Advances in Clinical Chemistry最新文献

筛选
英文 中文
Advances in exosome analysis. 外泌体分析的进展。
2区 医学
Advances in Clinical Chemistry Pub Date : 2023-01-01 DOI: 10.1016/bs.acc.2022.09.002
Arnau Pallares-Rusiñol, Mireia Bernuz, Silio Lima Moura, Carolina Fernández-Senac, Rosanna Rossi, Mercè Martí, María Isabel Pividori
{"title":"Advances in exosome analysis.","authors":"Arnau Pallares-Rusiñol,&nbsp;Mireia Bernuz,&nbsp;Silio Lima Moura,&nbsp;Carolina Fernández-Senac,&nbsp;Rosanna Rossi,&nbsp;Mercè Martí,&nbsp;María Isabel Pividori","doi":"10.1016/bs.acc.2022.09.002","DOIUrl":"https://doi.org/10.1016/bs.acc.2022.09.002","url":null,"abstract":"<p><p>There is growing demand for novel biomarkers that detect early stage disease as well as monitor clinical management and therapeutic strategies. Exosome analysis could provide the next advance in attaining that goal. Exosomes are membrane encapsulated biologic nanometric-sized particles of endocytic origin which are released by all cell types. Unfortunately, exosomes are exceptionally challenging to characterize with current technologies. Exosomes are between 30 and 200nm in diameter, a size that makes them out of the sensitivity range to most cell-oriented sorting or analysis platforms, i.e., traditional flow cytometers. The most common methods for targeting exosomes to date typically involve purification followed by the characterization and the specific determination of their cargo. The whole procedure is time consuming, requiring thus skilled personnel as well as laboratory facilities and benchtop instrumentation. The most relevant methodology for exosome isolation, characterization and quantification is addressed in this chapter, including the most up-to-date approaches to explore the potential usefulness of exosomes as biomarkers in liquid biopsies and in advanced nanomedicine.</p>","PeriodicalId":50872,"journal":{"name":"Advances in Clinical Chemistry","volume":"112 ","pages":"69-117"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10539456","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Preface. 前言。
2区 医学
Advances in Clinical Chemistry Pub Date : 2023-01-01 DOI: 10.1016/S0065-2423(23)00008-2
Gregory S Makowski
{"title":"Preface.","authors":"Gregory S Makowski","doi":"10.1016/S0065-2423(23)00008-2","DOIUrl":"https://doi.org/10.1016/S0065-2423(23)00008-2","url":null,"abstract":"","PeriodicalId":50872,"journal":{"name":"Advances in Clinical Chemistry","volume":"112 ","pages":"xiii"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10601277","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preface. 前言。
2区 医学
Advances in Clinical Chemistry Pub Date : 2023-01-01 DOI: 10.1016/S0065-2423(23)00022-7
Gregory S Makowski
{"title":"Preface.","authors":"Gregory S Makowski","doi":"10.1016/S0065-2423(23)00022-7","DOIUrl":"https://doi.org/10.1016/S0065-2423(23)00022-7","url":null,"abstract":"","PeriodicalId":50872,"journal":{"name":"Advances in Clinical Chemistry","volume":"113 ","pages":"xi-xii"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10829223","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fluid biomarkers in Alzheimer's disease. 阿尔茨海默病的液体生物标志物。
2区 医学
Advances in Clinical Chemistry Pub Date : 2023-01-01 DOI: 10.1016/bs.acc.2022.09.006
Joel Simrén, Anders Elmgren, Kaj Blennow, Henrik Zetterberg
{"title":"Fluid biomarkers in Alzheimer's disease.","authors":"Joel Simrén,&nbsp;Anders Elmgren,&nbsp;Kaj Blennow,&nbsp;Henrik Zetterberg","doi":"10.1016/bs.acc.2022.09.006","DOIUrl":"https://doi.org/10.1016/bs.acc.2022.09.006","url":null,"abstract":"<p><p>Alzheimer's disease (AD) characterization has progressed from being indexed using clinical symptomatology followed by neuropathological examination at autopsy to in vivo signatures using cerebrospinal fluid (CSF) biomarkers and positron emission tomography. The core AD biomarkers reflect amyloid-β plaques (A), tau pathology (T) and neurodegeneration (N), following the ATN schedule, and are now being introduced into clinical routine practice. This is an important development, as disease-modifying treatments are now emerging. Further, there are now reproducible data on CSF biomarkers which reflect synaptic pathology, neuroinflammation and common co-pathologies. In addition, the development of ultrasensitive techniques has enabled the core CSF biomarkers of AD pathophysiology to be translated to blood (e.g., phosphorylated tau, amyloid-β and neurofilament light). In this chapter, we review where we stand with both core and novel CSF biomarkers, as well as the explosion of data on blood biomarkers. Also, we discuss potential applications in research aiming to better understand the disease, as well as possible use in routine clinical practice and therapeutic trials.</p>","PeriodicalId":50872,"journal":{"name":"Advances in Clinical Chemistry","volume":"112 ","pages":"249-281"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10539453","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Evolving markers in amyotrophic lateral sclerosis. 肌萎缩性侧索硬化症的进化标志物。
2区 医学
Advances in Clinical Chemistry Pub Date : 2023-01-01 DOI: 10.1016/bs.acc.2023.02.002
Xu Chen, Lu Zhou, Can Cui, Jiangwei Sun
{"title":"Evolving markers in amyotrophic lateral sclerosis.","authors":"Xu Chen,&nbsp;Lu Zhou,&nbsp;Can Cui,&nbsp;Jiangwei Sun","doi":"10.1016/bs.acc.2023.02.002","DOIUrl":"https://doi.org/10.1016/bs.acc.2023.02.002","url":null,"abstract":"<p><p>Amyotrophic lateral sclerosis (ALS) is a relatively rare but fatal neurodegenerative disease with the progressive loss of both upper and lower motor neurons. Although electromyography, imaging and multi-omics technologies have suggested numerous functional, structural, circulating and microbiota markers for ALS, no clinically validated markers have, as yet, been identified. Here we summarize the advances to characterize markers underlying ALS pathophysiology as well as their potential use in diagnosis, prognosis and therapy.</p>","PeriodicalId":50872,"journal":{"name":"Advances in Clinical Chemistry","volume":"114 ","pages":"225-246"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9945693","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Heterogeneity in major depressive disorder: The need for biomarker-based personalized treatments. 重度抑郁症的异质性:基于生物标志物的个性化治疗的需要。
2区 医学
Advances in Clinical Chemistry Pub Date : 2023-01-01 DOI: 10.1016/bs.acc.2022.09.001
Shayam Suseelan, Graziano Pinna
{"title":"Heterogeneity in major depressive disorder: The need for biomarker-based personalized treatments.","authors":"Shayam Suseelan,&nbsp;Graziano Pinna","doi":"10.1016/bs.acc.2022.09.001","DOIUrl":"https://doi.org/10.1016/bs.acc.2022.09.001","url":null,"abstract":"<p><p>Major Depressive Disorder (MDD) or depression is a pathological mental condition affecting millions of people worldwide. Identification of objective biological markers of depression can provide for a better diagnostic and intervention criteria; ultimately aiding to reduce its socioeconomic health burden. This review provides a comprehensive insight into the major biomarker candidates that have been implicated in depression neurobiology. The key biomarker categories are covered across all the \"omics\" levels. At the epigenomic level, DNA-methylation, non-coding RNA and histone-modifications have been discussed in relation to depression. The proteomics system shows great promise with inflammatory markers as well as growth factors and neurobiological alterations within the endocannabinoid system. Characteristic lipids implicated in depression together with the endocrine system are reviewed under the metabolomics section. The chapter also examines the novel biomarkers for depression that have been proposed by studies in the microbiome. Depression affects individuals differentially and explicit biomarkers identified by robust research criteria may pave the way for better diagnosis, intervention, treatment, and prediction of treatment response.</p>","PeriodicalId":50872,"journal":{"name":"Advances in Clinical Chemistry","volume":"112 ","pages":"1-67"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10539458","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Biosensors for saliva biomarkers. 用于唾液生物标志物的生物传感器。
2区 医学
Advances in Clinical Chemistry Pub Date : 2023-01-01 DOI: 10.1016/bs.acc.2022.11.001
Elif Burcu Aydın, Muhammet Aydın, Mustafa Kemal Sezgintürk
{"title":"Biosensors for saliva biomarkers.","authors":"Elif Burcu Aydın,&nbsp;Muhammet Aydın,&nbsp;Mustafa Kemal Sezgintürk","doi":"10.1016/bs.acc.2022.11.001","DOIUrl":"https://doi.org/10.1016/bs.acc.2022.11.001","url":null,"abstract":"<p><p>The analysis of salivary biomarkers has gained interest and is advantageous for simple, safe, and non-invasive testing in diagnosis as well as treatment. This chapter explores the importance of saliva biomarkers and summarizes recent advances in biosensor fabrication. The identification of diagnostic, prognostic and therapeutic markers in this matrix enables more rapid and frequent testing when combined with the use of biosensor technology. Challenges and future goals are highlighted and examined.</p>","PeriodicalId":50872,"journal":{"name":"Advances in Clinical Chemistry","volume":"113 ","pages":"1-41"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10820268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Advances in TB testing. 结核病检测的进展。
2区 医学
Advances in Clinical Chemistry Pub Date : 2023-01-01 DOI: 10.1016/bs.acc.2023.03.003
Jayson V Pagaduan, Ghaith Altawallbeh
{"title":"Advances in TB testing.","authors":"Jayson V Pagaduan,&nbsp;Ghaith Altawallbeh","doi":"10.1016/bs.acc.2023.03.003","DOIUrl":"https://doi.org/10.1016/bs.acc.2023.03.003","url":null,"abstract":"<p><p>Globally, tuberculosis (TB) was the leading cause of death from a single infectious agent until the coronavirus (COVID-19) pandemic. In 2020, an estimated 10 million people fell ill with TB and a total of 1.5 million people died from the disease. About one-quarter of the global population, almost two billion people, is estimated to be latently infected with Mycobacterium tuberculosis (MTB). Although latent TB infection (LTBI) is asymptomatic and noncontagious, about 5-10% of LTBI patients have a lifetime risk of progression to active TB. The diagnosis and treatment of active cases are extremely vital for TB control programs. However, achieving the End TB goal of 2035 without the ability to identify and treat the pool of latently infected individuals will be a big challenge. To do so, improved technology to provide more accurate diagnostic tools and accessibility are crucial. Therefore, this chapter covers the current WHO-endorsed tests and advances in diagnostic and screening tests for active and latent TB.</p>","PeriodicalId":50872,"journal":{"name":"Advances in Clinical Chemistry","volume":"115 ","pages":"33-62"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056534/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10538653","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Translational proteomics and phosphoproteomics: Tissue to extracellular vesicles. 翻译蛋白质组学和磷酸化蛋白质组学:从组织到细胞外囊泡。
2区 医学
Advances in Clinical Chemistry Pub Date : 2023-01-01 DOI: 10.1016/bs.acc.2022.09.003
Xiaofeng Wu, Anton B Iliuk, W Andy Tao
{"title":"Translational proteomics and phosphoproteomics: Tissue to extracellular vesicles.","authors":"Xiaofeng Wu,&nbsp;Anton B Iliuk,&nbsp;W Andy Tao","doi":"10.1016/bs.acc.2022.09.003","DOIUrl":"https://doi.org/10.1016/bs.acc.2022.09.003","url":null,"abstract":"<p><p>We are currently experiencing a rapidly developing era in terms of translational and clinical medical sciences. The relatively mature state of nucleic acid examination has significantly improved our understanding of disease mechanism and therapeutic potential of personalized treatment, but misses a large portion of phenotypic disease information. Proteins, in particular phosphorylation events that regulates many cellular functions, could provide real-time information for disease onset, progression and treatment efficacy. The technical advances in liquid chromatography and mass spectrometry have realized large-scale and unbiased proteome and phosphoproteome analyses with disease relevant samples such as tissues. However, tissue biopsy still has multiple shortcomings, such as invasiveness of sample collection, potential health risk for patients, difficulty in protein preservation and extreme heterogeneity. Recently, extracellular vesicles (EVs) have offered a great promise as a unique source of protein biomarkers for non-invasive liquid biopsy. Membranous EVs provide stable preservation of internal proteins and especially labile phosphoproteins, which is essential for effective routine biomarker detection. To aid efficient EV proteomic and phosphoproteomic analyses, recent developments showcase clinically-friendly EV techniques, facilitating diagnostic and therapeutic applications. Ultimately, we envision that with streamlined sample preparation from tissues and EVs proteomics and phosphoproteomics analysis will become routine in clinical settings.</p>","PeriodicalId":50872,"journal":{"name":"Advances in Clinical Chemistry","volume":"112 ","pages":"119-153"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10539455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Biochemistry and pathophysiology of the Transient Potential Receptor Vanilloid 6 (TRPV6) calcium channel. 瞬时电位受体香草样蛋白6 (TRPV6)钙通道的生物化学和病理生理。
2区 医学
Advances in Clinical Chemistry Pub Date : 2023-01-01 DOI: 10.1016/bs.acc.2022.11.002
Valerie Walker, Geerten W Vuister
{"title":"Biochemistry and pathophysiology of the Transient Potential Receptor Vanilloid 6 (TRPV6) calcium channel.","authors":"Valerie Walker,&nbsp;Geerten W Vuister","doi":"10.1016/bs.acc.2022.11.002","DOIUrl":"https://doi.org/10.1016/bs.acc.2022.11.002","url":null,"abstract":"<p><p>TRPV6 is a Transient Receptor Potential Vanilloid (TRPV) cation channel with high selectivity for Ca<sup>2+</sup> ions. First identified in 1999 in a search for the gene which mediates intestinal Ca<sup>2+</sup> absorption, its far more extensive repertoire as a guardian of intracellular Ca<sup>2+</sup> has since become apparent. Studies on TRPV6-deficient mice demonstrated additional important roles in placental Ca<sup>2+</sup> transport, fetal bone development and male fertility. The first reports of inherited deficiency in newborn babies appeared in 2018, revealing its physiological importance in humans. There is currently strong evidence that TRPV6 also contributes to the pathogenesis of some common cancers. The recently reported association of TRPV6 deficiency with non-alcoholic chronic pancreatitis suggests a role in normal pancreatic function. Over time and with greater awareness of TRPV6, other disease-associations are likely to emerge. Powerful analytical tools have provided invaluable insights into the structure and operation of TRPV6. Its roles in Ca<sup>2+</sup> signaling and carcinogenesis, and the use of channel inhibitors in cancer treatment are being intensively investigated. This review first briefly describes the biochemistry and physiology of the channel, and analytical methods used to investigate these. The focus subsequently shifts to the clinical disorders associated with abnormal expression and the underlying pathophysiology. The aims of this review are to increase awareness of this channel, and to draw together findings from a wide range of sources which may help to formulate new ideas for further studies.</p>","PeriodicalId":50872,"journal":{"name":"Advances in Clinical Chemistry","volume":"113 ","pages":"43-100"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9153268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信