CELL-POPULATIONS PRESENT IN THE NOCTURNAL PERITONEAL EFFLUENT OF PATIENTS ON CONTINUOUS AMBULATORY PERITONEAL-DIALYSIS AND THEIR RELATIONSHIP WITH PERITONEAL FUNCTION AND INCIDENCE OF PERITONITIS
Mf. Decastro et al., CELL-POPULATIONS PRESENT IN THE NOCTURNAL PERITONEAL EFFLUENT OF PATIENTS ON CONTINUOUS AMBULATORY PERITONEAL-DIALYSIS AND THEIR RELATIONSHIP WITH PERITONEAL FUNCTION AND INCIDENCE OF PERITONITIS, Peritoneal dialysis international, 14(3), 1994, pp. 265-270
Objective: To study the relationship between peritoneal effluent cells
and infection rate and to relate this population with functional char
acteristics. Design: Prospective, longitudinal, and comparative study.
Setting: Outpatient continuous ambulatory peritoneal dialysis (CAPD)
unit of a university medical center. Participants:Seventy-one uninfect
ed patients, treated for 0 - 156 months on CAPD, in stable condition w
ere studied (33 female, 38 male). Interventions: Nocturnal peritoneal
effluent (NPE) was drained with EDTA (2.5 mmol/L) at 37-degrees-C and
centrifuged at 2500 rpm for 9 minutes. Measurements: Accumulated perit
oneal inflammation days/year and ultrafiltration/diffusion (mass trans
fer coefficients (MTCs) for small molecules) capacities were recorded.
Cellular count (cells/night) was performed using a Neubauer chamber.
Macrophage function was assessed by cytochemical (lysosomal enzyme con
tent: ANAE, beta-glucuronidase, acid phosphatase) and immunohistochemi
cal procedures (expression of membrane antigens, CD4, 11b, 11c, 14, 16
, 25, 35, and 71). Results: The macrophage is the most frequently appe
aring cell in the NPE. Cell count decreases over time on CAPD (from 20
x 10(6) to 5 x 10(6) after the first year). Intrapatient variability
was low, but interpatient differences were marked. Mesothelial cell co
unt remained stable over time (0.25 - 0.5 X 10(6)). Four of our patien
ts showed a ''transforming'' change in these cells. Previous incidence
of peritonitis and values of functional measurements did not correlat
e with cell count or expressions of macrophage function (lysosome enzy
me content and percentage of cells expressing different membrane antig
ens). Conclusion: There is difficulty interpreting the results on peri
toneal effluent cells and their relationship with the incidence of per
itonitis and functional characteristics of the peritoneum. No definite
conclusions can be drawn other than the great interpatient and intrap
atient variability. The presence of abnormal peritoneal cells with und
etermined origin and function suggests the need for periodic studies o
f peritoneal effluent cells on long-term CAPD patients.