From the Alix School of Medicine (S.H.), Department of Health Sciences Research (M.M.M., R.S.), and Department of Neurology (P.T., J.E.A., J.H.B., R.S.), Mayo Clinic, Rochester, MN.
Neurology. 2020 Feb 25;94(8):e764-e773. doi: 10.1212/WNL.0000000000008995. Epub 2020 Jan 28.
To determine the association between traumatic brain injury (TBI) and any clinically diagnosed α-synucleinopathy including Parkinson disease (PD), dementia with Lewy bodies (DLB), PD dementia (PDD), and multiple system atrophy (MSA).
Using the medical records-linkage system of the Rochester Epidemiology Project, we identified incident cases of α-synucleinopathies in Olmsted County, Minnesota, from 1991 to 2010, matching by age (±1 year) at symptom onset and sex to controls. We reviewed records of cases and controls to detect TBI prior to clinical-motor onset of any α-synucleinopathies. We based severity (possible, probable, and definite) upon the Mayo Classification System for TBI Severity. Using conditional-logistic regression, we calculated the odds ratio (OR) of all α-synucleinopathies and type, adjusting for coffee intake and smoking.
TBI frequency was lower among cases (7.0%) than controls (8.2%). No association was found between TBI and all α-synucleinopathies in multivariable analyses (OR 0.90, 95% confidence interval [CI] 0.54-1.52). No association presented when examining the number of TBIs, TBI severity, time between TBI exposure and index date, age at index date, or sex. When stratifying by each individual α-synucleinopathy, we did not identify any associations between TBI and PD, DLB, or PDD. Among the MSA group, 1 (6.4%) and 0 controls experienced a TBI (OR could not be estimated).
In this nested case-control population-based analysis, TBI was not associated with subsequent α-synucleinopathies in general or any individual α-synucleinopathy. This did not change based on the temporality or the severity of the TBI. Our findings may be limited by the study power.
确定创伤性脑损伤(TBI)与任何临床诊断的α-突触核蛋白病之间的关联,包括帕金森病(PD)、路易体痴呆(DLB)、PD 痴呆(PDD)和多系统萎缩(MSA)。
利用明尼苏达州罗切斯特流行病学项目的医疗记录-链接系统,我们在 1991 年至 2010 年间确定了明尼苏达州奥尔姆斯特德县的α-突触核蛋白病的发病病例,通过发病前的年龄(±1 岁)和性别与对照组相匹配。我们审查了病例和对照组的记录,以发现任何α-突触核蛋白病临床运动发作前的 TBI。我们根据 Mayo 创伤性脑损伤严重程度分类系统确定严重程度(可能、可能和明确)。使用条件逻辑回归,我们计算了所有α-突触核蛋白病和类型的优势比(OR),调整了咖啡摄入量和吸烟因素。
病例组(7.0%)的 TBI 频率低于对照组(8.2%)。多变量分析未发现 TBI 与所有α-突触核蛋白病之间存在关联(OR 0.90,95%置信区间[CI]0.54-1.52)。当我们分别检查 TBI 的数量、TBI 严重程度、TBI 暴露与索引日期之间的时间、索引日期的年龄或性别时,也没有发现 TBI 与 PD、DLB 或 PDD 之间存在关联。在 MSA 组中,1 名(6.4%)患者和 0 名对照者经历了 TBI(无法估计 OR)。
在这项基于嵌套病例对照的人群分析中,TBI 与一般的α-突触核蛋白病或任何特定的α-突触核蛋白病均无关联。这一结果不受 TBI 的时间性或严重程度的影响。我们的发现可能受到研究能力的限制。