학술논문

The Longitudinal Early‐onset Alzheimer's Disease Study (LEADS): Framework and methodology
Document Type
article
Source
Alzheimer's & Dementia. 17(12)
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Brain Disorders
Alzheimer's Disease
Clinical Research
Neurosciences
Dementia
Neurodegenerative
Acquired Cognitive Impairment
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
Aging
Biomedical Imaging
4.1 Discovery and preclinical testing of markers and technologies
2.1 Biological and endogenous factors
4.2 Evaluation of markers and technologies
Detection
screening and diagnosis
Aetiology
Neurological
Alzheimer Disease
Aniline Compounds
Autopsy
Biomarkers
Brain
Cognitive Dysfunction
Early Diagnosis
Female
Humans
Longitudinal Studies
Magnetic Resonance Imaging
Male
Middle Aged
National Institute on Aging (U.S.)
Positron-Emission Tomography
Stilbenes
United States
Alzheimer&apos
s disease
early‐
onset
EOAD
LEADS
YOAD
young onset
LEADS Consortium
Alzheimer's disease
early-onset
Geriatrics
Clinical sciences
Biological psychology
Language
Abstract
Patients with early-onset Alzheimer's disease (EOAD) are commonly excluded from large-scale observational and therapeutic studies due to their young age, atypical presentation, or absence of pathogenic mutations. The goals of the Longitudinal EOAD Study (LEADS) are to (1) define the clinical, imaging, and fluid biomarker characteristics of EOAD; (2) develop sensitive cognitive and biomarker measures for future clinical and research use; and (3) establish a trial-ready network. LEADS will follow 400 amyloid beta (Aβ)-positive EOAD, 200 Aβ-negative EOnonAD that meet National Institute on Aging-Alzheimer's Association (NIA-AA) criteria for mild cognitive impairment (MCI) or AD dementia, and 100 age-matched controls. Participants will undergo clinical and cognitive assessments, magnetic resonance imaging (MRI), [18 F]Florbetaben and [18 F]Flortaucipir positron emission tomography (PET), lumbar puncture, and blood draw for DNA, RNA, plasma, serum and peripheral blood mononuclear cells, and post-mortem assessment. To develop more effective AD treatments, scientists need to understand the genetic, biological, and clinical processes involved in EOAD. LEADS will develop a public resource that will enable future planning and implementation of EOAD clinical trials.