Citations 898

P1‐178: Frequency of cerebral infarcts in probable dementia with lewy bodies

Alzheimer's & Dementia | December 15, 2015 | Volume: 11 | Issue: 7S_Part_9 | Pages: No page available

10.1016/j.jalz.2015.06.377

P2‐285: Characteristics, caregiver evaluations, and telephone call volume of a frontotemporal dementia caregiver educational and support program

Alzheimer's & Dementia | December 15, 2015 | Volume: 11 | Issue: 7S_Part_13 | Pages: No page available

10.1016/j.jalz.2015.06.826

IC‐P‐061: Frequency and distribution of cerebral microbleeds in dementia with lewy bodies

Alzheimer's & Dementia | December 15, 2015 | Volume: 11 | Issue: 7S_Part_1 | Pages: No page available

10.1016/j.jalz.2015.06.082

Globular Glial Tauopathy Presenting as Semantic Variant Primary Progressive Aphasia

JAMA Neurology | November 16, 2015 | Volume: 73 | Issue: 1 | Pages: 123

10.1001/jamaneurol.2015.2711 | PMID 26571405

Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders

Neurology | November 11, 2015 | Volume: 85 | Issue: 23 | Pages: 2016-2025

10.1212/wnl.0000000000002170 | PMID 26561290

Spectrum of cognition short of dementia

Neurology | October 10, 2015 | Volume: 85 | Issue: 19 | Pages: 1712-1721

10.1212/wnl.0000000000002100 | PMID 26453643

Role of β-Amyloidosis and Neurodegeneration in Subsequent Imaging Changes in Mild Cognitive Impairment

JAMA Neurology | October 5, 2015 | Volume: 72 | Issue: 12 | Pages: 1475

10.1001/jamaneurol.2015.2323 | PMID 26437123

Basal ganglia T1 hyperintensity in LGI1-autoantibody faciobrachial dystonic seizures

Neurology Neuroimmunology & Neuroinflammation | October 2, 2015 | Volume: 2 | Issue: 6 | Pages: No page available

10.1212/nxi.0000000000000161 | PMID 26468474

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies

Neurology | September 3, 2015 | Volume: 85 | Issue: 19 | Pages: 1680-1686

10.1212/wnl.0000000000001946 | PMID 26333800

Association of traumatic brain injury with subsequent neurological and psychiatric disease: a meta-analysis

Journal of Neurosurgery | August 28, 2015 | Volume: 124 | Issue: 2 | Pages: 511-526

10.3171/2015.2.jns14503 | PMID 26315003

OBJECT Mild traumatic brain injury (TBI) has been proposed as a risk factor for the development of Alzheimer’s disease, Parkinson’s disease, depression, and other illnesses. This study’s objective was to determine the association of prior mild TBI with the subsequent diagnosis (that is, at least 1 year postinjury) of neurological or psychiatric disease. METHODS All studies from January 1995 to February 2012 reporting TBI as a risk factor for diagnoses of interest were identified by searching PubMed, study references, and review articles. Reviewers abstracted the data and assessed study designs and characteristics. RESULTS Fifty-seven studies met the inclusion criteria. A random effects meta-analysis revealed a significant association of prior TBI with subsequent neurological and psychiatric diagnoses. The pooled odds ratio (OR) for the development of any illness subsequent to prior TBI was 1.67 (95% CI 1.44–1.93, p < 0.0001). Prior TBI was independently associated with both neurological (OR 1.55, 95% CI 1.31–1.83, p < 0.0001) and psychiatric (OR 2.00, 95% CI 1.50–2.66, p < 0.0001) outcomes. Analyses of individual diagnoses revealed higher odds of Alzheimer’s disease, Parkinson’s disease, mild cognitive impairment, depression, mixed affective disorders, and bipolar disorder in individuals with previous TBI as compared to those without TBI. This association was present when examining only studies of mild TBI and when considering the influence of study design and characteristics. Analysis of a subset of studies demonstrated no evidence that multiple TBIs were associated with higher odds of disease than a single TBI. CONCLUSIONS History of TBI, including mild TBI, is associated with the development of neurological and psychiatric illness. This finding indicates that either TBI is a risk factor for heterogeneous pathological processes or that TBI may contribute to a common pathological mechanism.