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Jerusalem Perinatal Study (JPS)
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Sample details

The JPS originally aimed to investigate hypertensive disorders of pregnancy in Israel. It has since been extended to examine the developmental origins of cardiometabolic risk and explore the mechanisms underlying the associations between perinatal characteristics and the development of risk for adult chronic disease. The JPS cohort consists of all 92,000 children born to 44,000 mothers in West Jerusalem from 1964 to 1976. At baseline, participants were either interviewed antenatally or postnatally, or their information was collected from hospital records during the recruitment period. Participants have been followed up passively through linked government and healthcare data. A subset of participants were also interviewed when the children were 18 to 19 years old. The JPS Family Follow-up study was launched in 2007 and follows a subset of the children, as well as their siblings and fathers.

Study design
Cohort - primary caregiver and child, Cohort

Number of participants at first data collection

92,408 (children)

44,067 (mothers)

871 (fathers)

68 (siblings)

Age at first data collection

Birth (children)

Varied (mothers)

Varied (fathers)

Varied (siblings)

Participant year of birth

1964 - 1976 (children)

Varied (mothers)

Varied (fathers)

Varied (siblings)

Participant sex
All

Representative sample at baseline?
No

Sample features

Caregiver and child dyad
Family members
Father and child dyad
Mother and child dyad
Siblings
Dataset details

Country

Israel

Year of first data collection

1964 (children)

1964 (mothers)

2007 (fathers)

2007 (siblings)

Primary Institutions

Ashkelon Academic College (המכללה האקדמית אשקלון)

Hadassah Medical Center (הָמֶרְכָּז הָרְפוּאִי הֲדַסָּה)

Hebrew University of Jerusalem (הַאוּנִיבֶרְסִיטָה הַעִבְרִית בִּירוּשָׁלַיִם, HUJI)

Links

doi.org/10.1016/j.annepidem.2022.03.007

doi.org/10.1016/j.annepidem.2007.07.099

doi.org/10.1093/ije/dyv120

doi.org/10.1038/s41366-021-00802-9

doi.org/10.1159/000133837

Funders

Israel Science Foundation (ISF)

Israel National Institute for Health Policy Research

Ministry of Health (מִשְׂרַד הַבְּרִיאוּת)

National Alliance for Research on Schizophrenia & Depression (NARSAD) (now known as Brain & Behaviour Research Foundation; BBRF)

National Institutes of Health (NIH)

Ongoing?
Yes

Data types collected

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

Engagement

  • None
  • Keywords

    Birth defects
    Diabetes
    Diet and nutrition
    Genetics
    Lifestyle factors
    Metabolism
    Obesity
    Perinatal health
    Relationships
    Socioeconomics

    Consortia and dataset groups

    International Childhood Cancer Cohort Consortium (I4C)
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