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Titlebook: Biomarkers for Huntington‘s Disease; Improving Clinical O Elizabeth A. Thomas,Georgia M. Parkin Book 2023 The Editor(s) (if applicable) and

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发表于 2025-3-21 17:50:24 | 显示全部楼层 |阅读模式
期刊全称Biomarkers for Huntington‘s Disease
期刊简称Improving Clinical O
影响因子2023Elizabeth A. Thomas,Georgia M. Parkin
视频video
发行地址Presents the latest advances in the development of digital biomarkers for use in Huntington’s disease.Reviews the current status of fluid biomarkers for Huntington‘s disease.Explores the function of b
学科分类Contemporary Clinical Neuroscience
图书封面Titlebook: Biomarkers for Huntington‘s Disease; Improving Clinical O Elizabeth A. Thomas,Georgia M. Parkin Book 2023 The Editor(s) (if applicable) and
影响因子Huntington’s disease (HD) is a fatal, inherited, neurodegenerative disorder, characterized by chorea, motor instabilities, psychiatric manifestations and cognitive decline. Early genetic testing provides an opportunity for clinical interventions aimed at delaying onset and/or slowing progression of disease; however, current treatments for HD are limited, with only two FDA-approved drugs available to manage chorea. Encouragingly, however, several disease-modifying treatment approaches are in the therapeutic pipeline, with more than 200 clinical studies, and many more preclinical studies, in the works. Robust and reliable biomarkers are needed to predict disease onset, monitor disease progression and assess treatment responses. More specifically, biomarkers to stratify patients for clinical trials and biomarkers to track drug efficacy will certainly lead to improved clinical trial design and success. This book represents the first book focused solely on biomarkers for HD and represents adistinct resource that will be informative, not only for clinicians and those involved in clinical trial design, but also for a wide range of neurodegenerative disease researchers. This edited volume
Pindex Book 2023
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,Konflikte in der Wirtschaftsprüfung,with the diagnosis and management of this disorder. This chapter then reviews the different classes of CSF biomarkers that have been studied in HD, including neurotransmitters, amino acids, proteins, metabolites, metals, and microRNAs. CSF levels of mutant huntingtin and neurofilament light chain ar
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,Konflikte in der Wirtschaftsprüfung,apter will review findings from the literature that have explored saliva as a non-invasive biofluid for biomarker research in Huntington’s disease and have identified factors, such as huntingtin, cortisol, uric acid and cytokines, in saliva that track with features of the disease. These studies offe
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Wolfgang H. C. Junge,Martina Jungedetecting early HD pathophysiology before clinical onset. This chapter will provide an overview of the functional and physiological MRI studies conducted in the premanifest and early-stage HD patients, as well as in preclinical HD models, focusing on discussing the potential of different MRI measure
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Konflikte um die Aneignung von Landmutant huntingtin within inflammatory cells have been demonstrated. As circulating markers of inflammation has been shown to mirror brain inflammatory changes in HD, this has raised the possibility that these markers could be useful as markers of disease features. This chapter aims to summarize curr
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Beiträge zum Diversity ManagementHowever, several case reports of individuals with the HTT mutation and ALS-like syndrome suggest potential interactions and involvement of TDP-43 in the pathophysiology and phenotype of some individuals with HD. Investigations into other PolyQ diseases, such as Spinocerebellar Ataxias, have provided
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