ID

45480

Beschrijving

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

Trefwoorden

  1. 13-12-22 13-12-22 - Chiara Middel
Houder van rechten

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

Geüploaded op

13 december 2022

DOI

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Licentie

Creative Commons BY 4.0

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dbGaP phs000743 METSIM (METabolic Syndrome In Men) Study

Sample ID, analyte type, and exome chip genotyping batch of participants in the "METSIM (METabolic Syndrome In Men) Study GWAS and Exome Chip" project.

pht004825
Beschrijving

pht004825

Alias
UMLS CUI [1,1]
C3846158
Sample ID
Beschrijving

SAMPLE_ID

Datatype

string

Alias
UMLS CUI [1,1]
C1299222
Analyte Type
Beschrijving

ANALYTE_TYPE

Datatype

string

Alias
UMLS CUI [1,1]
C4744818
Exome Chip genotyping batch
Beschrijving

batch_exomechip

Datatype

text

Alias
UMLS CUI [1,1]
C0600596
UMLS CUI [1,2]
C3178814

Similar models

Sample ID, analyte type, and exome chip genotyping batch of participants in the "METSIM (METabolic Syndrome In Men) Study GWAS and Exome Chip" project.

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
pht004825
C3846158 (UMLS CUI [1,1])
SAMPLE_ID
Item
Sample ID
string
C1299222 (UMLS CUI [1,1])
ANALYTE_TYPE
Item
Analyte Type
string
C4744818 (UMLS CUI [1,1])
Item
Exome Chip genotyping batch
text
C0600596 (UMLS CUI [1,1])
C3178814 (UMLS CUI [1,2])
Code List
Exome Chip genotyping batch
CL Item
Feb 2012 (1)
CL Item
Aug 2013 (2)

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