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早期生活压力与端粒长度:探究两者的关联及其可能的机制——对现有证据基础、研究方法和基础生物学的批判性综述。

Early life stress and telomere length: investigating the connection and possible mechanisms: a critical survey of the evidence base, research methodology and basic biology.

机构信息

Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.

出版信息

Bioessays. 2012 Nov;34(11):943-52. doi: 10.1002/bies.201200084. Epub 2012 Sep 19.

DOI:10.1002/bies.201200084
PMID:22991129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3557830/
Abstract

How can adverse experiences in early life, such as maltreatment, exert such powerful negative effects on health decades later? The answer may lie in changes to DNA. New research suggests that exposure to stress can accelerate the erosion of DNA segments called telomeres. Shorter telomere length correlates with chronological age and also disease morbidity and mortality. Thus, telomere erosion is a potential mechanism linking childhood stress to health problems later in life. However, an array of mechanistic, methodological, and basic biological questions must be addressed in order to translate telomere discoveries into clinical applications for monitoring health and predicting disease risk. This paper covers the current state of the science and lays out new research directions.

摘要

早年生活中的逆境经历,如虐待,如何能在几十年后对健康产生如此强大的负面影响?答案可能在于 DNA 的变化。新的研究表明,暴露于压力下会加速称为端粒的 DNA 片段的磨损。端粒较短与实际年龄以及疾病发病率和死亡率相关。因此,端粒磨损是将儿童期压力与以后生活中的健康问题联系起来的潜在机制。然而,为了将端粒发现转化为监测健康和预测疾病风险的临床应用,必须解决一系列机制、方法和基本生物学问题。本文涵盖了该科学的现状,并提出了新的研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3666/3557830/b6ac0fd969f5/nihms432712f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3666/3557830/e0b397dd893c/nihms432712f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3666/3557830/b6ac0fd969f5/nihms432712f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3666/3557830/e0b397dd893c/nihms432712f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3666/3557830/b6ac0fd969f5/nihms432712f2.jpg

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PLoS Genet. 2012;8(5):e1002696. doi: 10.1371/journal.pgen.1002696. Epub 2012 May 17.
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Telomerase gene therapy in adult and old mice delays aging and increases longevity without increasing cancer.端粒酶基因治疗可延缓成年和老年小鼠衰老并延长寿命,而不增加癌症风险。
EMBO Mol Med. 2012 Aug;4(8):691-704. doi: 10.1002/emmm.201200245. Epub 2012 May 15.
3
Telomere length, oxidative stress, and antioxidant status in elderly men in Zutphen and Crete.
欧洲儿童家庭富裕程度与皮质醇分泌及端粒长度的关联
EBioMedicine. 2025 Jul;117:105793. doi: 10.1016/j.ebiom.2025.105793. Epub 2025 Jun 5.
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Cortisol, dehydroepiandrosterone, and depressive symptoms as pathways from child abuse to obesity.皮质醇、脱氢表雄酮以及抑郁症状作为儿童虐待与肥胖之间的关联路径。
Health Psychol. 2025 Apr 17. doi: 10.1037/hea0001513.
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Telomere Dynamics in Post-Traumatic Stress Disorder: A Critical Synthesis.创伤后应激障碍中的端粒动力学:一项批判性综述
Biomedicines. 2025 Feb 18;13(2):507. doi: 10.3390/biomedicines13020507.
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Early origins of health and disease risk: The case for investigating adverse exposures and biological aging in utero, across childhood, and into adolescence.健康与疾病风险的早期起源:关于研究子宫内、儿童期及青春期不良暴露与生物衰老的案例
Child Dev Perspect. 2023 Dec;17(3-4):149-156. doi: 10.1111/cdep.12488. Epub 2023 Oct 16.
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The biology of aging in a social world: Insights from free-ranging rhesus macaques.社会世界中的衰老生物学:来自自由放养恒河猴的见解。
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5
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10
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