ID

45564

Descrizione

Principal Investigator: Dharambir Sanghera, PhD, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA MeSH: Diabetes Mellitus, Type 2,Obesity https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000583 The Punjabi Sikh population is a well-defined, carefully collected homogeneous sample from northern India and the US. It has unique characteristics, which are ideal for genetic studies. Sikhs are *strictly* a non-smoking population and about 50% of participants are life-long vegetarians. All subjects included in the genome-wide association studies (GWAS) were recruited from one geographical location. Our population demonstrates a strong familial clustering of type 2 diabetes and related cardio-metabolic disorders that may be genetic and we believe that the contribution of alleles at specific loci are likely to be unique to Punjabi Asians compared to Europeans. Our group first showed that the association of a common variant at rs9939609 in the *FTO* (fat mass and obesity) gene in South Asians was independent of BMI (PMID:18598350) in contrast to Europeans where the association of same variant with T2D is mediated through obesity (PMID:17434869). These findings were later confirmed in an independent sample of South Indians (PMID:19005641), Pakistanis (PMID:21294771), and even East and South Asians in a large meta-analyses study comprising 96,551 individuals (PMID: 22109280). Earlier reported association of *MTNR1B* with fasting glucose concentrations and type 2 diabetes in European GWAS could not be confirmed in our Sikh cohort. On the other hand, our study revealed, for the first time, a significant protective association of another less common variant in *MTNR1B* with fasting glucose levels that was modulated by obesity. Ours was the first report that suggested that the low CETP activity was associated with higher CAD risk (PMID:22143414) in South Asians and that the genetic effects are significantly modulated by environmental factors (alcohol consumption). Our recent GWAS on type 2 diabetes has identified a novel locus at chromosome 13q12 in the *SGCG* gene (p=1.82x10sup-8/sup) associated with type 2 diabetes (PMID:23300278) in Punjabi Sikhs. From these findings, we are optimistic that our resource will provide new insights to gene functions in the diabetic pathway and better help researchers to understand and translate these insights to novel therapeutic treatment and early prevention to T2D that may be important beyond Indians.

collegamento

https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000583

Keywords

  1. 13/01/23 13/01/23 - Nelly Zental
Titolare del copyright

Dharambir Sanghera, PhD, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA

Caricato su

13 gennaio 2023

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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dbGaP phs000583 Asian Indian Diabetic Heart Study (AIDHS)

Eligibility Criteria

Inclusion and exclusion criteria
Descrizione

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
*Inclusion:*
Descrizione

Elig.phs000583.v1.p1.1

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1512693
The study sample consists of individuals who self-reported no South Indian (Dravidian) admixture and membership in the North Indian Punjabi Sikh community. Punjabi families originating from Punjab (Pakistan or India), Haryana, Jammu and Kashmir were included. Only individuals who reported that all four rand grandparents were Punjabi Sikhs of North Indian origin, who had Punjabi surnames and who spoke the Punjabi language, were included.
Descrizione

Elig.phs000583.v1.p1.2

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3875091
UMLS CUI [1,2]
C0337471
UMLS CUI [1,3]
C0079946
UMLS CUI [1,4]
C0574343
UMLS CUI [1,5]
C1277063
UMLS CUI [1,6]
C0421448
UMLS CUI [1,7]
C0424925
UMLS CUI [1,8]
C0021201
*Exclusion:*
Descrizione

Elig.phs000583.v1.p1.3

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0680251
Excluded from the sample were half-siblings, adopted individuals, and individuals with type I diabetes (T1DM) or a family member with T1DM, the rare form of T2DM subtype (MODY), or secondary diabetes (e.g., hemochromatosis, pancreatitis). The selection of controls was based on a fasting glucose of <100.8 mg/dL or a 2h glucose <141.0 mg/dL. Subjects with impaired fasting glucose (IFG) or impaired glucose tolerance (IGT) were excluded when data were analyzed for association of variants with T2D.
Descrizione

Elig.phs000583.v1.p1.4

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0425382
UMLS CUI [1,2]
C0337505
UMLS CUI [2,1]
C0271637
UMLS CUI [2,2]
C0271636
UMLS CUI [3,1]
C0241889
UMLS CUI [3,2]
C0271637
UMLS CUI [3,3]
C0271636
UMLS CUI [4,1]
C0342276
UMLS CUI [5,1]
C0271640
UMLS CUI [6,1]
C0009932
UMLS CUI [6,2]
C5147071
UMLS CUI [6,3]
C0392201
UMLS CUI [6,4]
C0438251

Similar models

Eligibility Criteria

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000583.v1.p1.1
Item
*Inclusion:*
boolean
C1512693 (UMLS CUI [1,1])
Elig.phs000583.v1.p1.2
Item
The study sample consists of individuals who self-reported no South Indian (Dravidian) admixture and membership in the North Indian Punjabi Sikh community. Punjabi families originating from Punjab (Pakistan or India), Haryana, Jammu and Kashmir were included. Only individuals who reported that all four rand grandparents were Punjabi Sikhs of North Indian origin, who had Punjabi surnames and who spoke the Punjabi language, were included.
boolean
C3875091 (UMLS CUI [1,1])
C0337471 (UMLS CUI [1,2])
C0079946 (UMLS CUI [1,3])
C0574343 (UMLS CUI [1,4])
C1277063 (UMLS CUI [1,5])
C0421448 (UMLS CUI [1,6])
C0424925 (UMLS CUI [1,7])
C0021201 (UMLS CUI [1,8])
Elig.phs000583.v1.p1.3
Item
*Exclusion:*
boolean
C0680251 (UMLS CUI [1,1])
Elig.phs000583.v1.p1.4
Item
Excluded from the sample were half-siblings, adopted individuals, and individuals with type I diabetes (T1DM) or a family member with T1DM, the rare form of T2DM subtype (MODY), or secondary diabetes (e.g., hemochromatosis, pancreatitis). The selection of controls was based on a fasting glucose of <100.8 mg/dL or a 2h glucose <141.0 mg/dL. Subjects with impaired fasting glucose (IFG) or impaired glucose tolerance (IGT) were excluded when data were analyzed for association of variants with T2D.
boolean
C0425382 (UMLS CUI [1,1])
C0337505 (UMLS CUI [1,2])
C0271637 (UMLS CUI [2,1])
C0271636 (UMLS CUI [2,2])
C0241889 (UMLS CUI [3,1])
C0271637 (UMLS CUI [3,2])
C0271636 (UMLS CUI [3,3])
C0342276 (UMLS CUI [4,1])
C0271640 (UMLS CUI [5,1])
C0009932 (UMLS CUI [6,1])
C5147071 (UMLS CUI [6,2])
C0392201 (UMLS CUI [6,3])
C0438251 (UMLS CUI [6,4])

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