Hiroshi IKEGAMI Osaka University Graduate School of Medicine Genetics of type 1 diabetes in Japanese (similarity to and difference from Caucasian populations)

Slides:



Advertisements
Similar presentations
Identification of rheumatoid arthritis-associated PADI4, SLC22A4/A5, FCRL3 & PTPN22 International Symposium on Inflammatory Diseases of Barrier Organs.
Advertisements

Adiponectin: Understanding the regulation of a metabolically important protein hormone. Bethany Schaffer Personalized Medicine and Genomics May 29, 2012.
1 of 25 Sequence Variation in Ensembl. 2 of 25 Outline SNPs SNPs in Ensembl Linkage disequilibrium SNPs in BioMart DAS sources.
Understanding GWAS Chip Design – Linkage Disequilibrium and HapMap Peter Castaldi January 29, 2013.
Association Mapping David Evans. Outline Definitions / Terminology What is (genetic) association? How do we test for association? When to use association.
Applying haplotype models to association study design Natalie Castellana June 7, 2005.
Can genotyping help to diagnose coeliac disease?
Positional Cloning LOD Sib pairs Chromosome Region Association Study Genetics Genomics Physical Mapping/ Sequencing Candidate Gene Selection/ Polymorphism.
A dynamic program algorithm for haplotype block partitioning Zhang, et. al. (2002) PNAS. 99, 7335.
Genotype Susceptibility And Integrated Risk Factors for Complex Diseases Weidong Mao Dumitru Brinza Nisar Hundewale Stefan Gremalshi Alexander Zelikovsky.
SNP Selection University of Louisville Center for Genetics and Molecular Medicine January 10, 2008 Dana Crawford, PhD Vanderbilt University Center for.
Genetics of Diabetes and Its Complications: Layers of Complexity University of Pittsburgh October 23, 2001 Craig L. Hanis, Ph.D. Human Genetics Center.
GENETIC FACTORS IN DIABETES MELLITUS. Birmingham Study A random sample of 4886 birth. Comparison between the most valid data: 2432North European babies.
Lecture 22 Autoimmunity.
Introduction Basic Genetic Mechanisms Eukaryotic Gene Regulation The Human Genome Project Test 1 Genome I - Genes Genome II – Repetitive DNA Genome III.
Bernard Keavney Institute of Human Genetics University of Newcastle, UK. Recent developments in genetic epidemiology relevant to PURE.
Rs Vanessa Burns Gene 210 SNP. rs Involved in lung vascular development and skeletogenesis PrrX1-/- mice are embryonic lethal – Cleft palate.
Journal Club 埼玉医科大学 総合医療センター 内分泌・糖尿病内科 Department of Endocrinology and Diabetes, Saitama Medical Center, Saitama Medical University 松田 昌文 Matsuda, Masafumi.
Association study of 5-HT2A genes with schizophrenia in the Malaysian population: A Multiethnic Meta- analysis Study Shiau Foon Tee* 1, Tze Jen Chow 1,
Case(Control)-Free Multi-SNP Combinations in Case-Control Studies Dumitru Brinza and Alexander Zelikovsky Combinatorial Search (CS) for Disease-Association:
The genetic bases BY Casey Jaroche
A single-nucleotide polymorphism tagging set for human drug metabolism and transport Kourosh R Ahmadi, Mike E Weale, Zhengyu Y Xue, Nicole Soranzo, David.
Chapter 25 Chapter 25 Genetic Determinants of Osteoporosis Copyright © 2013 Elsevier Inc. All rights reserved.
Figure S1. Quantile-quantile plot in –log10 scale for the individual studies The red line represents concordance of observed and expected values. The shaded.
Introduction : Recent progress of genetic studies in rheumatology JCR 2009 April 24, 2009 Tokyo, Japan IMS-UT Ryo Yamada.
Biology 101 DNA: elegant simplicity A molecule consisting of two strands that wrap around each other to form a “twisted ladder” shape, with the.
Molecular & Genetic Epi 217 Association Studies
CS177 Lecture 10 SNPs and Human Genetic Variation
NAD(P)H: Quinone Oxidoreductase 1 (NQO1) Pro187Ser Polymorphism and the Risk of Lung Cancer: A Meta-Analysis Chun Chao, Zuo-Feng Zhang, Julien Berthiller,
Two RANTES gene polymorphisms and their haplotypes in patients with myocardial infarction from two Slavonic populations Two RANTES gene polymorphisms and.
10/07/08 Journal Club Simone Sanna-Cherchi. OUTLINE Basis of Admixture Mapping as strategy do identify disease-associated genes Papers Implications.
BGRS 2006 SEARCH FOR MULTI-SNP DISEASE ASSOCIATION D. Brinza, A. Perelygin, M. Brinton and A. Zelikovsky Georgia State University, Atlanta, GA, USA 123.
Complement Factor H Polymorphism in Age- Related Macular Degeneration* *Klein RJ, et al. Science. 2005; 308:
Host genetic diversity Genome-wide approaches. Affected sib analysis Take full sibs, preferably of the same sex should share many environmental variables.
Risk Prediction of Complex Disease David Evans. Genetic Testing and Personalized Medicine Is this possible also in complex diseases? Predictive testing.
H.J. Muller. T. Dobzhansky Mutation Rates at Human STR Loci, Measured in Paternity Tests STR SystemMaternal Meioses (%)Paternal Meioses (%) TH015/42100.
Genetic Testing and the Prevention of Type 1 Diabetes Janice S. Dorman, Ph.D. September 4, 2001.
Role of CTLA-4 polymorphism in susceptibility to type 1 diabetes: Results of a family and a case-control study in Southern Tunisia Immunology Department,
Design and Validation of Methods Searching for Risk Factors in Genotype Case- Control Studies Dumitru Brinza Alexander Zelikovsky Department of Computer.
Genetic Association Study Principles: Andrew C. Heath.
KAWASAKI DISEASE RISK-ASSOCIATED SNPS As Identified by Lee et al., 2012 Jennifer Przybylo.
Admixture Mapping Controlled Crosses Are Often Used to Determine the Genetic Basis of Differences Between Populations. When controlled crosses are not.
Gene-based Large Scale LD-mapping of Rheumatoid Arthritis-associated Genes and Variation in Associated Polymorphisms Among Ethnic Groups PADI4, SLC22A4/A5.
DRD2 Gene in Alcohol Dependence 국립중앙의료원 이 소 희. Background Dopamine – Reward behavior (Wise & Rompre, 1989) – Alcoholism Mesolimbic dopamine system – 5.
Date of download: 5/27/2016 Copyright © The American College of Cardiology. All rights reserved. From: Causal Assessment of Serum Urate Levels in Cardiometabolic.
R2. 하효정 / 윤휘중 교수님 NEJM Introduction  Transplantation of hematopoietic cells  acute GVHD ?  The recipient and donor are HLA-DPB1–mismatched.
EBF FLJ31951UBLCP1 IL12B B36 Position Genes LD Regions Genotyped Markers Chr5 (q33.3) rs rs Figure 1. Physical map of 360kb around IL12B.
SCANNING OF CANDIDATE GENES FOR THE SUSCEPTIBILITY OF KAWASAKI DISEASE IN THE HLA REGION Lee JK, Kim JJ, Kim S, Choi IH, Kim KJ, Hong SJ, Seo EJ, Yoo HW,
Genetic Analysis in Human Disease Kim R. Simpfendorfer, PhD Robert S.Boas Center for Genomics & Human Genetics The Feinstein Institute for Medical Research.
1 Finding disease genes: A challenge for Medicine, Mathematics and Computer Science Andrew Collins, Professor of Genetic Epidemiology and Bioinformatics.
Date of download: 11/12/2016 Copyright © 2016 American Medical Association. All rights reserved. From: Influence of Child Abuse on Adult DepressionModeration.
Student of Cellular and Molecular biology
Copyright © 2014 American Medical Association. All rights reserved.
Genetics of common complex diseases: a view from Iceland
Xiaole Shirley Liu STAT115/STAT215/
ASSOCIATIONS BETWEEN ANXA11 RS C/T, BTNL2 RS G/A, HLA CLASS I AND II POLYMORPHISMS AND SARCOIDOSIS EVOLUTION Manuel Vaz1, Bruno Lima2, Natália.
Come my friend. Let’s forget the cares of tomorrow
Case Study #2 Session 1, Day 3, Liu
Association of functional genetic variants of CTLA4 with reduced serum CTLA4 protein levels and increased risk of idiopathic recurrent miscarriages  Maneesh.
Figure 1 Allele frequency and effect size for ALS-associated genes
Genetic Testing and the Prevention of Type 1 Diabetes
Host genetic diversity
Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population  S. Maeda, N. Osawa, T. Hayashi, S. Tsukada, M.
Emily C. Walsh, Kristie A. Mather, Stephen F
A Flexible Bayesian Framework for Modeling Haplotype Association with Disease, Allowing for Dominance Effects of the Underlying Causative Variants  Andrew.
The Genetic of Earwax Wet earwax is a dominant allele!
Figure 2 LocusZoom plots
Table 2 Rs number, gene, OR, 95% CI, and permutation p value for the statistical significant variants resulted from allelic association analysis association.
Benjamin A. Rybicki, José L. Walewski, Mary J
CaQTL analysis identifies genetic variants affecting human islet cis-RE use. caQTL analysis identifies genetic variants affecting human islet cis-RE use.
Presentation transcript:

Hiroshi IKEGAMI Osaka University Graduate School of Medicine Genetics of type 1 diabetes in Japanese (similarity to and difference from Caucasian populations) IDS8, Awaji Yumebutai ( October 8, 2005 )

General populationSibling Japanese0.01 ~ 0.02% Caucasian0.4 % Caucasian6% ( s = 15) ? Familiar clustering of type 1 diabetes Japanese3.8%( s > 100) Ikegami H et al. Endocrine J 1996

Susceptibility genes for type 1 diabetes Major gene : HLA(IDDM1)  -cell specificity : INS(IDDM2) negative regulator : CTLA4(IDDM12) SUMO4(IDDM5) PTPN22

Association of DRB1 alleles with type 1 diabetes Type 1 diabetesControlsORP (n=264)(n=314) DRB1 * %17.2%2.45 < * %13.1% * %14.6%0.11 < Kawabata Y et al. Diabetes 51: , 2002

JapaneseDRB1*0405-DQB1*0401 (DR4) DRB1*0901-DQB1*0303 (DR9) CaucasiansDRB1*0301-DQB1*0201 (DR3) DRB1*0401-DQB1*0302 (DR4) Disease susceptible HLA-haplotypes

JapaneseCaucasian DRB1-DQB1 Type 1 diabetes HF 1) Type 1 diabetes HF haplotype susceptibility susceptibility DRB1*0405-DQB1*0401 susceptiblepresent unknown rare DRB1*0901-DQB1*0303 susceptiblepresent unknownrare DRB1*0301-DQB1*0201 unknownraresusceptiblepresent DRB1*0401-DQB1*0302 unknownraresusceptiblepresent DRB1*1501-DQB1*0602 protectivepresentprotectivepresent Different haplotypes are associated with type 1 diabetes in Japanese and Caucasian populations 1)HF: Haplotype frequency,

JapaneseDRB1*0405-DQB1*0401 (DR4) DRB1*0901-DQB1*0303 (DR9) CaucasiansDRB1*0301-DQB1*0201 (DR3) DRB1*0401-DQB1*0302 (DR4) Very high risk genotype DRB1*0301 /0401 (DR3/4) High risk genotypes for type 1 diabetes (Caucasians)

Kawabata Y et al. Diabetes 51: , Odds Ratio DRB1*0405 / DRB1* DRB1*0405 / X 2.8 DRB1*0901 / DRB1*0901 DRB1*0901 / Y Disease-associated genotypes in Japanese ( DRB1*0405 vs. DRB1*0901 haplotype )

JapaneseDRB1*0405-DQB1*0401 (DR4) DRB1*0901-DQB1*0303 (DR9) CaucasiansDRB1*0301-DQB1*0201 (DR3) DRB1*0401-DQB1*0302 (DR4) Very high risk genotype ( Japanese ) DRB1*0901 /0901 (DR9/9) High risk genotypes for type 1 diabetes (Japanese)

JapaneseDRB1*0405-DQB1*0401 (DR4) DRB1*0901-DQB1*0303 (DR9) CaucasiansDRB1*0301-DQB1*0201 (DR3) DRB1*0401-DQB1*0302 (DR4) HLA haplotypes associated with type 1 diabetes KoreanDRB1*0301-DQB1*0201 (DR3) DRB1*0405-DQB1*0401 (DR4) DRB1*0901-DQB1*0303 (DR9)

DR9 homozygosity confers susceptibility to type 1 diabetes DR4DR Odds ratio :homo :hetero JapaneseKorean JapaneseKorean Kawabata Y et al. Diabetes 51: , 2002

Susceptibility genes for type 1 diabetes Major gene : HLA(IDDM1)  -cell specificity : INS(IDDM2) negative regulator : CTLA4(IDDM12) SUMO4(IDDM5)

Association of INS-VNTR with type 1 diabetes -596 VNTR -23 HphI 4.1 kb region of IDDM2 Class IIIhaplotype Class III  protective Class Ihaplotype Class I + susceptible TH INS IGF2 VNTR Type 1 diabetes susceptibility

Frequency of class I INS-VNTR tended to be higher in type 1 diabetes than in controls Controls CasesOdds ratio France 1 55%84%4.2 UK 2 59%76%2.2 Japan 3 94%99% 1 Lucassen et al.Nature Genet 4:305, Bennet et al.Nature Genet 9:284, Kawaguchi et al. BBRC 233:283, 1997

Susceptibility genes for type 1 diabetes Major gene : HLA(IDDM1)  -cell specificity : INS(IDDM2) negative regulator : CTLA4(IDDM12) PTPN22 SUMO4(IDDM5)

NATURE |VOL 423 | 29 MAY 2003 |

Association of CTLA4 with autoimmune diseases (Caucasian populations) Odds ratio(95% CI) Graves’s disease1.51( ) Hashimoto thyroiditis1.45( ) Type 1 diabetes1.14( ) SNP: +6230G>A (rs ) Ueda H et al. Nature 2003

Arg620Trp (R620W) of PTPN22 was consistently reported to be associated with autoimmune diseases in Caucasian populations Odds ratio (95%CI) Type 1 diabetesN. American ( ) Italian ( ) UK ( ) Caucasian 3 (C/T)1.7( ) (T/T)3.4( ) Graves's disease ( ) RA ( ) SLE 5 (C/T)1.37 ( ) (T/T)4.37 ( ) 1 Nat Genet 36:337, 2004, 2 Diabetes 53:3020, 2004, 3 Diabetes 54:906, Am J Hum Genet 75:330, 2004, 5 Am J Hum Genet 75:504, 2004

estimated by EM algorithm ( Haploview v2.03 ) SUMO4 2176bp M55V MAP3K7IP2 Exon 7 Exon 6 438C>T -504A>GM55V438C>Tfrequency Haplotype AGAC49.6% Haplotype BAGT35.9% Haplotype CAAC14.4% -504A>G D’: 1.0 for single pair of SNPs SUMO4 SNPs identified by re-sequencing in Japanese

SUMO4 ( M55V ) is associated with type 1 diabetes (Japanese and Koreans) *Mantel-Haenszel test CasesControlsOR(95%CI)p (n=541)(n=743) Japanese59% 50% Koreans58%44%1.46 ( )0.0008* Noso S et al. Poster #098 Diabetes ( in press)

Asian, Guo et al. 2004* Korean, Park et al Japanese, Noso et al Korean, Noso et al Caucasian, Guo et al UK, Smyth et al. 2005* Canadian, Paterson et al Meta-analysis

Asian, Guo et al. 2004* Korean, Park et al Japanese, Noso et al Korean, Noso et al Caucasian, Guo et al UK, Smyth et al. 2005* Canadian, Paterson et al Total (n=28,151) Meta-analysis Asian (n=4720) Caucasian (n=23,431) Summary OR:1.29 [95%CI: ] p = 4.0 x Summary OR:1.02 (95%CI: ) p = 0.25 (NS) p value against homogeneity 0.16 (NS)

%CI ( Caucasian) 95%CI ( Asian) Total (n=28,151) Meta-analysis Asian, Guo et al. 2004* Korean, Park et al Japanese, Noso et al Korean, Noso et al Asian (n=4720) Caucasian, Guo et al UK, Smyth et al. 2005* Canadian, Paterson et al Caucasian (n=23,431) Summary OR:1.29 [95%CI: ] p = 4.0 x Summary OR:1.02 (95%CI: ) p = 0.25 (NS) SUMO4 M55V is associated with type 1 diabetes in Asians, but not in Caucasians. Noso S et al. Poster #098 Diabetes ( in press)

Reasons for apparent differences in susceptibility alleles for type 1 diabetes between Japanese and Caucasian populations Association Reasons for apparent Caucasian Japanese difference HLAyesyes allele difference INSyesyes allele frequency CTLA4yesrestricted clinical subtype PTPN22yes unknown allele absent SUMO4? yes heterogeneity?