Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
Stem Cell Res ; 79: 103501, 2024 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-39029293

RESUMO

Apolipoprotein E (APOE)is the gene with greatest genetic risk for Alzheimer's disease (AD). We successfully established a human induced pluripotent stem cell(iPSC) line from a woman mutated by APOE gene. The cell line was isolated from this woman's peripheral blood mononuclear cells using a non-integrated Sendai virus, which retained the original genotype, showed a normal karyotype, highly expressed pluripotent markers and could differentiate into three germ layers.


Assuntos
Apolipoproteínas E , Células-Tronco Pluripotentes Induzidas , Mutação , Humanos , Células-Tronco Pluripotentes Induzidas/metabolismo , Células-Tronco Pluripotentes Induzidas/citologia , Feminino , Apolipoproteínas E/genética , Apolipoproteínas E/metabolismo , Linhagem Celular , Diferenciação Celular , Cariótipo , Leucócitos Mononucleares/metabolismo , Leucócitos Mononucleares/citologia
2.
BMJ Open ; 14(7): e082404, 2024 Jul 13.
Artigo em Inglês | MEDLINE | ID: mdl-39002963

RESUMO

INTRODUCTION: The efficacy of multitarget neuroprotective drug DL-3-n-butylphthalide (NBP) in improving cognitive function has been confirmed in patients with vascular cognitive impairment without dementia. However, its efficacy in patients with symptomatic predementia phase of Alzheimer's disease remains uncertain. This study aims to evaluate the efficacy and safety of NBP in improving cognitive function in patients with mild cognitive impairment (MCI) through a clinical randomised controlled trail. METHODS AND ANALYSIS: This study is a 12-month, randomised, double-blind, placebo-controlled, multicentric trial, involving 270 patients with MCI. Subjects are randomly assigned to receive either NBP soft capsule (200 mg, three times per day) or placebo with an allocation ratio of 1:1. The efficacy and safety of NBP are assessed by comparing the results of neuropsychological, neuroimaging and laboratory tests between the two groups. The primary endpoint is the change in Alzheimer's Disease Assessment Scale-Cognitive Subscale after 12 months. All patients will be monitored for adverse events. ETHICS AND DISSEMINATION: This study involving human participants has been reviewed and approved by Ethics Committee of Xuan Wu Hospital (No.2017058). The participants provide their written informed consent to participate in this study. Results will be published in peer-reviewed medical journals and disseminated to healthcare professionals at local and international conferences. PROTOCOL VERSION: V 3.0, 3 September 2022. TRIAL REGISTRATION NUMBER: ChiCTR1800018362.


Assuntos
Benzofuranos , Disfunção Cognitiva , Fármacos Neuroprotetores , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Benzofuranos/uso terapêutico , Benzofuranos/efeitos adversos , Cognição/efeitos dos fármacos , Disfunção Cognitiva/tratamento farmacológico , Método Duplo-Cego , Estudos Multicêntricos como Assunto , Fármacos Neuroprotetores/uso terapêutico , Fármacos Neuroprotetores/efeitos adversos , Testes Neuropsicológicos , Ensaios Clínicos Controlados Aleatórios como Assunto , Resultado do Tratamento
3.
Stem Cell Res ; 77: 103398, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38552354

RESUMO

Genetic polymorphism of apolipoprotein E (APOE) confers differential susceptibility to Alzheimer's disease (AD), and APOE ɛ4 variants is the most powerful risk factor for this disease. Here, we report the generation of a human induced pluripotent stem cell (iPSC) line carrying the APOE ɛ4/ɛ4 genotype from peripheral blood mononuclear cells (PBMCs) isolated from a male with a family history of AD utilizing non-integrative Sendai virus vector. The iPSC maintains their original genotype, highly express endogenous pluripotency markers, displays a normal karyotype, and retains the ability to differentiate into cells representative of the three germ layers.


Assuntos
Apolipoproteínas E , Células-Tronco Pluripotentes Induzidas , Humanos , Células-Tronco Pluripotentes Induzidas/metabolismo , Células-Tronco Pluripotentes Induzidas/citologia , Masculino , Apolipoproteínas E/genética , Apolipoproteínas E/metabolismo , Mutação , Linhagem Celular , Diferenciação Celular , Leucócitos Mononucleares/metabolismo , Leucócitos Mononucleares/citologia
SELEÇÃO DE REFERÊNCIAS
Detalhe da pesquisa