Literature DB >> 26153518

Evaluation of cholesterol metabolism in cerebrotendinous xanthomatosis.

Andrea Mignarri1, Alessandro Magni2, Marina Del Puppo2, Gian Nicola Gallus3, Ingemar Björkhem4, Antonio Federico3, Maria Teresa Dotti3.   

Abstract

BACKGROUND: Cerebrotendinous xanthomatosis (CTX) is a treatable bile acid disorder caused by mutations of CYP27A1. The pathogenesis of neurological damage has not been completely explained. Oral chenodeoxycholic acid (CDCA) can lead to clinical stabilization, but in a subgroup of patients the disease progresses despite treatment. In the present study, we aimed at clarifying cholesterol metabolism abnormalities and their response to CDCA treatment, in order to identify reliable diagnostic and prognostic markers and understand if differences exist between stable patients and those with neurological progression.
METHODS: We enrolled 19 untreated CTX patients and assessed serum profile of bile acids intermediates, oxysterols, cholesterol, lathosterol, and plant sterols. Then we performed a long-term follow up during CDCA therapy, and compared biochemical data with neurological outcome.
RESULTS: We observed increase of cholestanol, 7α-hydroxy-4-cholesten-3-one (7αC4), lathosterol, and plant sterols, whereas 27-hydroxycholesterol (27-OHC) was extremely low or absent. CDCA treatment at a daily dose of 750 mg normalized all biochemical parameters except for 7αC4 which persisted slightly higher than normal in most patients, and 27-OHC which was not modified by therapy. Biochemical evaluation did not reveal significant differences between stable and worsening patients. DISCUSSION: Cholestanol and 7αC4 represent important markers for CTX diagnosis and monitoring of therapy. Treatment with CDCA should aim at normalizing serum 7αC4 as well as cholestanol, since 7αC4 better mirrors 7α-hydroxylation rate and is thought to be correlated with cholestanol accumulation in the brain. Assessment of serum 27-OHC is a very good tool for biochemical diagnosis at any stage of disease. Lathosterol and plant sterols should be considered as additional markers for diagnosis and monitoring of therapy. Further studies including long-term assessment of bile acid intermediates in cerebrospinal fluid are needed in patients who show clinical progression despite treatment.

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Year:  2015        PMID: 26153518     DOI: 10.1007/s10545-015-9873-1

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  43 in total

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4.  Interobserver agreement for the assessment of handicap in stroke patients.

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5.  Crossing the barrier: net flux of 27-hydroxycholesterol into the human brain.

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6.  Feedback regulation of bile acid synthesis in primary human hepatocytes: evidence that CDCA is the strongest inhibitor.

Authors:  Ewa Ellis; Magnus Axelson; Anna Abrahamsson; Gösta Eggertsen; Anders Thörne; Grzegorz Nowak; Bo-Göran Ericzon; Ingemar Björkhem; Curt Einarsson
Journal:  Hepatology       Date:  2003-10       Impact factor: 17.425

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8.  Measurement of serum 7alpha-hydroxy-4-cholesten-3-one (or 7alphaC4), a surrogate test for bile acid malabsorption in health, ileal disease and irritable bowel syndrome using liquid chromatography-tandem mass spectrometry.

Authors:  M Camilleri; A Nadeau; W J Tremaine; J Lamsam; D Burton; S Odunsi; S Sweetser; R Singh
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9.  Chronic diarrhea and juvenile cataracts: think cerebrotendinous xanthomatosis and treat.

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10.  On the mechanism of cerebral accumulation of cholestanol in patients with cerebrotendinous xanthomatosis.

Authors:  Ute Panzenboeck; Ulla Andersson; Magnus Hansson; Wolfgang Sattler; Steve Meaney; Ingemar Björkhem
Journal:  J Lipid Res       Date:  2007-02-26       Impact factor: 5.922

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  13 in total

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3.  Levels of 7alpha-hydroxycholesterol and/or 7alpha-hydroxy-4-cholest-3-one are the optimal biochemical markers for the evaluation of treatment of cerebrotendinous xanthomatosis.

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5.  Treatment with chenodeoxycholic acid in cerebrotendinous xanthomatosis: clinical, neurophysiological, and quantitative brain structural outcomes.

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Review 6.  [Congenital disorders of lipoprotein metabolism].

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7.  Brain diffusion tensor imaging changes in cerebrotendinous xanthomatosis reversed with treatment.

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Review 8.  Epidemiology, diagnosis, and treatment of cerebrotendinous xanthomatosis (CTX).

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Review 10.  Conventional MRI findings in hereditary degenerative ataxias: a pictorial review.

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