A 71-year-old woman was admitted to hospital because of poor glycemic control and liver dysfunction. Although the patient's diabetes had been well-controlled with glibenclamide and pioglitazone, the pioglitazone had been discontinued because of an adverse effect on body weight gain and edema. The patient's Hb A
1c level subsequently rose from 7% to 11.6%. At admission, her BMI was 40.8kg/m
2 and she exhibited hypertension, hyperlipidemia, and microalbuminuria. A lacunar brain infarction was also diagnosed. The patient's fasting blood glucose level was 302mg/d
l, her serum IRI was 14.7μU/m
l, a hypoglycemic response was not obtained on an insulin tolerance test, and her fasting bloodg lucose was 219mg/d
l, and her postprandial blood glucose was 457mg/dl at an insulin dosage of 1U/kg body weight. Although she did not drink alcohol, she exhibited mild liver dysfdnction: AST, 80U/
l; ALT, 70U/
l;γGTP, 102U/l. A liver biopsy was performed, and the histological findings were compatible with a diagnosis of NASH. When 6mg of glimepiride, a sulfonylurea with an insulin-sensitizing extrapancreatic effect, was added to the patient's insulin therapy, her blood glucose control improved markedly: fasting blood glucose, 76mg/d
l; postprandial blood glucose, 135mg/d
l; insulin dosage, 0.5U/kg body weight. When insulin or oral hypoglycemic agents alone fail to control blood glucose in patients with type 2 diabetic associated with NASH, a combination therapy of glimepiride and insulin is recommended.
View full abstract