Naoufel Gaddour
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Naoufel Gaddour has a total of 36 co-authors. Here are the top co-authors by number of shared publications:
- Abderrahmen Merghni
Laboratory of Antimicrobial Resistance LR99ES09, Faculty of Medicine of Tunis, University of Tunis El Manar, Tunis 1007, Tunisia
3 shared publications - Clara Gonzalez de Los Reyes Gavilan
Institute of Health Research of the Principality of Asturias (ISPA), 33011 Oviedo, Asturias, Spain
3 shared publications - Maha Mastouri
Laboratory of Transmissible Diseases and Biologically Active Substances LR99ES27, Faculty of Pharmacy of Monastir, University of Monastir, Monastir 5000, Tunisia
3 shared publications - Mariem Chamtouri
Department of Microbiology and Biochemistry of Dairy Products, Instituto de Productos Lácteos de Asturias (IPLA-CSIC), 33300 Villaviciosa, Spain
3 shared publications Asma Guedria
Department of Child and Adolescent Psychiatry, University of Monastir, Monastir, Tunisia
2 shared publications- Silvia Arboleya
Institute of Health Research of the Principality of Asturias (ISPA), 33011 Oviedo, Asturias, Spain
2 shared publications
Latest Publications
- Open Access
- 30 December 2025
- Published by Springer Nature in Discover Mental Health
- Vol. 5 (1) , 211
Patterns of early exposure to screens by children with ASD
To further explore and discuss the characteristics of exposure to screens in Autism Spectrum Disorder in the Tunisian context. This case control study explored the exposure to TV in 150 children with ASD, aged 1 to 4 years old in comparison to a comparable group of 150 typically developing children. Results showed Significant differences were observed between groups regarding the age of television viewing onset (4 vs. 14 months) and daily viewing duration (7 h vs. <1 h). Children with ASD predominantly viewed television alone, showing preference for repetitive content such as music videos, with viewing occurring throughout the day. Television exposure served as both a child-occupying strategy and a parental soothing technique, and was associated with increased autistic symptomatology. While acknowledging methodological limitations, this study suggests that the impact of early intensive screen exposure warrants further investigation in ASD populations.
- 30 December 2025
- Published by Springer Nature in Discover Mental Health
- Vol. 5 (1) , 211
Open AccessPatterns of early exposure to screens by children with ASD
To further explore and discuss the characteristics of exposure to screens in Autism Spectrum Disorder in the Tunisian context. This case control study explored the exposure to TV in 150 children with ASD, aged 1 to 4 years old in comparison to a comparable group of 150 typically developing children. Results showed Significant differences were observed between groups regarding the age of television viewing onset (4 vs. 14 months) and daily viewing duration (7 h vs. <1 h). Children with ASD predominantly viewed television alone, showing preference for repetitive content such as music videos, with viewing occurring throughout the day. Television exposure served as both a child-occupying strategy and a parental soothing technique, and was associated with increased autistic symptomatology. While acknowledging methodological limitations, this study suggests that the impact of early intensive screen exposure warrants further investigation in ASD populations.
- 10 December 2025
- Published by Springer Nature in Molecular Neurobiology
- Vol. 63 (1) , 280
Genetic Association and Functional Prediction of PTEN and TSC1 3′UTR Variants in Autism Spectrum Disorder Among Tunisian Patients
ASD etiology may be influenced by non-coding single-nucleotide polymorphisms (SNPs) in 3' untranslated regions (3'UTRs). These variations can affect post-transcriptional regulation by altering RNA structure and miRNA binding patterns. PTEN and TSC1, two key regulators of the PI3K/AKT/mTOR signaling pathway, are promising candidate genes for ASD. We performed a case-control study involving 108 individuals diagnosed with ASD and 184 healthy matched controls from the Tunisian population. Four specific 3'UTR SNPs (PTEN: rs701848, rs34140758; TSC1: rs739442, rs2809244) were analyzed through genotyping. Statistical associations were assessed using various genetic inheritance models, with multivariate logistic regression adjusting for gender, family psychiatric history, and parental age. A thorough bioinformatics approach was applied, which included miRNASNP-v3 for predicting altered miRNA binding sites, RNAhybrid for calculating the minimum free energy (MFE) of miRNA-mRNA duplexes, PhyloP and phastCons for evolutionary conservation analysis, and mfold for modeling RNA secondary structures. PTEN rs701848 showed a significant statistical association with ASD risk that remained significant after correction for multiple testing (corrected p < .0004), while TSC1 rs739442 showed a suggestive association (p = .009, corrected p = .036). Systematic functional assessment using multi-criteria evaluation identified rs701848 as having high predicted functional impact (extensive miRNA binding changes, including loss of neurodevelopmental miR-129 sites, high conservation (PhyloP = 2.24), and altered RNA stability), while rs739442 showed moderate impact, and rs2809244 minimal predicted functional significance. For mutant alleles, RNA structure modeling showed slight decreases in mRNA stability, which might affect transcript accessibility to regulatory factors. Evolutionary conservation analysis demonstrated that rs701848 and rs34140758 reside in highly conserved areas, whereas rs739442 and rs2809244 are in less evolutionarily conserved regions. By integrating population-genetics data with bioinformatics predictions, this study supports the relevance of non-coding SNPs as biological risk factors for ASD. It emphasizes their functional significance in modulating post-transcriptional gene regulation mechanisms.
- 10 December 2025
- Published by Springer Nature in Molecular Neurobiology
- Vol. 63 (1) , 280
Genetic Association and Functional Prediction of PTEN and TSC1 3′UTR Variants in Autism Spectrum Disorder Among Tunisian Patients
ASD etiology may be influenced by non-coding single-nucleotide polymorphisms (SNPs) in 3' untranslated regions (3'UTRs). These variations can affect post-transcriptional regulation by altering RNA structure and miRNA binding patterns. PTEN and TSC1, two key regulators of the PI3K/AKT/mTOR signaling pathway, are promising candidate genes for ASD. We performed a case-control study involving 108 individuals diagnosed with ASD and 184 healthy matched controls from the Tunisian population. Four specific 3'UTR SNPs (PTEN: rs701848, rs34140758; TSC1: rs739442, rs2809244) were analyzed through genotyping. Statistical associations were assessed using various genetic inheritance models, with multivariate logistic regression adjusting for gender, family psychiatric history, and parental age. A thorough bioinformatics approach was applied, which included miRNASNP-v3 for predicting altered miRNA binding sites, RNAhybrid for calculating the minimum free energy (MFE) of miRNA-mRNA duplexes, PhyloP and phastCons for evolutionary conservation analysis, and mfold for modeling RNA secondary structures. PTEN rs701848 showed a significant statistical association with ASD risk that remained significant after correction for multiple testing (corrected p < .0004), while TSC1 rs739442 showed a suggestive association (p = .009, corrected p = .036). Systematic functional assessment using multi-criteria evaluation identified rs701848 as having high predicted functional impact (extensive miRNA binding changes, including loss of neurodevelopmental miR-129 sites, high conservation (PhyloP = 2.24), and altered RNA stability), while rs739442 showed moderate impact, and rs2809244 minimal predicted functional significance. For mutant alleles, RNA structure modeling showed slight decreases in mRNA stability, which might affect transcript accessibility to regulatory factors. Evolutionary conservation analysis demonstrated that rs701848 and rs34140758 reside in highly conserved areas, whereas rs739442 and rs2809244 are in less evolutionarily conserved regions. By integrating population-genetics data with bioinformatics predictions, this study supports the relevance of non-coding SNPs as biological risk factors for ASD. It emphasizes their functional significance in modulating post-transcriptional gene regulation mechanisms.
- Open Access
- 22 October 2024
- Published by MDPI AG in Journal of Fungi
- Vol. 10 (11) , 730
Characterization of Yeast Isolated from the Gut Microbiota of Tunisian Children with Autism Spectrum Disorder
Research on the microbiota–gut–brain axis in autism has primarily focused on bacteria, with limited attention to fungi. There is a growing interest in understanding the involvement of fungi, particularly Candida, in patients with autism spectrum disorder. The aim of this study was to assess the prevalence, antifungal susceptibility profiles and virulence factors of Candida isolates from the guts of Tunisian children with autism. Twenty-eight children with autism and forty-six controls were enrolled. Candida isolates from the faecal samples were identified using biochemical and molecular methods; antifungal susceptibility testing was determined by the EUCAST broth microdilution method and virulence factors, including biofilm formation, cell surface hydrophobicity and phospholipase and proteinase activities, were assessed in vitro. As a result, Candida was detected in 13 children with autism (46.4%) and 14 control children (30.4%). Candida albicans was found to be the most common species isolate in the faeces of both groups of children. Antifungal susceptibility profiles showed that one Candida isolate was resistant to amphotericin B and anidulafungin (3.7%), six were resistant to micafungin (22.2%) and five were resistant to fluconazole (18.5%). All Candida isolates were biofilm producers. Of the twenty-seven isolates, only four showed phospholipase activity (14.8%), eight showed aspartyl-proteinase activity (29.6%) and nine were hydrophobic (33.3%). These results highlight the presence of Candida in the guts of children with autism, as well as the ability to express multiple virulence factors and the antifungal resistance, and they emphasize the need for further studies to confirm intestinal Candida colonization and its potential role in autism.
- 22 October 2024
- Published by MDPI AG in Journal of Fungi
- Vol. 10 (11) , 730
Open AccessCharacterization of Yeast Isolated from the Gut Microbiota of Tunisian Children with Autism Spectrum Disorder
Research on the microbiota–gut–brain axis in autism has primarily focused on bacteria, with limited attention to fungi. There is a growing interest in understanding the involvement of fungi, particularly Candida, in patients with autism spectrum disorder. The aim of this study was to assess the prevalence, antifungal susceptibility profiles and virulence factors of Candida isolates from the guts of Tunisian children with autism. Twenty-eight children with autism and forty-six controls were enrolled. Candida isolates from the faecal samples were identified using biochemical and molecular methods; antifungal susceptibility testing was determined by the EUCAST broth microdilution method and virulence factors, including biofilm formation, cell surface hydrophobicity and phospholipase and proteinase activities, were assessed in vitro. As a result, Candida was detected in 13 children with autism (46.4%) and 14 control children (30.4%). Candida albicans was found to be the most common species isolate in the faeces of both groups of children. Antifungal susceptibility profiles showed that one Candida isolate was resistant to amphotericin B and anidulafungin (3.7%), six were resistant to micafungin (22.2%) and five were resistant to fluconazole (18.5%). All Candida isolates were biofilm producers. Of the twenty-seven isolates, only four showed phospholipase activity (14.8%), eight showed aspartyl-proteinase activity (29.6%) and nine were hydrophobic (33.3%). These results highlight the presence of Candida in the guts of children with autism, as well as the ability to express multiple virulence factors and the antifungal resistance, and they emphasize the need for further studies to confirm intestinal Candida colonization and its potential role in autism.
- Open Access
- 24 August 2023
- Published by MDPI AG in Microbiology Research
- Vol. 14 (3) , 1225-1237
Lactobacilli Profile in Faecal Samples of Tunisian Children Diagnosed with Autism Spectrum Disorder
Alterations in faecal lactobacilli in autistic children have been reported, but little is known related to age and disorder severity. We used a culture-based method and partial 16S rRNA gene sequencing to isolate and identify lactobacilli strains from faeces of Tunisian autistic children (ASD group) and compared them with strains isolated from siblings (SIB) and children from the general population (GP). The ASD group displayed an increased number of different species compared to SIB and GP. Differences in species abundance with age accounted for a significant decrease in the abundance of Lactiplantibacillus plantarum/Lactiplantibacillus pentosus isolates in the GP at the age of 8–10 years compared to the age of 4–7 years, and to a significantly lower abundance of Lacticaseibacillus rhamnosus in the ASD group with respect to SIB and the GP at the age of 8–10 years. Simpson’s and Shannon–Wiener indices showed a more pronounced species diversity increase with age in the GP group compared to the ASD and SIB groups. Minor differences were found in lactobacilli prevalence and in species diversity between children with severe and mild-to-moderate ASD. Overall, we found substantial differences in the profile of faecal lactobacilli species in the ASD and GP groups at the age of 8–10 years.
- 24 August 2023
- Published by MDPI AG in Microbiology Research
- Vol. 14 (3) , 1225-1237
Open AccessLactobacilli Profile in Faecal Samples of Tunisian Children Diagnosed with Autism Spectrum Disorder
Alterations in faecal lactobacilli in autistic children have been reported, but little is known related to age and disorder severity. We used a culture-based method and partial 16S rRNA gene sequencing to isolate and identify lactobacilli strains from faeces of Tunisian autistic children (ASD group) and compared them with strains isolated from siblings (SIB) and children from the general population (GP). The ASD group displayed an increased number of different species compared to SIB and GP. Differences in species abundance with age accounted for a significant decrease in the abundance of Lactiplantibacillus plantarum/Lactiplantibacillus pentosus isolates in the GP at the age of 8–10 years compared to the age of 4–7 years, and to a significantly lower abundance of Lacticaseibacillus rhamnosus in the ASD group with respect to SIB and the GP at the age of 8–10 years. Simpson’s and Shannon–Wiener indices showed a more pronounced species diversity increase with age in the GP group compared to the ASD and SIB groups. Minor differences were found in lactobacilli prevalence and in species diversity between children with severe and mild-to-moderate ASD. Overall, we found substantial differences in the profile of faecal lactobacilli species in the ASD and GP groups at the age of 8–10 years.
- Open Access
An Overview on Fecal Profiles of Amino Acids and Related Amino-Derived Compounds in Children with Autism Spectrum Disorder in Tunisia
Autism spectrum disorder (ASD) is a neurodevelopmental pathology characterized by the impairment of social interaction, difficulties in communication, and repetitive behaviors. Alterations in the metabolism of amino acids have been reported. We performed a chromatographic analysis of fecal amino acids, ammonium, biogenic amines, and gamma aminobutyric acid (GABA) in Tunisian autistic children from 4 to 10 years, and results were compared with their siblings (SIB) and children from the general population (GP). ASD presented significantly higher levels of fecal amino acids than SIB and GP; differences being more pronounced in younger (4–7 years) than in older (8–10 years) individuals whereas no changes were found for the remaining compounds. Lower levels of histidine were the only difference related with severe symptoms of autism (CARS scale). A linear discriminant analysis (LDA) based on fecal amino acid profiles clearly separated ASD, SIB, and GP at 4 to 7 years but not at more advanced age (8–10 years), evidencing more pronounced alterations in younger children. The relationship of fecal amino acids with autism needs deeper research integrating blood analytical parameters, brain metabolism, and intestinal microbiota. Fecal amino acids could be targeted for designing personalized diets to prevent or minimize cognitive impairments associated with ASD.
Open AccessAn Overview on Fecal Profiles of Amino Acids and Related Amino-Derived Compounds in Children with Autism Spectrum Disorder in Tunisia
Autism spectrum disorder (ASD) is a neurodevelopmental pathology characterized by the impairment of social interaction, difficulties in communication, and repetitive behaviors. Alterations in the metabolism of amino acids have been reported. We performed a chromatographic analysis of fecal amino acids, ammonium, biogenic amines, and gamma aminobutyric acid (GABA) in Tunisian autistic children from 4 to 10 years, and results were compared with their siblings (SIB) and children from the general population (GP). ASD presented significantly higher levels of fecal amino acids than SIB and GP; differences being more pronounced in younger (4–7 years) than in older (8–10 years) individuals whereas no changes were found for the remaining compounds. Lower levels of histidine were the only difference related with severe symptoms of autism (CARS scale). A linear discriminant analysis (LDA) based on fecal amino acid profiles clearly separated ASD, SIB, and GP at 4 to 7 years but not at more advanced age (8–10 years), evidencing more pronounced alterations in younger children. The relationship of fecal amino acids with autism needs deeper research integrating blood analytical parameters, brain metabolism, and intestinal microbiota. Fecal amino acids could be targeted for designing personalized diets to prevent or minimize cognitive impairments associated with ASD.
- Open Access
- 14 August 2019
- Published by Morressier GmbH
Impact of Parents psychiatric disorders on the evolution of children Autism spectrum disorder
Impact of Parents psychiatric disorders on the evolution of children Autism spectrum disorder Authors Name: Nabli R. Brahim T. Gaddour N; university of Monastir-Tunisia Introduction: Having a parent with a psychiatric disorder have an impact on the well being and the development of the child. Is there an influence on the evolution of the Autism spectrum disorder (ASD) by this
- 14 August 2019
- Published by Morressier GmbH
Open AccessImpact of Parents psychiatric disorders on the evolution of children Autism spectrum disorder
Impact of Parents psychiatric disorders on the evolution of children Autism spectrum disorder Authors Name: Nabli R. Brahim T. Gaddour N; university of Monastir-Tunisia Introduction: Having a parent with a psychiatric disorder have an impact on the well being and the development of the child. Is there an influence on the evolution of the Autism spectrum disorder (ASD) by this
- 5 April 2017
- Published by SAGE Publications in Journal of Attention Disorders
- Vol. 22 (2) , 154-162
ADHD in Tunisian Adolescents: Prevalence and Associated Factors
Objective: The aims of the study were to determine the prevalence of ADHD in a population of high school students and to explore the factors associated with this disorder. Method: This was a cross-sectional study that had included 447 high school students. The diagnosis of ADHD was made by the Adult ADHD Self-Report Scale translated in Arabic language. The sociodemographic and clinical characteristics were evaluated by a preestablished questionnaire. The self-esteem was assessed by the Rosenberg Self-Esteem Scale. Results: The prevalence of ADHD was 18.1%. The logistic regression analysis showed an association between the diagnosis of ADHD and the bad relationships with parents (odds ratio [OR] = 16.43; p < 10-3), the presence of personal psychiatric antecedents (OR = 12.16; p < 10-3), internet misuse (OR = 2.39; p = .014), and maltreatment antecedents (OR = 3.16; p = .009). Conclusion: The prevalence of ADHD in this study was one of the highest prevalence reported. The factors associated with ADHD may have diagnostic and therapeutic implications.
- 5 April 2017
- Published by SAGE Publications in Journal of Attention Disorders
- Vol. 22 (2) , 154-162
ADHD in Tunisian Adolescents: Prevalence and Associated Factors
Objective: The aims of the study were to determine the prevalence of ADHD in a population of high school students and to explore the factors associated with this disorder. Method: This was a cross-sectional study that had included 447 high school students. The diagnosis of ADHD was made by the Adult ADHD Self-Report Scale translated in Arabic language. The sociodemographic and clinical characteristics were evaluated by a preestablished questionnaire. The self-esteem was assessed by the Rosenberg Self-Esteem Scale. Results: The prevalence of ADHD was 18.1%. The logistic regression analysis showed an association between the diagnosis of ADHD and the bad relationships with parents (odds ratio [OR] = 16.43; p < 10-3), the presence of personal psychiatric antecedents (OR = 12.16; p < 10-3), internet misuse (OR = 2.39; p = .014), and maltreatment antecedents (OR = 3.16; p = .009). Conclusion: The prevalence of ADHD in this study was one of the highest prevalence reported. The factors associated with ADHD may have diagnostic and therapeutic implications.
- 1 June 2015
- Published by Elsevier in L'Encéphale
- Vol. 41 (3) , 215-220
Impulsivité et problèmes d’internalisation et d’externalisation chez l’adolescent
- 1 June 2015
- Published by Elsevier in L'Encéphale
- Vol. 41 (3) , 215-220
Impulsivité et problèmes d’internalisation et d’externalisation chez l’adolescent