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Optimal Growth of Preterm Infants With Growth Restriction

Body Composition, Metabolic Programming and Long Term Outcome of Growth Restricted Preterm Infants Under Different Nutritional Management A Prospective Randomized Controlled Multicenter Trial

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02999945
Acronym
OPTIGROW
Enrollment
0
Registered
2016-12-21
Start date
2019-03-31
Completion date
2022-01-31
Last updated
2019-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adiposity, Diabetes, Growth Failure, Neurologic Deficits

Keywords

preterm infants, SGA infants, IUGR infants, growth, body composition, metabolomics, microbiome, adiposity markers, metabolic programming, neurodevelopmental outcome

Brief summary

In this prospective randomized controlled multi center trial the investigators stratify Very Low Birthweight (VLBW)-infants with growth retardation in small for gestational age (SGA) or intrauterine growth restricted (IUGR) - infants and aim to investigate the impact of a nutritional management with enhanced nutrients from discharge up to the 52nd week of postconceptional age on growth, body composition, metabolic programming, metabolomics, microbiome and long term neurodevelopmental outcome. In this study, the investigators will evaluate the difference in metabolic profiles of SGA and IUGR preterm infants. The investigators will further longitudinally assess, how different nutritional interventions affect the altered pathways in the first year of life and identify, in combination with data available from metabolic markers, microbiome and breast milk analysis, potential pathways resulting in increased disease risk later in life.

Detailed description

Prematurity is the leading cause for mortality and morbidity in newborns with very low birth weight (VLBW) infants (\< 1500g birth weight) at highest risk. Ten to thirty percent of VLBW infants are also born too small for their gestational age defined by a birth weight below the 10th percentile. In daily neonatal intensive care, consequential long term-follow up and most studies all growth restricted premature infants are treated the same, importantly this includes the nutritional management after birth. However, different groups of patients with different causal pathologies are subsumed under the definition growth restriction or born too small. One group of growth restricted patients refers to the infants born constitutionally small or small for gestational age (SGA). The other group refers to infants with an intrauterine growth restriction (IUGR) caused by a complex antenatal pathology. Consequently, the nutritional management after birth is very important to minimize the potential risk for developing obesity, diabetes and cardiovascular diseases later in life and to achieve optimal growth. So far we do not consider the different underlying pathomechanisms of growth restriction in our nutritional concepts for preterm infants and therefore cause long-term consequences. The European society of pediatric gastroenterology, hematology and nutrition (ESPGHAN) recommends to feed enhanced nutrients up to 52nd week of gestation in all growth restricted preterm infants- regardless if they are SGA or IUGR premature. Actually, reliable data guaranteeing that the recommended enhanced nutrients strategy providing extra nutrients up to 52 weeks for SGA and IUGR infants is safe and effective for both groups in terms of long-term growth and metabolic programming are lacking. A total of 348 preterm infants born and discharged below the 10th percentile at term will be included in the study and stratified according to SGA or IUGR by a combination of antenatal ultrasound parameters and growth parameters (including 10% screening failures and 20% drop out. Furthermore IUGR and SGA growth restricted preterm infants will be stratified according to breastfeeding or formula feeding and randomized in one of the following groups: Standard nutrients group (breastfeeding or starter formula) or Enhanced nutrients group (fortified breast milk or post-discharge formula. Body composition measurements will be performed by air displacement plethysmography - a non-invasive method. Anthropometric measurements will be performed by measuring weight, height and head circumference. Furthermore, parameters of metabolic programming, metabolomics, the stool microbiome and neurodevelopmental outcome will be determined. Additionally, the stool microbiome will be characterized from infant stool samples and compared between the two groups. After an interventional period of three months infants will be followed up until 2 years of age.

Interventions

DIETARY_SUPPLEMENTSGA-enhanced nutrients

Infants will receive fortified breast milk (\>50% meals/d fortified, 1,4 g protein, 85 kcal/100ml, FM85, Nestle ®) or post discharge formula (2g protein; 73-75 kcal/100ml; Aptamil PDF, Milupa® or Beba F Nestle® ) between discharge and 52nd week of gestation (three months after term

DIETARY_SUPPLEMENTIUGR-enhanced nutrients

Infants will receive fortified breast milk (\>50% meals/d fortified, 1,4 g protein, 85 kcal/100ml, FM85, Nestle ®) or post discharge formula (2g protein; 73-75 kcal/100ml; Aptamil PDF, Milupa® or Beba F Nestle® ) between discharge and 52nd week of gestation (three months after term

OTHERSGA-standard nutrients

Infants will receive unfortified breast milk (65-70kcal/100ml) or starter formula (1,2- 1,3g protein, 66 kcal/100ml Beba Pre Pro Start, Nestle® or Aptamil Pre, Milupa ®) between discharge and 52nd week of gestation (three months after term)

OTHERIUGR-standard nutrients

Infants will receive unfortified breast milk (65-70kcal/100ml) or starter formula (1,2- 1,3g protein, 66 kcal/100ml Beba Pre Pro Start, Nestle® or Aptamil Pre, Milupa ®) between discharge and 52nd week of gestation (three months after term)

Sponsors

Medical University of Graz
CollaboratorOTHER
Ludwig-Maximilians - University of Munich
CollaboratorOTHER
University Hospital Tuebingen
CollaboratorOTHER
University of Erlangen-Nürnberg Medical School
CollaboratorOTHER
University of Milan
CollaboratorOTHER
Poznan University of Medical Sciences
CollaboratorOTHER
Lund University
CollaboratorOTHER
Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 42 Weeks
Healthy volunteers
Yes

Inclusion criteria

* Preterm infants with a birth weight \<1500g and birth weight \<10th percentile. * Weight at term \<10th percentile * Informed consent

Exclusion criteria

* Genetic or metabolic diseases with the primary effect on growth * Necrotizing enterocolitis * Intraventricular hemorrhage (IVH) \>Grade II * Periventricular leukomalacia (PVL) Stage III * Genetic or metabolic disorders * Bronchopulmonary dysplasia

Design outcomes

Primary

MeasureTime frameDescription
Fat Free Mass3 monthsFat free mass measured by body plethysmography

Secondary

MeasureTime frameDescription
anthropometry-weight24 monthsweight in grams
anthropometry-HC24 monthshead circumference in cm
anthropometry-z-score24 monthsz-scores
parameters of metabolic programming- IGF112 monthsIGF-1in ng/ml
parameters of metabolic programming-IGF312 monthsIGF-3 in ng/ml
parameters of metabolic programming-IGF-BP12 monthsIGF-BP in ng/ml
parameters of metabolic programming-Leptin12 monthsLeptin in ng/ml
anthropometry-length24 monthslength in cm
neurodevelopmental outcome24monthsBayley scales
metabolomics12 monthsMetabolomic analysis will determine around 200 metabolites covering polar lipids (SOFIA), acylcarnitines (CARN), non-esterified fatty acids (NEFA) and amino acids (AA). Data will be acquired according to retention time and mass transition on triple quadrupole mass spectrometer, controlled by Analyst. All metabolite concentrations are reported in µmol/L
stool microbiome24 months
macronutrients in breastmilk-fat6 monthsFat will be analysed by modified Mojonnierether extraction (g/100ml)
macronutrients in breastmilk-Lactose6 monthsLactose will be determined by Lactose analysis method: LC-MS/MS (g/100ml)
macronutrients in breastmilk-protein6 monthsProtein will be determined by elemental analysis (g/100ml)
parameters of metabolic programming-Adiponectin12 monthsAdiponectin in mcg/ml

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026