Independent relationships between renal mechanisms and systemic flow, but not resistance to flow in primary hypertension in Africa. Issue 12 (12th December 2021)

• Record Type: Journal Article
• Authors: Malan, Nico; Norton, Gavin R.; Peterson, Vernice R.; Yusuf, Suraj M.; Libhaber, Elena; Libhaber, Carlos D.; Mmopi, Keneilwe N.; Bello, Hamza; Masiu, Mohlabani; Da Silva Fernandes, Daniel; Tade, Grace; Mthembu, Nonhlanhla; Peters, Ferande; Dessein, Patrick H.; Sareli, Pinhas; Woodiwiss, Angela J.
• Is Part Of: Journal of hypertension. Volume 39:Issue 12(2021)
• Page Start: 2446
• Page End: 2454
• Publication Date: 2021-12-12
• Subjects: Africa -- aortic flow -- renal function -- stroke volume -- systemic vascular resistance; Hypertension -- Periodicals; Hypertension -- Periodicals; 616.132005
• DOI: 10.1097/HJH.0000000000002968
• Languages: English
• ISSNs: 1473-5598

Abstract

Abstract : Supplemental Digital Content is available in the text Abstract : Aims: Whether renal mechanisms of hypertension primarily translate into increases in systemic vascular resistance (SVR) in all populations is uncertain. We determined whether renal mechanisms associate with either increases in SVR (and impedance to flow) or systemic flow in a community of African ancestry. Method: In a South African community sampled across the full adult age range ( n = 546), we assessed stroke volume (SV), peak aortic flow (Q), SVR, characteristic impedance (Zc) and total arterial compliance (TAC) from velocity and diameter measurements in the outflow tract (echocardiography) and central arterial pressures. Renal changes were determined from creatinine clearance (glomerular filtration rate, GFR) and fractional Na + excretion (FeNa + ) (derived from 24-h urine collections). Results: Independent of confounders (including MAP and pressures generated by the product of Q and Zc), SV (and hence cardiac output) ( P < 0.0001) and Q ( P < 0.01), but not SVR, Zc or TAC ( P = 0.09–0.20) were independently associated with decreases in both GFR (index of nephron number) and FeNa + . Through an interactive effect ( P < 0.0001), the impact of GFR on SV or Q was strongly determined by FeNa + and vice versa . The relationship between the GFR-FeNa + interaction and either SV or Q was noted in those above or below 50 years of age, although neither GFR, FeNa + nor the interaction were independently associated with SVR, Zc or TAC at any age. Conclusion: Across the full adult lifespan, in groups of African ancestry, renal mechanisms of hypertension translate into increases in systemic flow rather than into resistance or impedance to flow.