Publication: Long-Term Outcomes of Chenodeoxycholic Acid Therapy for Cerebrotendinous Xanthomatosis: A Nationwide Study on Prognostic Factors and Treatment Response
| dc.authorwosid | Kasapkara, Çiğdem/Aaw-5228-2021 | |
| dc.authorwosid | Yildiz, Yilmaz/Aaj-8666-2020 | |
| dc.authorwosid | Erdol, Sahin/Hsf-7083-2023 | |
| dc.authorwosid | Gunes, Dilek/Hlp-7750-2023 | |
| dc.authorwosid | Kor, Deniz/G-5183-2018 | |
| dc.authorwosid | Akgün, Abdurrahman/Htp-0625-2023 | |
| dc.authorwosid | Ozturk Hismi, Burcu/Aah-6558-2019 | |
| dc.contributor.author | Zubarioglu, Tanyel | |
| dc.contributor.author | Kadioglu-Yilmaz, Banu | |
| dc.contributor.author | Kose, Engin | |
| dc.contributor.author | Teke-Kisa, Pelin | |
| dc.contributor.author | Balci, Mehmet Cihan | |
| dc.contributor.author | Yazici, Havva | |
| dc.contributor.author | Aktuglu-Zeybek, Cigdem | |
| dc.contributor.authorID | Yildiz, Yilmaz/0000-0001-9076-1388 | |
| dc.contributor.authorID | Zubarioglu, Tanyel/0000-0002-7159-4008 | |
| dc.contributor.authorID | Balci, Mehmet Cihan/0000-0003-2167-8139 | |
| dc.date.accessioned | 2025-12-11T01:25:16Z | |
| dc.date.issued | 2025 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_US |
| dc.department-temp | [Zubarioglu, Tanyel; Kiykim, Ertugrul; Aktuglu-Zeybek, Cigdem] Istanbul Univ Cerrahpasa, Cerrahpasa Med Fac, Div Pediat Nutr & Metab, Istanbul, Turkiye; [Kadioglu-Yilmaz, Banu] Konya Selcuk Univ, Div Pediat Nutr & Metab, Med Fac, Konya, Turkiye; [Kose, Engin; Eminoglu, Fatma Tuba] Ankara Univ, Fac Med, Dept Pediat Metab, Ankara, Turkiye; [Kose, Engin; Eminoglu, Fatma Tuba] Ankara Univ, Rare Dis Applicat & Res Ctr, Ankara, Turkiye; [Teke-Kisa, Pelin; Arslan, Nur] Dokuz Eylul Univ, Div Pediat Nutr & Metab, Med Fac, Izmir, Turkiye; [Balci, Mehmet Cihan] Istanbul Univ, Istanbul Fac Med, Div Nutr & Metab, Istanbul, Turkiye; [Yazici, Havva; Canda, Ebru] Ege Univ, Div Pediat Nutr & Metab, Med Fac, Izmir, Turkiye; [Ozturk-Hismi, Burcu; Genc, Emine] Marmara Univ, Div Pediat Metab Disorders, Sch Med, Istanbul, Turkiye; [Akgun, Abdurrahman] Firat Univ, Dept Pediat, Div Pediat Metab Dis, Sch Med, Elazig, Turkiye; [Kor, Deniz] Cukurova Univ, Div Pediat Nutr & Metab, Med Fac, Adana, Turkiye; [Yildiz, Sevil] Hlth Sci Univ, Bursa Yuksek Ihtisas Training & Res Hosp, Div Pediat Nutr & Metab, Bursa, Turkiye; [Kilic-Yildirim, Gonca] Eskisehir Osmangazi Univ, Fac Med, Pediat Nutr & Metab Unit, Eskisehir, Turkiye; [Soyucen, Erdogan] Akdeniz Univ, Dept Pediat, Div Inherited Pediat Metab Dis, Fac Med, Antalya, Turkiye; [Akcali, Aylin] Gaziantep Univ, Dept Neurol, Fac Med, Gaziantep, Turkiye; [Yildiz, Yilmaz] Hacettepe Univ, Fac Med, Dept Pediat, Div Pediat Metab, Ankara, Turkiye; [Durmus, Asli] Hlth Sci Univ, Trabzon Kanuni Training & Res Hosp, Div Pediat Nutr & Metab, Trabzon, Turkiye; [Gunes, Dilek] Bagcilar Training & Res Hosp, Div Inborn Metab Dis, Istanbul, Turkiye; [Soylu-Ustkoyuncu, Pembe] Hlth Sci Univ, Kayseri City Educ & Res Hosp, Dept Pediat, Pediat Metab Dis Unit, Kayseri, Turkiye; [Kasapkara, cigdem Seher] Ankara Yildirim Beyazit Univ, Ankara Bilkent City Hosp, Dept Pediat Metab, Ankara, Turkiye; [Erdol, Sahin] Uludag Univ, Dept Pediat, Div Metab, Fac Med, Bursa, Turkiye; [Goksoy, Emine] Adnan Menderes Univ, Div Pediat Nutr & Metab, Med Fac, Aydin, Turkiye; [Akar, Halil Tuna] Ankara Etlik City Hosp, Pediat Metab Dis Unit, Ankara, Turkiye; [Ekmekci, Ahmet Hakan] Konya Selcuk Univ, Dept Neurol, Med Fac, Konya, Turkiye; [Hanagasi, Hasmet Ayhan] Istanbul Univ, Istanbul Fac Med, Dept Neurol, Istanbul, Turkiye; [Ozer, Isil] Ondokuz Mayis Univ, Fac Med, Dept Pediat Metab, Samsun, Turkiye; [Ozer, Isil] Kafkas Univ, Div Pediat Nutr & Metab, Med Fac, Kars, Turkiye; [Gunduz, Ayseguel] Istanbul Univ Cerrahpasa, Cerrahpasa Med Fac, Dept Neurol, Istanbul, Turkiye | en_US |
| dc.description | Yildiz, Yilmaz/0000-0001-9076-1388; Zubarioglu, Tanyel/0000-0002-7159-4008; Balci, Mehmet Cihan/0000-0003-2167-8139; | en_US |
| dc.description.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. | en_US |
| dc.description.woscitationindex | Science Citation Index Expanded | |
| dc.identifier.doi | 10.1002/jimd.70069 | |
| dc.identifier.issn | 0141-8955 | |
| dc.identifier.issn | 1573-2665 | |
| dc.identifier.issue | 4 | en_US |
| dc.identifier.pmid | 40702717 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.uri | https://doi.org/10.1002/jimd.70069 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/43599 | |
| dc.identifier.volume | 48 | en_US |
| dc.identifier.wos | WOS:001544865900022 | |
| dc.identifier.wosquality | Q2 | |
| dc.language.iso | en | en_US |
| dc.publisher | Wiley | en_US |
| dc.relation.ispartof | Journal of Inherited Metabolic Disease | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Cerebrotendinous | en_US |
| dc.subject | Chenodeoxycholic Acid | en_US |
| dc.subject | Prognosis | en_US |
| dc.subject | Xanthomatosis | en_US |
| dc.title | Long-Term Outcomes of Chenodeoxycholic Acid Therapy for Cerebrotendinous Xanthomatosis: A Nationwide Study on Prognostic Factors and Treatment Response | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication |
