Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/56868
Title: Cerebral microvascular blood flow and CO2 reactivity in pulmonary arterial hypertension
Authors: Treptow, Erika [UNIFESP]
Oliveira, Mayron Faria [UNIFESP]
Soares, Aline [UNIFESP]
Ramos, Roberta Pulcheri [UNIFESP]
Medina, Luiz [UNIFESP]
Lima, Rita [UNIFESP]
Alencar, Maria Clara [UNIFESP]
Ferreira, Eloara Vieira [UNIFESP]
Ota-Arakaki, Jaquelina Sonoe [UNIFESP]
Tufik, Sergio [UNIFESP]
Nery, Luiz Eduardo [UNIFESP]
Bittencourt, Lia Rita Azeredo [UNIFESP]
Neder, Jose Alberto [UNIFESP]
Keywords: Cerebral blood flow
Carbon dioxide
Pulmonary hypertension
Ventilation
Near-infrared spectroscopy
Issue Date: 2016
Publisher: Elsevier Science Bv
Citation: Respiratory Physiology & Neurobiology. Amsterdam, v. 233, p. 60-65, 2016.
Abstract: Hypocapnia and endothelial dysfunction might impair microvascular cerebral blood flow (CBFmicr) and cerebrovascular reactivity to CO2 (CVRCO2). Pulmonary arterial hypertension (PAH) is characteristically associated with chronic alveolar hyperventilation and microvascular endothelial dysfunction. We therefore determined CBFmicr (pre-frontal blood flow index (BFI) by the indocyanine green-near infrared spectroscopy methodology) during hypocapnia and hypercapnia in 25 PAH patients and 10 gender- and age-matched controls. Cerebral BFI was lower in patients than controls at similar transcutaneous PCO2 (PtcCO(2)) levels in both testing conditions. In fact, while BFI increased from hypocapnia to hypercapnia in all controls, it failed to increase in 17/25 (68%) patients. Thus, BFI increased to a lesser extent from hypo to hypercapnia ("Delta") in patients, i.e., they showed lower Delta BFI/Delta PtcCO(2) ratios than controls. In conclusion, CBFmicr and CVRCO2 are lessened in clinically stable, mildly-impaired patients with PAH. These abnormalities might be associated with relevant clinical outcomes (hyperventilation and dyspnea, cognition, cerebrovascular disease) being potentially amenable to pharmacological treatment. (C) 2016 Elsevier B.V. All rights reserved.
URI: https://repositorio.unifesp.br/handle/11600/56868
ISSN: 1569-9048
Other Identifiers: http://dx.doi.org/10.1016/j.resp.2016.08.001
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