Limitations of stratifying sib-pair data in common disease linkage studies: An example using chromosome 10p14-10q11 in type 1 diabetes

被引:7
作者
Johnson, GCL
Koeleman, BPC
Todd, JA
机构
[1] Univ Cambridge, Cambridge Inst Med Res, JDRF WT Diabet & Inflammat Lab, Cambridge CB2 2XY, England
[2] Leiden Univ, Med Ctr, Dept Immunohaematol & Bloodbank, Leiden, Netherlands
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2002年 / 113卷 / 02期
关键词
linkage analysis; stratification; heterogeneity; common disease; type; 1; diabetes;
D O I
10.1002/ajmg.10737
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
IDDM10 on chromosome 10p11-q11 has been identified as a putative diabetes susceptibility locus through affected sib-pair (ASP) linkage analysis in UK nuclear families [Davies et al., 1994: Nature 371:130-136; Reed et al., 1997: Hum Mol Genet 6:1011-1016; Mein et al., 1998: Nat Genet 19:297-300]. We extended analysis of linkage to type 1 diabetes in this region by typing a total of 61 markers in a maximum of 418 UK sib-pairs (UK418; peak MLS = 3.84). We then stratified the dataset based on analyses performed previously by both our group [Mein et al., 1998: Nat Genet 19:297-300] and others [Paterson et al., 1999: Hum Hered 49:197-204; Paterson and Petronis, 1999a: Am J Med Genet 84:15-19; Paterson and Petronis, 2000a: J Med Genet 37:186-191; Paterson and Petronis, 2000b: Eur J Hum Genet 8:145-148] and used a permutation procedure to assess the significance of the results. We conclude that the results obtained had a high probability of occurring by chance alone. These data highlight the limitations of stratifying small datasets (n < 500) by additional criteria and the recurrent problems of multiple testing in genetic analysis. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:158 / 166
页数:9
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