Tamao Tsukie
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View article: Association of Plasma Placental Growth Factor with White Matter Hyperintensities in Alzheimer’s Disease
Association of Plasma Placental Growth Factor with White Matter Hyperintensities in Alzheimer’s Disease Open
Autopsy studies have shown that Alzheimer’s disease (AD) often coexists with cerebrovascular injury, affecting cognitive outcomes and the effectiveness of anti-amyloid-beta (Aβ) drugs. No fluid biomarkers of cerebrovascular injury have bee…
View article: Association of plasma placental growth factor with white matter hyperintensities in Alzheimer’s disease
Association of plasma placental growth factor with white matter hyperintensities in Alzheimer’s disease Open
Background The global prevalence of dementia, particularly Alzheimer’s disease (AD), is increasing. With the introduction of anti-β-amyloid (Aβ) antibody drugs, the accurate in vivo diagnosis of AD has become crucial. Autopsy studies have …
View article: Association of rare <i>APOE</i> missense variants with Alzheimer's disease in the Japanese population
Association of rare <i>APOE</i> missense variants with Alzheimer's disease in the Japanese population Open
Background Little is known about the rare missense variants (RMVs) of APOE in East Asians, including the Japanese, and their association with Alzheimer's disease (AD) and lipid metabolism. Objective To identify APOE RMVs in the Japanese po…
View article: Clinical utility of CSF Aβ38 in Japanese research and clinical cohorts
Clinical utility of CSF Aβ38 in Japanese research and clinical cohorts Open
INTRODUCTION Previous studies have reported that cerebrospinal fluid (CSF) amyloid beta (Aβ42/Aβ38) performs comparably to Aβ42/Aβ40 in predicting amyloid positron emission tomography (PET) positivity in White cohorts. However, this findin…
View article: CSF α‐synuclein reflects neurodegeneration in Alzhiemer's disease
CSF α‐synuclein reflects neurodegeneration in Alzhiemer's disease Open
Background The aim of this study is to investigate the clinical significance of cerebrospinal fluid (CSF) α‐synuclein (αSyn), a presynaptic protein, in Alzheimer's disease (AD) continuum. Method We analyzed 177 CSF samples obtained from pa…
View article: Application of blood biomarkers for the future anti‐Aβ antibody therapy in Japan
Application of blood biomarkers for the future anti‐Aβ antibody therapy in Japan Open
Background With the approval of Lecanemab in Japan following the U.S., biomarker‐based diagnosis of AD will be required in daily practice. However, PET or CSF are limited by cost, low availability, and invasiveness. In addition, frequent M…
View article: Clinical Characteristics of Progressive Supranuclear Palsy Subtypes Defined by AT(N) CSF Biomarkers
Clinical Characteristics of Progressive Supranuclear Palsy Subtypes Defined by AT(N) CSF Biomarkers Open
Background Progressive supranuclear palsy (PSP) may show concomitant neuropathological findings such as Alzheimer's disease (AD)‐related pathologies. Recent advances in CSF biomarkers enabled the estimation of neuropathological changes in …
View article: <i>APOE</i> rare missense variants in Japan
<i>APOE</i> rare missense variants in Japan Open
Background APOE is well recognized to be the most influential susceptibility gene for Alzheimer’s disease (AD). For the wild‐type allele, e3 , it is known that the e4 allele is a risk for AD, while the e2 allele is protective. Recently, ge…
View article: Association of rare<i>APOE</i>missense variants with Alzheimer's disease in the Japanese population
Association of rare<i>APOE</i>missense variants with Alzheimer's disease in the Japanese population Open
Background: APOE is a major susceptibility gene for Alzheimer's disease (AD). Recent studies in Europe and the US have identified rare missense variants (RMVs) in APOE which are significantly associated with AD. However, little is known re…
View article: Application of AT(N) classification using two CSF A‐markers and two CSF N‐markers to Alzheimer’s Clinical Syndrome (ACS) and non‐ACS
Application of AT(N) classification using two CSF A‐markers and two CSF N‐markers to Alzheimer’s Clinical Syndrome (ACS) and non‐ACS Open
Background Cerebrospinal fluid (CSF) biomarkers reflect the pathological process underlying Alzheimer’s disease (AD) and improve the accuracy of AD diagnosis. AT(N) classification using these CSF biomarkers has been used within the researc…
View article: AT(N) Classification and Clinical Characterization by CSF Biomarkers in Patients with Corticobasal Syndrome
AT(N) Classification and Clinical Characterization by CSF Biomarkers in Patients with Corticobasal Syndrome Open
Background Corticobasal syndrome (CBS) is clinically characterized by asymmetric cortical and extrapyramidal deficits. CBS is caused by various pathological conditions including primary tauopathy and Alzheimer’s disease (AD). To clarify wh…
View article: The clinical application of optimized AT(N) classification in Alzheimer’s clinical syndrome (ACS) and non-ACS conditions
The clinical application of optimized AT(N) classification in Alzheimer’s clinical syndrome (ACS) and non-ACS conditions Open
We aimed to assess the utility of AT(N) classification in clinical practice. We measured the cerebrospinal fluid levels of amyloid-β (Aβ) 42, Aβ40, phosphorylated tau, total tau, and neurofilament light chain (NfL) in samples from 230 pati…
View article: The Clinical Application of Optimized AT(N) Classification in Alzheimer’s Clinical Syndrome (ACS) and non-ACS Conditions
The Clinical Application of Optimized AT(N) Classification in Alzheimer’s Clinical Syndrome (ACS) and non-ACS Conditions Open
Background Cerebrospinal fluid (CSF) biomarkers reflect the pathological process underlying Alzheimer’s disease (AD) and improve the accuracy of AD diagnosis. AT(N) classification using these CSF biomarkers was applied to define AD continu…
View article: Different AT(N) profiles and clinical progression classified by two different N markers using total tau and neurofilament light chain in cerebrospinal fluid
Different AT(N) profiles and clinical progression classified by two different N markers using total tau and neurofilament light chain in cerebrospinal fluid Open
Background The AT(N) classification was proposed for categorising individuals according to biomarkers. However, AT(N) profiles may vary depending on the markers chosen and the target population. Methods We stratified 177 individuals who pa…
View article: Clinical correlations of cerebrospinal fluid biomarkers including neuron-glia 2 and neurofilament light chain in patients with multiple system atrophy
Clinical correlations of cerebrospinal fluid biomarkers including neuron-glia 2 and neurofilament light chain in patients with multiple system atrophy Open
Our results suggest CSF levels of NG2 and NfL as possible diagnostic and prognostic biomarkers in MSA. Further study is necessary to validate these findings.
View article: Effects of an essential amino acid mixture on behavioral and psychological symptoms of dementia and executive function in patients with Alzheimer's disease: A double‐blind, randomized, placebo‐controlled exploratory clinical trial
Effects of an essential amino acid mixture on behavioral and psychological symptoms of dementia and executive function in patients with Alzheimer's disease: A double‐blind, randomized, placebo‐controlled exploratory clinical trial Open
Background The increasing number of dementia patients has become a global social problem. Amino acids are known to be used as precursors of neurotransmitters in the brain. Amino acid mixtures as a supplement may be used as a solution to Al…
View article: Correlated levels of cerebrospinal fluid pathogenic proteins in drug‐naïve Parkinson's disease
Correlated levels of cerebrospinal fluid pathogenic proteins in drug‐naïve Parkinson's disease Open
Background Toxic oligomeric α‐synuclein (αS; O‐αS) has been suggested to play a central role in the pathogenesis of Lewy body diseases such as Parkinson's disease (PD). Cerebrospinal fluid (CSF) levels of αS, O‐αS, total and phosphorylated…
View article: P1‐233: CSF BIOMARKERS OF ALZHEIMER'S CLINICAL SYNDROME
P1‐233: CSF BIOMARKERS OF ALZHEIMER'S CLINICAL SYNDROME Open
It has been shown that cerebrospinal fluid (CSF) β-amyloid1-42 (Aβ1-42) levels show an inverse correlation with brain amyloid plaques, whereas total tau (t-tau) and phosphorylated tau (p-tau) levels correlate with the number of neurofibril…
View article: Correlated levels of cerebrospinal fluid pathogenic proteins in drug-naïve Parkinson’s disease
Correlated levels of cerebrospinal fluid pathogenic proteins in drug-naïve Parkinson’s disease Open
CSF levels of αS are correlated with some clinical symptoms and CSF levels of other pathogenic proteins in drug-naïve PD patients. These correlations suggest a central role for interaction and aggregation of αS with Aβ1-42, tau, and phosph…
View article: Additional file 1: of Correlated levels of cerebrospinal fluid pathogenic proteins in drug-naïve Parkinson’s disease
Additional file 1: of Correlated levels of cerebrospinal fluid pathogenic proteins in drug-naïve Parkinson’s disease Open
All data used during this study. (XLSX 13 kb)
View article: Longitudinal clinical and neuro-radiological findings in a patient with leukoencephalopathy with brain calcifications and cysts (Labrune syndrome)
Longitudinal clinical and neuro-radiological findings in a patient with leukoencephalopathy with brain calcifications and cysts (Labrune syndrome) Open
View article: P2‐172: Transcriptome Profile of Peripheral Blood from Patients with Alzheimer's Disease by Rna‐Seq Analysis
P2‐172: Transcriptome Profile of Peripheral Blood from Patients with Alzheimer's Disease by Rna‐Seq Analysis Open
There is growing demand for blood-based biomarkers for neurodegenerative dementias including Alzheimer’s disease (AD), because blood sampling is less invasive and easily available. Enrollment of qualified participants into clinical trials …
View article: Systematic review and meta-analysis of Japanese familial Alzheimer’s disease and FTDP-17
Systematic review and meta-analysis of Japanese familial Alzheimer’s disease and FTDP-17 Open
Mutations in APP, PSEN1 and PSEN2 as the genetic causes of familial Alzheimer's disease (FAD) have been found in various ethnic populations. A substantial number of FAD pedigrees with mutations have been reported in the Japanese population…