Related Experiment Video
Updated: Aug 16, 2026

Isolation of Neonatal Extrahepatic Cholangiocytes
Published on: June 5, 2014
Lipid intolerance in newborns is associated with hepatic dysfunction but not infection
1Department of Pediatrics and Adolescent Medicine, St Louis, University School of Medicine, Mo, USA.
Objective:
To examine the hypothesis that fat intolerance in newborns who receive intravenous lipid is related to both infection and liver dysfunction.
Design:
Prospective survey.
Setting:
Tertiary intensive care nursery.
Patients:
All newborns who were admitted to the neonatal intensive care unit during a 20-month period and received parenteral lipid for 2 or more weeks were eligible for the study. Of 279 newborns who received parenteral nutrition, 162 met eligibility criteria and form the basis of this report.
Interventions:
None.
Main Outcome Measure:
Fat intolerance as defined by a serum triglyceride level of 1.69 mmol/L or greater (> or = 150 mg/dL).
Results:
Triglyceride levels were similar in infected and noninfected patients. Newborns with hypertriglyceridemia were more likely to have liver dysfunction (P < .001) or growth retardation (P < .01), but not infections. Hypertriglyceridemia was approximately twice as likely (P < .05) in newborns with either growth retardation or liver dysfunction.
Conclusions:
Liver dysfunction and fetal growth retardation were associated with lipid intolerance in newborns who received intravenous fat. Infection does not appear to be independently associated with hypertriglyceridemia. In the absence of liver dysfunction or growth retardation, there is no a priori reason to limit intravenous lipid use in the presence of infection. Close monitoring of triglyceride levels with adjustments in lipid dose is warranted, especially in small, sick newborns who are at highest risk for hypertriglyceridemia.
Related Concept Videos
Lipid Digestion
Development of Immunocompetence
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...

