A systems based approach to integrating genetic and longitudinal omics data to support diagnosis and prediction of common chronic disease
Lead Research Organisation:
King's College London
Department Name: Genetics and Molecular Medicine
Abstract
New technologies are providing opportunities to measure health and disease in many novel ways. The data produced is complex and hard to decipher even by clinicians and health workers. This proposal will investigate how we can use modern molecular techniques which measure in blood the activity and expression of genes and the signatures of chemical reactions (metabolites) in the cell to help predict early disease. To do this we need to explore how global gene expression and metabolites alter over time and how these longitudinal changes along with other new molecular and genetic techniques (called omics) can be used to explore disease mechanisms and susceptibility in ageing populations. To explore the biology of "omic" variability, and to lay the foundation for the clinical integration of genetic and genomic data, we will investigate the longitudinal relationships of cellular and genomic phenotypes, including global gene expression and metabolites, in 700 twins over 7 years, measured at three time-periods. The study subjects derive from the TwinsUK cohort on whom there is already extensive clinical information and cross-sectional genetic and genomic data. Building on these existing data, and making use of the specific methodological opportunities and advantages afforded by the twin design, we will explore how these genomic traits track and vary over time, determine how such variation relates to underlying genetic variation, and explore the joint contribution of genetic and genomic data to disease risk and onset. We will also explore the potential value of monitoring changes in these and other situations within an integrated personalised medicine framework. We will use and develop new analysis approaches to integrate these complex data sets and suggest which changes might play a role in clinically relevant tratis and disease itself. This study will provide novel insights into disease understanding and stimulate larger-scale efforts to combine modern genetic and genomic data for clinical benefit in the future. These studies will pave the way for individualised medicine.
Technical Summary
This proposal will investigate the longitudinal relationships of cellular and genomic phenotypes, including global gene expression and metabolites, in 700 twins over 7 years, measured at three time-periods. To increase compliance some of the blood sampling will be performed by post as well as by routine visits. We have been using postal blood methods for the last ten years and found it works well for the assays without loss of quality and local GPs are happy to cooperate. So far 98% of samples arrive within 48 hours of blood draw. We will use RNA seq in fasting whole blood for the transcriptomics to be performed in Geneva and non-targeted Mass Spec Metabolon platform for the metabolomics performed by Metabolon Inc in the USA. We have extensively used both methods previously. The study subjects derive from the extensive TwinsUK cohort (www.twinsUK.ac.uk/phenotypes) on whom there is already extensive clinical information and cross-sectional genetic and genomic data. We will use and develop systems analysis approaches to integrate these complex data sets and make causal inferences. In particular, we will develop novel robust analytical approaches, which will combine methods for investigating multidimensional association between sets of high dimensional data with dimension reduction approaches and characterisation of internal co-variation structure in each data set. Initial cross-sectional integrative analysis will be extended to the longitudinal set-up to investigate changes in omics profiles, and predictive modelling of clinically relevant traits incorporating several types of omics phenotypes will be performed.
Planned Impact
The principal beneficiaries of the research will be:
i) Academics as outlined in the "academic beneficiaries" section;
ii) Industry and biotechnology companies, in a position to exploit the improved biological understanding we will provide to develop novel products (see below);
iii) The public sector (NHS, policy-makers), provided the research generates translational advances that provide more cost effective means of managing disease;
iv) The wider public, if those translational advances provide more effective strategies for the prediction, treatment and prevention of chronic diseases.
The academic benefits will be manifest through:
i) The generation of new knowledge related to chronic disease progression with the potential to contribute to amelioration of the social, economic and personal costs of these conditions
ii) The development of a unique biosample and data set available to other researchers;
iii) The development and promulgation of novel methods for analysis of complex longitudinal data sets;
iv) The aggregation through collaboration of additional expertise in this area;
v) Improved training of researchers in the specific areas of research activity, and in the development of cross-disciplinary expertise.
The broader economic and social impact will be manifest through:
i) Economic benefits to pharma and biotechnology companies (including "spin-outs" with potential for attracting "inwards" investment) able to exploit actionable translational opportunities with respect to the development of novel prognostic and
therapeutic approaches that build on the associations we detect;
ii) Benefits to those developing and marketing omics assays, in terms of defining additional content, and expanding markets (research initially, but potentially for clinical use);
iii) Improved effectiveness of public services if the biological insights result in better ways of predicting, treating and preventing late-onset disease (novel treatments, better diagnostics, improved strategies for stratifying risk and response to interventions);
iv) Maximising value of next-generation sequencing data collected within systems such as the NHS for other purposes, by augmenting the value of such data for late onset disease prediction;
v) Improved health outcomes (less disease-related morbidity and mortality) if the work leads to effective clinical translation, resulting in further personal, social and economic benefits.
It is important to be realistic about the true timelines for effective clinical translation. As we make clear in the grant, a complete understanding, particularly of the relationships between omics biomarkers and disease-related outcomes, requires accrual of those outcomes over time (thereby strengthening the ability to separate out causal and reactive changes in omics phenotypes). We see the research proposed as providing enablement (in terms of methods, data sets, and paradigms) that will support efforts to integrate genetic and genomic data relevant to late-onset diseases. Despite all the talk of a genomics-based health care "revolution", the list of indications is so far (rightly) focused around cancer, rare diseases, infectious diseases and pharmacogenetics, and a measured description of the value of whole genome sequencing (for example) to common, late-onset disease has been lacking. Based on our extensive experience of complex trait genetics we believe that the value of DNA sequence alone (or any omic alone) will be limited in terms of risk stratification for most diseases. It will require both integration of these different data types, plus additional longitudinal clinical phenotypes (which we argue are best derived from omics data) to achieve the levels of overall specificity and
sensitivity needed to trigger a specific preventative intervention or invasive diagnostic test. We believe this project will play a crucial role in enabling such a reconfiguration of health care delivery.
i) Academics as outlined in the "academic beneficiaries" section;
ii) Industry and biotechnology companies, in a position to exploit the improved biological understanding we will provide to develop novel products (see below);
iii) The public sector (NHS, policy-makers), provided the research generates translational advances that provide more cost effective means of managing disease;
iv) The wider public, if those translational advances provide more effective strategies for the prediction, treatment and prevention of chronic diseases.
The academic benefits will be manifest through:
i) The generation of new knowledge related to chronic disease progression with the potential to contribute to amelioration of the social, economic and personal costs of these conditions
ii) The development of a unique biosample and data set available to other researchers;
iii) The development and promulgation of novel methods for analysis of complex longitudinal data sets;
iv) The aggregation through collaboration of additional expertise in this area;
v) Improved training of researchers in the specific areas of research activity, and in the development of cross-disciplinary expertise.
The broader economic and social impact will be manifest through:
i) Economic benefits to pharma and biotechnology companies (including "spin-outs" with potential for attracting "inwards" investment) able to exploit actionable translational opportunities with respect to the development of novel prognostic and
therapeutic approaches that build on the associations we detect;
ii) Benefits to those developing and marketing omics assays, in terms of defining additional content, and expanding markets (research initially, but potentially for clinical use);
iii) Improved effectiveness of public services if the biological insights result in better ways of predicting, treating and preventing late-onset disease (novel treatments, better diagnostics, improved strategies for stratifying risk and response to interventions);
iv) Maximising value of next-generation sequencing data collected within systems such as the NHS for other purposes, by augmenting the value of such data for late onset disease prediction;
v) Improved health outcomes (less disease-related morbidity and mortality) if the work leads to effective clinical translation, resulting in further personal, social and economic benefits.
It is important to be realistic about the true timelines for effective clinical translation. As we make clear in the grant, a complete understanding, particularly of the relationships between omics biomarkers and disease-related outcomes, requires accrual of those outcomes over time (thereby strengthening the ability to separate out causal and reactive changes in omics phenotypes). We see the research proposed as providing enablement (in terms of methods, data sets, and paradigms) that will support efforts to integrate genetic and genomic data relevant to late-onset diseases. Despite all the talk of a genomics-based health care "revolution", the list of indications is so far (rightly) focused around cancer, rare diseases, infectious diseases and pharmacogenetics, and a measured description of the value of whole genome sequencing (for example) to common, late-onset disease has been lacking. Based on our extensive experience of complex trait genetics we believe that the value of DNA sequence alone (or any omic alone) will be limited in terms of risk stratification for most diseases. It will require both integration of these different data types, plus additional longitudinal clinical phenotypes (which we argue are best derived from omics data) to achieve the levels of overall specificity and
sensitivity needed to trigger a specific preventative intervention or invasive diagnostic test. We believe this project will play a crucial role in enabling such a reconfiguration of health care delivery.
Organisations
Publications
Zhang X
(2023)
PPI-Induced Changes in Plasma Metabolite Levels Influence Total Hip Bone Mineral Density in a UK Cohort.
in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Moayyeri A
(2018)
Metabolomic Pathways to Osteoporosis in Middle-Aged Women: A Genome-Metabolome-Wide Mendelian Randomization Study.
in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Baird DA
(2019)
Identification of Novel Loci Associated With Hip Shape: A Meta-Analysis of Genomewide Association Studies.
in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Louca P
(2022)
Body mass index mediates the effect of the DASH diet on hypertension: Common metabolites underlying the association.
in Journal of human nutrition and dietetics : the official journal of the British Dietetic Association
Mangino M
(2016)
Integrated multiomics approach identifies calcium and integrin-binding protein-2 as a novel gene for pulse wave velocity.
in Journal of hypertension
Nogal A
(2022)
Incremental Value of a Panel of Serum Metabolites for Predicting Risk of Atherosclerotic Cardiovascular Disease.
in Journal of the American Heart Association
Hysi P
(2022)
Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels
in Metabolites
Patel S
(2022)
Combined genetic deletion of GDF15 and FGF21 has modest effects on body weight, hepatic steatosis and insulin resistance in high fat fed mice.
in Molecular metabolism
Bar N
(2020)
A reference map of potential determinants for the human serum metabolome.
in Nature
Odhams CA
(2019)
Interferon inducible X-linked gene CXorf21 may contribute to sexual dimorphism in Systemic Lupus Erythematosus.
in Nature communications
Description | Adipose Multi-omics in TwinsUK |
Amount | $250,000 (USD) |
Organisation | Foundation for the National Institutes of Health (FNIH) |
Sector | Charity/Non Profit |
Country | United States |
Start | 11/2022 |
End | 03/2024 |
Description | BBSRC CASE Studentship |
Amount | £42,000 (GBP) |
Organisation | Biotechnology and Biological Sciences Research Council (BBSRC) |
Sector | Public |
Country | United Kingdom |
Start | 05/2018 |
End | 05/2022 |
Description | Diverging dynamic resilience: Using twins to identify frailty drivers independent of shared genetics in the context of the COVID-19 pandemic |
Amount | $6,188,000 (USD) |
Organisation | Wellcome Trust |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 08/2023 |
End | 08/2026 |
Description | HDR UK London Substantive Site |
Amount | £1,167,000 (GBP) |
Funding ID | London Substantive Site |
Organisation | Health Data Research UK |
Sector | Private |
Country | United Kingdom |
Start | 03/2018 |
End | 03/2023 |
Description | Identification of regulatory genomic networks underlying skin ageing |
Amount | £110,026 (GBP) |
Funding ID | BB/V509656/1 |
Organisation | Biotechnology and Biological Sciences Research Council (BBSRC) |
Sector | Public |
Country | United Kingdom |
Start | 08/2020 |
End | 09/2024 |
Description | MRC Project Grant "Genetic and environmental determinants of age-acquired skewed X-inactivation and escape from X-inactivation" |
Amount | £775,000 (GBP) |
Funding ID | MR/R023131/1 |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 09/2018 |
End | 09/2021 |
Description | NIH Type 2 Diabetes Accelerating Medicine Partnership, Sub-Award |
Amount | £56,000 (GBP) |
Organisation | National Institutes of Health (NIH) |
Sector | Public |
Country | United States |
Start | 03/2019 |
End | 03/2020 |
Description | Targeted metabolomics of urine samples to understand the role of the gut microbiota in food polyphenol metabolism |
Amount | £9,990 (GBP) |
Organisation | Chronic Disease Research Foundation |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 01/2020 |
End | 12/2020 |
Description | The Genetics Society Conference Grant for PhD Students |
Amount | £750 (GBP) |
Organisation | The Genetics Society |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 05/2018 |
End | 09/2018 |
Description | TwinsUK: A longitudinal epidemiological and genomic resource |
Amount | £2,462,449 (GBP) |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 01/2024 |
End | 12/2028 |
Description | Wellcome Longitudinal Population Studes Award "TwinsUK (2019-2022) - An Epidemiological and Genomic Resource" |
Amount | £3,000,000 (GBP) |
Organisation | Wellcome Trust |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 05/2019 |
End | 12/2022 |
Description | BBC1 - Easy ways to live well |
Form Of Engagement Activity | A broadcast e.g. TV/radio/film/podcast (other than news/press) |
Part Of Official Scheme? | No |
Geographic Reach | National |
Primary Audience | Public/other audiences |
Results and Impact | How your diet impacts your gut microbes and this affects your health |
Year(s) Of Engagement Activity | 2019 |
URL | https://www.bbc.co.uk/programmes/articles/5kq6JpLyGD38BMGYGKVMxQn/ten-simple-things-you-can-do-to-li... |
Description | Biogerontology Conference |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Industry/Business |
Results and Impact | Invited speaker to International cconference informing clinicians about advances in microbiome science and interactions between the microbiome and host health. |
Year(s) Of Engagement Activity | 2019 |
Description | Royal Society and Academy of Medical Sciences conference on Healthy ageing |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | National |
Primary Audience | Professional Practitioners |
Results and Impact | Presentation about the genetic drivers of ageing and longevity and how we might harness our current understanding of genetics to increase healthy lifespan |
Year(s) Of Engagement Activity | 2020 |
URL | https://royalsociety.org/science-events-and-lectures/2020/02/tof-healthy-ageing/ |
Description | TWINS 2017: The Joint 4th World Congress on Twin Pregnancy and 16th Congress of the International Society of Twin Studies (ISTS) |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Postgraduate students |
Results and Impact | Talk at a conference that aims to further research and public education in all fields related to twins and twin studies, for the mutual benefit of twins and their families and the scientific community. |
Year(s) Of Engagement Activity | 2017 |
URL | https://www.mcascientificevents.eu/wp-content/uploads/2017/05/Scientific-Programme-29.05.pdf |
Description | Talk at the KCL School of Life Course Sciences research meeting (CLR 2018) |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Professional Practitioners |
Results and Impact | Talk (by CLR) at the King's College London School of Life Course Sciences postdoctoral association research meeting, London, UK (2018), on the topic of "Exploring host-gut microbiota metabolic crosstalk in prospective cases of T2D". |
Year(s) Of Engagement Activity | 2018 |
Description | World Precision Medicine Congress 2017 |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | National |
Primary Audience | Industry/Business |
Results and Impact | Talk at World Precision Medicine Congress 2017 which brings together academia, industry and healthcare to discuss and debate key challenges and opportunities within: Diagnostics | Big Data | Genomics | Infrastructure | Investment| Rare Diseases | Oncology |Neuroscience |Diabetes| |
Year(s) Of Engagement Activity | 2017 |
URL | http://www.globaleventslist.elsevier.com/events/2017/05/world-precision-medicine-congress-2017/ |