3. Electronic Theses and Dissertations (ETDs) - All submissions
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Item Adverse effects of aortic backward waves in a group of African Ancestry(2017) Sibiya, Moekanyi JeffreyAlthough brachial blood pressure (BP) is a well-recognized risk factor for predicting cardiovascular events, aspects of aortic BP may enhance risk prediction. Pulse pressure (PP) is amplified from the aorta to peripheral arteries and variations in differences between brachial and aortic PP (PP amplification) are determined by factors that influence either the aortic forward (Pf) or backward (Pb)(reflected) pressure waves. Although aortic Pb may be more important than Pf in mediating cardiovascular risk, the best approach to assessing backward wave function (augmentation pressures [Pa] and index [AIx] or wave separation analysis); the relative impact of aortic Pb versus Pf on cardiovascular damage; and whether the ability of aortic-to-brachial PP amplification (PPamp) to add to risk prediction reflects backward or forward wave effects, is uncertain. In the present thesis I therefore first assessed in 808 community participants whether gender influences relations between Pa or AIx and left ventricular mass (LVM), a well-accepted end-organ measure. Aortic haemodynamics were determined using radial applanation tonometry and SphygmoCor software and LVM from echocardiography. In men, both AIx derived from Pa/central aortic PP (Pa/PPc) (p<0.01) and AIx derived from the second peak/first peak (P2/P1) of the aortic pulse wave (p<0.0005) were associated with LVM. In contrast, in women neither AIx derived from Pa/PPc (p=0.08) nor AIx derived from P2/P1 (p=0.17) were associated with LVM. Both the strength of the correlations (p<0.001 and p<0.0005) and the slope of the AIx-LVM relationships (p=0.001 and p<0.0005) were greater in men as compared to women. Therefore, in the present study I show that AIx is independently associated with LVMI in men, but not in women. I subsequently evaluated whether in women, measures of aortic systolic pressure augmentation (Pa or AIx) underestimate the effects of reflected waves on cardiovascular risk or whether Pb plays little role in cardiovascular risk prediction. In the same community sample I therefore evaluated sex-specific contributions of reflected (Pb and the reflection index [RI]) versus augmented (Pa and AIx) pressure wave indices to iii variations in PPc (n=1185, 65.0% women), and LVM (n=793, 64.9% women). Aortic Pb and Pf were determined using wave separation analysis. In both women and in men, independent of confounders, RI and Pb contributed more than Pf, whilst Pa and AIx contributed less than incident wave pressure (Pi) to variations in PPc (p<0.0001 for comparison of partial r values). In both men and in women Pb contributed more than Pf (p<0.05) to variations in LVM. Although in men Pa (partial r=0.33, p<0.0001) contributed to a similar extent as Pi ((partial r=0.34, p<0.0001) to variations in LVMI, in women Pa (partial r=0.05, p=0.36) failed to contribute to LVM, whilst Pi was significantly associated with LVM (partial r=0.30, p<0.0001). Similar results were obtained with AIx as opposed to Pa in the regression models. Therefore, in both women and in men, Pb is more closely associated with PPc and LVM than Pf, but indices of aortic pressure augmentation markedly underestimate these effects, particularly in women. As the relative impact of aortic Pb as compared to Pf on cardiovascular damage independent of brachial BP is uncertain, in 1174 participants from a community sample I subsequently assessed the relative impact of Pb and Pf on variations in LVM (n=786), aortic pulse wave velocity (PWV)(n=1019), carotid intima-media thickness (IMT)(n=578), transmitral early-to-late LV diastolic velocity (E/A)(n=779) and estimated glomerular filtration rate (eGFR)(n=1174). Independent of mean arterial pressure and confounders, PPc and both Pb and Pf were associated with end-organ measures or damage (p<0.05 to <0.0001). With adjustments for brachial PP and confounders, Pb remained directly associated with LVM (partial r=0.10, p<0.01), PWV (partial r=0.28, p<0.0001), and IMT (partial r=0.28, p<0.0001), and inversely associated with E/A (partial r=-0.31, p<0.0001) and eGFR (partial r=-0.14, p<0.0001). Similar relations were noted with the presence of end-organ damage (p<0.05 to <0.0001). In contrast, with adjustments for brachial PP and confounders, Pf no longer retained direct relations with LVM, PWV, and IMT or inverse relations with E/A and eGFR. Adjustments for Pb, but not Pf diminished brachial PP-independent relationships between PPc and end-organ measures. Thus, although both Pf and Pb contribute to end-organ measures and damage, independent of brachial iv BP, the impact of aortic BP is accounted for largely by Pb. PPamp is independently associated with cardiovascular outcomes. However, the aortic functional change most likely to account for this effect is uncertain. In 706 community participants I subsequently aimed to identify the aortic functional change that accounts for relations between PPamp and LVM. In multivariate models with the inclusion of brachial PP, 1/PPamp (partial r=0.12, p<0.005), Pb (partial r=0,09, p<0.05), and aortic PWV (partial r=0.09, p<0.05) were independently associated with LVMI. Similarly, in multivariate models with the inclusion of brachial PP, 1/PPamp (p<0.005), Pb (p<0.01), and aortic PWV (p<0.01) were independently associated with LV hypertrophy (LVH). With adjustments for Pb, the brachial PP-independent relationships between 1/PPamp and LVMI or LVH were abolished (p>0.08 for both). However, adjustments for PWV failed to modify brachial PP-independent relations between 1/PPamp and LVMI or LVH. Hence, independent relations between PPamp and LVM or LVH are largely accounted for by Pb. In conclusion, in the present thesis I show that the use of augmented pressures underestimates the impact of reflected pressure wave effects on end-organs, particularly in women; that brachial BP-independent relations between aortic BP and end organs is determined largely by Pb and that relations between PPamp and end organ measures is largely accounted for by Pb. These findings add to our understanding of the adverse effects of aortic functional changes on the cardiovascular system and suggest cost-effective approaches to add to risk prediction.Item Severe hypertension in two emergency departments of Netcare Management (Pty) Limited hospitals, Johannesburg, South Africa.(2014-03-28) Kabongo, DiuluHypertension is the major cause of cardio-vascular diseases and contributes to 13.5% of premature deaths worldwide. With a 10–year risk to develop organ damages estimated at 30%, severe hypertension exposes even more patients to premature death. Severe hypertension is a type of hypertension with systolic blood pressure ≥ 180mmHg and/or diastolic blood pressure ≥ 110 mmHg that may present with or without symptoms/signs or target organ damages, and may be classified accordingly as asymptomatic (without symptoms/signs) severe hypertension, hypertension urgency (with symptoms/signs, no target organ damage) or hypertension emergency (with target organ damage). Hypertension urgency and hypertension emergency are considered hypertension crisis. This study aimed to establish the socio-demographic and clinical characteristics of the patients who presented with severe hypertension at the Emergency Departments of two private hospitals of the Netcare Management (Pty) Limited in Johannesburg during the period from the 1st of January 2010 to 30th April 2011. These patients presumably receive quality health care and may not be expected to develop severe hypertension. Therefore, this study would contribute to efforts to identify patients at risk and those who may benefit from preventive measures. The methodology of this study was a retrospective, transversal and comparative study. One thousand and forty-two patients were included in the study. All of these participants had a medical aid cover or were able to pay for medical consultation at a private hospital. Data were collected from an electronic database, the Medibank™, and from manual patients’ registers kept in each hospital’s Emergency Department. Severe hypertension was found among 1.7% of all patients who presented to the studied emergency departments. Only 817 patients were classified in the different subtypes of SH. Asymptomatic severe hypertension was the most common (83.4%) type of severe hypertension and hypertension emergency was the least common (4.8%). At Mulbarton Hospital, 50.2% of severe hypertension patients were male and at Linksfield Hospital, 60.3% were female. Male patients were younger than female patients. White patients and elderly were mostly affected by severe hypertension in the studied population. Systolic blood pressures were similar among the different races and genders. Black patients had higher diastolic blood pressure compared to white patients. White patients were older and may have had a tendency of isolated systolic hypertension. Overall, the most common symptoms/signs in hypertension urgency were chest pains (46.4%), headache (34.0%) and epistaxis (11.3%). The most common target organ damages in hypertension emergency were stroke (58.9%), left ventricular failure/congestive cardiac failure (28.2%) and seizures (12.8%). None of the studied characteristics could be claimed predictors of hypertension crisis. Also, there was no association between seasons and days of presentation and onset of severe hypertension in each hospitals. Further studies are required to include other factors that are known to affect the occurrence of severe hypertension, such as co-morbidities, smoking, alcohol intake and poor adherence to medication by known hypertensive patients. Also, risk factors contributing to the occurrence of SH among younger black patients need to be analysed.Item Central blood pressure in an urban developing community in South Africa(2012-06-15) Redelinghuys, MichelleContemporary notions of the adverse effects of blood pressure (BP) incorporate the increasingly recognised damaging effects of not only distending pressure (indexed by mean arterial pressure-MAP) but also pulse pressure (PP) (the difference between systolic and diastolic BP) on the cardiovascular system. Although the factors which determine brachial artery PP are similar to those affecting central (aortic) PP (PPc), some factors may affect central PP preferentially, and thus PP calculated from brachial artery BP measurement may not closely reflect the PP that accounts for cardiovascular damage. In order that therapeutic strategies are developed that modify PPc independent of distending pressures, there is considerable interest in the pathophysiological mechanisms that explain increases in PPc. In this regard, aortic PP is comprised of the forward or incident pressure component (P1), which is largely determined by stroke volume, aortic compliance or stiffness and aortic diameter; and the augmented pressure component (AP), which is determined by wave reflection. Whilst currently employed antihypertensive agents may modify AP independent of distending pressures, there is little evidence to indicate a similar effect on the structural aortic changes responsible for P1. Although changes in AP as opposed to P1 largely account for age-related increases in PPc across the adult lifespan in normotensives, the relative contribution of AP and P1 to PPc in communities with a high prevalence of uncontrolled BP is unknown. In 1015 randomly recruited participants (range 16-88 years) from a community sample, 37.7% of whom had uncontrolled BP, I demonstrated that independent of MAP and other confounders, P1 contributes as much as AP to age-related increases in PPc and to variations in PPc across the adult lifespan. As no previous studies have assessed the relationship between P1 and cardiovascular damage, in 503 randomly recruited participants from a community with a high prevalence of uncontrolled BP, the relative contribution of P1 and AP to increases in left ventricular mass index (LVMI) was subsequently evaluated. In this regard, independent of distending pressures, P1 was associated with LVMI, highlighting the need to understand the iii potential mechanisms which contribute to P1. Could the pathophysiological mechanisms that determine hypertension account for the contribution of P1 to PPc? In this regard, I evaluated the potential role of three mechanisms. First, in 635 randomly selected participants with 24-hour urine samples that met with pre-specified quality control criteria, I provide the first data to demonstrate that urinary sodium-to-potassium ratio (an index of Na+ and K+ intake) is independently associated with PPc, but not brachial PP independent of distending pressures, a relationship that could be accounted for by changes in both AP and P1, but not aortic pulse wave velocity. Second, I explored the possibility that low grade inflammation as indexed by circulating high-sensitivity C-reactive protein concentrations (hs-CRP) may contribute toward PPc and the component pressures. In this regard, although hs-CRP has been associated with changes in central haemodynamics in small study samples, in a large community sample of participants these findings could not be reproduced. However, in that study the community had a low prevalence of risk-related hs-CRP concentrations. In 836 randomly recruited participants from a population sample with a high prevalence of risk-related hs-CRP concentrations (~57%), although on univariate analysis I showed that hs-CRP was strongly associated with PPc and the component pressures, this relationship did not persist with adjustments for confounders. Last I evaluated the potential contribution of genetic factors toward PPc and the component pressures. Although three prior studies had demonstrated heritability of PPc, AP and P1, two studies failed to adjust for MAP and a third assessed the heritability in females only. In none of these studies was the contribution of aortic PWV to the heritability estimates of PPc, AP and P1 assessed. In 568 participants from 183 nuclear families, I showed that independent of MAP, multivariable adjusted PPc, AP, P1 and PWV aggregated in families and were inherited. However, adjustments for aortic PWV failed to modify the extent of intrafamilial aggregation and heritability of PPc, AP, or P1. In conclusion, in the present thesis I have advanced our understanding of the mechanisms responsible for increases in PPc. In this regard, I provide evidence to suggest that independent of distending pressures and stroke volume, P1 accounts for a significant iv proportion of the age-related increases in PPc and the variability of PPc across the adult lifespan in communities with a high prevalence of uncontrolled hypertension; that P1 contributes substantially to the relationship between PPc and LVMI; and that PPc and both the AP and P1 component pressures are associated with a urinary index of salt intake as well as genetic factors, but not to an index of low-grade inflammation. These findings suggest that to achieve optimal cardiovascular risk reduction in hypertension, therapeutic strategies that target the aortic structural changes responsible for P1 are likely to be required across the adult lifespan, and that this therapy must in-part address the impact of salt intake and genetic factors, but not necessarily low-grade inflammation on PPc.