Abstract
(3.9 ng/ml), CLD (6.8 ng/ml), healthy control (6.6 ng/ml), [p = 0.02, 0.001, 0.001]. The Hepcidin/Iron ratio was found to be lowest (3.9%) in ACLF-MOF, compared to ACLF (19%) and CLD (22%) [p < 0.01], Hepcidin/ferritin ratio was similarly lowest in ACLF-MOF (6.1%) than in ACLF (12%) or CLD (51%) [p< 0.01]. Hepcidin/transferrin ratio was again lowest (37%) in ACLF-MOF than ACLF (84%), CLD (90%) [p < 0.01] and the ratio of Hepcidin/ceruloplasmin was 35%, 62% and 93% [<0.01] respectively. Circulating hepcidin levels inversely correlated to serum iron indices [r = −0.464, p = 0.003] in ACLF. ACLF patients with decreased circulating hepcidin and increased serum iron levels showed a significantly lower survival [p = 0.001, hazards ratio 13.19, CI 4.9–35.21], and higher development of MOF. Conclusions: The ratio of hepcidin to other iron regulating proteins and total iron levels is reduced in patients with ACLF; more so in those with multiorgan failure. Altered levels of circulating iron and iron regulating proteins may help in predicting outcome and developing new treatment strategies in ACLF patients.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.