Is There More to Blood Volume Pulse Than Heart Rate Variability

Total Page:16

File Type:pdf, Size:1020Kb

Is There More to Blood Volume Pulse Than Heart Rate Variability Biofeedback ©Association for Applied Psychophysiology & Biofeedback Volume 35, Issue 2, pp. 54-61 www.aapb.org SPECIAL TOPICS Is There More to Blood Volume Pulse Than Heart Rate Variability, Respiratory Sinus Arrhythmia, and Cardiorespiratory Synchrony? Erik Peper, PhD,1 Rick Harvey, PhD,1 I-Mei Lin, MA,2 Hana Tylova,1 and Donald Moss, PhD3 1San Francisco State University, San Francisco, CA; 2National Chung Cheng University, Taiwan; 3Saybrook Graduate School, San Francisco, CA Keywords: blood volume pulse, heart rate variability, respiratory sinus arrhythmia, cardiorespiratory synchrony A growing body of research reports the health benefi ts sympathetic-parasympathetic imbalance, new HRV training of training heart rate variability (HRV), and the clinical protocols could be employed as well. use of HRV training protocols has increased dramatically Measuring HRV, the beat-to-beat variability in the sinus in recent years. Many of the home training devices and rhythm over a given period of time, is usually done by many of the sophisticated biofeedback instrumentation calculating the standard deviation of the average of normal- systems rely on the blood volume pulse (BVP) sensor, or to-normal heart beats (SDNN or SDANN). This statistical photoplethysmograph, because it is more user friendly than index has health implications, predicting morbidity and the electrocardiogram used in medical settings. However, mortality. We will elaborate later on this relationship between the BVP signal is valuable in its own right, not merely HRV and health (Kleiger, Miller, Bigger, & Moss, 1987). as a convenient measure of HRV. This article explores the There are many technologies that can estimate the beat- methodology of BVP recording, the underlying physiology, to-beat variability in the sinus rhythm over a given period and the potential benefi ts from BVP treatment and training protocols. For example, the shape of the BVP waveform refl ects arterial changes correlated with hypertension. In Table. Alphabet soup of abbreviations addition, BVP training offers promise for the treatment of migraine and the monitoring of human sexual arousal. BVA Blood volume amplitude BVP Blood volume pulse Studies of methods for training improvement in heart rate variability (HRV), respiratory sinus arrhythmia (RSA), CRS Cardiorespiratory synchrony and cardiorespiratory synchrony (CRS) are promising EKG Electrocardiography areas of current research, expanding our knowledge of new clinical applications and training procedures for improving ECG Electrocardiography sympathetic-parasympathetic balance (see Table for the FFT Fast Fourier transform expansion of the abbrevations in text). For example, research HR Heart rate by Lehrer and colleagues (Lehrer et al., 2006; Lehrer et al., 2004) has demonstrated that HRV training in patients with HRV Heart rate variability asthma reduces their asthma severity. Similarly, research NN Normal-to-normal beat (interbeat interval) by Del Pozo and colleagues (Del Pozo, Del Pozo Scher, & PPG Photoplethysmography Guarneri, 2004) has shown that cardiac patients can improve their HRV. In addition, Giardino, Chan, and Borson (2004) PTT Pulse transit time reported a benefi t for patients with chronic obstructive RSA Respiratory sinus arrhythmia pulmonary disease using HRV training and an exercise protocol. It appears that learning to increase HRV results SDANN Standard deviation of average normal-to-normal in strengthening sympathetic-parasympathetic balance beat (also known as SDNN: standard deviation Biofeedback of the normal-to-normal beat) Ô and offers hope for many chronic illnesses (Gevirtz, 2003). Whereas clinical applications and feedback training of RSA SDAHR Standard deviation of average heart rate or CRS have been used to address illness affected by the Summer 2007 54 Peper, Harvey, Lin, Tylova, Moss Figure 2. Blood volume pulse, blood volume amplitude, heart rate, and Figure 1. Blood volume pulse, blood volume amplitude, heart rate, and respiration during training designed to increase cardiorespiratory synchrony. respiration before training. of time using measures of the volume of blood that passes breaths per minute with a corresponding heart rate of 73 over a photoplethysmographic (PPG) sensor with each beats per minute (SD = 10.1 beats). pulse, also called blood volume pulse (BVP). Recently, HRV Whereas designing training protocols for improving training using BVP measurements has escaped out of the HRV or RSA/CRS is possible using BVP technologies, the laboratory and into the marketplace. BVP training devices BVP signal holds even greater promise as a tool for use in are commercially available as portable units such as the improving other clinical applications and training protocols. StressEraser and the emWave or as units built for use with The remainder of this article explores various components computers such as the FreezeFramer or the Journey to Wild of the BVP technology. Divine. By using these BVP training devices, individuals can become aware of factors that increase or decrease their Background HRV. For example, excessive sensory arousal; shallow, rapid The BVP signal is derived with a PPG sensor that measures breathing; and excessive emotions of fear, worry, anger, changes in blood volume in arteries and capillaries by shining or panic will decrease HRV. On the other hand, reducing an infrared light (a light-emitting diode) through the tissues. sensory arousal, breathing slowly at approximately fi ve to This infrared light is selectively transmitted, backscattered, seven breaths per minute, and experiencing emotions of refl ected, and absorbed. The amount of light that returns appreciation and love will increase HRV. In clinical settings, to a PPG sensor’s photodetector is proportional to the practitioners use sophisticated multichannel biofeedback volume of blood in the tissue. The PPG signal represents systems to train clients to increase HRV and CRS. In most an average of all blood volume in the arteries, capillaries, clinical settings, heart rate information is derived from a and any other tissue through which the light passed. The BVP signal rather than from an electrocardiography (ECG) PPG signal depends on the thickness and composition of the signal. Whereas the ECG signal is more precise (e.g., with tissue beneath the sensor and the position of the source and fewer movement artifacts), applying an ECG sensor is also receiver of the infrared light. more cumbersome and obtrusive compared to applying a Most PPG sensors can be placed anywhere on the body, BVP sensor (e.g., without gel or tape or placement on a chest). from the earlobe to the vaginal wall, with the fi nger as the Using PPG feedback devices alone and/or in conjunction most common location for recording a BVP signal. The PPG with respiratory feedback devices such as respiratory strain sensor measures relative changes in the perfusion of the Biofeedback gauges, clients can learn to increase HRV/RSA, as shown in blood through the tissue underneath the sensor. For example, Figures 1 and 2. changes in the BVP signal can indicate relative changes in The participant data from Figure 1 represent an average the vascular bed due to vasodilation or vasoconstriction Ô respiration rate of 14 breaths per minute, with a corresponding (increase or decrease in blood perfusion) as well as changes Summer 2007 heart rate of 68 beats per minute (SD = 5.0 beats). The data in the elasticity of the vascular walls, refl ecting changes in from Figure 2 represent an average respiration rate of 7 blood pressure. Because the blood volume in the arteries and 55 Blood Volume Pulse Figure 3. Heart rate is derived from measures of blood volume pulse by Figure 4. Recording of the heart rate derived from the raw blood volume pulse measuring the interbeat interval and then transforming this information into during the baseline period. The average heart rate included a segment of very beats per minute. For example, the interbeat interval of 0.80 seconds is equal rapid heart beat refl ecting movement artifact rather than a true increase in to a heart rate of 75 beats per minute, whereas the interbeat interval of 0.93 average heart rate. seconds is equal to a heart rate of 64.5. capillary bed increases with each arterial pulsation, heart rate can be estimated from the BVP signal. Heart rate, or the number of heartbeats per minute, is calculated by estimating the time interval between the heartbeats, called the interbeat interval. The time in seconds of the interbeat interval is divided into 60 seconds to calculate the beat-by-beat heart rate, as shown in Figure 3. The time between each beat can vary; therefore, the estimated beat-by-beat heart rate can also vary. There are two estimates of the variability of the heart rate: variability estimated by the SDANN or variability estimated by the standard deviation of the average beat-by-beat heart rate (SDAHR). A methodological issue includes the fact that the raw BVP signal must be artifact free before meaning is Figure 5. When movement artifact is excluded from the signal shown in Figure assigned to the SDANN and SDAHR measures of variability 4, the actual heart rate is estimated at 61.05 beats per minute. in the heart rate data. The next section address artifacts in the BVP signal. This dialogue illustrates issues related to artifacts in the Inspecting the Raw BVP Signal for Artifacts BVP data. The data included movement artifacts, as shown in When analyzing average heart rates, it is important to Figure 4. After eliminating the movement artifact as shown eliminate artifacts before calculating estimates of HRV. Heart in Figure 5, the heart rate information was nearly fi ve beats rate averages calculated from the data may not be reliable if lower. Note also that in this participant, there was a slight artifacts exist, as illustrated in the following vignette: increase in heart rate during the stressful imagery rehearsal once the segments of data affected by artifact were removed. What happened? He reported increased arousal during Once movement artifacts are removed from BVP the stressful imagery, yet his heart rate was higher during estimates of heart rate, the BVP measure of HRV becomes the initial baseline condition.
Recommended publications
  • Blood Volume and Circulation Time in Children
    Arch Dis Child: first published as 10.1136/adc.11.61.21 on 1 February 1936. Downloaded from BLOOD VOLUME AND CIRCULATION TIME IN CHILDREN BY H. SECKEL, M.D., Late of the University Children's Clinic, Cologne. This paper is based mainly on the results of the author's own research work on blood volume and circulation time in cases of normal and sick children. The following methods were used:- 1. The colorimetric method for determining the circulating plasma volume, and the haematocrit method for estimating the volume of the total circulating blood; and 2. The histamine rash method for estimating the minimum circulation time of the blood. By means of these two methods there is determined only that portion of the total blood volume which is in rapid circulation, the other part, the so-called stored or depot blood, which is moving slowly or is almost stationary, being neglected. The organs which may act as blood depots are the spleen, the liver, the intestines, the sub-papillary plexus of the skin http://adc.bmj.com/ and possibly the muscles. The greater part of the capillary system of these organs is quite extensive enough to supply stored-up blood as and when required to the more rapid circulation or alternatively, withdraw rapidly circulating blood and store it. This action is regulated by the autonomic nervous system. The circulating blood volume as de-termined by the above methods is not absolutely fixed in quantity but chatnges within wide limits, according to the physiological or pathological conditions under on September 25, 2021 by guest.
    [Show full text]
  • Relationship Between Vasodilatation and Cerebral Blood Flow Increase in Impaired Hemodynamics: a PET Study with the Acetazolamide Test in Cerebrovascular Disease
    CLINICAL INVESTIGATIONS Relationship Between Vasodilatation and Cerebral Blood Flow Increase in Impaired Hemodynamics: A PET Study with the Acetazolamide Test in Cerebrovascular Disease Hidehiko Okazawa, MD, PhD1,2; Hiroshi Yamauchi, MD, PhD1; Hiroshi Toyoda, MD, PhD1,2; Kanji Sugimoto, MS1; Yasuhisa Fujibayashi, PhD2; and Yoshiharu Yonekura, MD, PhD2 1PET Unit, Research Institute, Shiga Medical Center, Moriyama, Japan; and 2Biomedical Imaging Research Center, Fukui Medical University, Fukui, Japan Key Words: acetazolamide; cerebrovascular disease; cerebral The changes in cerebral blood flow (CBF) and arterial-to- blood volume; vasodilatory capacity; cerebral perfusion pressure capillary blood volume (V0) induced by acetazolamide (ACZ) are expected to be parallel each other in the normal circula- J Nucl Med 2003; 44:1875–1883 tion; however, it has not been proven that the same changes in those parameters are observed in patients with cerebro- vascular disease. To investigate the relationship between changes in CBF, vasodilatory capacity, and other hemody- namic parameters, the ACZ test was performed after an The ability of autoregulation to maintain the cerebral 15O-gas PET study. Methods: Twenty-two patients with uni- blood flow (CBF), which resides in the cerebral circulation lateral major cerebral arterial occlusive disease underwent despite transient changes in systemic mean arterial blood 15 PET scans using the H2 O bolus method with the ACZ test pressure, has been shown to occur via the mechanism of 15 after the O-gas steady-state method. CBF and V0 for each arteriolar vasodilatation in the cerebral circulation (1). The subject were calculated using the 3-weighted integral vasodilatory change in the cerebral arteries is assumed for method as well as the nonlinear least-squares fitting method.
    [Show full text]
  • Frequency Response of Blood Flow Autoregulation
    FREQUENCY RESPONSE OF BLOOD FLOW AUTOREGULATION NICHOLAS BRATTO∗, AFRAH HANEK, AND DAVID WENDL FACULTYADVISORS:DR.HYEJINKIMANDDR.YULIAHRISTOVA INDUSTRYMENTOR:DR.SEBASTIANACOSTA Abstract. Autoregulation is the capability of an organ such as the brain, heart, and kidney to maintain a constant blood flow over a series of changes in arterial pressure within their vascular beds. Since the organs in the humany bod demand a steady delivery of blood and bio–agents to sustain their metabolic activity, autoregulation is crucial in protecting the organs from both over and under perfusion of blood. The impairment of autoregulation may lead to neurological, renal, and other complications. In this study, we analyze a simplified and recently developed mathematical model of blood flow autoregulation based on a system of nonlinear ordinary differential equations. Utilizing this model, we develop the optimal and realistic wall–compliance profiles of the blood vessels. Using the realistic wall–compliance profile, we then findthefrequencyresponseoftheautoregulationsystem. Thefrequencyresponsecanbeusedtodetermine whetheranorganisautoregulatingornotgivensomeinputfrequency. 1. Introduction Autoregulation is an extremely important mechanism that keeps blood flow and volume stable in the circulatory system. The circulatory system regulates the blood flow and supply of nutrients, vitamins, minerals,oxygen,carbondioxide,hormones,metabolicwasteandmoretomeetfunctionalneedsoftissues, muscles,andorgans. Thebasiccomponentsofthesystemconsistsoftheheart,arteries,capillarybeds,and
    [Show full text]
  • Jugular Venous Pressure
    NURSING Jugular Venous Pressure: Measuring PRACTICE & SKILL What is Measuring Jugular Venous Pressure? Measuring jugular venous pressure (JVP) is a noninvasive physical examination technique used to indirectly measure central venous pressure(i.e., the pressure of the blood in the superior and inferior vena cava close to the right atrium). It is a part of a complete cardiovascular assessment. (For more information on cardiovascular assessment in adults, see Nursing Practice & Skill ... Physical Assessment: Performing a Cardiovascular Assessment in Adults ) › What: Measuring JVP is a screening mechanism to identify abnormalities in venous return, blood volume, and right heart hemodynamics › How: JVP is determined by measuring the vertical distance between the sternal angle and the highest point of the visible venous pulsation in the internal jugular vein orthe height of the column of blood in the external jugular vein › Where: JVP can be measured in inpatient, outpatient, and residential settings › Who: Nurses, nurse practitioners, physician assistants, and treating clinicians can measure JVP as part of a complete cardiovascular assessment What is the Desired Outcome of Measuring Jugular Venous Pressure? › The desired outcome of measuring JVP is to establish the patient’s JVP within the normal range or for abnormal JVP to be identified so that appropriate treatment may be initiated. Patients’ level of activity should not be affected by having had the JVP measured ICD-9 Why is Measuring Jugular Venous Pressure Important? 89.62 › The JVP is
    [Show full text]
  • Hemodynamic Effects of Pneumonia: II
    Hemodynamic effects of pneumonia: II. Expansion of plasma volume Raj Kumar, … , Herbert Benson, Walter H. Abelmann J Clin Invest. 1970;49(4):799-805. https://doi.org/10.1172/JCI106293. Previous work has demonstrated that approximately one-third of patients with pneumonia have a hypodynamic circulatory response. This response is characterized by an abnormally wide arteriovenous oxygen difference, a low cardiac output, increased peripheral resistance, and an increased hematocrit. This state was found to abate in convalescence. In an attempt to elucidate the pathogenesis of this hypodynamic state, nine additional patients were studied hemodynamically during the acute phase of pneumonia before and during acute expansion of blood volume by low molecular weight dextran (seven patients) or normal saline (two patients). Five patients were restudied before and during acute blood volume expansion in convalescence. Three patients with pneumonia had a normal arteriovenous oxygen difference (< 5.5 vol%), and six patients were hypodynamic in that their arteriovenous oxygen differences were greater than 5.5 vol%. With expansion of blood volume in the acute phase of pneumonia, all patients showed an increase in cardiac output, a decrease in arteriovenous oxygen difference, and a decrease in peripheral vascular resistance; however, the percentage change in the hypodynamic patients was not as great as occurred in the patients with normal hemodynamics nor as great as occurred when restudied in convalescence. Likewise, all patients had a normal or near normal hemodynamic profile in convalescence. In addition, ventricular function in the acute phase of pneumonia was depressed. The findings suggest […] Find the latest version: https://jci.me/106293/pdf Hemodynamic Effects of Pneumonia II.
    [Show full text]
  • Blood Vessels and Circulation
    19 Blood Vessels and Circulation Lecture Presentation by Lori Garrett © 2018 Pearson Education, Inc. Section 1: Functional Anatomy of Blood Vessels Learning Outcomes 19.1 Distinguish between the pulmonary and systemic circuits, and identify afferent and efferent blood vessels. 19.2 Distinguish among the types of blood vessels on the basis of their structure and function. 19.3 Describe the structures of capillaries and their functions in the exchange of dissolved materials between blood and interstitial fluid. 19.4 Describe the venous system, and indicate the distribution of blood within the cardiovascular system. © 2018 Pearson Education, Inc. Module 19.1: The heart pumps blood, in sequence, through the arteries, capillaries, and veins of the pulmonary and systemic circuits Blood vessels . Blood vessels conduct blood between the heart and peripheral tissues . Arteries (carry blood away from the heart) • Also called efferent vessels . Veins (carry blood to the heart) • Also called afferent vessels . Capillaries (exchange substances between blood and tissues) • Interconnect smallest arteries and smallest veins © 2018 Pearson Education, Inc. Module 19.1: Blood vessels and circuits Two circuits 1. Pulmonary circuit • To and from gas exchange surfaces in the lungs 2. Systemic circuit • To and from rest of body © 2018 Pearson Education, Inc. Module 19.1: Blood vessels and circuits Circulation pathway through circuits 1. Right atrium (entry chamber) • Collects blood from systemic circuit • To right ventricle to pulmonary circuit 2. Pulmonary circuit • Pulmonary arteries to pulmonary capillaries to pulmonary veins © 2018 Pearson Education, Inc. Module 19.1: Blood vessels and circuits Circulation pathway through circuits (continued) 3. Left atrium • Receives blood from pulmonary circuit • To left ventricle to systemic circuit 4.
    [Show full text]
  • Study and Evaluation of Palmar Blood Volume Pulse for Heart Rate Monitoring in a Multimodal Framework
    Study and Evaluation of Palmar Blood Volume Pulse for Heart Rate Monitoring in a Multimodal Framework Hugo Silva1;2, Joana Sousa1;2 and Hugo Gamboa1;3 1PLUX - Wireless Biosignals, S.A., Av. 5 de Outubro, n. 70 - 6, 1050-059 Lisbon, Portugal 2IT - Instituto Superior Tecnico,´ Av. Rovisco Pais, n. 1, 1049-001 Lisboa, Portugal 3CEFITEC - Faculdade de Cienciasˆ e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica, Portugal Abstract. Within the field of biosignal acquisition and processing, there is a growing need for combining multiple modalities. Clinical psychology is an area where this is often the case, and one example are the studies where heart rate and electrodermal activity need to be acquired simultaneously. Both of these pa- rameters are typically measured in distinct anatomical regions (the former at the chest, and the later at the hand level), which raises wearability issues as in some cases two independent devices are used; finger clip sensors already enable heart rate measurement at the hand level, however they can be limiting for free living and quality of life activities. In this paper we perform a study and evaluation of an experimental blood volume pulse sensor, to assess the feasibility of measuring the heart rate at the hand palms, and thus enabling the design of more convenient systems for multimodal data acquisition. 1 Introduction Blood Volume Pulse (BVP) sensors are a commonly used method for assessing the cardiovascular activity at the arterial level [1]. Their operating principle is based on photoplethysmography, that is, by externally applying a light source in the visible or invisible wavelengths to the tissues, and measuring the amount of light that reaches a photodetector [2].
    [Show full text]
  • Altered Blood Volume Regulation in Sustained Essential Hypertension: a Hemodynamic Study
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Kidney International, Vol. 8 (1975), p. 42—47 Altered blood volume regulation in sustained essential hypertension: A hemodynamic study MICHEL E. SAFAR, GERARD M. LONDON, YVES A. WEIss and PAUL L. MILLIEZ Hemodynamic Laboratory, Hypertension Research Center, Hospital Broussais,Paris, France Altered blood volume regulation in sustained essential hyper- sion normale comme système de réfèrence, une evaluation quan- tension: A hemodynamic study. Cardiac and renal hemodynamics titative du trouble de Ia regulation volCmique des hypertendus and total blood volume were determined in 28 normal subjects est proposee. Chez ces patients, Ia valeur de Ia résistance pen- and 60 patients with untreated essential well-established hyper- pherique correspond a deux valeurs du volume sanguin: Ia tension. Endogenous creatinine clearance was within normal valeur mesurée et Ia valeur theorique, extrapolée a partir de Ia ranges and sodium intake was 110 mEq/day. A significant courbe normale. La difference entre ces deux valeurs est appelée negative volume-resistance relationship was observed both in "variation relative en volume sanguin" et utilisée comme normal subjects (P< 0.005) and hypertensive patients (P< 0.001). modéle mathématique. Chez les hypertendus, Ic volume sanguin In comparison with the normal curve, the hypertensive curve has mesuré est rCduit (P< 0,001) alors que Ia "variation relative en two characteristics: 1) the curve was reset on the right-hand side volume sanguin" augmente (P< 0,001). Cette "augmentation and, 2) the slope was significantly shallower, indicating a reduced relative" est correlée directement avec Ia pression artérielle dia- ability to decrease the volume per unit rise in resistance.
    [Show full text]
  • Cardiac Output
    Overview of Human Anatomy and Physiology: Cardiac Output Introduction Welcome to the Overview of Human Anatomy and Physiology course on the Cardiac System. This module, Cardiac Output, discusses measurement of heart activity and factors that affect activity. After completing this module, you should be able to: 1. Define stroke volume and cardiac output. 2. Discuss the relationship between heart rate, stroke volume, and cardiac output. 3. Identify the factors that control cardiac output. Measurement Cardiac Output The activity of the heart can be quantified to provide information on its health and efficiency. One important measurement is cardiac output (CO), which is the volume of blood ejected by the left ventricle each minute. Heart rate and stroke volume determine cardiac output. Heart rate (HR) is the number of heartbeats in one minute. The volume of blood ejected by the left ventricle during a heartbeat is the stroke volume (SV), which is measured in milliliters. Equation Cardiac output is calculated by multiplying the heart rate and the stroke volume. Average Values Cardiac output is the amount of blood pumped by the left ventricle--not the total amount pumped by both ventricles. However, the amount of blood within the left and right ventricles is almost equal, approximately 70 to 75 mL. Given this stroke volume and a normal heart rate of 70 beats per minute, cardiac output is 5.25 L/min. Relationships When heart rate or stroke volume increases, cardiac output is likely to increase also. Conversely, a decrease in heart rate or stroke volume can decrease cardiac output. What factors regulate increases and decreases in cardiac output? Regulation Factors Regulating Cardiac Output Factors affect cardiac output by changing heart rate and stroke volume.
    [Show full text]
  • Cardiac Output and Distribution of Blood Volume in Central and Peripheral Circulations in Hypertensive and Normotensive Man* MILOS ULRYCH, EDWARD D
    Br Heart J: first published as 10.1136/hrt.31.5.570 on 1 September 1969. Downloaded from Brit. Heart J., 1969, 31, 570. Cardiac Output and Distribution of Blood Volume in Central and Peripheral Circulations in Hypertensive and Normotensive Man* MILOS ULRYCH, EDWARD D. FROHLICH, ROBERT C. TARAZI, HARRIET P. DUSTAN, AND IRVINE H. PAGE From the Research Division, Cleveland Clinic, Cleveland, Ohio, U.S.A. Most haemodynamic studies of arterial hyper- blood volume expansion since intravascular volume tension have been concerned with cardiac output was, if anything, decreased (Tarazi et al., 1969). and peripheral resistance (Page and McCubbin, The possibility remained that output might be 1965). Some, additionally, have investigated re- raised through a redistribution of intravascular gional distribution of blood flow and vascular volume from peripheral veins to the cardiopulmon- resistances, whereas only a few, dealing with circu- ary capacitance bed, even if total blood volume were lation in the extremities, were designed to provide diminished. The present study describes the rela- information about the venous segment of the circu- tions among cardiopulmonary blood volume, total lation (Wood, 1961; Caliva et al., 1963a, b). These blood volume, cardiac output, and arterial blood studies of the capacitance segment in hypertension pressure in normal subjects, in patients with dealt only with regional circulations; there has been essential hypertension, or with hypertension no report on the relationships of total blood volume accompanying renal arterial disease. This was to its distribution between the central and peripheral made possible by the recent development of circulations, to cardiac output, or to systemic arterial methods for determination of cardiopulmonary http://heart.bmj.com/ pressure in hypertensive patients.
    [Show full text]
  • The Renin-Angiotensin-Aldosterone System in Patients with Cystic Fibrosis of the Pancreas
    Pcdiat. Res. 5:626-C32 (1971) Aldosterone renin angiotensin sodium cystic fibrosis of sweat the pancreas The Renin-Angiotensin-Aldosterone System in Patients with Cystic Fibrosis of the Pancreas A. P. SIMOPOULOS'191, A. LAPEY, T. F. BOAT, P. A. DI SANT' AGNESE, AND F. C. BARTTER Endocrinology Branch, National Heart and Lung Institute, and Pediatric Metabolism Branch, National Institute of Arthritis and Metabolic Diseases, National Institutes of Health, Bethcsda, Maryland, USA Extract Patients with cystic fibrosis of the pancreas (CFP) have elevated plasma renin activity, supine renin 497-595 compared with a normal value of 228 ± 133 ng/100 ml plasma on 109 mEq sodium intake/24 hr, but have normal renin release mechanisms as far as postural changes are concerned, since the renin activity increases normally with the upright posture; upright renin, 594-875 compared with a normal value of 359 ± 210 ng/100 ml plasma on the same sodium intake. The high aldosterone secretion rates (ASR), 161 —4-45 compared with a normal value of 90 ± 31 /jg/24 hr, seen on 109 mEq sodium intake were probably secondary to the abnormally high renin release. The same can be said for the lack of adequate suppression to normal of both renin and ASR on 249 mEq sodium intake/24 hr, supine renin 205-544 compared with a normal value of 97 ± 71 ng/100 ml plasma; upright renin 845-893 compared with a normal value of 212 ±61 ng/100 ml plasma; ASR on the same intake, 93-333 compared with a normal value of 62.15 ± 27.8 /ug/24 hr.
    [Show full text]
  • Angiotensin-Converting Enzyme 2 (ACE2) As a Potential Diagnostic and Prognostic Biomarker for Chronic Inflammatory Lung Diseases
    G C A T T A C G G C A T genes Review Angiotensin-Converting Enzyme 2 (ACE2) as a Potential Diagnostic and Prognostic Biomarker for Chronic Inflammatory Lung Diseases Dejan Marˇceti´c 1,2 , Miroslav Samaržija 2, Andrea Vuki´cDugac 2,† and Jelena Kneževi´c 3,4,*,† 1 Department of Internal and Pulmonary Diseases, General Hospital Virovitica, Ljudevita Gaja 21, 33000 Virovitica, Croatia; [email protected] 2 Department of Lung Diseases Jordanovac, Zagreb University Hospital Centre, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia; [email protected] (M.S.); [email protected] (A.V.D.) 3 Laboratory for Advanced Genomics, Division of Molecular Medicine, Ruder¯ Boškovi´cInstitute, 10000 Zagreb, Croatia 4 Faculty of Dental Medicine and Health, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia * Correspondence: [email protected] † These authors share senior authorship. Abstract: Chronic inflammatory lung diseases are characterized by uncontrolled immune response in the airways as their main pathophysiological manifestation. The lack of specific diagnostic and thera- peutic biomarkers for many pulmonary diseases represents a major challenge for pulmonologists. The majority of the currently approved therapeutic approaches are focused on achieving disease re- mission, although there is no guarantee of complete recovery. It is known that angiotensin-converting Citation: Marˇceti´c,D.; Samaržija, M.; enzyme 2 (ACE2), an important counter-regulatory component of the renin–angiotensin–aldosterone Vuki´cDugac, A.; Kneževi´c,J. system (RAAS), is expressed in the airways. It has been shown that ACE2 plays a role in systemic Angiotensin-Converting Enzyme 2 regulation of the cardiovascular and renal systems, lungs and liver by acting on blood pressure, (ACE2) as a Potential Diagnostic and Prognostic Biomarker for Chronic electrolyte balance control mechanisms and inflammation.
    [Show full text]