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38 Plasma proteomic signature of motoric cognitive risk syndrome
OBJECTIVES/GOALS: Motoric cognitive risk (MCR) is a pre-dementia syndrome characterized by slow gait and subjective cognitive complaints. In the Atherosclerosis Risk in Communities (ARIC) study, we aim to (1) identify plasma proteins and protein modules associated with MCR and (2) compare the proteo...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10129631/ http://dx.doi.org/10.1017/cts.2023.131 |
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author | Gomez, Gabriela T. Sathyan, Sanish Chen, Jingsha Fornage, Myriam Schlosser, Pascal Peng, Zhongsheng Cordon, Jenifer Palta, Priya Sullivan, Kevin J. Tin, Adrienne Windham, B. Gwen Gottesman, Rebecca F. Coresh, Josef Barzilai, Nir Milman, Sofiya Verghese, Joe Walker, Keenan A. |
author_facet | Gomez, Gabriela T. Sathyan, Sanish Chen, Jingsha Fornage, Myriam Schlosser, Pascal Peng, Zhongsheng Cordon, Jenifer Palta, Priya Sullivan, Kevin J. Tin, Adrienne Windham, B. Gwen Gottesman, Rebecca F. Coresh, Josef Barzilai, Nir Milman, Sofiya Verghese, Joe Walker, Keenan A. |
author_sort | Gomez, Gabriela T. |
collection | PubMed |
description | OBJECTIVES/GOALS: Motoric cognitive risk (MCR) is a pre-dementia syndrome characterized by slow gait and subjective cognitive complaints. In the Atherosclerosis Risk in Communities (ARIC) study, we aim to (1) identify plasma proteins and protein modules associated with MCR and (2) compare the proteomic signature of MCR to that of mild cognitive impairment (MCI). METHODS/STUDY POPULATION: Nondemented ARIC participants were classified by MCR status (yes/no) according to a memory questionnaire and 4-meter walk. MCI status (yes/no) was classified by expert diagnosis using standardized criteria. We measured 4,877 proteins in plasma collected at ARIC Visit 5 (late-life) and Visit 2 (midlife) utilizing the SomaScan4 proteomic assay. Multivariable logistic regression”adjusted for demographic variables, kidney function, cardiovascular risk factors, and APOE4 status”related each protein to MCR at late-life. An FDR corrected P RESULTS/ANTICIPATED RESULTS: Proteome-wide association study among 4076 ARIC participants (mean age=75; 58% women, 17% Black, 4% MCR+, 21% MCI+; MCR+ and MCI+ groups overlapped) at late-life identified 26 MCR-associated proteins involved in metabolism, vascular/visceral smooth muscle, and extracellular matrix organization. At an uncorrected P DISCUSSION/SIGNIFICANCE: This proteomic characterization of MCR identifies novel plasma proteins and networks, both distinct from and overlapping with those of MCI, thus highlighting the partially divergent mechanisms underlying these pre-dementia syndromes. These findings may be leveraged toward dementia prognostication and targeted therapeutic approaches. |
format | Online Article Text |
id | pubmed-10129631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101296312023-04-26 38 Plasma proteomic signature of motoric cognitive risk syndrome Gomez, Gabriela T. Sathyan, Sanish Chen, Jingsha Fornage, Myriam Schlosser, Pascal Peng, Zhongsheng Cordon, Jenifer Palta, Priya Sullivan, Kevin J. Tin, Adrienne Windham, B. Gwen Gottesman, Rebecca F. Coresh, Josef Barzilai, Nir Milman, Sofiya Verghese, Joe Walker, Keenan A. J Clin Transl Sci Biostatistics, Epidemiology, and Research Design OBJECTIVES/GOALS: Motoric cognitive risk (MCR) is a pre-dementia syndrome characterized by slow gait and subjective cognitive complaints. In the Atherosclerosis Risk in Communities (ARIC) study, we aim to (1) identify plasma proteins and protein modules associated with MCR and (2) compare the proteomic signature of MCR to that of mild cognitive impairment (MCI). METHODS/STUDY POPULATION: Nondemented ARIC participants were classified by MCR status (yes/no) according to a memory questionnaire and 4-meter walk. MCI status (yes/no) was classified by expert diagnosis using standardized criteria. We measured 4,877 proteins in plasma collected at ARIC Visit 5 (late-life) and Visit 2 (midlife) utilizing the SomaScan4 proteomic assay. Multivariable logistic regression”adjusted for demographic variables, kidney function, cardiovascular risk factors, and APOE4 status”related each protein to MCR at late-life. An FDR corrected P RESULTS/ANTICIPATED RESULTS: Proteome-wide association study among 4076 ARIC participants (mean age=75; 58% women, 17% Black, 4% MCR+, 21% MCI+; MCR+ and MCI+ groups overlapped) at late-life identified 26 MCR-associated proteins involved in metabolism, vascular/visceral smooth muscle, and extracellular matrix organization. At an uncorrected P DISCUSSION/SIGNIFICANCE: This proteomic characterization of MCR identifies novel plasma proteins and networks, both distinct from and overlapping with those of MCI, thus highlighting the partially divergent mechanisms underlying these pre-dementia syndromes. These findings may be leveraged toward dementia prognostication and targeted therapeutic approaches. Cambridge University Press 2023-04-24 /pmc/articles/PMC10129631/ http://dx.doi.org/10.1017/cts.2023.131 Text en © The Association for Clinical and Translational Science 2023 https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is unaltered and is properly cited. The written permission of Cambridge University Press must be obtained for commercial re-use or in order to create a derivative work. |
spellingShingle | Biostatistics, Epidemiology, and Research Design Gomez, Gabriela T. Sathyan, Sanish Chen, Jingsha Fornage, Myriam Schlosser, Pascal Peng, Zhongsheng Cordon, Jenifer Palta, Priya Sullivan, Kevin J. Tin, Adrienne Windham, B. Gwen Gottesman, Rebecca F. Coresh, Josef Barzilai, Nir Milman, Sofiya Verghese, Joe Walker, Keenan A. 38 Plasma proteomic signature of motoric cognitive risk syndrome |
title | 38 Plasma proteomic signature of motoric cognitive risk syndrome |
title_full | 38 Plasma proteomic signature of motoric cognitive risk syndrome |
title_fullStr | 38 Plasma proteomic signature of motoric cognitive risk syndrome |
title_full_unstemmed | 38 Plasma proteomic signature of motoric cognitive risk syndrome |
title_short | 38 Plasma proteomic signature of motoric cognitive risk syndrome |
title_sort | 38 plasma proteomic signature of motoric cognitive risk syndrome |
topic | Biostatistics, Epidemiology, and Research Design |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10129631/ http://dx.doi.org/10.1017/cts.2023.131 |
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