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Epigenetic scores for the circulating proteome as tools for disease prediction.
Gadd, Danni A; Hillary, Robert F; McCartney, Daniel L; Zaghlool, Shaza B; Stevenson, Anna J; Cheng, Yipeng; Fawns-Ritchie, Chloe; Nangle, Cliff; Campbell, Archie; Flaig, Robin; Harris, Sarah E; Walker, Rosie M; Shi, Liu; Tucker-Drob, Elliot M; Gieger, Christian; Peters, Annette; Waldenberger, Melanie; Graumann, Johannes; McRae, Allan F; Deary, Ian J; Porteous, David J; Hayward, Caroline; Visscher, Peter M; Cox, Simon R; Evans, Kathryn L; McIntosh, Andrew M; Suhre, Karsten; Marioni, Riccardo E.
Affiliation
  • Gadd DA; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom.
  • Hillary RF; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom.
  • McCartney DL; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom.
  • Zaghlool SB; Department of Physiology and Biophysics, Weill Cornell Medicine-Qatar, Education City, Doha, Qatar.
  • Stevenson AJ; Computer Engineering Department, Virginia Tech, Blacksburg, United States.
  • Cheng Y; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom.
  • Fawns-Ritchie C; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom.
  • Nangle C; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom.
  • Campbell A; Department of Psychology, University of Edinburgh, Edinburgh, United Kingdom.
  • Flaig R; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom.
  • Harris SE; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom.
  • Walker RM; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom.
  • Shi L; Department of Psychology, University of Edinburgh, Edinburgh, United Kingdom.
  • Tucker-Drob EM; Lothian Birth Cohorts, University of Edinburgh, Edinburgh, United Kingdom.
  • Gieger C; Centre for Clinical Brain Sciences, Chancellor's Building, University of Edinburgh, Edinburgh, United Kingdom.
  • Peters A; Department of Psychiatry, University of Oxford, Oxford, United Kingdom.
  • Waldenberger M; Department of Psychology, The University of Texas at Austin, Austin, United States.
  • Graumann J; Population Research Center, The University of Texas at Austin, Austin, United States.
  • McRae AF; Research Unit Molecular Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
  • Deary IJ; Institute of Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
  • Porteous DJ; German Center for Cardiovascular Research (DZHK), partner site Munich Heart Alliance, Munich, Germany.
  • Hayward C; German Center for Diabetes Research (DZD), Neuherberg, Germany.
  • Visscher PM; Institute of Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
  • Cox SR; German Center for Cardiovascular Research (DZHK), partner site Munich Heart Alliance, Munich, Germany.
  • Evans KL; German Center for Diabetes Research (DZD), Neuherberg, Germany.
  • McIntosh AM; Research Unit Molecular Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
  • Suhre K; Institute of Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
  • Marioni RE; German Center for Cardiovascular Research (DZHK), partner site Munich Heart Alliance, Munich, Germany.
Elife ; 112022 01 13.
Article in En | MEDLINE | ID: mdl-35023833
Although our genetic code does not change throughout our lives, our genes can be turned on and off as a result of epigenetics. Epigenetics can track how the environment and even certain behaviors add or remove small chemical markers to the DNA that makes up the genome. The type and location of these markers may affect whether genes are active or silent, this is, whether the protein coded for by that gene is being produced or not. One common epigenetic marker is known as DNA methylation. DNA methylation has been linked to the levels of a range of proteins in our cells and the risk people have of developing chronic diseases. Blood samples can be used to determine the epigenetic markers a person has on their genome and to study the abundance of many proteins. Gadd, Hillary, McCartney, Zaghlool et al. studied the relationships between DNA methylation and the abundance of 953 different proteins in blood samples from individuals in the German KORA cohort and the Scottish Lothian Birth Cohort 1936. They then used machine learning to analyze the relationship between epigenetic markers found in people's blood and the abundance of proteins, obtaining epigenetic scores or 'EpiScores' for each protein. They found 109 proteins for which DNA methylation patterns explained between at least 1% and up to 58% of the variation in protein levels. Integrating the 'EpiScores' with 14 years of medical records for more than 9000 individuals from the Generation Scotland study revealed 130 connections between EpiScores for proteins and a future diagnosis of common adverse health outcomes. These included diabetes, stroke, depression, various cancers, and inflammatory conditions such as rheumatoid arthritis and inflammatory bowel disease. Age-related chronic diseases are a growing issue worldwide and place pressure on healthcare systems. They also severely reduce quality of life for individuals over many years. This work shows how epigenetic scores based on protein levels in the blood could predict a person's risk of several of these diseases. In the case of type 2 diabetes, the EpiScore results replicated previous research linking protein levels in the blood to future diagnosis of diabetes. Protein EpiScores could therefore allow researchers to identify people with the highest risk of disease, making it possible to intervene early and prevent these people from developing chronic conditions as they age.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / DNA Methylation / Proteome / Diabetes Mellitus / Epigenomics / Neoplasms Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Elife Year: 2022 Document type: Article Affiliation country: United kingdom Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / DNA Methylation / Proteome / Diabetes Mellitus / Epigenomics / Neoplasms Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Elife Year: 2022 Document type: Article Affiliation country: United kingdom Country of publication: United kingdom