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NIA‐AA Alzheimer's Disease Framework: Clinical Characterization of Stages

BACKGROUND: To operationalize the National Institute on Aging – Alzheimer's Association (NIA‐AA) Research Framework for Alzheimer's Disease 6‐stage continuum of clinical progression for persons with abnormal amyloid. METHODS: The Mayo Clinic Study of Aging is a population‐based longitudina...

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Autores principales: Petersen, Ronald C., Wiste, Heather J., Weigand, Stephen D., Fields, Julie A., Geda, Yonas E., Graff‐Radford, Jonathan, Knopman, David S., Kremers, Walter K., Lowe, Val, Machulda, Mary M., Mielke, Michelle M., Stricker, Nikki H., Therneau, Terry M., Vemuri, Prashanthi, Jack, Clifford R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131266/
https://www.ncbi.nlm.nih.gov/pubmed/33772866
http://dx.doi.org/10.1002/ana.26071
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author Petersen, Ronald C.
Wiste, Heather J.
Weigand, Stephen D.
Fields, Julie A.
Geda, Yonas E.
Graff‐Radford, Jonathan
Knopman, David S.
Kremers, Walter K.
Lowe, Val
Machulda, Mary M.
Mielke, Michelle M.
Stricker, Nikki H.
Therneau, Terry M.
Vemuri, Prashanthi
Jack, Clifford R.
author_facet Petersen, Ronald C.
Wiste, Heather J.
Weigand, Stephen D.
Fields, Julie A.
Geda, Yonas E.
Graff‐Radford, Jonathan
Knopman, David S.
Kremers, Walter K.
Lowe, Val
Machulda, Mary M.
Mielke, Michelle M.
Stricker, Nikki H.
Therneau, Terry M.
Vemuri, Prashanthi
Jack, Clifford R.
author_sort Petersen, Ronald C.
collection PubMed
description BACKGROUND: To operationalize the National Institute on Aging – Alzheimer's Association (NIA‐AA) Research Framework for Alzheimer's Disease 6‐stage continuum of clinical progression for persons with abnormal amyloid. METHODS: The Mayo Clinic Study of Aging is a population‐based longitudinal study of aging and cognitive impairment in Olmsted County, Minnesota. We evaluated persons without dementia having 3 consecutive clinical visits. Measures for cross‐sectional categories included objective cognitive impairment (OBJ) and function (FXN). Measures for change included subjective cognitive impairment (SCD), objective cognitive change (ΔOBJ), and new onset of neurobehavioral symptoms (ΔNBS). We calculated frequencies of the stages using different cutoff points and assessed stability of the stages over 15 months. RESULTS: Among 243 abnormal amyloid participants, the frequencies of the stages varied with age: 66 to 90% were classified as stage 1 at age 50 but at age 80, 24 to 36% were stage 1, 32 to 47% were stage 2, 18 to 27% were stage 3, 1 to 3% were stage 4 to 6, and 3 to 9% were indeterminate. Most stage 2 participants were classified as stage 2 because of abnormal ΔOBJ only (44–59%), whereas 11 to 21% had SCD only, and 9 to 13% had ΔNBS only. Short‐term stability varied by stage and OBJ cutoff points but the most notable changes were seen in stage 2 with 38 to 63% remaining stable, 4 to 13% worsening, and 24 to 41% improving (moving to stage 1). INTERPRETATION: The frequency of the stages varied by age and the precise membership fluctuated by the parameters used to define the stages. The staging framework may require revisions before it can be adopted for clinical trials. ANN NEUROL 2021;89:1145–1156
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spelling pubmed-81312662021-06-01 NIA‐AA Alzheimer's Disease Framework: Clinical Characterization of Stages Petersen, Ronald C. Wiste, Heather J. Weigand, Stephen D. Fields, Julie A. Geda, Yonas E. Graff‐Radford, Jonathan Knopman, David S. Kremers, Walter K. Lowe, Val Machulda, Mary M. Mielke, Michelle M. Stricker, Nikki H. Therneau, Terry M. Vemuri, Prashanthi Jack, Clifford R. Ann Neurol Research Articles BACKGROUND: To operationalize the National Institute on Aging – Alzheimer's Association (NIA‐AA) Research Framework for Alzheimer's Disease 6‐stage continuum of clinical progression for persons with abnormal amyloid. METHODS: The Mayo Clinic Study of Aging is a population‐based longitudinal study of aging and cognitive impairment in Olmsted County, Minnesota. We evaluated persons without dementia having 3 consecutive clinical visits. Measures for cross‐sectional categories included objective cognitive impairment (OBJ) and function (FXN). Measures for change included subjective cognitive impairment (SCD), objective cognitive change (ΔOBJ), and new onset of neurobehavioral symptoms (ΔNBS). We calculated frequencies of the stages using different cutoff points and assessed stability of the stages over 15 months. RESULTS: Among 243 abnormal amyloid participants, the frequencies of the stages varied with age: 66 to 90% were classified as stage 1 at age 50 but at age 80, 24 to 36% were stage 1, 32 to 47% were stage 2, 18 to 27% were stage 3, 1 to 3% were stage 4 to 6, and 3 to 9% were indeterminate. Most stage 2 participants were classified as stage 2 because of abnormal ΔOBJ only (44–59%), whereas 11 to 21% had SCD only, and 9 to 13% had ΔNBS only. Short‐term stability varied by stage and OBJ cutoff points but the most notable changes were seen in stage 2 with 38 to 63% remaining stable, 4 to 13% worsening, and 24 to 41% improving (moving to stage 1). INTERPRETATION: The frequency of the stages varied by age and the precise membership fluctuated by the parameters used to define the stages. The staging framework may require revisions before it can be adopted for clinical trials. ANN NEUROL 2021;89:1145–1156 John Wiley & Sons, Inc. 2021-04-06 2021-06 /pmc/articles/PMC8131266/ /pubmed/33772866 http://dx.doi.org/10.1002/ana.26071 Text en © 2021 The Authors. Annals of Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Petersen, Ronald C.
Wiste, Heather J.
Weigand, Stephen D.
Fields, Julie A.
Geda, Yonas E.
Graff‐Radford, Jonathan
Knopman, David S.
Kremers, Walter K.
Lowe, Val
Machulda, Mary M.
Mielke, Michelle M.
Stricker, Nikki H.
Therneau, Terry M.
Vemuri, Prashanthi
Jack, Clifford R.
NIA‐AA Alzheimer's Disease Framework: Clinical Characterization of Stages
title NIA‐AA Alzheimer's Disease Framework: Clinical Characterization of Stages
title_full NIA‐AA Alzheimer's Disease Framework: Clinical Characterization of Stages
title_fullStr NIA‐AA Alzheimer's Disease Framework: Clinical Characterization of Stages
title_full_unstemmed NIA‐AA Alzheimer's Disease Framework: Clinical Characterization of Stages
title_short NIA‐AA Alzheimer's Disease Framework: Clinical Characterization of Stages
title_sort nia‐aa alzheimer's disease framework: clinical characterization of stages
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131266/
https://www.ncbi.nlm.nih.gov/pubmed/33772866
http://dx.doi.org/10.1002/ana.26071
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