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Genotype-based treatment of type 2 diabetes with an α2A-adrenergic receptor antagonist.

  • Yunzhao Tang
  • Annika Axelsson
  • Peter Spégel
  • Lotta Andersson
  • Hindrik Mulder
  • Leif Groop
  • Erik Renström
  • Anders Rosengren
Publishing year: 2014
Language: English
Pages: 139-257
Publication/Series: Science Translational Medicine
Volume: 6
Issue: 257
Document type: Journal article
Publisher: American Association for the Advancement of Science (AAAS)

Abstract english

The feasibility of exploiting genomic information for individualized treatment of polygenic diseases remains uncertain. A genetic variant in ADRA2A, which encodes the α2A-adrenergic receptor (α2AAR), was recently associated with type 2 diabetes. This variant causes receptor overexpression and impaired insulin secretion; thus, we hypothesized that blocking α2AAR pharmacologically could improve insulin secretion in patients with the risk genotype. A total of 50 type 2 diabetes patients were recruited on the basis of ADRA2A genotype for a randomized placebo-controlled intervention study with the α2AAR antagonist yohimbine. The patients received 0, 10, or 20 mg of yohimbine at three separate visits. The primary endpoint was insulin secretion at 30 min (Ins30) during an oral glucose tolerance test (OGTT). Patients with the risk variant had 25% lower Ins30 than those without risk genotype. After administration of 20 mg of yohimbine, Ins30 was enhanced by 29% in the risk group, making secretion similar to patients carrying the low-risk allele. The corrected insulin response and disposition index in individuals with the high-risk (but not low-risk) allele were improved by 59 ± 18% and 43 ± 14%, respectively. The beneficial effect of yohimbine was not a consequence of improved insulin sensitivity. In summary, the data show that the insulin secretion defect in patients carrying the ADRA2A risk genotype can be corrected by α2AAR antagonism. The findings show that knowledge of genetic risk variants can be used to guide therapeutic interventions that directly target the underlying pathophysiology and demonstrate the potential of individualized genotype-specific treatment of type 2 diabetes.


  • Endocrinology and Diabetes


  • Islet patophysiology
  • Diabetes and Endocrinology
  • Molecular Metabolism
  • ISSN: 1946-6242
Peter Spegel
E-mail: peter [dot] spegel [at] chem [dot] lu [dot] se


Centre for Analysis and Synthesis


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