慢性的脳外傷の稀少性に関する研究(Mount Sinai Study Finds Chronic Traumatic Encephalopathy Rare Among Individuals With Isolated Brain Injuries)

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2025-10-23 マウントサイナイ医療システム

マウントサイナイ医科大学の研究チームは、単発的な脳外傷を負った人々の脳を剖検解析し、慢性外傷性脳症(CTE)が非常にまれであることを報告した。研究では、スポーツ選手や軍人など反復的外傷を受けた症例と比較し、単発外傷患者のCTE発症率は1%未満であることが確認された。多くのケースでは、血管周囲のタウ蛋白沈着や神経変性の特徴は認められず、外傷後脳障害とCTEを混同すべきでないと指摘している。これにより、単発の脳震盪や事故が必ずしもCTEを引き起こすわけではないことが明確となり、診断基準の再評価が求められる。研究成果は『JAMA Neurology』誌に掲載され、脳外傷と神経変性疾患の関係を再定義する重要な知見とされる。

<関連情報>

外傷性脳損傷後遺症プロジェクトにおける慢性外傷性脳症の神経病理学的変化:地域剖検コホートにおける知見 Chronic traumatic encephalopathy neuropathologic change in the Late Effects of Traumatic Brain Injury project: Findings in a community autopsy cohort

Enna Selmanovic, BS, Alan C Seifert, PhD, Bradley N Delman, MD, Ariel Pruyser, BS, Emma L Thorn, MA, Amber L Nolan, MD, PhD, C Dirk Keene, MD, PhD, Jamie M Walker, MD, PhD, John F Crary, MD, PhD, Patrick R Hof, MD …
Journal of Neuropathology & Experimental Neurology  Published:18 October 2025
DOI:https://doi.org/10.1093/jnen/nlaf117

Neocortical phosphorylated tau pathology in the CTE-NC cases. (A, B) Case 1 (A) with high CTE-NC and Case 2 (B) with indeterminate staging of CTE-NC, visible as aggregates of neuronal and astroglial tau in a perivascular distribution in neocortex; subcortical neuronal tau deposition was also significant (not shown). (C, D) Case 3 (indeterminate CTE-NC) with abnormal neuronal and astroglial tau aggregates in the temporal lobe adjacent to evidence of subpial aging-related tau astrogliopathy (ARTAG, arrow) (C) and in the locus coeruleus (D). (E-H) Cases 4 (E), 5 (F), 6 (G), and 7 (H) with lesser but distinct perivascular neocortical tau deposition indicative of low CTE-NC. Abbreviation: CTE-NC: chronic traumatic encephalopathy-neuropathologic change. Scale bar = 200 µm.

Abstract

Chronic traumatic encephalopathy-neuropathologic change (CTE-NC) has been studied in contact sport athletes with repetitive head impacts (RHI), but its association with isolated traumatic brain injury (iTBI) and non-sport RHI in the community remains unclear. Forty-seven consecutive donor brains from the Late Effects of TBI Project underwent comprehensive neuropathologic evaluation. Seven (14.9%; median age, seventh decade) had CTE-NC, defined as perivascular neuronal tau at the depth of sulcus. Four had 4 “low” CTE-NC burden, 1 “high,” and 2 “indeterminate.” Ex vivo neuroimaging in 5 facilitated histological sampling of subtle changes otherwise likely to be overlooked. Five of the 7 CTE-NC donors reportedly had substantial RHI exposure: football (n = 3), boxing (n = 1), military and interpersonal violence (n = 1), and child abuse (n = 1). One CTE-NC case had no known RHI exposure but had 2 severe iTBIs sustained 30 and 3 years prior to death. Donors without CTE-NC had variable patterns of head trauma: RHI exposure (college football, n = 4), some RHI (n = 21, 17 of whom also had ≥1 iTBI), and ≥1 iTBI but no RHI (n = 15). These findings converge with prior reports that CTE is largely associated with extensive RHI and is infrequent in a cohort with varying TBI exposures.

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