Literature DB >> 26678054

The Concordance and Heritability of Type 2 Diabetes in 34,166 Twin Pairs From International Twin Registers: The Discordant Twin (DISCOTWIN) Consortium.

Gonneke Willemsen1, Kirsten J Ward2, Christopher G Bell2, Kaare Christensen3, Jocelyn Bowden4, Christine Dalgård3, Jennifer R Harris5, Jaakko Kaprio6, Robert Lyle7, Patrik K E Magnusson8, Karen A Mather4, Juan R Ordoňana9, Francisco Perez-Riquelme10, Nancy L Pedersen8, Kirsi H Pietiläinen6, Perminder S Sachdev4, Dorret I Boomsma1, Tim Spector2.   

Abstract

Twin pairs discordant for disease may help elucidate the epigenetic mechanisms and causal environmental factors in disease development and progression. To obtain the numbers of pairs, especially monozygotic (MZ) twin pairs, necessary for in-depth studies while also allowing for replication, twin studies worldwide need to pool their resources. The Discordant Twin (DISCOTWIN) consortium was established for this goal. Here, we describe the DISCOTWIN Consortium and present an analysis of type 2 diabetes (T2D) data in nearly 35,000 twin pairs. Seven twin cohorts from Europe (Denmark, Finland, Norway, the Netherlands, Spain, Sweden, and the United Kingdom) and one from Australia investigated the rate of discordance for T2D in same-sex twin pairs aged 45 years and older. Data were available for 34,166 same-sex twin pairs, of which 13,970 were MZ, with T2D diagnosis based on self-reported diagnosis and medication use, fasting glucose and insulin measures, or medical records. The prevalence of T2D ranged from 2.6% to 12.3% across the cohorts depending on age, body mass index (BMI), and national diabetes prevalence. T2D discordance rate was lower for MZ (5.1%, range 2.9-11.2%) than for same-sex dizygotic (DZ) (8.0%, range 4.9-13.5%) pairs. Across DISCOTWIN, 720 discordant MZ pairs were identified. Except for the oldest of the Danish cohorts (mean age 79), heritability estimates based on contingency tables were moderate to high (0.47-0.77). From a meta-analysis of all data, the heritability was estimated at 72% (95% confidence interval 61-78%). This study demonstrated high T2D prevalence and high heritability for T2D liability across twin cohorts. Therefore, the number of discordant MZ pairs for T2D is limited. By combining national resources, the DISCOTWIN Consortium maximizes the number of discordant MZ pairs needed for in-depth genotyping, multi-omics, and phenotyping studies, which may provide unique insights into the pathways linking genes to the development of many diseases.

Entities:  

Keywords:  discordant twins; heterogeneity; international comparison; prevalence; type 2 diabetes

Mesh:

Year:  2015        PMID: 26678054     DOI: 10.1017/thg.2015.83

Source DB:  PubMed          Journal:  Twin Res Hum Genet        ISSN: 1832-4274            Impact factor:   1.587


  49 in total

1.  DNA methylation associated with healthy aging of elderly twins.

Authors:  Sangkyu Kim; Jennifer Wyckoff; Anne-T Morris; Annemarie Succop; Ally Avery; Glen E Duncan; S Michal Jazwinski
Journal:  Geroscience       Date:  2018-08-22       Impact factor: 7.713

Review 2.  Postpartum glucose intolerance: an updated overview.

Authors:  Ida Pastore; Eusebio Chiefari; Raffaella Vero; Antonio Brunetti
Journal:  Endocrine       Date:  2017-08-14       Impact factor: 3.633

Review 3.  The genetics of human ageing.

Authors:  David Melzer; Luke C Pilling; Luigi Ferrucci
Journal:  Nat Rev Genet       Date:  2019-11-05       Impact factor: 53.242

4.  Neurocognitive impairment in type 2 diabetes: evidence for shared genetic aetiology.

Authors:  Josephine Mollon; Joanne E Curran; Samuel R Mathias; Emma E M Knowles; Phoebe Carlisle; Peter T Fox; Rene L Olvera; Harald H H Göring; Amanda Rodrigue; Laura Almasy; Ravi Duggirala; John Blangero; David C Glahn
Journal:  Diabetologia       Date:  2020-02-04       Impact factor: 10.122

5.  Heritability of Type 2 Diabetes in the Washington State Twin Registry.

Authors:  Ally R Avery; Glen E Duncan
Journal:  Twin Res Hum Genet       Date:  2019-04       Impact factor: 1.587

6.  Assessment of the potential role of natural selection in type 2 diabetes and related traits across human continental ancestry groups: comparison of phenotypic with genotypic divergence.

Authors:  Robert L Hanson; Cristopher V Van Hout; Wen-Chi Hsueh; Alan R Shuldiner; Sayuko Kobes; Madhumita Sinha; Leslie J Baier; William C Knowler
Journal:  Diabetologia       Date:  2020-09-04       Impact factor: 10.122

7.  Mediation analysis in a case-control study when the mediator is a censored variable.

Authors:  Jian Wang; Jing Ning; Sanjay Shete
Journal:  Stat Med       Date:  2018-11-12       Impact factor: 2.373

8.  Estimation of indirect effect when the mediator is a censored variable.

Authors:  Jian Wang; Sanjay Shete
Journal:  Stat Methods Med Res       Date:  2017-01-30       Impact factor: 3.021

9.  In Silico Preliminary Association of Ammonia Metabolism Genes GLS, CPS1, and GLUL with Risk of Alzheimer's Disease, Major Depressive Disorder, and Type 2 Diabetes.

Authors:  Jeddidiah W D Griffin; Ying Liu; Patrick C Bradshaw; Kesheng Wang
Journal:  J Mol Neurosci       Date:  2018-02-13       Impact factor: 3.444

Review 10.  Dietary Fat and the Genetic Risk of Type 2 Diabetes.

Authors:  Germán D Carrasquilla; Hermina Jakupović; Tuomas O Kilpeläinen
Journal:  Curr Diab Rep       Date:  2019-11-04       Impact factor: 4.810

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