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有氧运动训练对轻度认知障碍非裔美国老年人DNA甲基化的影响:基因、运动与记忆研究——GEMS-I

Aerobic Exercise Training-Induced Changes on DNA Methylation in Mild Cognitively Impaired Elderly African Americans: Gene, Exercise, and Memory Study - GEMS-I.

作者信息

Ngwa Julius S, Nwulia Evaristus, Ntekim Oyonumo, Bedada Fikru B, Kwabi-Addo Bernard, Nadarajah Sheeba, Johnson Steven, Southerland William M, Kwagyan John, Obisesan Thomas O

机构信息

Division of Cardiovascular Medicine, Department of Internal Medicine, Howard University, Washington, DC, United States.

Department of Psychiatry and Behavioral Sciences, Howard University, Washington, DC, United States.

出版信息

Front Mol Neurosci. 2022 Jan 17;14:752403. doi: 10.3389/fnmol.2021.752403. eCollection 2021.

Abstract

BACKGROUND

DNA methylation at CpG sites is a vital epigenetic modification of the human genome affecting gene expression, and potentially, health outcomes. However, evidence is just budding on the effects of aerobic exercise-induced adaptation on DNA methylation in older mild cognitively impaired (MCI) elderly African American (AAs). Therefore, we examined the effects of a 6-month aerobic exercise-intervention on genome-wide DNA methylation in elderly AA MCI volunteers.

DESIGN

Elderly AA volunteers confirmed MCI assigned into a 6-month program of aerobic exercise (eleven participants) underwent a 40-min supervised-training 3-times/week and controls (eight participants) performed stretch training. Participants had maximal oxygen consumption (VOmax) test and Genome-wide methylation levels at CpG sites using the Infinium HumanMethylation450 BeadChip assay at baseline and after a 6-month exercise program. We computed false discovery rates (FDR) using Sidak to account for multiplicity of tests and performed quantitative real-time polymerase chain-reaction (qRT-PCR) to confirm the effects of DNA methylations on expression levels of the top 5 genes among the aerobic participants. CpG sites identified from aerobic-exercise participants were similarly analyzed by the stretch group to quantify the effects of exercise-induced methylation changes among the group of stretch participants.

RESULTS

Eleven MCI participants (aerobic: 73% females; mean age 72.3 ± 6.6 years) and eight MCI participants (stretch: 75% female; mean age 70.6 ± 6.7 years) completed the training. Aerobic exercise-training was associated with increases in VOmax and with global hypo- and hypermethylation changes. The most notable finding was CpG hypomethylation within the body of the gene ( = 5.4 × 10), a Golgi-associated protein, involved in intracellular protein trafficking including amyloid precursor protein. qRT-PCR confirmed a nearly twofold increased expression of . Other top findings with FDR -value < 10, include hypomethylations of (8.8 × 10), (6.1 × 10), (2.1 × 10) and (9.8 × 10).

CONCLUSION

We conclude that genome-wide DNA methylation patterns is associated with exercise training-induced methylation changes. Identification of methylation changes around genes previously shown to interact with amyloid biology, intracellular protein trafficking, and lipoprotein regulations provide further support to the likely protective effect of exercise in MCI. Future studies in larger samples are needed to confirm our findings.

摘要

背景

CpG位点的DNA甲基化是人类基因组重要的表观遗传修饰,影响基因表达,并可能影响健康状况。然而,关于有氧运动诱导的适应性对老年轻度认知障碍(MCI)非裔美国人(AA)DNA甲基化影响的证据才刚刚出现。因此,我们研究了为期6个月的有氧运动干预对老年AA MCI志愿者全基因组DNA甲基化的影响。

设计

确诊为MCI的老年AA志愿者被分配到一个为期6个月的有氧运动项目中(11名参与者),他们每周接受3次、每次40分钟的监督训练,而对照组(8名参与者)进行伸展训练。参与者在基线时以及在进行6个月的运动项目后,进行了最大摄氧量(VOmax)测试,并使用Infinium HumanMethylation450 BeadChip分析法检测了CpG位点的全基因组甲基化水平。我们使用Sidak方法计算错误发现率(FDR)以考虑多重检验,并进行定量实时聚合酶链反应(qRT-PCR)以确认有氧运动参与者中前5个基因的DNA甲基化对表达水平的影响。伸展训练组对有氧运动参与者中鉴定出的CpG位点进行了类似分析,以量化伸展训练组中运动诱导的甲基化变化的影响。

结果

11名MCI参与者(有氧运动组:73%为女性;平均年龄72.3±6.6岁)和8名MCI参与者(伸展训练组:75%为女性;平均年龄70.6±6.7岁)完成了训练。有氧运动训练与VOmax增加以及全基因组的低甲基化和高甲基化变化相关。最显著的发现是基因体内的CpG低甲基化(=5.4×10),该基因是一种与高尔基体相关的蛋白质,参与包括淀粉样前体蛋白在内的细胞内蛋白质运输。qRT-PCR证实基因表达增加了近两倍。其他FDR值<10的主要发现包括基因(8.8×10)、基因(6.1×10)、基因(2.1×10)和基因(9.8×10)的低甲基化。

结论

我们得出结论,全基因组DNA甲基化模式与运动训练诱导的甲基化变化相关。对先前显示与淀粉样生物学、细胞内蛋白质运输和脂蛋白调节相互作用的基因周围甲基化变化的鉴定,进一步支持了运动对MCI可能具有的保护作用。需要在更大样本中进行进一步研究以证实我们的发现。

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