Effects of two different lipid emulsions on antioxidant status, lipid peroxidation and parenteral nutrition- related cholestasis in premature babies, a randomized-controlled study
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Updated: Feb 5, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Hacer Yapicioglu Yildizdas1, Burak Poyraz1, Guluzar Atli2
1Cukurova University, Faculty of Medicine, Department of Paediatrics, Division of Neonatology, Turkey.
Insights
Fish oil-based lipid emulsions (FMOS) reduced cholestasis in preterm neonates compared to olive oil-soybean oil (OO/SO) emulsions. Both lipid types showed similar effects on lipid peroxidation and other morbidities in the short term.
Area of Science:
- Neonatal nutrition
- Parenteral nutrition
- Lipid emulsions
Background:
- Olive oil-soybean oil (OO/SO) lipid emulsions (LE) lack essential ω-3 PUFAs like EPA and DHA.
- Fish oil-based LEs, such as FMOS, are rich in EPA and DHA and differ in antioxidant and phytosterol content from OO/SO LEs.
Purpose of the Study:
- To investigate the effects of FMOS versus OO/SO lipid emulsions on cholestasis, antioxidant enzyme levels, and lipid peroxidation in preterm neonates.
Main Methods:
- Preterm neonates (≤32 weeks gestational age and/or ≤1500 g) were randomized to receive either FMOS or OO/SO LE.
- Levels of catalase, superoxide dismutase (SOD), glutathione peroxidase (GPx), and thiobarbituric acid reactive substances (TBARS) were measured.
- Cholestasis incidence and time to regain birth weight were recorded.
Main Results:
- Cholestasis was significantly lower in the FMOS group (0% vs. 18.2%).
- Neonates in the FMOS group regained birth weight earlier.
- While OO/SO showed higher initial TBARS levels, by day 28, TBARS levels were similar, and SOD levels were higher in the OO/SO group.
Conclusions:
- FMOS lipid emulsions are associated with a significant reduction in cholestasis in preterm neonates compared to OO/SO.
- Both FMOS and OO/SO lipid emulsions demonstrate comparable effects on lipid peroxidation and short-term morbidities, excluding cholestasis.
Background:
Olive oil-soybean oil (OO/SO) based lipid emulsions (LE) lack ω-3 PUFAs eicosapentaenoic acid -EPA and docosahexaenoic acid- DHA, which have clinical benefits on inflammatory processes. Fish oil based LEs are good sources of DHA and EPA. Fish oil, MCT, Olive oil and Soya oil (FMOS) lipid is one of the fish oil containing LEs supplemented with high levels of α-tocopherol and lower levels of phytosterol compared to OO/SO lipid emulsions. We investigated the effects of OO/SO and FMOS lipid preparations on cholestasis, levels of antioxidant enzymes and lipid peroxidation.
Methods:
Preterm neonates ≤32 gestational weeks age and/or ≤1500 g were randomly assigned to receive either FMOS or OO/SO in the first day of life. Catalase, superoxide dismutase (SOD), glutathione peroxidase (GPx) and thiobarbituric acid reactive substances (TBARS) levels in the first day of life, 7th day of lipid use and 28th day of life were measured and cholestasis during parenteral nutrition was recorded.
Results:
34 and 33 patients were in FMOS and OO/SO lipid groups respectively. Although the TBARS levels were higher in the first day of life and 7th day of LEs in OO/SO lipid group (p=0.014 and p=0.022), on the 28th day of life TBARS level was similar and SOD level was higher (p=0.014) in OO/SO group. Cholestasis was significantly lower in FMOS lipid group (0% vs. 18.2%), (p=0.011) and neonates regained birth weight earlier (p=0.006). There was no significant difference in other morbidities.
Conclusions:
FMOS and OO/SO lipid emulsions have similar effects on lipid peroxidation on 28th day of life and on morbidities in short term period except for cholestasis.
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