2010
DOI: 10.1016/j.jalz.2010.03.006
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Clinical core of the Alzheimer's disease neuroimaging initiative: Progress and plans

Abstract: The Clinical Core of the Alzheimer's Disease Neuroimaging Initiative (ADNI) has provided clinical, operational and data management support to ADNI since its inception. This paper reviews the activities and accomplishments of the core in support of ADNI aims. These include the enrollment and follow-up of over 800 subjects in the three original cohorts: healthy controls, amnestic MCI (now referred to as late MCI, or LMCI) and mild Alzheimer's disease (AD) in the first phase of ADNI (ADNI 1), with baseline longit… Show more

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Cited by 417 publications
(345 citation statements)
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“…At eligibility, participants underwent medical history and record review, a clinical interview (including a functional questionnaire and Clinical Dementia Rating17 with the informant), and neuropsychological assessment. Participants were excluded for a cognitive diagnosis other than normal cognition (NC), early MCI,18 or MCI19; contraindication to magnetic resonance imaging; history of neurological disease (eg, stroke); prevalent heart failure; major psychiatric illness; head injury with loss of consciousness >5 minutes; and systemic or terminal illness affecting follow‐up examination participation. At enrollment, participants completed a comprehensive evaluation, including (but not limited to) fasting blood draw, physical examination, a clinical interview, medication review, neuropsychological assessment, and cardiac magnetic resonance (CMR) imaging.…”
Section: Methodsmentioning
confidence: 99%
“…At eligibility, participants underwent medical history and record review, a clinical interview (including a functional questionnaire and Clinical Dementia Rating17 with the informant), and neuropsychological assessment. Participants were excluded for a cognitive diagnosis other than normal cognition (NC), early MCI,18 or MCI19; contraindication to magnetic resonance imaging; history of neurological disease (eg, stroke); prevalent heart failure; major psychiatric illness; head injury with loss of consciousness >5 minutes; and systemic or terminal illness affecting follow‐up examination participation. At enrollment, participants completed a comprehensive evaluation, including (but not limited to) fasting blood draw, physical examination, a clinical interview, medication review, neuropsychological assessment, and cardiac magnetic resonance (CMR) imaging.…”
Section: Methodsmentioning
confidence: 99%
“…Inclusion required participants be ≥60 years, speak English, have adequate auditory and visual acuity, and have a reliable study partner. As part of a comprehensive screening, participants were excluded for a cognitive diagnosis other than NC, early MCI,13 or MCI,12 magnetic resonance imaging contraindication, history of neurological disease (eg, multiple sclerosis, stroke), heart failure, major psychiatric illness, head injury with loss of consciousness >5 minutes, or a systemic or terminal illness affecting follow‐up participation. At enrollment, participants completed a comprehensive examination, including (but not limited to) fasting blood draw, physical examination, clinical interview, medication review, neuropsychological assessment, echocardiogram, cardiac magnetic resonance, and multimodal brain magnetic resonance imaging.…”
Section: Methodsmentioning
confidence: 99%
“…18 Clinical assessment data were also obtained, including the Mini-Mental State Examination, Clinical Dementia Rating Scale, and the Alzheimer's Disease Assessment Scale-cognitive subscale. 19 The clinical assessments had been completed within 14 days of the MR imaging scans. Diagnostic categorization (AD, MCI, and HC) had been made by ADNI site physicians in accordance with the National Institute of Neurologic and Communicative Disorders and Stroke/Alzheimer Disease and Related Disorders Association (NINCDS/ADRDA) criteria and reviewed by ADNI clinical monitors.…”
Section: Datamentioning
confidence: 99%