Elastic net-based prediction of IFN-β treatment response of patients with multiple sclerosis using time series microarray gene expression profiles

被引:12
|
作者
Fukushima, Arika [1 ]
Sugimoto, Masahiro [2 ,3 ,4 ]
Hiwa, Satoru [1 ]
Hiroyasu, Tomoyuki [1 ]
机构
[1] Doshisha Univ, Grad Sch Life & Med Sci, Kyoto, Japan
[2] Tokyo Med Univ, Res & Dev Ctr Minimally Invas Therapies Hlth Prom, Shinjuku Ku, Tokyo 1608402, Japan
[3] Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970052, Japan
[4] Univ Tsukuba, Res & Dev Ctr Precis Med, Tsukuba, Ibaraki 3058550, Japan
基金
日本学术振兴会;
关键词
INTERFERON-BETA; REGULARIZATION; REGRESSION; SELECTION; CELLS;
D O I
10.1038/s41598-018-38441-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
INF-beta has been widely used to treat patients with multiple sclerosis (MS) in relapse. Accurate prediction of treatment response is important for effective personalization of treatment. Microarray data have been frequently used to discover new genes and to predict treatment responses. However, conventional analytical methods suffer from three difficulties: high-dimensionality of datasets; high degree of multicollinearity; and achieving gene identification in time-course data. The use of Elastic net, a sparse modelling method, would decrease the first two issues; however, Elastic net is currently unable to solve these three issues simultaneously. Here, we improved Elastic net to accommodate time-course data analyses. Numerical experiments were conducted using two time-course microarray datasets derived from peripheral blood mononuclear cells collected from patients with MS. The proposed methods successfully identified genes showing a high predictive ability for INF-beta treatment response. Bootstrap sampling resulted in an 81% and 78% accuracy for each dataset, which was significantly higher than the 71% and 73% accuracy obtained using conventional methods. Our methods selected genes showing consistent differentiation throughout all time-courses. These genes are expected to provide new predictive biomarkers that can influence INF-beta treatment for MS patients.
引用
收藏
页数:11
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