Fas/Fas-Ligand pathway is impaired in patients with type 2 diabetes. Influence of hypertension and insulin resistance

Diabetes Metab. 2005 Feb;31(1):47-54. doi: 10.1016/s1262-3636(07)70166-0.

Abstract

Objectives: In type 2 diabetic patients with no cardiac history or symptoms, 1) to evaluate whether the soluble forms of Fas (sFas) and Fas-ligand (sFasL), involved in apoptosis, may be markers of silent coronary disease or related to hypertension or microangiopathic complications; 2) to examine the effect of short-term glycemic control on sFas and sFasL.

Methods: (1) sFas and sFasL were measured with the ELISA method in 44 asymptomatic diabetic patients, 33 with hypertension, and with a normal myocardial scintigraphy (n=14), with silent myocardial ischemia (SMI) and without (n=15) or with (n=15) significant coronary stenoses; and in 14 controls; (2) sFas and sFasL were measured in 15 poorly controlled diabetic patients before and after 7 days of CSII treatment.

Results: (1) sFas and sFasL differed in the four groups of patients (p=0.003 each). sFas was significantly higher in the patients with SMI without (p=0.035) and with coronary stenoses (p=0.002) than in the control group. sFasL was lower in the three groups of diabetic patients (p<0.05 each) than in control group. In the diabetic population, sFas correlated positively with hypertension (p=0.021), and sFasL negatively with hypertension (p=0.027) and HOMA index in the non-insulin treated patients (p=0.049); (2) sFas did not differ before or after CSII, and there was a marginal decrease in sFasL.

Conclusion: Fas-mediated apoptosis is involved in type 2 diabetes and might be associated with hypertension and/or its vascular consequences. sFasL might be affected by insulin resistance. sFas and sFasL are not effective markers of SMI.

MeSH terms

  • Adult
  • Blood Glucose / metabolism
  • Blood Pressure
  • Body Mass Index
  • Coronary Disease / blood
  • Coronary Disease / immunology
  • Diabetes Complications / blood
  • Diabetes Complications / immunology*
  • Diabetes Mellitus, Type 2 / immunology*
  • Fas Ligand Protein
  • Female
  • Humans
  • Hypertension / immunology*
  • Insulin Resistance / immunology*
  • Lipids / blood
  • Male
  • Membrane Glycoproteins / blood
  • Membrane Glycoproteins / physiology*
  • Pulse
  • fas Receptor / blood
  • fas Receptor / physiology*

Substances

  • Blood Glucose
  • FASLG protein, human
  • Fas Ligand Protein
  • Lipids
  • Membrane Glycoproteins
  • fas Receptor