MRI and pathology of REM sleep behavior disorder in dementia with Lewy bodies

被引:55
|
作者
Murray, Melissa E. [1 ]
Ferman, Tanis J.
Boeve, Bradley F.
Przybelski, Scott A.
Lesnick, Timothy G.
Liesinger, Amanda M. [1 ]
Senjem, Matthew L.
Gunter, Jeffrey L.
Preboske, Gregory M.
Lowe, Val J.
Vemuri, Prashanthi
Dugger, Brittany N. [1 ]
Knopman, David S.
Smith, Glenn E.
Parisi, Joseph E.
Silber, Michael H.
Graff-Radford, Neill R.
Petersen, Ronald C.
Jack, Clifford R., Jr.
Dickson, Dennis W. [1 ]
Kantarci, Kejal
机构
[1] Mayo Clin, Dept Neurosci, Jacksonville, FL 32224 USA
关键词
ALZHEIMERS-DISEASE; FOCAL ATROPHY; CLASSIFICATION; DIAGNOSIS; SUBTYPES; AUTOPSY; DLB;
D O I
10.1212/01.wnl.0000435299.57153.f0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To determine structural MRI and digital microscopic characteristics of REM sleep behavior disorder in individuals with low-, intermediate-, and high-likelihood dementia with Lewy bodies (DLB) at autopsy. Methods: Patients with autopsy-confirmed low-, intermediate-, and high-likelihood DLB, according to the probability statement recommended by the third report of the DLB Consortium, and antemortem MRI, were identified (n = 75). The clinical history was assessed for presence (n = 35) and absence (n = 40) of probable REM sleep behavior disorder (pRBD), and patients' antemortem MRIs were compared using voxel-based morphometry. Pathologic burdens of phospho-tau, beta-amyloid, and a-synuclein were measured in regions associated with early neuropathologic involvement, the hippocampus and amygdala. Results: pRBD was present in 21 patients (60%) with high-likelihood, 12 patients (34%) with intermediate-likelihood, and 2 patients (6%) with low-likelihood DLB. Patients with pRBD were younger, more likely to be male (p <= 0.001), and had a more frequent neuropathologic diagnosis of diffuse (neocortical) Lewy body disease. In the hippocampus and amygdala, phospho-tau and b-amyloid burden were lower in patients with pRBD compared with those without pRBD (p < 0.01). a-Synuclein burden did not differ in the hippocampus, but trended in the amygdala. Patients without pRBD had greater atrophy of temporoparietal cortices, hippocampus, and amygdala (p < 0.001) than those with pRBD; atrophy of the hippocampus (p = 0.005) and amygdala (p = 0.02) were associated with greater phospho-tau burdens in these regions. Conclusion: Presence of pRBD is associated with a higher likelihood of DLB and less severe Alzheimer-related pathology in the medial temporal lobes, whereas absence of pRBD is characterized by Alzheimer-like atrophy patterns on MRI and increased phospho-tau burden.
引用
收藏
页码:1681 / 1689
页数:9
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