Abstract. We saw a 57-yr-old female non-insulin dependent diabetes mellitus (NIDDM) patient with antiinsulin antibody, in whom insulin-like growth factor-I (IGF-I) was shown to be effective as a blood glucose-lowering agent. Due to the presence of the antibody, the patient suffered from postprandial hyperglycemia and frequent hypoglycemia, which were uncontrollable even by multiple insulin injection therapy. In contrast to insulin injection (0.24 IU/kg body wt) which showed a delayed glucoselowering effect, subcutaneous injection of recombinant human IGF-I (0.05-0.1 mg/kg body wt) caused a quick fall in plasma glucose levels. Prolongation of the glucose-lowering effect of "rapid-acting" insulin frequently caused subsequent hypoglycemia in this patient, but the effect of IGF-I seemed to have disappeared within the first three hours.Key words: IGF-I, Antiinsulin antibody (Endocrine Journal 42:101-105,1995) ANTIINSULIN antibody, which can frequently be identified in patients receiving long-term insulin injection therapy, often causes both a delayed onset and prolongation of insulin effects. This is often associated with unexpected hypoglycemia, and thus the presence of antiinsulin antibody is frequently found in "brittle-type" diabetes.We recently had a female patient with non-insulin dependent diabetes mellitus (NIDDM) who suffered from frequent hypo-and hyperglycemia due to the presence of antiinsulin antibody. As a step to exploring the potential of insulin-like growth factor-I (IGF-I) use for diabetic patients, the effect of IGF-I as a glucose-lowering agent in this NIDDM case was examined. A 57-yr-old Japanese woman with a 26-year history of diabetes mellitus. She started using porcine insulin 13 years ago and then human insulin 6 years ago, when multiple insulin injection therapy was introduced. The daily profile of the plasma glucose level revealed typical postprandial hyperglycemia that was uncontrollable even by preprandial subcutaneous injection of "rapid-acting" insulin; the plasma glucose concentration, which had been 90 mg/dl before breakfast, rose up to 292 mg/dl two hours after it (2 h 15 min after injection of 0.33 IU/ kg body wt insulin). Thus the "rapid-acting" insulin showed a delayed and yet prolonged glucose-lowering effect in this patient. When the present trial was performed, the patient took a "rapid -acting" insulin injection twice daily (0.33 IU/kg body wt in the morning and 0.16 IU/kg body wt in the evening) and her fasting serum C-