Diabetes Research and Clinical Practice
Volume 88, Issue 1 , Pages 76-80, April 2010

C358A missense polymorphism of the endocannabinoid degrading enzyme fatty acid amide hydrolase (FAAH) and insulin resistance in patients with diabetes mellitus type 2

Institute of Endocrinology and Nutrition, Medicine School and Unit of Investigation, Hospital Rio Hortega, University of Valladolid, C/Los perales 16, Simancas 47130, RETICEF RD056/0013, Valladolid, Spain

Received 11 November 2009; received in revised form 7 December 2009; accepted 14 December 2009. published online 07 January 2010.

Abstract 

Background

The polymorphism 385 C/A of FAAH has been associated with overweight and obesity. The aim of our study was to investigate the relationship of polymorphism (cDNA 385 CA) of FAAH gene on obesity parameters in patients with diabetes mellitus type 2.

Design

A population of 70 patients with diabetes mellitus type 2 was analyzed. An anthropometric and biochemical nutritional assessment was performed. The statistical analysis was performed for the combined C358A and A358A as a group and wild type C358C as second group.

Results

Fifty-five patients (78.7%) had genotype C358C (wild type group) and 15 (21.3%) patients C358A (14 patients, 20.6%) or A358A (1 patient, 0.7%) (mutant group). BMI (38.9±6.4 vs. 39.2±5.7, p<0.05), weight (96.8±17.6kg vs. 102.5±16.8kg, p<0.05), fat mass (42.1±16.1kg. vs. 46.9±11.1kg, p<0.05), waist circumference (115.9±12.8cm vs. 121.3±12.8cm, p<0.05), insulin (22.5±18.8mUI/L vs. 33.9±17.1UI/L, p<0.05) and TNF-alpha (6.1±3.4pg/mL vs. 8.4±3.2pg/mL, p<0.05) were higher in mutant type group than wild type. Adiponectin levels (33.3±20.8ng/mL vs. 22.3±10.8ng/mL, p<0.05) were higher in wild type group than mutant type group.

Conclusion

There is an association of the mutant type group A358C and A358A of FAAH with a worse cardiovascular profile (weight, body mass index, waist circumference, insulin,TNF-alpha and adiponectin levels) than wild type group.

Keywords: Diabetes mellitus, FAAH, Insulin resistance, Polymorphism

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PII: S0168-8227(09)00544-0

doi:10.1016/j.diabres.2009.12.019

Diabetes Research and Clinical Practice
Volume 88, Issue 1 , Pages 76-80, April 2010