Department of Neurology, Washington University School of Medicine, St. Louis, MO, United States.
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States.
Parkinsonism Relat Disord. 2018 May;50:23-28. doi: 10.1016/j.parkreldis.2018.02.008. Epub 2018 Feb 9.
Gastrointestinal (GI) dysfunction precedes the motor symptoms of Parkinson's disease (PD) by several years. PD patients have abnormal aggregation of intestinal α-synuclein, the accumulation of which may be promoted by inflammation. The relationship between intestinal α-synuclein aggregates and central nervous system neuropathology is unknown. Recently, we observed a possible inverse association between inflammatory bowel disease (IBD) and PD as part of a predictive model of PD. Therefore, the objective of this study was to examine the relationship between PD risk and IBD and IBD-associated conditions and treatment.
Using a case-control design, we identified 89,790 newly diagnosed PD cases and 118,095 population-based controls >65 years of age using comprehensive Medicare data from 2004-2009 including detailed claims data. We classified IBD using International Classification of Diseases version 9 (ICD-9) diagnosis codes. We used logistic regression to calculate odds ratios (ORs) and 95% confidence intervals (CIs) to evaluate the association between PD and IBD. Covariates included age, sex, race/ethnicity, smoking, Elixhauser comorbidities, and health care use.
PD was inversely associated with IBD overall (OR = 0.85, 95% CI 0.80-0.91) and with both Crohn's disease (OR = 0.83, 95% CI 0.74-0.93) and ulcerative colitis (OR = 0.88, 95% CI 0.82-0.96). Among beneficiaries with ≥2 ICD-9 codes for IBD, there was an inverse dose-response association between number of IBD ICD-9 codes, as a potential proxy for IBD severity, and PD (p-for-trend = 0.006).
IBD is associated with a lower risk of developing PD.
胃肠道(GI)功能障碍在帕金森病(PD)的运动症状出现前数年就已出现。PD 患者的肠道α-突触核蛋白异常聚集,其聚集可能受到炎症的促进。肠道α-突触核蛋白聚集与中枢神经系统神经病理学之间的关系尚不清楚。最近,我们在帕金森病预测模型的一部分中观察到炎症性肠病(IBD)和 PD 之间可能存在负相关关系。因此,本研究的目的是研究 PD 风险与 IBD 以及 IBD 相关疾病和治疗之间的关系。
我们使用病例对照设计,使用 2004-2009 年综合医疗保险数据(包括详细的索赔数据),从 89790 名新诊断的 PD 病例和 118095 名年龄在 65 岁以上的人群中确定病例和对照。我们使用国际疾病分类第 9 版(ICD-9)诊断代码来分类 IBD。我们使用逻辑回归计算优势比(OR)和 95%置信区间(CI),以评估 PD 与 IBD 之间的关联。协变量包括年龄、性别、种族/民族、吸烟、Elixhauser 合并症和医疗保健使用情况。
PD 与 IBD 总体呈负相关(OR=0.85,95%CI 0.80-0.91),与克罗恩病(OR=0.83,95%CI 0.74-0.93)和溃疡性结肠炎(OR=0.88,95%CI 0.82-0.96)均呈负相关。在具有≥2 个 IBD ICD-9 代码的受益人中,IBD ICD-9 代码的数量与 PD 之间存在反向剂量反应关联(趋势检验 p 值=0.006),这可能是 IBD 严重程度的一个代理。
IBD 与 PD 的发病风险降低相关。