Several investigators have reported that more than half of African-American persons with new diagnoses of
diabetic ketoacidosis have clinical, metabolic, and immunologic features of
type 2 diabetes during follow-up. These patients are usually obese, have a strong family history of diabetes, have a low prevalence of autoimmune markers, and lack a genetic association with HLA. Their initial presentation is acute, with a few days to weeks of
polyuria,
polydipsia, and
weight loss and lack of a precipitating cause of metabolic decompensation. At presentation, they have markedly impaired insulin secretion and
insulin action, but intensified diabetic management results in significant improvement in beta-cell function and
insulin sensitivity sufficient to allow discontinuation of
insulin therapy within a few months of follow-up. On discontinuation of
insulin therapy, the period of near-normoglycemic remission may last for a few months to several years. The absence of autoimmune markers and the presence of measurable insulin secretion have proven useful in predicting near-normoglycemic remission and long-term
insulin dependence in adult patients with a history of
diabetic ketoacidosis. This clinical presentation is commonly reported in African and African-American persons but is also observed in Hispanic persons and those from other minority ethnic groups. The underlying mechanisms for beta-cell dysfunction in
ketosis-prone
type 2 diabetes are not known; however, preliminary evidence suggests an increased susceptibility to
glucose desensitization.