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焦虑障碍青少年的 DNA 甲基化:一项纵向研究。

DNA methylation in adolescents with anxiety disorder: a longitudinal study.

机构信息

Anxiety Disorders Outpatient Program for Children and Adolescents, Universidade Federal do Rio Grande do Sul, UFRGS/Hospital de Clínicas de Porto Alegre, HCPA, Porto Alegre, Brazil.

Post Graduate Program in Neuroscience, Institute of Basic Sciences/Health, Universidade Federal do Rio Grande do Sul, UFRGS, Porto Alegre, Brazil.

出版信息

Sci Rep. 2018 Sep 14;8(1):13800. doi: 10.1038/s41598-018-32090-1.

Abstract

Anxiety disorders (AD) typically manifest in children and adolescents and might persist into adulthood. However, there are still few data concerning epigenetic mechanisms associated with onset, persistence or remission of AD over time. We investigated a cohort of adolescents and young adults at baseline (age; 13.19 ± 2.38) and after 5 years and classified them according to the AD diagnosis and their longitudinal trajectories into 4 groups: (1) Typically Developing Comparisons (TDC; control group, n = 14); (2) Incident (AD in the second evaluation only, n = 11); (3) Persistent (AD in both evaluations, n = 14) and (4) Remittent (AD in the first evaluation only, n = 8). DNA methylation was evaluated with the Infinium HumanMethylation450 BeadChip from saliva samples collected at both evaluations. Gene set enrichment analysis was applied to consider biological pathways. We found decreased DNA methylation in TDC group while the chronic cases of AD presented hypermethylation in central nervous system development pathways. Moreover, we showed that this persistent group also presented hypermethylation while the other three groups were associated with hypomethylation in nervous system development pathway. Incidence and remission groups were associated with increased and decreased methylation in neuron development pathways, respectively. Larger studies are likely to detect specific genes relevant to AD.

摘要

焦虑障碍(AD)通常在儿童和青少年中表现出来,并可能持续到成年期。然而,关于与 AD 的发病、持续或缓解相关的表观遗传机制的数据仍然很少。我们调查了一组青少年和年轻人,他们在基线时(年龄;13.19±2.38)和 5 年后进行了分类,并根据 AD 的诊断和他们的纵向轨迹分为 4 组:(1)典型发育对照(TDC;对照组,n=14);(2)新发病例(仅在第二次评估中患有 AD,n=11);(3)持续性(在两次评估中均患有 AD,n=14)和(4)缓解性(仅在第一次评估中患有 AD,n=8)。我们从两次评估时收集的唾液样本中使用 Infinium HumanMethylation450 BeadChip 评估了 DNA 甲基化。应用基因集富集分析来考虑生物学途径。我们发现 TDC 组的 DNA 甲基化减少,而 AD 的慢性病例在中枢神经系统发育途径中表现出过度甲基化。此外,我们还表明,该持续性组也表现出过度甲基化,而其他三组与神经系统发育途径中的低甲基化相关。发病和缓解组分别与神经元发育途径中的增加和减少的甲基化相关。更大的研究可能会检测到与 AD 相关的特定基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92e9/6138655/8d55c6581c21/41598_2018_32090_Fig1_HTML.jpg

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