Cholic acid as a treatment for cerebrotendinous xanthomatosis in adults

被引:28
|
作者
Mandia, Daniele [1 ]
Chaussenot, Annabelle [2 ]
Besson, Gerard [3 ]
Lamari, Foudil [4 ]
Castelnovo, Giovanni [5 ]
Curot, Jonathan [6 ,7 ]
Duval, Fanny [8 ]
Giral, Philippe [9 ,10 ]
Lecerf, Jean-Michel [11 ,12 ]
Roland, Dominique [13 ]
Pierdet, Heloise [1 ]
Douillard, Claire [14 ]
Nadjar, Yann [1 ]
机构
[1] Hop La Pitie Salpetriere, Neurol Dept, Reference Ctr Lysosomal Dis, Neurogenet & Metab Unit, 47-83 Blvd Hop, F-75013 Paris, France
[2] Hop Archet 2, Serv Genet Med, Ctr Reference Malad Mitochondriales, 151 Route St Antoine Ginestiere,BP 3079, F-06202 Nice 3, France
[3] CHU Grenoble, Unite Neurol Gen, Pole Psychiat Neurol & Reeduc Neurol, Serv Neurol, Site Nord Hop Albert Michallon,Blvd Chantourne, F-38043 Grenoble 9, France
[4] Hop La Pitie Salpetriere, Biochim Malad Neurometabol, Dept Biochim Metabol, 47-83 Blvd Hop, F-75013 Paris, France
[5] CHU Caremeau, Neurol Dept, Pl Prof Debre, F-30029 Nimes, France
[6] Toulouse Univ Hosp, Dept Neurol, F-31059 Toulouse, France
[7] CNRS, UMR 5549, Ctr Rech Cerveau & Cognit, F-31052 Toulouse, France
[8] CHU Bordeaux, Dept Neurol, Nerve Muscle Unit, Pellegrin Hosp, F-33076 Bordeaux, France
[9] Sorbonne Univ, INSERM, UMR S1166, ICAN, Paris, France
[10] Hop Pitie, AP HP, Dept Endocrinol Metab, Paris, France
[11] Inst Pasteur, Serv Nutr & Activite Phys, 1 Rue Prof Calmette, F-59019 Lille, France
[12] CHRU Lille, Hop Claude Huriez, Serv Med Interne, F-59037 Lille, France
[13] Ctr Genet Humaine, Inst Pathol & Genet ASBL, Ctr Agree Malad Hereditaires Metab, Ave Georges Lemaitre 25, B-6041 Gosselies, Belgium
[14] Lille Univ Hosp, Endocrinol & Metab Dept, Huriez Hosp, 1 Rue Polonovski, F-59037 Lille, France
关键词
Cerebrotendineous xanthomatosis; Cholic acid; Cholestanol; Chenodeoxycholic acid; CHENODEOXYCHOLIC ACID; CHOLESTEROL; DIAGNOSIS; PATIENT;
D O I
10.1007/s00415-019-09377-y
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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-naive patient and one non-treatment-naive 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.
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收藏
页码:2043 / 2050
页数:8
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