脊髓损伤继发性并发症的生物标志物。

Q1 Biochemistry, Genetics and Molecular Biology Current Pharmacology Reports Pub Date : 2022-02-01 Epub Date: 2021-12-02 DOI:10.1007/s40495-021-00268-3
Hani Alostaz, Li Cai
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引用次数: 2

摘要

回顾目的:在美国,由于车祸、跌倒、暴力或运动损伤等事件,每年每百万人中就有40人发生脊髓损伤(SCI)。脊髓损伤引起的继发性并发症是危及生命的,应尽早治疗。在某些情况下,患者可能出现的并发症并不完全明显,直到为时已晚。因此,需要生物标志物来评估脊髓损伤后继发并发症的水平。由于有几种并发症会产生不同的预警信号,不同的生物标志物可能对脊髓损伤患者的早期发现、维持和长期护理有益。近期研究发现:对各种脊髓损伤及其相关并发症,如神经性疼痛和深静脉血栓形成的生物标志物进行了大量研究。近年来,随着细胞和分子、全基因组转录组分析、生物信息学和临床研究发现生物标志物,研究范围不断扩大。生物标志物可以早期预测脊髓损伤继发性并发症的严重程度。摘要:本文综述了近年来有关脊髓损伤继发性并发症的常见生物标志物的研究进展。我们强调已经测试过的可靠的生物标志物,如硬化蛋白、NGF、d -二聚体、抑癌素M (OSM)、微生物群和c反应蛋白,这些都是有价值的,具有临床重要性。这篇综述还强调了生物标志物的持续研究,因为它们可以为脊髓损伤后的继发性并发症提供有价值的细胞和分子见解。
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Biomarkers from Secondary Complications in Spinal Cord Injury.

Purpose of review: In the USA, spinal cord injury (SCI) occurs in 40 people per million every year due to events such as car accidents, falls, violence, or sports injury. Secondary complications that arise from SCI are life-threatening and should be treated as early as possible. In some cases, it is not completely obvious what complication a patient may have until it is too late. Therefore, biomarkers are required to assess the levels of secondary complications after SCI. As there are several complications that pose different warning signs, different biomarkers may be beneficial in early detection, maintenance, and long-term care for patients with SCI.

Recent findings: Numerous studies have been conducted on biomarkers in various SCI and its related complications, such as neuropathic pain and deep vein thrombosis. In recent years, research has expanded with biomarkers discovered by cellular and molecular, genome-wide transcriptomic analysis, bioinformatics, and clinical studies. Biomarkers have allowed early prediction of the severity of secondary complications due to SCI.

Summary: In this review, we summarize recent studies on the common biomarkers for the secondary complications related to SCI. We highlight the reliable biomarkers that have been tested, e.g., sclerostin, NGF, D-dimer, oncostatin M (OSM), microbiota, and C-reactive protein, which are valuable and with clinical importance. This review also emphasizes continuing research in biomarkers as they can provide valuable cellular and molecular insight into secondary complications after SCI.

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来源期刊
Current Pharmacology Reports
Current Pharmacology Reports Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
9.30
自引率
0.00%
发文量
35
期刊介绍: Current Pharmacology Reports will: publish cutting-edge reviews on subjects pertinent to all aspects of pharmacology, including drug discovery and development.provide incisive, insightful, and balanced contributions from international leading experts.interest a wide readership of basic scientists and translational investigators in academia and in industry. The Current Pharmacology Reports journal accomplishes its goal by appointing international authorities to serve as Section Editors in key subject areas, such as: epigenetics and epigenomics, chemoinformatics and rational drug design and target discovery, drug delivery and biomaterial, pharmacogenomics and molecular targets and biomarkers, chemical/drug/molecular toxicology, absorption, distribution, metabolism and elimination (ADME), pharmacokinetics (PK) and pharmacodynamics (PD), Modeling & Simulation (M&S) and pharmacometrics, and other related topics in pharmacology including neurology/central nervous system (CNS), cardiovascular, metabolic diseases, cancer, among others. Section Editors for Current Pharmacology Reports select topics for which leading experts contribute comprehensive review articles that emphasize new developments and recently published papers of major importance, highlighted by annotated reference lists. An Editorial Board of internationally diverse members suggests topics of special interest to their country/region and ensures that topics are current and include emerging research. Commentaries from well-known figures in the field are also provided. This journal publishes on a bi-monthly schedule.Please submit here: https://www.editorialmanager.com/phar/default.aspx
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