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法医遗传标记揭示的关于我们的信息是否超出了应有的范畴?(综述)

Do forensic genetic markers disclose more information about us than they should? (A review).

作者信息

Fuente Carlota Manglano de la, Palomo-Díez Sara

机构信息

Medicine Faculty, Complutense University of Madrid, Madrid, Spain.

Health Legislation, Psychiatry and Pathology Department, Medicine Faculty, The Complutense University of Madrid, Madrid, Spain.

出版信息

Int J Legal Med. 2025 May;139(3):935-943. doi: 10.1007/s00414-024-03395-w. Epub 2025 Jan 8.

DOI:10.1007/s00414-024-03395-w
PMID:39775034
Abstract

The 20 established STRs that make up the CoDIS package must comply with national and international privacy rights and legal policies. Current research reveals that it is possible that certain genetic markers, used in forensic contexts, may show information about other neighboring markers that could reflect certain private characteristics of individuals. Therefore, we will aim to find out, through a literature review, whether there may indeed be associations between some of the STRs alleles established by CoDIS and medical and phenotypic conditions, with the aim of checking whether this problem has a real basis. To carry out this review, a systematic search has been carried out in different databases, as well as a critical evaluation of the articles collected and a synthesis of all the relevant studies. The results generally show that private phenotypic data of the individual can be known from certain STRs established by CoDIS, due to their association with neighboring genes. However, most of the papers state that practically none of the established associations offer proof of causality, but rather a relationship between some STRs and a phenotype.

摘要

构成联合DNA索引系统(CODIS)软件包的20个既定短串联重复序列(STR)必须符合国家和国际隐私权及法律政策。当前研究表明,在法医背景下使用的某些基因标记可能会显示有关其他相邻标记的信息,而这些信息可能反映个体的某些隐私特征。因此,我们旨在通过文献综述来查明CODIS确定的某些STR等位基因与医学和表型状况之间是否确实存在关联,以核查这一问题是否有实际依据。为进行此次综述,我们在不同数据库中进行了系统检索,并对所收集的文章进行了批判性评估以及对所有相关研究进行了综合分析。结果总体显示,由于CODIS确定的某些STR与相邻基因存在关联,个体的隐私表型数据可能会由此被知晓。然而,大多数论文指出,实际上已确立的关联几乎都没有提供因果关系的证据,而只是表明某些STR与一种表型之间存在关联。

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本文引用的文献

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A Treg-related riskscore model may improve the prognosis evaluation of colorectal cancer.一种与调节性T细胞相关的风险评分模型可能会改善结直肠癌的预后评估。
J Gene Med. 2024 Feb;26(2):e3668. doi: 10.1002/jgm.3668.
2
Could routine forensic STR genotyping data leak personal phenotypic information?常规法医 STR 基因分型数据会泄露个人表型信息吗?
Forensic Sci Int. 2022 Jun;335:111311. doi: 10.1016/j.forsciint.2022.111311. Epub 2022 Apr 18.
3
Patterns of de novo tandem repeat mutations and their role in autism.从头开始的串联重复突变模式及其在自闭症中的作用。
Nature. 2021 Jan;589(7841):246-250. doi: 10.1038/s41586-020-03078-7. Epub 2021 Jan 13.
4
The impact of short tandem repeat variation on gene expression.短串联重复序列变异对基因表达的影响。
Nat Genet. 2019 Nov;51(11):1652-1659. doi: 10.1038/s41588-019-0521-9. Epub 2019 Nov 1.
5
A reference haplotype panel for genome-wide imputation of short tandem repeats.全基因组短串联重复序列遗传数据推断的参考单体型面板
Nat Commun. 2018 Oct 23;9(1):4397. doi: 10.1038/s41467-018-06694-0.
6
Linkage disequilibrium matches forensic genetic records to disjoint genomic marker sets.连锁不平衡将法医遗传记录与不相交的基因组标记集匹配。
Proc Natl Acad Sci U S A. 2017 May 30;114(22):5671-5676. doi: 10.1073/pnas.1619944114. Epub 2017 May 15.
7
Characterization of the standard and recommended CODIS markers.标准和推荐的联合DNA索引系统(CODIS)标记的特征描述
J Forensic Sci. 2013 Jan;58 Suppl 1(Suppl 1):S169-72. doi: 10.1111/j.1556-4029.2012.02253.x. Epub 2012 Aug 24.
8
The analysis of the entire HLA, partial non-HLA and HPV for Chinese women with cervical cancer.对中国宫颈癌女性患者的全人类白细胞抗原、部分非人类白细胞抗原及人乳头瘤病毒进行分析。
J Med Virol. 2008 Oct;80(10):1808-13. doi: 10.1002/jmv.21251.
9
Activation of signal transducer and activator of transcription 5 is required for progression of autochthonous prostate cancer: evidence from the transgenic adenocarcinoma of the mouse prostate system.信号转导及转录激活因子5的激活是原位前列腺癌进展所必需的:来自小鼠前列腺转基因腺癌系统的证据。
Cancer Res. 2003 Dec 15;63(24):8757-62.
10
Dopamine D3 receptor gene polymorphism and violent behavior: relation to impulsiveness and ADHD-related psychopathology.多巴胺D3受体基因多态性与暴力行为:与冲动性及注意缺陷多动障碍相关精神病理学的关系
J Neural Transm (Vienna). 2003 May;110(5):561-72. doi: 10.1007/s00702-002-0805-5.