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DIABETIC KETOACIDOSIS: A COMMON DEBUT OF DIABETES AMONG AFRICAN AMERICANS WITH TYPE 2 DIABETES

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ENDOCRINE PRACTICE
卷 23, 期 8, 页码 971-978

出版社

AMER ASSOC CLINICAL ENDOCRINOLOGISTS
DOI: 10.4158/EP161679.RA

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资金

  1. American Diabetes Association [1-14-LLY-36]
  2. Public Health Service Grant from the Clinical and Translational Science Award program [UL1 RR025008]
  3. National Institutes of Health and National Center for Research Resources [1P30DK111024-01]

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Objective: More than half of African Americans (AA) with a new diagnosis of diabetic ketoacidosis have clinical and metabolic features of type 2 diabetes during follow-up. This particular presentation of diabetes has been termed as ketosis-prone type 2 diabetes (KPDM) or atypical diabetes. Methods: We review the epidemiology, diagnosis, pathophysiology, and acute and long-term management of AA with KPDM and compare these similarities to patients with type 2 diabetes. Results: In contrast to the long-term insulin requirement of auto-immune type 1 diabetes, patients with KPDM are able to discontinue insulin after a few months of therapy and maintain acceptable glycemic control for many years on either diet or oral agents. Patients with KPDM have significant impairment of both insulin secretion and insulin action at presentation; however, at the time of near-normoglycemia remission, insulin secretion and action improve to levels similar to hyperglycemic patients with ketosis-resistant type 2 diabetes. In the long term, however, patients with KPDM have a decline in beta-cell function similar to patients with type 2 diabetes. Recent studies indicate that treatment with metformin and dipeptidyl peptidase-4 inhibitors can prolong the period of near-normoglycemia remission for several years compared to placebo therapy. Conclusion: KPDM is a unique but common presentation of newly diagnosed African Americans with type 2 diabetes.

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