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Auteur Ilknur BINGUL |
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Peripheral markers of nitrosative stress in children with autism spectrum disorder and bipolar disorder comorbidity during euthymic phase / Ali KARAYAGMURLU ; Canan KUCUKGERGIN ; Ilknur BINGUL ; Murat COSKUN in Research in Autism Spectrum Disorders, 109 (November 2023)
[article]
Titre : Peripheral markers of nitrosative stress in children with autism spectrum disorder and bipolar disorder comorbidity during euthymic phase Type de document : Texte imprimé et/ou numérique Auteurs : Ali KARAYAGMURLU, Auteur ; Canan KUCUKGERGIN, Auteur ; Ilknur BINGUL, Auteur ; Murat COSKUN, Auteur Article en page(s) : 102259 Langues : Anglais (eng) Mots-clés : Autism spectrum disorder Bipolar disorder Biomarker Nitrosative stress Nitric oxide 3-nitrotyrosine Nitric oxide synthetase Index. décimale : PER Périodiques Résumé : Background Bipolar Disorder (BD) is often comorbid with Autism Spectrum Disorder (ASD) (Skokauskas & Frodl, 2015). However, to our knowledge, the etiological pathways of BD comorbidity in individuals with ASD was not given a particular focus in the literature. The present study aims to investigate the link between BD comorbidity and nitrosative stress in children and adolescents with ASD. Method The case group consisted of 41 participants with comorbid ASD and BD, while the control group consisted of 39 participants with ASD who did not have any past or present mood disorders. As indicators of nitrosative stress, serum levels of NO (Nitric Oxide), NO2/NO3 (Nitrite/Nitrate), 3-NT (3-Nitrotyrosine) and NOS-I (Nitric Oxide Synthetase-I) were compared between groups. Results Serum levels of NO and 3-NT were significantly higher in the case group. As the phenomenological findings of BD, the age of onset was 10.5, mixed attack rate was 70%, seasonality rate was 63.8%, and sub-threshold symptoms were seen in 36.6% of the cases. Conclusion The present study indicated a relationship between BD comorbidity and nitrosative stress cascade among children and adolescents with ASD. Further studies with larger samples are needed to better understand the etiology of BD comorbidity in patients with ASD. En ligne : https://doi.org/10.1016/j.rasd.2023.102259 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517
in Research in Autism Spectrum Disorders > 109 (November 2023) . - 102259[article] Peripheral markers of nitrosative stress in children with autism spectrum disorder and bipolar disorder comorbidity during euthymic phase [Texte imprimé et/ou numérique] / Ali KARAYAGMURLU, Auteur ; Canan KUCUKGERGIN, Auteur ; Ilknur BINGUL, Auteur ; Murat COSKUN, Auteur . - 102259.
Langues : Anglais (eng)
in Research in Autism Spectrum Disorders > 109 (November 2023) . - 102259
Mots-clés : Autism spectrum disorder Bipolar disorder Biomarker Nitrosative stress Nitric oxide 3-nitrotyrosine Nitric oxide synthetase Index. décimale : PER Périodiques Résumé : Background Bipolar Disorder (BD) is often comorbid with Autism Spectrum Disorder (ASD) (Skokauskas & Frodl, 2015). However, to our knowledge, the etiological pathways of BD comorbidity in individuals with ASD was not given a particular focus in the literature. The present study aims to investigate the link between BD comorbidity and nitrosative stress in children and adolescents with ASD. Method The case group consisted of 41 participants with comorbid ASD and BD, while the control group consisted of 39 participants with ASD who did not have any past or present mood disorders. As indicators of nitrosative stress, serum levels of NO (Nitric Oxide), NO2/NO3 (Nitrite/Nitrate), 3-NT (3-Nitrotyrosine) and NOS-I (Nitric Oxide Synthetase-I) were compared between groups. Results Serum levels of NO and 3-NT were significantly higher in the case group. As the phenomenological findings of BD, the age of onset was 10.5, mixed attack rate was 70%, seasonality rate was 63.8%, and sub-threshold symptoms were seen in 36.6% of the cases. Conclusion The present study indicated a relationship between BD comorbidity and nitrosative stress cascade among children and adolescents with ASD. Further studies with larger samples are needed to better understand the etiology of BD comorbidity in patients with ASD. En ligne : https://doi.org/10.1016/j.rasd.2023.102259 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517