Department of Neurology, University of Kentucky Medical Center, Kentucky Neuroscience Institute, 740 S Limestone Dr, Lexington, KY 40536, USA.
Department of Neurology, University of Kentucky Medical Center, Kentucky Neuroscience Institute, 740 S Limestone Dr, Lexington, KY 40536, USA.
Mult Scler Relat Disord. 2021 Jun;51:102942. doi: 10.1016/j.msard.2021.102942. Epub 2021 Apr 9.
We investigated if anti-tumor necrosis factor-α (anti-TNF-α) drugs used in the treatment of inflammatory bowel disease (IBD) alter the incidence of MS and if so, to understand the magnitude of such an effect.
This is a retrospective cohort study of data from Truven Health Market Scan administrative claims database. The patients included in the study had to be ≥ 18 years of age. The presence of IBD was based on at least 2 claims of International Classification of Diseases (ICD-9 or 10) diagnosis codes. The IBD diagnosis index date had to precede the MS diagnosis index date for inclusion in the study. The diagnosis of multiple sclerosis (MS) was defined as having at least 2 claims for the disease (ICD 9, 340 and ICD 10 codes, G35) and at least one prescription claim for any of the drugs that were defined as MS therapy.
Patients with IBD had 1.32 times the risk of MS incidence compared to healthy controls (adjusted incidence rate ratio (IRR): 1.32; 95% CI: 1.03 - 1.71; p = .0312). Patients with IBD exposed to anti-TNF-α therapies had a 43% increase in the incidence of MS compared to those with IBD without exposure (adjusted incidence rate: 1.43; 95% CI: .062 - 3.32; p = .3989). Among CD patients treated anti-TNF-α medications an increase in the incidence of MS, compared to CD patients not exposed to such medications was observed (IRR = 2.62; 95% CI: 1.00 to 6.83; p = 0.049), statistically significant. After adjusting for age/gender, patients with CD using anti-TNF-α agents had an increase of incidence in MS (adjusted IRR: 2.24; 95% CI: 0.85 - 5.94; p = .1035) but it was not statistically significant.
Use of anti-TNF-α drugs in CD was associated with a statistically significant increase in the incidence of MS but this effect was lost when controlled for age/gender.
我们研究了治疗炎症性肠病(IBD)的抗肿瘤坏死因子-α(anti-TNF-α)药物是否会改变多发性硬化症(MS)的发病率,如果是,那么要了解这种影响的程度。
这是一项来自 Truven Health Market Scan 行政索赔数据库的回顾性队列研究。研究纳入的患者必须年满 18 岁。IBD 的存在基于至少 2 次国际疾病分类(ICD-9 或 10)诊断代码的索赔。IBD 诊断索引日期必须先于 MS 诊断索引日期,以便纳入研究。多发性硬化症(MS)的诊断定义为至少有 2 次疾病的索赔(ICD 9,340 和 ICD 10 代码,G35)和至少一次规定的任何一种被定义为 MS 治疗的药物的处方索赔。
与健康对照组相比,IBD 患者的 MS 发病率风险增加了 1.32 倍(校正发病率比(IRR):1.32;95%置信区间:1.03-1.71;p=0.0312)。与未暴露于抗 TNF-α 治疗的 IBD 患者相比,暴露于抗 TNF-α 治疗的 IBD 患者的 MS 发病率增加了 43%(校正发病率:1.43;95%置信区间:0.062-3.32;p=0.3989)。与未接受此类药物治疗的 CD 患者相比,接受抗 TNF-α 药物治疗的 CD 患者的 MS 发病率增加(IRR=2.62;95%置信区间:1.00-6.83;p=0.049),具有统计学意义。在校正年龄/性别后,使用抗 TNF-α 药物的 CD 患者 MS 发病率增加(校正 IRR:2.24;95%置信区间:0.85-5.94;p=0.1035),但无统计学意义。
在 CD 中使用抗 TNF-α 药物与 MS 发病率的统计学显著增加相关,但在控制年龄/性别后,这种作用消失了。