阿尔法降钙素基因相关肽、神经肽 Y 和物质 P 作为多发性硬化症诊断、疾病活动性和严重程度的生物标记物。

IF 2.7 4区 医学 Q3 NEUROSCIENCES CNS & neurological disorders drug targets Pub Date : 2024-01-01 DOI:10.2174/1871527322666230403130540
Maha S Al-Keilani, Basima A Almomani, Saied A Jaradat, Nour A Al-Sawalha, Majdi Al Qawasmeh
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引用次数: 0

摘要

背景:α-降钙素基因相关肽(aCGRP)、神经肽Y(NPY)和P物质(SP)是近年来新出现的神经肽,它们是强有力的免疫调节因子,有望成为多发性硬化症(MS)的新型生物标记物和治疗靶点:该研究旨在检测多发性硬化症患者与健康对照者血清中aCGRP、NPY和SP的水平及其与疾病活动和严重程度的关系:采用酶联免疫吸附法测定多发性硬化症患者以及年龄和性别匹配的健康对照组的血清水平:结果:我们纳入了 67 名多发性硬化症患者:结果:我们纳入了 67 名多发性硬化症患者:61 名复发缓解型多发性硬化症 (RR-MS) 和 6 名进行性多发性硬化症 (PR-MS),以及 67 名健康对照组。发现多发性硬化症患者的血清 NPY 水平低于健康对照组(P < 0.001)。与 RR-MS (p = 0.007)和健康对照组(p = 0.001)相比,PR-MS 患者的血清 aCGRP 水平较高,且与 EDSS 呈正相关(r = 0.270,p = 0.028)。RR-MS 和 PR-MS 患者的血清 NPY 水平明显高于健康对照组(分别为 p < 0.001 和 p = 0.001),轻度或中度/重度患者的血清 NPY 水平低于健康对照组(p < 0.001)。SP水平与多发性硬化症病程(r = -0.279,p = 0.022)和当前DMT病程(r = -0.315,p = 0.042)之间存在显著的反相关性:结论:与健康对照组相比,多发性硬化症患者的血清 NPY 水平较低。结论:与健康对照组相比,多发性硬化症患者的血清中 NPY 水平较低。由于血清中 aCGRP 水平与疾病活动和严重程度显著相关,因此它是一种潜在的疾病进展标志物。
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Alpha Calcitonin Gene-related Peptide, Neuropeptide Y, and Substance P as Biomarkers for Diagnosis and Disease Activity and Severity in Multiple Sclerosis.

Background: Alpha calcitonin gene-related peptide (aCGRP), neuropeptide Y (NPY), and substance P (SP) are neuropeptides that have emerged recently as potent immunomodulatory factors with potential as novel biomarkers and therapeutic targets in multiple sclerosis (MS).

Objective: The study aimed to detect serum levels of aCGRP, NPY, and SP in MS patients versus healthy controls and their association with disease activity and severity.

Methods: Serum levels were measured in MS patients and age and sex-matched healthy controls using ELISA.

Results: We included 67 MS patients: 61 relapsing-remitting MS (RR-MS) and 6 progressive MS (PR-MS), and 67 healthy controls. Serum NPY level was found to be lower in MS patients than in healthy controls (p < 0.001). Serum aCGRP level was higher in PR-MS compared to RR-MS (p = 0.007) and healthy controls (p = 0.001), and it positively correlated with EDSS (r = 0.270, p = 0.028). Serum NPY level was significantly higher in RR-MS and PR-MS than in healthy controls (p < 0.001 and p = 0.001, respectively), and it was lower in patients with mild or moderate/severe disease than in healthy controls (p < 0.001). Significant inverse correlations were found between SP level and MS disease duration (r = -0.279, p = 0.022) and duration of current DMT (r = -0.315, p = 0.042).

Conclusion: Lower serum levels of NPY were revealed in MS patients compared to healthy controls. Since serum levels of aCGRP are significantly associated with disease activity and severity, it is a potential disease progression marker.

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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
158
审稿时长
6-12 weeks
期刊介绍: Aims & Scope CNS & Neurological Disorders - Drug Targets aims to cover all the latest and outstanding developments on the medicinal chemistry, pharmacology, molecular biology, genomics and biochemistry of contemporary molecular targets involved in neurological and central nervous system (CNS) disorders e.g. disease specific proteins, receptors, enzymes, genes. CNS & Neurological Disorders - Drug Targets publishes guest edited thematic issues written by leaders in the field covering a range of current topics of CNS & neurological drug targets. The journal also accepts for publication original research articles, letters, reviews and drug clinical trial studies. As the discovery, identification, characterization and validation of novel human drug targets for neurological and CNS drug discovery continues to grow; this journal is essential reading for all pharmaceutical scientists involved in drug discovery and development.
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