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Metabolomic Profiles in Jamaican Children With and Without Autism Spectrum Disorder.
Yazdani, Akram; Samms-Vaughan, Maureen; Saroukhani, Sepideh; Bressler, Jan; Hessabi, Manouchehr; Tahanan, Amirali; Grove, Megan L; Gangnus, Tanja; Putluri, Vasanta; Kamal, Abu Hena Mostafa; Putluri, Nagireddy; Loveland, Katherine A; Rahbar, Mohammad H.
Afiliación
  • Yazdani A; Division of Clinical and Translational Sciences, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Samms-Vaughan M; Biostatistics/Epidemiology/Research Design (BERD) Component, Center for Clinical and Translational Sciences (CCTS), The University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Saroukhani S; Department of Child & Adolescent Health, The University of the West Indies (UWI), Mona Campus, Kingston 7, Jamaica.
  • Bressler J; Division of Clinical and Translational Sciences, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Hessabi M; Biostatistics/Epidemiology/Research Design (BERD) Component, Center for Clinical and Translational Sciences (CCTS), The University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Tahanan A; Human Genetics Center, Department of Epidemiology, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Grove ML; Biostatistics/Epidemiology/Research Design (BERD) Component, Center for Clinical and Translational Sciences (CCTS), The University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Gangnus T; Biostatistics/Epidemiology/Research Design (BERD) Component, Center for Clinical and Translational Sciences (CCTS), The University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Putluri V; Human Genetics Center, Department of Epidemiology, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Kamal AHM; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA.
  • Putluri N; Advanced Technology Core, Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
  • Loveland KA; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA.
  • Rahbar MH; Advanced Technology Core, Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
J Autism Dev Disord ; 2024 Jul 20.
Article en En | MEDLINE | ID: mdl-39033254
ABSTRACT
Autism spectrum disorder (ASD) is a complex neurodevelopmental condition with a wide range of behavioral and cognitive impairments. While genetic and environmental factors are known to contribute to its etiology, metabolic perturbations associated with ASD, which can potentially connect genetic and environmental factors, remain poorly understood. Therefore, we conducted a metabolomic case-control study and performed a comprehensive analysis to identify significant alterations in metabolite profiles between children with ASD and typically developing (TD) controls in order to identify specific metabolites that may serve as biomarkers for the disorder. We conducted metabolomic profiling on plasma samples from participants in the second phase of Epidemiological Research on Autism in Jamaica, an age and sex-matched cohort of 200 children with ASD and 200 TD controls (2-8 years old). Using high-throughput liquid chromatography-mass spectrometry techniques, we performed a targeted metabolite analysis, encompassing amino acids, lipids, carbohydrates, and other key metabolic compounds. After quality control and missing data imputation, we performed univariable and multivariable analysis using normalized metabolites while adjusting for covariates, age, sex, socioeconomic status, and child's parish of birth. Our findings revealed unique metabolic patterns in children with ASD for four metabolites compared to TD controls. Notably, three metabolites were fatty acids, including myristoleic acid, eicosatetraenoic acid, and octadecenoic acid. The amino acid sarcosine exhibited a significant association with ASD. These findings highlight the role of metabolites in the etiology of ASD and suggest opportunities for the development of targeted interventions.
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Texto completo: 1 Bases de datos: MEDLINE País/Región como asunto: Caribe ingles / Jamaica Idioma: En Revista: J Autism Dev Disord / J. autism dev. disord / Journal of autism and developmental disorders Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE País/Región como asunto: Caribe ingles / Jamaica Idioma: En Revista: J Autism Dev Disord / J. autism dev. disord / Journal of autism and developmental disorders Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos