自闭症谱系障碍的早期生物标志物揭晓——我们了解到了什么?

IF 3.6 3区 医学 Q1 PATHOLOGY
Daniel A Rossignol, Richard E Frye
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引用次数: 0

摘要

在美国,每31名儿童中就有1名患有自闭症谱系障碍(ASD),这凸显了早期发现和干预的迫切需要。确定可靠的早期生物标志物可以彻底改变ASD的诊断,并通过及时的治疗策略改善结果。涉及领域:本综述探讨了导致ASD的母亲、父亲和环境风险因素,包括免疫失调、代谢状况、毒物暴露以及胎盘和羊膜因素。生物标志物有助于识别这些因素。专家意见:未来对孕产妇健康和生物标志物的研究对于预测ASD风险和制定个性化干预措施至关重要。多组学、成像、表观遗传学和人工智能驱动的分析技术的进步可以提高生物标志物的准确性,从而实现早期检测和靶向治疗。然而,诸如生物标志物可靠性和ASD异质性等挑战必须通过大规模验证研究和跨学科合作来解决,以便将这些发现有效地转化为临床实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early biomarker for autism spectrum disorder unveiled - what are we learning?

Introduction: Autism Spectrum Disorder (ASD) affects 1 in 31 children in the U.S. highlighting the urgent need for early detection and intervention. Identifying reliable early biomarkers could revolutionize ASD diagnosis and improve outcomes by enabling timely therapeutic strategies.

Areas covered: This review explores maternal, paternal, and environmental risk factors contributing to ASD, including immune dysregulation, metabolic conditions, toxicant exposures, and placental and amniotic factors. Biomarkers aid in identifying these factors.

Expert opinion: Future research in maternal health and biomarkers is crucial for predicting ASD risk and developing personalized interventions. Advances in multi-omics, imaging, epigenetics, and AI-driven analysis can improve biomarker accuracy, enabling earlier detection and targeted therapies. However, challenges such as biomarker reliability and ASD heterogeneity must be addressed through large-scale validation studies and interdisciplinary collaboration to translate these discoveries into clinical practice effectively.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
71
审稿时长
1 months
期刊介绍: Expert Review of Molecular Diagnostics (ISSN 1473-7159) publishes expert reviews of the latest advancements in the field of molecular diagnostics including the detection and monitoring of the molecular causes of disease that are being translated into groundbreaking diagnostic and prognostic technologies to be used in the clinical diagnostic setting. Each issue of Expert Review of Molecular Diagnostics contains leading reviews on current and emerging topics relating to molecular diagnostics, subject to a rigorous peer review process; editorials discussing contentious issues in the field; diagnostic profiles featuring independent, expert evaluations of diagnostic tests; meeting reports of recent molecular diagnostics conferences and key paper evaluations featuring assessments of significant, recently published articles from specialists in molecular diagnostic therapy. Expert Review of Molecular Diagnostics provides the forum for reporting the critical advances being made in this ever-expanding field, as well as the major challenges ahead in their clinical implementation. The journal delivers this information in concise, at-a-glance article formats: invaluable to a time-constrained community.
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