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Janus Serum Bank Cohort in Norway
Janus Serum Bank Cohort in Norway logo
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Sample details

The Janus Serum Bank Cohort in Norway is a resource for research on the early detection and causes of cancer. Participants were initially recruited through four health surveys: Oslo Study 1 (1972-73), the Norwegian Counties Study (1974-88), the Age 40 Programme (1982-99), and the TROFINN Health Study (2001-03). Participants were also recruited from Red Cross blood donation lists beginning in 1973. Participants are from 18 of the 19 regions in Norway and were aged between 18 and 65 years at baseline, depending on where they were recruited. Follow-up periods vary depending on the health survey from which participants were recruited. As of 2024, the cohort includes over 318,000 individuals. As of December 2023, over 120,000 cancer cases were found in the Janus donors.

Study design
Biobank, Cohort

Number of participants at first data collection

318,628 (participants)

Recruitment is ongoing

Age at first data collection

18 - 65 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Blood donors
Cancer patients
Dataset details

Country

Norway

Year of first data collection

1973

Primary Institutions

Cancer Registry of Norway (Kreftregisteret)

Norwegian Institute of Public Health (Folkehelseinstituttet, FHI, NIPH)

Ullevål University Hospital (now known as Oslo University Hospital, Ullevål, Oslo universitetssykehus, Ullevål)

Links

kreftregisteret.no/en/Research/Janus-Serum-Bank/

doi.org/10.1093/ije/dyw302

Profile paper DOI

doi.org/10.1093/ije/dyw027

Funders

Cancer Registry of Norway (Kreftregisteret)

Norwegian Cancer Society (Kreftforeningen, NCS)

Research Council of Norway (Norges forskningsråd)

Ongoing?
Yes

Data types collected

dataLinkage
Quantitative data collection
  • Activity log (e.g. food, sleep, exercise)
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
Features

Engagement

  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Alcohol use
    Biological samples/biospecimens
    Cancer registry
    Comorbidity
    Diet and nutrition
    Lifestyle factors
    Noncommunicable diseases
    Physical activity and exercise
    Smoking

    Consortia and dataset groups

    AGRICOH
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