scholarly journals Expression analyses of the mitochondrial complex I 75-kDa subunit in early onset schizophrenia and autism spectrum disorder: increased levels as a potential biomarker for early onset schizophrenia

2009 ◽  
Vol 19 (5) ◽  
pp. 441-448 ◽  
Author(s):  
Regina Taurines ◽  
Johannes Thome ◽  
J. Catharina Duvigneau ◽  
Sarah Forbes-Robertson ◽  
Liya Yang ◽  
...  
2017 ◽  
Vol 41 (S1) ◽  
pp. S457-S458
Author(s):  
N. Zvereva ◽  
N. Simashkova ◽  
A. Koval-Zaitsev

IntroductionAutism spectrum disorder and early onset schizophrenia have many similar symptoms, however, these are different disorders. It is important to identify the main similarities\differences in the structure of cognitive impairment to define further assistance these children correctly. We distinguished two options for cognitive defect (total and partial) in children with schizophrenia.AimsComparison of cognitive functions at children with autism spectrum disorder and early onset schizophrenia.ObjectivesTwo groups with autism spectrum disorder (ASD1 – 22 patients of MHRC mean age 8.9; ASD2 – 27 pupils of special school mean age 7,4). Two groups with early onset schizophrenia (F20.8 – 16 patients of MHRC mean age 10,2; F21 – 18 patients of MHRC mean age 10.0).MethodsBattery of pathopsychological tests for assessing cognitive functions (memory, attention, thinking), test figures of Leeper for visual perception. Z-scales were used for estimation of cognitive deficit or defect.ResultsPatients demonstrate variety of cognitive functioning. Normal cognitive functioning: ASD1* – 22%, F20.8 – 18%, F21* – 50% (* – P ≤ 0.05); partial cognitive defect: ASD1 – 27%, F20.8 – 18%, F21 – 22%; total cognitive defect: ASD1** – 50%, F20.8 – 64%, F21** – 27% (** – P ≤ 0.01). ASD1 and F20 were the worth in thinking. Children ASD1 and ASD2 demonstrate similar success in recognizing Leeper's figures.ConclusionsThere are some common features of cognitive development in children with severe forms of ASD and early onset schizophrenia, first of all in thinking.No significant differences obtained between severe – mild forms of autistic disorders in visual perception (ASD1 and ASD2).Disclosure of interestThe authors have not supplied their declaration of competing interest.


2015 ◽  
Vol 24 (14) ◽  
pp. 3948-3955 ◽  
Author(s):  
Claire Angebault ◽  
Majida Charif ◽  
Naig Guegen ◽  
Camille Piro-Megy ◽  
Benedicte Mousson de Camaret ◽  
...  

2020 ◽  
Vol 146 ◽  
pp. 350-356
Author(s):  
Huimin Fu ◽  
Wenwen Deng ◽  
Lulu Yao ◽  
Miaozi Gong ◽  
Shenghan Lai ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Richard E. Frye ◽  
Loïc Lionnard ◽  
Indrapal Singh ◽  
Mohammad A. Karim ◽  
Hanane Chajra ◽  
...  

AbstractAutism spectrum disorder (ASD) is a neurodevelopmental disorder that is associated with unique changes in mitochondrial metabolism, including elevated respiration rates and morphological alterations. We examined electron transport chain (ETC) complex activity in fibroblasts derived from 18 children with ASD as well as mitochondrial morphology measurements in fibroblasts derived from the ASD participants and four typically developing controls. In ASD participants, symptoms severity was measured by the Social Responsiveness Scale and Aberrant Behavior Checklist. Mixed-model regression demonstrated that alterations in mitochondrial morphology were associated with both ETC Complex I+III and IV activity as well as the difference between ETC Complex I+III and IV activity. The subgroup of ASD participants with relative elevation in Complex IV activity demonstrated more typical mitochondrial morphology and milder ASD related symptoms. This study is limited by sample size given the invasive nature of obtaining fibroblasts from children. Furthermore, since mitochondrial function is heterogenous across tissues, the result may be specific to fibroblast respiration. Previous studies have separately described elevated ETC Complex IV activity and changes in mitochondrial morphology in cells derived from children with ASD but this is the first study to link these two findings in mitochondrial metabolism. The association between a difference in ETC complex I+III and IV activity and normal morphology suggests that mitochondrial in individuals with ASD may require ETC uncoupling to function optimally. Further studies should assess the molecular mechanisms behind these unique metabolic changes.Trial registration: Protocols used in this study were registered in clinicaltrials.gov as NCT02000284 and NCT02003170.


2003 ◽  
Vol 21 (6) ◽  
pp. 582-586 ◽  
Author(s):  
Paule Bénit ◽  
Réjane Beugnot ◽  
Dominique Chretien ◽  
Irina Giurgea ◽  
Pascale De Lonlay-Debeney ◽  
...  

2020 ◽  
Vol 38 (4) ◽  
pp. 992-1000
Author(s):  
Mingyang Zou ◽  
Dexin Li ◽  
Luxi Wang ◽  
Ling Li ◽  
Shu Xie ◽  
...  

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