Lingjun Yan, Yu Huang, Bingqin Xie, Zilin Liu, Lan Luo, Baochang He, Chenyu Ding, Wenhua Fang, Yuanxiang Lin, Dezhi Kang, Fa Chen
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Weighted logistic regression analysis was used to evaluate the association between periodontitis/clinical periodontal parameters and migraine. Mediation analysis was performed to explore the potential mediating role of inflammatory response. A cohort study including 1909 participants with migraine disease was further conducted to assess the associations between periodontitis/clinical periodontal parameters and mortality from all causes, cardiovascular disease (CVD), and cancer in participants with migraine disease using Cox proportional hazards models. Death outcomes were ascertained by linkage to National Death Index records through December 31, 2018.</p><p><strong>Results: </strong>Periodontitis was positively associated with migraine (odds ratio [OR] 1.29, 95% confidence interval [CI] 1.01-1.65). Each 1-unit rise in attachment loss and pocket depth was linked to a 17.5% (OR 1.18, 95% CI 1.08-1.29) and 28.1% (OR 1.28, 95% CI 1.08-1.51) increase in migraine risk, respectively. Mediation analyses revealed that leukocyte, monocyte, and lymphocyte counts mediated 17.9%, 7.3%, and 20.1%, respectively, of the association between periodontitis and migraine. During a median follow-up of 17.7 years among 1909 participants with migraine disease, periodontitis was associated with greater all-cause mortality (hazard ratio 1.82, 95% CI 1.25-2.66), but was not significantly associated with mortality from CVD or cancer among participants with migraine disease. Similar association patterns were also observed for attachment loss and pocket depth.</p><p><strong>Conclusions: </strong>This study provides evidence that periodontitis and clinical periodontal parameters were significantly associated with migraine as well as all-cause mortality in people with migraine disease. These findings underscore the importance of considering periodontal health in the prevention and management strategies for migraine disease.</p>","PeriodicalId":12844,"journal":{"name":"Headache","volume":" ","pages":""},"PeriodicalIF":5.4000,"publicationDate":"2024-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Association of periodontitis and periodontal parameters with migraine and mortality in people with migraine disease: A nationally representative observational study.\",\"authors\":\"Lingjun Yan, Yu Huang, Bingqin Xie, Zilin Liu, Lan Luo, Baochang He, Chenyu Ding, Wenhua Fang, Yuanxiang Lin, Dezhi Kang, Fa Chen\",\"doi\":\"10.1111/head.14893\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To investigate the association of periodontitis and clinical periodontal parameters with migraine as well as mortality among people with migraine disease.</p><p><strong>Background: </strong>Periodontitis has been shown to increase the systemic inflammatory burden thereby promoting various systemic health outcomes; however, the evidence regarding the relationship between periodontitis and migraine is scarce.</p><p><strong>Methods: </strong>A cross-sectional study was performed, and it included 13,108 participants from the National Health and Nutrition Examination Survey (1999-2004). Weighted logistic regression analysis was used to evaluate the association between periodontitis/clinical periodontal parameters and migraine. Mediation analysis was performed to explore the potential mediating role of inflammatory response. A cohort study including 1909 participants with migraine disease was further conducted to assess the associations between periodontitis/clinical periodontal parameters and mortality from all causes, cardiovascular disease (CVD), and cancer in participants with migraine disease using Cox proportional hazards models. Death outcomes were ascertained by linkage to National Death Index records through December 31, 2018.</p><p><strong>Results: </strong>Periodontitis was positively associated with migraine (odds ratio [OR] 1.29, 95% confidence interval [CI] 1.01-1.65). Each 1-unit rise in attachment loss and pocket depth was linked to a 17.5% (OR 1.18, 95% CI 1.08-1.29) and 28.1% (OR 1.28, 95% CI 1.08-1.51) increase in migraine risk, respectively. 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引用次数: 0
摘要
目的:探讨牙周炎和临床牙周参数与偏头痛的关系以及偏头痛患者的死亡率。背景:牙周炎已被证明会增加全身炎症负担,从而促进各种全身健康结果;然而,关于牙周炎和偏头痛之间关系的证据很少。方法:采用横断面研究方法,纳入1999-2004年全国健康与营养调查的13108名参与者。采用加权logistic回归分析来评估牙周炎/临床牙周参数与偏头痛之间的关系。通过中介分析探讨炎症反应的潜在中介作用。一项包括1909名偏头痛患者的队列研究进一步使用Cox比例风险模型来评估牙周炎/临床牙周参数与偏头痛患者全因死亡率、心血管疾病(CVD)和癌症之间的关系。通过与截至2018年12月31日的国家死亡指数记录的联系来确定死亡结果。结果:牙周炎与偏头痛呈正相关(优势比[OR] 1.29, 95%可信区间[CI] 1.01-1.65)。附着丧失和口袋深度每增加1个单位,偏头痛风险分别增加17.5% (OR 1.18, 95% CI 1.08-1.29)和28.1% (OR 1.28, 95% CI 1.08-1.51)。中介分析显示,白细胞、单核细胞和淋巴细胞计数分别介导牙周炎和偏头痛之间关联的17.9%、7.3%和20.1%。在1909名偏头痛患者17.7年的中位随访期间,牙周炎与更高的全因死亡率相关(风险比1.82,95% CI 1.25-2.66),但与偏头痛患者心血管疾病或癌症的死亡率无显著相关性。类似的关联模式也观察到附着损失和口袋深度。结论:本研究提供了证据,证明牙周炎和临床牙周参数与偏头痛以及偏头痛患者的全因死亡率显著相关。这些发现强调了在偏头痛的预防和管理策略中考虑牙周健康的重要性。
Association of periodontitis and periodontal parameters with migraine and mortality in people with migraine disease: A nationally representative observational study.
Objective: To investigate the association of periodontitis and clinical periodontal parameters with migraine as well as mortality among people with migraine disease.
Background: Periodontitis has been shown to increase the systemic inflammatory burden thereby promoting various systemic health outcomes; however, the evidence regarding the relationship between periodontitis and migraine is scarce.
Methods: A cross-sectional study was performed, and it included 13,108 participants from the National Health and Nutrition Examination Survey (1999-2004). Weighted logistic regression analysis was used to evaluate the association between periodontitis/clinical periodontal parameters and migraine. Mediation analysis was performed to explore the potential mediating role of inflammatory response. A cohort study including 1909 participants with migraine disease was further conducted to assess the associations between periodontitis/clinical periodontal parameters and mortality from all causes, cardiovascular disease (CVD), and cancer in participants with migraine disease using Cox proportional hazards models. Death outcomes were ascertained by linkage to National Death Index records through December 31, 2018.
Results: Periodontitis was positively associated with migraine (odds ratio [OR] 1.29, 95% confidence interval [CI] 1.01-1.65). Each 1-unit rise in attachment loss and pocket depth was linked to a 17.5% (OR 1.18, 95% CI 1.08-1.29) and 28.1% (OR 1.28, 95% CI 1.08-1.51) increase in migraine risk, respectively. Mediation analyses revealed that leukocyte, monocyte, and lymphocyte counts mediated 17.9%, 7.3%, and 20.1%, respectively, of the association between periodontitis and migraine. During a median follow-up of 17.7 years among 1909 participants with migraine disease, periodontitis was associated with greater all-cause mortality (hazard ratio 1.82, 95% CI 1.25-2.66), but was not significantly associated with mortality from CVD or cancer among participants with migraine disease. Similar association patterns were also observed for attachment loss and pocket depth.
Conclusions: This study provides evidence that periodontitis and clinical periodontal parameters were significantly associated with migraine as well as all-cause mortality in people with migraine disease. These findings underscore the importance of considering periodontal health in the prevention and management strategies for migraine disease.
期刊介绍:
Headache publishes original articles on all aspects of head and face pain including communications on clinical and basic research, diagnosis and management, epidemiology, genetics, and pathophysiology of primary and secondary headaches, cranial neuralgias, and pains referred to the head and face. Monthly issues feature case reports, short communications, review articles, letters to the editor, and news items regarding AHS plus medicolegal and socioeconomic aspects of head pain. This is the official journal of the American Headache Society.