Skip to main content
. 2010 Oct 5;11:26. doi: 10.1186/1471-2369-11-26

Table 3.

Plasma concentration of vasopressin (p-AVP) and plasma osmolaririty (p-osm) during urine diluting test.

Baseline Post
0-60
Post
60-120
Post
120-180
Post
180-240
Post
240-300
P
(GLM-within)
AVP (pmol/l)
Group 1
1.00(0.40)
0.7(0.10) *
0.60(0.25)*
0.70(0.35)*
0.90(0.65)
1.00(0.45)
0.000
Group 2
0.75(0.45)
0.60(0.08)*
0.60(0.18)*
0.60(0.10)*
0.70(0.60)
0.80(0.45)
Group 3
0.70(0.53)
0.60(0.08)*
0.60(0.15)*
0.60(0.15)*
0.65(0.63)
0.80(0.60)
Group 4
1.80(1.85)
1.10(0.83)*
1.10(0.88)*
1.30(0.93)*
1.50(0.85)*
1.65(1.25)*
P (GLM-between)
0.000
P (Kruskal-Wallis)
0.000
0.000
0.000
0.000
0.001
0.002

P-osm (mosmol/l)
Group 1
290(6)
283(3) *
284(6)*
287(5)*
286(5)*
287(4)
0.000
Group 2
288(7)
283(8)*
284(8)*
286(9)*
286(9)*
288(8)
Group 3
291(11)
285(7)*
287(9)*
289(6)*
288(4)*
289(6)*
Group 4
305(14)
299(15)*
298(14)*
297(14)*
297(14)*
299(13)*
P (GLM-between)
0.000
P (Kruskal-Wallis) 0.000 0.000 0.000 0.000 0.000 0.000

Blood samples were drawn after a baseline period of 120 minutes, and after the end of five consecutive periods each of one hour duration (Post 0-60, Post 60-120, Post 120-180, Post 180-240, and Post 240-300. An oral water load of 20 ml/kg body weight was given during the first 15 minutes of the Post 0-60 period. Group 1 comprised healthy control subjects (n = 10). Groups 2-4 comprised patients with chronic kidney disease or hyperension (Group 2 (n = 14), e-GFR ≥ 90 ml/min; Group 3 (n = 11), 60 ml/min ≤ e-GFR < 90 ml/min; and Group 4 (n = 16), 15 ml/min < e-GFR ≤ 60 ml/min).

Median with Interquartile Range in brackets. A General Linear Model (GLM) for Repeated Measures was used for comparison within and between groups. Kruskal-Wallis's test was used to analyze differences between groups during the diluting test. Wilcoxon's signed rank test was used in each group to analyze significant deviations from baseline (* = P < 0.05).