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      Dynamic cerebral autoregulation is attenuated in young fit women

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          Abstract

          Young women exhibit higher prevalence of orthostatic hypotension with presyncopal symptoms compared to men. These symptoms could be influenced by an attenuated ability of the cerebrovasculature to respond to rapid blood pressure ( BP) changes [dynamic cerebral autoregulation ( dCA)]. The influence of sex on dCA remains unclear. dCA in 11 fit women (25 ± 2 years) and 11 age‐matched men (24 ± 1 years) was compared using a multimodal approach including a sit‐to‐stand ( STS) and forced BP oscillations (repeated squat‐stand performed at 0.05 and 0.10 Hz). Prevalence of initial orthostatic hypotension ( IOH; decrease in systolic ≥ 40 mmHg and/or diastolic BP ≥ 20 mmHg) during the first 15 sec of STS was determined as a functional outcome. In women, the decrease in mean middle cerebral artery blood velocity ( MCAv mean) following the STS was greater (−20 ± 8 vs. −11 ± 7 cm sec −1; P = 0.018) and the onset of the regulatory change (time lapse between the beginning of the STS and the increase in the conductance index ( MCAv mean/mean arterial pressure) was delayed ( P = 0.007). Transfer function analysis gain during 0.05 Hz squat‐stand was ~48% higher in women (6.4 ± 1.3 vs. 3.8 ± 2.3 cm sec −1 mmHg −1; P = 0.017). Prevalence of IOH was comparable between groups (women: 4/9 vs. men: 5/9, P = 0.637). These results indicate the cerebrovasculature of fit women has an attenuated ability to react to rapid changes in BP in the face of preserved orthostasis, which could be related to higher resting cerebral blood flow allowing women to better face transient hypotension.

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          Most cited references37

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          Consensus statement on the definition of orthostatic hypotension, neurally mediated syncope and the postural tachycardia syndrome.

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            Cerebral autoregulation dynamics in humans.

            We studied the response of cerebral blood flow to acute step decreases in arterial blood pressure noninvasively and nonpharmacologically in 10 normal volunteers during normocapnia, hypocapnia, and hypercapnia. The step (approximately 20 mm Hg) was induced by rapidly deflating thigh blood pressure cuffs following a 2-minute inflation above systolic blood pressure. Instantaneous arterial blood pressure was measured by a new servo-cuff method, and cerebral blood flow changes were assessed by transcranial Doppler recording of middle cerebral artery blood flow velocity. In hypocapnia, full restoration of blood flow to the pretest level was seen as early as 4.1 seconds after the step decrease in blood pressure, while the response was slower in normocapnia and hypercapnia. The time course of cerebrovascular resistance was calculated from blood pressure and blood flow recordings, and rate of regulation was determined as the normalized change in cerebrovascular resistance per second during 2.5 seconds just after the step decrease in blood pressure. The reference for normalization was the calculated change in cerebrovascular resistance that would have nullified the effects of the step decrease in arterial blood pressure on cerebral blood flow. The rate of regulation was 0.38, 0.20, and 0.11/sec in hypocapnia, normocapnia, and hypercapnia, respectively. There was a highly significant inverse relation between rate of regulation and PaCO2 (p less than 0.001), indicating that the response rate of cerebral autoregulation in awake normal humans is profoundly dependent on vascular tone.
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              Utility of transcranial Doppler ultrasound for the integrative assessment of cerebrovascular function.

              There is considerable utility in the use of transcranial Doppler ultrasound (TCD) to assess cerebrovascular function. The brain is unique in its high energy and oxygen demand but limited capacity for energy storage that necessitates an effective means of regional blood delivery. The relative low cost, ease-of-use, non-invasiveness, and excellent temporal resolution of TCD make it an ideal tool for the examination of cerebrovascular function in both research and clinical settings. TCD is an efficient tool to access blood velocities within the cerebral vessels, cerebral autoregulation, cerebrovascular reactivity to CO(2), and neurovascular coupling, in both physiological states and in pathological conditions such as stroke and head trauma. In this review, we provide: (1) an overview of TCD methodology with respect to other techniques; (2) a methodological synopsis of the cerebrovascular exam using TCD; (3) an overview of the physiological mechanisms involved in regulation of the cerebral blood flow; (4) the utility of TCD for assessment of cerebrovascular pathology; and (5) recommendations for the assessment of four critical and complimentary aspects of cerebrovascular function: intra-cranial blood flow velocity, cerebral autoregulation, cerebral reactivity, and neurovascular coupling. The integration of these regulatory mechanisms from an integrated systems perspective is discussed, and future research directions are explored. Copyright © 2011 Elsevier B.V. All rights reserved.
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                Author and article information

                Contributors
                patrice.brassard@kin.ulaval.ca
                Journal
                Physiol Rep
                Physiol Rep
                10.1002/(ISSN)2051-817X
                PHY2
                physreports
                Physiological Reports
                John Wiley and Sons Inc. (Hoboken )
                2051-817X
                16 January 2019
                January 2019
                : 7
                : 2 ( doiID: 10.1002/phy2.2019.7.issue-2 )
                : e13984
                Affiliations
                [ 1 ] Department of Kinesiology Faculty of Medicine Université Laval Québec Canada
                [ 2 ] Research center of the Institut universitaire de cardiologie et de pneumologie de Québec Québec Canada
                [ 3 ] Concussion Research Laboratory Health and Exercise Sciences University of British Columbia Okanagan British Columbia Canada
                [ 4 ] Neurovascular Research Laboratory Faculty of Life Sciences and Education University of South Wales South Wales United Kingdom
                Author notes
                [*] [* ] Correspondence

                Patrice Brassard, Department of Kinesiology, Faculty of Medicine, PEPS ‐ Université Laval, 2300 rue de la Terrasse, room 0290‐H, Québec (Qc) GIV OA6, Canada.

                Tel: 418 656‐2131 (ext. 5621)

                Fax: 418 656‐4537

                E‐mail: patrice.brassard@ 123456kin.ulaval.ca

                Author information
                https://orcid.org/0000-0003-0498-7095
                https://orcid.org/0000-0002-6254-5044
                Article
                PHY213984
                10.14814/phy2.13984
                6335382
                30652420
                13dc0286-dbcb-4230-8ee9-b658bf49e92b
                © 2019 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 21 December 2018
                : 28 December 2018
                Page count
                Figures: 3, Tables: 2, Pages: 12, Words: 7905
                Funding
                Funded by: Ministère de l’Éducation du Loisir et du Sport du Québec
                Funded by: Foundation of the Institut universitaire de cardiologie et de pneumologie de Québec
                Funded by: Société québécoise d'hypertension artérielle
                Funded by: Fonds de recherche du Québec‐Santé (FRQS)
                Funded by: Royal Society Wolfson Research Fellow
                Award ID: #WM170007
                Categories
                Cardiovascular Physiology
                Central Nervous System
                Ageing and Degeneration
                Original Research
                Original Research
                Custom metadata
                2.0
                phy213984
                January 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.5.4 mode:remove_FC converted:16.01.2019

                brain,cerebral blood flow,cerebral pressure–flow relationship,dynamic cerebral autoregulation,sex differences

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