[48] Other research has implicated PM2.5 in irregular heart rhythm, reduced heart rate variability (decreased vagal tone), and most notably heart failure.[48][49] PM2.5 is also linked to carotid artery thickening and increased risk of acute myocardial infarction.[48][49]
Cardiovascular risk assessment
Existing cardiovascular disease or a previous cardiovascular event, such as a heart attack or stroke, is the strongest predictor of a future cardiovascular event.[50] Age, sex, smoking, blood pressure, blood lipids and diabetes are important predictors of future cardiovascular disease in people who are not known to have cardiovascular disease.[51] These measures, and sometimes others, may be combined into composite risk scores to estimate an individual's future risk of cardiovascular disease.[50] Numerous risk scores exist although their respective merits are debated.[52] Other diagnostic tests and biomarkers remain under evaluation but currently these lack clear-cut evidence to support their routine use. They include family history, coronary artery calcification score, high sensitivity C-reactive protein (hs-CRP), ankle–brachial pressure index, lipoprotein subclasses and particle concentration, lipoprotein(a), apolipoproteins A-I and B, fibrinogen, white blood cell count, homocysteine, N-terminal pro B-type natriuretic peptide (NT-proBNP), and markers of kidney function.[53][54] High blood phosphorus is also linked to an increased risk.[55]
Occupational exposure
Main article: Occupational cardiovascular disease
Little is known about the relationship between work and cardiovascular disease, but links have been established between certain toxins, extreme heat and cold, exposure to tobacco smoke, and mental health concerns such as stress and depression.[56]
Chemical risk factors
A 2015 SBU-report looking at non-chemical factors found an association for those:[57]
- with mentally stressful work with a lack of control over their working situation — with an effort-reward imbalance[57]
- who experience low social support at work; who experience injustice or experience insufficient opportunities for personal development; or those who experience job insecurity[57]
- those who work night schedules; or have long working weeks[57]
- those who are exposed to noise[57]
Specifically the risk of stroke was also increased by exposure to ionizing radiation.[57] Hypertension develops more often in those who experience job strain and who have shift-work.[57] Differences between women and men in risk are small, however men risk suffering and dying of heart attacks or stroke twice as often as women during working life.[57]
Non-chemical risk factors
A 2017 SBU report found evidence that workplace exposure to silica dust, engine exhaust or welding fumes is associated with heart disease.[58] Associations also exist for exposure to arsenic, benzopyrenes, lead, dynamite, carbon disulphide, carbon monoxide, metalworking fluids and occupational exposure to tobacco smoke.[58] Working with the electrolytic production of aluminium or the production of paper when the sulphate pulping process is used is associated with heart disease.[58] An association was also found between heart disease and exposure to compounds which are no longer permitted in certain work environments, such as phenoxy acids containing TCDD(dioxin) or asbestos.[58]
Workplace exposure to silica dust or asbestos is also associated with pulmonary heart disease.There is evidence that workplace exposure to lead, carbon disulphide, phenoxyacids containing TCDD, as well as working in an environment where aluminium is being electrolytically produced, is associated with stroke.[58]
Somatic mutations
As of 2017, evidence suggests that certain leukemia-associated mutations in blood cells may also lead to increased risk of cardiovascular disease. Several large-scale research projects looking at human genetic data have found a robust link between the presence of these mutations, a condition known as clonal hematopoiesis, and cardiovascular disease-related incidents and mortality.[59]
Pathophysiology
Density-Dependent Colour Scanning Electron Micrograph SEM (DDC-SEM) of cardiovascular calcification, showing in orange calcium phosphate spherical particles (denser material) and, in green, the extracellular matrix (less dense material)
[60]
Population-based studies show that atherosclerosis, the major precursor of cardiovascular disease, begins in childhood. The Pathobiological Determinants of Atherosclerosis in Youth (PDAY) study demonstrated that intimal lesions appear in all the aortas and more than half of the right coronary arteries of youths aged 7–9 years.[61]
This is extremely important considering that 1 in 3 people die from complications attributable to atherosclerosis. In order to stem the tide, education and awareness that cardiovascular disease poses the greatest threat, and measures to prevent or reverse this disease must be taken.
Obesity and diabetes mellitus are often linked to cardiovascular disease,[62] as are a history of chronic kidney disease and hypercholesterolaemia.[63] In fact, cardiovascular disease is the most life-threatening of the diabetic complications and diabetics are two- to four-fold more likely to die of cardiovascular-related causes than nondiabetics.[64][65][66]
Screening
Screening ECGs (either at rest or with exercise) are not recommended in those without symptoms who are at low risk.[67] This includes those who are young without risk factors.[68] In those at higher risk the evidence for screening with ECGs is inconclusive.[67]
Additionally echocardiography, myocardial perfusion imaging, and cardiac stress testing is not recommended in those at low risk who do not have symptoms.[69]
Some biomarkers may add to conventional cardiovascular risk factors in predicting the risk of future cardiovascular disease; however, the clinical value of some biomarkers is questionable.[70][71]
The NIH recommends lipid testing in children beginning at the age of 2 if there is a family history of heart disease or lipid problems.[72] It is hoped that early testing will improve lifestyle factors in those at risk such as diet and exercise.[73]
Screening and selection for primary prevention interventions has traditionally been done through absolute risk using a variety of scores (ex. Framingham or Reynolds risk scores).[74] This stratification has separated people who receive the lifestyle interventions (generally lower and intermediate risk) from the medication (higher risk). The number and variety of risk scores available for use has multiplied, but their efficacy according to a 2016 review was unclear due to lack of external validation or impact analysis.[75] Risk stratification models often lack sensitivity for population groups and do not account for the large number of negative events among the intermediate and low risk groups.[74] As a result, future preventative screening appears to shift toward applying prevention according to randomized trial results of each intervention rather than large-scale risk assessment.
Prevention
Up to 90% of cardiovascular disease may be preventable if established risk factors are avoided.[76][77] Currently practiced measures to prevent cardiovascular disease include:
- Tobacco cessation and avoidance of second-hand smoke.[78] Smoking cessation reduces risk by about 35%.[79]
- A low-fat, low-sugar, high-fiber diet including whole grains and fruit and vegetables.[78][80][81] Dietary interventions are effective in reducing cardiovascular risk factors over a year, but the longer term effects of such interventions and their impact on cardiovascular disease events is uncertain.[82]
- At least 150 minutes (2 hours and 30 minutes) of moderate exercise per week.[83][84] Exercise-based cardiac rehabilitation reduces risk of subsequent cardiovascular events by 26%,[85] but there have been few high quality studies of the benefits of exercise training in people with increased cardiovascular risk but no history of cardiovascular disease.[86]
- Limit alcohol consumption to the recommended daily limits;[78] People who moderately consume alcoholic drinks have a 25–30% lower risk of cardiovascular disease.[87][88] However, people who are genetically predisposed to consume less alcohol have lower rates of cardiovascular disease[89] suggesting that alcohol itself may not be protective. Excessive alcohol intake increases the risk of cardiovascular disease[90][88] and consumption of alcohol is associated with increased risk of a cardiovascular event in the day following consumption.[88]
- Lower blood pressure, if elevated. A 10 mmHg reduction in blood pressure reduces risk by about 20%.[91]
- Decrease non-HDL cholesterol.[92][93] Statin treament reduces cardiovascular mortality by about 31%.[94]
- Decrease body fat if overweight or obese.[95] The effect of weight loss is often difficult to distinguish from dietary change, and evidence on weight reducing diets is limited.[96] In observational studies of people with severe obesity, weight loss following bariatric surgery is associated with a 46% reduction in cardiovascular risk.[97]
- Decrease psychosocial stress.[98] This measure may be complicated by imprecise definitions of what constitute psychosocial interventions.[99] Mental stress–induced myocardial ischemia is associated with an increased risk of heart problems in those with previous heart disease.[100] Severe emotional and physical stress leads to a form of heart dysfunction known as Takotsubo syndrome in some people.[101] Stress, however, plays a relatively minor role in hypertension.[102] Specific relaxation therapies are of unclear benefit.[103][104]
Most guidelines recommend combining preventive strategies. A 2015 Cochrane Review found some evidence that interventions aiming to reduce more than one cardiovascular risk factor may have beneficial effects on blood pressure, body mass index and waist circumference; however, evidence was limited and the authors were unable to draw firm conclusions on the effects on cardiovascular events and mortality.[105] For adults without a known diagnosis of hypertension, diabetes, hyperlipidemia, or cardiovascular disease, routine counseling to advise them to improve their diet and increase their physical activity has not been found to significantly alter behavior, and thus is not recommended.[106] Another Cochrane review suggested that simply providing people with a cardiovascular disease risk score may reduce cardiovascular disease risk factors by a small amount compared to usual care.[107] However, there was some uncertainty as to whether providing these scores had any effect on cardiovascular disease events. It is unclear whether or not dental care in those with periodontitis affects their risk of cardiovascular disease.[108]
Diet
See also: Saturated fat and cardiovascular disease and Salt and cardiovascular disease
A diet high in fruits and vegetables decreases the risk of cardiovascular disease and death.[109] Evidence suggests that the Mediterranean diet may improve cardiovascular outcomes.[110] There is also evidence that a Mediterranean diet may be more effective than a low-fat diet in bringing about long-term changes to cardiovascular risk factors (e.g., lower cholesterol level and blood pressure).[111] The DASH diet (high in nuts, fish, fruits and vegetables, and low in sweets, red meat and fat) has been shown to reduce blood pressure,[112] lower total and low density lipoprotein cholesterol[113] and improve metabolic syndrome;[114] but the long-term benefits outside the context of a clinical trial have been questioned.[115] A high fiber diet appears to lower the risk.[116]
Total fat intake does not appear to be an important risk factor.[117][118] A diet high in trans fatty acids, however, does increase rates of cardiovascular disease.[118][119] Worldwide, dietary guidelines recommend a reduction in saturated fat.[120] However, there are some questions around the effect of saturated fat on cardiovascular disease in the medical literature.[119][121] Reviews from 2014 and 2015 did not find evidence of harm from saturated fats.[119][121] A 2012 Cochrane review found suggestive evidence of a small benefit from replacing dietary saturated fat by unsaturated fat.[122] A 2013 meta analysis concludes that substitution with omega 6 linoleic acid (a type of unsaturated fat) may increase cardiovascular risk.[120] Replacement of saturated fats with carbohydrates does not change or may increase risk.[123][124] Benefits from replacement with polyunsaturated fat appears greatest;[118][125] however, supplementation with omega-3 fatty acids (a type of polysaturated fat) does not appear to have an effect.[126]
A 2014 Cochrane review found unclear benefit of recommending a low-salt diet in people with high or normal blood pressure.[127] In those with heart failure, after one study was left out, the rest of the trials show a trend to benefit.[128][129] Another review of dietary salt concluded that there is strong evidence that high dietary salt intake increases blood pressure and worsens hypertension, and that it increases the number of cardiovascular disease events; both as a result of the increased blood pressure and, quite likely, through other mechanisms.[130][131] Moderate evidence was found that high salt intake increases cardiovascular mortality; and some evidence was found for an increase in overall mortality, strokes, and left ventricular hypertrophy.[130]
Medication
Blood pressure medication reduces cardiovascular disease in people at risk,[91] irrespective of age,[132] the baseline level of cardiovascular risk,[133] or baseline blood pressure.[134] The commonly-used drug regimens have similar efficacy in reducing the risk of all major cardiovascular events, although there may be differences between drugs in their ability to prevent specific outcomes.[135] Larger reductions in blood pressure produce larger reductions in risk,[135] and most people with high blood pressure require more than one drug to achieve adequate reduction in blood pressure.[136]
Statins are effective in preventing further cardiovascular disease in people with a history of cardiovascular disease.[137] As the event rate is higher in men than in women, the decrease in events is more easily seen in men than women.[137] In those at risk, but without a history of cardiovascular disease (primary prevention), statins decrease the risk of death and combined fatal and non-fatal cardiovascular disease.[138] A United States guideline recommends statins in those who have a 12% or greater risk of cardiovascular disease over the next ten years.[139] Niacin, fibrates and CETP Inhibitors, while they may increase HDL cholesterol do not affect the risk of cardiovascular disease in those who are already on statins.[140]
Anti-diabetic medication may reduce cardiovascular risk in people with Type 2 Diabetes, although evidence is not conclusive.[141] A meta-analysis in 2009 including 27,049 participants and 2,370 major vascular events showed a 15% relative risk reduction in cardiovascular disease with more-intensive glucose lowering over an average follow-up period of 4.4 years, but an increased risk of major hypoglycemia.[142]
Aspirin has been found to be of only modest benefit in those at low risk of heart disease as the risk of serious bleeding is almost equal to the benefit with respect to cardiovascular problems.[143] In those at very low risk it is not recommended.[144] The United States Preventive Services Task Force recommends against use of aspirin for prevention in women less than 55 and men less than 45 years old; however, in those who are older it is recommends in some individuals.[145]
The use of vasoactive agents for people with pulmonary hypertension with left heart disease or hypoxemic lung diseases may cause harm and unnecessary expense.[146]
Physical activity
A systematic review estimated that inactivity is responsible for 6% of the burden of disease from coronary heart disease worldwide.[147] The authors estimated that 121,000 deaths from coronary heart disease could have been averted in Europe in 2008, if physical inactivity had been removed. A Cochrane review found some evidence that yoga has beneficial effects on blood pressure and cholesterol, but studies included in this review were of low quality.[148]
Dietary supplements
While a healthy diet is beneficial, the effect of antioxidant supplementation (vitamin E, vitamin C, etc.) or vitamins has not been shown to protect against cardiovascular disease and in some cases may possibly result in harm.[149][150] Mineral supplements have also not been found to be useful.[151] Niacin, a type of vitamin B3, may be an exception with a modest decrease in the risk of cardiovascular events in those at high risk.[152][153] Magnesium supplementation lowers high blood pressure in a dose dependent manner.[154] Magnesium therapy is recommended for people with ventricular arrhythmia associated with torsades de pointes who present with long QT syndrome as well as for the treatment of people with digoxin intoxication-induced arrhythmias.[155] There is no evidence to support omega-3 fatty acid supplementation.[156]
Management
Cardiovascular disease is treatable with initial treatment primarily focused on diet and lifestyle interventions.[2] Influenza may make heart attacks and strokes more likely and therefore influenza vaccination may decrease the chance of cardiovascular events and death in people with heart disease.[157]
Proper CVD management necessitates a focus on MI and stroke cases due to their combined high mortality rate, keeping in mind the cost-effectiveness of any intervention, especially in developing countries with low or middle income levels.[74] Regarding MI, strategies using aspirin, atenolol, streptokinase or tissue plasminogen activator have been compared for quality-adjusted life-year (QALY) in regions of low and middle income. The costs for a single QALY for aspirin, atenolol, streptokinase, and t-PA were $25, $630–$730, and $16,000, respectively. Aspirin, ACE inhibitors, beta blockers, and statins used together for secondary CVD prevention in the same regions showed single QALY costs of $300–400.
Epidemiology
Cardiovascular diseases deaths per million persons in 2012
318–925
926–1,148
1,149–1,294
1,295–1,449
1,450–1,802
1,803–2,098
2,099–2,624
2,625–3,203
3,204–5,271
5,272–10233
Disability-adjusted life year for cardiovascular diseases per 100,000 inhabitants in 2004[12]
no data
<900
900–1650
1650–2300
2300–3000
3000–3700
3700–4400
4400–5100
5100–5800
5800–6500
6500–7200
7200–7900
>7900
Cardiovascular diseases are the leading cause of death worldwide and in all regions except Africa.[158] In 2008, 30% of all global death was attributed to cardiovascular diseases. Death caused by cardiovascular diseases are also higher in low- and middle-income countries as over 80% of all global deaths caused by cardiovascular diseases occurred in those countries. It is also estimated that by 2030, over 23 million people will die from cardiovascular diseases each year.
It is estimated that 60% of the world's cardiovascular disease burden will occur in the South Asian subcontinent despite only accounting for 20% of the world's population. This may be secondary to a combination of genetic predisposition and environmental factors. Organizations such as the Indian Heart Association are working with the World Heart Federation to raise awareness about this issue.[159]
Research
See also: Timeline of cardiovascular disease
There is evidence that cardiovascular disease existed in pre-history,[160] and research into cardiovascular disease dates from at least the 18th century.[161] The causes, prevention, and/or treatment of all forms of cardiovascular disease remain active fields of biomedical research, with hundreds of scientific studies being published on a weekly basis.
Recent areas of research include the link between inflammation and atherosclerosis[162] the potential for novel therapeutic interventions,[163] and the genetics of coronary heart disease.[164]
References
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- ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab Shanthi Mendis; Pekka Puska; Bo Norrving; World Health Organization (2011). Global Atlas on Cardiovascular Disease Prevention and Control (PDF). World Health Organization in collaboration with the World Heart Federation and the World Stroke Organization. pp. 3–18. ISBN 978-92-4-156437-3. Archived (PDF) from the original on 2014-08-17.
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External links
Classification |
V · T · D
- ICD-10: I51.6
- ICD-9-CM: 429.2
- MeSH: D002318
- DiseasesDB: 28808
|
- Cardiovascular disease at Curlie (based on DMOZ)
- European Guidelines on cardiovascular disease prevention in clinical practice (version 2012)
- Heart Disease MedicineNet Slides, photos, descriptions
Cardiovascular disease (heart) (I00–I52, 390–429)
|
Ischaemic |
Coronary disease |
- Coronary artery disease (CAD)
- Coronary artery aneurysm
- Spontaneous coronary artery dissection (SCAD)
- Coronary thrombosis
- Coronary vasospasm
- Myocardial bridge
|
Active ischemia |
- Angina pectoris
- Prinzmetal's angina
- Stable angina
- Acute coronary syndrome
- Myocardial infarction
- Unstable angina
|
Sequelae |
- hours
- Hibernating myocardium
- Myocardial stunning
- days
- weeks
- Aneurysm of heart / Ventricular aneurysm
- Dressler syndrome
|
|
Layers |
Pericardium |
- Pericarditis
- Acute
- Chronic / Constrictive
- Pericardial effusion
- Cardiac tamponade
- Hemopericardium
|
Myocardium |
- Myocarditis
- Cardiomyopathy
- Dilated
- Hypertrophic
- Restrictive
- Loeffler endocarditis
- Cardiac amyloidosis
- Endocardial fibroelastosis
- Arrhythmogenic right ventricular dysplasia
|
Endocardium /
valves |
Endocarditis |
- infective endocarditis
- Subacute bacterial endocarditis
- non-infective endocarditis
- Libman–Sacks endocarditis
- Nonbacterial thrombotic endocarditis
|
Valves |
- mitral
- regurgitation
- prolapse
- stenosis
- aortic
- tricuspid
- pulmonary
|
|
|
Conduction /
arrhythmia |
Bradycardia |
- Sinus bradycardia
- Sick sinus syndrome
- Heart block: Sinoatrial
- AV
- Intraventricular
- Bundle branch block
- Right
- Left
- Left anterior fascicle
- Left posterior fascicle
- Bifascicular
- Trifascicular
- Adams–Stokes syndrome
|
Tachycardia
(paroxysmal and sinus) |
Supraventricular |
- Atrial
- Junctional
- AV nodal reentrant
- Junctional ectopic
|
Ventricular |
- Accelerated idioventricular rhythm
- Catecholaminergic polymorphic
- Torsades de pointes
|
|
Premature contraction |
- Atrial
- Junctional
- Ventricular
|
Pre-excitation syndrome |
- Lown–Ganong–Levine
- Wolff–Parkinson–White
|
Flutter / fibrillation |
- Atrial flutter
- Ventricular flutter
- Atrial fibrillation
- Ventricular fibrillation
|
Pacemaker |
- Ectopic pacemaker / Ectopic beat
- Multifocal atrial tachycardia
- Pacemaker syndrome
- Parasystole
- Wandering pacemaker
|
Long QT syndrome |
- Andersen–Tawil
- Jervell and Lange-Nielsen
- Romano–Ward
|
Cardiac arrest |
- Sudden cardiac death
- Asystole
- Pulseless electrical activity
- Sinoatrial arrest
|
Other / ungrouped |
- hexaxial reference system
- Right axis deviation
- Left axis deviation
- QT
- T
- ST
- Osborn wave
- ST elevation
- ST depression
- Strain pattern
|
|
Cardiomegaly |
- Ventricular hypertrophy
- Left
- Right / Cor pulmonale
- Atrial enlargement
|
Other |
- Cardiac fibrosis
- Heart failure
- Diastolic heart failure
- Cardiac asthma
- Rheumatic fever
|
Cardiovascular disease (vessels) (I70–I99, 440–456)
|
Arteries, arterioles
and capillaries |
Inflammation |
- Arteritis
- Buerger's disease
|
Peripheral artery disease |
Arteriosclerosis |
- Atherosclerosis
- Foam cell
- Fatty streak
- Atheroma
- Intermittent claudication
- Critical limb ischemia
- Monckeberg's arteriosclerosis
- Arteriolosclerosis
- Hyaline
- Hyperplastic
- Cholesterol
- LDL
- Oxycholesterol
- Trans fat
|
Stenosis |
- Carotid artery stenosis
- Renal artery stenosis
|
Other |
- Aortoiliac occlusive disease
- Degos disease
- Erythromelalgia
- Fibromuscular dysplasia
- Raynaud's phenomenon
|
|
Aneurysm / dissection /
pseudoaneurysm |
- torso: Aortic aneurysm
- Abdominal aortic aneurysm
- Thoracic aortic aneurysm
- Aneurysm of sinus of Valsalva
- Aortic dissection
- Coronary artery aneurysm
- head / neck
- Intracranial aneurysm
- Intracranial berry aneurysm
- Carotid artery dissection
- Vertebral artery dissection
- Familial aortic dissection
|
Vascular malformation |
- Arteriovenous fistula
- Arteriovenous malformation
- Telangiectasia
- Hereditary hemorrhagic telangiectasia
|
Vascular nevus |
- Cherry hemangioma
- Halo nevus
- Spider angioma
|
|
Veins |
Inflammation |
|
Venous thrombosis /
Thrombophlebitis |
- primarily lower limb
- abdomen
- Hepatic veno-occlusive disease
- Budd–Chiari syndrome
- May–Thurner syndrome
- Portal vein thrombosis
- Renal vein thrombosis
- upper limb / torso
- Mondor's disease
- Paget–Schroetter disease
- head
- Cerebral venous sinus thrombosis
- Post-thrombotic syndrome
|
Varicose veins |
- Gastric varices
- Portacaval anastomosis
- Caput medusae
- Esophageal varices
- Hemorrhoid
- Varicocele
|
Other |
- Chronic venous insufficiency
- Chronic cerebrospinal venous insufficiency
- Superior vena cava syndrome
- Inferior vena cava syndrome
- Venous ulcer
|
|
Arteries or veins |
- Angiopathy
- Macroangiopathy
- Microangiopathy
- Embolism
- Pulmonary embolism
- Cholesterol embolism
- Paradoxical embolism
- Thrombosis
- Vasculitis
|
Blood pressure |
Hypertension |
- Hypertensive heart disease
- Hypertensive emergency
- Hypertensive nephropathy
- Essential hypertension
- Secondary hypertension
- Renovascular hypertension
- Benign hypertension
- Pulmonary hypertension
- Systolic hypertension
- White coat hypertension
|
Hypotension |
|
|
Certain conditions originating in the perinatal period / fetal disease (P, 760–779)
|
Maternal factors and
complications of pregnancy,
labour and delivery |
placenta: |
- Placenta praevia
- Placental insufficiency
- Twin-to-twin transfusion syndrome
|
chorion/amnion: |
|
umbilical cord: |
- Umbilical cord prolapse
- Nuchal cord
- Single umbilical artery
|
|
Length of gestation
and fetal growth |
- Small for gestational age/Large for gestational age
- Preterm birth/Postmature birth
- Intrauterine growth restriction
|
Birth trauma |
- scalp
- Cephalhematoma
- Chignon
- Caput succedaneum
- Subgaleal hemorrhage
- Brachial plexus lesion
- Erb's palsy
- Klumpke paralysis
|
By system |
Respiratory |
- Intrauterine hypoxia
- Infant respiratory distress syndrome
- Transient tachypnea of the newborn
- Meconium aspiration syndrome
- pleural disease
- Pneumothorax
- Pneumomediastinum
- Wilson–Mikity syndrome
- Bronchopulmonary dysplasia
|
Cardiovascular |
- Pneumopericardium
- Persistent fetal circulation
|
Haemorrhagic and
hematologic disease |
- Vitamin K deficiency
- Haemorrhagic disease of the newborn
- HDN
- ABO
- Anti-Kell
- Rh c
- Rh D
- Rh E
- Hydrops fetalis
- Hyperbilirubinemia
- Kernicterus
- Neonatal jaundice
- Velamentous cord insertion
- Intraventricular hemorrhage
- Germinal matrix hemorrhage
- Anemia of prematurity
|
Digestive |
- Ileus
- Necrotizing enterocolitis
- Meconium peritonitis
|
Integument and
thermoregulation |
- Erythema toxicum
- Sclerema neonatorum
|
Nervous system |
- Perinatal asphyxia
- Periventricular leukomalacia
|
Musculoskeletal |
- Gray baby syndrome
- muscle tone
- Congenital hypertonia
- Congenital hypotonia
|
|
Infectious |
- Vertically transmitted infection
- Neonatal infection
- Congenital rubella syndrome
- Neonatal herpes simplex
- Mycoplasma hominis infection
- Ureaplasma urealyticum infection
- Omphalitis
- Neonatal sepsis
- Group B streptococcal infection
- Neonatal conjunctivitis
|
Other |
- Miscarriage
- Perinatal mortality
- Stillbirth
- Infant mortality
- Neonatal withdrawal
|
Symptoms and signs relating to the cardiovascular system (R00–R03, 785)
|
Chest pain |
- Referred pain
- Angina
- Aerophagia
|
Auscultation |
- Heart sounds
- Split S2
- S3
- S4
- Gallop rhythm
- Heart murmur
- Systolic
- Diastolic
- Continuous
- Pericardial friction rub
- Heart click
- Bruit
|
Pulse |
- Tachycardia
- Bradycardia
- Pulsus tardus et parvus
- Pulsus paradoxus
- doubled
- Pulsus bisferiens
- Dicrotic pulse
- Pulsus bigeminus
- Pulsus alternans
- Pulse deficit
|
Vascular disease |
|
Other |
- Palpitations
- Cœur en sabot
- Jugular venous pressure
- Hyperaemia
|
Shock |
- Cardiogenic
- Hypovolemic
- Distributive
|
Eponymous medical signs for circulatory system
|
Heart disease |
Heart murmur |
- Systolic heart murmur: Benign paediatric heart murmur (Still's murmur)
- Diastolic heart murmur: Pulmonic regurgitation (Graham Steell murmur)
- Aortic insufficiency (Austin Flint murmur) Carey Coombs murmur
- Mitral regurgitation (Presystolic murmur)
|
Aortic insufficiency |
- Watson's water hammer pulse/Corrigan pulse
- De Musset's sign
- Duroziez's sign
- Müller's sign
- Quincke's sign
- Austin Flint murmur
- Mayne's sign
|
Other endocardium |
- endocarditis: Roth's spot
- Janeway lesion/Osler's node
- Bracht-Wachter bodies
|
Pericardium |
- Cardiac tamponade/Pericardial effusion: Beck's triad
- Ewart's sign
|
Other |
- rheumatic fever: Anitschkow cell
- Aschoff body
- angina pectoris (Levine's sign)
|
|
Vascular disease |
Arterial |
- aortic aneurysm (Cardarelli's sign, Oliver's sign)
- pulmonary embolism (McConnell's sign)
- radial artery sufficiency (Allen's test)
- pseudohypertension (Osler's sign)
- thrombus (Lines of Zahn)
- Adson's sign
- arteriovenous fistula (Nicoladoni sign)
|
Venous |
- Friedreich's sign
- Caput medusae
- Kussmaul's sign
- DVT
- Bancroft's sign
- Homans sign
- Lisker's sign
- Louvel's sign
- Lowenberg's sign
- Peabody's sign
- Pratt's sign
- Rose's sign
- Trendelenburg test
- superior vena cava syndrome (Pemberton's sign)
|
|
Authority control |
- GND: 4024666-8
- NDL: 00575113
|