三叉神经痛及其合并症:全国性疾病轨迹研究。

IF 5.9 1区 医学 Q1 ANESTHESIOLOGY PAIN® Pub Date : 2024-10-01 DOI:10.1097/j.pain.0000000000003428
Jacob Worm, Isabella Friis Jørgensen, Ólafur Birgir Davídsson, Henrik Hjalgrim, Timo Röder, Sisse Rye Ostrowski, Ole Birger Pedersen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Erik Sørensen, Henrik Ullum, Gyða Björnsdóttir, Thorgeir Thorgeirsson, Hreinn Stefánsson, Ólafur Árni Sveinsson, Kári Stefánsson, Henrik Winther Schytz, Lars Bendtsen, Søren Brunak, Thomas Folkmann Hansen, Stine Maarbjerg
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引用次数: 0

摘要

摘要:人们对三叉神经痛的危险因素和合并症了解有限,这种疾病的特点是阵发性单侧面部剧烈疼痛,女性发病率较高。我们的目标是通过分析全国范围内的疾病轨迹,确定与三叉神经痛相关的时间性合并症。利用 1994 年至 2018 年期间丹麦全国患者登记册中 720 万名独特个体的数据,将每个确诊为三叉神经痛的个体与 10,000 名匹配对照者进行比较,以确定并发疾病。在性别分层的疾病轨迹中确定了连续的疾病关联。Cox 回归分析研究了卡马西平或奥卡西平治疗与加巴喷丁、普瑞巴林或拉莫三嗪治疗相比是否与中风风险相关。最后,我们研究了三叉神经痛基因分型个体的中风多基因风险评分及其与中风发病率的关系。我们纳入了 7141 名三叉神经痛患者(64.2% 为女性,诊断时平均年龄为 58.7 岁),并确定了 18 种与三叉神经痛相关的疾病。确诊后,三叉神经痛与 9 种疾病相关,包括缺血性中风(相对风险 1.55)。卡马西平或奥卡西平治疗会增加缺血性中风的风险(危险比为 1.78;95% 置信区间为 1.47-2.17);但中风的多基因风险与此没有关联。在丹麦人群中,三叉神经痛的诊断与系统疾病轨迹显示的 27 种疾病在时间上相关。三叉神经痛本身及其一线治疗(而非中风多基因风险评分)与缺血性中风风险的增加有关,这表明应常规评估三叉神经痛患者的血管风险因素。
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Trigeminal neuralgia and its comorbidities: a nationwide disease trajectory study.

Abstract: There is a limited understanding of risk factors and comorbidities in trigeminal neuralgia, a disease characterized by paroxysms of severe unilateral facial pain and a higher incidence in women. We aim to identify temporally associated comorbidities involving trigeminal neuralgia by analyzing nationwide disease trajectories. Using data from 7.2 million unique individuals in the Danish National Patient Register between 1994 and 2018, each individual diagnosed with trigeminal neuralgia was compared with 10,000 matched controls to identify co-occurring diseases. The sequential disease associations were identified in sex-stratified disease trajectories. A Cox-regression analysis investigated whether treatment with carbamazepine or oxcarbazepine, as compared with gabapentin, pregabalin, or lamotrigine, was associated with stroke risk. Finally, we investigated the stroke polygenic risk score and its association with stroke incidence in a subset of genotyped individuals with trigeminal neuralgia. We included 7141 individuals with trigeminal neuralgia (64.2% female, mean age at diagnosis 58.7 years) and identified 18 diseases associated with subsequent trigeminal neuralgia. After diagnosis, trigeminal neuralgia was associated with 9 diseases, including ischemic stroke (relative risk 1.55). Carbamazepine or oxcarbazepine treatment increased the ischemic stroke risk (hazard ratio 1.78; 95% confidence interval 1.47-2.17); however, the polygenic risk of stroke showed no association. In the Danish population, a trigeminal neuralgia diagnosis is temporally associated with 27 diseases revealed in systematic disease trajectories. Trigeminal neuralgia itself and its first-line treatment, but not a stroke polygenic risk score, was associated with an increased risk of ischemic stroke indicating that vascular risk factors should be routinely assessed in individuals with trigeminal neuralgia.

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来源期刊
PAIN®
PAIN® 医学-临床神经学
CiteScore
12.50
自引率
8.10%
发文量
242
审稿时长
9 months
期刊介绍: PAIN® is the official publication of the International Association for the Study of Pain and publishes original research on the nature,mechanisms and treatment of pain.PAIN® provides a forum for the dissemination of research in the basic and clinical sciences of multidisciplinary interest.
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