PMID- 19247846 OWN - NLM STAT- MEDLINE DCOM- 20091008 LR - 20090519 IS - 1502-7708 (Electronic) IS - 0036-5521 (Linking) VI - 44 IP - 6 DP - 2009 TI - MCP-1 and MIP3-alpha serum levels in acute liver failure and molecular adsorbent recirculating system (MARS) treatment: a pilot study. PG - 745-51 LID - 10.1080/00365520902770086 [doi] AB - OBJECTIVE: The CC chemokines monocyte chemoattractant protein-1 (MCP-1) and macrophage inflammatory protein-3 alpha (MIP3-alpha) may be involved in the pathogenesis of acute liver failure (ALF) and acute-on-chronic liver failure (ACLF). In ALF and ACLF, the molecular adsorbent recirculating system (MARS) has been used to support liver function. Enhancement of MCP-1, as seen in other extracorporeal support systems such as haemodialysis, might thus have mitigated the beneficial effects of the MARS system in acute hepatic failure. MATERIAL AND METHODS: Serum concentrations of MCP-1 and MIP3-alpha were measured in 10 patients with ALF or ACLF treated with MARS. Thirteen patients suffering from chronic hepatic failure (CHF) and 15 healthy individuals served as controls. RESULTS: Baseline MCP-1 serum concentrations were significantly increased in ALF and ACLF patients as compared to patients with CHF (p=0.0027 and p=0.0046, respectively) and controls (p=0.0006 and p=0.0012, respectively). MIP3-alpha serum concentrations were also significantly enhanced in the ALF and ACLF groups as compared with those in CHF patients (p=0.0002 and p=0.0003, respectively) and controls (p<0.0001 and p<0.0001, respectively). Moreover, MIP3-alpha levels were significantly increased in CHF patients as compared to controls (p=0.0002). MCP-1 and MIP3-alpha concentrations did not change significantly during MARS treatment in ALF and ACLF patients. CONCLUSIONS: The CC chemokines MCP-1 and MIP3-alpha are increased in ALF and ACLF patients. MARS had no effect on MCP-1 and MIP3-alpha serum concentrations in patients with ALF and ACLF, and yielded no evidence of any harmful effects of the increase of these potentially hepatocidal chemokines. FAU - Roth, Georg A AU - Roth GA AD - Department of Anaesthesiology, General Intensive Care and Pain Medicine, Center for Physiology, Pathophysiology and Immunology, Medical University of Vienna, Vienna, Austria. georg.roth@meduniwien.ac.at FAU - Faybik, Peter AU - Faybik P FAU - Hetz, Hubert AU - Hetz H FAU - Ankersmit, Hendrik J AU - Ankersmit HJ FAU - Hoetzenecker, Konrad AU - Hoetzenecker K FAU - Bacher, Andreas AU - Bacher A FAU - Thalhammer, Theresia AU - Thalhammer T FAU - Krenn, Claus G AU - Krenn CG LA - eng PT - Comparative Study PT - Journal Article PL - England TA - Scand J Gastroenterol JT - Scandinavian journal of gastroenterology JID - 0060105 RN - 0 (CCL2 protein, human) RN - 0 (CCL20 protein, human) RN - 0 (Chemokine CCL2) RN - 0 (Chemokine CCL20) SB - IM MH - Adolescent MH - Adult MH - Case-Control Studies MH - Chemokine CCL2/*blood MH - Chemokine CCL20/*blood MH - Female MH - Humans MH - Liver Failure, Acute/*blood MH - Male MH - Middle Aged MH - Pilot Projects EDAT- 2009/02/28 09:00 MHDA- 2009/10/09 06:00 CRDT- 2009/02/28 09:00 PHST- 2009/02/28 09:00 [entrez] PHST- 2009/02/28 09:00 [pubmed] PHST- 2009/10/09 06:00 [medline] AID - 909086361 [pii] AID - 10.1080/00365520902770086 [doi] PST - ppublish SO - Scand J Gastroenterol. 2009;44(6):745-51. doi: 10.1080/00365520902770086.