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Scientific Concept of the National Cohort (status ... - Nationale Kohorte

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A.2 <strong>Scientific</strong> background and rationale for study elements<br />

wise, knowledge <strong>of</strong> <strong>the</strong> possible effects <strong>of</strong> cardiac dysfunction on cognitive function and risk<br />

<strong>of</strong> neurodegenerative disease is scarce.<br />

There is a need to better understand <strong>the</strong> determinants underlying development and progression<br />

<strong>of</strong> diastolic dysfunction in HFPEF in order to address <strong>the</strong> epidemic <strong>of</strong> heart failure<br />

in <strong>the</strong> population. Identifying modifiable risk factors <strong>of</strong> HFPEF (in order to improve prevention)<br />

and improved models for predicting progression from subclinical stages <strong>of</strong> left ventricular<br />

cardiac diastolic dysfunction to clinically overt heart failure are important aims <strong>of</strong><br />

<strong>the</strong> <strong>National</strong> <strong>Cohort</strong>. It is also important to help disentangle possible different pathophysiological<br />

mechanisms underlying HFPEF and HFREF and to investigate specific causes <strong>of</strong><br />

death in subjects with HFPEF versus subjects with HFREF (e.g., sudden cardiac death,<br />

arrhythmia-related deaths, and o<strong>the</strong>r causes <strong>of</strong> death). In <strong>the</strong> <strong>National</strong> <strong>Cohort</strong>, heart failure<br />

and cardiac (dys)function at baseline will be assessed by symptoms, questionnaires, and<br />

3D-Echocardiography, supplemented by cardiac MRI, according to scientific recommendations<br />

/ guidelines 43 , ESC Task Force 48 .<br />

Assessment <strong>of</strong> heart failure:<br />

Examinations and questionnaires (at baseline and during reassessment)<br />

Level 1: Questionnaires,<br />

3D-Echocardiography<br />

MRI program: Cardiac MRI<br />

Active follow-up (and medical verification <strong>of</strong> self-reports):<br />

Self-report <strong>of</strong> physician-diagnosed heart failure<br />

Atrial fibrillation is <strong>the</strong> most common cardiac arrhythmia in developed countries, with<br />

an overall prevalence <strong>of</strong> 1-2% in <strong>the</strong> general population and a marked age-dependent increase,<br />

with a remaining life-time risk <strong>of</strong> about 25% in 40-year-old subjects 49 . The ageadjusted<br />

incidence and prevalence <strong>of</strong> atrial fibrillation seem to be increasing in Europe and<br />

North America 50 , and <strong>the</strong> prevalence <strong>of</strong> atrial fibrillation is expected to more than triple in <strong>the</strong><br />

next 50 years 51 . Atrial fibrillation is associated with significant morbidity and mortality; it is<br />

a known cause <strong>of</strong> “cryptogenic” stroke and is associated with cerebral white matter lesions<br />

and cognitive dysfunction 52, 53 . A number <strong>of</strong> clinical risk factors for atrial fibrillation have been<br />

identified; however, characterization <strong>of</strong> lifestyle factors, genes, and novel biomarkers for<br />

risk <strong>of</strong> atrial fibrillation is still in its infancy. Fur<strong>the</strong>rmore, <strong>the</strong> information about risk factors<br />

for asymptomatic atrial fibrillation and regarding progression from paroxysmal to persistent<br />

and permanent atrial fibrillation is insufficient 50 .<br />

Assessment <strong>of</strong> atrial fibrillation:<br />

Examinations (at baseline and during reassessment)<br />

Level 1: Questionnaire<br />

10-s, 12-lead ECG<br />

Level 2: Long-term ECG<br />

Active follow-up (and medical verification <strong>of</strong> self-reports):<br />

Self-report <strong>of</strong> physician-diagnosed arrythmia (and use <strong>of</strong> antiarrhythmic drugs)<br />

Cerebrovascular diseases such as ischemic or hemorrhagic stroke pertain both to <strong>the</strong><br />

group <strong>of</strong> cardiovascular and neurologic diseases. Owing to <strong>the</strong>ir close link to cognitive impairments<br />

originating from vascular changes (including vascular dementia and vascular<br />

depression), <strong>the</strong> cerebrovascular diseases will be detailed fur<strong>the</strong>r in Sect. A.2.2.4 on neurologic<br />

and psychiatric diseases, below. In <strong>the</strong> <strong>National</strong> <strong>Cohort</strong>, we will regard <strong>the</strong> research<br />

25<br />

A.2

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