Evidence map›Paper›PMID 27590926›Full record

ArticleMolecular genetics and metabolism2016

Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disorders.

J Vockley, J Charrow, J Ganesh, M Eswara, G A Diaz, E McCracken, R Conway, G M Enns, J Starr, R Wang and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular genetics and metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Guideline
  2. Trial
  3. Trial
  4. No effect of triheptanoin on exercise performance in McArdle disease.Annals of clinical and translational neurology · 2019
    Trial
  5. Trial
  6. Trial
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. The Physiological and Pathological Role of Acyl-CoA Oxidation.International journal of molecular sciences · 2023
    Review
  17. Article
  18. Review
  19. Article
  20. 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

13 authors at 9 institutions in 1 country.

J VockleyChildren's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA. Electronic address: vockleyg@upmc.edu.
J CharrowAnn & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
J GaneshCooper University, Camden, NJ, USA.
M EswaraSutter Medical Center, Sacramento, CA, USA.
G A DiazMt. Sinai School of Medicine, New York, NY, USA.
E McCrackenChildren's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
R ConwayChildren's Hospital of Michigan, Detroit, MI, USA.
G M EnnsLucile Packard Children's Hospital Stanford, Palo Alto, CA, USA.
J StarrChildren's Hospital of Orange County, Orange, CA, USA.
R WangChildren's Hospital of Orange County, Orange, CA, USA.
J E AbdenurChildren's Hospital of Orange County, Orange, CA, USA.
J Sanchez-de-ToledoChildren's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
D L MarsdenUltragenyx Pharmaceutical, Inc., Novato, CA, USA.
Children's Hospital of Orange County · USChildren's Hospital of Pittsburgh · USChildren's Hospital of Michigan · USCooper University Hospital · USLucile Packard Children's Hospital · USLurie Children's Hospital · USMount Sinai Hospital · USSutter Medical Center · USUltragenyx Pharmaceutical (United States) · US

Funding

Inborn Errors of Long Chain Fat MetabolismR01DK078775 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VOCKLEY, GERARD · 2008 to 2019
$4.5M
NIDDK NIH HHS R01 DK078775
6 · The paper itself

Abstract

Long-chain fatty acid oxidation disorders (LC-FAOD) can cause cardiac hypertrophy and cardiomyopathy, often presenting in infancy, typically leading to death or heart transplant despite ongoing treatment. Previous data on triheptanoin treatment of cardiomyopathy in LC-FAOD suggested a clinical benefit on heart function during acute failure. An additional series of LC-FAOD patients with critical emergencies associated with cardiomyopathy was treated with triheptanoin under emergency treatment or compassionate use protocols. Case reports from 10 patients (8 infants) with moderate or severe cardiomyopathy associated with LC-FAOD are summarized. The majority of these patients were detected by newborn screening, with follow up confirmatory testing, including mutation analysis; all patients were managed with standard treatment, including medium chain triglyceride (MCT) oil. While on this regimen, they presented with acute heart failure requiring hospitalization and cardiac support (ventilation, ECMO, vasopressors) and, in some cases, resuscitation. The patients discontinued MCT oil and began treatment with triheptanoin, an investigational drug. Triheptanoin is expected to provide anaplerotic metabolites, to replace deficient TCA cycle intermediates and improve effective energy metabolism. Cardiac function was measured by echocardiography and ejection fraction (EF) was assessed. EF was moderately to severely impaired prior to triheptanoin treatment, ranging from 12-45%. Improvements in EF began between 2 and 21days following initiation of triheptanoin, and peaked at 33-71%, with 9 of 10 patients achieving EF in the normal range. Continued treatment was associated with longer-term stabilization of clinical signs of cardiomyopathy. The most common adverse event observed was gastrointestinal distress. Of the 10 patients, 7 have continued on treatment, 1 elected to discontinue due to tolerability issues, and 2 patients died from other causes. Two of the case histories illustrate that cardiomyopathy may also develop later in childhood and/or persist into adulthood. Overall, the presented cases suggest a therapeutic effect of triheptanoin in the management of acute cardiomyopathy associated with LC-FAOD.

Indexed as

AdolescentCardiomyopathiesChildChild, PreschoolClinical Trials as TopicEnergy MetabolismFatty AcidsFemaleHumansInfantInfant, NewbornLipid Metabolism, Inborn ErrorsMaleOxidation-ReductionTriglyceridesFatty AcidsTriglyceridestriheptanoinCardiomyopathyFatty acid oxidation disordersMetabolic disordersTriheptanoin

Identifiers

PMID27590926
PMCPMC5083220
OpenAlexW2518161914

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.