Evidence map›Paper›PMID 39375714›Full record

ArticleItalian journal of pediatrics2024

Triheptanoin in patients with long-chain fatty acid oxidation disorders: clinical experience in Italy.

Francesco Porta, Arianna Maiorana, Vincenza Gragnaniello, Elena Procopio, Serena Gasperini, Roberta Taurisano, Marco Spada, Carlo Dionisi-Vici, Alberto Burlina

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Article in Italian journal of pediatrics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

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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.

Francesco PortaDepartment of Paediatrics, University of Turin, Turin, Italy.
Arianna MaioranaDivision of Metabolic Diseases and Hepatology, Bambino Gesù Children‛s Hospital IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy.
Vincenza GragnanielloDivision of Inherited Metabolic Diseases, Department of Women and Children‛s Health, Reference Centre for Expanded Newborn Screening, University Hospital, Padua, Italy.
Elena ProcopioMetabolic and Neuromuscular Unit, Meyer Children‛s Hospital IRCCS, Florence, Italy.
Serena GasperiniDepartment of Paediatrics, Fondazione IRCCS San Gerardo Dei Tintori, Monza, Italy.
Roberta TaurisanoDivision of Metabolic Diseases and Hepatology, Bambino Gesù Children‛s Hospital IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy.
Marco SpadaDepartment of Paediatrics, University of Turin, Turin, Italy.
Carlo Dionisi-Vici *Division of Metabolic Diseases and Hepatology, Bambino Gesù Children‛s Hospital IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy. carlo.dionisivici@opbg.net.
Alberto Burlina *Division of Inherited Metabolic Diseases, Department of Women and Children‛s Health, Reference Centre for Expanded Newborn Screening, University Hospital, Padua, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLong-chain fatty acid oxidation disorders (LC-FAOD) are rare and potentially life-threatening diseases that cause deficient energy production and accumulation of toxic metabolites. Despite dietary management, adherence to maximum fasting guidelines, restricted long-chain triglyceride intake and supplementation with medium-chain triglyceride (MCT) oil (current standard of care), most patients experience recurrent decompensation episodes that can require hospitalisation. Herein, we analysed the effectiveness and safety of triheptanoin (a highly purified, synthetic medium odd-chain triglyceride) treatment in a cohort of Italian patients with LC-FAOD.

methodsThis retrospective, nationwide study included nine patients with LC-FAOD who switched from standard therapy with MCT oil to triheptanoin oral liquid. Data were collected between 2018 and 2022. Clinical outcome measures were the number and duration of intercurrent catabolic episodes and number and duration of metabolic decompensation episodes requiring hospitalisation. Creatine kinase (CK) levels and treatment-related adverse effects were also reported.

resultsPatients were provided a mean ± standard deviation (SD) triheptanoin dose of 1.5 ± 0.9 g/kg/day in four divided administrations, which accounted for 23.9 ± 8.9% of patients' total daily caloric intake. Triheptanoin treatment was started between 2.7 and 16 years of age and was continued for 2.2 ± 0.9 years. The number of intercurrent catabolic episodes during triheptanoin treatment was significantly lower than during MCT therapy (4.3 ± 5.3 vs 22.0 ± 22.2; p = 0.034), as were the number of metabolic decompensations requiring hospitalisation (mean ± SD: 2.0 ± 2.5 vs 18.3 ± 17.7; p = 0.014), and annualised hospitalisation rates and duration. Mean CK levels (outside metabolic decompensation episodes) were lower with triheptanoin treatment versus MCT oil for seven patients. No intensive care unit admissions were required during triheptanoin treatment. Epigastric pain and diarrhoea were recorded as adverse effects during both MCT and triheptanoin treatment.

conclusionsThe significant improvement in clinical outcome measures after the administration of triheptanoin highlights that this treatment approach can be more effective than MCT supplementation in patients with LC-FAOD. Triheptanoin was well tolerated and decreased the number of intercurrent catabolic episodes, metabolic decompensation episodes requiring hospitalisation, and the annualised rate and duration of hospitalisations.

Indexed as

Lipid Metabolism, Inborn ErrorsTriglyceridesAdolescentChildChild, PreschoolFatty AcidsFemaleHumansItalyMaleRetrospective StudiesTreatment OutcomeFatty AcidsTriglyceridestriheptanoinInherited metabolic disordersLong-chain fatty acid oxidation disordersMedium-chain triglyceride oilTriheptanoin

Identifiers

PMID39375714
PMCPMC11460043

What Socratic holds

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Registered trials

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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 Socratic graph.