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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
The Association Between Selected Molecular Biomarkers and Ambulatory Blood Pressure Patterns in African Chronic
Abiodun Moshood Adeoye1,2, Oladimeji Adebayo1, Busayo Abiola1
1Department of Medicine, University College Hospital, Ibadan, Nigeria.
Insights
This study investigates blood pressure variations in African patients with chronic kidney disease (CKD), examining genetic and environmental factors to improve cardiovascular event prevention. Findings will aid in targeted interventions for CKD patients.
Area of Science:
- Nephrology
- Cardiology
- Genetics
- Environmental Health
Background:
- Chronic kidney disease (CKD) is a growing health crisis in sub-Saharan Africa.
- Abnormal blood pressure variations in CKD increase cardiovascular risks.
- Determinants of ambulatory blood pressure in African CKD patients remain understudied.
Purpose of the Study:
- To identify phenomic, genetic, and environmental factors influencing ambulatory blood pressure patterns in African CKD and hypertensive patients.
- To compare these determinants with normotensive controls.
- To develop targeted interventions for cardiovascular event prevention.
Main Methods:
- Longitudinal study of 200 CKD patients, 200 hypertensives without CKD, and 200 healthy controls.
- Collection of demographic, clinical, electrocardiography, echocardiography, and 24-hour ambulatory blood pressure data.
- Analysis of biomarkers (e.g., albumin-creatinine ratio, CRP, homocysteine) and DNA for genetic polymorphisms.
Main Results:
- Recruitment of 239 participants is complete.
- Follow-up phase, data analysis, and publications are ongoing.
- Expected to provide insights into blood pressure variability in the study population.
Conclusions:
- The study will enable phenotypic and genotypic stratification of Nigerian CKD patients based on blood pressure variations.
- Findings will inform targeted interventions and medication timing to improve patient prognosis.
- Aims to reduce cardiovascular morbidity and mortality in CKD patients.
Background:
Chronic kidney disease (CKD) is a burgeoning epidemic in sub-Saharan Africa. Abnormal blood pressure variations are prevalent in CKD and potentiate the risk of cardiovascular morbidity and mortality. Certain genetic variants (angiotensin II receptor type 1 1166 A>C and angiotensin-converting enzyme insertion and deletion polymorphisms) and biomarkers such as interleukin-6, tumor necrosis factor, soluble (s) E-selectin, homocysteine, and highly sensitive C-reactive protein have been shown to affect blood pressure variability among non-African CKD, hypertensive. and nonhypertensive CKD population. However, the contributions of the pattern, genetic, and environmental determinants of ambulatory blood pressure in African CKD have not been characterized. Understanding these interactions may help to develop interventions to prevent major cardiovascular events among people with CKD.
Objective:
The overarching objective of this study is to identify, document, and develop approaches to address related phenomic, genetic, and environmental determinants of ambulatory blood pressure patterns in African CKD and non-CKD hypertensive patients compared with normotensive controls.
Methods:
This is a longitudinal short-term follow-up study of 200 adult subjects with CKD and 200 each of age-matched hypertensives without CKD and apparently healthy controls. Demographic information, detailed clinical profile, electrocardiography, echocardiography, and 24-hr ambulatory blood pressure measurements will be obtained. Blood samples will be collected to determine albumin-creatinine ratio, fasting plasma glucose, lipid profile, electrolytes, urea and creatinine, C-reactive protein, serum homocysteine, fibroblast growth factor-23, and complete blood count, while 2 mL blood aliquot will be collected in EDTA (ethylenediaminetetraacetic acid) tubes and mixed using an electronic rolling system to prevent blood clots and subsequently used for DNA extraction and genetic analysis.
Results:
A total of 239 participants have been recruited so far, and it is expected that the recruitment phase will be complete in June 2020. The follow-up phase will continue with data analysis and publications of results.
Conclusions:
This study will help stratify Nigerian CKD patients phenotypically and genotypically in terms of their blood pressure variations with implications for targeted interventions and timing of medications to improve prognosis.
International Registered Report Identifier (Irrid):
DERR1-10.2196/14820.
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