The relationship between the inheritance of diabetes, microangiopathies and obesity was examined in 97 patients with NIDDM who had been diagnosed as diabetes before the age of 25 years and referred to the Diabetes Center of the Tokyo Women's Medical College from 1980 to 1984 (51 males and 46 femeles; the age at diabetes, diagnosis of 18.4±4.2 years [mean±SD]; the duration of diabetes 7.1±6.4 years). At the same time 127 patients diagnosed as having IDDM before the age of 25 years (60 males and 67 females; the age at diabetes, diagnosis of 11.8±5.9 years; the duration of diabetes 10.5±7.2 years) during hospital visits were used as the control group.
The percentage of probands with diabetic first degree relatives was 49.0% for NIDDM, and 11.9% for IDDM (p<0.005). For NIDDM, MODY was defined as follows:(1) every affected person had an affected parent, (2) there was direct vertical transmission through three generations, (3) the ratio of affected: unaffected children of diabetic parents was 1: 1. All other cases of NIDDM except MODY were defined as NIDDY. 11.5% of the NIDDM were designated as MODY. Incidences of MODY detected before the age of 20 years and between 20 and 24 years were 19.2% and 2.3%, respectively (p<0.025).
Patients with past histories of obesity amounted to 30.9% for NIDDM and 3.9% for IDDM (p<0.005). None of the MODY patients had past histories of obesity, whereas 35.3% of NIDDY patients did.
Among NIDDM patients the rates of those with simple and with proliferative retinopathy were 22.1% and 14.7% respectively, although these rates in IDDM patients were 43.7% and 9.5% respectively. Retinopathy was found in 41.7%(simple, 25.0%; proliferative, 16.7%) of the patients with MODY, and 36.1%(simple, ≥21.7%; proliferative, 14.5%) of those with NIDDY. The rate of patients with nephropathy was 14.7% for NIDDM and 10.3% for IDDM. Nephropathy was indicated in 16.7% of the patients with MODY, and 14.5% of those with NIDDY. These findings suggest that severe microagniopathies occur in patients with NIDDM to the same degree as in patients with IDDM, and that there were various heterogeneities with or without microangiopathies in MODY.
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