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Scottish Diabetes Research Network Type 1 Bioresource Study (SDRNT1BIO)
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Sample details

SDRNT1BIO is an ongoing cohort study of over 6,000 patients across Scotland. Eligible participants were adults aged 16 years and above with a clinical diagnosis of Type 1 Diabetes Mellitus, Monogenic Diabetes, or Latent Autoimmune Disease of Adulthood. Recruitment was focused on 10 of the 14 National Health Service (NHS) Board regions in Scotland, with certain boards excluded due to remote geographical locations and low population density. The main sampling frame used was the comprehensive SCI-Diabetes electronic health care record, a national register of patients with diagnosed diabetes. Recruitment was primarily undertaken at diabetes outpatient clinics, with some additional recruitment in renal units. Baseline data collection took place between 1 December 2010 and 29 November 2013.

Study design
Biobank, Cohort - clinical

Number of participants at first data collection

6,127 (participants)

Recruitment is ongoing

Age at first data collection

≥ 16 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
Broadly representative of the Scottish national adult population with Type 1 Diabetes Mellitus.

Sample features

Diabetes patients
Patients and clinical populations
Dataset details
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Countries

Scotland, United Kingdom of Great Britain and Northern Ireland

Year of first data collection

2010

Primary Institutions

University of Edinburgh (University o Edinburgh, Oilthigh Dhùn Èideann)

Links

scottish-diabetes-research-network-t1-bioresource.ed.ac.uk/

diabetes-healthnet.ac.uk/default.aspx

Profile paper DOI

doi.org/10.1093/ije/dyw152

Funders

Chief Scientist Office

Diabetes UK

Scottish Diabetes Research Network

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – unspecified
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Medical birth registry
  • Mortality data
Features

Engagement

  • Patients, service users, lived experience involvement
  • Community engagement
  • Keywords

    Biological samples/biospecimens
    Biomarkers
    Diabetes
    Environmental determinants
    Genetics
    Patient data
    Socioeconomics
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