Long-Term Outcomes of Chenodeoxycholic Acid Therapy for Cerebrotendinous Xanthomatosis: A Nationwide Study on Prognostic Factors and Treatment Response

IF 3.8 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Tanyel Zubarioglu, Banu Kadıoğlu-Yılmaz, Engin Köse, Pelin Teke-Kısa, Mehmet Cihan Balcı, Havva Yazıcı, Burcu Özturk-Hişmi, Abdurrahman Akgün, Deniz Kor, Sevil Yıldız, Gonca Kılıç-Yıldırım, Erdoğan Soyuçen, Aylin Akçalı, Yılmaz Yıldız, Aslı Durmuş, Dilek Güneş, Pembe Soylu-Üstkoyuncu, Çiğdem Seher Kasapkara, Şahin Erdöl, Emine Göksoy, Halil Tuna Akar, Haluk Gümüş, Ahmet Hakan Ekmekçi, Fatma Tuba Eminoğlu, Nur Arslan, Haşmet Ayhan Hanağası, Ebru Canda, Emine Genç, Işıl Özer, Ayşegül Gündüz, Ertuğrul Kıykım, Çiğdem Aktuğlu-Zeybek
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Abstract

Cerebrotendinous xanthomatosis (CTX) is a treatable neurometabolic disorder. Chenodeoxycholic acid (CDCA) is the first-line treatment and can potentially halt disease progression if initiated before neurologic symptoms appear. This nationwide, multicenter study evaluates the long-term effects of treatment in 86 genetically confirmed patients with CTX receiving CDCA for ≥ 6 months, focusing on neurologic and extraneurologic outcomes, prognostic factors, and biochemical response. Clinical and biochemical parameters were recorded at baseline and follow-up, and neurological outcomes were assessed using neurological disability scores. Our results indicate a critical age of 28 years for the start of treatment. Patients diagnosed before 28 years showed 100% neurological stabilization or improvement, whereas patients diagnosed later had a higher rate of disease progression (p < 0.05). CDCA effectively stabilized or improved pyramidal and cerebellar symptoms, although myoclonus and parkinsonism remained less responsive. Psychiatric symptoms showed a lower treatment response, with psychosis being the most refractory finding. CDCA resulted in a strong and sustained reduction in cholestanol levels, although biochemical response did not always correlate with clinical improvement. Longer diagnostic delay and presence of anxiety and pyramidal/cerebellar symptoms were associated with poorer outcomes. Notably, a cholestatic child, for whom liver transplantation had initially been considered, recovered completely under CDCA therapy. Our results show that early diagnosis and initiation of CDCA therapy significantly improve neurological outcomes in CTX. However, even in late-diagnosed patients, treatment continues to be beneficial, demonstrating that it is never too late to start therapy. Biochemical response does not always predict clinical improvement; multidisciplinary follow-up is essential.

Abstract Image

鹅去氧胆酸治疗脑腱黄瘤病的长期疗效:一项关于预后因素和治疗反应的全国性研究
脑腱黄瘤病(CTX)是一种可治疗的神经代谢疾病。鹅去氧胆酸(CDCA)是一线治疗,如果在神经系统症状出现之前开始治疗,可能会阻止疾病进展。这项全国范围内的多中心研究评估了86例接受CDCA治疗≥6个月的遗传确诊CTX患者的长期治疗效果,重点关注神经系统和外神经系统预后、预后因素和生化反应。在基线和随访时记录临床和生化参数,并使用神经功能障碍评分评估神经预后。我们的结果表明,28岁是开始治疗的关键年龄。28岁前确诊的患者神经系统100%稳定或改善,而28岁后确诊的患者疾病进展率更高(p < 0.05)。CDCA有效地稳定或改善锥体和小脑症状,尽管肌阵挛和帕金森病仍然反应较差。精神科症状表现出较低的治疗反应,精神病是最难治愈的症状。尽管生化反应并不总是与临床改善相关,但CDCA导致了胆固醇水平的强烈和持续的降低。较长的诊断延迟、焦虑和锥体/小脑症状的出现与较差的预后相关。值得注意的是,一名胆汁淤积的儿童,最初考虑进行肝移植,在CDCA治疗下完全恢复。我们的研究结果表明,早期诊断和开始CDCA治疗可显著改善CTX的神经预后。然而,即使在晚期诊断的患者中,治疗仍然是有益的,这表明开始治疗永远不会太晚。生化反应并不总能预测临床改善;多学科随访至关重要。
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来源期刊
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease 医学-内分泌学与代谢
CiteScore
9.50
自引率
7.10%
发文量
117
审稿时长
4-8 weeks
期刊介绍: The Journal of Inherited Metabolic Disease (JIMD) is the official journal of the Society for the Study of Inborn Errors of Metabolism (SSIEM). By enhancing communication between workers in the field throughout the world, the JIMD aims to improve the management and understanding of inherited metabolic disorders. It publishes results of original research and new or important observations pertaining to any aspect of inherited metabolic disease in humans and higher animals. This includes clinical (medical, dental and veterinary), biochemical, genetic (including cytogenetic, molecular and population genetic), experimental (including cell biological), methodological, theoretical, epidemiological, ethical and counselling aspects. The JIMD also reviews important new developments or controversial issues relating to metabolic disorders and publishes reviews and short reports arising from the Society''s annual symposia. A distinction is made between peer-reviewed scientific material that is selected because of its significance for other professionals in the field and non-peer- reviewed material that aims to be important, controversial, interesting or entertaining (“Extras”).
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