What are cardiovascular diseases?


Cardiovascular diseases (CVDs) include a broad range of disorders affecting either blood vessels, mostly the arteries, or the heart. One of the major causes of CVD is atherosclerosis, a disease of the vessel wall often manifesting at multiple sites and characterised by deposition of lipids, inflammation, and cellular proliferation. Atherosclerosis can affect the arteries nourishing the heart (coronary artery disease), the brain (cerebrovascular disease), and the periphery. Consequently, blood flow to organs can be compromised chronically (angina pectoris or cerebral ischemia) or acutely (myocardial infarction or stroke).

Another major disease is heart failure in which the heart is unable to pump enough blood into circulation. Its causes include atherosclerosis, toxic damage, metabolic disorders, but also genetic factors. Other CVDs of the heart are arrhythmias, valve diseases, or aneurysms (bulges of the vessel wall).

Are there any latest developments in in vitro diagnostics (IVD) for the early detection or risk profiling of CVDs?


State-of-the-art risk assessment is accomplished by combining a few important clinical attributes like age, sex, smoking, and diabetes mellitus with a few generic laboratory values like low-density lipoprotein and high-density lipoprotein cholesterol and triglycerides in risk calculators. Research of the last decade has consistently proven that newer biomarkers including natriuretic peptides (also used for the diagnosis of heart failure), cardiac troponins (cardiac damage, also used for the diagnosis of acute myocardial infarction) or cystatin C (a kidney function marker), or most recently ceramides (bioactive sphingolipids) are individually or in combination better markers for CVD risk.

Significant progress has also been made in the identification of measurable “polygenic” genetic risk factors for CVD which are commonly combined into polygenic risk scores and have the potential to refine risk assessment and open new avenues for CVD precision medicine. In the future, further innovations in early detection and risk profiling for CVDs will emerge through machine learning algorithms and artificial intelligence that consolidate and exploit different diagnostic technologies (clinical, imaging, circulating metabolites and proteins, genetics).

CVDs are a leading cause of death globally. How can they be treated?


In addition to lifestyle changes and drugs, medical invasive procedures are available to treat CVDs. Angioplasty and stenting are applied immediately after myocardial infarction to re-open occluded coronary arteries or in chronic coronary artery disease to reduce myocardial ischemia and angina pectoris. In severe coronary artery disease, coronary artery bypass surgery may be needed to restore blood flow. Damaged heart valves can be replaced surgically or by catheterisation. Arrhythmias are treated with pacemakers, implantable cardioverter defibrillators or ablation of abnormal heart tissue.

Any risk factors should be controlled rigorously following such procedures to halt or slow down disease progression. Current research into primary and secondary prevention focuses on tailoring therapeutic strategies to the individual needs of patients according to specific risk stratification algorithms.

How does an early diagnosis help in preventing and treating CVDs?


As mentioned, CVDs develop gradually from the second or the third decade of life onwards due to long-term exposure to risk factors. Both the severity of a risk factor and the time of exposure are crucial. For instance, CVD risk follows the number of cigarettes smoked per day and the number of years smoked, known as pack-years. Because it may be difficult to reverse atherosclerosis upon late intervention, it is crucial to recognise any CVD risks early, maintain a healthy lifestyle, and initiate medical treatment early if considered necessary.