Treatment of Mitochondrial Diabetes with a Peroxisome Proliferator-activated Receptor (PPAR)-gamma Agonist

Intern Med. 2016;55(9):1143-7. doi: 10.2169/internalmedicine.55.4418. Epub 2016 May 1.

Abstract

The 3243 A>G mutation in mitochondrial DNA is the most common cause of monogenic diabetes mellitus in Japan. A 45-year-old woman with mitochondrial diabetes and significant insulin resistance presented with hypoadiponectinemia despite a normal amount of visceral fat. Three months of treatment with pioglitazone (PIO) improved her blood glucose profile and response to the 75-g oral glucose tolerance test. These changes were accompanied by the amelioration of her insulin resistance and the impairment of early-phase insulin secretion. Her serum adiponectin levels increased to the normal range. In this case of mitochondrial diabetes, PIO was effective for glycemic control.

Publication types

  • Case Reports

MeSH terms

  • Adiponectin / blood
  • Adiponectin / deficiency
  • Blood Glucose / metabolism
  • DNA, Mitochondrial / genetics
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / genetics
  • Female
  • Glucose Tolerance Test
  • Humans
  • Hypoglycemic Agents / therapeutic use*
  • Insulin / blood
  • Insulin Resistance / physiology
  • Metabolism, Inborn Errors / drug therapy
  • Metabolism, Inborn Errors / etiology
  • Middle Aged
  • Mitochondria / drug effects
  • PPAR gamma / agonists*
  • Pedigree
  • Pioglitazone
  • Thiazolidinediones / therapeutic use*

Substances

  • ADIPOQ protein, human
  • Adiponectin
  • Blood Glucose
  • DNA, Mitochondrial
  • Hypoglycemic Agents
  • Insulin
  • PPAR gamma
  • Thiazolidinediones
  • Pioglitazone

Supplementary concepts

  • Hypoadiponectinemia