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Guinea-Bissau Twin Registry
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Sample details

The Guinea-Bissau Twin Registry was established by the Bandim Health Project (BHP), which maintains a health and demographic surveillance system (HDSS) in Bissau, the capital of Guinea-Bissau. The study aims to describe the twinning rate and mortality patterns among newborn twins, including mortality risk factors and hospitalization patterns, and to focus particularly on risk factors for metabolic disorders. The Guinea-Bissau Twin Registry includes two cohorts: almost 2,500 newborns born between 2009 and 2013 at a local hospital and around 1,000 young people aged 5 to 30 years registered with the Bandim HDSS. Each cohort includes both twins and singleton controls. Baseline assessment occurred shortly after birth for the newborn cohort with follow-up after 2, 6, and 12 months, and afterward at 6-month intervals until 2013. The young cohort underwent baseline assessment from 2009 to 2011 and continues to be regularly followed up through the HDSS.

Study design
Cohort - birth, Cohort - twin, Registry

Number of participants at first data collection

1,783 (twins - newborn cohort)

673 (singleton controls - newborn cohort)

574 (twins - young cohort)

463 (singleton controls - young cohort)

Age at first data collection

Birth (newborn cohort)

5 - 30 years (young cohort)

Participant year of birth

2009 - 2013 (newborn cohort)

Varied (young cohort)

Participant sex
All

Representative sample at baseline?
No

Sample features

Children and young people
Dizygotic and monozygotic twins
Newborns, infants and babies
Singletons
Young adults
Dataset details

Country

Guinea-Bissau

Year of first data collection

2009

Primary Institutions

Bandim Health Project (Projecto de Saúde Bandim, BHP)

Odense University Hospital (Odense Universitetshospital, OUH)

University of Southern Denmark (Syddansk Universitet, SDU)

Links

bandim.org/

doi.org/10.1017/thg.2012.90

Profile paper DOI

doi.org/10.1017/thg.2019.39

Funders

Bandim Health Project (BHP)

Ongoing?
Yes

Data types collected

dataLinkage
Quantitative data collection
  • Interview – face-to-face
  • 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

  • None
  • Keywords

    Biological samples/biospecimens
    Epigenetics
    Human development
    Infant health
    Infant mortality
    Low birth weight
    Young adulthood

    Consortia and dataset groups

    COllaborative project of Development of Anthropometrical measures in Twins (CODATwins) project
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