PRIME Study
- Start Year
- 1991
- Supplementary Information
- The PRIME Study in Belfast was conducted by the Queen's University of Belfast, Centre for Public Health, Institute of Clinical Science, Northern Ireland, UK. The PRIME Study in Strasbourg was conducted by the Department of Epidemiology and Public Health, University of Strasbourg, France. The PRIME Study in Toulouse was conducted by the Department of Epidemiology, National Institute of Health and Medical Research, Unit 558, Toulouse, France. The PRIME Study in Lille was conducted by the French National Institute of Health and Medical Research (INSERM), Pasteur Institute, Lille, France.
Visit PRIME
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Design
- Study design
- Cohort
- Follow Up
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In Belfast, deaths were obtained from the Business Services Organisation (BSO) and the General Register Office. Annual Follow-up Questionnaire was sent to all participants each year and some of the answers to this questionnaire led to further enquiry for hospitals/GPs.
In Strasbourg, Toulouse and Lille, deaths were obtained from the town hall or municipal corporation of the city (birth place). Annual Follow-up Questionnaire was sent to all participants each year and some of the answers to this questionnaire led to further enquiry for hospitals/GPs.
- Supplementary Information
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Deaths and cardiovascular events are followed up in all cohorts for the harmonized MORGAM data. Diabetes and cancers are additionally followed up for the PRIME Belfast cohort. See the detailed information on follow-up procedures used for MORGAM data in the cohort descriptions in the MORGAM e-publication (separate pages for Belfast, Strasbourg, Toulouse, and Lille).
For PRIME Belfast, deaths are followed up locally beyond the time period covered in the MORGAM data.
Marker Paper
PRIME Study Group (prepared by Yarnell JWG). The PRIME Study: classical risk factors do not explain the several fold differences in risk of coronary heart disease between France and Northern Ireland. Q J Med. 1998; 91: 667-676.
PUBMED 10024924
Recruitment
- Sources of Recruitment
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- Individuals
Number of participants
- Number of participants
- 10,600
- Number of participants with biosamples
- 3,000
Data Access
Availability of data and biosamples
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| Biosamples | |
| Other |
Description of the access procedures
Access to the local data and biosamples is approved on a case-by-case basis. For more information about data request please contact the study representative.
For access to the harmonized MORGAM data from many MORGAM Centres, one should seek a collaboration with any of the Centre which can submit a publication proposal to the MORGAM/BiomarCaRE Steering Group.
Availability of access information
By contacting the study representative