In Search of Biomarkers to Guide Interventions in Autism Spectrum Disorder: A Systematic Review

自闭症谱系障碍 生物标志物 自闭症 样本量测定 临床试验 心理学 系统回顾 荟萃分析 生物标志物发现 临床研究设计 梅德林 生物信息学 精神科 临床心理学 医学 内科学 蛋白质组学 生物 统计 基因 生物化学 数学
作者
Mara Parellada,Álvaro Andreu-Bernabeu,Mónica Burdeus-Olavarrieta,Antonia San José Cáceres,Elena Urbiola,Linda L. Carpenter,Nina V. Kraguljac,William M. McDonald,Charles B. Nemeroff,Carolyn I. Rodríguez,Alik S. Widge,Matthew W. State,Stephan Sanders
出处
期刊:American Journal of Psychiatry [American Psychiatric Association]
卷期号:180 (1): 23-40 被引量:116
标识
DOI:10.1176/appi.ajp.21100992
摘要

OBJECTIVE: The aim of this study was to catalog and evaluate response biomarkers correlated with autism spectrum disorder (ASD) symptoms to improve clinical trials. METHODS: A systematic review of MEDLINE, Embase, and Scopus was conducted in April 2020. Seven criteria were applied to focus on original research that includes quantifiable response biomarkers measured alongside ASD symptoms. Interventional studies or human studies that assessed the correlation between biomarkers and ASD-related behavioral measures were included. RESULTS: A total of 5,799 independent records yielded 280 articles for review that reported on 940 biomarkers, 755 of which were unique to a single publication. Molecular biomarkers were the most frequently assayed, including cytokines, growth factors, measures of oxidative stress, neurotransmitters, and hormones, followed by neurophysiology (e.g., EEG and eye tracking), neuroimaging (e.g., functional MRI), and other physiological measures. Studies were highly heterogeneous, including in phenotypes, demographic characteristics, tissues assayed, and methods for biomarker detection. With a median total sample size of 64, almost all of the reviewed studies were only powered to identify biomarkers with large effect sizes. Reporting of individual-level values and summary statistics was inconsistent, hampering mega- and meta-analysis. Biomarkers assayed in multiple studies yielded mostly inconsistent results, revealing a "replication crisis." CONCLUSIONS: There is currently no response biomarker with sufficient evidence to inform ASD clinical trials. This review highlights methodological imperatives for ASD biomarker research necessary to make definitive progress: consistent experimental design, correction for multiple comparisons, formal replication, sharing of sample-level data, and preregistration of study designs. Systematic "big data" analyses of multiple potential biomarkers could accelerate discovery.
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