High rate of functional cure in infants with chronic hepatitis B following a definite duration of antiviral treatment
View abstract on PubMed
Summary
This summary is machine-generated.Antiviral treatment with Lamivudine and Interferon-alfa can lead to a functional cure in infants with chronic hepatitis B. This study shows high success rates for achieving undetectable HBV DNA and HBeAg seroconversion.
Area Of Science
- Pediatrics
- Hepatology
- Virology
Background
- Limited data exists on antiviral therapies for infants diagnosed with chronic hepatitis B (CHB).
- Investigating the efficacy of antiviral treatment for achieving a functional cure in infants with CHB is crucial.
Purpose Of The Study
- To assess the effectiveness of antiviral treatment in achieving a functional cure for CHB in infants.
- To evaluate the virological response and safety of Lamivudine plus Interferon-alfa therapy in this population.
Main Methods
- A real-world study involving 21 infants (median age 9 months) with HBeAg-positive CHB.
- Treatment involved initial Lamivudine monotherapy, with Interferon-alfa added after 12 months of age.
- Analysis of virological responses, functional cure rates, and safety over 36 months.
Main Results
- All infants achieved viral suppression, with undetectable HBV DNA in a median of 6 months.
- HBeAg seroconversion occurred in 20 out of 21 infants within a median of 7 months.
- 19 out of 21 infants achieved a functional cure within a median of 9 months; no serious adverse events were reported.
Conclusions
- Infants under one year with CHB can achieve a high probability of functional cure with Lamivudine add-on Interferon-alfa therapy.
- A defined duration of antiviral treatment is effective for achieving sustained virological response and functional cure.
Related Concept Videos
Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the...
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...
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...
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...
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...
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...

