ASSOCIATION OF POLYMORPHISM IN THE INTERFERON-GAMMA GENE WITH IDDM
Citation
T. Awata et al., ASSOCIATION OF POLYMORPHISM IN THE INTERFERON-GAMMA GENE WITH IDDM, Diabetologia, 37(11), 1994, pp. 1159-1162
Categorie Soggetti
Endocrynology & Metabolism","Medicine, General & Internal
SICI code
0012-186X(1994)37:11<1159:AOPITI>2.0.ZU;2-N
Abstract
Cytokines may play important roles in the pathogenesis of insulin-depe
ndent diabetes mellitus (IDDM). We analysed a dinucleotide repeat poly
morphism within the first intron of the interferon gamma (IFN-gamma) g
ene in Japanese diabetic patients (175 IDDM and 145 non-insulin-depend
ent diabetes mellitus) and 267 control subjects. A significant differe
nce was observed in the global allele distribution of the polymorphism
between the IDDM and control groups (p = 0.039). The difference from
the control group was more evident in the patients whose insulin thera
py started within 1 year from onset (p = 0.006) or in the young-onset
(< 10 years) patients (p = 0.0006). The alleles ''3'' and ''6'' were i
ncreased in the IDDM patients, and a significant increase in the frequ
ency of the ''3/6'' genotype was observed in the IDDM patient group (9
.1 %, RR 2.9, p = 0.010), in the patients with initial insulin therapy
less than 1 year from onset (10.6 %, RR 3.4, p = 0.004), or in the yo
ung-onset patients (16.7 %, RR 5.7, p = 0.0003) in comparison to the c
ontrol subjects (3.4 %). There was a tendency towards frequent occurre
nce of clinical characteristics which reflect young or abrupt onset of
diabetes or both, and depletion of insulin secretion capacity in the
patients with ''3/6'' or ''6/6'' in comparison to the patients with ot
her genotypes. These results suggest that the IFN-gamma gene region ma
y contribute to the pathogenesis of IDDM and could be a genetic marker
for IDDM.