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Prohepcidin, Inflammation and Iron Homeostasis in Hemodialysis Patients With Chronic Hepatitis C

I

Istanbul University

Status

Completed

Conditions

Hepatitis C
Renal Failure Chronic Requiring Hemodialysis

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this study is to address questions regarding the link among hepcidin, hematological iron markers, inflammation and hepatitis C in HD patients. In attempt to address this issue, we planned to measure serum levels of hepcidin prohormone (pro-hepcidin), inflammatory and iron parameters.

Full description

Hepatitis C virus (HCV) infection is the most common cause of chronic liver disease in the world and also common among chronic hemodialysis (HD) patients. Patients with chronic HCV often have increased liver iron, a condition associated with reduced sustained response to antiviral therapy, more rapid progression to cirrhosis, and development of hepatocellular carcinoma; however, little is known about the mechanism of iron accumulation in the liver. Recently identified hepcidin, a 25-amino acid peptide hormone exclusively synthesized in the liver, is thought to be a key regulator for iron homeostasis and is induced by infection and inflammation. Hepcidin expression is modulated by iron stores, so that it decreases in iron deficiency to facilitate iron absorption while it increases in iron repletion to prevent pathological overload. Interleukin (IL)-6 has been proposed as a major inducer of hepcidin, via direct transcriptional activation of hepatic hepcidin expression by binding to its receptor complex containing gp130 to activate janus kinase (JAK) and activator of transcription 3 (STAT 3).

Enrollment

80 patients

Sex

All

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Chronic hemodialysis patients

Exclusion criteria

  • Patients positive for hepatitis B virus surface antigen (HBsAg)
  • Patients previously diagnosed nonrenal cause of anemia other than iron deficiency
  • Patients with an evidence of active or occult bleeding
  • Patients received blood transfusion within the past 4 months
  • Patients with a history of malignancy, end-stage liver disease, or chronic hypoxia
  • Patients with a history of recent hospitalization or infection requiring antibiotics within the past 4 weeks.

Trial design

80 participants in 3 patient groups

HCV (+)
Description:
Hemodialysis patients with chronic hepatitis C
HCV (-)
Description:
Hemodialysis patients without chronic hepatitis C
Control
Description:
Healthy volunteers

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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