Cerebral blood flow autoregulation in ischemic heart failure

  • J. R. Caldas
  • , R. B. Panerai*
  • , V. J. Haunton
  • , J. P. Almeida
  • , G. S.R. Ferreira
  • , L. Camara
  • , R. C. Nogueira
  • , E. Bor-Seng-Shu
  • , M. L. Oliveira
  • , R. R.V. Groehs
  • , L. Ferreira-Santos
  • , M. J. Teixeira
  • , F. R.B.G. Galas
  • , T. G. Robinson
  • , F. B. Jatene
  • , L. A. Hajjar
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

<jats:p> Patients with ischemic heart failure (iHF) have a high risk of neurological complications such as cognitive impairment and stroke. We hypothesized that iHF patients have a higher incidence of impaired dynamic cerebral autoregulation (dCA). Adult patients with iHF and healthy volunteers were included. Cerebral blood flow velocity (CBFV, transcranial Doppler, middle cerebral artery), end-tidal CO<jats:sub>2</jats:sub> (capnography), and arterial blood pressure (Finometer) were continuously recorded supine for 5 min at rest. Autoregulation index (ARI) was estimated from the CBFV step response derived by transfer function analysis using standard template curves. Fifty-two iHF patients and 54 age-, gender-, and BP-matched healthy volunteers were studied. Echocardiogram ejection fraction was 40 (20–45) % in iHF group. iHF patients compared with control subjects had reduced end-tidal CO<jats:sub>2</jats:sub> (34.1 ± 3.7 vs. 38.3 ± 4.0 mmHg, P &lt; 0.001) and lower ARI values (5.1 ± 1.6 vs. 5.9 ± 1.0, P = 0.012). ARI &lt;4, suggestive of impaired CA, was more common in iHF patients (28.8 vs. 7.4%, P = 0.004). These results confirm that iHF patients are more likely to have impaired dCA compared with age-matched controls. The relationship between impaired dCA and neurological complications in iHF patients deserves further investigation. </jats:p>
Original languageEnglish
Pages (from-to)R108-R113
Number of pages0
JournalAmerican Journal of Physiology-Regulatory, Integrative and Comparative Physiology
Volume312
Issue number1
DOIs
Publication statusPublished - 1 Jan 2017

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