The project is designed as a large scale, cross-sectional study. This research seeks to identify physical fitness and cardiovascular parameters that best resemble underlying cardiovascular risk with age. Further, it will examine which physical fitness markers are impaired most in heart failure.
Cardiovascular (CV) diseases including heart failure are the leading causes of morbidity, with age being the primary risk factor. The combination of age-related organic functional impairment and reduced physical fitness can drastically impact an individual's healthspan. One's lifespan can potentially be prolonged by the preservation or improvement of physical fitness. However, it remains unclear as to which biomarkers are most suitable for distinguishing between healthy aging and the impaired organ function associated with heart failure. Therefore, a comprehensive assessment of the components of physical fitness and CV function will be performed to identify the most important factors contributing to aging in relation to both health and disease. This cross-sectional investigation will consist of two parts: the COmPLETE-Health (C-Health) and COmPLETE-Heart (C-Heart) studies. C-Health will examine the aging trajectories of physical fitness components and CV properties in a healthy population sample aged between 20 and 100 years (n = 490). Separately, C-Heart will assess the same markers in patients at different stages of chronic heart failure (n = 80). The primary outcome to determine the difference between C-Health and C-Heart will be cardiorespiratory fitness as measured by cardiopulmonary exercise testing on a bicycle ergometer. Secondary outcomes will include walking speed, balance, isometric strength, peak power, and handgrip strength. Physical activity as a behavioural component will be assessed objectively via accelerometry. Further, CV assessments will include pulse wave velocity; retinal, arterial, and venous diameters; brachial and retinal arterial endothelial function; carotid intima-media thickness; and systolic and diastolic function. The health distances for C-Health and C-Heart will be calculated using the methodology based on statistical (Mahalanobis) distance applied to measurements of quantitative biomarkers. This research seeks to identify physical fitness and CV biomarkers that best resemble underlying CV risk with age. Further, it will examine which physical fitness markers are impaired most in heart failure. The presented integrative approach could define new recommendations for diagnostic guidance in aging. Ultimately, this study is expected to offer a better understanding of which functional characteristics should be specifically targeted in primary and secondary prevention to achieve an optimal healthspan.
Study Type
OBSERVATIONAL
Enrollment
678
Physical Activity
Department for Sport, Exercise and Health, Section Sports and Exercise Medicine, University of Basel
Basel, Switzerland
Cardiorespiratroy Fitness
Maximal Oxygen uptake measured by cardiopulmonary exercise testing (VO2peak) in L/min
Time frame: 3 hours after inclusion in study
Ventilatory Efficiency
VE/VCO2 measured by cardiopulmonary exercise testing ((L/min)/(L/min))
Time frame: 3 hours after inclusion in study
Oxygen Uptake Efficiency
The Oxygen Uptake Efficiency Slope is defined as the regression slope 'a' in V̇O2 = a × log VE +b measured by cardiopulmonary exercise testing.
Time frame: 3 hours after inclusion in study
Gait speed
Gait speed measured by an inertial sensor system in m/s.
Time frame: 1.5 hours after inclusion in study
Standing balance
The cumulative sway path (cm) serves as a measure of postural control.
Time frame: 2.5 hours after inclusion in study
Hand grip strength
Measured by a handheld dynamometer. Maximal achieved grip strength (kg) is recorded.
Time frame: 2.5 hours after inclusion in study
Power of leg muscles
Peak power measured by countermovement jump performed on a force plate. Reported in N/kg
Time frame: 2.5 hours after inclusion in study
Arterial stiffness
Meausred by an noninvasive vascular screening system. Reported as brachial-ankle pulse wave velocity (baPWV).
Time frame: 0.5 hours after inclusion in study
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Endothelial function
Meausred as flow mediated dilation (FMD) by ultrasound reported as %.
Time frame: 1 hours after inclusion in study
Left ventricular ejection fraction
Meausred by echocardiography reported as %.
Time frame: 1 hour after inclusion in study
Carotid-intima-media thickness
Carotid intima-media thickness (mm) is measured by 2D ultrasound instrument.
Time frame: 1 hour after inclusion in study
Retinal arterial and venous diameters
Measured by static retinal vessel analysis. Diameters will be averaged to central retinal arteriolar and venular equivalents (CRAE and CRVE) and the arteriolar-to-venular diameter ratio will be calculated from the CRAE and CRVE.
Time frame: 7-30 days after inclusion in study
Retinal endothelial function
Measured by dynamic retinal vessel analysis reported as %.
Time frame: 7-30 days after inclusion in study