A. Matsuda et T. Kuzuya, RELATIONSHIP BETWEEN OBESITY AND CONCORDANCE RATE FOR TYPE-2 (NON-INSULIN-DEPENDENT) DIABETES-MELLITUS AMONG TWINS, Diabetes research and clinical practice, 26(2), 1994, pp. 137-143
In order to analyse the relationship of genetic factors and the role o
f obesity in the pathogenesis of Type 2 (noninsulin-dependent) diabete
s mellitus, we compared body mass index (BMI) and other parameters in
71 monozygotic and 17 dizygotic twins (MZT and DZT) with Type 2 diabet
es, and analysed the relationship of maximal BMI in the past (max BMI)
with the concordance and discordance for diabetes. Data were collecte
d by mail from the members of the Japan Diabetes Society. Concordance
rate for diabetes was higher in MZT than in DZT (72% vs. 41%, P = 0.01
7). Concordance rate in MZT varied in relation to the max BMI of the i
ndex twins who developed diabetes earlier. It was higher in non-obese
and slightly obese groups (82% and 80% for those with max BMI < 24 and
24-27.9, respectively) than in obese group (36%, max BMI greater than
or equal to 28) (P = 0.003). In MZT, diabetic twins of discordant pai
rs were significantly more obese at the survey and in the past than in
dex twins of concordant pairs (mean BMI: 23.9 vs. 21.7, P = 0.007; mea
n max BMI, 27.7 vs. 24.3, P = 0.001). A similar tendency of difference
s in BMI was also observed in DZT. Intrapair comparison in discordant
MZT and DZT pairs showed that diabetic twins were more obese than nond
iabetic cotwins (mean max BMI, 27.7 vs. 24.7, P = 0.004 for MZT; and 2
7.3 vs. 23.9, P = 0.002 for DZT). In concor dant DZT pairs, index twin
s with earlier onset of diabetes had been less obese than cotwins (mea
n max BMI, 23.6 vs. 26.0, P = 0.004). In conclusion, the comparison of
the max BMI in twins suggests that the degree of diabetogenic role of
obesity varies in heterogeneous genetic background. The index twins o
f discordant pairs had been more obese than those of concordant pairs,
suggesting that obesity plays a more important role in those with wea
ker genetic susceptibility for diabetes.