Neuropsychiatric symptoms and lifelong mental activities in cerebral amyloid angiopathy - a cross-sectional study

被引:0
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作者
Doerner, Marc [1 ,2 ]
Tyndall, Anthony [3 ]
Hainc, Nicolin [3 ]
von Kaenel, Roland [2 ]
Neumann, Katja [4 ]
Euler, Sebastian [2 ]
Schreiber, Frank [1 ,4 ]
Arndt, Philipp [1 ,4 ]
Fuchs, Erelle [5 ]
Garz, Cornelia [1 ,4 ]
Glanz, Wenzel [1 ,6 ]
Butryn, Michaela [1 ,6 ]
Schulze, Jan Ben [2 ]
Schiebler, Sarah Lavinia Florence [2 ]
John, Anna-Charlotte [4 ]
Hildebrand, Annkatrin [4 ]
Hofmann, Andreas B. [7 ]
Machetanz, Lena [8 ]
Kirchebner, Johannes [8 ]
Tacik, Pawel [9 ,10 ]
Grimm, Alexander [11 ,12 ]
Jansen, Robin [13 ]
Pawlitzki, Marc [13 ]
Henneicke, Solveig [1 ,4 ]
Bernal, Jose [1 ,6 ]
Perosa, Valentina [14 ]
Duezel, Emrah [1 ,6 ]
Meuth, Sven G. [13 ]
Vielhaber, Stefan [4 ]
Mattern, Hendrik [1 ,15 ,16 ]
Schreiber, Stefanie [1 ,4 ,15 ]
机构
[1] Helmholtz Assoc, German Ctr Neurodegenerat Dis DZNE, D-39120 Magdeburg, Germany
[2] Univ Zurich, Univ Hosp Zurich, Dept Consultat Liaison Psychiat & Psychosomat Med, Culmannstr 8, CH-8091 Zurich, Switzerland
[3] Univ Zurich, Univ Hosp Zurich, Clin Neurosci Ctr, Dept Neuroradiol, CH-8091 Zurich, Switzerland
[4] Otto von Guericke Univ, Dept Neurol, D-39120 Magdeburg, Germany
[5] Otto von Guericke Univ, Dept Neuroradiol, D-39120 Magdeburg, Germany
[6] Otto von Guericke Univ, Inst Cognit Neurol & Dementia Res, D-39120 Magdeburg, Germany
[7] Univ Zurich, Univ Hosp Psychiat Zurich, Dept Psychiat Psychotherapy & Psychosomat, CH-8032 Zurich, Switzerland
[8] Univ Zurich, Univ Hosp Psychiat Zurich, Dept Forens Psychiat, CH-8032 Zurich, Switzerland
[9] Univ Hosp Bonn, Dept Parkinsons Dis Sleep & Movement Disorders, D-53127 Bonn, Germany
[10] Helmholtz Assoc, German Ctr Neurodegenerat Dis DZNE, D-53127 Bonn, Germany
[11] Eberhard Karls Univ Tubingen, Tuebingen Univ Hosp, Ctr Neurol, D-72076 Tubingen, Germany
[12] Eberhard Karls Univ Tubingen, Hertie Inst Clin Brain Res, D-72076 Tubingen, Germany
[13] Heinrich Heine Univ, Dept Neurol, D-40225 Dusseldorf, Germany
[14] Massachusetts Gen Hosp, J Philip Kistler Stroke Res Ctr, Boston, MA 02114 USA
[15] Ctr Behav Brain Sci CBBS, D-39120 Magdeburg, Germany
[16] Otto von Guericke Univ, Biomed Magnet Resonance, D-39120 Magdeburg, Germany
关键词
Cerebral amyloid angiopathy; Neuropsychiatric symptoms; Depression; Lifelong mental activities; Alzheimer's disease; White matter hyperintensities; Magnetic resonance imaging; SMALL VESSEL DISEASE; RATING-SCALE; FUNCTIONAL IMPAIRMENT; SUPERFICIAL SIDEROSIS; ALZHEIMERS-DISEASE; ASSOCIATION; DEPRESSION; DEMENTIA; DYSFUNCTION; APATHY;
D O I
10.1186/s13195-024-01519-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundWhile several studies in cerebral amyloid angiopathy (CAA) focus on cognitive function, data on neuropsychiatric symptoms (NPS) and lifelong mental activities in these patients are scarce. Since NPS are associated with functional impairment, faster cognitive decline and faster progression to death, replication studies in more diverse settings and samples are warranted.MethodsWe prospectively recruited n = 69 CAA patients and n = 18 cognitively normal controls (NC). The number and severity of NPS were assessed using the Alzheimer's Disease (AD) Assessment Scale's (ADAS) noncognitive subscale. We applied different regression models exploring associations between NPS number or severity and group status (CAA vs. NC), CAA severity assessed with magnetic resonance imaging (MRI) or cognitive function (Mini-Mental State Examination (MMSE), ADAS cognitive subscale), adjusting for age, sex, years of education, arterial hypertension, AD pathology, and apolipoprotein E status. Mediation analyses were performed to test indirect effects of lifelong mental activities on CAA severity and NPS.ResultsPatients with CAA had 4.86 times (95% CI 2.20-10.73) more NPS and 3.56 units (95% CI 1.94-5.19) higher expected NPS severity than NC. Higher total CAA severity on MRI predicted 1.14 times (95% CI 1.01.-1.27) more NPS and 0.57 units (95% CI 0.19-0.95) higher expected NPS severity. More severe white matter hyperintensities were associated with 1.21 times more NPS (95% CI 1.05-1.39) and 0.63 units (95% CI 0.19-1.08) more severe NPS. NPS number (MMSE mean difference - 1.15, 95% CI -1.67 to -0.63; ADAS cognitive mean difference 1.91, 95% CI 1.26-2.56) and severity (MMSE - 0.55, 95% CI -0.80 to -0.30; ADAS cognitive mean difference 0.89, 95% CI 0.57-1.21) predicted lower cognitive function. Greater lifelong mental activities partially mediated the relationship between CAA severity and NPS (indirect effect 0.05, 95% CI 0.0007-0.13), and greater lifelong mental activities led to less pronounced CAA severity and thus to less NPS (indirect effect - 0.08, 95% CI -0.22 to -0.002).DiscussionThis study suggests that NPS are common in CAA, and that this relationship may be driven by CAA severity. Furthermore, NPS seem to be tied to lower cognitive function. However, lifelong mental activities might mitigate the impact of NPS in CAA.
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页数:11
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