Evidence map›Paper›PMID 31295363›Full record

Trial reportJournal of inherited metabolic disease2019

Higher dietary protein intake preserves lean body mass, lowers liver lipid deposition, and maintains metabolic control in participants with long-chain fatty acid oxidation disorders.

Melanie B Gillingham, Gabriela Elizondo, Annie Behrend, Dietrich Matern, Dale A Schoeller, Cary O Harding, Jonathan Q Purnell

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of inherited metabolic disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 3 pooled it
0.8field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 3 syntheses or guidelines pooled it, 14 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Clinical manifestations and management of fatty acid oxidation disorders.Reviews in endocrine & metabolic disorders · 2020
    Review
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

7 authors at 4 institutions in 1 country.

Melanie B GillinghamDepartment of Molecular and Medical Genetics, Oregon Health and Science University, Portland, Oregon.ORCID 0000-0003-0897-8268
Gabriela ElizondoDepartment of Molecular and Medical Genetics, Oregon Health and Science University, Portland, Oregon.
Annie BehrendDepartment of Molecular and Medical Genetics, Oregon Health and Science University, Portland, Oregon.
Dietrich MaternBiochemical Genetics Laboratory, Mayo Clinic, Rochester, Minnesota.
Dale A SchoellerDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin.
Cary O HardingDepartment of Molecular and Medical Genetics, Oregon Health and Science University, Portland, Oregon.
Jonathan Q PurnellKnight Cardiovascular Institute, Oregon Health and Science University, Portland, Oregon.
Oregon Health & Science University · USOregon Department of Human Services · USMayo Clinic · USUniversity of Wisconsin–Madison · US

Funding

Oregon Clinical and Translational Research Institute - The National COVID Cohort Collaborative (N3C)UL1TR002369 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Cynthia D Morris, Christopher G. Slatore · 2017 to 2026
$78.4M
Oregon Clinical and Translational Research InstituteUL1TR000128 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI ELLISON, DAVID H · 2012 to 2015
$28.7M
Role of Fatty Acid Oxidation Defects in Insulin SensitivityR01DK102813 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI GILLINGHAM, MELANIE B, PURNELL, JONATHAN Q. · 2015 to 2018
$2.4M
Fatty Acid Oxidation Disorders & Body Weight RegulationK01DK071869 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI GILLINGHAM, MELANIE B · 2006 to 2009
$421k
NCATS NIH HHS UL1 TR000128NCATS NIH HHS UL1 TR002369NIDDK NIH HHS K01 DK071869NIDDK NIH HHS R01 DK102813
6 · The paper itself

Abstract

Medical nutrition therapy for long-chain fatty acid oxidation disorders (LC-FAODs) currently emphasizes fasting avoidance, restricted dietary long-chain fatty acid intake, supplementation with medium chain triglycerides, and increased carbohydrate intake. We hypothesize that increasing dietary protein intake relative to carbohydrate intake would preserve metabolic control yet induce physical benefits including reduced hepatic lipogenesis. Therefore, we compared two dietary approaches with similar fat intake but different carbohydrate to protein ratios in participants diagnosed with LC-FAODs. Thirteen participants were enrolled and randomized into either a high-protein (PRO) or a high-carbohydrate (CHO) diet for 4 months. Baseline and 4-month assessments included body composition, ectopic lipid deposition, and resting energy expenditure. End of study assessments also included total energy expenditure, metabolic responses to oral feedings, and whole-body fatty acid oxidation capacity. At the end of the dietary intervention, both groups had similar energy expenditure, fat and glucose oxidation rates, and glucolipid responses to mixed meal and oral glucose loads. Neither dietary group experienced worsening symptoms related to their LC-FAOD. Compared to the CHO group, the PRO group exhibited increased blood levels of short-chain acylcarnitines, reduced intrahepatic lipid content, and maintained lean body mass while the CHO group lost lean mass. In patients with LC-FAODs, increasing protein intake maintained metabolic control, reduced liver fat without risk of metabolic decompensation, and helped preserve lean body mass. We propose that a modest increase in dietary protein along with fasting avoidance and fat restriction may improve body composition and energy expenditure in patients with LC-FAODs.

Indexed as

AdolescentAdultBody CompositionChildDietary CarbohydratesDietary ProteinsEnergy MetabolismFatty AcidsFemaleGlucoseHumansLipid MetabolismLipid Metabolism, Inborn ErrorsLiverMaleOxidation-ReductionDietary CarbohydratesDietary ProteinsFatty AcidsGlucoseTriglyceridesbody compositiondietary proteinenergy expenditurefatty acid oxidation disordersintrahepatic lipids

Identifiers

PMID31295363
PMCPMC7452215
OpenAlexW2959389076

What OpenQuestion holds

Textmetadata
LicenceTDM
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.