Individualized Nutrition to Optimize Preterm Infant Growth and Neurodevelopment

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeUp to 4
SponsorChildren's National Research Institute

About this trial

Human milk has several well-established benefits but does not adequately meet the increased nutritional demands of the growing preterm infant, necessitating additional nutrient supplementation in a process known as fortification. In U.S. neonatal intensive care units (NICUs), human milk is primarily supplemented using standardized fortification, in which a multicomponent fortifier is added to human milk to achieve assumed nutrient content based on standard milk reference values. However, this method does not account for the significant variability in human milk composition or in preterm infant metabolism, and up to half of all very premature infants experience poor growth and malnutrition using current nutritional practices. Poor postnatal growth has adverse implications for the developing preterm brain and long-term neurodevelopment.

Recent advances allow for individualized methods of human milk fortification, including adjustable and targeted fortification. Adjustable fortification uses laboratory markers of protein metabolism (BUN level) to estimate an infant's protein requirements. In targeted fortification, a milk sample is analyzed to determine its specific macronutrient and energy content, with additional macronutrient supplementation provided as needed to achieve goal values. Emerging data suggest that both methods are safe and effective for improving growth, however information on their comparable efficacy and neurodevelopmental implications are lacking, particularly using advanced quantitative brain MRI (qMRI) techniques.

Through this prospective, randomized-controlled trial, the investigators will compare the impact of individualized human milk fortification on somatic growth and neurodevelopment in preterm infants. Infants will be randomized to receive one of three nutritional interventions: standardized (control group), adjustable, or targeted human milk fortification. Infants will undergo their assigned nutritional intervention until term-equivalent age or discharge home, whichever is achieved first. Brain qMRI will be performed at term-corrected age, and neurodevelopmental follow-up will be performed through 5 years of age.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Birth gestational age (GA) of ≤32 weeks

Postnatal age ≤4 weeks at time of enrollment

Maternal plan to provide human milk to infant, and consent to providing donor human milk if insufficient maternal milk supply

Maternal age > 18 years old

Disqualifiers

Formula feeding prior to 36 weeks PMA or discharge home (whichever achieved first), either secondary to parental preference or medical necessity

Dysmorphic features or congenital anomalies suggestive of a genetic syndrome, metabolic disorder, chromosomal abnormality, or congenital infection

Dysgenetic or major destructive brain lesions detected by head ultrasound before enrollment

Trial design

Design model

Parallel

Treatments tested in this trial

  • Standardized Fortification

    Dietary supplement

    Fortification with liquid, bovine-based HMF to assumed human milk content of 24kcal/oz

  • Adjustable Fortification

    Dietary supplement

    Additional liquid protein supplementation to maintain serum BUN levels within goal range (9-14mmol/dL)

  • Adjustable Fortification

    Dietary supplement

    Additional liquid protein and/or MCT oil supplementation to maintain protein, fat, and energy intake within goal range based upon mid-infrared human milk analysis

Treatment groups

150 Participants
are divided into 3 treatment groups
Group A: Standardized FortificationActive comparator 1 intervention
Group B: AdjustableExperimental treatment 2 interventions
Group C: TargetedExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Weight Gain Velocity

Weight gain velocity (grams per kilogram per day)

Time frame
Study enrollment through nutritional intervention endpoint (term-equivalent age (40 weeks PMA [postmenstrual age]) or discharge home, whichever is achieved first)
2

Length Growth Velocity

Length growth velocity (centimeters per week)

Time frame
Study enrollment through nutritional intervention endpoint (term-equivalent age (40 weeks PMA [postmenstrual age]) or discharge home, whichever is achieved first)
3

Head Circumference Growth Velocity

Head circumference growth velocity (centimeters per week)

Time frame
Study enrollment through nutritional intervention endpoint (term-equivalent age (40 weeks PMA [postmenstrual age]) or discharge home, whichever is achieved first)
4

Total and Regional Brain Volumes

Total and regional (cortical and deep gray matter, white matter, amygdala-hippocampus, brainstem, cerebellum) brain volumes by MRI

Time frame
Term-equivalent age (38 to 41 weeks postmenstrual age)

Secondary outcomes

Other outcomes

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