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Part 4: Inflammation and Fibrosis |
1 Division of Nephrology,2 Department of Medicine, and Kidney, Urinary Bladder and Metabolic Syndrome Research Unit, Faculty of Medicine, Chulalongkorn University, Bangkok; 3 Division of Internal Medicine, Trat Hospital, Trat;4 Banphaeo Hospital, Samutsakorn;5 and Renal Unit, Internal Medicine Department, Sappasitthiprasong Hospital, Ubon Ratchathani, Thailand;6 and Department of International Health, Johns Hopkins Bloomberg School of Public Health,7 and Renal Asia, Regional Medical Affairs, Seoul, Korea.
Correspondence to: Talerngsak Kanjanabuch, Division of Nephrology, Department
of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok 10330
Thailand.
golfnephro{at}hotmail.com
Background: Continuous exposure of the peritoneal membrane
to dialysis solutions during long-term dialysis results in mesothelial cell
loss, peritoneal membrane damage, and thereby, ultrafiltration (UF) failure, a
major determinant of mortality in patients on continuous ambulatory peritoneal
dialysis (CAPD). Unfortunately, none of tests available today can predict
long-term UF decline. Here, we propose a new tool to predict such a
change.
Patients and Methods: Mesothelial cells from 8-hour
overnight effluents (1.36% glucose dialysis solution) were harvested,
co-stained with cytokeratin (a mesothelial marker) and TUNEL (an apoptotic
marker), and were counted using flow cytometry in 48 patients recently started
on CAPD. Adequacy of dialysis, UF, nutrition status, dialysate cancer antigen
125 (CA125), and a peritoneal equilibration test (3.86% glucose peritoneal
dialysis solution) were simultaneously assessed and were re-evaluated 1 year
later.
Results: The numbers of total and apoptotic mesothelial
cells were 0.19 ± 0.19 million and 0.08 ± 0.12 million cells per
bag, respectively. Both numbers correlated well with the levels of end
dialysate-to-initial dialysate (D/D0) glucose, dialysate-to-plasma
(D/P) creatinine, and sodium dipping. Notably, the counts of cells of both
types in patients with diabetes or with high or high-average transport were
significantly greater than the equivalent counts in nondiabetic patients or
those with low or low-average transport. A cut-off of 0.06 million total
mesothelial cells per bag had sensitivity of 1 and a specificity of 0.75 in
predicting a further decline in D/D0 glucose and a sensitivity of
0.86 and a specificity of 0.63 to predict a further decline in UF over a
1-year period. In contrast, dialysate CA125 and other measured parameters had
low predictive values.
Conclusions: The greater the loss of exfoliated cells, the
worse the expected decline in UF. The ability of a count of mesothelial cells
to predict a future decline in UF warrants further investigation in clinical
practice.
KEY WORDS: Cancer antigen 125; CA125; continuous ambulatory peritoneal dialysis; CAPD; exfoliated mesothelial cells; mesothelial cell mass; ultrafiltration failure.
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