Protein metabolism in the extremely low-birth weight infant

S C Kalhan1, S Iben

  • 1Robert Schwartz, MD, Center for Metabolism & Nutrition, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA. sck@po.cwru.edu

Clinics in Perinatology
|February 26, 2000
PubMed

Insights

Very preterm infants exhibit high protein breakdown, unresponsive to nutrient intake. Current interventions for nitrogen accretion in extremely low birth weight (ELBW) infants have not improved growth, possibly due to insufficient calorie and nitrogen delivery.

Area of Science:

  • Neonatal physiology and metabolism
  • Pediatric nutrition and growth

Background:

  • Extensive data exist on nutrient and protein impact on infant growth, plasma amino acids, and nitrogen balance.
  • Limited studies have investigated in vivo protein metabolism dynamics in micropremie or extremely low birth weight (ELBW) infants.

Purpose of the Study:

  • To examine the dynamic aspects of protein metabolism in very preterm infants, including micropremies and ELBW infants.
  • To understand the responsiveness of protein turnover and breakdown to nutrient administration in this vulnerable population.

Main Methods:

  • In vivo examination of protein metabolism dynamics.
  • Analysis of protein turnover and breakdown rates.
  • Assessment of responsiveness to nutrient administration and specific interventions.

Main Results:

  • Very preterm infants demonstrate high rates of protein turnover and breakdown, potentially due to immaturity or illness.
  • High rates of proteolysis show limited responsiveness to nutrient administration.
  • Interventions like insulin, human growth hormone, or glutamine have not enhanced protein accretion or growth.

Conclusions:

  • Protein metabolism in very preterm and ELBW infants is characterized by high proteolysis that is not readily influenced by nutrient intake.
  • Current strategies to promote nitrogen accretion have been ineffective, possibly limited by inadequate calorie and nitrogen delivery.

Related Concept Videos

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...
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...
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...
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...