Md. Anvar et al., The concentration of protein-compounds in interstitial tissue of patients with chronic critical limb ischaemia and oedema, VASA, 30(1), 2001, pp. 14-20
Background: Many of chronic critical limb ischaemia (CLI) patients have dis
tal leg and foot oedema. Previous electronmicroscopic studies have shown th
at chronic severe ischaemia ma), cause hypoxic damage of the capillary endo
thelium, including morphological changes i.e. multiplicated/thickened basal
lamina, and formation of interendothelial gaps. To assess the functional c
onsequences of these morphologic derangements, where proteins can leak thro
ugh, we investigated the composition of the interstitial fluid in oedematou
s ischaemic limbs.
Patients and methods: Nine female and 3 male patients with a mean age of 79
+/- 7.9 years were included. All had unilateral CLI and peripheral pitting
oedema. Leg and foot volume was measured with wafer displacement volumetry
. Blister suction technique was used to collect subcutaneous interstitial f
luid. The concentration of albumin, transferin, immmoglobulin G and alpha (
2)-macroglobulin in plasma and blister fluid was measured by immunoturbidim
etry. Nine patients, 8 women and 1 man with a mean age of 83 +/- 5.5 years
with a proximal femur fracture sewed as an age-matched control group.
Results: The mean concentration of albumin in blister fluid was significant
ly lower in the patients, whereas the mean concentration of alpha (2)-macro
globulin in blister fluid did not differ between patients and controls. Mea
n ratio between concentrations in blister and serum of albumin, transferin
and immunoglobulin G in the limbs with CLI and oedema were significantly lo
wer than respective values in the control group. However there was no signi
ficant difference in the ratio of alpha (2)-macroglobulin between these gro
ups.
Conclusion: A higher transcapillary concentration gradient for proteins in
CLI limbs signifies an increase in the net osmotic pressure gradient across
the capillary wall, which may be a potential oedema limiting factor