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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00006071naa a2201009 4500
001oai:gup.ub.gu.se/253869
003SwePub
008240528s2017 | |||||||||||000 ||eng|
024a https://gup.ub.gu.se/publication/2538692 URI
024a https://doi.org/10.1186/s12883-017-0846-x2 DOI
040 a (SwePub)gu
041 a eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Lane, C. A.4 aut
2451 0a Study protocol: Insight 46-a neuroscience sub-study of the MRC National Survey of Health and Development
264 c 2017-04-18
264 1b Springer Science and Business Media LLC,c 2017
520 a Background: Increasing age is the biggest risk factor for dementia, of which Alzheimer's disease is the commonest cause. The pathological changes underpinning Alzheimer's disease are thought to develop at least a decade prior to the onset of symptoms. Molecular positron emission tomography and multi-modal magnetic resonance imaging allow key pathological processes underpinning cognitive impairment -including a-amyloid depostion, vascular disease, network breakdown and atrophy -to be assessed repeatedly and non-invasively. This enables potential determinants of dementia to be delineated earlier, and therefore opens a pre-symptomatic window where intervention may prevent the onset of cognitive symptoms. Methods/design: This paper outlines the clinical, cognitive and imaging protocol of "Insight 46", a neuroscience sub-study of the MRC National Survey of Health and Development. This is one of the oldest British birth cohort studies and has followed 5362 individuals since their birth in England, Scotland and Wales during one week in March 1946. These individuals have been tracked in 24 waves of data collection incorporating a wide range of health and functional measures, including repeat measures of cognitive function. Now aged 71 years, a small fraction have overt dementia, but estimates suggest that similar to 1/3 of individuals in this age group may be in the preclinical stages of Alzheimer's disease. Insight 46 is recruiting 500 study members selected at random from those who attended a clinical visit at 60-64 years and on whom relevant lifecourse data are available. We describe the sub-study design and protocol which involves a prospective two time-point (0, 24 month) data collection covering clinical, neuropsychological, beta-amyloid positron emission tomography and magnetic resonance imaging, biomarker and genetic information. Data collection started in 2015 (age 69) and aims to be completed in 2019 (age 73). Discussion: Through the integration of data on the socioeconomic environment and on physical, psychological and cognitive function from 0 to 69 years, coupled with genetics, structural and molecular imaging, and intensive cognitive and neurological phenotyping, Insight 46 aims to identify lifetime factors which influence brain health and cognitive ageing, with particular focus on Alzheimer's disease and cerebrovascular disease. This will provide an evidence base for the rational design of disease-modifying trials.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Neurovetenskaper0 (SwePub)301052 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Neurosciences0 (SwePub)301052 hsv//eng
653 a Epidemiology
653 a Life course
653 a Genetics
653 a Alzheimer's Disease
653 a Ageing
653 a Magnetic resonance imaging
653 a short-term-memory
653 a entirely irrelevant distractors
653 a subjective cognitive
653 a decline
653 a familial alzheimers-disease
653 a british birth cohort
653 a rating-scale
653 a educational-attainment
653 a informant interview
653 a parkinsons-disease
653 a multiple-sclerosis
653 a Neurosciences & Neurology
700a Parker, T. D.4 aut
700a Cash, D. M.4 aut
700a Macpherson, K.4 aut
700a Donnachie, E.4 aut
700a Murray-Smith, H.4 aut
700a Barnes, A.4 aut
700a Barker, S.4 aut
700a Beasley, D. G.4 aut
700a Bras, J.4 aut
700a Brown, D.4 aut
700a Burgos, N.4 aut
700a Byford, M.4 aut
700a Cardoso, M. J.4 aut
700a Carvalho, A.4 aut
700a Collins, J.4 aut
700a De Vita, E.4 aut
700a Dickson, J. C.4 aut
700a Epie, N.4 aut
700a Espak, M.4 aut
700a Henley, S. M. D.4 aut
700a Hoskote, C.4 aut
700a Hutel, M.4 aut
700a Klimova, J.4 aut
700a Malone, I. B.4 aut
700a Markiewicz, P.4 aut
700a Melbourne, A.4 aut
700a Modat, M.4 aut
700a Schrag, A.4 aut
700a Shah, S.4 aut
700a Sharma, N.4 aut
700a Sudre, C. H.4 aut
700a Thomas, D. L.4 aut
700a Wong, A.4 aut
700a Zhang, H.4 aut
700a Hardy, J.4 aut
700a Zetterberg, Henrik,d 1973u Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry4 aut0 (Swepub:gu)xzethe
700a Ourselin, S.4 aut
700a Crutch, S. J.4 aut
700a Kuh, D.4 aut
700a Richards, M.4 aut
700a Fox, N. C.4 aut
700a Schott, J. M.4 aut
710a Göteborgs universitetb Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi4 org
773t Bmc Neurologyd : Springer Science and Business Media LLCg 17q 17x 1471-2377
856u https://bmcneurol.biomedcentral.com/track/pdf/10.1186/s12883-017-0846-x
8564 8u https://gup.ub.gu.se/publication/253869
8564 8u https://doi.org/10.1186/s12883-017-0846-x

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