Helsinki Birth Cohort Study

The main aim of HBCS is to assess the importance of early life factor on later health outcomes taking into account adult lifestyle, socioeconomic factors and genetic factors.

Overview

Acronym
HBCS
Investigators
Prof. Johan Eriksson
University of Helsinki
Contacts
Prof. Johan Eriksson
University of Helsinki

General Design

Study design
Cohort
Start - End Year
1934 -
General Information on Follow Up (profile, frequency)

13 345 people born 1934-44 have been followed-up longitudinally – of them 2003 have been participating in a clinical study at several time points starting in 1995.

Recruitment Target
  • Individuals
Number of Participants
13,345
Number of Participants with Biological Samples
2,003

Access

Availability of data and biosamples

Possible Access to Data
Possible Access to Biosamples
Other

Marker Papers

Barker DJ, Osmond C, Forsén TJ, Kajantie E, Eriksson JG. Trajectories of growth among children who have coronary events as adults. The New England Journal of Medicine, 2005; 353(17): 1802-9.

PUBMED 16251536

Supplementary Information

For access to the data and biosamples please apply to HBCS’s steering committee.

Timeline

Population

HBCS population

The HBCS cohort is composed of men and women born as singletons at Helsinki University Central Hospital during 1934-44, who attended child welfare clinics in the city of Helsinki and who were still resident in Finland in 1971.

Selection Criteria

Newborns
Countries
  • Finland
Supplementary Information about selection criteria

The participants had to have been born as singletons at Helsinki University Central Hospital during 1934-44, have attended child welfare clinics in the city of Helsinki.

Sources of Recruitment

General Population
  • Selected sample

Sample Size

Number of Participants
13,345
Number of Participants with Biological Samples
2,003
Supplementary information about number of participants

Baseline (at birth): 13 345 participants

Socioeconomic data: 13 345 participants

Follow-up 1: 4515 participants

Clinical Evaluation: 2003 participants

Follow-up 2: 1078 participants

Follow-up 3: 1080 participants

Data Collection Events

# Name Data sources Data sources - Biosamples Start End
0 HBCS - Baseline
  • Physical measures
  • Other : Medical records
1934 1946
1 HBCS - Socioeconomic information from registries
  • Administrative databases
1944 2001
2 HBCS - Follow-up 1
  • Questionnaires
2000 2000
3 HBCS - Mortality
  • Administrative databases
2000 (November) 2010 (December)
4 HBCS - Clinical Evaluation
  • Questionnaires
  • Physical measures
  • Biosamples
  • Administrative databases
  • Blood
2001 (August) 2004 (March)
5 HBCS - Follow-up 2
  • Questionnaires
2004 (April) 2005 (June)
6 HBCS - Follow-up 3
  • Questionnaires
  • Physical measures
  • Biosamples
  • Blood
2011 (October) 2013 (April)

Participating Studies

Acronym Name Study design Countries

Harmonization Initiatives Included

Acronym Name

Datasets

Name Data Collection Events Variables

Areas of Information Collected

Socio-demographic and economic characteristics
Death
Lifestyle and behaviours
Physical measures and assessments
Birth, pregnancy and reproductive health history
Laboratory measures
Perception of health, quality of life, development and functional limitations
Cognition, personality and psychological measures and assessments
Diseases
Life events, life plans, beliefs and values
Symptoms and signs
Preschool, school and work life
Medication and supplements
Social environment and relationships
Non-pharmacological interventions
Physical environment
Health and community care services utilization
Administrative information

Variables Content Summary

Areas of Information Collected
No Areas of Information Collected
No Scales Collected
Areas of Information Collected per per Population and Data Collection Event
No Areas of Information Collected
No Scales Collected

Networks

Acronym Name Harmonization Initiatives Individual Studies
Last Update: 2026-02-17T18:05:16.297