TY - JOUR
T1 - Advanced glycation end products are associated with immature angiogenesis and peritoneal dysfunction in patients on peritoneal dialysis
AU - Nakano, Toshiaki
AU - Mizumasa, Tohru
AU - Kuroki, Yusuke
AU - Eriguchi, Masahiro
AU - Yoshida, Hisako
AU - Taniguchi, Masatomo
AU - Masutani, Kosuke
AU - Tsuruya, Kazuhiko
AU - Kitazono, Takanari
N1 - Funding Information:
We thank Hideko Noguchi, Hiroshi Fujii, and Mikio Munakata for their excellent technical assistance. We also thank Ellen Knapp, PhD, from Edanz Group (www.edanzediting.com/ac) for editing a draft of this manuscript. The author(s) disclosed receipt of the following financial support with respect to the research, authorship, and/or publication of this article: This work was supported by the 19th Baxter PD fund Award and partly by a JSPS KAKENHI Grant-in-Aid for Scientific Research C [No. 23590400].
Funding Information:
We thank Hideko Noguchi, Hiroshi Fujii, and Mikio Munakata for their excellent technical assistance. We also thank Ellen Knapp, PhD, from Edanz Group (www.edanzediting.com/ac ) for editing a draft of this manuscript. Declaration of conflicting interests The author(s) declared no conflict of interest with respect to the research, authorship, and/or publication of this article. Funding The author(s) disclosed receipt of the following financial support with respect to the research, authorship, and/or publication of this article: This work was supported by the 19th Baxter PD fund Award and partly by a JSPS KAKENHI Grant-in-Aid for Scientific Research C [No. 23590400].
Publisher Copyright:
© The Author(s) 2020.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Background: Deposition of advanced glycation end products (AGEs) is frequently found in the peritoneum of patients on peritoneal dialysis (PD). Angiogenesis is also observed in the peritoneum. However, the clinical significance of AGEs and angiogenesis in the peritoneum is not fully understood. We evaluated the maturation of capillary vessels and investigated whether AGEs are associated with angiogenesis and peritoneal function in the peritoneal membrane. Methods: Peritoneum obtained when PD catheters were removed from 61 patients with PD was analyzed. The peritoneum was immunohistochemically stained with anti-CD34 (for endothelial cells), anti-alpha smooth muscle actin (αSMA) (for pericytes), and anti-AGE antibodies. We defined CD34-positive and αSMA-negative vessels as immature capillary vessels in peritoneal membranes using serial sections. We evaluated the associations between vessel density, peritoneal function (dialysate-to-plasma ratio for creatinine (D/P creatinine)), and the degree of AGE deposition. Results: AGE accumulation in the interstitium was positively associated with the duration of PD (p < 0.01). AGE accumulation in the interstitium and vascular wall was positively correlated with the use of acidic solution (p < 0.05) and the maximum value of D/P creatinine (p < 0.05). AGE accumulation in the vascular wall was significantly associated with immature capillary density (CD34+/αSMA−) in the peritoneum (p < 0.01). Vessel density was not significantly correlated with the last measurement of D/P creatinine (p = 0.126, r = 0.202), However, immature capillary density was positively correlated with the last measurement of D/P creatinine (p < 0.05, r = 0.278). Conclusions: AGE accumulation is significantly associated with immature angiogenesis and peritoneal dysfunction in patients undergoing PD.
AB - Background: Deposition of advanced glycation end products (AGEs) is frequently found in the peritoneum of patients on peritoneal dialysis (PD). Angiogenesis is also observed in the peritoneum. However, the clinical significance of AGEs and angiogenesis in the peritoneum is not fully understood. We evaluated the maturation of capillary vessels and investigated whether AGEs are associated with angiogenesis and peritoneal function in the peritoneal membrane. Methods: Peritoneum obtained when PD catheters were removed from 61 patients with PD was analyzed. The peritoneum was immunohistochemically stained with anti-CD34 (for endothelial cells), anti-alpha smooth muscle actin (αSMA) (for pericytes), and anti-AGE antibodies. We defined CD34-positive and αSMA-negative vessels as immature capillary vessels in peritoneal membranes using serial sections. We evaluated the associations between vessel density, peritoneal function (dialysate-to-plasma ratio for creatinine (D/P creatinine)), and the degree of AGE deposition. Results: AGE accumulation in the interstitium was positively associated with the duration of PD (p < 0.01). AGE accumulation in the interstitium and vascular wall was positively correlated with the use of acidic solution (p < 0.05) and the maximum value of D/P creatinine (p < 0.05). AGE accumulation in the vascular wall was significantly associated with immature capillary density (CD34+/αSMA−) in the peritoneum (p < 0.01). Vessel density was not significantly correlated with the last measurement of D/P creatinine (p = 0.126, r = 0.202), However, immature capillary density was positively correlated with the last measurement of D/P creatinine (p < 0.05, r = 0.278). Conclusions: AGE accumulation is significantly associated with immature angiogenesis and peritoneal dysfunction in patients undergoing PD.
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U2 - 10.1177/0896860819878344
DO - 10.1177/0896860819878344
M3 - Article
C2 - 32063152
AN - SCOPUS:85077567211
SN - 0896-8608
VL - 40
SP - 67
EP - 75
JO - Peritoneal Dialysis International
JF - Peritoneal Dialysis International
IS - 1
ER -