Effect of Triheptanoin on Caudate Atrophy and Motor Scores in Patients With Early-Stage Huntington Disease

This study provides Class I evidence that triheptanoin does not slow caudate atrophy compared with placebo over 6 months in patients with early HD.

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Publication Details

Journal
Neurology
Published
2024-12-30
DOI
https://doi.org/10.1212/wnl.0000000000210194
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Effect of Triheptanoin on Caudate Atrophy and Motor Scores in Patients With Early-Stage Huntington Disease

Mariana Atencio, Fleur Veldkamp, Camille Giron, Alexandra Dürr et al.
4 links
Neurology
Genetic Neurodegenerative Diseases
article

Effect of Triheptanoin on Caudate Atrophy and Motor Scores in Patients With Early-Stage Huntington Disease

Mariana Atencio, Fleur Veldkamp, Camille Giron, Alexandra Dürr, Marie-Pierre Luton, Élodie Hainque, Fanny Mochel, Isaac Adanyeguh, Chris Ottolenghi, Kasper F. van der Zwaan, Abdourahmane Diallo, Emma M. Coppen, Aurélie Méneret, Milou Jacobs, Éric Vicaut, Raymund A.C. Roos, Magali Barbier, Rabab Debs
article en

Abstract

This study provides Class I evidence that triheptanoin does not slow caudate atrophy compared with placebo over 6 months in patients with early HD.

NeurologyVol. 104(2)
Centre National de la Recherche Scientifique (FR), University of Minnesota (US), Inserm (FR), Université Paris Cité (FR), Leiden University Medical Center (NL), Sorbonne Université (FR), Assistance Publique – Hôpitaux de Paris (FR), Hôpital Fernand-Widal (FR), Institut de Psychiatrie et Neurosciences de Paris (FR), Institut du Cerveau (FR), Resonance Research (United States) (US), Institut des Maladies Génétiques Imagine (FR)
Biogen, Ultragenyx Pharmaceutical, Agence Nationale de la Recherche, Servier, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 74%
Genetic Neurodegenerative Diseases
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