Objectives: To study the association of the single nucleotide polymorphisms (SNPs) of the adenylyl cyclase IX () gene at rs1967309, rs2230739, rs2601814, rs2601825, rs2601796, and rs2283497 loci and gene-environment interaction with childhood bronchial asthma (asthma for short).
Methods: A total of 123 children with asthma who attended the hospital from March 2019 to September 2021 were enrolled as the asthma group, among whom 84 (68.3%) had mild-to-moderate attacks and 39 (31.7%) had severe attacks. A total of 124 healthy children were enrolled as the control group. The association of the SNPs and haplotypes of the gene at the above 6 loci with the susceptibility to childhood asthma was evaluated. The method of generalized multifactor dimensionality reduction was used to analyze gene-environment interaction.
Results: Polymorphisms were observed for the gene at the above six loci in both the asthma and control groups, and there were significant differences in genotype and allele frequencies at the rs1967309 locus between the two groups (<0.05). There was no significant difference in the distribution frequency of haplotypes TA and GG between the asthma and control groups (>0.05). The generalized multifactor dimensionality reduction analysis showed interaction between rs1967309 locus and allergen contact (<0.05), which increased the risk of asthma (=1.585, <0.05).
Conclusions: The rs1967309 locus of the gene is associated with the susceptibility to childhood asthma, and the locus and allergen contact have a synergistic effect on the development of asthma.
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http://dx.doi.org/10.7499/j.issn.1008-8830.2204107 | DOI Listing |
Alzheimers Dement
December 2024
University of Michigan School of Public Health, Ann Arbor, MI, USA.
Background: Dementia is a prevalent neurodegenerative disease with risk attributed to both genetic and environmental factors. Multiple factors contribute to the etiology of dementia, and the relevant exposure window of susceptibility is likely before symptom onset. Conditions and the environment in the early life period have not yet been comprehensively tested for association with later-life dementia.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Hotchkiss Brain Institute, University of Calgary, Calgary, AB, Canada.
Background: Of the 12 modifiable dementia risk factors established by the Lancet Commission, only one addresses early life. However, the brain is highly plastic in early life. Adverse childhood experiences (ACE)-physical, emotional, and sexual abuse and neglect-can result in long-term reductions in brain volume.
View Article and Find Full Text PDFCase Reports Immunol
December 2024
Department of Medical Oncology and Hematology, Oncology Institute, Cleveland Clinic Abu Dhabi (CCAD), Abu Dhabi, UAE.
X-linked moesin-associated immunodeficiency (X-MAID) is a recently identified combined immunodeficiency caused by a mutation in the moesin () gene. It is characterized by cytopenias, hypogammaglobulinemia, poor immune response to vaccine antigens, and increased susceptibility to early-life infections. We report a patient with adult-onset neutropenia, lymphopenia, inadequate response to the pneumococcal polysaccharide vaccine (PPSV23), and recurrent bacterial infections associated with a hemizygous deletion.
View Article and Find Full Text PDFCurr Nutr Rep
January 2025
Department of Nutrition and Dietetics, Faculty of Health Sciences, Bursa Uludag University, Bursa, Turkey.
Endocrine disruptors (EDs) can mimic or interfere with hormones in the body, leading to non-communicable diseases, such as obesity, diabetes, and metabolic syndrome. Susceptibility to EDs increases during prenatal and postnatal life, a critical time window. This review aims to summarize the latest evidence on the relation of early life exposure to some EDs with obesity and the other metabolic disorders.
View Article and Find Full Text PDFIntroduction: Children with early childhood caries (ECC) show different caries severities and susceptibility in different tooth types and location in the oral cavity. The study aimed to investigate differences in the oral microbiome in ECC subjects stratified according to the severity of caries and between more and less caries prone teeth within the same subjects.
Methods: Supragingival plaque from the upper and lower anterior regions in the oral cavity of subjects were collected in 3 groups of increasing caries severity, G1 - Molar (M) caries only; G2 - Molar and Upper Anterior (UA) caries; and G3 - M + UA + lower anterior (LA) caries were obtained followed by microbiome analysis.
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