Evaluation of the Neurodevelopmental Status for Urea Cycle Disorders: Based on Clinical Experience
dc.authorid | TEKMENURAY-UNAL, AYSEL/0000-0001-8730-3968 | |
dc.authorid | Bozaci, Ayse Ergul/0000-0002-9783-1016 | |
dc.authorid | Mutlu Albayrak, Hatice/0000-0001-5624-3878 | |
dc.authorscopusid | 57201619907 | |
dc.authorscopusid | 57963234400 | |
dc.authorscopusid | 57879099300 | |
dc.authorscopusid | 57192270096 | |
dc.authorscopusid | 57464245200 | |
dc.authorscopusid | 18233751800 | |
dc.authorscopusid | 57206379419 | |
dc.authorwosid | Ozbek, mehmetnuri/LNR-5794-2024 | |
dc.authorwosid | taş, ibrahim/ABG-8476-2020 | |
dc.authorwosid | Bozaci, Ergul/JBJ-5349-2023 | |
dc.authorwosid | TEKMENURAY-UNAL, AYSEL/IWM-4732-2023 | |
dc.authorwosid | Mutlu Albayrak, Hatice/A-3635-2017 | |
dc.contributor.author | Bozaci, Ayse Ergul | |
dc.contributor.author | Goksoy, Emine | |
dc.contributor.author | Unal, Aysel Tekmenuray | |
dc.contributor.author | Albayrak, Hatice Mutlu | |
dc.contributor.author | Tas, Ibrahim | |
dc.contributor.author | Kanar, Berat | |
dc.contributor.author | Kose, Melis | |
dc.date.accessioned | 2025-02-15T19:33:56Z | |
dc.date.available | 2025-02-15T19:33:56Z | |
dc.date.issued | 2023 | |
dc.department | Artuklu University | en_US |
dc.department-temp | [Bozaci, Ayse Ergul; Tas, Ibrahim] Diyarbakir Childrens Hosp, Clin Pediat Nutr & Metab, Diyarbakir, Turkiye; [Goksoy, Emine] Gaziantep Cengiz Gokcek Obstet & Gynecol & Childre, Clin Pediat Nutr & Metab, Gaziantep, Turkiye; [Unal, Aysel Tekmenuray] Univ Hlth Sci Turkey, Diyarbakir Gaziyaşargil Training & Res Hosp, Clin Med Genet, Diyarbakir, Turkiye; [Albayrak, Hatice Mutlu] Gaziantep Childrens Hosp, Pediat Neurol Clin, Gaziantep, Turkiye; [Kanar, Berat] Diyarbakir Childrens Hosp, Clin Neonatol, Diyarbakir, Turkiye; [Ozbek, Mehmet Nuri] Mardin Artuklu Univ, Dept Pediat, Div Pediat Endocrinol & Metab, Fac Med, Mardin, Turkiye; [Kose, Melis] Childrens Hosp Philadelphia, Mitochondrial Med Frontier Program, Philadelphia, PA USA; [Bozaci, Ayse Ergul] Manisa City Hosp, Div Pediat Endocrinol, Manisa, Turkiye | en_US |
dc.description | TEKMENURAY-UNAL, AYSEL/0000-0001-8730-3968; Bozaci, Ayse Ergul/0000-0002-9783-1016; Mutlu Albayrak, Hatice/0000-0001-5624-3878 | en_US |
dc.description.abstract | Aim: Urea cycle disorders (UCD) still have poor neurological outcomes despite early diagnosis and treatment. We aimed to present the neurological outcomes of UCD patients and to determine the main simple and accessible factors affecting these outcomes. Materials and Metkods: This was a descriptive cross-sectional study conducted in two pediatric metabolism centers on 29 patients from 25 unrelated families who were diagnosed and followed with UCD based on clinical presentation, neurological parameters, biochemical measurements, and molecular analysis.Results: Within the study population, the most common diagnosis was argininosuccinate synthase deficiency in 13 (44.82%) patients, followed by N-acetylglutamate synthase deficiency in five patients (17.24%), ornithine transcarbamylase deficiency in four patients (13.79%), arginase 1 deficiency in three patients (10.34%), carbamoyl phosphate synthase 1 deficiency in three patients (10.34%), and argininosuccinate lyase deficiency in one patient (3.44%). Peak ammonia levels were observed to be significantly higher in those patients with delayed milestones and patients who had Denver II <-2 standard deviation score results (p=0.032, p=0.026). Effect sizes were large in both groups. Delayed milestones were noted in 17 (94.4%) of the cases with peak ammonia >500 mu mol/L (n=18). Those patients with abnormal neurological parameters had a significantly higher mean number of hyperammonemic episodes per year. Extracorporeal detoxification was given to eight patients, in combination with therapeutic hypothermia in two patients. Rapid regression was observed in brain edema in those who underwent therapeutic hypothermia.Conclusion: Our study emphasizes the effect of peak ammonia levels and the frequency of hyperammonemic episodes on neurological outcomes. There were still poor neurocognitive outcomes despite extracorporeal detoxification. This highlights the need to reassess current treatment strategies, including the threshold for starting extracorporeal detoxification if ammonia levels exceed 500 mu mol/L. The use of therapeutic hypothermia by experienced teams may be promising due to its brain edema-reducing effects. | en_US |
dc.description.provenance | Submitted by GCRIS Admin (gcris@artuklu.edu.tr) on 2025-02-15T19:33:56Z No. of bitstreams: 0 | en |
dc.description.provenance | Made available in DSpace on 2025-02-15T19:33:56Z (GMT). No. of bitstreams: 0 Previous issue date: 2023 | en |
dc.description.woscitationindex | Emerging Sources Citation Index | |
dc.identifier.citationcount | 0 | |
dc.identifier.doi | 10.4274/jpr.galenos.2023.96992 | |
dc.identifier.issn | 2147-9445 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.scopus | 2-s2.0-85208449663 | |
dc.identifier.scopusquality | N/A | |
dc.identifier.uri | https://doi.org/10.4274/jpr.galenos.2023.96992 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12514/5944 | |
dc.identifier.volume | 10 | en_US |
dc.identifier.wos | WOS:001144653500007 | |
dc.language.iso | en | en_US |
dc.publisher | Galenos Publ House | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Urea Cycle Disorders | en_US |
dc.subject | Hyperammonemia | en_US |
dc.subject | Citrullinemia | en_US |
dc.subject | Inborn Errors Of Metabolism | en_US |
dc.subject | Therapeutic Hypothermia | en_US |
dc.title | Evaluation of the Neurodevelopmental Status for Urea Cycle Disorders: Based on Clinical Experience | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication |