Shifting the trajectory of therapeutic development for neurological and psychiatric disorders

被引:0
|
作者
Krainc, Dimitri [1 ]
Martin, William J. [2 ]
Casey, Bradford [3 ]
Jensen, Frances E. [4 ]
Tishkoff, Sarah [5 ,6 ]
Potter, William Z.
Hyman, Steven E. [7 ,8 ]
机构
[1] Northwestern Univ, Simpson Querrey Ctr Neurogenet, Feinberg Sch Med, Davee Dept Neurol, Chicago, IL 60611 USA
[2] Johnson & Johnson Innovat Med, San Diego, CA USA
[3] Michael J Fox Fdn Parkinsons Res, New York, NY USA
[4] Univ Penn, Perelman Sch Med, Dept Neurol, Philadelphia, PA USA
[5] Univ Penn, Dept Genet, Philadelphia, PA USA
[6] Univ Penn, Dept Biol, Philadelphia, PA USA
[7] Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA
[8] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
关键词
ANTISENSE OLIGONUCLEOTIDE TOFERSEN; NEUROFILAMENT LIGHT-CHAIN; DRUG DEVELOPMENT; CELL DIVERSITY; RISK; MITOCHONDRIAL; DISEASE; ALS;
D O I
10.1126/scitranslmed.adg4775
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Clinical trials for central nervous system disorders often enroll patients with unrecognized heterogeneous diseases, leading to costly trials that have high failure rates. Here, we discuss the potential of emerging technologies and datasets to elucidate disease mechanisms and identify biomarkers to improve patient stratification and monitoring of disease progression in clinical trials for neuropsychiatric disorders. Greater efforts must be centered on rigorously standardizing data collection and sharing of methods, datasets, and analytical tools across sectors. To address health care disparities in clinical trials, diversity of genetic ancestries and environmental exposures of research participants and associated biological samples must be prioritized.
引用
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页数:10
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