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1.
Prz Gastroenterol ; 16(4): 352-357, 2021.
Article in English | MEDLINE | ID: mdl-34976244

ABSTRACT

INTRODUCTION: A common comorbidity in autism spectrum disorder (ASD) children is gastrointestinal problems, and a possible link between active gastrointestinal inflammation and autism has been suggested. Faecal calprotectin (FC) is a non-invasive marker for of gastrointestinal inflammation. AIM: To study the level of FC as a marker of bowel inflammation in children with ASD and its possible relation to gastrointestinal manifestations. MATERIAL AND METHODS: Calprotectin levels were assessed in stool samples of 40 ASD children. Autism severity was assessed by the Childhood Autism Rating Scale (CARS). Severity of gastrointestinal symptoms was assessed using a modified version of the 6-Item Gastrointestinal Severity Index (6-GSI) questionnaire. A control group of 40 healthy children matched for age and sex with the cases was also included to compare their levels of FC. RESULTS: Gastrointestinal symptoms were present in 82.5% of children with autism; the most reported offensive stool odour (70%) and the least diarrhoea (17.5%), and a high 6-GSI score was observed in 35% of ASD children. FC levels were elevated in 35% of the cases and in 25% of the control group. The mean levels of FC of cases were significantly elevated compared to levels of controls. FC levels positively correlated with severity of gastrointestinal symptoms (6-GSI) in autistic patients. There was positive correlation between CARS and 6-GSI. CONCLUSIONS: Gastrointestinal manifestations are a common comorbidity in autistic patients. ASD patients have significantly higher FC levels than healthy controls. FC levels are strongly correlated with the severity of gastrointestinal manifestations in ASD children. So, gastrointestinal manifestations among autistic patients could be caused by gastrointestinal inflammation.

2.
J Mol Neurosci ; 71(1): 153-161, 2021 Jan.
Article in English | MEDLINE | ID: mdl-32607756

ABSTRACT

The role of the gut microbiota in triggering autism is a rapidly emerging field of research. Gut microbiota have been incriminated because autistic children often have gastrointestinal symptoms. Pathogenic gut bacteria in children with autism spectrum disorders (ASD) have been reported. The present study aimed to assess Clostridium difficile in the stool of children with ASD and its relation to gastrointestinal (GI) comorbidities, autism severity, and sensory impairment. The study included 58 ASD patients, 45 of their neurotypical siblings, and 45 unrelated controls. Childhood Autism Rating Scale (CARS) was used to assess the severity of autism. Sensory problems were evaluated using the Short Sensory Profile (SSP). GI symptoms were assessed with a modified six-item GI Severity Index (6-GSI) questionnaire. Quantitative real-time PCR was done for the detection and quantitation of C. difficile and its toxins A and B. C. difficile was detected in 25.9%, 40%, and 15.6% of ASD cases, siblings, and unrelated control respectively. Regarding toxin A and B production, 73.3%, 77.8%, and 71.4% of C. difficile in positive ASD, siblings, and unrelated control cases respectively were toxigenic. There was no statistically significant difference between the three groups as regards C. difficile qualitative, quantitative, and toxin production results. In conclusion, C. difficile is not specifically prevalent in the gut of children with ASD. Although most of the strains are toxigenic, there were no GI symptoms in the control groups and no statistically significant association with GI Severity Index in autistic cases. Gastrointestinal dysfunction and sensory impairment are common comorbidities in ASD.


Subject(s)
Autism Spectrum Disorder/complications , Clostridioides difficile/isolation & purification , Gastrointestinal Diseases/etiology , Gastrointestinal Microbiome , Sensation Disorders/etiology , Autism Spectrum Disorder/microbiology , Bacterial Proteins/analysis , Bacterial Toxins/analysis , Child , Child, Preschool , Clostridioides difficile/pathogenicity , Comorbidity , Enterotoxins/analysis , Feces/microbiology , Female , Gastrointestinal Diseases/microbiology , Humans , Male , Real-Time Polymerase Chain Reaction , Sensation Disorders/microbiology , Severity of Illness Index , Siblings
3.
J Mol Neurosci ; 70(6): 887-896, 2020 Jun.
Article in English | MEDLINE | ID: mdl-32062762

ABSTRACT

The role of gut microbiome was recently raised in the pathogenesis of neurodevelopmental disorders including autism spectrum disorder (ASD). The aim of this study was to elucidate changes in gut microbiome in Egyptian autistic children and its possible correlation with the severity of autism and gastrointestinal (GI) symptoms. The gut bacterial microbiome of 41 ASD children, 45 siblings, and 45 healthy controls were analyzed using quantitative SYBR Green real-time PCR technique targeting 16S rRNA of selected bacteria. The gut microbiome of ASD children and their siblings contained a higher relative abundance of Bacteroides as well as Ruminococcus than controls. Prevotella/Bacteroides (P/B) ratio and Firmicutes/Bacteroidetes (F/B) were significantly lower in both ASD cases and their siblings. The only difference between the autistic cases and their siblings was the significantly higher level of Bifidobacterium in siblings, which appears to offer them a protective role. There was no correlation between the altered gut microbiome and the severity of autism or GI symptoms. The current study showed an evidence of changes in the gut microbiome of autistic children compared to the unrelated control. However, the microbiome profile of siblings was more like that of autistic children than that of unrelated controls indicating that gut microbiota is affected by dietary habits, living conditions together with host genetic factors.


Subject(s)
Autism Spectrum Disorder/microbiology , Gastrointestinal Microbiome , Bacteroides/genetics , Bacteroides/pathogenicity , Bifidobacterium/genetics , Bifidobacterium/pathogenicity , Child , Child, Preschool , Female , Firmicutes/genetics , Firmicutes/pathogenicity , Humans , Infant , Male , Prevotella/genetics , Prevotella/pathogenicity , RNA, Ribosomal, 16S/genetics , Tertiary Care Centers/statistics & numerical data
4.
Int J Pediatr Otorhinolaryngol ; 104: 36-42, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29287877

ABSTRACT

OBJECTIVES: This study was carried out to assess various skills of central auditory processing (CAP) in children with autism spectrum disorders (ASD) and to evaluate the efficacy of auditory training in these children. METHODS: This study is a non-randomized clinical experiment. 30 high functioning ASD children aged from 7 to 12 years were included in the study. They underwent behavioral assessments of CAP skills with subsequent remediation by dichotic training therapy for the children who revealed dichotic deficits. RESULTS: Scores of CAP skills in ASD children are wide-ranging from completely normal to substantially defective and generally lower than those of typically developing children. By auditory training, ASD children improved their dichotic deficits as well as other untrained areas of auditory and language processing skills. CONCLUSIONS: A group of ASD children showed different degrees of abnormalities in CAP that could be measured behaviorally and achieved benefits from auditory training in improving their dichotic listening, auditory and language processing skills.


Subject(s)
Auditory Perception/physiology , Auditory Perceptual Disorders/therapy , Autism Spectrum Disorder/complications , Cognitive Remediation/methods , Auditory Perceptual Disorders/etiology , Child , Female , Humans , Male
5.
Int J Pediatr Otorhinolaryngol ; 78(12): 2297-300, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25468467

ABSTRACT

AIM: To study the auditory profile at different levels of the auditory system in children with ASD and to verify the role of (Central) auditory processing disorder as an essential pathology of the autistic disorder or as an associated co-morbidity, and to establish the correlation between CAP findings and the language delay in these cases. PATIENTS: The study included 30 children with definite autistic disorder according to DSM-IV-TR criteria and ADI-R among those attending the outpatient neuropsychiatry clinic of Alexandria University Children Hospital at El Shatby. An informed consent was taken from all patients in this part of the study. Confidentiality of the records was maintained. METHODS: All cases were subjected to complete history taking and examination; special assessment to language skills and evoked potentials were done. RESULTS: The results concluded that (central) auditory processing disorder is an essential pathology of the autistic disorder. Autistic children possess a dysfunctioning or an immature central auditory nervous system at both the brainstem and cortical levels.


Subject(s)
Autistic Disorder/complications , Language Development Disorders/etiology , Child , Child, Preschool , Evoked Potentials, Auditory, Brain Stem , Female , Humans , Language Development Disorders/diagnosis , Male
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