Lecture 17: Cardiac/Vascular risk factors Flashcards

1
Q

what is the atherosclerosis?

A

Atherosclerosis (most common type of arteriosclerosis): multifactorial inflammatory disease of the intima, manifesting at points of hemodynamic shear stress

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2
Q

endothelial dysfunction in early atherogenesis leads too…

A

–Invasion of inflammatory cells (mainly monocytes and lymphocytes) through the disrupted endothelial barrier
–Adhesion of platelets to the damaged vessel wall → platelets release inflammatory mediators (e.g., cytokines) and platelet-derived growth factor (PDGF)
–PDGF stimulates migration and proliferation of smooth muscle cells (SMC) in the tunica intima and mediates differentiation of fibroblasts into myofibroblasts
Inflammation of the vessel wall

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3
Q

what causes chronic stress on endothelium?

A

arterial hypertension and turbulence

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4
Q

what substance causes migration of smooth muscle cells into tunic intima?

A

PDGF

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5
Q

how fatty streaks are formed (early atherosclerotic lesion)

A
  • -inflammation of the vessel wall
  • -LDL enters through the damaged vessel wall, accumulates, and is oxidized by free radicals.
  • -Macrophages and SMCs ingest cholesterol from oxidized LDL and transform into foam cells.
  • -Foam cells accumulate to form fatty streaks (early atherosclerotic lesions).
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6
Q

how fibrous plaques are formed?

A
  • -lipid-laden macrophages and SMCs produce extracellular matrix (e.g., collagen) → development of a fibrous plaque (atheroma)
  • -Macrophages, smooth muscle cells, lymphocytes and extracellular matrix form a fibrous cap, which covers a necrotic center, consisting of foam cells, free cholesterol crystals, and cellular debris.
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7
Q

why? fibrous plaque is ruptured?

A
  • -inlammatory cells in the atheroma (e.g., macrophages) secrete matrix metalloproteinases → weakening of the fibrous cap of the plaque due to the breakdown of extracellular matrix → minor stress ruptures the fibrous cap
  • -Plaque rupture → exposure of thrombogenic material (e.g., collagen) → thrombus formation with vascular occlusion or spreading of thrombogenic material
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8
Q

what are the manifestations of atherosclerosis?

A
  • -Coronary Heart Disease (CHD), manifested by myocardial infarction (MI), angina pectoris, heart failure, and coronary death
  • -CerebroVascular Disease (CVD), manifested by stroke and transient ischaemic attack
  • -Peripheral Artery (or Vascular) Disease (PAD or PVD), manifested by intermittent claudication
  • -Aortic Atherosclerosis and thoracic or abdominal aortic aneurysm (AAA)
  • -Vascular Diseases of the Kidney – renal artery stenosis and/or ischaemic nephropathy
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9
Q

what is the epidemiology of cardiovascular diseases?

A
  • -In 2012, CVD was estimated to result in 17.3 million deaths worldwide.
  • -By 2030 more than 23 million people will die annually from CVDs (WHO estimate).
  • -Most common cause of death in Ireland.
  • -Accounts for 36% of all deaths.
  • -Approximately, 10,000 people die in Ireland from cardiovascular disease.
  • -Also a major cause of disability worldwide.
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10
Q

primary vs secondary prevention?

A
  • -Primary prevention: Avoid occurrence of disease

- -Secondary prevention: Reduce risk of recurrence and retard progression of existing disease

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11
Q

what is primary prevention?

A
  • -Prevent the onset of specific diseases via risk reduction by altering behaviors or exposures that can lead to disease, or by enhancing resistance to the effects of exposure to a disease agent.
  • -Primarily decrease the incidence, and in turn, decrease the prevalence of disease.
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12
Q

examples of primary prevention?

A
  • -Immunization
  • -Lifestyle modification ( smoking cessation, eating habits, dental care)
  • -Fortification of salt with iodine to prevent iodine deficiency
  • -Fluoridation of toothpaste, water, and salt to reduce the risk of dental caries
  • -Fortification of food with folic acid to reduce the prevalence of neural tube defects
  • -Health legislation ( smoking cessation, eating habits, dental care)
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13
Q

what is secondary prevention??

A
  • -Early detection of disease in asymptomatic patients to promote early intervention, and to prevent further progression and complications from the disease.
  • -Consists of a 2-step process: screening test to identify the disease and a follow-up for management of the disease.
  • -Secondary prevention testing measures are not intended to be diagnostic!
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14
Q

screening is an example of primary or secondary prevention?

A

secondary

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15
Q

examples of secondary prevention?

A
  • -General medical examination (“checkup”): blood pressure measurement for hypertension
  • -Laboratory testing (lipid panel, HIV, etc.)
  • -Other screening tests ( colonoscopy, mammography, etc.)
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16
Q

what are the non-modifiable risk factors of CVDs?

A
  • -Age
  • -Gender
  • -Family History (Genetics)
  • -Race
  • -Personal History
17
Q

what are the modifiable risk factors of CVDs?

A
  • -Smoking
  • -Hypertension
  • -Cholesterol
  • -Diabetes
  • -Obesity / Diet Quantity (Calories)
  • -Diet Quality
    1) Excesses: Salt, Sugar, Excess Fats
    2) Deficiencies: Fruits, Vegetables, Omega-3 Fats
  • -Lack of Fitness
  • -Renal Dysfunction/Failure
  • -Psychosocial factors
  • -Alcohol
18
Q

what is the most important factor in lowering the risk for CVs?

A
  • -Risk of recurrent MI in patients who have had an MI falls by 50% within one year of smoking cessation
  • -Benefits are seen regardless of how long and how much the patient smoked
19
Q

Pulse pressure is the best predictor of CVD in all age groups. True/False

A

False

  • -With increasing age, there was a gradual shift from DBP to SBP and then to PP as predictors of CHD risk”.
  • -Age <50 years; DBP best
  • -Age 50-59 years; DBP = SBP = PP
  • -Age > 60 years; PP best
20
Q

what is the most common cause of death in DM?

A

CVD

  • -People with type 2 diabetes die 5-10 years before people without diabetes and most of this excess mortality is due to cardiovascular disease
  • -High blood glucose and glycosylated haemoglobin levels also correlated with increased cardiovascular risk
21
Q

how exercise protects against CVD?

A
  • -Result from the benefits of exercise in
  • -reducing blood pressure
  • -controlling blood cholesterol levels
  • -improving glucose control in diabetes
  • -weight reduction
22
Q

how much exercise is recommended to prevent CVDs?

A
  • -30 minutes of brisk activity on
  • -most preferably every day of the week at
  • -50-75 percent of maximum heart rate.
23
Q

does obesity increase the risk of CVD?

A
  • -Associated with other risk factors (Particularly Hypertension, Dyslipidaemia & Diabetes)
  • -Also independently predicts occurrence of CHD and stroke
24
Q

what are the effects of weight loss on plasm lipid levels?

A

During active weight loss, serum HDL-cholesterol concentrations decrease, but later increase once weight loss stabilizes. The greatest improvements in serum lipid concentrations tend to occur in the first 4 to 8 weeks of weight loss. The degree of improvement in triglyceride and cholesterol concentrations is related to the amount of weight lost, and weight regain leads to relapse in serum lipid levels. At 2 years, a sustained weight loss of 5% is sufficient to maintain the reduction in serum triglyceride concentrations, whereas serum total and LDL-cholesterol revert toward baseline unless a 10% weight loss is maintained

25
Q

what are the other risk factors of CVD?

A
  • -Alcohol - lack of moderate alcohol intake may be a risk factor
  • -Psychosocial factors - may contribute to development of atherosclerosis as well as acute MI and cardiac death
  • -Chronic kidney disease - associated with increased risk of CHD; leading cause of death in patients with CKD is cardiovascular disease.
  • -Inflammatory markers – raised CRP has been associated with increased risk but role in uncertain
  • -HIV – higher rates of CHD in HIV+ patients compared with HIV- controls even after correction for traditional risk factors
  • -Infection – possible role
26
Q

what is the risk factor clustering?

A
  • -Diabetics very likely to be hypertensive, obese and dyslipidaemic which contributes to the vascular risk burden.
  • -Patients with hypertension very likely to have other risk factors.
27
Q

what factor increases the risk of CVDs in diabetics?

A

The presence of hypertension further increases the already high risk of cardiovascular (CV) disease associated with type 2 diabetes. There is an approximate 2-fold increased risk of CV disease in hypertensive vs. normotensive patients with diabetes; similarly, patients with diabetes have a 2-fold increased risk for CV disease than patients without diabetes. The combination of diabetes and hypertension gives an approximate 4-fold increase in CV risk over the nondiabetic, normotensive population.

28
Q

what are the measures of primordial prevention- whole population reduction of risk factor levels?

A

1) Every adult should know their numbers
- -BP < 140/90
- -total Cholesterol < 5.0 mmol/l
- -LDL Cholesterol < 3.0 mmol/l
- -HDL Cholesterol > 1.0 mmol/l
- -Fasting Glucose < 6.5 mmol/l
2) Smoking
- -Taxation
- -Smoking in work-place/enclosed spaces ban
- -Plain labeling with prominent warnings
3) Healthy diet to be promoted
- -Labelling of constituents
- -Taxation policy
- -School provision of fruit
- -Ban on junk food advertising to children
- -Targets for salt reduction in processed foods.
4) Exercise facilitation
- -School programs
- -Provision of walkways -Sli na Slainte

29
Q

what lifestyle changes should be performed to reduce the risk of CVDs?

A

1) Stop smoking
2) Diet
- -Reduce calories, saturated fat, and salt
- -Reduce packaged, processed and take-aways
- -Increase fish, fruit, and vegetables
3) Alcohol in moderation
- -<17 units/week males and <11units/week for females
4) Regular exercise

30
Q

what are the antiplatelet drugs used for primary/secondary prevention of CVD?

A
  • -Aspirin

- -Clopidogrel

31
Q

what are the lipid-lowering drugs used for primary/secondary prevention of CVD?

A
  • -Statins
  • -Fibrates
  • -Cholesterol absorption inhibitors
  • -PCSK9 inhibitors
32
Q

what are the BP-lowering drugs used for primary/secondary prevention of CVD?

A

ACE-Inhibitors/ARBs
Calcium-channel blockers
Diuretics

33
Q

what are the hypoglycemics drugs used for primary/secondary prevention of CVD?

A
  • -Biguanides
  • -Sulphonylureas
  • -Glitazones
  • -Acarbose
  • -Insulin
34
Q

what are the anti-obesity drugs used for primary/secondary prevention of CVD?

A
  • -Orlistat

- -Sibutramine

35
Q

what is metabolic syndrome?

A

A constellation of medical conditions that increase the risk for cardiovascular disease, type 2 diabetes mellitus, and fatty liver. Presence of ≥ 3 of the following conditions (or already receiving medical treatment for them):

  • -Insulin resistance: fasting glucose ≥ 100 mg/dL
  • -Elevated blood pressure: ≥ 130/85 mm Hg
  • -Elevated triglycerides: ≥ 150 mg/dL
  • -Low HDL-C: in men < 40 mg/dL; in women < 50 mg/dL
  • -Abdominal obesity: waist circumference ≥ 102 cm in men; ≥ 88 cm in women
36
Q

what type of obesity particularly increases the risk of CVD?

A

Abdominal obesity
Whereas obesity in general is a known risk factor for many diseases, the accumulation of fat in visceral tissue (abdominal obesity) has been particularly associated with an atherogenic and hyperglycemic state.