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Nippon-Honolulu-San Francisco Study (Ni-Hon-San Study)
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Sample details

The Ni-Hon-San study began in 1965 to compare coronary heart disease and its risk factors among Japanese men in Hiroshima and Nagasaki (Japan), Honolulu (Hawaii), and the San Francisco Bay Area (California). The Japan cohort included 2,141 men selected from the Adult Health Study (AHS) in Hiroshima and Nagasaki. Participants had been assessed biennially since 1958 and participated in the baseline Ni-Hon-San assessments from 1965 to 1966. The Hawaii cohort included 8,006 Japanese men living on Oahu, Honolulu, who participated in the Honolulu Heart Program and were assessed at baseline from 1965 to 1968. The California cohort included 1,844 Japanese American men living in eight counties of the San Francisco Bay Area. Participants were recruited through a 1967 census and examined at baseline from 1969 to 1970. All participants were born between 1900 and 1919. Follow-up in Japan includes biennial reexaminations and mortality surveillance. In Hawaii, follow-up includes assessments at two and six years after baseline, and routine hospital and mortality surveillance. In California, mortality surveillance was maintained for two years.

Study design
Cohort

Number of participants at first data collection

2,141 (Japan cohort)

8,006 (Hawaii cohort)

1,844 (California cohort)

Age at first data collection

45 - 69 years (participants)

Participant year of birth

1900 - 1919 (participants)

Participant sex
Male

Representative sample at baseline?
No

Sample features

Adults
Middle-aged people
Population-based sample
Dataset details
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Countries

Japan, United States of America

Year of first data collection

1965 (Japan cohort)

1965 (Hawaii cohort)

1969 (California cohort)

Primary Institutions

Kuakini Medical Center (KMC)

National Heart, Lung, and Blood Institute (NHLBI)

Radiation Effects Research Foundation (放射線影響研究所, RERF)

University of Minnesota

Links

rerf.or.jp/en/glossary/nihonsan-en/

epi.umn.edu/cvdepi/study-synopsis/nihonsan-study/

doi.org/10.2188/jea.6.4sup_197

doi.org/10.1093/oxfordjournals.aje.a112185

Funders

No funding information available

Ongoing?
Yes

Data types collected

dataLinkage
Quantitative data collection
  • Activity log (e.g. food, sleep, exercise)
  • 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
  • Mortality data
Features

Engagement

  • None
  • Keywords

    Anthropometry
    Biological samples/biospecimens
    Blood pressure
    Cardiovascular health and disease
    Electrocardiograms
    Family health history
    Lifestyle factors
    Lung health
    Medical history
    Morbidity and mortality
    Risk factors
    Sociodemographics
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