Potential use of microRNA-590 biomarkers verses plasma calcitonin gene-related peptide for diagnosis of migraine

Hany Mohamed El Deeb, Rasha Said Amr, Dina Elsayed Gaber
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Abstract

Many biomarkers have been investigated for migraine diagnosis, giving insights into the pathophysiology of migraine, treatment response, and for the development of new treatment strategies. Over the years, many substances, for example, neurotransmitters, neuropeptides, glio transmitters, and hormones, have been suggested as possible biomarkers for migraine. The literature demonstrates that miRNAs may play a role in migraine. The aim of this study was to compare serum mi RNA and calcitonin gene-related peptide in Migraineurs. 43 Migraineurs and 43 age and sex-matched controls were included in the study serum miRNA 590 of Migraineurs and controls were assessed by high content serum miRNA arrays. miRNA was compared to serum calcitonin gene-related peptide in both groups. Expression of miRNA-590 in serum is detected by real time PCR (q-PCR) Measurement of serum CGRP by ELISA (enzyme-linked immunosorbent assay) technique. 43 patients (86% females) mean age was 35.56 ± 9.45 and 43 controls (93% females) mean age was37.26 ± 9.15 which were age and sex matched with no statistically significant difference regarding age and sex (fisher extract) FE p = 0.483, p = 0.400, respectively. Regarding the level of miR-590-5p among patients and controls, Table 1 shows that miR-590-5p was significantly higher among cases (mean = 5.90 ± 21.22) than among controls mean = 3.32 ± 5.73 and *p = 0.027 reading the level of CGRP among patients and controls Table 2 shows that CGRP was significantly higher among cases (mean = 172 ± 110) than among controls mean = 66.43 ± 8.89 and *p ≤ 0.001. Regarding the relation between migraine type with miR-590-5p and CGRP among cases miR-590-5p had a higher mean among cases with episodic migraine mean = 11.58 ± 32.40 in comparison with chronic migraine mean = 1.81 ± 1.68 and this was statistically significant *p = 0.013. MicroRNA-590 can be used as a biomarker of migraine and has a comparable result to CGRP.
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将 microRNA-590 生物标记物与血浆降钙素基因相关肽用于偏头痛诊断的可能性
人们研究了许多用于偏头痛诊断的生物标志物,从而深入了解偏头痛的病理生理学、治疗反应以及新治疗策略的开发。多年来,许多物质,如神经递质、神经肽、胶质递质和激素,都被认为可能是偏头痛的生物标志物。文献表明,miRNAs 可能在偏头痛中发挥作用。本研究旨在比较偏头痛患者的血清 mi RNA 和降钙素基因相关肽。研究采用高含量血清 miRNA 阵列评估了 43 名偏头痛患者和 43 名年龄与性别匹配的对照组患者的血清 miRNA 590。采用实时 PCR(q-PCR)技术检测血清中 miRNA-590 的表达,采用酶联免疫吸附试验(ELISA)技术测量血清降钙素相关肽。43 名患者(86% 为女性)的平均年龄为(35.56 ± 9.45)岁,43 名对照组患者(93% 为女性)的平均年龄为(37.26 ± 9.15)岁,年龄和性别匹配,年龄和性别差异无统计学意义(fisher extract)FE p = 0.483,p = 0.400。关于患者和对照组的 miR-590-5p 水平,表 1 显示,病例中 miR-590-5p 显著高于对照组(平均值=5.90±21.22),平均值=3.32±5.73,*p = 0.027;关于患者和对照组的 CGRP 水平,表 2 显示,病例中 CGRP 显著高于对照组(平均值=66.43±8.89),平均值=172±110,*p ≤ 0.001。关于偏头痛类型与 miR-590-5p 和 CGRP 的关系,在病例中,发作性偏头痛病例的 miR-590-5p 平均值 = 11.58 ± 32.40,高于慢性偏头痛病例的平均值 = 1.81 ± 1.68,这在统计学上有显著意义 *p = 0.013。MicroRNA-590可用作偏头痛的生物标志物,其结果与CGRP相当。
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