PharmFreq:临床重要药物基因等位基因变异的人种地理综合图谱。

IF 16.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Nucleic Acids Research Pub Date : 2024-11-14 DOI:10.1093/nar/gkae1016
Roman Tremmel, Yitian Zhou, Mahamadou D Camara, Sofiene Laarif, Erik Eliasson, Volker M Lauschke
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引用次数: 0

摘要

药物代谢酶、药物转运体以及人类主要组织相容性复合体编码基因的基因多态性导致了药物疗效和安全性的个体差异。在不同的人群中,这种药物基因变异的程度、模式和复杂性都大不相同。在此,我们介绍了全球药物基因频率信息库 PharmFreq,该信息库汇总了来自 144 个国家超过 1200 项研究的超过 1000 万个个体的 658 个等位基因变异的频率数据。大多数研究是在东亚和欧洲人群中进行的,分别占所有研究的 29.4% 和 26.6%。我们发现,每个国家的研究数量和总体队列规模与人口规模(R = 0.55,P= 3*10-9)和国家国内生产总值(R = 0.43,P= 2*10-6)显著相关,总体人口覆盖率从爱沙尼亚的 5%到美国的 5%不等。
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PharmFreq: a comprehensive atlas of ethnogeographic allelic variation in clinically important pharmacogenes.

Genetic polymorphisms in drug metabolizing enzymes, drug transporters as well as in genes encoding the human major histocompatibility complex contribute to inter-individual differences in drug efficacy and safety. The extent, pattern and complexity of such pharmacogenetic variation differ drastically across human populations. Here, we present PharmFreq, a global repository of pharmacogenetic frequency information that aggregates frequency data of 658 allelic variants from over 10 million individuals collected from >1200 studies across 144 countries. Most investigations were conducted in East Asian and European populations, accounting for 29.4 and 26.6% of all studies, respectively. We find that the number of studies per country and aggregated cohort size correlated significantly with population size (R = 0.55, P= 3*10-9) and country gross domestic product (R = 0.43, P= 2*10-6) with overall population coverage varying between 5% in Estonia to < 0.001% in many countries in Sub-Saharan Africa and Asia. All frequency data are openly accessible via a web-based interactive dashboard at pharmfreq.com that facilitates the exploration, visualization and analysis of country- and population-specific data and their inferred phenotypic consequences. PharmFreq thus presents a comprehensive, freely available resource for pharmacogenetic variant frequencies that can inform about ethnogeographic pharmacogenomic diversity and reveal important inequities that help to focus future research efforts into underrepresented populations.

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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
期刊最新文献
RASP v2.0: an updated atlas for RNA structure probing data. SPathDB: a comprehensive database of spatial pathway activity atlas. PharmFreq: a comprehensive atlas of ethnogeographic allelic variation in clinically important pharmacogenes. SETDB1 activity is globally directed by H3K14 acetylation via its Triple Tudor Domain. The secondary metabolism collaboratory: a database and web discussion portal for secondary metabolite biosynthetic gene clusters.
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