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创伤性脑损伤与临床诊断的α-突触核蛋白病的关系:一项病例对照研究。

Traumatic brain injury preceding clinically diagnosed α-synucleinopathies: A case-control study.

机构信息

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.

出版信息

Neurology. 2020 Feb 25;94(8):e764-e773. doi: 10.1212/WNL.0000000000008995. Epub 2020 Jan 28.

Abstract

OBJECTIVE

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).

METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

目的

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)。

方法

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。

结果

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)。

结论

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。

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