Mam. Mateijsen et al., Vascular and interstitial changes in the peritoneum of CAPD patients with peritoneal sclerosis, PERIT DIA I, 19(6), 1999, pp. 517-525
Objective:To analyze morphological changes in the peritoneum of peritoneal
sclerosis (PS) patients. Emphasis was put on vascular abnormalities, becaus
e the continuous exposure to glucose-based dialysis solutions could cause d
iabetiform changes and because longitudinal transport studies suggested the
development of a large peritoneal vascular surface area.
Design: Peritoneal biopsies from continuous ambulatory peritoneal dialysis
(CAPD) patients were investigated in two studies. Diabetic patients were ex
cluded. In study 1, 11 PS biopsies were compared to three control groups va
rying in duration of CAPD treatment: 0 months (n = 15), 2 - 25 months (n =
7), and > 25 months CAPD (n = 7). The second study was a case-control study
, comparing six biopsies from the long-term control group to six PS biopsie
s, matched for age and duration of CAPD. All biopsies were scored for prese
nce and type of fibrosis [Picro Sirius red, type IV collagen, alpha-smooth
muscle actin (alpha SMA)] and for neoangiogenesis (factor VIII). Thickening
of vascular walls by type IV collagen and vasodilation of capillaries were
measured by computer-aided planimetry.
Results: In study 1 the presence of sclerosing fibrosis, deposition of inte
rstitial type IV collagen, and the number of myofibroblasts (alpha SMA-posi
tive cells) was greater in the PS biopsies than biopsies from all control g
roups (p < 0.002). Moreover, the number of vessels per field was higher in
PS biopsies (p < 0.01). Vascular wall thickening of small arteries (p < 0.0
08) and vasodilation of capillaries were found in PS biopsies compared to a
ll control groups (p (0.007). The second study revealed differences in the
presence of sclerosis but not in the extent of fibrosis between PS biopsies
and their controls. The number of vessels per field in PS biopsies was hig
her compared to controls (p = 0.04). Also, thickening of the vascular wall
was more marked in PS biopsies (p = 0.03). Vasodilation of capillaries was
greater in PS biopsies than in controls (p = 0.07).
Conclusion: Fibrosis of the peritoneum may precede peritoneal sclerosis. Th
e deposition of type IV collagen and the presence of myofibroblasts in the
interstitial layer could be part of a pathologic process similar to the sca
rring in diabetic nephropathy. Neoangiogenesis and thickening of the vascul
ar wall by type IV collagen are consistent with glucose-induced microangiop
athy. These abnormalities and the vasodilation of the capillaries can expla
in the high dialysate-to-plasma ratios or mass transfer area coefficients o
f low molecular weight solutes that can be found in long-term CAPD patients
.