Growth, Safety and Tolerance in Infants Fed Rice Protein Hydrolysate Formula: The GRITO Randomised Controlled Trial

Anaïs Lemoine1, Antonio Nieto-García2, María Nieto-Cid2

  • 1Service de Nutrition et Gastro-Entérologie Pédiatrique, Hôpital Armand Trousseau AP HP, Sorbonne Université, 75571 Paris, France.

Nutrients
|January 11, 2025
PubMed

Insights

Hydrolysed rice formula (HRF) supports appropriate growth and tolerance acquisition in infants with cow's milk protein allergy (CMPA), showing comparable safety and efficacy to extensively hydrolysed formula (eHF).

Area of Science:

  • Pediatric Nutrition
  • Allergy and Immunology
  • Gastroenterology

Background:

  • Cow's milk protein allergy (CMPA) affects a significant number of infants.
  • Hydrolysed rice formula (HRF) is a common alternative, but growth concerns exist compared to extensively hydrolysed formula (eHF).

Purpose of the Study:

  • To compare the growth, safety, and tolerance acquisition in infants diagnosed with CMPA when fed either HRF or eHF.
  • To evaluate anthropometric measurements and adverse events in infants with CMPA on different formulas.

Main Methods:

  • A multicentre, prospective, randomized, double-blind, placebo-controlled trial.
  • 105 infants with CMPA were randomized to receive either HRF or eHF for 12 months.
  • Primary outcome: change in weight-for-length Z-score; secondary outcomes: anthropometrics, tolerability, adverse events.

Main Results:

  • No significant differences in weight-for-length Z-scores between HRF and eHF groups (p=0.28).
  • Normal growth patterns observed across all anthropometric variables in both groups.
  • Similar safety profiles and tolerability, with a trend towards faster tolerance acquisition in the HRF group.

Conclusions:

  • HRF is a safe and effective option for managing CMPA, supporting appropriate growth and tolerance development.
  • HRF demonstrates comparable outcomes to eHF in infants with CMPA.
  • HRF can be considered a suitable alternative in CMPA management.

Related Concept Videos

Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
4.2K
Bioavailability Study Design: Absolute Versus Relative Bioavailability01:27

Bioavailability Study Design: Absolute Versus Relative Bioavailability

Bioavailability is a crucial pharmacokinetic parameter that quantifies the proportion of an administered drug that reaches the systemic circulation and is available for therapeutic action. Regulatory agencies mandate the assessment of bioavailability, typically measured as the area under the drug plasma concentration-versus-time curve (AUC), to ensure the efficacy and safety of pharmaceutical products. These evaluations are categorized as absolute and relative bioavailability studies.Absolute...
658
Bioavailability Study Design: Single Versus Multiple Dose Studies01:11

Bioavailability Study Design: Single Versus Multiple Dose Studies

Bioavailability studies are essential for understanding how a drug is absorbed, distributed, metabolized, and excreted in the body. These studies assess the extent and rate at which the active pharmaceutical agent becomes available at the site of action. The design of bioavailability studies can involve single-dose or multiple-dose regimens, each with distinct advantages and limitations.Single-dose studies are the preferred approach due to their simplicity and reduced drug exposure for...
388
Bioavailability Study Design: Healthy Subjects Versus Patients01:15

Bioavailability Study Design: Healthy Subjects Versus Patients

Bioavailability studies are essential for evaluating a drug's therapeutic efficacy and understanding its absorption patterns under various physiological conditions. Conducting such studies on target patient populations provides more relevant data by simulating real-world disease states. However, practical challenges often necessitate the use of young, healthy adult volunteers as study subjects.Patients may exhibit altered drug absorption patterns due to the effects of the disease itself,...
252
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
1.0K
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...
975