Effect of changing the lipid component of home parenteral nutrition in adults.


Journal

Clinical nutrition (Edinburgh, Scotland)
ISSN: 1532-1983
Titre abrégé: Clin Nutr
Pays: England
ID NLM: 8309603

Informations de publication

Date de publication:
06 2019
Historique:
received: 18 01 2018
revised: 09 05 2018
accepted: 27 05 2018
pubmed: 17 6 2018
medline: 2 6 2020
entrez: 17 6 2018
Statut: ppublish

Résumé

The effect of different lipid emulsions (LEs) within the parenteral nutrition (PN) regimen of adult home PN (HPN) patients is not clear. This study investigated the effect of changing adult HPN patients from a soybean oil based LE (Intralipid) to either a fish oil containing LE (providing n-3 fatty acids) (SMOFLipid) or an olive oil based LE (ClinOleic). Thirty two adults receiving long-term HPN with Intralipid as the LE were transferred to receive either SMOFLipid (n = 13) or ClinOleic (n = 19) for 60 days. Liver function markers, cholesterol, triglycerides, a full profile of fatty acids, and several cytokines were measured at study entry and after 60 days. SMOFLipid did not affect liver function markers, blood lipids or plasma cytokines. ClinOleic lowered both gamma-glutamyltranspeptidase (P = 0.044) and interleukin-8 (P = 0.030) concentrations. Both LEs induced marked changes in the fatty acid profile of plasma. SMOFLipid resulted in significant decreases in the proportions of linoleic acid, several other n-6 fatty acids and the essential fatty acid (EFA) deficiency indicator mead acid and significant increases in the proportions of the n-3 fatty acids eicosapentaenoic acid and docosahexaenoic acid. ClinOleic resulted in significant decreases in the proportions of some saturated fatty acids, linoleic acid, several n-6 fatty acids, all n-3 fatty acids and mead acid and a significant increase in the proportion of oleic acid. The ratio of mead to arachidonic acid in plasma was not altered by either SMOFLipid or ClinOleic. No patient had a mead acid to arachidonic acid ratio of >0.2, the cut-off used to indicate EFA deficiency. Both SMOFLipid and ClinOleic significantly alter the fatty acid profile of plasma in adult HPN patients previously using Intralipid. Neither LE induces EFA deficiency in these patients. SMOFLipid did not alter liver function markers or inflammation. In contrast, ClinOleic decreased some, though not all, markers of liver function and inflammation. SMOFLipid and ClinOleic may both be considered for use in adult HPN patients.

Sections du résumé

BACKGROUND
The effect of different lipid emulsions (LEs) within the parenteral nutrition (PN) regimen of adult home PN (HPN) patients is not clear. This study investigated the effect of changing adult HPN patients from a soybean oil based LE (Intralipid) to either a fish oil containing LE (providing n-3 fatty acids) (SMOFLipid) or an olive oil based LE (ClinOleic).
METHODS
Thirty two adults receiving long-term HPN with Intralipid as the LE were transferred to receive either SMOFLipid (n = 13) or ClinOleic (n = 19) for 60 days. Liver function markers, cholesterol, triglycerides, a full profile of fatty acids, and several cytokines were measured at study entry and after 60 days.
RESULTS
SMOFLipid did not affect liver function markers, blood lipids or plasma cytokines. ClinOleic lowered both gamma-glutamyltranspeptidase (P = 0.044) and interleukin-8 (P = 0.030) concentrations. Both LEs induced marked changes in the fatty acid profile of plasma. SMOFLipid resulted in significant decreases in the proportions of linoleic acid, several other n-6 fatty acids and the essential fatty acid (EFA) deficiency indicator mead acid and significant increases in the proportions of the n-3 fatty acids eicosapentaenoic acid and docosahexaenoic acid. ClinOleic resulted in significant decreases in the proportions of some saturated fatty acids, linoleic acid, several n-6 fatty acids, all n-3 fatty acids and mead acid and a significant increase in the proportion of oleic acid. The ratio of mead to arachidonic acid in plasma was not altered by either SMOFLipid or ClinOleic. No patient had a mead acid to arachidonic acid ratio of >0.2, the cut-off used to indicate EFA deficiency.
CONCLUSION
Both SMOFLipid and ClinOleic significantly alter the fatty acid profile of plasma in adult HPN patients previously using Intralipid. Neither LE induces EFA deficiency in these patients. SMOFLipid did not alter liver function markers or inflammation. In contrast, ClinOleic decreased some, though not all, markers of liver function and inflammation. SMOFLipid and ClinOleic may both be considered for use in adult HPN patients.

Identifiants

pubmed: 29907355
pii: S0261-5614(18)30214-0
doi: 10.1016/j.clnu.2018.05.028
pii:
doi:

Substances chimiques

ClinOleic 0
Cytokines 0
Emulsions 0
Fat Emulsions, Intravenous 0
Fatty Acids 0
Fish Oils 0
Olive Oil 0
Phospholipids 0
Plant Oils 0
Triglycerides 0
soybean oil, phospholipid emulsion 0
Soybean Oil 8001-22-7
Cholesterol 97C5T2UQ7J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1355-1361

Informations de copyright

Copyright © 2018. Published by Elsevier Ltd.

Auteurs

Sylwia Osowska (S)

Department of General Surgery and Clinical Nutrition, Warsaw Medical University, Warsaw, Poland. Electronic address: sylwiao@hotmail.com.

Marek Kunecki (M)

Centre of Clinical Nutrition, Pirogow Hospital, Lodz, Poland.

Jacek Sobocki (J)

Department of General Surgery and Clinical Nutrition, Warsaw Medical University, Warsaw, Poland.

Joanna Tokarczyk (J)

Centre of Clinical Nutrition, Pirogow Hospital, Lodz, Poland.

Krystyna Majewska (K)

Department of General Surgery and Clinical Nutrition, Warsaw Medical University, Warsaw, Poland.

Mohamed Omidi (M)

Department of General Surgery and Clinical Nutrition, Warsaw Medical University, Warsaw, Poland.

Marek Radkowski (M)

Immunopathology Department, Warsaw Medical University, Warsaw, Poland.

Helena L Fisk (HL)

Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.

Philip C Calder (PC)

Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom; NIHR Southampton Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust, University of Southampton, Southampton, United Kingdom.

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Classifications MeSH