S. Galatius et al., Plasma clearance of polyfructosan and extracellular body fluid distribution in idiopathic dilated cardiomyopathy and after heart transplantation, AM J CARD, 85(7), 2000, pp. 843-848
Citations number
30
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
The total extracellular fluid volume and distribution in plasma and interst
itial spaces, and the microvascular permeability properties were studied in
16 nonedematous patients with congestive heart failure (CHF) due to idiopa
thic dilated cardiomyopathy and 17 such patients who underwent heart transp
lantation (HT) by analyzing the 3-hour plasma disappearance curve of polyfr
uctosan. Eighteen healthy subjects served as controls. Polyfructosan (3.5 k
D) is an extracellular marker and inulin analog transported almost solely b
y diffusion. The initial capillary membrane plasma clearance (i.e., the per
meability-surface area product), the interstitial plasma clearance determin
ed at 10 minutes (clearance[10]), and the extracellular volume were determi
ned from the poly fructosan curves. I-131-albumin was used as a plasma volu
me reference. Permeability-surface area product was elevated in both patien
t groups (6.6 +/- 1.9 ml/kg/min in the CHF group and 6.7 +/- 2.0 ml/kg/min
in the HT group vs 5.1 +/- 1.3 ml/kg/min in controls, p <0.01 for both), wh
ereas clearance(10) was normalized in the HT group (4.5 +/- 0.9 ml/kg/min i
n the HT group, 4.4 +/- 0.7 ml/kg/min in controls vs 5.0 +/- 0.9 ml/kg/min
in the CHF group, p <0.1 and p <0.05, respectively), The normalization of i
nterstitial plasma clearance of polyfructosan was associated with time sinc
e HT (r = 0.49, p <0.05). Plasma volumes were similar in all 3 groups (41 /- 8 ml/kg in controls, 44 +/- 13 in the CHF group and 39 +/- 8 in the HT g
roup). In contrast, total extracellular volume was elevated in both patient
s groups (177 +/- 27 ml/kg in the CHF group and 173 +/- 27 in the HT group
vs 152 +/- 12 in controls, p <0.01), The results strongly suggest a microva
scular permeability defect in both patient groups that perhaps plays a role
in the extravascular distribution of the excess extracellular fluid volume
. (C)2000 by Excerpta Medico, Inc.