Spectrum of tau pathologies in Huntington's disease

被引:28
作者
Baskota, Swikrity Upadhyay [1 ]
Lopez, Oscar L. [2 ,3 ]
Greenamyre, J. Timothy [2 ,4 ]
Kofler, Julia [1 ]
机构
[1] Univ Pittsburgh, Dept Pathol, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA
[4] Univ Pittsburgh, Pittsburgh Inst Neurodegenerat Dis, Pittsburgh, PA USA
关键词
CHRONIC TRAUMATIC ENCEPHALOPATHY; AMYOTROPHIC-LATERAL-SCLEROSIS; ALZHEIMERS ASSOCIATION GUIDELINES; FRONTOTEMPORAL LOBAR DEGENERATION; NEUROPATHOLOGIC ASSESSMENT; INTRANUCLEAR INCLUSIONS; NATIONAL INSTITUTE; FUS; PROTEIN; FUS/TLS;
D O I
10.1038/s41374-018-0166-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Huntington's disease (HD) is an autosomal dominant disorder caused by a trinucleotide expansion in the huntingtin gene. Recently, a new role for tau has been implicated in the pathogenesis of HD, whereas others have argued that postmortem tau pathology findings are attributable to concurrent Alzheimer's disease pathology. The frequency of other well-defined common age-related tau pathologies in HD has not been examined in detail. In this single center, retrospective analysis, we screened seven cases of Huntington's disease (5 females, 2 males, age at death: 47-73 years) for neuronal and glial tau pathology using phospho-tau immunohistochemistry. All seven cases showed presence of neuronal tau pathology. Five cases met diagnostic criteria for primary age-related tauopathy (PART), with three cases classified as definite PART and two cases as possible PART, all with a Braak stage of I. One case was diagnosed with low level of Alzheimer's disease neuropathologic change. In the youngest case, rare perivascular aggregates of tau-positive neurons, astrocytes and processes were identified at sulcal depths, meeting current neuropathological criteria for stage 1 chronic traumatic encephalopathy (CTE). Although the patient had no history of playing contact sports, he experienced several falls, but no definitive concussions during his disease course. Three of the PART cases and the CTE-like case showed additional evidence of aging-related tau astrogliopathy. None of the cases showed significant tau pathology in the striatum. In conclusion, while we found evidence for tau hyperphosphorylation and aggregation in all seven of our HD cases, the tau pathology was readily classifiable into known diagnostic entities and most likely represents non-specific age- or perhaps trauma-related changes. As the tau pathology was very mild in all cases and not unexpected for a population of this age range, it does not appear that the underlying HD may have promoted or accelerated tau accumulation.
引用
收藏
页码:1068 / 1077
页数:10
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