Severity in the genomic age: the significance of lived experience to understandings of severity.

IF 3.7 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Amarpreet Kaur
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Abstract

This article explores the significance of lived experience to understandings of severity in the genomic age. It draws upon data from structured interviews with 21 people living with monogenic conditions in England. The article argues that while lived experiences are subjective, participants consider the severity of disease by the impact a condition has on a person's quality of life and mental health; both of these interplays are influenced by social, economic, and environmental factors. The three factors and considerations to the impact of living with disease on mental health are generally absent from current frameworks designed to assess severity for clinical applications of genomic technologies such as preimplantation genetic testing (PGT). This article describes ways in which such factors impact the quality of life and the mental health of people living with genetic conditions. It also indicates what lived experiences, which illustrate the impact of these factors, have to offer policy-makers when they are assessing the concept of severity or seriousness of genetic conditions for applications of existing and potential genomic technologies in the genomic age.

基因组时代的严重性:生活经验对理解严重性的意义。
本文探讨了生活经验对于理解基因组时代严重性的重要意义。文章借鉴了对英格兰 21 名单基因疾病患者进行的结构化访谈数据。文章认为,虽然生活经验是主观的,但参与者会根据病情对个人生活质量和心理健康的影响来考虑疾病的严重程度;这两种因素的相互作用都受到社会、经济和环境因素的影响。在目前为基因组技术临床应用(如植入前基因检测(PGT))而设计的严重性评估框架中,一般都没有考虑到这三个因素以及带病生活对心理健康的影响。本文介绍了这些因素如何影响遗传病患者的生活质量和心理健康。文章还指出,在基因组时代,决策者在评估现有和潜在基因组技术应用中遗传病严重程度的概念时,生活经验能说明这些因素的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Journal of Human Genetics
European Journal of Human Genetics 生物-生化与分子生物学
CiteScore
9.90
自引率
5.80%
发文量
216
审稿时长
2 months
期刊介绍: The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community. Key areas include: -Monogenic and multifactorial disorders -Development and malformation -Hereditary cancer -Medical Genomics -Gene mapping and functional studies -Genotype-phenotype correlations -Genetic variation and genome diversity -Statistical and computational genetics -Bioinformatics -Advances in diagnostics -Therapy and prevention -Animal models -Genetic services -Community genetics
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