Evaluation of Polygenic Risk Score for Prediction of Childhood Onset and Severity of Asthma

被引:0
作者
Savelieva, Olga [1 ,2 ,3 ]
Karunas, Alexandra [1 ,2 ,4 ]
Prokopenko, Inga [5 ]
Balkhiyarova, Zhanna [5 ]
Gilyazova, Irina [1 ,4 ]
Khidiyatova, Irina [1 ]
Khusnutdinova, Elza [1 ,2 ,3 ,4 ]
机构
[1] Russian Acad Sci, Inst Biochem & Genet, Subdiv Ufa Fed Res Ctr, Ufa 450054, Russia
[2] Ufa Univ Sci & Technol, Fed State Budgetary Educ Inst Higher Educ, Lab Genom & Postgenom Technol, Ufa 450076, Russia
[3] St Petersburg State Univ, Fed State Budgetary Educ Inst Higher Educ, Fac Biol, St Petersburg 199034, Russia
[4] Bashkir State Med Univ, Fed State Budgetary Educ Inst Higher Educ, Dept Med Genet & Fundamental Med, Russian Minist Hlth, Ufa 450008, Russia
[5] Univ Surrey, Dept Clin & Expt Med, Guildford GU2 7XH, England
关键词
asthma; polymorphism; polygenic score; pharmacogenetics; association; GENOME-WIDE ASSOCIATION; GENE; POLYMORPHISMS; PHENOTYPES; RECEPTOR; GLCCI1;
D O I
10.3390/ijms26010103
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Asthma is a common complex disease with susceptibility defined through an interplay of genetic and environmental factors. Responsiveness to asthma treatment varies between individuals and is largely determined by genetic variability. The polygenic score (PGS) approach enables an individual risk of asthma and respective response to drug therapy. PGS models could help to predict the individual risk of asthma using 26 SNPs of drug pathway genes involved in the metabolism of glucocorticosteroids (GCS), and beta-2-agonists, antihistamines, and antileukotriene drugs associated with the response to asthma treatment within GWAS were built. For PGS, summary statistics from the Trans-National Asthma Genetic Consortium GWAS meta-analysis, and genotype data for 882 individuals with asthma/controls from the Volga-Ural region, were used. The study group was comprised of Russian, Tatar, Bashkir, and mixed ethnicity individuals with asthma (N = 378) aged 2-18 years. and individuals without features of atopic disease (N = 504) aged 4-67 years from the Volga-Ural region. The DNA samples for the study were collected from 2000 to 2021. The drug pathway genes' PGS revealed a higher odds for childhood asthma risk (p = 2.41 x 10-12). The receiver operating characteristic (ROC) analysis showed an Area Under the Curve, AUC = 0.63. The AUC of average significance for moderate-to-severe and severe asthma was observed (p = 5.7 x 10-9, AUC = 0.64). Asthma drug response pathway gene variant PGS models may contribute to the development of modern approaches to optimise asthma diagnostics and treatment.
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页数:12
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