Department of Internal Medicine, China Medical University Hospital, Taichung, Taiwan; School of Medicine, College of Medicine, China Medical University, Taichung, Taiwan.
School of Medicine, College of Medicine, China Medical University, Taichung, Taiwan; Trauma and Emergency Center, China Medical University Hospital, Taichung, Taiwan.
Pain Physician. 2018 Mar;21(2):E149-E156.
Inflammation may trigger migraine development through neurovascular reactions in the brain. Most of the migraine patients, particularly the younger ones, do not have any risk factors for this disease. Hence, we assessed whether chronic osteomyelitis (COM), a chronic inflammatory disease, increases the risk of migraine.
We aim to evaluate the risk of migraine among female and middle-age COM patients with a large patient sample.
A retrospective cohort study was conducted in this study.
The data used in this study were extracted from the Taiwan National Health Insurance (NHI) Research Database.
A study group with 2,012 COM patients and 8,048 randomly chosen gender- and age-matched controls were chosen from the Taiwan NHI Research Database (NHIRD) from the start of 2000 to the end of 2009. The risk of migraine was estimated with Cox proportional regression model. Both COM and control groups were followed-up until the occurrence of migraine during the study period (2000-2011). Prevalent covariates, such as age, gender, hypertension, diabetes, hyperlipidemia, stroke, coronary artery disease, depression, anxiety, sleep disorder, bipolar disorder, and epilepsy, were included for further evaluation. The hazard ratio (HR) of migraine was measured with Cox proportional hazard regression model. The primary outcome was the overall migraine risk among COM patients, and the secondary outcome was the migraine risk among COM patients lacking the comorbidities. Additional outcomes included migraine risk among COM patients in different age and gender subgroups.
The overall migraine risk was increased in COM patients (adjusted hazard ratio [aHR] 1.74, 95% confidence interval [CI] 1.14-2.65). Even without any prevalent comorbidities, COM patients still exhibited an increased risk of migraine (aHR 2.05, 95% CI 1.06-3.97) than the controls did. Moreover, this risk was relatively higher in COM patients aged < 40 and 45-54 years (aHR 2.07, 95% CI 0.97-4.46 and aHR 2.11, 95% CI 0.97-4.57, respectively) than in their counterparts. Female COM patients had a relatively higher migraine risk (aHR 1.85, 95% CI 1.05-3.24) than male patients did (aHR 1.68, 95% CI 0.89-3.16).
The messages about personal behaviors were unavailable in the Taiwan NHIRD. Other neurovascular risk factors that might increase migraine cannot be excluded completely in this research.
An association between COM and increased risk of migraine was shown in this study. The results suggest that COM is a significant migraine predictor, and thus imply the necessity for rigorous migraine prevention in COM patients, especially female and younger ones.
Inflammation, migraine, chronic osteomyelitis, Taiwan National Health Insurance Research Database.
炎症可能通过大脑中的神经血管反应引发偏头痛的发生。大多数偏头痛患者,尤其是年轻患者,没有这种疾病的任何危险因素。因此,我们评估了慢性骨髓炎(COM)这一慢性炎症性疾病是否会增加偏头痛的风险。
我们旨在使用大样本量的女性和中年 COM 患者来评估偏头痛的风险。
这是一项回顾性队列研究。
本研究的数据来自于台湾全民健康保险(NHI)研究数据库。
从台湾全民健康保险研究数据库(NHIRD)中选择了 2012 例 COM 患者和 8048 名随机性别和年龄匹配的对照者,纳入了从 2000 年初到 2009 年底的研究人群。使用 Cox 比例风险回归模型估计偏头痛的风险。COM 组和对照组均在研究期间(2000-2011 年)内进行随访,直到偏头痛发生。为进一步评估,纳入了年龄、性别、高血压、糖尿病、高血脂、中风、冠心病、抑郁、焦虑、睡眠障碍、双相情感障碍和癫痫等常见合并症的协变量。使用 Cox 比例风险回归模型测量偏头痛的风险比(HR)。主要结局是 COM 患者的总体偏头痛风险,次要结局是无合并症的 COM 患者的偏头痛风险。其他结局包括 COM 患者在不同年龄和性别亚组中的偏头痛风险。
COM 患者的总体偏头痛风险增加(调整后的 HR [aHR] 1.74,95%置信区间 [CI] 1.14-2.65)。即使没有任何现患合并症,COM 患者的偏头痛风险(aHR 2.05,95%CI 1.06-3.97)也高于对照组。此外,与年龄<40 岁和 45-54 岁的患者相比,COM 患者的这种风险相对较高(aHR 2.07,95%CI 0.97-4.46 和 aHR 2.11,95%CI 0.97-4.57)。与男性患者相比(aHR 1.68,95%CI 0.89-3.16),女性 COM 患者的偏头痛风险相对较高(aHR 1.85,95%CI 1.05-3.24)。
在台湾 NHIRD 中没有关于个人行为的信息。在本研究中不能完全排除其他可能增加偏头痛的神经血管危险因素。
本研究表明 COM 与偏头痛风险增加之间存在关联。结果表明,COM 是偏头痛的一个重要预测因子,因此意味着需要对 COM 患者,尤其是女性和年轻患者进行严格的偏头痛预防。
炎症,偏头痛,慢性骨髓炎,台湾全民健康保险研究数据库。