Evidence and Perspectives for Choline Supplementation during Parenteral Nutrition-A Narrative Review.

betaine cholestasis choline hepatosteatosis liver disease methyl donors parenchymal integrity parenteral nutrition phosphatidylcholine preterm infants

Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
14 Jun 2024
Historique:
received: 02 05 2024
revised: 03 06 2024
accepted: 09 06 2024
medline: 27 6 2024
pubmed: 27 6 2024
entrez: 27 6 2024
Statut: epublish

Résumé

Choline is an essential nutrient, with high requirements during fetal and postnatal growth. Tissue concentrations of total choline are tightly regulated, requiring an increase in its pool size proportional to growth. Phosphatidylcholine and sphingomyelin, containing a choline headgroup, are constitutive membrane phospholipids, accounting for >85% of total choline, indicating that choline requirements are particularly high during growth. Daily phosphatidylcholine secretion via bile for lipid digestion and very low-density lipoproteins for plasma transport of arachidonic and docosahexaenoic acid to other organs exceed 50% of its hepatic pool. Moreover, phosphatidylcholine is required for converting pro-apoptotic ceramides to sphingomyelin, while choline is the source of betaine as a methyl donor for creatine synthesis, DNA methylation/repair and kidney function. Interrupted choline supply, as during current total parenteral nutrition (TPN), causes a rapid drop in plasma choline concentration and accumulating deficit. The American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.) defined choline as critical to all infants requiring TPN, claiming its inclusion in parenteral feeding regimes. We performed a systematic literature search in Pubmed with the terms "choline" and "parenteral nutrition", resulting in 47 relevant publications. Their results, together with cross-references, are discussed. While studies on parenteral choline administration in neonates and older children are lacking, preclinical and observational studies, as well as small randomized controlled trials in adults, suggest choline deficiency as a major contributor to acute and chronic TPN-associated liver disease, and the safety and efficacy of parenteral choline administration for its prevention. Hence, we call for choline formulations suitable to be added to TPN solutions and clinical trials to study their efficacy, particularly in growing children including preterm infants.

Identifiants

pubmed: 38931230
pii: nu16121873
doi: 10.3390/nu16121873
pii:
doi:

Substances chimiques

Choline N91BDP6H0X

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : University of Tübingen
ID : Open Access Publishing Fund

Auteurs

Wolfgang Bernhard (W)

Department of Neonatology, University Children's Hospital, 72076 Tübingen, Germany.

Katrin A Böckmann (KA)

Department of Neonatology, University Children's Hospital, 72076 Tübingen, Germany.

Michaela Minarski (M)

Department of Neonatology, University Children's Hospital, 72076 Tübingen, Germany.

Cornelia Wiechers (C)

Department of Neonatology, University Children's Hospital, 72076 Tübingen, Germany.

Annegret Busch (A)

Pharmaceutical Department, University Hospital, 72076 Tübingen, Germany.

Daniela Bach (D)

Pharmaceutical Department, University Hospital, 72076 Tübingen, Germany.

Christian F Poets (CF)

Department of Neonatology, University Children's Hospital, 72076 Tübingen, Germany.

Axel R Franz (AR)

Department of Neonatology, University Children's Hospital, 72076 Tübingen, Germany.
Center for Pediatric Clinical Studies, University Children's Hospital, 72076 Tübingen, Germany.

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Classifications MeSH