-
Články
- Časopisy
- Kurzy
- Témy
- Kongresy
- Videa
- Podcasty
Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in and Enrichment for Risk Variants in Lean Compared to Obese Cases
Common diseases such as type 2 diabetes are phenotypically heterogeneous. Obesity is a major risk factor for type 2 diabetes, but patients vary appreciably in body mass index. We hypothesized that the genetic predisposition to the disease may be different in lean (BMI<25 Kg/m2) compared to obese cases (BMI≥30 Kg/m2). We performed two case-control genome-wide studies using two accepted cut-offs for defining individuals as overweight or obese. We used 2,112 lean type 2 diabetes cases (BMI<25 kg/m2) or 4,123 obese cases (BMI≥30 kg/m2), and 54,412 un-stratified controls. Replication was performed in 2,881 lean cases or 8,702 obese cases, and 18,957 un-stratified controls. To assess the effects of known signals, we tested the individual and combined effects of SNPs representing 36 type 2 diabetes loci. After combining data from discovery and replication datasets, we identified two signals not previously reported in Europeans. A variant (rs8090011) in the LAMA1 gene was associated with type 2 diabetes in lean cases (P = 8.4×10−9, OR = 1.13 [95% CI 1.09–1.18]), and this association was stronger than that in obese cases (P = 0.04, OR = 1.03 [95% CI 1.00–1.06]). A variant in HMG20A—previously identified in South Asians but not Europeans—was associated with type 2 diabetes in obese cases (P = 1.3×10−8, OR = 1.11 [95% CI 1.07–1.15]), although this association was not significantly stronger than that in lean cases (P = 0.02, OR = 1.09 [95% CI 1.02–1.17]). For 36 known type 2 diabetes loci, 29 had a larger odds ratio in the lean compared to obese (binomial P = 0.0002). In the lean analysis, we observed a weighted per-risk allele OR = 1.13 [95% CI 1.10–1.17], P = 3.2×10−14. This was larger than the same model fitted in the obese analysis where the OR = 1.06 [95% CI 1.05–1.08], P = 2.2×10−16. This study provides evidence that stratification of type 2 diabetes cases by BMI may help identify additional risk variants and that lean cases may have a stronger genetic predisposition to type 2 diabetes.
Vyšlo v časopise: Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in and Enrichment for Risk Variants in Lean Compared to Obese Cases. PLoS Genet 8(5): e32767. doi:10.1371/journal.pgen.1002741
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1002741Souhrn
Common diseases such as type 2 diabetes are phenotypically heterogeneous. Obesity is a major risk factor for type 2 diabetes, but patients vary appreciably in body mass index. We hypothesized that the genetic predisposition to the disease may be different in lean (BMI<25 Kg/m2) compared to obese cases (BMI≥30 Kg/m2). We performed two case-control genome-wide studies using two accepted cut-offs for defining individuals as overweight or obese. We used 2,112 lean type 2 diabetes cases (BMI<25 kg/m2) or 4,123 obese cases (BMI≥30 kg/m2), and 54,412 un-stratified controls. Replication was performed in 2,881 lean cases or 8,702 obese cases, and 18,957 un-stratified controls. To assess the effects of known signals, we tested the individual and combined effects of SNPs representing 36 type 2 diabetes loci. After combining data from discovery and replication datasets, we identified two signals not previously reported in Europeans. A variant (rs8090011) in the LAMA1 gene was associated with type 2 diabetes in lean cases (P = 8.4×10−9, OR = 1.13 [95% CI 1.09–1.18]), and this association was stronger than that in obese cases (P = 0.04, OR = 1.03 [95% CI 1.00–1.06]). A variant in HMG20A—previously identified in South Asians but not Europeans—was associated with type 2 diabetes in obese cases (P = 1.3×10−8, OR = 1.11 [95% CI 1.07–1.15]), although this association was not significantly stronger than that in lean cases (P = 0.02, OR = 1.09 [95% CI 1.02–1.17]). For 36 known type 2 diabetes loci, 29 had a larger odds ratio in the lean compared to obese (binomial P = 0.0002). In the lean analysis, we observed a weighted per-risk allele OR = 1.13 [95% CI 1.10–1.17], P = 3.2×10−14. This was larger than the same model fitted in the obese analysis where the OR = 1.06 [95% CI 1.05–1.08], P = 2.2×10−16. This study provides evidence that stratification of type 2 diabetes cases by BMI may help identify additional risk variants and that lean cases may have a stronger genetic predisposition to type 2 diabetes.
Zdroje
1. VoightBFScottLJSteinthorsdottirVMorrisAPDinaC 2010 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet 42 579 589
2. DupuisJLangenbergCProkopenkoISaxenaRSoranzoN 2010 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet 42 105 116
3. QiLCornelisMCKraftPStanyaKJLinda KaoWH 2010 Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. Hum Mol Genet 19 2706 2715
4. TsaiFJYangCFChenCCChuangLMLuCH 2010 A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. PLoS Genet 6 e1000847 doi:10.1371/journal.pgen.1000847
5. YamauchiTHaraKMaedaSYasudaKTakahashiA 2010 A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B. Nat Genet 42 864 868
6. ShuXOLongJCaiQQiLXiangYB 2010 Identification of new genetic risk variants for type 2 diabetes. PLoS Genet 6 e1001127 doi:10.1371/journal.pgen.1001127
7. KoonerJSSaleheenDSimXSehmiJZhangW 2011 Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. Nat Genet
8. LyssenkoVNagornyCLErdosMRWierupNJonssonA 2009 Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion. Nat Genet 41 82 88
9. ProkopenkoILangenbergCFlorezJCSaxenaRSoranzoN 2009 Variants in MTNR1B influence fasting glucose levels. Nat Genet 41 77 81
10. FreathyRMMook-KanamoriDOSovioUProkopenkoITimpsonNJ 2010 Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nat Genet 42 430 435
11. PerryJRWeedonMNLangenbergCJacksonAULyssenkoV 2010 Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes. Hum Mol Genet 19 535 544
12. TuomiTCarlssonALiHIsomaaBMiettinenA 1999 Clinical and genetic characteristics of type 2 diabetes with and without GAD antibodies. Diabetes 48 150 157
13. PearsonERFlechtnerINjolstadPRMaleckiMTFlanaganSE 2006 Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations. N Engl J Med 355 467 477
14. TimpsonNJLindgrenCMWeedonMNRandallJOuwehandWH 2009 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. Diabetes 58 505 510
15. CauchiSNeadKTChoquetHHorberFPotocznaN 2008 The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies. BMC Med Genet 9 45
16. CauchiSChoquetHGutierrez-AguilarRCapelFGrauK 2008 Effects of TCF7L2 polymorphisms on obesity in European populations. Obesity (Silver Spring) 16 476 482
17. GueyLTKravicJMelanderOBurttNPLaramieJM 2011 Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants. Genet Epidemiol
18. SpeliotesEKWillerCJBerndtSIMondaKLThorleifssonG 2010 Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet 42 937 948
19. ZhouKBellenguezCSpencerCCBennettAJColemanRL 2011 Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. Nat Genet 43 117 120
20. SoranzoNSannaSWheelerEGiegerCRadkeD 2010 Common variants at 10 genomic loci influence hemoglobin A(C) levels via glycemic and nonglycemic pathways. Diabetes 59 3229 3239
21. SaxenaRHivertMFLangenbergCTanakaTPankowJS 2010 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Nat Genet 42 142 148
22. GoringHHCurranJEJohnsonMPDyerTDCharlesworthJ 2007 Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes. Nat Genet 39 1208 1216
23. IdaghdourYCzikaWShiannaKVLeeSHVisscherPM 2010 Geographical genomics of human leukocyte gene expression variation in southern Morocco. Nat Genet 42 62 67
24. HeapGATrynkaGJansenRCBruinenbergMSwertzMA 2009 Complex nature of SNP genotype effects on gene expression in primary human leucocytes. BMC Med Genomics 2 1
25. DixonALLiangLMoffattMFChenWHeathS 2007 A genome-wide association study of global gene expression. Nat Genet 39 1202 1207
26. StrangerBENicaACForrestMSDimasABirdCP 2007 Population genomics of human gene expression. Nat Genet 39 1217 1224
27. KwanTBenovoyDDiasCGurdSProvencherC 2008 Genome-wide analysis of transcript isoform variation in humans. Nat Genet 40 225 231
28. HeinzenELGeDCroninKDMaiaJMShiannaKV 2008 Tissue-specific genetic control of splicing: implications for the study of complex traits. PLoS Biol 6 e1 doi:10.1371/journal.pbio.1000001
29. ZellerTWildPSzymczakSRotivalMSchillertA 2010 Genetics and beyond–the transcriptome of human monocytes and disease susceptibility. PLoS ONE 5 e10693 doi:10.1371/journal.pone.0010693
30. EmilssonVThorleifssonGZhangBLeonardsonASZinkF 2008 Genetics of gene expression and its effect on disease. Nature 452 423 428
31. GreenawaltDMDobrinRChudinEHatoumIJSuverC 2011 A survey of the genetics of stomach, liver, and adipose gene expression from a morbidly obese cohort. Genome Res 21 1008 1016
32. KompassKSWitteJS 2011 Co-regulatory expression quantitative trait loci mapping: method and application to endometrial cancer. BMC Med Genomics 4 6
33. WebsterJAGibbsJRClarkeJRayMZhangW 2009 Genetic control of human brain transcript expression in Alzheimer disease. Am J Hum Genet 84 445 458
34. SchadtEEMolonyCChudinEHaoKYangX 2008 Mapping the genetic architecture of gene expression in human liver. PLoS Biol 6 e107 doi:10.1371/journal.pbio.0060107
35. InnocentiFCooperGMStanawayIBGamazonERSmithJD 2011 Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue. PLoS Genet 7 e1002078 doi:10.1371/journal.pgen.1002078
36. GrundbergEKwanTGeBLamKCKokaV 2009 Population genomics in a disease targeted primary cell model. Genome Res 19 1942 1952
37. DingJGudjonssonJELiangLStuartPELiY 2010 Gene expression in skin and lymphoblastoid cells: Refined statistical method reveals extensive overlap in cis-eQTL signals. Am J Hum Genet 87 779 789
38. DimasASDeutschSStrangerBEMontgomerySBBorelC 2009 Common regulatory variation impacts gene expression in a cell type-dependent manner. Science 325 1246 1250
39. HanBEskinE 2011 Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies. Am J Hum Genet 88 586 598
40. AntinozziPAGarcia-DiazAHuCRothmanJE 2006 Functional mapping of disease susceptibility loci using cell biology. Proc Natl Acad Sci U S A 103 3698 3703
41. JiangFXHarrisonLC 2005 Convergence of bone morphogenetic protein and laminin-1 signaling pathways promotes proliferation and colony formation by fetal mouse pancreatic cells. Exp Cell Res 308 114 122
42. VasirBAielloLPYoonKHQuickelRRBonner-WeirS 1998 Hypoxia induces vascular endothelial growth factor gene and protein expression in cultured rat islet cells. Diabetes 47 1894 1903
43. Bonner-WeirSTanejaMWeirGCTatarkiewiczKSongKH 2000 In vitro cultivation of human islets from expanded ductal tissue. Proc Natl Acad Sci U S A 97 7999 8004
44. GaoRUstinovJPulkkinenMALundinKKorsgrenO 2003 Characterization of endocrine progenitor cells and critical factors for their differentiation in human adult pancreatic cell culture. Diabetes 52 2007 2015
45. JiangFXGeorges-LabouesseEHarrisonLC 2001 Regulation of laminin 1-induced pancreatic beta-cell differentiation by alpha6 integrin and alpha-dystroglycan. Mol Med 7 107 114
46. JiangFXCramDSDeAizpuruaHJHarrisonLC 1999 Laminin-1 promotes differentiation of fetal mouse pancreatic beta-cells. Diabetes 48 722 730
47. GeutskensSBHomo-DelarcheFPleauJMDurantSDrexhageHA 2004 Extracellular matrix distribution and islet morphology in the early postnatal pancreas: anomalies in the non-obese diabetic mouse. Cell Tissue Res 318 579 589
48. HuCOliverJAGoldbergMRAl-AwqatiQ 2001 LRP: a new adhesion molecule for endothelial and smooth muscle cells. Am J Physiol Renal Physiol 281 F739 750
49. WilliamsRCMullerYLHansonRLKnowlerWCMasonCC 2011 HLA-DRB1 reduces the risk of type 2 diabetes mellitus by increased insulin secretion. Diabetologia 54 1684 1692
Štítky
Genetika Reprodukčná medicína
Článek Functional Centromeres Determine the Activation Time of Pericentric Origins of DNA Replication inČlánek Dynamic Deposition of Histone Variant H3.3 Accompanies Developmental Remodeling of the TranscriptomeČlánek Integrin α PAT-2/CDC-42 Signaling Is Required for Muscle-Mediated Clearance of Apoptotic Cells inČlánek Prdm5 Regulates Collagen Gene Transcription by Association with RNA Polymerase II in Developing BoneČlánek Acquisition Order of Ras and p53 Gene Alterations Defines Distinct Adrenocortical Tumor Phenotypes
Článok vyšiel v časopisePLOS Genetics
Najčítanejšie tento týždeň
2012 Číslo 5- Gynekologové a odborníci na reprodukční medicínu se sejdou na prvním virtuálním summitu
- Je „freeze-all“ pro všechny? Odborníci na fertilitu diskutovali na virtuálním summitu
-
Všetky články tohto čísla
- Slowing Replication in Preparation for Reduction
- Chromosome Pairing: A Hidden Treasure No More
- Loss of Imprinting Differentially Affects REM/NREM Sleep and Cognition in Mice
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Regulation by the Noncoding RNA
- UDP-Galactose 4′-Epimerase Activities toward UDP-Gal and UDP-GalNAc Play Different Roles in the Development of
- Deletion of PTH Rescues Skeletal Abnormalities and High Osteopontin Levels in Mice
- Karyotypic Determinants of Chromosome Instability in Aneuploid Budding Yeast
- Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene:
- MicroRNA-277 Modulates the Neurodegeneration Caused by Fragile X Premutation rCGG Repeats
- Functional Centromeres Determine the Activation Time of Pericentric Origins of DNA Replication in
- Dynamic Deposition of Histone Variant H3.3 Accompanies Developmental Remodeling of the Transcriptome
- Scientist Citizen: An Interview with Bruce Alberts
- YY1 Regulates Melanocyte Development and Function by Cooperating with MITF
- Congenital Heart Disease–Causing Gata4 Mutation Displays Functional Deficits
- Recombination Drives Vertebrate Genome Contraction
- KATNAL1 Regulation of Sertoli Cell Microtubule Dynamics Is Essential for Spermiogenesis and Male Fertility
- Re-Patterning Sleep Architecture in through Gustatory Perception and Nutritional Quality
- Using Whole-Genome Sequence Data to Predict Quantitative Trait Phenotypes in
- Genome-Wide Analysis of GLD-1–Mediated mRNA Regulation Suggests a Role in mRNA Storage
- Meiotic Chromosome Pairing Is Promoted by Telomere-Led Chromosome Movements Independent of Bouquet Formation
- LINT, a Novel dL(3)mbt-Containing Complex, Represses Malignant Brain Tumour Signature Genes
- The H3K27 Demethylase UTX-1 Is Essential for Normal Development, Independent of Its Enzymatic Activity
- Suppresses Senescence Programs and Thereby Accelerates and Maintains Mutant -Induced Lung Tumorigenesis
- Genome-Wide Association of Pericardial Fat Identifies a Unique Locus for Ectopic Fat
- An Essential Role for Katanin p80 and Microtubule Severing in Male Gamete Production
- Identification of Genes That Promote or Antagonize Somatic Homolog Pairing Using a High-Throughput FISH–Based Screen
- Principles of Carbon Catabolite Repression in the Rice Blast Fungus: Tps1, Nmr1-3, and a MATE–Family Pump Regulate Glucose Metabolism during Infection
- Integrin α PAT-2/CDC-42 Signaling Is Required for Muscle-Mediated Clearance of Apoptotic Cells in
- Histone H3 Localizes to the Centromeric DNA in Budding Yeast
- Collapse of Telomere Homeostasis in Hematopoietic Cells Caused by Heterozygous Mutations in Telomerase Genes
- Hypersensitive to Red and Blue 1 and Its Modification by Protein Phosphatase 7 Are Implicated in the Control of Arabidopsis Stomatal Aperture
- Extent, Causes, and Consequences of Small RNA Expression Variation in Human Adipose Tissue
- TBC-8, a Putative RAB-2 GAP, Regulates Dense Core Vesicle Maturation in
- Regulating Repression: Roles for the Sir4 N-Terminus in Linker DNA Protection and Stabilization of Epigenetic States
- Common Genetic Determinants of Intraocular Pressure and Primary Open-Angle Glaucoma
- Prdm5 Regulates Collagen Gene Transcription by Association with RNA Polymerase II in Developing Bone
- Fitness Landscape Transformation through a Single Amino Acid Change in the Rho Terminator
- Repeated, Selection-Driven Genome Reduction of Accessory Genes in Experimental Populations
- Allelic Variation and Differential Expression of the mSIN3A Histone Deacetylase Complex Gene Promote Mammary Tumor Growth and Metastasis
- DNA Demethylation and USF Regulate the Meiosis-Specific Expression of the Mouse
- Knowledge-Driven Analysis Identifies a Gene–Gene Interaction Affecting High-Density Lipoprotein Cholesterol Levels in Multi-Ethnic Populations
- A Duplication CNV That Conveys Traits Reciprocal to Metabolic Syndrome and Protects against Diet-Induced Obesity in Mice and Men
- EMT Inducers Catalyze Malignant Transformation of Mammary Epithelial Cells and Drive Tumorigenesis towards Claudin-Low Tumors in Transgenic Mice
- Inactivation of a Novel FGF23 Regulator, FAM20C, Leads to Hypophosphatemic Rickets in Mice
- Genome-Wide Association for Abdominal Subcutaneous and Visceral Adipose Reveals a Novel Locus for Visceral Fat in Women
- Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in and Enrichment for Risk Variants in Lean Compared to Obese Cases
- New Insight into the History of Domesticated Apple: Secondary Contribution of the European Wild Apple to the Genome of Cultivated Varieties
- Activated Cdc42 Kinase Has an Anti-Apoptotic Function
- The Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in a Down Syndrome Mouse Model
- COP9 Signalosome Integrity Plays Major Roles for Hyphal Growth, Conidial Development, and Circadian Function
- Bmps and Id2a Act Upstream of Twist1 To Restrict Ectomesenchyme Potential of the Cranial Neural Crest
- Psip1/Ledgf p52 Binds Methylated Histone H3K36 and Splicing Factors and Contributes to the Regulation of Alternative Splicing
- The Number of X Chromosomes Causes Sex Differences in Adiposity in Mice
- Target Gene Analysis by Microarrays and Chromatin Immunoprecipitation Identifies HEY Proteins as Highly Redundant bHLH Repressors
- Acquisition Order of Ras and p53 Gene Alterations Defines Distinct Adrenocortical Tumor Phenotypes
- ELK1 Uses Different DNA Binding Modes to Regulate Functionally Distinct Classes of Target Genes
- Histone H1 Depletion Impairs Embryonic Stem Cell Differentiation
- IDN2 and Its Paralogs Form a Complex Required for RNA–Directed DNA Methylation
- Separation of DNA Replication from the Assembly of Break-Competent Meiotic Chromosomes
- Genomic Hypomethylation in the Human Germline Associates with Selective Structural Mutability in the Human Genome
- PLOS Genetics
- Archív čísel
- Aktuálne číslo
- Informácie o časopise
Najčítanejšie v tomto čísle- Inactivation of a Novel FGF23 Regulator, FAM20C, Leads to Hypophosphatemic Rickets in Mice
- Genome-Wide Association of Pericardial Fat Identifies a Unique Locus for Ectopic Fat
- Slowing Replication in Preparation for Reduction
- An Essential Role for Katanin p80 and Microtubule Severing in Male Gamete Production
Prihlásenie#ADS_BOTTOM_SCRIPTS#Zabudnuté hesloZadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.
- Časopisy