Genes related to cell adhesion pathway have been implicated in the genetic architecture of attention-deficit/hyperactivity disorder (ADHD). Cell adhesion molecule 1, encoded by gene, is a protein which facilitates cell adhesion, highly expressed in the human prefrontal lobe. This study aimed to evaluate the association of genotype with ADHD, executive function, and regional brain functions. The genotype data of 10-tag single nucleotide polymorphisms of for 1,040 children and adolescents with ADHD and 963 controls were used for case-control association analyses. Stroop color-word interference test, Rey-Osterrieth complex figure test, and trail making test were conducted to assess "inhibition," "working memory," and "set-shifting," respectively. A subsample (35 ADHD versus 56 controls) participated in the nested imaging genetic study. Resting-state functional magnetic resonance images were acquired, and the mean amplitude of low-frequency fluctuations (mALFF) were captured. Nominal significant genotypic effect of rs10891819 in "ADHD-alone" subgroup was detected ( = 0.008) with TT genotype as protective. The results did not survive multiple testing correction. No direct genetic effect was found for performance on executive function tasks. In the imaging genetic study for the "ADHD-whole" sample, rs10891819 genotype was significantly associated with altered mALFF in the right superior frontal gyrus (rSFG, peak = 3.85, corrected < 0.05). Specifically, the mALFFs in T-allele carriers were consistently higher than GG carriers in ADHD and control groups. Endophenotypic correlation analyses indicated a significant negative correlation between "word interference time" in Stroop (shorter "word interference time" indexing better inhibitory function) and mALFF in the rSFG ( = -0.29, = 0.006). Finally, mediation analysis confirmed significant indirect effects from "rs10891819 genotype (T-allele carriers)" "mALFF (rSFG)" to "inhibition ("word interference time")" (Sobel = -2.47; B = -2.61, 95% confidence interval -0.48 to -4.72; = 0.009). Our study offered preliminary evidence to implicate the roles of in relation to prefrontal brain activities, inhibition function, and ADHD, indicating a potential "gene-brain-behavior" relationship of the . Future studies with larger samples may specifically test these hypotheses generated by our exploratory findings.
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http://dx.doi.org/10.3389/fgene.2019.00882 | DOI Listing |
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CiRA Foundation, Research and Development Center, Osaka, Japan.
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Oral Microbiology, Bristol Dental School, University of Bristol, United Kingdom.
This review discusses the chemical properties, synthesis and detection, and biological functions of a molecular group of cis-2-unsaturated fatty acids, containing fatty acid carbon chains of various lengths and cis double-bond configurations, known as the diffusible signaling factor family (DSFF). Early postulation of the conserved nature of the DSFF among Gram-negative bacteria have now been challenged by the latest evidences that unraveled their presence in a various other distinct microorganisms. Over the last decade, a significant depth and breadth of understanding has been made on the multifaceted functions of DSFFs among bacteria, and their interactions with evolutionarily divergent fungi, plants insects and small animals.
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Laboratory of Molecular Microbiology (Micromol), Institute of Biomedical Sciences, Universidade Federal de Uberlndia, Uberlndia, Minas Gerais, Brazil.
In critically ill patients, the occurrence of multidrug-resistant infection is a significant concern, given its ability to acquire multidrug-resistant, form biofilms and secrete toxic effectors. In Brazil, limited data are available regarding the prevalence of dissemination, and the impact of the type III secretion system (T3SS) on toxin production and biofilm formation in clinical isolates of . This study investigates the dissemination of virulent harbouring the and genes, the presence of T3SS genes and their biofilm-forming capability.
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Department of Orthopaedics, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200233, China.
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