Dynamic cerebral autoregulation is impaired during submaximal isometric handgrip in patients with heart failure

Author:

Caldas J. R.123,Panerai R. B.45,Salinet A. M.,Seng-Shu E.2,Ferreira G. S. R.1,Camara L.1,Passos R. H.3,Galas F. R. B. G.1,Almeida J. P.,Nogueira R. C.2,de Lima Oliveira M.2,Robinson T. G.45,Hajjar L. A.6

Affiliation:

1. Department of Anesthesia, Heart Institute, University of Sao Paulo, Sao Paulo, Brazil

2. Department of Neurosurgery, Hospital das Clinicas, University of São Paulo, São Paulo, Brazil

3. Critical Care Unit, Hospital São Rafael, Salvador, Brazil

4. Department of Cardiovascular Sciences, University of Leicester, Leicester, United Kingdom

5. NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, United Kingdom

6. Department of Cardiopneumology, Heart Institute, University of Sao Paulo, São Paulo, Brazil

Abstract

The incidence of neurological complications, including stroke and cognitive dysfunction, is elevated in patients with heart failure (HF) with reduced ejection fraction. We hypothesized that the cerebrovascular response to isometric handgrip (iHG) is altered in patients with HF. Adults with HF and healthy volunteers were included. Cerebral blood velocity (CBV; transcranial Doppler, middle cerebral artery) and arterial blood pressure (BP; Finometer) were continuously recorded supine for 6 min, corresponding to 1 min of baseline and 3 min of iHG exercise, at 30% maximum voluntary contraction, followed by 2 min of recovery. The resistance-area product was calculated from the instantaneous BP-CBV relationship. Dynamic cerebral autoregulation (dCA) was assessed with the time-varying autoregulation index estimated from the CBV step response derived by an autoregressive moving-average time-domain model. Forty patients with HF and 23 BP-matched healthy volunteers were studied. Median left ventricular ejection fraction was 38.5% (interquartile range: 0.075%) in the HF group. Compared with control subjects, patients with HF exhibited lower time-varying autoregulation index during iHG, indicating impaired dCA ( P < 0.025). During iHG, there were steep rises in CBV, BP, and heart rate in control subjects but with different temporal patterns in HF, which, together with the temporal evolution of resistance-area product, confirmed the disturbance in dCA in HF. Patients with HF were more likely to have impaired dCA during iHG compared with age-matched control subjects. Our results also suggest an impairment of myogenic, neurogenic, and metabolic control mechanisms in HF. The relationship between impaired dCA and neurological complications in patients with HF during exercise deserves further investigation. NEW & NOTEWORTHY Our findings provide the first direct evidence that cerebral blood flow regulatory mechanisms can be affected in patients with heart failure during isometric handgrip exercise. As a consequence, eventual blood pressure modulations are buffered less efficiently and metabolic demands may not be met during common daily activities. These deficits in cerebral autoregulation are compounded by limitations of the systemic response to isometric exercise, suggesting that patients with heart failure may be at greater risk for cerebral events during exercise.

Publisher

American Physiological Society

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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