# Do different lipid emulsions affect brain development? A single-center retrospective analysis

**Authors:** Samuele Caruggi, Andrea Calandrino, Benedetta Corradi, Marcella Battaglini, Paolo Massirio, Francesco Vinci, Federica Mongelli, Alessia Pepe, Alessandro Parodi, Mariya Malova, Agata Zoia, Mariasavina Severino, Martina Resaz, Andrea Rossi, Luca Antonio Ramenghi

PMC · DOI: 10.3389/fnut.2026.1723062 · Frontiers in Nutrition · 2026-02-04

## TL;DR

This study investigates whether different lipid emulsions used in parenteral nutrition affect brain development and neurodevelopmental outcomes in preterm infants.

## Contribution

The study provides a retrospective analysis comparing brain maturation and neurodevelopment in preterm infants using two lipid emulsions.

## Key findings

- No statistically significant differences were found in brain maturation scores between the two lipid emulsion groups.
- Neurodevelopmental outcomes assessed at 2 years showed no significant differences between the groups.
- The study could not determine an optimal lipid emulsion for preterm infants based on the outcomes measured.

## Abstract

Preterm birth is a critical period for brain development, as extrauterine factors can impair growth and myelination, thereby increasing the risk of neurodevelopmental impairment. Adequate nutrition and rapid weight gain are associated with better cognitive outcomes, and the choice of lipid emulsion during parenteral nutrition may influence these results. SMOFlipid®, enriched with omega-3 long-chain polyunsaturated fatty acids, could reduce inflammation and oxidative stress, potentially lowering bronchopulmonary dysplasia (BPD) risk. This study compared brain maturation at term-equivalent age (TEA) using MRI and neurodevelopment at 2 years in infants receiving either SMOFlipid® or Intralipid®.

In this single-center retrospective observational cohort study, we included all very low birth weight (VLBW) infants admitted to the NICU of our institution between 2017 and 2021. Infants who underwent brain MRI at term-equivalent age and completed neurodevelopmental assessment at 2 years were included, and those with severe brain lesions were excluded. Patients were categorized into two groups based on the lipid emulsion administered during parenteral nutrition. The primary outcome was neurodevelopment at 24 months of corrected age (CA). The secondary outcome was brain maturation assessed by the total maturation score (TMS) on magnetic resonance imaging (MRI).

A total of 121 VLBW infants were included and categorized into two cohorts based on the lipid formulation administered: multi-component lipid emulsion (MLE) in 62 and soybean lipid emulsion (SLE) in 49 infants. TMS showed non-statistically significant differences among infants treated with SLE compared with those treated with MLE, as well as in neurodevelopmental outcomes assessed using Griffith’s scales.

Despite integrating brain imaging and clinical follow-up data, this study could not determine the optimal lipid emulsion for preterm infants.

## Linked entities

- **Diseases:** bronchopulmonary dysplasia (MONDO:0019091)

## Full-text entities

- **Diseases:** perinatal stroke (MESH:D066087), congenital malformations (OMIM:163000), brain injury (MESH:D001930), autism spectrum disorder (MESH:D000067877), brain lesions (MESH:D001927), CA (MESH:D000080041), epilepsy (MESH:D004827), cerebral palsy (MESH:D002547), intrauterine growth retardation (MESH:D005317), inflammation (MESH:D007249), VLBW (MESH:D001724), cerebral malformations (MESH:D020786), language delay (MESH:D007805), PLIC (MESH:D002062), preeclampsia (MESH:D011225), BPD (MESH:D001997), PDA (MESH:D004374), cholestasis (MESH:D002779), pulmonary (MESH:D008171), preterm complications (MESH:D047928), congenital infections (MESH:D007239), PVL (MESH:D007969), prematurity (MESH:C536271), IVH (MESH:D000074042), CBH (MESH:D020201), PVHI (MESH:D007238), hemorrhage (MESH:D006470), NEC (MESH:D020345), arteriovenous malformation (MESH:D001165), cytomegalovirus (MESH:D003586), WMI (MESH:D056784), ROP (MESH:D012178), weight gain (MESH:D015430), sepsis (MESH:D018805), placental abruption (MESH:D000037), neurodevelopmental impairment (MESH:D009422), cerebellar lesions (MESH:D002526), MLE (MESH:D011017), Diffuse white matter injury (MESH:D000070625), metabolic diseases (MESH:D008659), post-hemorrhagic hydrocephalus (MESH:D006849)
- **Chemicals:** paracetamol (MESH:D000082), PUFAs (MESH:D005231), soy bean oil (MESH:D013024), ibuprofen (MESH:D007052), MLE (-), olive oil (MESH:D000069463), fatty acid (MESH:D005227), Intralipid (MESH:C545823), alpha-tocopherol (MESH:D024502), DHA (MESH:D004281), lipid (MESH:D008055), MCT (MESH:C000709826), EPA (MESH:D015118), fish oil (MESH:D005395)
- **Species:** Glycine max (soybean, species) [taxon 3847], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913121/full.md

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Source: https://tomesphere.com/paper/PMC12913121