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  • Review Article   
  • Occup Med Health 2023, Vol 11(4): 469
  • DOI: 10.4172/2329-6879.1000469

Demographic and Lifestyle Characteristics of Parental Occupational Autism Spectrum Disorder

Michael Kens*
Department of Public Health Sciences, University of California, USA
*Corresponding Author: Michael Kens, Department of Public Health Sciences, University of California, USA, Email: kens1@gmail.com

Received: 05-Jul-2023 / Manuscript No. omha-23-103886 / Editor assigned: 07-Jul-2023 / PreQC No. omha-23-103886 (PQ) / Reviewed: 21-Jul-2023 / QC No. omha-23-103886 / Revised: 24-Jul-2023 / Manuscript No. omha-23-103886(R) / Accepted Date: 29-Jul-2023 / Published Date: 31-Jul-2023 DOI: 10.4172/2329-6879.1000469

Abstract

Repetitive behavior, impairment in reciprocal social interaction, difficulty communicating, and sensory sensitivities are all symptoms of autism spectrum disorder (ASD). ASD's etiology has been linked to both environmental and genetic factors. Gene-environment interaction research may shed light on the complexities of ASD's etiology and point the way toward potential ways to prevent it. SNPs from a wide range of targeted genes have only been used in a few studies to investigate how genes and environments affect autism risk. Due to their small size, higher absorption rates, rapid growth, development of cellular structures, and diminished capacity for detoxification of exogenous chemicals, the fetus, neonate, and young child are more susceptible to exposures. A few surveys refer to recreated discoveries that ecological variables are related with ASD.

Additionally, occupational exposures to parents have been found to be linked to ASD; in particular, working with solvents by parents. Solvents are metabolized into toxic secondary substances like methyl-butyl ketone and n-hexane, which are linked to abnormal white matter, smaller corpus callosum volume, and cerebellar atrophy. Solvents can be absorbed through the skin or the lungs. Cognitive delays, attention deficit hyperactivity disorder, delayed speech, and motor function are all seen in infants born to mothers who were exposed to solvents. Further supporting the link between solvents and the risk of ASD, mothers who were occupationally exposed to solvents were 1.5 times more likely to have a child with ASD than a child who was normally developing. Similarly, despite the overwhelming evidence from decades of genetic research that links ASD to multiple genes on virtually every chromosome, the majority of ASD cases cannot be explained. Causal pathways likely involve interactions between environmental, chemical, and physical agents that influence immune, endocrine, and neuro-developmental processes, as they do with the majority of complex diseases. Epigenetic changes, which are themselves influenced by environmental factors, are also linked to an increased risk of neurocognitive or behavioral impairments, according to increasing evidence.

Keywords

Demographic; Autism spectrum; Neurocognitive; Epigenetic changes; Neuro-developmental

Introduction

A population-based case-control study has previously been described as the Childhood Autism Risks from Genetics and Environment CHARGE study. In a nutshell, the CHARGE study enrolls children selected from birth records maintained by the California State Vital Statistics as well as children selected from the general population. Children between the ages of 2 and 5 who were born in California, reside in the catchment areas of a specified list of California Regional Centers that coordinate services for people with developmental disabilities, and live with at least one biological parent who speaks English or Spanish are eligible [1]. Youngsters with mental imbalance are distinguished through the California Branch of Formative Administrations, which manages the Territorial Place framework, and all inclusive community controls from state birth records are recurrence matched to the normal sex dissemination, as well as the age, furthermore, catchment region of the mental imbalance cases. 976 children and their parents who participated in the CHARGE study provided the National Institute for Occupational Safety and Health (NIOSH) with genetic, diagnosis, and basic demographic information. 423 of those were children with typical development (TD) serving as controls. The present study's sample consisted of 711 children, after excluding 265 participants with missing genetic data: 414 people with ASD, 297 people with TD, and their parents [2].

Method

Both the UC Davis MIND Institute and the UCLA Neuropsychiatric Institute evaluated each child. The Autism Diagnostic Observation Schedule-2 (ADOS-2) was used to assess ASD-disabled children, and their parents completed the Autism Diagnostic Interview-Revised (ADI-R) to confirm their child's diagnosis. Cognitive and adaptive function was evaluated using the Vineland Adaptive Behavior Scales (VABS) and the Mullen Scales of Early Learning (MSEL) (Mullen, 1995) [3]. The Social Communication Questionnaire (SCQ) was used to evaluate children from the general population (Rutter et al., 2003) ASD screening instrument they were considered to be typically developing (TD) if their SCQ scores were below 15 and their MSEL and VABS scores were within the normal range. The ADOS-2 was used to check for ASD in children who scored less than 15, and the ADI-R was filled out by their parents. The Risi algorithm was used to determine whether the child had ASD or not. 2.3. Collection of specimens and genotype analysis Study children gave a blood sample, and standard methods were used to isolate genomic DNA [4].

Result

Quality control and information cleaning was acted in Genotyping Control center, utilizing the 2-step process suggested in Affymetrix's Accepted procedures. After calling 175,000 well-characterized SNPs in the first step, samples with call rates below 95% were eliminated. Genotypes were called on the entire set of SNPs in samples that met the 95% call rate threshold. The mean call rate and number of SNPs were 675,367 prior to any quality control measures being implemented [5]. R and PLINK were used to clean up all of the subsequent data. Based on heterozygosity on the X chromosome, all individuals' reported sex was compared to their likely sex. The samples were eliminated if there was a mismatch between recorded and apparent sex. Three people were eliminated due to extremely low genotyping rates, and 30,601 SNPs were eliminated due to low call rates. Additionally, 12,370 SNPs with p-values below 10-4 that violated the Hardy-Weinberg equilibrium assumption were excluded from the analyses. There were no samples with unusually high levels of heterozygosity [6], which could indicate that the samples were contaminated. To measure cryptic relatedness, PLINK was utilized. Even using variants with high minor allele frequencies, testing revealed high levels of cryptic relatedness between a few individuals and the rest of the cohort. However, given that this cohort is multiethnic, it's possible that the apparent oversharing is a result of the population's structure [7].

Discussion

A population-based case-control study known as the CHildhood Autism Risks from Genetics and Environment CHARGE study has previously been described. In a nutshell, the CHARGE study enrolls children selected from birth records maintained by the California State Vital Statistics as well as children selected from the general population. Children between the ages of 2 and 5 who were born in California, reside in the catchment areas of a specified list of California Regional Centers that coordinate services for people with developmental disabilities, and live with at least one biological parent who speaks English or Spanish are eligible [8]. Youngsters with mental imbalance are distinguished through the California Branch of Formative Administrations, which manages the Territorial Place framework, and all inclusive community controls from state birth records are recurrence matched to the normal sex dissemination, as well as the age, furthermore, catchment region of the mental imbalance cases. 976 children and their parents who participated in the CHARGE study provided the National Institute for Occupational Safety and Health (NIOSH) with genetic, diagnosis, and basic demographic information. 423 of those were children with typical development (TD) serving as controls. The present study's sample consisted of 711 children, after excluding 265 participants with missing genetic data: 414 people with ASD, 297 people with TD, and their parents [9].

Data on the two moms and fathers, gathered through surveys, incorporated their age (years), training level, race/nationality, origin, smoking history, liquor use, provincial focus/geographic area of home, and installment strategy utilized for the youngster's conveyance (public or private). High school/GED or less, some college, Bachelor's degree, and graduate or professional degree were the categories for educational level [10]. There were three categories for birthplaces: Mexico, the United States, and locations outside of Mexico and the United States. Liquor use was gathered as none/low and middle/high [11-13].

Conclusion

Smoking was a yes/no dichotomy variable. There were five territorial communities: 1) North Bay, East Bay, San Andreas, and Golden Gate, 2) Valley Mt., Central Valley, and Kern, 3) All Los Angeles RCs, including Orange, San Diego Tricounties, and Inland, and 4) Redwood Coast, far Northern, and Alta. By adding up the education levels of both parents, the variable total years of education was calculated. The parents' ages were expressed in years, while the parents' ages were determined by taking the average of their ages. Race/ ethnicity was grouped as a result of the small numbers in some racial categories: non-Hispanic white; non-Hispanic black; Any Hispanic; or then again Other. Those who identified as American Indian, Alaska Native, Asian, Pacific Islander/Hawaiian Native, or multiracial fall into the "other" category. the percentage of each parent's exposure to solvent. Age in years, gender (male or female), date of birth, race or ethnicity, and length of breastfeeding (in months) were the child variables. Similar to the parents' race and ethnicity, race and ethnicity were categorized.

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Citation: Kens M (2023) Demographic and Lifestyle Characteristics of Parental Occupational Autism Spectrum Disorder. Occup Med Health 11: 469. DOI: 10.4172/2329-6879.1000469

Copyright: © 2023 Kens M. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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