Amino Acid and Acylcarnitine Profiles in Premature Neonates

Pediatrix

Status: Completed

Conditions: Prematurity; Parenteral Nutrition; Neonatal Screening

Study type: Observational

Funder types: Other

Identifiers

NCT00865150

PDX-001-08

Details and patient eligibility

About

Primary Hypotheses of the study include:

• Metabolic profiles are influenced by gestational age, chronological age, type and degree of nutritional support and illness
• Metabolic profiles differ between neonates who receive commercial formula and neonates who receive primarily human breast milk
• Neonates who develop parenteral associated cholestasis have metabolic markers that identify at risk patients (high serum urea nitrogen, citrulline, histidine, methionine, and succinyl carnitine and low thyroxine, serine and glutamate)
• Neonates that have hypothyroidism have abnormal metabolic profiles (low tyrosine levels)

Full description

Malnutrition is a common problem in the neonatal intensive care unit. Recent studies indicate that prematurely born neonates commonly develop a severe nutritional deficit during the first weeks after birth, referred to as extrauterine growth restriction. Despite an increase in growth during the second month of hospitalization, many neonates are ultimately discharged home having grown inadequately. The early nutritional deficit affects weight gain as well as growth in length and head circumference. Aggressive administration of parenteral amino acids to improve protein accretion rates in very preterm neonates has been supported in the literature. Although tolerance of high dose amino acids has been described, researchers acknowledge that sensitive tests to monitor amino acid toxicity are not readily available in the clinical setting.

The goals of this study are:

• To better define normal amino acid and acylcarnitine values and how they change in premature neonates
• To measure the effect nutritional support has (human breastmilk vs. formula) on amino acid and acylcarnitines profiles
• To measure the effect of illness (parenteral nutrition associated cholestasis) on amino acid and acylcarnitine profiles
• To better define abnormal metabolic profiles (low tyrosine levels) in neonates that have hypothyroidism.

Enrollment: 1,003 patients

Sex: All

Ages: 23 to 31 weeks old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

• Documentation of informed consent
• Inborn
• Less than or equal to twenty four (24) hours of age
• Gestational age between twenty three (23) weeks and 0/7 days and thirty one (31) weeks and 0/7 days as per the best estimate by the neonatologist
• If subject is transferred to another hospital, the ability to obtain follow-up data on outcomes
• No known major anomalies (inborn error of metabolism, chromosomal abnormalities, cyanotic congenital heart disease, gastroschisis, omphalocele, diaphragmatic hernia or other major gastrointestinal anomalies, major neurological injury or anomaly, and multiple congenital anomalies)

Exclusion Criteria

• Outborn (transferred for intensive care from another hospital)
• Greater than twenty four (24) hours of age
• Gestational age < 23 weeks or > 31 weeks
• Any known major congenital anomalies