Perfusion and pulsatile pressure: their relationship with target organ damage in the African-PREDICT study
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Abstract
Background Hypertension is the leading risk factor for subclinical target-organ damage (TOD) and cardiovascular
disease (CVD). Little is known about the relationship between different pressure measures and subclinical TOD,
especially in young populations. We compared the strength of associations of subclinical TOD markers with perfusion
and pulsatile pressure in young adults.
Methods A total of 1 187 young adults from the African-PREDICT study were included. Ambulatory mean arterial
pressure (MAP) and pulse pressure (PP) was obtained. Markers of subclinical TOD were measured and included left
ventricular mass index (LVMi), carotid intimamedia thickness (cIMT), carotidfemoral pulse wave velocity (cfPWV),
central retinal arteriolar equivalent (CRAE) and albumin to creatinine ratio (ACR).
Results Measures of sub-clinical TOD (cIMT, cfPWV and CRAE), associated stronger with perfusion pressure (all
p<0.001) than pulsatile pressure in unadjusted models. Stronger associations were found between cfPWV (adjusted
R2=0.26), CRAE (adjusted R2=0.12) and perfusion pressure (all p≤0.001) than pulsatile pressure independent of
several non-modifiable and modifiable risk factors.
Conclusions In young, healthy adults, perfusion pressure is more strongly associated with subclinical TOD markers
than pulsatile pressure. These findings contribute to the understanding of the development of early cardiovascular
changes and may guide future intervention strategies.
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Correspondence:
Yolandi Breet
21195706@nwu.ac.za
1
Hypertension in Africa Research Team (HART), North-West University,
Private Bag X 1290, Potchefstroom 2520, South Africa
2
MRC Research Unit for Hypertension and Cardiovascular Disease, NorthWest University, Potchefstroom, South Africa
Citation
Rooi, D., Botha-Le Roux, S. and Breet, Y., 2024. Perfusion and pulsatile pressure: their relationship with target organ damage in the African-PREDICT study. BMC Cardiovascular Disorders, 24(1), p.399. https://doi.org/10.1186/s12872-024-04071-y
