Assessing the Causal Relationship Between Various Immune Cells and Attention Deficit Hyperactivity Disorder: Mendelian Randomization Study.

IF 2.6 3区 心理学 Q2 BEHAVIORAL SCIENCES Brain and Behavior Pub Date : 2025-01-01 DOI:10.1002/brb3.70280
Qian Ge, Zhongyan Li, Weijing Meng, Chen Cai, Mengdi Qiu, Yafei Liu, Haibo Zhu
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Abstract

Background: Immune system modulation has been shown to have a significant impact on attention deficit hyperactivity disorder (ADHD). Mendelian randomization (MR) analysis was used in this study to investigate the potential role of different immune cells in the development of ADHD to provide therapy and preventative alternatives.

Methods: In this study, 731 immune cells and the risk of ADHD were examined using publicly accessible genetic data and a two-sample MR analysis. Included were four different types of immunological profiles: determinate cells (DC), proportional cells (PC), median brightness level (MBL), and morphological characteristics (MA). It was discovered that single-nucleotide polymorphisms (SNPs) are linked to ADHD. To evaluate the dependability of the results, we conducted sensitivity analysis (heterogeneity and pleiotropy) and employed supplementary MR techniques, such as the inverse variance weighted (IVW) and MR-Egger. Graphs are used to display the final findings of the pertinent analyses.

Results: Following MR analysis, immune cells associated with a few low p value phenotypes may influence ADHD, and these immune cells may serve as an inspiration for clinical treatment practices that aim to prevent and cure ADHD. Immune cell phenotypes that may both increase and worsen the likelihood of having ADHD were identified by IVW results. These included CD27 on memory B cells (OR = 1.066, 95% CI = 1.024-1.109, p = 2E-3) and CD27 on IgD-CD38- (OR = 1.059, 95% CI = 1.018-1.103, p = 5E-3), among others. Immune cell phenotypes that may act as a safeguard against ADHD included CD3 on resting Treg (OR = 0.925, 95% CI = 0.888-0.963, p = 1.5E-4) and SSC-A on monocytes (OR = 0.951, 95% CI = 0.924-0.980, p = 8.5E-4), among others. The primary findings and the outcomes of the sensitivity analysis matched.

Conclusions: This study provides a broad theoretical foundation for the development of immune-oriented therapeutic strategies in future clinical practice by demonstrating a potential genetic relationship between immune cells and ADHD. This study also advances our understanding of how to use the immune pathway to prevent and treat ADHD.

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评估各种免疫细胞与注意缺陷多动障碍之间的因果关系:孟德尔随机研究。
背景:免疫系统调节已被证明对注意缺陷多动障碍(ADHD)有重要影响。本研究使用孟德尔随机化(MR)分析来研究不同免疫细胞在ADHD发展中的潜在作用,以提供治疗和预防方案。方法:在这项研究中,使用可公开获取的遗传数据和两样本MR分析,检查了731个免疫细胞和ADHD的风险。包括四种不同类型的免疫图谱:确定细胞(DC)、比例细胞(PC)、中位亮度水平(MBL)和形态特征(MA)。人们发现单核苷酸多态性(snp)与多动症有关。为了评估结果的可靠性,我们进行了敏感性分析(异质性和多效性),并采用了补充MR技术,如逆方差加权(IVW)和MR- egger。图表用于显示相关分析的最终结果。结果:通过MR分析,与少数低p值表型相关的免疫细胞可能影响ADHD,这些免疫细胞可能为旨在预防和治疗ADHD的临床治疗实践提供灵感。免疫细胞表型可能增加或加重患ADHD的可能性,这是通过IVW结果确定的。其中包括记忆B细胞上的CD27 (OR = 1.066, 95% CI = 1.024-1.109, p = e2 -3)和IgD-CD38-上的CD27 (OR = 1.059, 95% CI = 1.018-1.103, p = 5E-3)等。可能作为预防ADHD的免疫细胞表型包括静息Treg上的CD3 (OR = 0.925, 95% CI = 0.888-0.963, p = 1.5E-4)和单核细胞上的SSC-A (OR = 0.951, 95% CI = 0.924-0.980, p = 8.5E-4)等。初步结果与敏感性分析结果相符。结论:本研究通过证明免疫细胞与ADHD之间潜在的遗传关系,为未来临床实践中免疫导向治疗策略的发展提供了广泛的理论基础。这项研究也促进了我们对如何使用免疫途径来预防和治疗多动症的理解。
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来源期刊
Brain and Behavior
Brain and Behavior BEHAVIORAL SCIENCES-NEUROSCIENCES
CiteScore
5.30
自引率
0.00%
发文量
352
审稿时长
14 weeks
期刊介绍: Brain and Behavior is supported by other journals published by Wiley, including a number of society-owned journals. The journals listed below support Brain and Behavior and participate in the Manuscript Transfer Program by referring articles of suitable quality and offering authors the option to have their paper, with any peer review reports, automatically transferred to Brain and Behavior. * [Acta Psychiatrica Scandinavica](https://publons.com/journal/1366/acta-psychiatrica-scandinavica) * [Addiction Biology](https://publons.com/journal/1523/addiction-biology) * [Aggressive Behavior](https://publons.com/journal/3611/aggressive-behavior) * [Brain Pathology](https://publons.com/journal/1787/brain-pathology) * [Child: Care, Health and Development](https://publons.com/journal/6111/child-care-health-and-development) * [Criminal Behaviour and Mental Health](https://publons.com/journal/3839/criminal-behaviour-and-mental-health) * [Depression and Anxiety](https://publons.com/journal/1528/depression-and-anxiety) * Developmental Neurobiology * [Developmental Science](https://publons.com/journal/1069/developmental-science) * [European Journal of Neuroscience](https://publons.com/journal/1441/european-journal-of-neuroscience) * [Genes, Brain and Behavior](https://publons.com/journal/1635/genes-brain-and-behavior) * [GLIA](https://publons.com/journal/1287/glia) * [Hippocampus](https://publons.com/journal/1056/hippocampus) * [Human Brain Mapping](https://publons.com/journal/500/human-brain-mapping) * [Journal for the Theory of Social Behaviour](https://publons.com/journal/7330/journal-for-the-theory-of-social-behaviour) * [Journal of Comparative Neurology](https://publons.com/journal/1306/journal-of-comparative-neurology) * [Journal of Neuroimaging](https://publons.com/journal/6379/journal-of-neuroimaging) * [Journal of Neuroscience Research](https://publons.com/journal/2778/journal-of-neuroscience-research) * [Journal of Organizational Behavior](https://publons.com/journal/1123/journal-of-organizational-behavior) * [Journal of the Peripheral Nervous System](https://publons.com/journal/3929/journal-of-the-peripheral-nervous-system) * [Muscle & Nerve](https://publons.com/journal/4448/muscle-and-nerve) * [Neural Pathology and Applied Neurobiology](https://publons.com/journal/2401/neuropathology-and-applied-neurobiology)
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