TY - JOUR
T1 - Citrulline as a marker for chemotherapy induced mucosal barrier injury in pediatric patients
AU - Van Vliet, Michel J.
AU - Tissing, Wim J.E.
AU - Rings, Edmond H.H.M.
AU - Koetse, Harma A.
AU - Stellaard, Frans
AU - Kamps, Willem A.
AU - De Bont, Eveline S.J.M.
PY - 2009/12/15
Y1 - 2009/12/15
N2 - Background. The currently used National Cancer Institute (NCI) adverse events criteria for mucosal barrier injury (MBI) are insufficient for use in children. We searched for objective, easily measurable indicators for MBI in children with cancer. Purpose. In children with acute myeloid leukemia, various MBI-related clinical and laboratory tests were investigated, reflecting clinical severity (NCI symptomatic adverse events criteria (gold standard), daily gut score (DGS)), inflammation (plasma and fecal interleukin-8 (IL-8), fecal calprotectin), enterocytic loss (plasma citrulline, ratio fecal human DNA/total DNA) and intestinal permeability (sugar absorption tests). Results. Intestinal MBI as detected by the NCI adverse events criteria was found in 55% of chemotherapy cycles, correlating well with the continuous DGS (n = 55, rho = 0.581; P<0.001). Intestinal cell loss as measured by the ratio fecal human DNA/total DNA and plasma citrulline correlated well with both NCI criteria (n = 61, rho = 0.357, P = 0.005 resp. n = 58, rho = -0.482; P<0.001) and DGS (n<54, rho = 0.352, P = 0.009 resp. n = 55, rho = -0.625; P<0.001). Plasma IL-8 correlated strongly to plasma citrulline (n = 46, rho = -0.627; P<0.001). Conclusions. MBI was reflected by parameters indicating inflammation (IL-8) and cell loss (plasma citrulline, ratio fecal human DNA/total DNA). We conclude that plasma citrulline might be a good parameter for MBI. Further studies are needed to show whether plasma citrulline can be used as a marker for MBI in future research.
AB - Background. The currently used National Cancer Institute (NCI) adverse events criteria for mucosal barrier injury (MBI) are insufficient for use in children. We searched for objective, easily measurable indicators for MBI in children with cancer. Purpose. In children with acute myeloid leukemia, various MBI-related clinical and laboratory tests were investigated, reflecting clinical severity (NCI symptomatic adverse events criteria (gold standard), daily gut score (DGS)), inflammation (plasma and fecal interleukin-8 (IL-8), fecal calprotectin), enterocytic loss (plasma citrulline, ratio fecal human DNA/total DNA) and intestinal permeability (sugar absorption tests). Results. Intestinal MBI as detected by the NCI adverse events criteria was found in 55% of chemotherapy cycles, correlating well with the continuous DGS (n = 55, rho = 0.581; P<0.001). Intestinal cell loss as measured by the ratio fecal human DNA/total DNA and plasma citrulline correlated well with both NCI criteria (n = 61, rho = 0.357, P = 0.005 resp. n = 58, rho = -0.482; P<0.001) and DGS (n<54, rho = 0.352, P = 0.009 resp. n = 55, rho = -0.625; P<0.001). Plasma IL-8 correlated strongly to plasma citrulline (n = 46, rho = -0.627; P<0.001). Conclusions. MBI was reflected by parameters indicating inflammation (IL-8) and cell loss (plasma citrulline, ratio fecal human DNA/total DNA). We conclude that plasma citrulline might be a good parameter for MBI. Further studies are needed to show whether plasma citrulline can be used as a marker for MBI in future research.
KW - Cancer
KW - Chemotherapy
KW - Childhood
KW - Laboratory tests
KW - Mucositis
UR - http://www.scopus.com/inward/record.url?scp=70449698426&partnerID=8YFLogxK
U2 - 10.1002/pbc.22210
DO - 10.1002/pbc.22210
M3 - Article
C2 - 19688831
AN - SCOPUS:70449698426
SN - 1545-5009
VL - 53
SP - 1188
EP - 1194
JO - Pediatric Blood and Cancer
JF - Pediatric Blood and Cancer
IS - 7
ER -