Big Data for Population Health



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Big Data for Population Health Prof Martin Landray Nuffield Department of Population Health Deputy Director, Big Data Institute, Li Ka Shing Centre for Health Information and Discovery University of Oxford

Li Ka Shing Centre for Health Information and Discovery New building: 7500 m 2 in heart of Oxford medical campus 350 BDI researchers (+ 200 population health scientists) Opening Autumn 2016 Innovation in Medical Science - Transformation in Human Health

The Oxford Big Data Institute The Oxford Big Data Institute Genomics and statistical genetics Infectious disease Large-scale trials & cohort studies Informatics, engineering & analytic methods Innovation in Medical Science - Transformation in Human Health

Founders and Directors Sir John Bell Regius professor of medicine Peter Donnelly Statistical and population genetics Sir Rory Collins Population health, UK Biobank Dominic Kwiatkowski Infection surveillance Gil McVean, director Computational genomics Martin Landray, deputy director Clinical trials & epidemiology

Big Data for Population Health Scale: Breadth: Length: Depth: Number of people (cases & controls) Range of exposures & outcomes Frequency & duration of observations Level of detail Using the power of data to understand disease, develop treatments, and improve healthcare

Big Data a strength of Oxford Study type Population Size Duration Prospective cohort General UK 2M 5-60 yrs General Overseas 2M 5-20 yrs Clinical trials Cardiovascular 100,000 5-20 yrs Renal 10,000 <10 yrs Screening 1M <4 yrs Maternal 20,000 5-15 yrs Routine datasets Oxfordshire 4M <50 yrs England 50M <45 yrs Mother-child 7M pairs <15 yrs Innovation in Medical Science - Transformation in Human Health

Value of routine data

The value of routine healthcare data: The return of Mumps within the UK Goldacre Lancet 2013

Large-scale randomized evidence: Lowering cholesterol reduces risk of vascular events 20,536 patients randomized to simvastatin vs placebo in the Heart Protection Study Heart Protection Study Collaborative Group Lancet 2011

Value of large numbers

Large numbers give clarity: Ischaemic heart diseases vs. Systolic BP Hazard Ratio (95% CI) 256 128 64 32 16 8 4 5000 people Age at risk: 80-89 70-79 60-69 50-59 40-49 256 128 64 32 16 8 4 50 000 people Age at risk: 80-89 70-79 60-69 50-59 40-49 256 128 64 32 16 8 4 500 000 people Age at risk: 80-89 70-79 60-69 50-59 40-49 2 2 2 1 1 1 120 140 160 180 Usual SBP (mmhg) 120 140 160 180 120 140 160 180 Usual SBP (mmhg) Usual SBP (mmhg) Lewington on behalf of the Prospective Studies Collaboration (unpublished)

500,000 participants recruited in 3.5 years 9M invites generated from NHS register 22 assessment centres in rented office space

Understanding the phenotype Consent / Questionnaire Cognition Diet Respiratory function Exercise / ECG MRI / DEXA Multi-modal brain MRI Physical activity Retinal imaging

Understanding the phenotype 500,000 100,000 200,000 450,000 Consent / Questionnaire Cognition Diet Respiratory function 5,000 95,000 Exercise / ECG MRI / DEXA 5,000 100,000 60,000 Multi-modal brain MRI Physical activity Retinal imaging

Data collection directly from participants: e.g. activity monitors 45% agree to wear device Completed by >80,000 UK Biobank participants

Exemplar data acquired during testing Example activities Wear around office 2 hours Swimming 3 minutes Squash 2 minutes

Visual inspection of one day s recording 1 hour 8.6M readings/day, 7 days/person, 100 000 people 6,000,000,000,000 readings Activity stops at 10:07pm

Turning samples into data Laboratory assays (500,000) haematology, biochemistry, disease biomarkers (2015-16) infectious disease panel (TBC) Genetic assays (500,000) 820k markers (Affymetrix) 250,000 SNPs in a whole-genome array 200,000 markers for known risk factor or disease associations, copy number variation, loss of function, and insertions/deletions 150,000 exome markers for high proportion of non-synonymous coding variants with allele frequency over 0.02% Imputation of >70M markers using reference sequence data (UK 10k; 1000 genomes phase III 2015-16) Genotyping data on first 150,000 participants released May 2015

Record linkage Death registries Cancer registries Environmental data Screening programmes Research data Pathology records Treatment records Primary care data Hospital records Built environment

Hospital admissions following recruitment (linkage to national hospital episode statistics) Osteoarthritis Ischaemic heart disease Asthma Diabetes mellitus Inflammatory bowel disease COPD & bronchiectasis Unipolar depression Cerebrovascular disease Kidney disease Rheumatoid arthritis Venous thrombo-embolism Glaucoma Liver cirrhosis Parkinson s disease Hip fracture Dementia Any diagnosis field Main diagnosis 0 10,000 20,000 30,000 40,000 Number of participants

The future

Big Data Collaborations & Opportunities Local Medicine, Engineering, Computer Science, Statistics NHS partnerships: Academic Health Science Centre / Network (n=3.3m) National UK Biobank, 100 000 Genomes, UK Dementia Platform NIHR Health Informatics Collaborative, Farr Institute MRC Hubs for Trials Methodology Research CRC Registered Clinical Trials Unit network International Stanford, Vanderbilt, Global Alliance Technology Google, Apple, irhythm, AliveCor Regulators FDA, EMA, MHRA, HRA Innovation in Medical Science - Transformation in Human Health

NIHR Health Informatics Collaborative (HIC) Chief Medical Officer s Grand Challenge: demonstrate use of routine clinical data for collaborative, translational research 5 Biomedical Research Centres Imperial, UCL, Guys & St Thomas, Cambridge, Oxford Exemplar therapeutic areas Task acute coronary syndrome, renal transplantation, ITU, cancer, infection establish clinical data repositories to known data standards automatic data flows from clinical systems framework for sharing data (and managing intellectual property) Innovation in Medical Science - Transformation in Human Health

Oxford Academic Health Science Centre (AHSC) Vision: an integrated & coordinated Big Data programme that underpins a world-class Learning Healthcare System Patient & public engagement setting agenda, building trust, collecting data, sharing information Clinical care delivery monitoring (individual & population needs) decision support (treatment, referral & discharge) Quality assurance assessment, comparison, improvement Discovery causes, mechanism, treatment, consequence of disease Evaluation service utilization, epidemiology, clinical trials, health economics Innovation in Medical Science - Transformation in Human Health

Acknowledgements Funding: Li Ka Shing Foundation Robertson Foundation British Heart Foundation Medical Research Council Cancer Research UK If you would like to know more: martin.landray@ndph.ox.ac.uk www.ndph.ox.ac.uk