Neuropsychiatric symptoms with focus on apathy and irritability in sporadic and hereditary cerebral amyloid angiopathy

被引:2
|
作者
Kaushik, Kanishk [1 ]
de Kort, Anna M. [2 ,3 ]
van Dort, Rosemarie [1 ]
van der Zwet, Reinier G. J. [1 ]
Siegerink, Bob [4 ]
Voigt, Sabine [1 ,5 ]
van Zwet, Erik W. [6 ]
van der Plas, Maaike C. [1 ]
Koemans, Emma A. [1 ]
Rasing, Ingeborg [1 ]
Kessels, Roy P. C. [3 ,7 ,8 ]
Middelkoop, Huub A. M. [1 ,9 ]
Schreuder, Floris H. B. M. [2 ,3 ]
Klijn, Catharina J. M. [2 ,3 ]
Verbeek, Marcel M. [2 ,3 ,10 ]
Terwindt, Gisela M. [1 ]
van Etten, Ellis S. [1 ]
Wermer, Marieke J. H. [1 ,11 ]
机构
[1] Leiden Univ Med Ctr LUMC, Neurol, Albinusdreef 2, NL-2300 RC Leiden, Netherlands
[2] Radboud Univ Med Ctr RUMC, Neurol, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands
[4] LUMC, Clin Epidemiol, Leiden, Netherlands
[5] LUMC, Radiol, Leiden, Netherlands
[6] LUMC, Biomed Data Sci, Leiden, Netherlands
[7] Med Psychol & RUMC Alzheimer Ctr, Nijmegen, Netherlands
[8] Vincent van Gogh Inst Psychiat, Venray, Netherlands
[9] Leiden Univ, Inst Psychol Hlth & Neuropsychol, Leiden, Netherlands
[10] RUMC, Lab Med, Nijmegen, Netherlands
[11] Univ Med Ctr Groningen, Neurol, Groningen, Netherlands
关键词
Cerebral amyloid angiopathy; CAA; Neuropsychiatric symptoms; ICH; Apathy; Irritability; Depression; Executive function; Processing speed; Cognitive decline; SMALL VESSEL DISEASE; MILD COGNITIVE IMPAIRMENT; DIAGNOSTIC-CRITERIA; PREVALENCE; DEMENTIA; SPEED; TRAIL; SET;
D O I
10.1186/s13195-024-01445-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Neuropsychiatric symptoms (NPS) may affect cognition, but their burden in cerebral amyloid angiopathy (CAA), one of the main causes of intracerebral hemorrhage (ICH) and dementia in the elderly, remains unclear. We investigated NPS, with emphasis on apathy and irritability in sporadic (sCAA) and Dutch-type hereditary (D-)CAA.Methods We included patients with sCAA and (pre)symptomatic D-CAA, and controls from four prospective cohort studies. We assessed NPS per group, stratified for history of ICH, using the informant-based Neuropsychiatric Inventory (NPI-Q), Starkstein Apathy scale (SAS), and Irritability Scale. We modeled the association of NPS with disease status, executive function, processing speed, and CAA-burden score on MRI and investigated sex-differences.Results We included 181 participants: 82 with sCAA (mean[SD] age 72[6] years, 44% women, 28% previous ICH), 56 with D-CAA (52[11] years, 54% women, n = 31[55%] presymptomatic), and 43 controls (69[9] years, 44% women). The NPI-Q NPS-count differed between patients and controls (sCAA-ICH+:adj.beta = 1.4[95%CI:0.6-2.3]; sCAA-ICH-:1.3[0.6-2.0]; symptomatic D-CAA:2.0[1.1-2.9]; presymptomatic D-CAA:1.2[0.1-2.2], control median:0[IQR:0-3]), but not between the different CAA-subgroups. Apathy and irritability were reported most frequently: n = 12[31%] sCAA, 19[37%] D-CAA had a high SAS-score; n = 12[29%] sCAA, 14[27%] D-CAA had a high Irritability Scale score. NPS-count was associated with decreased processing speed (adj.beta=-0.6[95%CI:-0.8;-0.4]) and executive function (adj.beta=-0.4[95%CI:-0.6;-0.1]), but not with radiological CAA-burden. Men had NPS more often than women.Discussion According to informants, one third to half of patients with CAA have NPS, mostly apathy, even in presymptomatic D-CAA and possibly with increased susceptibility in men. Neurologists should inform patients and caregivers of these disease consequences and treat or refer patients with NPS appropriately.
引用
收藏
页数:11
相关论文
共 50 条
  • [31] Amyloid-PET in sporadic cerebral amyloid angiopathy A diagnostic accuracy meta-analysis
    Charidimou, Andreas
    Farid, Karim
    Baron, Jean-Claude
    NEUROLOGY, 2017, 89 (14) : 1490 - 1498
  • [32] Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies
    Revesz, Tamas
    Holton, Janice L.
    Lashley, Tammaryn
    Plant, Gordon
    Frangione, Blas
    Rostagno, Agueda
    Ghiso, Jorge
    ACTA NEUROPATHOLOGICA, 2009, 118 (01) : 115 - 130
  • [33] PROGRESSIVE DEMENTIA, WITHOUT CEREBRAL-HEMORRHAGE, IN A PATIENT WITH HEREDITARY CEREBRAL AMYLOID ANGIOPATHY
    HAAN, J
    BAKKER, E
    JENNEKENSSCHINKEL, A
    ROOS, RAC
    CLINICAL NEUROLOGY AND NEUROSURGERY, 1992, 94 (04) : 317 - 318
  • [34] Alzheimer's disease associated with sporadic cerebral amyloid angiopathy in an elderly patient
    Guaquiere-Bernard, Odile
    Rouaud, Olivier
    Manckoundia, Patrick
    GERIATRICS & GERONTOLOGY INTERNATIONAL, 2015, 15 (06) : 811 - 812
  • [35] Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies
    Tamas Revesz
    Janice L. Holton
    Tammaryn Lashley
    Gordon Plant
    Blas Frangione
    Agueda Rostagno
    Jorge Ghiso
    Acta Neuropathologica, 2009, 118 : 115 - 130
  • [36] The hemorrhage caused by sporadic-type cerebral amyloid angiopathy occurs primarily in the cerebral sulci
    Takeda, Shigeki
    Hinokuma, Kaoru
    Yamazaki, Kazunori
    Onda, Kiyoshi
    Miyakawa, Teruo
    Ikuta, Fusahiro
    Arai, Hiroyuki
    NEUROPATHOLOGY, 2012, 32 (01) : 38 - 43
  • [37] Advancing diagnostic criteria for sporadic cerebral amyloid angiopathy: Study protocol for a multicenter MRI-pathology validation of Boston criteria v2.0
    Charidimou, Andreas
    Frosch, Matthew P.
    Salman, Rustam Al-Shahi
    Baron, Jean-Claude
    Cordonnier, Charlotte
    Hernandez-Guillamon, Mar
    Linn, Jennifer
    Raposo, Nicolas
    Rodrigues, Mark
    Romero, Jose Rafael
    Schneider, Julie A.
    Schreiber, Stefanie
    Smith, Eric E.
    van Buchem, Mark A.
    Viswanathan, Anand
    Wollenweber, Frank A.
    Werring, David J.
    Greenberg, Steven M.
    INTERNATIONAL JOURNAL OF STROKE, 2019, 14 (09) : 956 - 971
  • [38] Sensitivity of the Boston criteria version 2.0 in Dutch-type hereditary cerebral amyloid angiopathy
    van der Zwet, Rgj
    Koemans, Ea
    Voigt, S.
    van Dort, R.
    Rasing, I
    Kaushik, K.
    van Harten, Tw
    Schipper, Mr
    Terwindt, Gm
    van Osch, Mjp
    van Walderveen, Maa
    van Etten, Es
    Wermer, Mjh
    INTERNATIONAL JOURNAL OF STROKE, 2024, 19 (08) : 942 - 946
  • [39] Multiple Approaches to Diffusion Magnetic Resonance Imaging in Hereditary Cerebral Amyloid Angiopathy Mutation Carriers
    Schouten, Tijn M.
    de Vos, Frank
    van Rooden, Sanneke
    Bouts, Mark J. R. J.
    van Opstal, Anna M.
    Feis, Rogier A.
    Terwindt, Gisela M.
    Wermer, Marieke J. H.
    van Buchem, Mark A.
    Greenberg, Steven M.
    de Rooij, Mark
    Rombouts, Serge A. R. B.
    van der Grond, Jeroen
    JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2019, 8 (03):
  • [40] Migraine With Aura as Early Disease Marker in Hereditary Dutch-Type Cerebral Amyloid Angiopathy
    Koemans, Emma A.
    Voigt, Sabine
    Rasing, Ingeborg
    van Etten, Ellis S.
    van Zwet, Erik W.
    van Walderveen, Marianne A. A.
    Wermer, Marieke J. H.
    Terwindt, Gisela M.
    STROKE, 2020, 51 (04) : 1094 - 1099