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Abstract lntreductien and Aim 11the Werk Diabetes mellitus is a chronic metabolic disease with many acute and chronic complications. Chronic complications are mainly due to development of diabetic microangiopathy resulting in retinopathy, nephropathy and neuropathy (Bodausky eta!., 1982). IDDM is characterized by insulinopenia (Geuutlz, 1982). Insulin is synthesized in the beta cells of the islets of Langerhans as a precursor molecule, Proinsulin which is cleaved into insulin and a 31 aminoacid peptide called the connecting peptide or C-peptide. Insulin and C-peptide are secreted in equimolar amounts (Beisclzer, 1976). C-peptide analysis can provide an estimate of residual (3-cell function (Faber and Binder, 1977). Plasma C-peptide measurement have been used in research to calculate insulin secretory rate (Eato11 eta!., 1983). Epidemiological data suggest a strong relationship between the level of glycaemia and incidence and progression of retinopathy in IDDM. However the relationship of endogenous insulin secretion to diabetic retinopathy independent of glycemic control is not clear, some studies suggest a protective effect whereas others do not (Kleiu eta/., 1995). On the other hand higher fasting insulin and C-peptide levels were found to be associated with higher blood pressure (Every et al., 1993). (2} C!5J,rtroductii7Jt a!td Aim q(tlu: &ork The ann of this study is to assess the importance of C peptide as a measure of endogenous insulin secretion and to throw light on the relationship between level of C-peptide and prevalence of diabetic retinopathy, nephropathy and hype11ension. |