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Non-aspirin NSAIDs, cyclooxygenase-2 inhibitors and risk for cardiovascular events-stroke, acute myocardial infarction, and death from coronary heart disease.非阿司匹林类 NSAIDs、环氧化酶-2 抑制剂与心血管事件(卒、急性心肌梗死、冠心病死亡)风险。
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药物过度使用性头痛的基因组表达模式

Genomic expression patterns in medication overuse headaches.

作者信息

Hershey Andrew D, Burdine Danny, Kabbouche Marielle A, Powers Scott W

机构信息

University of Cincinnati, OH, USA.

出版信息

Cephalalgia. 2011 Jan;31(2):161-71. doi: 10.1177/0333102410373155. Epub 2010 Jun 2.

DOI:10.1177/0333102410373155
PMID:20974594
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4893192/
Abstract

BACKGROUND

Chronic daily headache (CDH) and chronic migraine (CM) are one of the most frequent problems encountered in neurology, are often difficult to treat, and frequently complicated by medication-overuse headache (MOH). Proper recognition of MOH may alter treatment outcome and prevent long term disability.

OBJECTIVE

This study identifies the unique genomic expression pattern MOH that respond to cessation of the overused medication.

METHODS

Baseline occurrence of MOH and typical pattern of response to medication cessation were measured from a large database. Whole blood samples from patients with CM with or without MOH were obtained and their genomic profile was assessed. Affymetrix human U133 plus2 arrays were used to examine the genomic expression patterns prior to treatment and 6-12 weeks later. Headache characterisation and response to treatment based on headache frequency and disability were compared.

RESULTS

Of 1311 patients reporting daily or continuous headaches, 513 (39.1%) reported overusing analgesic medication. At follow-up, 44.5% had a 50% or greater reduction in headache frequency, while 41.6% had no change. Blood genomic expression patterns were obtained on 33 patients with 19 (57.6%) overusing analgesic medication with a unique genomic expression pattern in MOH that responded to cessation of analgesics. Gene ontology of these samples indicated a significant number were involved with brain and immunological tissues, including multiple signalling pathways and apoptosis.

CONCLUSIONS

Blood genomic patterns can accurately identify MOH patients that respond to medication cessation. These results suggest that MOH involves a unique molecular biology pathway that can be identified with a specific biomarker.

摘要

背景

慢性每日头痛(CDH)和慢性偏头痛(CM)是神经病学中最常见的问题之一,通常难以治疗,且常并发药物过度使用性头痛(MOH)。正确识别MOH可能会改变治疗结果并预防长期残疾。

目的

本研究确定对停用过度使用药物有反应的MOH独特基因组表达模式。

方法

从一个大型数据库中测量MOH的基线发生率和药物戒断的典型反应模式。获取有或无MOH的CM患者的全血样本,并评估其基因组概况。使用Affymetrix人类U133 plus2芯片在治疗前和6 - 12周后检查基因组表达模式。比较基于头痛频率和残疾程度的头痛特征及对治疗的反应。

结果

在1311名报告每日或持续性头痛的患者中,513名(39.1%)报告过度使用止痛药物。随访时,44.5%的患者头痛频率降低了50%或更多,而41.6%的患者无变化。对33名过度使用止痛药物的患者进行了血液基因组表达模式检测,其中19名(57.6%)在MOH中有独特的基因组表达模式,对停用止痛药物有反应。这些样本的基因本体分析表明,大量基因与脑和免疫组织有关,包括多个信号通路和细胞凋亡。

结论

血液基因组模式可以准确识别对药物戒断有反应的MOH患者。这些结果表明,MOH涉及一条独特的分子生物学途径,可通过特定生物标志物识别。