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Hepcidin and iron metabolism disorders in patients with chronic kidney disease
Marija Jelić1, Tatjana Cvetković, Vidojko Djordjević
1Clinical Biochemical Laboratory, Military Hospital Nis, Nis, Serbia. jelicmarija1211@gmail.com
Insights
Hepcidin levels correlate with iron metabolism in chronic kidney disease (CKD) patients. This finding suggests hepcidin can help diagnose and monitor iron disorders in CKD.
Area of Science:
- Nephrology
- Hematology
- Biochemistry
Background:
- Hepcidin is implicated in iron metabolism disorders.
- Chronic kidney disease (CKD) affects iron homeostasis.
- Understanding hepcidin's role in CKD is crucial.
Purpose of the Study:
- To investigate the relationship between hepcidin concentration and iron metabolism parameters in CKD patients.
- To compare hepcidin levels across different stages of CKD.
Main Methods:
- 104 CKD patients (64 hemodialysis, 40 pre-dialysis) were studied.
- Patients received erythropoietin and iron supplementation.
- Iron status, anemia parameters, inflammation, and hepcidin levels were assessed, with hemodialysis patients stratified by ferritin levels.
Main Results:
- Hemodialysis patients exhibited lower red blood cell counts, hemoglobin, and transferrin saturation, but higher iron, ferritin, and hepcidin.
- Lower serum ferritin subgroups (<199 ng/mL) showed reduced inflammation markers (hsCRP) and improved iron status indicators.
- Hepcidin levels strongly correlated with serum ferritin, peaking in the lowest and highest ferritin groups.
Conclusions:
- Hepcidin may serve as a valuable biomarker for diagnosing and monitoring anemia and iron metabolism disturbances in CKD patients.
- Further research can elucidate hepcidin's precise role in CKD pathophysiology.
Background/Aim:
[corrected] Hepcidin may play a pathogenetic role in iron metobolism disorders. The aim of this study was to determine the correlation between hepcidin concentration and parameters of iron metabolism in patients with different stage of chronic kidney disease (CKD).
Methods:
The study involved 104 patients with CKD: 64 on hemodialysis (HD) and 40 patients in pre-dialysis stadium (pre-HD) with adequate erythropoetin therapy and iron supplementation. The HD group was divided in four subgroups according to the level of serum ferritin (up to 100; 100-199; 200-499 and over 500 ng/mL). Parameters of anemia, iron status, in flamation and hepcidin level were evaluated.
Results:
The HD patients had a significantly lower eritrocyte count, erythrocytes indexes, hemoglobin and transferrin saturation and significantly higher iron, ferritin, hepcidin and total iron binding capacity (TIBC). The HD subgroups up to 199 ng/mL of serum feritin had lower high-sensitivity C-reactive protein (hsCRP), iron and higher unbuffered iron binding capacity (UIBC), transferrin saturation and TIBC compared to the HD subgroups over 200 ng/mL. The lowest and the highest ferritin subgroups had the highest hepcidin level and it showed significant correlation with ferritin.
Conclusion:
Hepcidin may serve as a marker for better diagnosing and monitoring anemia and iron metabolism disorders in CKD.
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