Uric acid and unhealthy metabolic phenotype in Colombian children

Gina Gonzalez-Valencia1, Johana Hernandez2, Silvia Rueda2

  • 1Department of Pediatric Endocrinology, School of Medicine, University of Antioquia, Medellín, Colombia. ginagv.endoped@gmail.com.

Insights

Children with metabolically unhealthy obesity have higher uric acid (UA) levels than metabolically healthy peers. Elevated UA may serve as a marker for metabolic risk in pediatric obesity.

Area of Science:

  • Pediatric Endocrinology
  • Metabolic Health
  • Public Health

Background:

  • Childhood overweight and obesity present a growing public health challenge.
  • Identifying differential markers between metabolically healthy obese (MHO) and metabolically unhealthy obese (MUHO) children is crucial.
  • Uric acid (UA) is being investigated as a potential metabolic risk marker.

Purpose of the Study:

  • To evaluate differences in uric acid (UA) levels in children with overweight or obesity.
  • To classify children based on metabolic phenotype using the 2018 Damanhoury criteria.
  • To assess the relationship between UA levels and insulin resistance indices.

Main Methods:

  • Retrospective cross-sectional study of children aged 5-18 years.
  • Eighty patients were categorized into MHO (n=36) and MUHO (n=44) groups based on triglycerides, glucose, HDL-C, and blood pressure.
  • Student's t-test analyzed mean UA differences; correlations with insulin resistance indices were examined.

Main Results:

  • A statistically significant difference in UA levels was observed between MUHO (5.4 mg/dl) and MHO (4.5 mg/dl) groups (p=0.0069).
  • Moderate positive correlations were found between UA levels and the TyG ratio (0.4137) and TG/HDL index (0.3813).

Conclusions:

  • Uric acid levels are significantly higher in metabolically unhealthy obese children compared to metabolically healthy obese children.
  • Elevated UA levels correlate with markers of insulin resistance.
  • UA may serve as a valuable metabolic risk marker for evaluating pediatric overweight and obesity.
Abstract

Related Concept Videos

Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
925
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...
256
Overview of Protein Metabolism01:21

Overview of Protein Metabolism

Proteins are broken down into amino acids during digestion. Unlike fats and carbohydrates, which are stored for later use, proteins are not. Instead, amino acids are either used to produce ATP through oxidation or contribute to the creation of new proteins for the growth and repair of the body. Any surplus amino acids from the diet are converted into glucose or triglycerides rather than excreted.
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
4.1K
Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion01:20

Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion

Drug metabolism, a critical process in the liver, involves two primary phases: Phase I reactions and Phase II conjugation. Obesity introduces significant alterations in this metabolic process, primarily due to fatty infiltration of the liver, leading to conditions such as nonalcoholic fatty liver disease (NAFLD). This condition can modify the activities of both Phase I and II enzymes, impacting how drugs are metabolized in obese patients.Phase I metabolism sees variable effects across...
197
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu01:29

Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu

Genetic variations significantly influence drug response through pharmacokinetics, receptor interactions, and biologic milieu modifications. Pharmacokinetic alterations impact drug metabolism and clearance, affecting efficacy and toxicity. Variants in drug-metabolizing enzymes, such as CYP2C9 and CYP2C19, alter drug activation and elimination. For example, CYP2C9 loss-of-function variants require lower warfarin doses to prevent excessive bleeding, while CYP2C19 variants reduce clopidogrel...
10
Lethal Alleles02:41

Lethal Alleles

Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
18.3K