CCR5Delta32 genotype is associated with outcome in type 2 diabetes mellitus

Diabetes Res Clin Pract. 2009 Nov;86(2):140-5. doi: 10.1016/j.diabres.2009.08.013. Epub 2009 Sep 9.

Abstract

Aims: To test whether the genetic variant CCR5Delta32 in the CC-chemokine receptor 5, which is known to lead to CCR5 deficiency, is associated with mortality in type 2 diabetes patients.

Methods: We examined the effect of presence or absence of the CCR5Delta32 on overall and cardiovascular mortality risk in the Zwolle Outpatient Diabetes project Integrating Available Care (ZODIAC) cohort, a type 2 diabetes patient cohort.

Results: We studied 756 patients with a mean duration of follow-up of 5.4 (+/- 1.4) years. 194 patients died during follow up of which 83 were cardiovascular deaths. 144 subjects (19%) carried the CCR5Delta32 deletion. CCR5Delta32 carriers had an adjusted hazard ratio of 0.62 (95%CI: 0.40-0.96; p=0.03) for all-cause mortality and 0.63 (95%CI: 0.33-1.19; p=0.16) for cardiovascular mortality.

Conclusions: The presence of CCR5Delta32 is associated with better survival in type 2 diabetes patients. These data suggest that it is worthwhile to explore the protective potential of pharmacological blockade of CCR5 in type 2 diabetic patients.

MeSH terms

  • Age of Onset
  • Aged
  • Blood Pressure
  • Cardiovascular Diseases / genetics
  • Cardiovascular Diseases / mortality
  • Cohort Studies
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetes Mellitus, Type 2 / mortality
  • Diabetes Mellitus, Type 2 / therapy
  • Diabetic Angiopathies / genetics
  • Diabetic Angiopathies / mortality
  • Female
  • Follow-Up Studies
  • Genetic Variation
  • Genotype
  • Glomerular Filtration Rate
  • Glycated Hemoglobin / metabolism
  • Humans
  • Male
  • Middle Aged
  • Outpatients
  • Receptors, CCR5 / genetics*
  • Survivors / statistics & numerical data
  • Treatment Outcome

Substances

  • Glycated Hemoglobin A
  • Receptors, CCR5