Response to highly active antiretroviral therapy varies with age: the UK and Ireland Collaborative HIV Paediatric

AIDS (London, England)
|September 9, 2004
PubMed

Insights

Younger children show better immune recovery on highly active antiretroviral therapy (HAART) but poorer viral suppression. Age and baseline CD4% influence HAART response in children, impacting resistance risk.

Area of Science:

  • Pediatric Infectious Diseases
  • Immunology
  • Virology

Background:

  • Highly active antiretroviral therapy (HAART) is crucial for managing HIV-1 infection in children.
  • Understanding factors influencing HAART response is essential for optimizing treatment outcomes.
  • Age and immunological status (CD4%) are key considerations in pediatric HIV management.

Purpose of the Study:

  • To evaluate how age, CD4 percentage (CD4%), and plasma HIV-1 RNA levels affect HAART response in previously untreated children.
  • To identify specific patient characteristics that predict immunological and virological responses to HAART.

Main Methods:

  • A cohort study design was employed to analyze treatment responses.
  • Logistic and Cox regression models were used to examine associations between age at HAART initiation, CD4%, and HIV-1 RNA response.
  • Analyses were adjusted for sex, route of infection, and pre-HAART values.

Main Results:

  • Younger children and those with lower baseline CD4% showed greater CD4% increases at 6 months.
  • Older children were more likely to achieve HIV-1 RNA suppression (<400 copies/ml) at 6 months.
  • Immunological response (CD4% increase) was faster in younger children, while virological response (HIV-1 RNA decrease) was slower, potentially increasing resistance risk.

Conclusions:

  • Children achieve immunological responses to HAART regardless of baseline viral load or clinical status.
  • Younger children and those with lower CD4% exhibit superior immunological recovery but poorer virological response.
  • Age-related differences in HAART response necessitate tailored treatment strategies to mitigate resistance risk.
Abstract

Related Concept Videos

Retrovirus Life Cycles01:10

Retrovirus Life Cycles

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 retrovirus to...
Pharmacokinetics in Geriatric Patients: Effect of Age on Drug Absorption01:22

Pharmacokinetics in Geriatric Patients: Effect of Age on Drug Absorption

As individuals age, their body's physiology evolves, affecting drug pharmacokinetics. The most apparent changes occur in the gastrointestinal tract, where an increase in gastric pH, a delay in gastric emptying, and a reduction in gastrointestinal motility are observed. Remarkably, these changes do not substantially modify the absorption of orally administered drugs, particularly those absorbed via passive diffusion.Transdermal drug delivery emerges as a highly viable method for older adults due...
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...
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, compared...
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 a challenge in...
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...