Background and objectives Sympathetic overactivity and high levels of the endogenous inhibitor of NO synthase asymmetric dimethylarginine (ADMA) are prevalent risk factors in chronic kidney disease (CKD). Design, setting, participants, & measurements In 48 stage 2 to 4 CKD patients, we investigated the relationship between efferent postganglionic muscle sympathetic nerve traffic (microneurography) and circulating ADMA and analyzed the links between these risk factors and estimated GFR (eGFR), proteinuria, and different parameters of left ventricular (LV) geometry. Results CKD patients characterized by sympathetic nerve traffic values in the third tertile showed the highest ADMA levels, and this association was paralleled by a continuous, positive relationship between these two risk factors (r=0.32, P=0.03) independent of other confounders. Both sympathetic nerve traffic and ADMA were inversely related to eGFR and directly to proteinuria and LV geometry. Remarkably, the variance of eGFR, proteinuria, and LV geometry explained by sympathetic nerve traffic and ADMA largelyoverlapped because sympathetic nerve traffic but not ADMA was retained as a significant correlate of the eGFR (P<0.001) and of the relative wall thickness or the left ventricular mass index/LV volume ratio (P=0.05) in models including both risk factors. ADMA, but not sympathetic nerve traffic, emerged as anindependent correlate of proteinuria (P=0.003) in a model including the same covariates.Conclusions Sympathetic activity and ADMA may share a pathway leading to renal disease progression, proteinuria, and LV concentric remodeling in CKD patients. © 2011 by the American Society of Nephrology.

Grassi, G., Seravalle, G., Ghiadoni, L., Tripepi, G., Bruno, R., Mancia, G., et al. (2011). Sympathetic nerve traffic and asymmetric dimethylarginine in chronic kidney disease. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 6(11), 2620-2627 [10.2215/CJN.06970711].

Sympathetic nerve traffic and asymmetric dimethylarginine in chronic kidney disease

GRASSI, GUIDO;MANCIA, GIUSEPPE;
2011

Abstract

Background and objectives Sympathetic overactivity and high levels of the endogenous inhibitor of NO synthase asymmetric dimethylarginine (ADMA) are prevalent risk factors in chronic kidney disease (CKD). Design, setting, participants, & measurements In 48 stage 2 to 4 CKD patients, we investigated the relationship between efferent postganglionic muscle sympathetic nerve traffic (microneurography) and circulating ADMA and analyzed the links between these risk factors and estimated GFR (eGFR), proteinuria, and different parameters of left ventricular (LV) geometry. Results CKD patients characterized by sympathetic nerve traffic values in the third tertile showed the highest ADMA levels, and this association was paralleled by a continuous, positive relationship between these two risk factors (r=0.32, P=0.03) independent of other confounders. Both sympathetic nerve traffic and ADMA were inversely related to eGFR and directly to proteinuria and LV geometry. Remarkably, the variance of eGFR, proteinuria, and LV geometry explained by sympathetic nerve traffic and ADMA largelyoverlapped because sympathetic nerve traffic but not ADMA was retained as a significant correlate of the eGFR (P<0.001) and of the relative wall thickness or the left ventricular mass index/LV volume ratio (P=0.05) in models including both risk factors. ADMA, but not sympathetic nerve traffic, emerged as anindependent correlate of proteinuria (P=0.003) in a model including the same covariates.Conclusions Sympathetic activity and ADMA may share a pathway leading to renal disease progression, proteinuria, and LV concentric remodeling in CKD patients. © 2011 by the American Society of Nephrology.
Articolo in rivista - Articolo scientifico
sympathetic nervous traffic
English
2011
6
11
2620
2627
none
Grassi, G., Seravalle, G., Ghiadoni, L., Tripepi, G., Bruno, R., Mancia, G., et al. (2011). Sympathetic nerve traffic and asymmetric dimethylarginine in chronic kidney disease. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 6(11), 2620-2627 [10.2215/CJN.06970711].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/27097
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