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Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing

BACKGROUND: In the last decade, genomic studies have identified and replicated thousands of genetic associations with measures of health and disease and contributed to the understanding of the etiology of a variety of health conditions. Proteins are key biomarkers in clinical medicine and often drug...

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Autores principales: Austin, Thomas R., McHugh, Caitlin P., Brody, Jennifer A., Bis, Joshua C., Sitlani, Colleen M., Bartz, Traci M., Biggs, Mary L., Bansal, Nisha, Buzkova, Petra, Carr, Steven A., deFilippi, Christopher R., Elkind, Mitchell S. V., Fink, Howard A., Floyd, James S., Fohner, Alison E., Gerszten, Robert E., Heckbert, Susan R., Katz, Daniel H., Kizer, Jorge R., Lemaitre, Rozenn N., Longstreth, W. T., McKnight, Barbara, Mei, Hao, Mukamal, Kenneth J., Newman, Anne B., Ngo, Debby, Odden, Michelle C., Vasan, Ramachandran S., Shojaie, Ali, Simon, Noah, Smith, George Davey, Davies, Neil M., Siscovick, David S., Sotoodehnia, Nona, Tracy, Russell P., Wiggins, Kerri L., Zheng, Jie, Psaty, Bruce M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9255954/
https://www.ncbi.nlm.nih.gov/pubmed/35790642
http://dx.doi.org/10.1007/s10654-022-00888-z
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author Austin, Thomas R.
McHugh, Caitlin P.
Brody, Jennifer A.
Bis, Joshua C.
Sitlani, Colleen M.
Bartz, Traci M.
Biggs, Mary L.
Bansal, Nisha
Buzkova, Petra
Carr, Steven A.
deFilippi, Christopher R.
Elkind, Mitchell S. V.
Fink, Howard A.
Floyd, James S.
Fohner, Alison E.
Gerszten, Robert E.
Heckbert, Susan R.
Katz, Daniel H.
Kizer, Jorge R.
Lemaitre, Rozenn N.
Longstreth, W. T.
McKnight, Barbara
Mei, Hao
Mukamal, Kenneth J.
Newman, Anne B.
Ngo, Debby
Odden, Michelle C.
Vasan, Ramachandran S.
Shojaie, Ali
Simon, Noah
Smith, George Davey
Davies, Neil M.
Siscovick, David S.
Sotoodehnia, Nona
Tracy, Russell P.
Wiggins, Kerri L.
Zheng, Jie
Psaty, Bruce M.
author_facet Austin, Thomas R.
McHugh, Caitlin P.
Brody, Jennifer A.
Bis, Joshua C.
Sitlani, Colleen M.
Bartz, Traci M.
Biggs, Mary L.
Bansal, Nisha
Buzkova, Petra
Carr, Steven A.
deFilippi, Christopher R.
Elkind, Mitchell S. V.
Fink, Howard A.
Floyd, James S.
Fohner, Alison E.
Gerszten, Robert E.
Heckbert, Susan R.
Katz, Daniel H.
Kizer, Jorge R.
Lemaitre, Rozenn N.
Longstreth, W. T.
McKnight, Barbara
Mei, Hao
Mukamal, Kenneth J.
Newman, Anne B.
Ngo, Debby
Odden, Michelle C.
Vasan, Ramachandran S.
Shojaie, Ali
Simon, Noah
Smith, George Davey
Davies, Neil M.
Siscovick, David S.
Sotoodehnia, Nona
Tracy, Russell P.
Wiggins, Kerri L.
Zheng, Jie
Psaty, Bruce M.
author_sort Austin, Thomas R.
collection PubMed
description BACKGROUND: In the last decade, genomic studies have identified and replicated thousands of genetic associations with measures of health and disease and contributed to the understanding of the etiology of a variety of health conditions. Proteins are key biomarkers in clinical medicine and often drug-therapy targets. Like genomics, proteomics can advance our understanding of biology. METHODS AND RESULTS: In the setting of the Cardiovascular Health Study (CHS), a cohort study of older adults, an aptamer-based method that has high sensitivity for low-abundance proteins was used to assay 4979 proteins in frozen, stored plasma from 3188 participants (61% women, mean age 74 years). CHS provides active support, including central analysis, for seven phenotype-specific working groups (WGs). Each CHS WG is led by one or two senior investigators and includes 10 to 20 early or mid-career scientists. In this setting of mentored access, the proteomic data and analytic methods are widely shared with the WGs and investigators so that they may evaluate associations between baseline levels of circulating proteins and the incidence of a variety of health outcomes in prospective cohort analyses. We describe the design of CHS, the CHS Proteomics Study, characteristics of participants, quality control measures, and structural characteristics of the data provided to CHS WGs. We additionally highlight plans for validation and replication of novel proteomic associations. CONCLUSION: The CHS Proteomics Study offers an opportunity for collaborative data sharing to improve our understanding of the etiology of a variety of health conditions in older adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10654-022-00888-z.
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spelling pubmed-92559542022-07-06 Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing Austin, Thomas R. McHugh, Caitlin P. Brody, Jennifer A. Bis, Joshua C. Sitlani, Colleen M. Bartz, Traci M. Biggs, Mary L. Bansal, Nisha Buzkova, Petra Carr, Steven A. deFilippi, Christopher R. Elkind, Mitchell S. V. Fink, Howard A. Floyd, James S. Fohner, Alison E. Gerszten, Robert E. Heckbert, Susan R. Katz, Daniel H. Kizer, Jorge R. Lemaitre, Rozenn N. Longstreth, W. T. McKnight, Barbara Mei, Hao Mukamal, Kenneth J. Newman, Anne B. Ngo, Debby Odden, Michelle C. Vasan, Ramachandran S. Shojaie, Ali Simon, Noah Smith, George Davey Davies, Neil M. Siscovick, David S. Sotoodehnia, Nona Tracy, Russell P. Wiggins, Kerri L. Zheng, Jie Psaty, Bruce M. Eur J Epidemiol Cohort Profile BACKGROUND: In the last decade, genomic studies have identified and replicated thousands of genetic associations with measures of health and disease and contributed to the understanding of the etiology of a variety of health conditions. Proteins are key biomarkers in clinical medicine and often drug-therapy targets. Like genomics, proteomics can advance our understanding of biology. METHODS AND RESULTS: In the setting of the Cardiovascular Health Study (CHS), a cohort study of older adults, an aptamer-based method that has high sensitivity for low-abundance proteins was used to assay 4979 proteins in frozen, stored plasma from 3188 participants (61% women, mean age 74 years). CHS provides active support, including central analysis, for seven phenotype-specific working groups (WGs). Each CHS WG is led by one or two senior investigators and includes 10 to 20 early or mid-career scientists. In this setting of mentored access, the proteomic data and analytic methods are widely shared with the WGs and investigators so that they may evaluate associations between baseline levels of circulating proteins and the incidence of a variety of health outcomes in prospective cohort analyses. We describe the design of CHS, the CHS Proteomics Study, characteristics of participants, quality control measures, and structural characteristics of the data provided to CHS WGs. We additionally highlight plans for validation and replication of novel proteomic associations. CONCLUSION: The CHS Proteomics Study offers an opportunity for collaborative data sharing to improve our understanding of the etiology of a variety of health conditions in older adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10654-022-00888-z. Springer Netherlands 2022-07-05 2022 /pmc/articles/PMC9255954/ /pubmed/35790642 http://dx.doi.org/10.1007/s10654-022-00888-z Text en © Springer Nature B.V. 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Cohort Profile
Austin, Thomas R.
McHugh, Caitlin P.
Brody, Jennifer A.
Bis, Joshua C.
Sitlani, Colleen M.
Bartz, Traci M.
Biggs, Mary L.
Bansal, Nisha
Buzkova, Petra
Carr, Steven A.
deFilippi, Christopher R.
Elkind, Mitchell S. V.
Fink, Howard A.
Floyd, James S.
Fohner, Alison E.
Gerszten, Robert E.
Heckbert, Susan R.
Katz, Daniel H.
Kizer, Jorge R.
Lemaitre, Rozenn N.
Longstreth, W. T.
McKnight, Barbara
Mei, Hao
Mukamal, Kenneth J.
Newman, Anne B.
Ngo, Debby
Odden, Michelle C.
Vasan, Ramachandran S.
Shojaie, Ali
Simon, Noah
Smith, George Davey
Davies, Neil M.
Siscovick, David S.
Sotoodehnia, Nona
Tracy, Russell P.
Wiggins, Kerri L.
Zheng, Jie
Psaty, Bruce M.
Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing
title Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing
title_full Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing
title_fullStr Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing
title_full_unstemmed Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing
title_short Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing
title_sort proteomics and population biology in the cardiovascular health study (chs): design of a study with mentored access and active data sharing
topic Cohort Profile
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9255954/
https://www.ncbi.nlm.nih.gov/pubmed/35790642
http://dx.doi.org/10.1007/s10654-022-00888-z
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