Evidence map›Paper›PMID 31240164›Full record

ArticleJIMD reports2019

Formation of 3-hydroxyglutaric acid in glutaric aciduria type I: in vitro participation of medium chain acyl-CoA dehydrogenase.

Verena Peters, Marina Morath, Matthias Mack, Michael Liesert, Wolfgang Buckel, Georg F Hoffmann, Jerry Vockley, Sandro Ghisla, Johannes Zschocke

Open access · goldAbstract read
In one paragraph

Article in JIMD reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Odd-Chain Dicarboxylic Acid Feeding Produces a Glutaric Aciduria Type 1-Like Metabolic Signature in Mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  3. Article
  4. Human wild-type and D76N βFASEB bioAdvances · 2023
    Article
  5. Article
  6. Article
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 6 institutions in 3 countries.

Verena PetersCenter für Paediatric and Adolescent Medicine University of Heidelberg Germany.ORCID https://orcid.org/0000-0002-4649-0848
Marina MorathCenter für Paediatric and Adolescent Medicine University of Heidelberg Germany.
Matthias MackInstitut für Technische Mikrobiologie Hochschule Mannheim Germany.
Michael LiesertLaboratorium für Mikrobiologie, Fachbereich Biologie Philipps-Universität Marburg Germany.
Wolfgang BuckelLaboratorium für Mikrobiologie, Fachbereich Biologie Philipps-Universität Marburg Germany.
Georg F HoffmannCenter für Paediatric and Adolescent Medicine University of Heidelberg Germany.
Jerry VockleyDepartment of Pediatric and Human Genetics Children's Hospital of Pittsburgh and University of Pittsburgh Pittsburgh Pennsylvania.
Sandro GhislaDepartment of Biology, Section of Natural Sciences Universität Konstanz Germany.
Johannes ZschockeDivision of Human Genetics Medical University Innsbruck Austria.ORCID https://orcid.org/0000-0002-0046-8274
Heidelberg University · DEPhilipps University of Marburg · DEInnsbruck Medical University · ATTechnische Hochschule Mannheim · DEUniversity of Konstanz · DEUniversity of Pittsburgh · US

Funding

Characterization of Branched Chain Amino Acid Metabolism and Its DeficiencyR01DK109907 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VOCKLEY, GERARD · 2016 to 2024
$4.1M
NIDDK NIH HHS R01 DK109907
6 · The paper itself

Abstract

3-Hydroxyglutaric acid (3-OH-GA) in urine has been identified as the most reliable diagnostic marker for glutaric aciduria type I (GA I). We showed that hydratation of glutaconyl-CoA to 3-hydroxyglutaryl-CoA, which is subsequently hydrolyzed to 3-OH-GA, is efficiently catalyzed by 3-methylglutaconyl-CoA hydratase (3-MGH). We have now investigated whether mitochondrial acyl-CoA-dehydrogenases can convert glutaryl-CoA to glutaconyl-CoA. Short-chain acyl-CoA dehydrogenase (SCAD), medium-chain acyl-CoA dehydrogenase (MCAD), and long-chain acyl-CoA dehydrogenase (LCAD) accepted glutaryl-CoA as a substrate. The highest

Indexed as

3‐hydroxyglutaric acidacyl‐CoA dehydrogenaseglutaconyl‐CoAglutaric aciduria type Iglutaryl‐CoA

Identifiers

PMID31240164
PMCPMC6498835
OpenAlexW2944170987

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.