<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-24T16:01:16.371519550Z</responseDate><request verb="GetRecord" identifier="oai:repository.nwu.ac.za:10394/25384" metadataPrefix="dim">https://repository.nwu.ac.za/server/oai/request</request><GetRecord><record><header><identifier>oai:repository.nwu.ac.za:10394/25384</identifier><datestamp>2018-03-05T06:18:03Z</datestamp><setSpec>com_10394_26463</setSpec><setSpec>col_10394_26476</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor">Schutte, A E</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" authority="7e83c250-14fa-4ef7-bf4f-dae9291bb0c9" confidence="600">Gafane-Matemane, Lebo Francina</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2017-08-17T12:58:58Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2017-08-17T12:58:58Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2016</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/10394/25384</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">PhD (Physiology), North-West University, Potchefstroom Campus, 2017</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Motivation&#xd;
Blood pressure is decreasing globally, however, the prevalence of hypertension continues to&#xd;
increase in Sub-Saharan African countries such as South Africa. Populations of African ancestry&#xd;
are more likely to suffer from cardiovascular outcomes such as cerebrovascular accidents and&#xd;
heart disease due to hypertension, as compared to whites. The mechanisms involved are not&#xd;
clear, particularly the role of the renin-angiotensin-aldosterone system (RAAS). The RAAS is the&#xd;
master regulator of water, electrolyte and blood pressure balance. The rate-limiting enzyme of&#xd;
this cascade, namely renin, is usually suppressed in Africans and as a result low-renin&#xd;
hypertension is common in this population group. Low-renin hypertension is not a diagnosis, but&#xd;
rather a description. A lower renin level indicates that renin secretion in the kidney is inhibited by&#xd;
increasing blood pressure, possibly due to volume-overload. Features of low-renin hypertension&#xd;
include blood pressure sensitivity to increased salt intake; a poor response to angiotensin&#xd;
blockade; and a positive response to calcium channel blockers, aldosterone blockade or diuretics.&#xd;
It is therefore questionable whether the activation of the RAAS has a causal role in the&#xd;
development of hypertension and its associated complications in Africans. Relationships between&#xd;
the components of the RAAS and cardiovascular disease are well established in other&#xd;
populations, however such information in Africans is scant, particularly a detailed physiological&#xd;
description of the low renin phenotype.&#xd;
Aim: The overarching aim of this study was to examine the cardiovascular profile of a black South&#xd;
African population, and the associations of renin, aldosterone, and their ratio with cardiovascular haemodynamics. In addition, the study aimed to determine if the low renin phenotype is&#xd;
associated with an increased risk for cardiovascular- and all-cause mortality. Firstly, the frequency&#xd;
of low renin levels in a black and white population was determined as well as the associations&#xd;
between renin and cardiovascular responses to a laboratory stressor, the cold pressor test (CPT).&#xd;
It was then explored whether aldosterone and renin relate to surrogate measures of sympathetic&#xd;
activity. Lastly, the prognostic value of renin and its interactions with systolic blood pressure (SBP)&#xd;
for all-cause and cardiovascular mortality was investigated. Methodology: This thesis used data collected from the Sympathetic activity and Ambulatory Blood Pressure in&#xd;
Africans (SABPA) and Prospective Urban and Rural Epidemiology (PURE) studies. For the first&#xd;
objective, our study population consisted of 153 black and 188 white men and women (age range,&#xd;
20 to 65 years) from the SABPA study. Haemodynamic measurements included blood pressure&#xd;
(BP), heart rate (HR), stroke volume, total peripheral resistance (TPR) and Windkessel arterial&#xd;
compliance. Active plasma renin levels were determined at rest and when a stressor (CPT) was&#xd;
applied. Reactivity was calculated for each participant as the percentage change from the resting&#xd;
value. For the second objective, black (N=162) and white (N=206) participants (also from the&#xd;
SABPA study) with similar age range as aforementioned were included. The study population&#xd;
was stratified by low and high renin status and the focus was on the low renin groups. Ambulatory&#xd;
BP and HR were measured and night-time dipping calculated. Biochemical analyses were done&#xd;
for plasma renin and aldosterone, and then the aldosterone-to-renin ratio (ARR) was calculated.&#xd;
Noradrenaline and creatinine were determined in urine and the noradrenaline:creatinine ratio was&#xd;
calculated. Lastly, from the PURE study, plasma renin was determined in 1502 black men and&#xd;
women from urban and rural areas in South Africa (age ≥ 35 years), and mortality was assessed&#xd;
over five years. The population was divided into low and high renin groups based on the cut-off&#xd;
from the Renin III CISBIO kit. Results: Lower renin and elevated BP were apparent in blacks compared to whites at rest and during&#xd;
stress (both, P&lt;0.001). When a stressor was applied, HR increased more in blacks (P&lt;0.001),&#xd;
whereas stroke volume (P&lt;0.001) and arterial compliance (P=0.013) decreased more in blacks&#xd;
compared to their white counterparts. There was a positive association between TPR reactivity&#xd;
and renin reactivity in blacks only (β=0.17; P=0.041), while in whites diastolic BP reactivity was&#xd;
positively associated with renin reactivity (β=0.21; P=0.005).&#xd;
Furthermore, a high percentage of blacks exhibited a low renin status (80.9%) compared to whites&#xd;
(57.8%) (P&lt;0.001). In univariate and after multivariate analyses the following significant&#xd;
associations were evident only in low-renin blacks: noradrenaline:creatinine ratio associated&#xd;
positively with aldosterone (β=0.32, P=0.001), 24-hour HR associated positively with renin&#xd;
(β=0.17, P=0.041), while HR dipping associated negatively with aldosterone (β=-0.30, P=0.001)&#xd;
and ARR (β=-0.23, P=0.010). No significant findings were obtained in whites in the low renin&#xd;
group.&#xd;
Lastly, multivariable-adjusted Cox-regression analyses were performed. In the low renin group,&#xd;
SBP and renin*SBP interaction, but not renin, predicted both all-cause [(HR, 1.41; 95% CI, 1.07-&#xd;
1.87; P=0.014), (HR, 1.72, 95% CI, 1.05-2.83, P= 0.031)] and cardiovascular mortality [(HR, 1.87;&#xd;
95% CI, 1.16-3.01; P=0.010), (HR, 2.40; 95% CI, 1.06-5.46; P=0.037)]. In the total group, renin&#xd;
and SBP*renin predicted all-cause, but not cardiovascular mortality [(HR, 1.33; 95% CI, 1.07-&#xd;
1.65; P=0.011), (HR, 1.30; 95% CI, 1.06-1.60; P=0.012)]. In the high renin group, neither renin,&#xd;
SBP nor the renin*SBP predicted all-cause or cardiovascular mortality.&#xd;
Conclusion: The low renin phenotype (volume-loading hypertension) is eminent in the black South African&#xd;
population, and may be suggestive of an increased cardiovascular risk. Although blacks had&#xd;
supressed renin levels at rest and during acute stress, vascular resistance reactivity associated positively with renin reactivity only in the black population. These results suggest that even at low&#xd;
renin levels a sympathetic response evoked by stress is linked to increased peripheral vascular&#xd;
responses, which may contribute to elevated BP in blacks. Furthermore, in a black low-renin&#xd;
population, the observed associations of surrogate indices of sympathetic nerve activity with&#xd;
components of the RAAS suggest that higher aldosterone levels relative to renin may have&#xd;
detrimental effects on the heart, and that the effects of aldosterone may be coupled to sympathetic&#xd;
dominance. Lastly, the interaction of renin with SBP is predictive of all-cause and cardiovascular&#xd;
mortality only in Africans with low renin levels</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="thesistype" lang="en_US">Doctoral</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">en</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">North-West University (South Africa) , Potchefstroom Campus</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Black</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Renin</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Aldosterone</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Sympathetic nervous system</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Total peripheral resistance</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Hypertension</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Cardiovascular mortality</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">The cardiovascular profile of the low renin phenotype in a black South African population</dim:field>
   <dim:field mdschema="dc" element="type" lang="en_US">Thesis</dim:field>
   <dim:field mdschema="others" element="access-status">open.access</dim:field>
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