Your browser doesn't support javascript.
loading
Comparison of Diagnostic Performances Between Cerebrospinal Fluid Biomarkers and Amyloid PET in a Clinical Setting.
Jung, Na-Yeon; Kim, Eun Soo; Kim, Hyang-Sook; Jeon, Sumin; Lee, Myung Jun; Pak, Kyoungjune; Lee, Jae-Hyeok; Lee, Young Min; Lee, Kangyoon; Shin, Jin-Hong; Ko, Jun Kyeung; Lee, Jae Meen; Yoon, Jin A; Hwang, Chungsu; Choi, Kyung-Un; Lee, Eun Chong; Seong, Joon-Kyung; Huh, Gi Yeong; Kim, Dae-Seong; Kim, Eun-Joo.
Affiliation
  • Jung NY; Department of Neurology, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Republic of Korea.
  • Kim ES; Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Republic of Korea.
  • Kim HS; Department of Anesthesia and Pain Medicine, Pusan National University Hospital, School of Medicine, Pusan National University, Busan, Republic of Korea.
  • Jeon S; Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Republic of Korea.
  • Lee MJ; Department of Neurology, Pusan National University Hospital, Pusan National University School of Medicine and Medical Research Institute, Busan, Republic of Korea.
  • Pak K; Department of Neurology, Pusan National University Hospital, Pusan National University School of Medicine and Medical Research Institute, Busan, Republic of Korea.
  • Lee JH; Department of Nuclear Medicine, Pusan National University Hospital, Pusan National University School of Medicine, Busan, Republic of Korea.
  • Lee YM; Department of Neurology, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Republic of Korea.
  • Lee K; Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Republic of Korea.
  • Shin JH; Department of Psychiatry, Pusan National University Hospital, Pusan National University School of Medicine, Busan, Republic of Korea.
  • Ko JK; Department of Psychiatry, Pusan National University Hospital, Pusan National University School of Medicine, Busan, Republic of Korea.
  • Lee JM; Department of Neurology, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Republic of Korea.
  • Yoon JA; Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Republic of Korea.
  • Hwang C; Department of Neurosurgery, Medical Research Institute, Pusan National University Hospital, Busan, Republic of Korea.
  • Choi KU; Department of Neurosurgery, Medical Research Institute, Pusan National University Hospital, Busan, Republic of Korea.
  • Lee EC; Department of Rehabilitation Medicine, Pusan National University School of Medicine and Biomedical Research Institute, Pusan National University Hospital, Busan, Republic of Korea.
  • Seong JK; Department of Pathology, Pusan National University School of Medicine, Yangsan, Republic of Korea.
  • Huh GY; Department of Pathology, Pusan National University School of Medicine, Yangsan, Republic of Korea.
  • Kim DS; School of Biomedical Engineering, Korea University, Seoul, Republic of Korea.
  • Kim EJ; School of Biomedical Engineering, Korea University, Seoul, Republic of Korea.
J Alzheimers Dis ; 74(2): 473-490, 2020.
Article in En | MEDLINE | ID: mdl-32039853
ABSTRACT
The diagnostic performances of cerebrospinal fluid (CSF) biomarkers and amyloid positron emission tomography (PET) were compared by examining the association and concordance or discordance between CSF Aß1-42 and amyloid PET, after determining our own cut-off values for CSF Alzheimer's disease (AD) biomarkers. Furthermore, we evaluated the ability of CSF biomarkers and amyloid PET to predict clinical progression. CSF Aß1-42, t-tau, and p-tau levels were analyzed in 203 individuals [27 normal controls, 38 mild cognitive impairment (MCI), 62 AD dementia, and 76 patients with other neurodegenerative diseases] consecutively recruited from two dementia clinics. We used both visual and standardized uptake value ratio (SUVR)-based amyloid PET assessments for analyses. The association of CSF biomarkers with amyloid PET SUVR, hippocampal atrophy, and cognitive function were investigated by linear regression analysis, and the risk of conversion from MCI to AD dementia was assessed using a Cox proportional hazards model. CSF p-tau/Aß1-42 and t-tau/Aß1-42 exhibited the best diagnostic accuracies among the CSF AD biomarkers examined. Correlations were observed between CSF biomarkers and global SUVR, hippocampal volume, and cognitive function. Overall concordance and discordance between CSF Aß1-42 and amyloid PET was 77% and 23%, respectively. Baseline positive CSF Aß1-42 for MCI demonstrated a 5.6-fold greater conversion risk than negative CSF Aß1-42 .  However, amyloid PET findings failed to exhibit significant prognostic value. Therefore, despite presence of a significant correlation between the CSF Aß1-42 level and SUVR of amyloid PET, and a relevant concordance between CSF Aß1-42 and amyloid PET, baseline CSF Aß1-42 better predicted AD conversion.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Fragments / Biomarkers / Amyloid beta-Peptides / Positron-Emission Tomography / Amyloidogenic Proteins / Alzheimer Disease Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: J Alzheimers Dis Journal subject: GERIATRIA / NEUROLOGIA Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Fragments / Biomarkers / Amyloid beta-Peptides / Positron-Emission Tomography / Amyloidogenic Proteins / Alzheimer Disease Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: J Alzheimers Dis Journal subject: GERIATRIA / NEUROLOGIA Year: 2020 Document type: Article