Literature DB >> 33608041

Cognitive trajectories of patients with focal ß-amyloid deposition.

Si Eun Kim1,2, Byungju Lee3, Hyemin Jang1,4,5, Juhee Chin1,4,5, Ching Soong Khoo6, Yeong Sim Choe1,4,5,7, Ji Sun Kim1,4,5, Sung Hoon Kang1,4,5,8, Hang-Rai Kim1,4,5, Song Hwangbo1,4,5, Jee Hyang Jeong9, Soo Jin Yoon10, Kyung Won Park11, Eun-Joo Kim12, Bora Yoon13, Jae-Won Jang14, Jin Yong Hong15, Duk L Na1,4,5,7, Sang Won Seo1,4,5,16,17, Seong Hye Choi18, Hee Jin Kim19,20,21,22,23.   

Abstract

BACKGROUND: The presence of ß-amyloid (Aß) in the brain can be identified using amyloid PET. In clinical practice, the amyloid PET is interpreted based on dichotomous visual rating, which renders focal Aß accumulation be read as positive for Aß. However, the prognosis of patients with focal Aß deposition is not well established. Thus, we investigated cognitive trajectories of patients with focal Aß deposition.
METHODS: We followed up 240 participants (112 cognitively unimpaired [CU], 78 amnestic mild cognitive impairment [aMCI], and 50 Alzheimer's disease (AD) dementia [ADD]) for 2 years from 9 referral centers in South Korea. Participants were assessed with neuropsychological tests and 18F-flutemetamol (FMM) positron emission tomography (PET). Ten regions (frontal, precuneus/posterior cingulate (PPC), lateral temporal, parietal, and striatum of each hemisphere) were visually examined in the FMM scan, and participants were divided into three groups: No-FMM, Focal-FMM (FMM uptake in 1-9 regions), and Diffuse-FMM. We used mixed-effects model to investigate the speed of cognitive decline in the Focal-FMM group according to the cognitive level, extent, and location of Aß involvement, in comparison with the No- or Diffuse-FMM group.
RESULTS: Forty-five of 240 (18.8%) individuals were categorized as Focal-FMM. The rate of cognitive decline in the Focal-FMM group was faster than the No-FMM group (especially in the CU and aMCI stage) and slower than the Diffuse-FMM group (in particular in the CU stage). Within the Focal-FMM group, participants with FMM uptake to a larger extent (7-9 regions) showed faster cognitive decline compared to those with uptake to a smaller extent (1-3 or 4-6 regions). The Focal-FMM group was found to have faster cognitive decline in comparison with the No-FMM when there was uptake in the PPC, striatum, and frontal cortex.
CONCLUSIONS: When predicting cognitive decline of patients with focal Aß deposition, the patients' cognitive level, extent, and location of the focal involvement are important.

Entities:  

Keywords:  18F-flutemetamol PET; Alzheimer’s disease; Cognitive decline; Longitudinal studies; ß-Amyloid

Mesh:

Substances:

Year:  2021        PMID: 33608041      PMCID: PMC7896397          DOI: 10.1186/s13195-021-00787-7

Source DB:  PubMed          Journal:  Alzheimers Res Ther            Impact factor:   6.982


  24 in total

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Authors:  Thomas G Beach; Lucia I Sue; Douglas G Walker; Marwan N Sabbagh; Geidy Serrano; Brittany N Dugger; Monica Mariner; Kim Yantos; Jonette Henry-Watson; Glenn Chiarolanza; Jose A Hidalgo; Leslie Souders
Journal:  J Alzheimers Dis       Date:  2012       Impact factor: 4.472

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Journal:  Arch Neurol       Date:  2010-06

3.  Development of the Korean version of the Consortium to Establish a Registry for Alzheimer's Disease Assessment Packet (CERAD-K): clinical and neuropsychological assessment batteries.

Authors:  Jung H Lee; Kang U Lee; Dong Y Lee; Ki W Kim; Jin H Jhoo; Ju H Kim; Kun H Lee; Sung Y Kim; Sul H Han; Jong I Woo
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2002-01       Impact factor: 4.077

4.  Cognition and amyloid load in Alzheimer disease imaged with florbetapir F 18(AV-45) positron emission tomography.

Authors:  Paul B Rosenberg; D F Wong; S L Edell; J S Ross; A D Joshi; J R Brašić; Y Zhou; V Raymont; A Kumar; H T Ravert; R F Dannals; M J Pontecorvo; D M Skovronsky; C G Lyketsos
Journal:  Am J Geriatr Psychiatry       Date:  2013-03       Impact factor: 4.105

5.  Practice effects due to serial cognitive assessment: Implications for preclinical Alzheimer's disease randomized controlled trials.

Authors:  Terry E Goldberg; Philip D Harvey; Keith A Wesnes; Peter J Snyder; Lon S Schneider
Journal:  Alzheimers Dement (Amst)       Date:  2015-03-29

6.  Validation of an electronic image reader training programme for interpretation of [18F]flutemetamol β-amyloid PET brain images.

Authors:  Christopher J Buckley; Paul F Sherwin; Adrian P L Smith; Jan Wolber; Sharon M Weick; David J Brooks
Journal:  Nucl Med Commun       Date:  2017-03       Impact factor: 1.690

7.  Association of Longitudinal Cognitive Decline With Amyloid Burden in Middle-aged and Older Adults: Evidence for a Dose-Response Relationship.

Authors:  Michelle E Farrell; Kristen M Kennedy; Karen M Rodrigue; Gagan Wig; Gérard N Bischof; Jennifer R Rieck; Xi Chen; Sara B Festini; Michael D Devous; Denise C Park
Journal:  JAMA Neurol       Date:  2017-07-01       Impact factor: 18.302

8.  In vivo staging of regional amyloid deposition.

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9.  The Cortical Neuroanatomy Related to Specific Neuropsychological Deficits in Alzheimer's Continuum.

Authors:  Sung Hoon Kang; Yu Hyun Park; Daun Lee; Jun Pyo Kim; Juhee Chin; Yisuh Ahn; Seong Beom Park; Hee Jin Kim; Hyemin Jang; Young Hee Jung; Jaeho Kim; Jongmin Lee; Ji-Sun Kim; Bo Kyoung Cheon; Alice Hahn; Hyejoo Lee; Duk L Na; Young Ju Kim; Sang Won Seo
Journal:  Dement Neurocogn Disord       Date:  2019-10-02

10.  Longitudinal outcomes of amyloid positive versus negative amnestic mild cognitive impairments: a three-year longitudinal study.

Authors:  Byoung Seok Ye; Hee Jin Kim; Yeo Jin Kim; Na-Yeon Jung; Jin San Lee; Juyoun Lee; Young Kyoung Jang; Jin-Ju Yang; Jong-Min Lee; Jacob W Vogel; Duk L Na; Sang Won Seo
Journal:  Sci Rep       Date:  2018-04-03       Impact factor: 4.379

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2.  Influence of Subject-Specific Effects in Longitudinal Modelling of Cognitive Decline in Alzheimer's Disease.

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3.  Predicting conversion of brain β-amyloid positivity in amyloid-negative individuals.

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