Serum levels of advanced glycation end products and their receptors sRAGE and Galectin-3 in chronic pancreatitis

/Objectives: AGE and their receptors like RAGE and Galectin-3 can activate inflammatory pathways and have been associated with chronic inflammatory diseases. Several studies investigated the role of AGE, Galectin-3 and sRAGE in pancreatic diseases, whereas no comprehensive data for chronic pancreati...

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Veröffentlicht in:Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2020-03, Vol.20 (2), p.187-192
Hauptverfasser: Böhme, Richard, Becker, Carla, Keil, Bettina, Damm, Marko, Rasch, Sebastian, Beer, Sebastian, Schneider, Rick, Kovacs, Peter, Bugert, Peter, Riedel, Jan, Griesmann, Heidi, Ruffert, Claudia, Kaune, Tom, Michl, Patrick, Hesselbarth, Nico, Rosendahl, Jonas
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Sprache:eng
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Zusammenfassung:/Objectives: AGE and their receptors like RAGE and Galectin-3 can activate inflammatory pathways and have been associated with chronic inflammatory diseases. Several studies investigated the role of AGE, Galectin-3 and sRAGE in pancreatic diseases, whereas no comprehensive data for chronic pancreatitis (CP) are available. Serum samples from CP patients without an active inflammatory process (85 ACP; 26 NACP patients) and 40 healthy controls were collected. Levels of AGE, sRAGE and Galectin-3 were measured by ELISA. To exclude potential influences of previously described RAGE SNPs on detected serum levels, we analyzed variants rs207128, rs207060, rs1800625, and rs1800624 by melting curve technique in 378 CP patients and 338 controls. AGE and Galectin-3 serum levels were significantly elevated in both ACP and NACP patients compared to controls (AGE: 56.61 ± 3.043 vs. 31.71 ± 2.308 ng/mL; p 
ISSN:1424-3903
1424-3911
DOI:10.1016/j.pan.2019.12.013