Impaired fasting glucose (IFG) and impaired glucose tolerance (IGT) often coexist and as such represent a potent risk factor for subsequent development of type 2 diabetes. -Cell mass is ϳ50% deficient in IFG and ϳ65% deficient in type 2 diabetes. To establish the effect of a ϳ50% deficit in -cell mass on carbohydrate metabolism, we performed a ϳ50% partial pancreatectomy versus sham surgery in 14 dogs. Insulin secretion was quantified from insulin concentrations measured in the portal vein at 1-min sampling intervals under basal conditions, after a 30-g oral glucose, and during a hyperglycemic clamp. Insulin sensitivity was measured by a hyperinsulinemic-euglycemic clamp combined with isotope dilution. Partial pancreatectomy resulted in IFG and IGT. After partial pancreatectomy both basal and glucose-stimulated insulin secretion were decreased through the mechanism of a selective ϳ50 and ϳ80% deficit in insulin pulse mass, respectively (P < 0.05). These defects in insulin secretion were partially offset by decreased hepatic insulin clearance (P < 0.05). Partial pancreatectomy also caused a ϳ40% decrease in insulinstimulated glucose disposal (P < 0.05), insulin sensitivity after partial pancreatectomy being related to insulin pulse amplitude (r ؍ 0.9, P < 0.01). We conclude that a ϳ50% deficit in -cell mass can recapitulate the alterations in glucose-mediated insulin secretion and insulin action in humans with IFG and IGT. These data support a mechanistic role of a deficit in -cell mass in the evolution of IFG/IGT and subsequently type 2 diabetes. Diabetes 55: [2347][2348][2349][2350][2351][2352][2353][2354][2355][2356] 2006 T ype 2 diabetes is characterized by insulin resistance and impaired glucose-mediated insulin secretion (1,2). Although the basis for the defective insulin secretion remains unknown, a contributory factor may be the ϳ65% deficit in -cell mass (3,4). Interestingly, a relatively high proportion of living related donors who underwent a ϳ50% pancreatectomy subsequently developed diabetes (5). Also, humans with impaired fasting glucose (IFG) have a ϳ50% deficit in -cell mass (3), implying that a deficit in -cell mass may be important in the pathophysiology of type 2 diabetes.Further support for this hypothesis is provided by the observation that pharmacological or surgical reduction of -cell mass in rats (6,7), pigs (8), dogs (9 -12), or monkeys (13) results in defective insulin secretion and, depending on the extent of the induced deficit in -cell mass, diabetes or IFG. The purpose of the current study was to reproduce in dogs the ϳ50% deficit in -cell mass present in humans with IFG in order to address the following questions. First, does a 50% deficit in -cell mass lead to IFG and/or impaired glucose tolerance (IGT)? Second, does a ϳ50% deficit in -cell mass lead to impaired glucose-stimulated insulin secretion, and, if so, does this reproduce the pattern seen in humans with type 2 diabetes? Third, does a 50% deficit in -cell mass lead to a change in insulin sensitivity, and, ...