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Clinical and Biomarker Characteristics According to Clinical Spectrum of Alzheimer's Disease (AD) in the Validation Cohort of Korean Brain Aging Study for the Early Diagnosis and Prediction of AD.
Hwang, Jihye; Jeong, Jee Hyang; Yoon, Soo Jin; Park, Kyung Won; Kim, Eun-Joo; Yoon, Bora; Jang, Jae-Won; Kim, Hee Jin; Hong, Jin Yong; Lee, Jong-Min; Park, Hyuntae; Kang, Ju-Hee; Choi, Yong-Ho; Park, Gilsoon; Hong, Jinwoo; Byun, Min Soo; Yi, Dahyun; Kim, Yu Kyeong; Lee, Dong Young; Choi, Seong Hye.
Afiliação
  • Hwang J; Department of Neurology, Keimyung University Dongsan Medical Center, Daegu 41931, Korea. jh.hwang0110@gmail.com.
  • Jeong JH; Department of Neurology, Ewha Womans University School of Medicine, Seoul 07985, Korea. jjeong@ewha.ac.kr.
  • Yoon SJ; Department of Neurology, Eulji University School of Medicine, Daejeon 35233, Korea. trumind@eulji.ac.kr.
  • Park KW; Department of Neurology, Dong-A Medical Center, Dong-A University College of Medicine, Busan 49201, Korea. neuropark@dau.ac.kr.
  • Kim EJ; Department of Neurology, Pusan National University Hospital, Pusan National University School of Medicine and Medical Research Institute, Busan 49241, Korea. eunjookim@pusan.ac.kr.
  • Yoon B; Department of Neurology, Konyang University College of Medicine, Daejeon 35365, Korea. boradori3@naver.com.
  • Jang JW; Department of Neurology, Kangwon National University Hospital, Kangwon National University College of Medicine, Chuncheon 24289, Korea. light26@hanmail.net.
  • Kim HJ; Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea. evekhj.kim@samsung.com.
  • Hong JY; Department of Neurology, Yonsei University Wonju College of Medicine, Wonju 26426, Korea. jinyhong@yonsei.ac.kr.
  • Lee JM; Department of Biomedical Engineering, Hanyang University, Seoul 04763, Korea. ljm@hanyang.ac.kr.
  • Park H; Department of Health Care and Science, Dong-A University, Busan 49315, Korea. htpark@dau.ac.kr.
  • Kang JH; Department of Pharmacology, Inha University School of Medicine, Incheon 22212, Korea. johykang@inha.ac.kr.
  • Choi YH; Department of Biomedical Engineering, Hanyang University, Seoul 04763, Korea. chldydgh0128@hanyang.ac.kr.
  • Park G; Department of Biomedical Engineering, Hanyang University, Seoul 04763, Korea. pks1207@hanyang.ac.kr.
  • Hong J; Department of Biomedical Engineering, Hanyang University, Seoul 04763, Korea. jwhong1125@gmail.com.
  • Byun MS; Institute of Human Behavioral Medicine, Medical Research Center Seoul National University, Seoul 03080, Korea. bminsoo@gmail.com.
  • Yi D; Institute of Human Behavioral Medicine, Medical Research Center Seoul National University, Seoul 03080, Korea. dahyunyi@gmail.com.
  • Kim YK; Department of Nuclear Medicine, SMG-SNU Boramae Medical Center, Seoul 07061, Korea. yk3181@snu.ac.k.
  • Lee DY; Department of Neuropsychiatry, Seoul National University Hospital & Department of Seoul National University College of Medicine, Seoul 03080, Korea. selfpsy@snu.ac.kr.
  • Choi SH; Department of Neurology, Inha University School of Medicine, Incheon 22332, Korea. seonghye@inha.ac.kr.
J Clin Med ; 8(3)2019 Mar 11.
Article em En | MEDLINE | ID: mdl-30862124
ABSTRACT
We aimed to present the study design of an independent validation cohort from the Korean Brain Aging Study for the Early Diagnosis and Prediction of Alzheimer's disease (AD) (KBASE-V) and to investigate the baseline characteristics of the participants according to the AD clinical spectrum. We recruited 71 cognitively normal (CN) participants, 96 with subjective cognitive decline (SCD), 72 with mild cognitive impairment (MCI), and 56 with AD dementia (ADD). The participants are followed for three years. The Consortium to Establish a Registry for AD scores was significantly different between all of the groups. The logical memory delayed recall scores were significantly different between all groups, except between the MCI and ADD groups. The Mini-Mental State Examination score, hippocampal volume, and cerebrospinal fluid (CSF) amyloid-ß42 level were significant difference among the SCD, MCI, and ADD groups. The frequencies of participants with amyloid pathology according to PET or CSF studies were 8.9%, 25.6%, 48.3%, and 90.0% in the CN, SCD, MCI, and ADD groups, respectively. According to ATN classification, A+/T+/N+ or A+/T+/N- was observed in 0%, 15.5%, 31.0%, and 78.3% in the CN, SCD, MCI, and ADD groups, respectively. The KBASE-V showed a clear difference according to the AD clinical spectrum in neuropsychological tests and AD biomarkers.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article