A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: Genes, Brain and Behaviour (PISA)
This prospective cohort study, “Prospective Imaging Study of Ageing: Genes, Brain and Behaviour” (PISA) seeks to characterise the phenotype and natural history of healthy adult Australians at high future risk of Alzheimer’s disease (AD). In particular, we are recruiting midlife and older Australians...
Ausführliche Beschreibung
Autor*in: |
Michelle K. Lupton [verfasserIn] Gail A. Robinson [verfasserIn] Robert J. Adam [verfasserIn] Stephen Rose [verfasserIn] Gerard J. Byrne [verfasserIn] Olivier Salvado [verfasserIn] Nancy A. Pachana [verfasserIn] Osvaldo P. Almeida [verfasserIn] Kerrie McAloney [verfasserIn] Scott D Gordon [verfasserIn] Parnesh Raniga [verfasserIn] Amir Fazlollahi [verfasserIn] Ying Xia [verfasserIn] Amelia Ceslis [verfasserIn] Saurabh Sonkusare [verfasserIn] Qing Zhang [verfasserIn] Mahnoosh Kholghi [verfasserIn] Mohan Karunanithi [verfasserIn] Philip E Mosley [verfasserIn] Jinglei Lv [verfasserIn] Léonie Borne [verfasserIn] Jessica Adsett [verfasserIn] Natalie Garden [verfasserIn] Jurgen Fripp [verfasserIn] Nicholas G. Martin [verfasserIn] Christine C Guo [verfasserIn] Michael Breakspear [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Schlagwörter: |
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Übergeordnetes Werk: |
In: NeuroImage: Clinical - Elsevier, 2015, 29(2021), Seite 102527- |
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Übergeordnetes Werk: |
volume:29 ; year:2021 ; pages:102527- |
Links: |
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DOI / URN: |
10.1016/j.nicl.2020.102527 |
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Katalog-ID: |
DOAJ01684145X |
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520 | |a This prospective cohort study, “Prospective Imaging Study of Ageing: Genes, Brain and Behaviour” (PISA) seeks to characterise the phenotype and natural history of healthy adult Australians at high future risk of Alzheimer’s disease (AD). In particular, we are recruiting midlife and older Australians with high and low genetic risk of dementia to discover biological markers of early neuropathology, identify modifiable risk factors, and establish the very earliest phenotypic and neuronal signs of disease onset. PISA utilises genetic prediction to recruit and enrich a prospective cohort and follow them longitudinally. Online surveys and cognitive testing are used to characterise an Australia-wide sample currently totalling over 3800 participants. Participants from a defined at-risk cohort and positive controls (clinical cohort of patients with mild cognitive impairment or early AD) are invited for onsite visits for detailed functional, structural and molecular neuroimaging, lifestyle monitoring, detailed neurocognitive testing, plus blood sample donation. This paper describes recruitment of the PISA cohort, study methodology and baseline demographics. | ||
650 | 4 | |a Alzheimer’s disease | |
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653 | 0 | |a Computer applications to medicine. Medical informatics | |
653 | 0 | |a Neurology. Diseases of the nervous system | |
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700 | 0 | |a Stephen Rose |e verfasserin |4 aut | |
700 | 0 | |a Gerard J. Byrne |e verfasserin |4 aut | |
700 | 0 | |a Olivier Salvado |e verfasserin |4 aut | |
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700 | 0 | |a Christine C Guo |e verfasserin |4 aut | |
700 | 0 | |a Michael Breakspear |e verfasserin |4 aut | |
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10.1016/j.nicl.2020.102527 doi (DE-627)DOAJ01684145X (DE-599)DOAJ9f0815600a5b47a385ac99cd0a68dfe4 DE-627 ger DE-627 rakwb eng R858-859.7 RC346-429 Michelle K. Lupton verfasserin aut A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: Genes, Brain and Behaviour (PISA) 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier This prospective cohort study, “Prospective Imaging Study of Ageing: Genes, Brain and Behaviour” (PISA) seeks to characterise the phenotype and natural history of healthy adult Australians at high future risk of Alzheimer’s disease (AD). In particular, we are recruiting midlife and older Australians with high and low genetic risk of dementia to discover biological markers of early neuropathology, identify modifiable risk factors, and establish the very earliest phenotypic and neuronal signs of disease onset. PISA utilises genetic prediction to recruit and enrich a prospective cohort and follow them longitudinally. Online surveys and cognitive testing are used to characterise an Australia-wide sample currently totalling over 3800 participants. Participants from a defined at-risk cohort and positive controls (clinical cohort of patients with mild cognitive impairment or early AD) are invited for onsite visits for detailed functional, structural and molecular neuroimaging, lifestyle monitoring, detailed neurocognitive testing, plus blood sample donation. This paper describes recruitment of the PISA cohort, study methodology and baseline demographics. Alzheimer’s disease Neuroimaging Neuropsychology Genetic risk prediction Protocol At risk cohort Computer applications to medicine. Medical informatics Neurology. Diseases of the nervous system Gail A. Robinson verfasserin aut Robert J. Adam verfasserin aut Stephen Rose verfasserin aut Gerard J. Byrne verfasserin aut Olivier Salvado verfasserin aut Nancy A. Pachana verfasserin aut Osvaldo P. Almeida verfasserin aut Kerrie McAloney verfasserin aut Scott D Gordon verfasserin aut Parnesh Raniga verfasserin aut Amir Fazlollahi verfasserin aut Ying Xia verfasserin aut Amelia Ceslis verfasserin aut Saurabh Sonkusare verfasserin aut Qing Zhang verfasserin aut Mahnoosh Kholghi verfasserin aut Mohan Karunanithi verfasserin aut Philip E Mosley verfasserin aut Jinglei Lv verfasserin aut Léonie Borne verfasserin aut Jessica Adsett verfasserin aut Natalie Garden verfasserin aut Jurgen Fripp verfasserin aut Nicholas G. Martin verfasserin aut Christine C Guo verfasserin aut Michael Breakspear verfasserin aut In NeuroImage: Clinical Elsevier, 2015 29(2021), Seite 102527- (DE-627)735358869 (DE-600)2701571-3 22131582 nnns volume:29 year:2021 pages:102527- https://doi.org/10.1016/j.nicl.2020.102527 kostenfrei https://doaj.org/article/9f0815600a5b47a385ac99cd0a68dfe4 kostenfrei http://www.sciencedirect.com/science/article/pii/S2213158220303648 kostenfrei https://doaj.org/toc/2213-1582 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 29 2021 102527- |
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10.1016/j.nicl.2020.102527 doi (DE-627)DOAJ01684145X (DE-599)DOAJ9f0815600a5b47a385ac99cd0a68dfe4 DE-627 ger DE-627 rakwb eng R858-859.7 RC346-429 Michelle K. Lupton verfasserin aut A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: Genes, Brain and Behaviour (PISA) 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier This prospective cohort study, “Prospective Imaging Study of Ageing: Genes, Brain and Behaviour” (PISA) seeks to characterise the phenotype and natural history of healthy adult Australians at high future risk of Alzheimer’s disease (AD). In particular, we are recruiting midlife and older Australians with high and low genetic risk of dementia to discover biological markers of early neuropathology, identify modifiable risk factors, and establish the very earliest phenotypic and neuronal signs of disease onset. PISA utilises genetic prediction to recruit and enrich a prospective cohort and follow them longitudinally. Online surveys and cognitive testing are used to characterise an Australia-wide sample currently totalling over 3800 participants. Participants from a defined at-risk cohort and positive controls (clinical cohort of patients with mild cognitive impairment or early AD) are invited for onsite visits for detailed functional, structural and molecular neuroimaging, lifestyle monitoring, detailed neurocognitive testing, plus blood sample donation. This paper describes recruitment of the PISA cohort, study methodology and baseline demographics. Alzheimer’s disease Neuroimaging Neuropsychology Genetic risk prediction Protocol At risk cohort Computer applications to medicine. Medical informatics Neurology. Diseases of the nervous system Gail A. Robinson verfasserin aut Robert J. Adam verfasserin aut Stephen Rose verfasserin aut Gerard J. Byrne verfasserin aut Olivier Salvado verfasserin aut Nancy A. Pachana verfasserin aut Osvaldo P. Almeida verfasserin aut Kerrie McAloney verfasserin aut Scott D Gordon verfasserin aut Parnesh Raniga verfasserin aut Amir Fazlollahi verfasserin aut Ying Xia verfasserin aut Amelia Ceslis verfasserin aut Saurabh Sonkusare verfasserin aut Qing Zhang verfasserin aut Mahnoosh Kholghi verfasserin aut Mohan Karunanithi verfasserin aut Philip E Mosley verfasserin aut Jinglei Lv verfasserin aut Léonie Borne verfasserin aut Jessica Adsett verfasserin aut Natalie Garden verfasserin aut Jurgen Fripp verfasserin aut Nicholas G. Martin verfasserin aut Christine C Guo verfasserin aut Michael Breakspear verfasserin aut In NeuroImage: Clinical Elsevier, 2015 29(2021), Seite 102527- (DE-627)735358869 (DE-600)2701571-3 22131582 nnns volume:29 year:2021 pages:102527- https://doi.org/10.1016/j.nicl.2020.102527 kostenfrei https://doaj.org/article/9f0815600a5b47a385ac99cd0a68dfe4 kostenfrei http://www.sciencedirect.com/science/article/pii/S2213158220303648 kostenfrei https://doaj.org/toc/2213-1582 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 29 2021 102527- |
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Michelle K. Lupton misc R858-859.7 misc RC346-429 misc Alzheimer’s disease misc Neuroimaging misc Neuropsychology misc Genetic risk prediction misc Protocol misc At risk cohort misc Computer applications to medicine. Medical informatics misc Neurology. Diseases of the nervous system A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: Genes, Brain and Behaviour (PISA) |
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R858-859.7 RC346-429 A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: Genes, Brain and Behaviour (PISA) Alzheimer’s disease Neuroimaging Neuropsychology Genetic risk prediction Protocol At risk cohort |
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Michelle K. Lupton Gail A. Robinson Robert J. Adam Stephen Rose Gerard J. Byrne Olivier Salvado Nancy A. Pachana Osvaldo P. Almeida Kerrie McAloney Scott D Gordon Parnesh Raniga Amir Fazlollahi Ying Xia Amelia Ceslis Saurabh Sonkusare Qing Zhang Mahnoosh Kholghi Mohan Karunanithi Philip E Mosley Jinglei Lv Léonie Borne Jessica Adsett Natalie Garden Jurgen Fripp Nicholas G. Martin Christine C Guo Michael Breakspear |
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prospective cohort study of prodromal alzheimer’s disease: prospective imaging study of ageing: genes, brain and behaviour (pisa) |
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A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: Genes, Brain and Behaviour (PISA) |
abstract |
This prospective cohort study, “Prospective Imaging Study of Ageing: Genes, Brain and Behaviour” (PISA) seeks to characterise the phenotype and natural history of healthy adult Australians at high future risk of Alzheimer’s disease (AD). In particular, we are recruiting midlife and older Australians with high and low genetic risk of dementia to discover biological markers of early neuropathology, identify modifiable risk factors, and establish the very earliest phenotypic and neuronal signs of disease onset. PISA utilises genetic prediction to recruit and enrich a prospective cohort and follow them longitudinally. Online surveys and cognitive testing are used to characterise an Australia-wide sample currently totalling over 3800 participants. Participants from a defined at-risk cohort and positive controls (clinical cohort of patients with mild cognitive impairment or early AD) are invited for onsite visits for detailed functional, structural and molecular neuroimaging, lifestyle monitoring, detailed neurocognitive testing, plus blood sample donation. This paper describes recruitment of the PISA cohort, study methodology and baseline demographics. |
abstractGer |
This prospective cohort study, “Prospective Imaging Study of Ageing: Genes, Brain and Behaviour” (PISA) seeks to characterise the phenotype and natural history of healthy adult Australians at high future risk of Alzheimer’s disease (AD). In particular, we are recruiting midlife and older Australians with high and low genetic risk of dementia to discover biological markers of early neuropathology, identify modifiable risk factors, and establish the very earliest phenotypic and neuronal signs of disease onset. PISA utilises genetic prediction to recruit and enrich a prospective cohort and follow them longitudinally. Online surveys and cognitive testing are used to characterise an Australia-wide sample currently totalling over 3800 participants. Participants from a defined at-risk cohort and positive controls (clinical cohort of patients with mild cognitive impairment or early AD) are invited for onsite visits for detailed functional, structural and molecular neuroimaging, lifestyle monitoring, detailed neurocognitive testing, plus blood sample donation. This paper describes recruitment of the PISA cohort, study methodology and baseline demographics. |
abstract_unstemmed |
This prospective cohort study, “Prospective Imaging Study of Ageing: Genes, Brain and Behaviour” (PISA) seeks to characterise the phenotype and natural history of healthy adult Australians at high future risk of Alzheimer’s disease (AD). In particular, we are recruiting midlife and older Australians with high and low genetic risk of dementia to discover biological markers of early neuropathology, identify modifiable risk factors, and establish the very earliest phenotypic and neuronal signs of disease onset. PISA utilises genetic prediction to recruit and enrich a prospective cohort and follow them longitudinally. Online surveys and cognitive testing are used to characterise an Australia-wide sample currently totalling over 3800 participants. Participants from a defined at-risk cohort and positive controls (clinical cohort of patients with mild cognitive impairment or early AD) are invited for onsite visits for detailed functional, structural and molecular neuroimaging, lifestyle monitoring, detailed neurocognitive testing, plus blood sample donation. This paper describes recruitment of the PISA cohort, study methodology and baseline demographics. |
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title_short |
A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: Genes, Brain and Behaviour (PISA) |
url |
https://doi.org/10.1016/j.nicl.2020.102527 https://doaj.org/article/9f0815600a5b47a385ac99cd0a68dfe4 http://www.sciencedirect.com/science/article/pii/S2213158220303648 https://doaj.org/toc/2213-1582 |
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Gail A. Robinson Robert J. Adam Stephen Rose Gerard J. Byrne Olivier Salvado Nancy A. Pachana Osvaldo P. Almeida Kerrie McAloney Scott D Gordon Parnesh Raniga Amir Fazlollahi Ying Xia Amelia Ceslis Saurabh Sonkusare Qing Zhang Mahnoosh Kholghi Mohan Karunanithi Philip E Mosley Jinglei Lv Léonie Borne Jessica Adsett Natalie Garden Jurgen Fripp Nicholas G. Martin Christine C Guo Michael Breakspear |
author2Str |
Gail A. Robinson Robert J. Adam Stephen Rose Gerard J. Byrne Olivier Salvado Nancy A. Pachana Osvaldo P. Almeida Kerrie McAloney Scott D Gordon Parnesh Raniga Amir Fazlollahi Ying Xia Amelia Ceslis Saurabh Sonkusare Qing Zhang Mahnoosh Kholghi Mohan Karunanithi Philip E Mosley Jinglei Lv Léonie Borne Jessica Adsett Natalie Garden Jurgen Fripp Nicholas G. Martin Christine C Guo Michael Breakspear |
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R - General Medicine |
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doi_str |
10.1016/j.nicl.2020.102527 |
callnumber-a |
R858-859.7 |
up_date |
2024-07-03T23:13:29.022Z |
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|
score |
7.399455 |