Cholic acid as a treatment for cerebrotendinous xanthomatosis in adults.


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 16 01 2019
accepted: 15 05 2019
revised: 29 04 2019
pubmed: 23 5 2019
medline: 10 1 2020
entrez: 23 5 2019
Statut: ppublish

Résumé

Cerebrotendineous xanthomatosis (CTX) is an autosomal recessive disorder of bile acids synthesis. Patients may present with a variety of clinical manifestations: bilateral cataract and chronic diarrhea during childhood, then occurrence of neurological debilitating symptoms in adulthood (cognitive decline, motor disorders). Plasma cholestanol is used as a diagnostic marker of CTX, and to monitor the response to the treatment. Current treatment for CTX is chenodeoxycholic acid (CDCA), which was reported to improve and/or stabilize clinical status and decrease levels of plasma cholestanol. Rare published reports have also suggested a potential efficacy of cholic acid (CA) in patients with CTX. In this retrospective Franco-Belgian multicentric study, we collected data from 12 patients treated with CA, evaluating their clinical status, cholestanol levels and adverse effects during the treatment period. The population was divided in two subgroups: treatment-naive (who never had CDCA prior to CA) and non-treatment-naive patients (who had CDCA prior to CA introduction). We found that treatment with CA significantly and strongly reduced cholestanol levels in all patients. Additionally, 10 out of 12 patients clinically improved or stabilized with CA treatment. Worsening was noted in one treatment-naïve patient and one non-treatment-naïve patient, but both patients experienced similar outcomes with CDCA treatment as well. No adverse effects were reported from patients with CA treatment, whereas elevated transaminases were observed in some patients while they were treated with CDCA. In conclusion, these findings suggest that CA may be a suitable alternative treatment for CTX, especially in patients with side effects related to CDCA.

Identifiants

pubmed: 31115677
doi: 10.1007/s00415-019-09377-y
pii: 10.1007/s00415-019-09377-y
doi:

Substances chimiques

Cholestanol 8M308U816E
Cholesterol 97C5T2UQ7J
Cholic Acid G1JO7801AE

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2043-2050

Commentaires et corrections

Type : CommentIn

Références

Science. 1999 May 21;284(5418):1362-5
pubmed: 10334992
Science. 1999 May 21;284(5418):1365-8
pubmed: 10334993
Arch Neurol. 2000 Apr;57(4):520-4
pubmed: 10768627
Biochem Med. 1975 Sep;14(1):57-74
pubmed: 1212241
Neurol Sci. 2004 Oct;25(4):185-91
pubmed: 15549503
Neurol Sci. 2006 Jun;27(2):143-9
pubmed: 16816916
J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S241-5
pubmed: 19125350
J Inherit Metab Dis. 2016 Jan;39(1):75-83
pubmed: 26153518
Eur J Pediatr. 2016 Jan;175(1):143-6
pubmed: 26156051
Mol Genet Metab. 2015 Dec;116(4):298-304
pubmed: 26643207
Orphanet J Rare Dis. 2016 Apr 16;11:41
pubmed: 27084087
J Neurol. 2017 May;264(5):862-874
pubmed: 28324197
J Inherit Metab Dis. 2017 Nov;40(6):771-781
pubmed: 28980151
J Inherit Metab Dis. 2018 Sep;41(5):799-807
pubmed: 29560583
J Clin Lipidol. 2018 Sep - Oct;12(5):1169-1178
pubmed: 30017468
Clin Neurol Neurosurg. 1987;89(3):169-75
pubmed: 3665290
Clin Chim Acta. 1985 Oct 31;152(1-2):115-22
pubmed: 4053393
N Engl J Med. 1984 Dec 27;311(26):1649-52
pubmed: 6504105
J Neurol Sci. 1994 Aug;125(1):22-8
pubmed: 7964884

Auteurs

Daniele Mandia (D)

Neurology Department, Reference Center for Lysosomal Diseases, Neurogenetics and Metabolism Unit, Hôpital Pitié-Salpêtrière, 47-83 boulevard de l'Hôpital, 75013, Paris, France.

Annabelle Chaussenot (A)

Service de Génétique Médicale, Centre de Référence des Maladies Mitochondriales, Hôpital de l'Archet 2, 151 Route de Saint-Antoine de Ginestière, B.P.3079, 06202, Nice Cedex 3, France.

Gérard Besson (G)

Unité Neurologie générale, Pôle Psychiatrie, Neurologie et Rééducation Neurologique, Service de Neurologie, CHU de Grenoble site Nord-Hôpital Albert Michallon, boulevard de la Chantourne, CS10217, 38043, Grenoble Cedex 9, France.

Foudil Lamari (F)

UF Biochimie des maladies neurométaboliques-Département de Biochimie métabolique, Hôpital Pitié-Salpêtrière, 47-83 boulevard de l'Hôpital, 75013, Paris, France.

Giovanni Castelnovo (G)

Neurological Department, Centre hospitalo-universitaire Caremeau, place du Professeur Debré, 30029, Nîmes Cedex, France.

Jonathan Curot (J)

Department of Neurology, Toulouse University Hospital, 31059, Toulouse, France.
Centre de Recherche Cerveau et Cognition, CNRS, UMR5549, 31052, Toulouse, France.

Fanny Duval (F)

Department of Neurology (Nerve-Muscle Unit), CHU Bordeaux (Pellegrin Hospital), 33076, Bordeaux, France.

Philippe Giral (P)

Inserm, Institute of Cardiometabolism and Nutrition (ICAN), UMR_S1166, Sorbonne Université, Paris, France.
Department of Endocrinology-Metabolism, AP-HP, Hôpital de la Pitié, Paris, France.

Jean-Michel Lecerf (JM)

Service de Nutrition & Activité Physique, Institut Pasteur de Lille, 1, rue du professeur Calmette, 59019, Lille, France.
Service de Médecine Interne, Hôpital Claude Huriez-CHRU de Lille, 59037, Lille, France.

Dominique Roland (D)

Institut de Pathologie et de Génétique ASBL, Centre Agréé des Maladies Héréditaires du Métabolisme, Centre de Génétique Humaine, Avenue Georges Lemaitre, 25, 6041, Gosselies, Belgium.

Heloise Pierdet (H)

Neurology Department, Reference Center for Lysosomal Diseases, Neurogenetics and Metabolism Unit, Hôpital Pitié-Salpêtrière, 47-83 boulevard de l'Hôpital, 75013, Paris, France.

Claire Douillard (C)

Endocrinology and Metabolism Department, Lille University Hospital, C. Huriez Hospital, 1, rue Polonovski, 59037, Lille Cedex, France.

Yann Nadjar (Y)

Neurology Department, Reference Center for Lysosomal Diseases, Neurogenetics and Metabolism Unit, Hôpital Pitié-Salpêtrière, 47-83 boulevard de l'Hôpital, 75013, Paris, France. yann.nadjar@aphp.fr.

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