0 Ratings

ID

45480

Description

Principal Investigator: Markku Laakso, MD, PhD, University of Eastern Finland and Kuopio University Hospital, Kuopio, Finland MeSH: Metabolic Syndrome,Diabetes Mellitus, Type 2,Cardiovascular Diseases https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000743 The METSIM Study includes 10,197 men, aged from 45 to 73 years, randomly selected from the population register of the town of Kuopio, Eastern Finland, and examined in 2005-2010. The aim of the study is to investigate genetic and non-genetic factors associated with the risk of type 2 diabetes (T2D), cardiovascular disease (CVD), and insulin resistance-related traits in a cross-sectional and longitudinal setting. Study protocol includes collection of data on CVD risk factors (smoking, exercise, diet, history of chronic diseases including coronary heart disease, stroke, cardiac failure, medication, history of diabetes or early onset coronary heart disease in the family), questionnaire on the FINDRISC Score, measurement of height, weight, waist, hip, blood pressure, and bioimpedance for the evaluation of fat percentage. July 2016 - This first study release includes phenotype and whole exome sequencing data of n=982 participants in substudy: Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: Metabolic Syndrome in Men Study (METSIM) - phs001100.v2.p1. The second release (v2) includes phenotype data for the entire METSIM cohort and makes two additional substudies available, phs000919.v1.p1 and phs000752.v1.p1. *The METSIM Study v2 is utilized in the following dbGaP sub-studies.* To view genotypes, other molecular data, and derived variables collected in these sub-studies, please click on the following sub-studies below or in the "Sub-studies" section of this top-level study page phs000743.v2.p1 METSIM Study v2. - phs000752 METSIM FinMetSeq Exome Sequencing - phs000919 METSIM GWAS and Exome Chip - phs001100 METSIM T2D-GENES Exome Sequencing

Link

dbGaP-study=phs000743

Keywords

  1. 12/13/22 12/13/22 - Chiara Middel
Copyright Holder

Markku Laakso, MD, PhD, University of Eastern Finland and Kuopio University Hospital, Kuopio, Finland

Uploaded on

December 13, 2022

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :


    No comments

    In order to download data models you must be logged in. Please log in or register for free.

    dbGaP phs000743 METSIM (METabolic Syndrome In Men) Study

    Subject ID, family ID, father, mother, sex, and ID of monozygotic twins of participants in the "METSIM (METabolic Syndrome In Men) Study" project.

    pht010809
    Description

    pht010809

    Alias
    UMLS CUI [1,1]
    C3846158 (Other Coding)
    LOINC
    LA4728-7
    Family ID
    Description

    FAMILY_ID

    Data type

    string

    Alias
    UMLS CUI [1,1]
    C3669174 (Family pedigree identifier)
    LOINC
    LP173549-9
    Subject ID
    Description

    SUBJECT_ID

    Data type

    string

    Alias
    UMLS CUI [1,1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Father's Subject ID
    Description

    FATHER

    Data type

    string

    Alias
    UMLS CUI [1,1]
    C3669177 (Father identifier)
    LOINC
    MTHU047348
    UMLS CUI [1,2]
    C0030761 (genetic pedigree)
    Mother's Subject ID
    Description

    MOTHER

    Data type

    string

    Alias
    UMLS CUI [1,1]
    C3669352 (Mother identifier)
    LOINC
    MTHU047347
    UMLS CUI [1,2]
    C0030761 (genetic pedigree)
    Biological sex
    Description

    SEX

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0079399 (Gender)
    SNOMED
    263495000
    LOINC
    LP61312-2
    Twin ID for monozygotic twins and multiples. An MZ_TWIN_ID is not provided for dizygotic twins or multiples.
    Description

    MZ_TWIN_ID

    Data type

    string

    Alias
    UMLS CUI [1,1]
    C0041427 (Twin sibling (person))
    SNOMED
    11286003
    UMLS CUI [1,2]
    C2348585 (Clinical Trial Subject Unique Identifier)
    UMLS CUI [1,3]
    C0030761 (genetic pedigree)

    Similar models

    Subject ID, family ID, father, mother, sex, and ID of monozygotic twins of participants in the "METSIM (METabolic Syndrome In Men) Study" project.

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    pht010809
    C3846158 (UMLS CUI [1,1])
    FAMILY_ID
    Item
    Family ID
    string
    C3669174 (UMLS CUI [1,1])
    SUBJECT_ID
    Item
    Subject ID
    string
    C2348585 (UMLS CUI [1,1])
    FATHER
    Item
    Father's Subject ID
    string
    C3669177 (UMLS CUI [1,1])
    C0030761 (UMLS CUI [1,2])
    MOTHER
    Item
    Mother's Subject ID
    string
    C3669352 (UMLS CUI [1,1])
    C0030761 (UMLS CUI [1,2])
    Item
    Biological sex
    text
    C0079399 (UMLS CUI [1,1])
    Code List
    Biological sex
    CL Item
    Male (1)
    C0086582 (UMLS CUI [1,1])
    CL Item
    Female (2)
    C0086287 (UMLS CUI [1,1])
    CL Item
    Unknown (UNK)
    MZ_TWIN_ID
    Item
    Twin ID for monozygotic twins and multiples. An MZ_TWIN_ID is not provided for dizygotic twins or multiples.
    string
    C0041427 (UMLS CUI [1,1])
    C2348585 (UMLS CUI [1,2])
    C0030761 (UMLS CUI [1,3])

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial