Evidence map›Paper›PMID 30889905›Full record

ArticleNutrients2019

Choline Supplementation in Cystic Fibrosis-The Metabolic and Clinical Impact.

Wolfgang Bernhard, Robert Lange, Ute Graepler-Mainka, Corinna Engel, Jürgen Machann, Verena Hund, Anna Shunova, Andreas Hector, Joachim Riethmüller

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 28 citations in OpenAlex.

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  14. The Effect ofMetabolites · 2024
    Article
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  16. Choline supplements: An update.Frontiers in endocrinology · 2023
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Wolfgang BernhardDepartment of Neonatology, Children's Hospital, Eberhard-Karls-University, 72076 Tübingen, Germany. wolfgang.bernhard@med.uni-tuebingen.de.
Robert LangeDepartment of Neonatology, Children's Hospital, Eberhard-Karls-University, 72076 Tübingen, Germany. robert.lange@student.uni-tuebingen.de.
Ute Graepler-MainkaDepartment of General Pediatrics, Hematology and Oncology, Children's Hospital, Eberhard-Karls-University, 72076 Tübingen, Germany. ute.graepler-mainka@med.uni-tuebingen.de.
Corinna EngelCenter for Pediatric Clinical Studies, Children's Hospital, Eberhard-Karls-University, 72076 Tübingen, Germany. corinna.engel@med.uni-tuebingen.de.
Jürgen MachannDepartment of Diagnostic and Interventional Radiology, Medical Faculty, Eberhard-Karls-University, 72076 Tübingen, Germany. juergen.machann@med.uni-tuebingen.de.
Verena HundUniversity Pharmacy, Medical Faculty, Eberhard-Karls-University, 72076 Tübingen, Germany. verena.hund@med.uni-tuebingen.de.
Anna ShunovaDepartment of Neonatology, Children's Hospital, Eberhard-Karls-University, 72076 Tübingen, Germany. anna.shunova@med.uni-tuebingen.de.
Andreas HectorDepartment of General Pediatrics, Hematology and Oncology, Children's Hospital, Eberhard-Karls-University, 72076 Tübingen, Germany. Andreas.Hector@med.uni-tuebingen.de.
Joachim RiethmüllerDepartment of General Pediatrics, Hematology and Oncology, Children's Hospital, Eberhard-Karls-University, 72076 Tübingen, Germany. wolfgangbernhard246@gmail.com.
University Children's Hospital Tübingen · DEUniversity of Tübingen · DE

Funding

Margarete Müller Bull Stiftung, Stuttgart, Gertmany Phos-CF II
6 · The paper itself

Abstract

backgroundCholine is essential for the synthesis of liver phosphatidylcholine (PC), parenchymal maintenance, bile formation, and lipoprotein assembly to secrete triglycerides. In choline deficiency, the liver accretes choline/PC at the expense of lung tissue, thereby impairing pulmonary PC homoeostasis. In cystic fibrosis (CF), exocrine pancreas insufficiency results in impaired cleavage of bile PC and subsequent fecal choline loss. In these patients, the plasma choline concentration is low and correlates with lung function. We therefore investigated the effect of choline supplementation on plasma choline/PC concentration and metabolism, lung function, and liver fat.

methods10 adult male CF patients were recruited (11/2014⁻1/2016), and orally supplemented with 3 × 1 g choline chloride for 84 (84⁻91) days. Pre-/post-supplementation, patients were spiked with 3.6 mg/kg [methyl-D₉]choline chloride to assess choline/PC metabolism. Mass spectrometry, spirometry, and hepatic nuclear resonance spectrometry served for analysis.

resultsSupplementation increased plasma choline from 4.8 (4.1⁻6.2) µmol/L to 10.5 (8.5⁻15.5) µmol/L at d84 (

conclusionsCholine supplementation normalized plasma choline concentration and increased choline-containing PC precursor pools in adult CF patients. Improved lung function and decreased liver fat suggest that in CF correcting choline deficiency is clinically important. Choline supplementation of CF patients should be further investigated in randomized, placebo-controlled trials.

Indexed as

AdolescentAdultCholineCholine DeficiencyCystic FibrosisDietary SupplementsExocrine Pancreatic InsufficiencyFatty LiverForced Expiratory VolumeHumansLipid MetabolismLiverLungMaleMiddle AgedPhosphatidylcholinesCholinePhosphatidylcholinesTriglyceridescholine deficiencycholine supplementationcystic fibrosisliverlung functionmagnetic resonance spectroscopystable isotope labelingsteatosis

Identifiers

PMID30889905
PMCPMC6471815
OpenAlexW2921470996

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.