Key result
Aging in ovine heart failure is linked to higher resting heart rate and impaired chronotropic response.
Absolute Event Rate: 123% vs 105%
p-value: p=<0.05
Aging accelerates the development of impaired beta-adrenergic responsiveness and autonomic dysfunction during the progression of heart failure in an ovine model.
Aging may exacerbate autonomic imbalance in HF models; leaves open translation to age-specific human chronotropic management.
Heart failure (HF) is predominantly a disease of older adults and characterized by extensive sympatho-vagal imbalance leading to impaired reflex control of heart rate (HR). However, whether aging influences the development or extent of the autonomic imbalance in HF remains unclear. To address this, we used an ovine model of aging with tachypacing-induced HF to determine whether aging affects the chronotropic and inotropic responses to autonomic stimulation and reduction in heart rate variability (HRV) in HF. We find that aging is associated with increased cardiac dimensions and reduced contractility before the onset of tachypacing, and these differences persist in HF. Additionally, the chronotropic response to β-adrenergic stimulation was markedly attenuated in HF, and this occurred more rapidly in aged animals. By measuring HR during sequential autonomic blockade, our data are consistent with a reduced parasympathetic control of resting HR in aging, with young HF animals having an attenuated sympathetic influence on HR. Time-domain analyses of HR show a reduction in HRV in both young and aged failing animals, although HRV is lowest in aged HF. In conclusion, aging is associated with altered autonomic control and β-adrenergic responsiveness of HR, and these are exacerbated with the development of HF.
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Horn et al. (2015) studied Heart failure (n=39). Aging vs. Young sheep (18 months) was evaluated on Resting heart rate (p=<0.05). Aging in an ovine model of heart failure is associated with increased resting heart rate, reduced heart rate variability, and an earlier loss of chronotropic response to β-adrenergic stimulation.
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