Potential for Omega-3 Fatty Acids to Protect against the Adverse Effect of Phytosterols: Comparing Laboratory Outcomes in Adult Patients on Home Parenteral Nutrition Including Different Lipid Emulsions.

fish oil inflammation lipid emulsion liver parenteral nutrition phytosterol

Journal

Biology
ISSN: 2079-7737
Titre abrégé: Biology (Basel)
Pays: Switzerland
ID NLM: 101587988

Informations de publication

Date de publication:
24 Nov 2022
Historique:
received: 24 10 2022
revised: 19 11 2022
accepted: 21 11 2022
entrez: 23 12 2022
pubmed: 24 12 2022
medline: 24 12 2022
Statut: epublish

Résumé

the effect on liver function markers and inflammation of the different content of phytosterols in lipid emulsions (LEs) used in the parenteral nutrition (PN) regimen of adult home PN (HPN) patients is not clear. plasma phytosterol and cytokine concentrations, fatty acid composition, liver function markers, and triglycerides were measured in 58 adult HPN patients receiving one of three different LEs (soybean oil-based: Intralipid; olive oil-based: ClinOleic; containing fish oil: SMOFLipid). patients receiving Intralipid had higher plasma campesterol and stigmasterol concentrations than those receiving ClinOleic or SMOFLipid. Plasma sterol concentrations were not different between patients receiving ClinOleic and SMOFLipid. Differences in plasma fatty acids reflected the fatty acid composition of the LEs. Markers of liver function did not differ among the three groups. Blood triglycerides were higher with ClinOleic than with Intralipid or SMOFLipid. Total bilirubin correlated positively with the plasma concentrations of two of the phytosterols, ALT correlated positively with one, AST with one, and GGT with three. liver function markers correlate with plasma plant sterol concentrations in adult HPN patients. Adult HPN patients receiving SMOFLipid are more likely to have liver function markers and triglycerides within the normal range than those receiving ClinOleic or Intralipid. The omega-3 fatty acids in SMOFLipid may act to mitigate the adverse effects of plant sterols on liver function.

Sections du résumé

BACKGROUND BACKGROUND
the effect on liver function markers and inflammation of the different content of phytosterols in lipid emulsions (LEs) used in the parenteral nutrition (PN) regimen of adult home PN (HPN) patients is not clear.
METHODS METHODS
plasma phytosterol and cytokine concentrations, fatty acid composition, liver function markers, and triglycerides were measured in 58 adult HPN patients receiving one of three different LEs (soybean oil-based: Intralipid; olive oil-based: ClinOleic; containing fish oil: SMOFLipid).
RESULTS RESULTS
patients receiving Intralipid had higher plasma campesterol and stigmasterol concentrations than those receiving ClinOleic or SMOFLipid. Plasma sterol concentrations were not different between patients receiving ClinOleic and SMOFLipid. Differences in plasma fatty acids reflected the fatty acid composition of the LEs. Markers of liver function did not differ among the three groups. Blood triglycerides were higher with ClinOleic than with Intralipid or SMOFLipid. Total bilirubin correlated positively with the plasma concentrations of two of the phytosterols, ALT correlated positively with one, AST with one, and GGT with three.
CONCLUSIONS CONCLUSIONS
liver function markers correlate with plasma plant sterol concentrations in adult HPN patients. Adult HPN patients receiving SMOFLipid are more likely to have liver function markers and triglycerides within the normal range than those receiving ClinOleic or Intralipid. The omega-3 fatty acids in SMOFLipid may act to mitigate the adverse effects of plant sterols on liver function.

Identifiants

pubmed: 36552209
pii: biology11121699
doi: 10.3390/biology11121699
pmc: PMC9774711
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Sylwia Osowska (S)

Applied Pharmacy Department, Warsaw Medical University, 02-097 Warsaw, Poland.
Centre of Clinical Nutrition, Pirogow Hospital, 90-531 Lodz, Poland.

Marek Kunecki (M)

Centre of Clinical Nutrition, Pirogow Hospital, 90-531 Lodz, Poland.

Jacek Sobocki (J)

Department of General Surgery and Clinical Nutrition, Centre for Postgraduate Medical Education, 00-416 Warsaw, Poland.

Joanna Tokarczyk (J)

Centre of Clinical Nutrition, Pirogow Hospital, 90-531 Lodz, Poland.

Krystyna Majewska (K)

Department of General Surgery and Clinical Nutrition, Centre for Postgraduate Medical Education, 00-416 Warsaw, Poland.

Magdalena Burkacka (M)

Centre of Clinical Nutrition, Pirogow Hospital, 90-531 Lodz, Poland.

Marek Radkowski (M)

Department of Immunopathology, Warsaw Medical University, 02-097 Warsaw, Poland.

Magdalena Makarewicz-Wujec (M)

Institute of Pharmaceutical Care, University of Economics and Human Sciences, 01-043 Warsaw, Poland.

Helena L Fisk (HL)

School of Human Development and Health, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.

Sultan Mashnafi (S)

Department of Nutrition and Movement Sciences, NUTRIM School of Translational Research in Metabolism, Maastricht University, 6200 MD Maastricht, The Netherlands.

Sabine Baumgartner (S)

Department of Nutrition and Movement Sciences, NUTRIM School of Translational Research in Metabolism, Maastricht University, 6200 MD Maastricht, The Netherlands.

Jogchum Plat (J)

Department of Nutrition and Movement Sciences, NUTRIM School of Translational Research in Metabolism, Maastricht University, 6200 MD Maastricht, The Netherlands.

Philip C Calder (PC)

School of Human Development and Health, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
NIHR Southampton Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust and University of Southampton, Southampton SO16 6YD, UK.

Classifications MeSH