孟德尔随机化
全基因组关联研究
候选基因
注意缺陷多动障碍
优势比
遗传学
生物信息学
内科学
基因
医学
生物
精神科
单核苷酸多态性
基因型
遗传变异
作者
Detong Guo,Wenchao Sheng,Yingzi Cai,Jianbo Shu,C Cai
标识
DOI:10.1177/10870547231222219
摘要
BACKGROUND: Lipid metabolism plays an essential role in nervous system development. Cholesterol deficiency leads to a variety of neurodevelopmental disorders, such as autism spectrum disorder and fragile X syndrome. There have been a lot of efforts to search for biological markers associated with and causal to ADHD, among which lipid is one possible etiological factor that is quite widely studied. We aimed to evaluate the causal relationship between lipids traits, lipid-lowering drugs, and attention deficit hyperactivity disorder (ADHD) outcomes using Mendelian randomization (MR) studies. METHODS: We used summary data from genome-wide association studies to explore the causal relationships between circulating lipid-related traits and ADHD. Then, quantitative trait loci for the expression of lipid-lowering drug target genes and genetic variants associated with lipid traits were extracted. Summary-data-based MR and inverse-variance-weighted MR (IVW-MR) were used to investigate the correlation between the expression of these drug-target genes and ADHD. RESULTS: < .001). CONCLUSION: gene may be candidate drug target genes for the treatment of ADHD.
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