Disordered aldosterone-volume relationship in end-stage kidney disease

被引:24
作者
Bomback, Andrew S. [1 ]
Kshirsagar, Abhijit V. [2 ]
Ferris, Maria E. [2 ]
Klemmer, Philip J. [2 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Med, Div Nephrol, New York, NY 10032 USA
[2] Univ N Carolina, Dept Med, Div Nephrol & Hypertens, UNC Kidney Ctr, Chapel Hill, NC USA
关键词
aldosterone; chronic kidney disease; extracellular volume; haemodialysis; mineralocorticoid receptor blockers; HEMODIALYSIS-PATIENTS; PLASMA-ALDOSTERONE; DIALYSIS PATIENTS; BIOIMPEDANCE SPECTROSCOPY; BLOOD-PRESSURE; RENAL-DISEASE; ORGAN DAMAGE; ANEPHRIC MAN; NA+ STORAGE; DRY-WEIGHT;
D O I
10.1177/1470320309352353
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Introduction. Sodium loading, and subsequent volume expansion, suppresses aldosterone levels in individuals with normal renal function. We hypothesised that loss of renal function impairs this volume-aldosterone relationship. Materials and methods. With multifrequency bioimpedance spectroscopy, we measured total body water (TBW), extracellular volume (ECV), and intracellular volume in five haemodialysis patients at varied states of hydration and in five healthy volunteers during low-, normal-, and high-salt diets. Serum aldosterone, potassium, and C-reactive protein were measured simultaneously. Scatterplots and general estimating equations were used to examine the relationship among these variables. Results. In healthy volunteers with salt loading, and in haemodialysis subjects with increased inter-dialytic weight gain, expansion of ECV led to reciprocal declines in serum aldosterone concentrations. The relationship was more profound in healthy volunteers (p < 0.001) than in haemodialysis subjects (p=0.1). Notably, haemodialysis subjects posted consistently higher levels of ECV (median 49.6% TBW, IQR 43.9-51.8% compared to 41.1%, 39.9-42.8% in volunteers) and serum aldosterone (median 26.7 ng/dl, IQR 19.8-29.6 compared to 12.4 ng/dl, 8.8-16.0 in volunteers). Serum potassium did not appear to influence aldosterone concentration (p=0.9). Conclusions. The shift of the volume-aldosterone curve in haemodialysis subjects suggests that end-stage kidney disease is a state of high volume and inappropriately high aldosterone. These data have important clinical implications, as dialysis patients may benefit from both volume reduction and mineralocorticoid receptor blockade.
引用
收藏
页码:230 / 236
页数:7
相关论文
共 44 条
[1]   Dry-Weight Reduction in Hypertensive Hemodialysis Patients (DRIP) A Randomized, Controlled Trial [J].
Agarwal, Rajiv ;
Alborzi, Pooneh ;
Satyan, Sangeetha ;
Light, Robert P. .
HYPERTENSION, 2009, 53 (03) :500-U23
[2]  
[Anonymous], 2006, USRDS 2006 ANN DAT R
[3]   Aldosterone and end-organ damage [J].
Brown, NJ .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2005, 14 (03) :235-241
[4]   ESSENTIAL HYPERTENSION - RENIN AND ALDOSTERONE, HEART ATTACK AND STROKE [J].
BRUNNER, HR ;
BUHLER, FR ;
BARD, RH ;
BAER, L ;
GOODWIN, FT ;
NEWTON, MA ;
KRAKOFF, LR ;
LARAGH, JH .
NEW ENGLAND JOURNAL OF MEDICINE, 1972, 286 (09) :441-+
[5]   SURVIVAL AS AN INDEX OF ADEQUACY OF DIALYSIS [J].
CHARRA, B ;
CALEMARD, E ;
RUFFET, M ;
CHAZOT, C ;
TERRAT, JC ;
VANEL, T ;
LAURENT, G .
KIDNEY INTERNATIONAL, 1992, 41 (05) :1286-1291
[6]  
Charra B., 2003, NEPHRON PHYSIOL, V93, P94
[7]   Dispersion and absorption in dielectrics I. Alternating current characteristics [J].
Cole, KS ;
Cole, RH .
JOURNAL OF CHEMICAL PHYSICS, 1941, 9 (04) :341-351
[8]   MODULATION OF PLASMA ALDOSTERONE CONCENTRATION BY PLASMA POTASSIUM IN ANEPHRIC MAN IN ABSENCE OF A CHANGE IN POTASSIUM BALANCE [J].
COOKE, CR ;
HORVATH, JS ;
MOORE, MA ;
BLEDSOE, T ;
WALKER, WG .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (12) :3028-3032
[9]   REGULATION OF PLASMA ALDOSTERONE CONCENTRATION IN ANEPHRIC MAN AND RENAL-TRANSPLANT RECIPIENTS [J].
COOKE, CR ;
RUIZMAZA, F ;
KOWARSKI, A ;
MIGEON, CJ ;
WALKER, WG .
KIDNEY INTERNATIONAL, 1973, 3 (03) :160-166
[10]   Is it time for spironolactone therapy in dialysis patients? [J].
Covic, A ;
Gusbeth-Tatomir, P ;
Goldsmith, DJA .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2006, 21 (04) :854-858