Literature DB >> 13680298

Power of association test for detecting minor histocompatibility gene causing graft-versus-host disease following bone marrow transplantation [correction].

Jun Ohashi1,2, Etsuko Maruya3, Katsushi Tokunaga4, Hiroh Saji3.   

Abstract

Incompatibility of minor histocompatibility antigen (mHa) is a major cause of acute graft-versus-host disease (GVHD) following bone marrow transplantation in human leukocyte antigen (HLA)-matched donor-recipient pairs. To avoid acute GVHD, as many mHa genes as possible need to be identified. In this study, we introduce a comparison of two proportions as an association test for detecting mHa genes in HLA-matched pairs with and without GVHD. Assuming multiple mHa loci, each with two alleles, we evaluated the effects of (1). minor allele frequency of the mHa locus of interest (denoted by p), and (2). probability of GVHD developing in a donor-recipient pair being incompatible at an mHa locus (denoted by r) on the powers of association tests for unrelated pairs and for sib pairs. Our results showed that based on a candidate gene approach, an mHa gene with high p and r values can be detected by the association test with a small sample size. Application of the present method to the Japanese population revealed that the association test for unrelated pairs is more suitable for detecting an mHa gene with a high r value than that for sib pairs. The present method will be helpful to researchers who evaluate the power of association study in advance.

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Year:  2003        PMID: 13680298     DOI: 10.1007/s10038-003-0065-8

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  16 in total

1.  Comparison of statistical power between 2 * 2 allele frequency and allele positivity tables in case-control studies of complex disease genes.

Authors:  J Ohashi; S Yamamoto; N Tsuchiya; Y Hatta; T Komata; M Matsushita; K Tokunaga
Journal:  Ann Hum Genet       Date:  2001-03       Impact factor: 1.670

2.  Accurate power approximations for chi2-tests in case-control association studies of complex disease genes.

Authors:  M R Jackson; E Genin; M Knapp; J L Escary
Journal:  Ann Hum Genet       Date:  2002-07       Impact factor: 1.670

3.  Identification of classical minor histocompatibility antigen as cell-derived peptide.

Authors:  H J Wallny; H G Rammensee
Journal:  Nature       Date:  1990-01-18       Impact factor: 49.962

4.  Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs.

Authors:  N Risch
Journal:  Am J Hum Genet       Date:  1990-02       Impact factor: 11.025

5.  Minor histocompatibility antigens and marrow transplantation.

Authors:  N A Kernan; B Dupont
Journal:  N Engl J Med       Date:  1996-02-01       Impact factor: 91.245

Review 6.  Minor histocompatibility antigens.

Authors:  E Simpson; D Roopenian
Journal:  Curr Opin Immunol       Date:  1997-10       Impact factor: 7.486

7.  Evidence that CD31, CD49b, and CD62L are immunodominant minor histocompatibility antigens in HLA identical sibling bone marrow transplants.

Authors:  E Maruya; H Saji; S Seki; Y Fujii; K Kato; S Kai; A Hiraoka; K Kawa; Y Hoshi; K Ito; S Yokoyama; T Juji
Journal:  Blood       Date:  1998-09-15       Impact factor: 22.113

8.  A genetic analysis of human minor histocompatibility antigens demonstrates Mendelian segregation independent of HLA.

Authors:  G M Schreuder; J Pool; E Blokland; C van Els; A Bakker; J J van Rood; E Goulmy
Journal:  Immunogenetics       Date:  1993       Impact factor: 2.846

9.  HLA-identical sibling bone marrow transplantation in younger patients with chronic lymphocytic leukemia. European Group for Blood and Marrow Transplantation and the International Bone Marrow Transplant Registry.

Authors:  M Michallet; E Archimbaud; G Bandini; P A Rowlings; H J Deeg; G Gahrton; E Montserrat; C Rozman; A Gratwohl; R P Gale
Journal:  Ann Intern Med       Date:  1996-02-01       Impact factor: 25.391

10.  Strategy for mapping minor histocompatibility genes involved in graft-versus-host disease: a novel application of discordant sib pair methodology.

Authors:  K L Lunetta; J J Rogus
Journal:  Genet Epidemiol       Date:  1998       Impact factor: 2.135

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