Thesis (M. Tech.) -- Central University of Technology, Free State, 2010 / This main aim of this study was to assess patients in a general cardiology practice in order to determine the systolic and diastolic profiles of these patients. The aim was also to determine what effect life style and risk factors may have on the echocardiographic variables measured during such an examination. The specific aim of this study was the importance of not only examining the systolic function but the necessity to also examine the diastolic profile of patients. Life-style plays an important role, with the main culprit being obesity. Obesity was the single most important factor that affected the diastolic profile of patients seen in this study. With obesity a combination of other risk factors related to obesity was observed. Most abnormalities found due to these risk factors were associated with diastolic changes in the left ventricle. Echocardiography is routinely used in daily practice, but the diagnostic value of this tool can be enhanced if proper analyses of the systolic as well as the diastolic profiles are determined. Many cardiologists only measure the systolic function of the heart as an indication of the well- being of the left ventricle, although in this study it was proven that systolic function did not alter with ageing or with changes in the risk profile. Hundred-and-twelve patients, divided into three age groups, were evaluated in this study. Both systolic and diastolic variables were measured and analysed for abnormalities. None of these patients had systolic function abnormalities, although they had detectable anatomic changes due to ageing, obesity and hypertension. Several abnormalities were found on the diastolic profile of these patients. Muscle thickness increased due to obesity and hypertension and even with ageing, but with no significant abnormalities in the systolic function of the heart. There was a slight increase in the circumferential shortening of the left ventricle and that both the septal and longitudinal functions decreased with ageing. It is noteworthy that even where the systolic function remained normal in ageing subjects, their diastolic profiles changed significantly. Assessment of left ventricular function required a meticulous and systematic approach. In this study forty- one percent of patients visiting this general practice had abnormalities of their diastolic function although their systolic function was normal. It was found that with ageing, especially in the older age group, important abnormalities occur in their diastolic profile. The most common changes were that the E- peak velocity decreased and that the Apeak velocity of the trans-mitral flow increased. It seemed that passive filling decreased with ageing but that active filling increased simultaneously, causing the cardiac output to remain constant in older subjects. This is important to know because diseases affecting the atrium may have a profound effect on the cardiac output of older patients, even if they have normal systolic function, (due to the decreased passive filling they need their active filling or atrial contraction to support a normal cardiac output). An important marker will be to look at the ratio of the E/A- velocities in older patients to determine the ratio of active against passive filling. Other than that, a relatively new tool in echocardiography called tissue Doppler was used to determine what happened to the muscle with ageing. Here it was demonstrated that the different layers of the left ventricle acted differently with ageing. Results showed that the longitudinal fibres weakened with ageing although the circumferential fibres remained unchanged or even strengthened with ageing. It was apparent in this study that the traditional use of only systolic function may not be adequate when evaluating relative asymptomatic patients presenting at a general cardiology practice. It is important to also evaluate the diastolic profiles of these patients in order to scientifically quantify their heart health, even in asymptomatic patients. It is important to routinely evaluate the diastolic profile of patients so that early detection of these diastolic variables can be detected and timely consideration for its treatment can be given by their cardiologist. It is also important to take note of the significance of the obesity problem and the effect it has on the heart’s health. In conclusion, this study emphasizes the importance of the echocardiographic evaluation of diastolic cardiac function in addition to routine systolic evaluation in asymptomatic patients. This will enable the clinician to detect abnormalities early and tailor therapy accordingly. Lifestyle related risk factors, especially obesity, also have significant effects on diastolic cardiac function.

Orientadores: José Wilson Magalhães Bassani, Rosana Almada Bassani / Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia Elétrica e de Computação / Made available in DSpace on 2018-08-24T11:00:56Z (GMT). No. of bitstreams: 1 Oshiyama_NataliaFerreira_D.pdf: 4721295 bytes, checksum: 5ed8a9a173462afb13315f133bf426f8 (MD5) Previous issue date: 2014 / Resumo: O potencial de ação (PA), variação do potencial elétrico através da membrana (Em), é gerado por fluxos iônicos através de canais e transportadores, cuja função e expressão pode ser alterada por hormônios, neurotransmissores, drogas e toxinas. Trata-se de um sistema complexo, para o qual os modelos computacionais constituem ferramenta importante de estudo. No presente trabalho, foi desenvolvido um modelo de PA e transporte de Ca2+ em células ventriculares de ratos neonatos, para o que foi necessário medir a concentração intracelular de Na+ ([Na+]i) e a corrente de Na+ (INa) em cardiomiócitos isolados, sobre as quais há pouca informação na literatura, e as correntes de Ca2+ (ICa), transiente de saída (Ito) e retificadora tardia (IK) de K+, além do próprio PA para melhorar a precisão do modelo. Medições em miócitos de ratos adultos foram realizadas para comparação. Foi observada menor excitabilidade das células de ratos neonatos, o que poderia ser explicado por um deslocamento da curva de ativação de INa de ~10 mV para a direita, i.e., a ativação dos canais de Na+ ocorreu em Em menos negativos e numa faixa mais ampla de Em em miócitos de neonatos do que em células de adultos. Outra diferença encontrada foi com relação à densidade de INa, ~2 vezes maior em células de neonatos. O maior influxo de Na+ poderia causar um aumento da [Na+]i durante a atividade em células de recém-nascidos, que foi confirmado pela medição de [Na+]i. No entanto, não houve aumento significativo quando ICa e o trocador Na+/Ca2+ (NCX) foram inibidos, o que indica que o aumento da [Na+]i se deve mais ao efluxo de Ca2+ via NCX do que ao influxo pelos canais de Na+ do sarcolema. Além disso, observou- se maior duração do PA em miócitos de neonatos, que poderia ser explicada pela menor densidade observada de correntes repolarizantes (Ito e IK). No entanto, não foi detectada diferença entre idades na densidade de ICa. Dados de simulações mostraram que o retículo sarcoplasmático (RS) é a principal fonte do Ca2+ ativador da contração e que a liberação fracional de Ca2+ do RS nos ratos neonatos é menor que nos adultos, confirmando dados experimentais deste laboratório. Portanto, o modelo poderá ser utilizado para predizer possíveis alterações eletrofisiológicas dos cardiomiócitos de ratos neonatos em diferentes condições. / Abstract: The action potential (AP), a change in electrical potential across the membrane (Em), is generated by ionic fluxes through channels and transporters, of which function and expression may be affected by hormones, neurotransmitters, drugs and toxins. Computational models constitute an important tool for the study of this highly non-linear and complex system. In this work, a model of AP and Ca2+ transport in ventricular cells of neonatal rats was developed. It was necessary to measure the intracellular Na+ concentration ([Na+]i) and the Na+ current (INa), for which information in the literature is scarce, and the Ca2+ current (ICa), as well as the outward transient (Ito) and delayed rectifier (IK) K+ currents, in addition to the AP itself, to improve the accuracy of the model. Measurements from adult rat myocytes were also made in order to compare these developmental phases. It was observed that neonatal rat cells are less excitable, which could be explained by a ~10 mV shift to the right of the channel activation curve, i.e., Na+ channels activation occured at less negative Em value and over a higher range of Em compared to adult cells. On the other hand, INa density was twice as great as that in adults. This might promote increase in [Na+]i during activity in cells from newborns, which was confirmed by measurement of [Na+]i. Nonetheless, significant Na+ accumulation was suppressed when ICa and the Na+ / Ca2+ exchanger (NCX) were inhibited, which indicates that the increase in [Na+]i probably depends more on Ca2+ efflux via NCX than on the influx through sarcolemmal Na+ channels. The longer AP duration in neonatal myocytes could be explained by the lower density of the repolarizing currents (Ito and IK). However, age-dependent difference in ICa density was not observed. Simulation data agreed with experimental data from this laboratory regarding the sarcoplasmic reticulum (SR) as the main source of Ca2+ during excitation-contraction coupling and the lower SR fractional release in neonatal than in adult myocytes. In conclusion, the present model may be used to predict possible electrophysiological alterations in developing cardiomyocytes under different conditions. / Doutorado / Engenharia Biomedica / Doutora em Engenharia Elétrica

Ten caucasian male quadriplegics were compared with eight sedentary caucasian male controls in regards to left ventricular dimensions and mass obtained from echocardiograrns. The interventricular septum (IVS), left ventricular posterior wall (LVPW) and left ventricular internal diameter (LVII) were within normal limits for both groups. However, the INS in the SCI were significantly thicker than controls (p <0.05). Myocardial thickness was larger in SCI subjects (p <0.05). Absolute left ventricular mass (LVM) and total left ventricular volume was not different ( p > 0.05), but SCI subjects had significantly greater LVM to lean body mass ratios. Echocardiographically, SCI patients demonstrate concentric hypertrophy. This suggests adaptive response to chronic increase in afterload pressure secondary to their daily activities and muscle spasticity.

Thesis (PhD)-- Stellenbosch University, 2013. / ENGLISH ABSTRACT: This dissertation considers automatic segmentation of the left cardiac ventricle in short axis magnetic resonance images. The presence of papillary muscles near the endocardium border makes simple threshold based segmentation difficult. The endo- and epicardium are modelled as two series of radii which are inter-related using features describing shape and motion. Image features are derived from edge information from human annotated images. The features are combined within a Conditional Random Field (CRF) – a discriminatively trained probabilistic model. Loopy belief propagation is used to infer segmentations when an unsegmented video sequence is given. Powell’s method is applied to find CRF parameters by minimising the difference between ground truth annotations and the inferred contours. We also describe how the endocardium centre points are calculated from a single human-provided centre point in the first frame, through minimisation of frame alignment error. We present and analyse the results of segmentation. The algorithm exhibits robustness against inclusion of the papillary muscles by integrating shape and motion information. Possible future improvements are identified. / AFRIKAANSE OPSOMMING: Hierdie proefskrif bespreek die outomatiese segmentasie van die linkerhartkamer in kortas snit magnetiese resonansie beelde. Die teenwoordigheid van die papillêre spiere naby die endokardium grens maak eenvoudige drumpel gebaseerde segmentering moeilik. Die endo- en epikardium word gemodelleer as twee reekse van die radiusse wat beperk word deur eienskappe wat vorm en beweging beskryf. Beeld eienskappe word afgelei van die rand inligting van mens-geannoteerde beelde. Die funksies word gekombineer binne ’n CRF (Conditional Random Field) – ’n diskriminatief afgerigte waarskynlikheidsverdeling. “Loopy belief propagation” word gebruik om segmentasies af te lei wanneer ’n ongesegmenteerde video verskaf word. Powell se metode word toegepas om CRF parameters te vind deur die minimering van die verskil tussen mens geannoteerde segmentasies en die afgeleide kontoere. Ons beskryf ook hoe die endokardium se middelpunte bereken word vanaf ’n enkele mens-verskafte middelpunt in die eerste raam, deur die minimering van ’n raambelyningsfout. Ons analiseer die resultate van segmentering. Die algoritme vertoon robuustheid teen die insluiting van die papillêre spiere deur die integrasie van inligting oor die vorm en die beweging. Moontlike toekomstige verbeterings word geïdentifiseer.

Synchronous contraction and relaxation of the myocardium is required to optimize cardiac function. Regional timing of contraction and relaxation is dyssynchronous in many patients with heart failure. Cardiac resynchronization therapy (CRT) is a highly successful treatment for dyssynchronous heart failure. Patients are currently selected for CRT using surface electrocardiogram QRS duration as a measure of dyssynchrony. However, up to 30% of patients selected for CRT show no improvement. This poor response rate may in part be explained by the poor correlation between mechanical dyssynchrony and QRS duration. Thus, better methods to quantify mechanical dyssynchrony in the heart may improve the poor CRT response rate. The overall goal of this project was to develop better methods to diagnose dyssynchrony in the left ventricle (LV). We developed two new methods with different approaches. The first method improved upon existing tissue-Doppler based echocardiographic diagnosis of dyssynchrony by utilizing a cross-correlation (XC) function to quantify dyssynchrony during post-processing as opposed to the quantitatively simplistic time-to-peak analysis that is currently utilized. The second method utilized standard cine cardiac magnetic resonance (CMR) images to quantify the dyssynchrony in the flow of blood within the LV, which may represent a more direct, physiologically relevant measure of dyssynchrony. Specific aim 1 demonstrated that the new XC delay parameters can be quantified accurately with a stationary region of interest and therefore require significantly less post-processing time to calculate compared to the time-to-peak dyssynchrony parameters. Specific aim 2 showed that XC delays are superior to existing time-to-peak dyssynchrony parameters at discriminating patients with LV dyssynchrony from those with normal function. The time-to-peak parameters showed dyssynchrony in approximately half of the normal, healthy volunteers while the XC delay parameters had nearly perfect diagnostic accuracy. The results of specific aim 3 showed that XC delays could diagnose acute, pacing-induced dyssynchrony in young, healthy children with 79% accuracy while the time-to-peak parameters showed accuracies of 71%, 57% and 57%. Specific aim 4 showed that CMR-based quantification of LV internal flow can be used to discriminate patients with dyssynchronous heart failure from normal controls with 95% accuracy.

Indiana University-Purdue University Indianapolis (IUPUI) / 17-β estradiol (E2) exerts protective effects in hypoxia-induced pulmonary hypertension (HPH) via endothelial cell estrogen receptor (ER)-dependent mechanisms. However, the effects of hypoxia on ER expression in the pulmonary-right ventricle (RV) axis remain unknown. Based on previous data suggesting a role of ER-β in mediating E2 protection, we hypothesized that hypoxia selectively up-regulates ER-β in the lung and pulmonary endothelial cells. In our Male Sprague-Dawley rat model, chronic hypoxia exposure (10% FiO2) resulted in a robust HPH phenotype associated with significant increases in ER- β but not ER-α protein in the lung via western blotting. More importantly, this hypoxia-induced ER-β increase was not replicated in the RV, left ventricle (LV) or in the liver. Hence, hypoxia-induced ER-β up-regulation appears to be lung-specific. Ex vivo, hypoxia exposure time-dependently up-regulated ER-β but not ER-α in cultured primary rat pulmonary artery endothelial cells (RPAECs) exposed to hypoxia (1% O2) for 4, 24 or 72h. Furthermore, the hypoxia induced ER-β protein abundance, while not accompanied by increases in its own transcript, was associated with ER-β nuclear translocation, suggesting increase in activity as well as post-transcriptional up-regulation of ER-β. Indeed, the requirement for ER-β activation was indicated in hypoxic ER-βKO mice where administration of E2 failed to inhibit hypoxia-induced pro-proliferative ERK1/2 signaling. Interestingly, HIF-1α accumulation was noted in lung tissue of hypoxic ER-βKO mice; consistent with previously reported negative feedback of ER-β on HIF-1α protein and transcriptional activation. In RAPECs, HIF-1 stabilization and overexpression did not replicate the effects of ER- β up-regulation seen in gas hypoxia; suggestive that HIF-1α is not sufficient for ER-β up- regulation. Similarly, HIF-1 inhibition with chetomin did not result in ER-β down-regulation. HIF-1α knockdown in RPAECs in hypoxic conditions is currently being investigated. Hypoxia increases ER- β, but not ER-α in the lung and lung vascular cells. Interpreted in context of beneficial effects of E2 on hypoxic PA and RV remodeling, our data suggest a protective role for ER-β in HPH. The mechanisms by which hypoxia increases ER-β appears to be post-transcriptional and HIF-1α independent. Elucidating hypoxia-related ER-β signaling pathways in PAECs may reveal novel therapeutic targets in HPH.

Indiana University-Purdue University Indianapolis (IUPUI) / Recent advancements in the management of systemic glucose regulation in obesity/T2DM include drug therapies designed to utilize components of the incretin system specifically related to glucagon-like peptide 1 (GLP-1). More recently, GLP-1 has been investigated for potential cardioprotective effects. Several investigations have revealed that acute/sub-acute intravenous administration of GLP-1 significantly reduces myocardial infarct size following ischemia/reperfusion injury and improves cardiac contractile function in the settings of coronary artery disease, myocardial ischemia/reperfusion injury, and heart failure. Despite an abundance of data indicating that intravenous infusion of GLP-1 is cardioprotective, information has been lacking on the cardiac effects of iv GLP-1 in the MetS or T2DM population. Some important questions this study aimed to address are 1) what are the direct, dose-dependent cardiac effects of GLP-1 in-vivo 2) are the cardiac effects influenced by cardiac demand (MVO2) and/or ischemia, 3) does GLP-1 effect myocardial blood flow, glucose uptake or total oxidative metabolism in human subjects, and 4) are the cardiac effects of GLP-1 treatment impaired in the settings of obesity/MetS and T2DM. Initial studies conducted in canines demonstrated that GLP-1 had no direct effect on coronary blood flow in-vivo or vasomotor tone in-vitro, but preferentially increased myocardial glucose uptake in ischemic myocardium independent of effects on cardiac contractile function or coronary blood flow. Parallel translational studies conducted in the humans and Ossabaw swine demonstrate that iv GLP-1 significantly increases myocardial glucose uptake at rest and in response to increases in cardiac demand (MVO2) in lean subjects, but not in the settings of obesity/MetS and T2DM. Further investigation in isolated cardiac tissue from lean and obese/MetS swine indicate that this impairment in GLP-1 responsiveness is related to attenuated activation of p38-MAPK, independent of alterations in GLP-1 receptor expression or PKA-dependent signaling. Our results indicate that the affects of GLP-1 to reduce cardiac damage and increase left ventricular performance may be impaired by obesity/MetS and T2DM.