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No linkage of P187S polymorphism in NAD(P)H: Quinone oxidoreductase (NQO1/DIA4) and type 1 diabetes in the Danish population
Author(s) -
Kristiansen Ole P.,
Larsen Zenia M.,
Johannesen Jesper,
Nerup Jørn,
MandrupPoulsen Thomas,
Pociot Flemming
Publication year - 1999
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/(sici)1098-1004(1999)14:1<67::aid-humu8>3.0.co;2-5
Subject(s) - biology , genetics , linkage disequilibrium , haplotype , population , type 2 diabetes , offspring , genotype , gene , diabetes mellitus , endocrinology , medicine , pregnancy , environmental health
Recent genome screening studies have identified novel regions of possible interest for susceptibility to type 1 diabetes. One of these is a 30‐35 cM region mapping to 16q22‐q24 ( D16S515‐D16S520 ), where also the gene encoding NAD(P)H: quinone oxidoreductase ( NQO1 ) maps. Data has suggested association of a polymorphism (P187S) in the NQO1 gene and type 1 diabetes. NQO1 is involved in protection against oxidative stress, which is likely to be involved in β‐cell destruction. By use of the transmission disequilibrium test (TDT), we analyzed the P187S polymorphism for association to type 1 diabetes in a population‐based sample of 247 Danish nuclear type 1 diabetic families. Random transmission patterns were observed to all affected offspring (p tdt = 0.82), to index cases (p tdt = 0.77), as well as to unaffected offspring (p tdt = 0.93). Hence, the NQO1 polymorphism is not likely to be an etiological mutation underlying the reported linkage of the 16q22‐q24 region. Hum Mutat 14:67–70, 1999. © 1999 Wiley‐Liss, Inc.