Hepcidin and iron parameters in children with anemia of chronic disease and iron deficiency anemia

Gunjan Mahajan1, Sunita Sharma1, Jagdish Chandra2

  • 1Department of Pathology, Lady Hardinge Medical College, New Delhi, India.

Blood Research
|October 19, 2017
PubMed

Insights

Hepcidin aids in distinguishing anemia of chronic disease (ACD) from iron deficiency anemia (IDA). This biomarker also helps identify iron deficiency in ACD patients, guiding appropriate therapy selection.

Area of Science:

  • Pediatric Hematology
  • Clinical Biochemistry
  • Iron Metabolism

Background:

  • Anemia of chronic disease (ACD) and iron deficiency anemia (IDA) are common, often overlapping anemias.
  • Hepcidin, a key regulator of iron metabolism, is a novel biomarker for iron status assessment.
  • Differentiating ACD from IDA and identifying coexistent iron deficiency in ACD is clinically significant.

Purpose of the Study:

  • To investigate the role of serum hepcidin and conventional iron parameters in differentiating ACD from IDA in children.
  • To identify children with ACD who also have iron deficiency (ID).
  • To assess the utility of hepcidin in guiding therapeutic decisions for pediatric anemia.

Main Methods:

  • A comparative study involving 30 pediatric cases each of ACD and IDA, plus 30 age/sex-matched controls.
  • ACD cases were subcategorized into pure ACD and ACD with coexistent ID.
  • Analysis included complete blood count, inflammatory markers (CRP, IL-6), iron studies, soluble transferrin receptor (sTfR), and serum hepcidin.

Main Results:

  • Serum hepcidin levels were significantly elevated in pure ACD patients (143.85±42.76 ng/mL) compared to IDA patients (6.01±2.83 ng/mL) and controls (24.96±9.09 ng/mL).
  • ACD patients with coexistent ID exhibited significantly lower serum hepcidin (10.0±2.97 ng/mL) compared to pure ACD patients.
  • Elevated sTfR levels in ACD patients correlated with reduced hepcidin, indicating coexistent iron deficiency.

Conclusions:

  • Serum hepcidin is a valuable biomarker for differentiating pediatric ACD from IDA.
  • Hepcidin measurement effectively identifies iron deficiency in children with ACD.
  • These findings support the use of hepcidin assays to guide targeted anemia therapy.
Abstract

Related Concept Videos

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test01:22

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test

In clinical practice, the direct measurement of hepatic blood flow to evaluate liver function presents significant challenges due to the intricate and specialized nature of the necessary techniques. Consequently, healthcare professionals often rely on empirical estimates derived from thorough patient examinations and liver function tests to gauge liver health. Among the tools at their disposal, the Child–Pugh and MELD scoring systems stand out for their ability to categorize and assess...
223
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
269
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow01:26

Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow

Chronic liver disease significantly impacts drug metabolism due to alterations in hepatic blood flow and enzyme accessibility. This disruption affects the body's pharmacokinetics—the movement and processing of drugs within the system. Key enzymes crucial for metabolizing medications become less accessible, changing how drugs are processed and utilized. Furthermore, liver disease influences the synthesis of plasma proteins, such as albumin and globulins, which play critical roles in drug...
270
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
346
Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
298
Pharmacokinetics in Pediatric Patients: Drug Distribution01:17

Pharmacokinetics in Pediatric Patients: Drug Distribution

Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight,...
350