ID

45959

Descrição

Principal Investigator: Michael Boehnke, University of Michigan, Ann Arbor, MI, USA MeSH: Diabetes Mellitus, Type 2 https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000867 The Finland-United States Investigation of NIDDM Genetics (FUSION) study is a long-term effort to identify genetic variants that predispose to type 2 diabetes (T2D) or that impact the variability of T2D-related quantitative traits. The initial effort involved linkage analysis of affected-sibling-pair (ASP) families based on over 5,000 individuals living in Finland, and association fine mapping based on these family members and additional T2D cases and controls. We completed a genome-wide association scan on 1161 T2D cases and 1174 normal glucose tolerant (NGT) controls. Individual-level data is available for the 919 T2D cases and 787 NGT controls who reconsented to the use of their data or are deceased (phs000100). In addition, we selected these 919 T2D cases and a matched set of 919 NGT controls (774 overlapping with GWAS) for targeted sequencing of 78 genes associated with glucose, insulin, and/or lipids. 400 of these T2D cases were also chosen for whole-exome sequencing (phs000702).

Link

dbGaP study=phs000867

Palavras-chave

Versões (1)
  1. 16/03/2024 16/03/2024 - Madita Rudolph
Titular dos direitos

Michael Boehnke, University of Michigan, Ann Arbor, MI, USA

Transferido a

16 de março de 2024

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

dbGaP phs000867 The Finland-United States Investigation of NIDDM Genetics (FUSION) Study

Inglês

Eligibility Criteria

8 Formulários  
Inclusion and exclusion criteria
Descrição

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
*Cases*: T2D cases were selected from FUSION ASP families, each reporting at least one T2D sibling, and from Finrisk 2002, a Finnish population-based risk factor survey. T2D was defined by WHO 1999 criteria of fasting plasma glucose >= 7.0 mmol/l or 2-h plasma glucose >= 11.1 mmol/l, by report of diabetes medication use, or based on medical record review. FUSION cases with known or probable type 1 diabetes among their first degree relatives were excluded.
Descrição

Elig.phs000867.v1.p1.1

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1706256
UMLS CUI [1,2]
C1512693
UMLS CUI [1,3]
C0011860
UMLS CUI [1,4]
C0037047
UMLS CUI [1,5]
C0035648
UMLS CUI [2,1]
C1706256
UMLS CUI [2,2]
C0680251
UMLS CUI [2,3]
C0011854
UMLS CUI [2,4]
C1517194
*Controls*: NGT controls for GWAS were selected from FUSION, including subjects from Vantaa, Finland, who were NGT at ages 65 and 70 years, and spouses of FUSION subjects, and from Finrisk 2002. Additional NGT controls for sequencing were selected from D2D 2004, Finrisk 1987, Health 2000, and the Savitaipale Diabetes Study. NGT was defined by WHO 1999 criteria of fasting glucose < 6.1 mmol/l and 2-h glucose < 7.8 mmol/l. Controls were frequency-matched to the cases as described in the sub-study descriptions.
Descrição

Elig.phs000867.v1.p1.2

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0009932
UMLS CUI [1,2]
C1512693
UMLS CUI [1,3]
C0438251
Voltar ao início da página

Similar models

Eligibility Criteria

8 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000867.v1.p1.1
Item
*Cases*: T2D cases were selected from FUSION ASP families, each reporting at least one T2D sibling, and from Finrisk 2002, a Finnish population-based risk factor survey. T2D was defined by WHO 1999 criteria of fasting plasma glucose >= 7.0 mmol/l or 2-h plasma glucose >= 11.1 mmol/l, by report of diabetes medication use, or based on medical record review. FUSION cases with known or probable type 1 diabetes among their first degree relatives were excluded.
boolean
C1706256 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
C0011860 (UMLS CUI [1,3])
C0037047 (UMLS CUI [1,4])
C0035648 (UMLS CUI [1,5])
C1706256 (UMLS CUI [2,1])
C0680251 (UMLS CUI [2,2])
C0011854 (UMLS CUI [2,3])
C1517194 (UMLS CUI [2,4])
Elig.phs000867.v1.p1.2
Item
*Controls*: NGT controls for GWAS were selected from FUSION, including subjects from Vantaa, Finland, who were NGT at ages 65 and 70 years, and spouses of FUSION subjects, and from Finrisk 2002. Additional NGT controls for sequencing were selected from D2D 2004, Finrisk 1987, Health 2000, and the Savitaipale Diabetes Study. NGT was defined by WHO 1999 criteria of fasting glucose < 6.1 mmol/l and 2-h glucose < 7.8 mmol/l. Controls were frequency-matched to the cases as described in the sub-study descriptions.
boolean
C0009932 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
C0438251 (UMLS CUI [1,3])
Voltar ao início da página 

Contacto

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Ajuda

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