It is generally assumed that the male:female (M:F) ratio in patients with type 1 (insulin-dependent) diabetes mellitus (IDDM) is 1. A recent survey, however, revealed that high incidence countries (mainly European) have a high M:F ratio and low incidence ones (Asian and African) have a low M:F ratio(1) We have now analysed the M:F ratio according to genotype at the major locus, the major histocompatibility complex (MHC; IDDM1). There are two main IDDM1 susceptibility haplotypes, HLA-DR3 and -DR4, which are present in 95% of Caucasian cases(2-4). We report here that in medium/high incidence Caucasian populations from the United States of America, United Kingdom and Sardinia (1307 cases), the bias in male incidence is largely restricted to the DR3/X category of patients (X not equal DR4) with a M:F ratio of 1.7 (P = 9.3 x 10(-7)), compared with a ratio of 1.0 in the DR4/Y category (Y not equal DR3). This is additional evidence for significant heterogeneity between the aetiology of 'DR4-associated' and 'DR3-associated' diabetes(5-13). We analysed linkage of type 1 diabetes to chromosome X, and as expected, most of the linkage to Xp13-p11 was in the DR3/X affected sib-pair families (n=97; peak multipoint Mts at DXS1068 = 3.5, P = 2.7 x 10(-4); single point MLS = 4.5, P = 2.7 x 10(-5)). This is evidence for aetiological heterogeneity at the IDDM1/MHC locus and, therefore, in the search for non-MHC loci in type 1 diabetes, conditioning of linkage data by HLA type is advised.
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|Titolo:||A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patients|
|Data di pubblicazione:||1998|
|Appare nelle tipologie:||1.1 Articolo in rivista|