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从群体遗传学角度看多基因疾病的未来预防性基因治疗。

Future Preventive Gene Therapy of Polygenic Diseases from a Population Genetics Perspective.

机构信息

Centre for Computational Evolution, University of Auckland, Auckland 1010, New Zealand.

Department of Computer Science, University of Auckland, Auckland 1010, New Zealand.

出版信息

Int J Mol Sci. 2019 Oct 10;20(20):5013. doi: 10.3390/ijms20205013.

Abstract

With the accumulation of scientific knowledge of the genetic causes of common diseases and continuous advancement of gene-editing technologies, gene therapies to prevent polygenic diseases may soon become possible. This study endeavored to assess population genetics consequences of such therapies. Computer simulations were used to evaluate the heterogeneity in causal alleles for polygenic diseases that could exist among geographically distinct populations. The results show that although heterogeneity would not be easily detectable by epidemiological studies following population admixture, even significant heterogeneity would not impede the outcomes of preventive gene therapies. Preventive gene therapies designed to correct causal alleles to a naturally-occurring neutral state of nucleotides would lower the prevalence of polygenic early- to middle-age-onset diseases in proportion to the decreased population relative risk attributable to the edited alleles. The outcome would manifest differently for late-onset diseases, for which the therapies would result in a delayed disease onset and decreased lifetime risk; however, the lifetime risk would increase again with prolonging population life expectancy, which is a likely consequence of such therapies. If the preventive heritable gene therapies were to be applied on a large scale, the decreasing frequency of risk alleles in populations would reduce the disease risk or delay the age of onset, even with a fraction of the population receiving such therapies. With ongoing population admixture, all groups would benefit over generations.

摘要

随着对常见疾病遗传原因的科学知识的积累和基因编辑技术的不断进步,预防多基因疾病的基因疗法可能很快成为可能。本研究旨在评估此类疗法的群体遗传学后果。计算机模拟用于评估地理上不同人群中可能存在的多基因疾病因果等位基因的异质性。结果表明,尽管在人群混合后进行的流行病学研究可能不易检测到异质性,但即使存在显著的异质性,也不会妨碍预防性基因疗法的效果。旨在将因果等位基因校正为自然发生的核苷酸中性状态的预防性基因疗法将降低多基因早至中年发病疾病的流行率,比例为编辑等位基因归因的人群相对风险降低。对于发病较晚的疾病,其结果会有所不同,因为这些疗法会导致疾病发病延迟和终生风险降低;然而,随着人口预期寿命的延长,终生风险会再次增加,这可能是此类疗法的后果。如果大规模应用预防性可遗传基因疗法,人群中风险等位基因的频率降低将降低疾病风险或延迟发病年龄,即使只有一部分人群接受此类疗法。随着人口的不断混合,所有群体都会在几代人中受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65c0/6834143/1c0c586d82ed/ijms-20-05013-g0A1.jpg

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