Key result
Macroalbuminuria linked to ~43% lower microvascular endothelial response in older hypertensive men.
Cross-Sectional (n=66)
Single-blind
No
Effect estimate: β= -0.37 (95% CI -0.55 to -0.08)
p-value: p=0.01
Microvascular endothelial dysfunction is strongly associated with greater albuminuria and CKD in older hypertensive adults, independent of diabetes and blood pressure, suggesting a systemic microvascular mechanism for their excess cardiovascular risk.
Should not yet change practice in older hypertensive men; leaves open whether macroalbuminuria signals broader microvascular risk needing longitudinal confirmation.
BACKGROUND: Impairment in glomerular endothelial function likely plays a major role in the development of albuminuria and CKD progression. Glomerular endothelial dysfunction may reflect systemic microvascular dysfunction, accounting in part for the greater cardiovascular risk in patients with albuminuria. Prior studies of vascular function in CKD have focused on conduit artery function or those with ESRD, and have not examined microvascular endothelial function with albuminuria. METHODS: We conducted a cross-sectional study among older hypertensive male veterans with stage 1-4 CKD, and hypertensive controls without CKD. Microvascular function was quantified by two distinct Laser-Doppler flowmetry (LDF) measures: peak responses to 1) post-occlusive reactive hyperemia (PORH) and 2) thermal hyperemia (TH), measured on forearm skin. Associations of each LDF measure with albuminuria, eGFR, and CKD status were estimated using correlation coefficients and multiple linear regression, accounting for potential confounders. RESULTS: Among 66 participants (mean age 69.2 years), 36 had CKD (mean eGFR 46.1 cc/min/1.73 m(2); 30.6 % with overt albuminuria). LDF responses to PORH and TH were 43 and 39 % significantly lower in multivariate analyses among those with macroalbuminuria compared to normoalbuminuria, (β= - 0.42, p = 0.009 and β= -0.37, p = 0.01, respectively). Those with CKD had a 23.9 % lower response to PORH compared to controls (p = 0.02 after adjustment). In contrast, TH responses did not differ between those with and without CKD. CONCLUSIONS: Microvascular endothelial function was strongly associated with greater albuminuria and CKD, independent of diabetes and blood pressure. These findings may explain in part the excess systemic cardiovascular risk associated with albuminuria and CKD.
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Seliger et al. (2016) conducted a cross-sectional in Chronic kidney disease and hypertension (n=66). Macroalbuminuria vs. Normoalbuminuria was evaluated on Microvascular endothelial function measured by post-occlusive reactive hyperemia (PORH) LDF response (β= -0.37, 95% CI -0.55 to -0.08, p=0.01). Macroalbuminuria was associated with a 43% lower microvascular endothelial response to post-occlusive reactive hyperemia compared to normoalbuminuria among older hypertensive men.
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