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A Clinical Trial Assessing the Safety, Efficacy, and Delivery of Olive-Oil-Based Three-Chamber Bags for Parenteral Nutrition
Published on: September 20, 2019
The metabolic effects of two different lipid emulsions used in parenterally fed premature infants--a randomized
Gamze Demirel1, Serife Suna Oguz, Istemi Han Celik
1Division of Neonatology, Zekai Tahir Burak Maternity Teaching Hospital, Ankara, Turkey. kgamze@hotmail.com
Insights
Soybean oil lipid emulsions in very low birth weight infants showed lower very low-density lipoprotein and free carnitine levels. Olive oil emulsions resulted in higher free carnitine and lower hexanoyl carnitine, potentially impacting sepsis risk.
Area of Science:
- Neonatal nutrition
- Biochemistry
- Pediatric intensive care
Background:
- Parenteral nutrition is crucial for very low birth weight infants.
- Lipid emulsions are a key component of parenteral nutrition.
- Different lipid sources may have distinct metabolic effects.
Purpose of the Study:
- To compare the impact of soybean oil versus olive oil-based lipid emulsions on plasma lipids and acylcarnitines in very low birth weight infants.
- To investigate potential differences in metabolic profiles and clinical implications.
Main Methods:
- A randomized comparative study involving 40 very low birth weight infants (≤32 weeks gestational age).
- Infants received either soybean oil-based (Intralipid®) or olive oil-based (Clinoleic®) lipid emulsions.
- Plasma lipid concentrations and acylcarnitine profiles were assessed.
Main Results:
- No significant differences in triglyceride, cholesterol, HDL, or LDL levels between groups.
- Lower very low-density lipoprotein levels were observed in the soybean oil group (p<0.05).
- Significantly lower free carnitine and higher hexanoyl carnitine levels were found in the soybean oil group compared to the olive oil group.
Conclusions:
- Soybean oil-based emulsions may influence lipid metabolism and carnitine status in VLBW infants.
- Altered acylcarnitine profiles in the soybean oil group suggest potential impacts on mitochondrial fatty acid transport.
- The findings highlight the need for careful selection of lipid emulsions in neonatal parenteral nutrition to optimize metabolic outcomes and potentially mitigate risks like sepsis.
Objective:
To compare the effects of two different lipid emulsions, based on soybean oil and olive oil respectively on plasma lipid concentrations and acylcarnitine profile of very low birth weight infants.
Design:
Randomized comparative study.
Patients And Methods:
Forty very low birth weight infants, ≤32 weeks of gestational age and receiving at least 40% of the calorie taken by parenteral nutrition from lipid solution at 14th day of life were evaluated. Group I (n=20) received soybean oil based lipid emulsion (Intralipid®) and Group II (n=20) received olive oil based lipid emulsion (Clinoleic®).
Main Outcome Measures:
Plasma lipid concentrations and acylcarnitine profile were assessed.
Results:
Triglyceride, cholesterol, high and low density lipoprotein levels, liver function tests were similar between two groups whereas very low density lipoprotein level was statistically lower in Group I (p<0.05). Free carnitine levels were 15.73±10.67 in Group I and 34.25±22.18 μM in Group II (p=0.012) and hexanoyl carnitine levels 2.18±2.10 in Group I and 0.38±0.12 μM in Group II, respectively (p=0.005). Plasma medium chain acylcarnitine levels were significantly higher in Group I.
Conclusions:
Low levels of very low density lipoprotein in Group I may be a way of hemostasis to keep the serum triglyceride within normal levels. Lower free carnitine levels in soybean oil-based group is the result of carnitine need during the mitochondrial transport of long chain fatty acids. In Group I, due to the inefficient transport of medium chain fatty acids into the mitochondria, medium chain acylcarnitines accumulate in plasma. This may be the reason of lower carnitine levels in Group I. We suggest that higher levels of hexanoyl carnitine, reflecting defective mitochondrial transport of hexanoyl which leads immunsupression, may be the cause of higher sepsis risk in Group I.
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