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±ÛÁ¦¸ñ :     Çѱ¹Àο¡¼­ PSMA6 (rs1048990)¿Í PSMB5 (rs2230087) À¯ÀüÀÚ ´ÙÇü¼º°ú Á¦2Çü ´ç´¢º´°úÀÇ ¿¬°ü¼º
 

±èÈñ°æ, ±è¼ö¿ø, µµÀ±Á¤, ±è»õ·Ò, ±è¹Ì°æ, ¹Ú±Ù±Ô, ±èÇý¼ø, ¹Ú°æ¼ö, À¯  ¹Î, ±èÁ¤±¹, ±èº¸¿Ï, ÀÌÀαÔ. Çѱ¹Àο¡¼­ PSMA6 (rs1048990)¿Í PSMB5 (rs2230087) À¯ÀüÀÚ ´ÙÇü¼º°ú Á¦2Çü ´ç´¢º´°úÀÇ ¿¬°ü¼º

KOREAN DIABETES JOURNAL  Á¦32±Ç, Á¦3È£,  2008³â pp204-214

Background: The 26S ubiquitin-proteasome system (UPS) is a principal proteolytic pathway of intracellular molecules regulating apoptosis, cell cycle, cell proliferation or differentiation, inflammation and etc. The recent study suggests that the rs1048990 (C/G) polymorphism of the proteasome subunit ¥á type 6 (PSMA6) gene is associated with the increase of the risk of myocardial infarction by the dysregulation of I¬ÜB degradation. We hypothesized that 26S UPS is important in the development of insulin resistance and type 2 diabetes (T2DM) by controlling the degradation of I¬ÜB and insulin receptor substances as a substrate. We therefore investigated whether the rs1048990 (C/G) polymorphism of PSMA6 gene and the rs2230087 (G/A) polymorphism of proteasome subunit ¥â type 5 gene (PSMB5), that is chymotrypsin-like protease determining the rate of proteolysis, are associated with susceptibility to T2DM in Korean subjects. Methods: We examined the polymorphisms of these genes in 309 diabetic subjects and 170 non-diabetic
controls. The polymorphisms of rs1048990 (C/G) and rs2230087 (G/A) were genotyped by real-time PCR. Results: The frequency of the G allele of rs1048990 (C/G) and the A allele of rs2230087 (G/A) polymorphisms was significantly higher in diabetic patients (28% and 13%) compared to that in controls (13% and 1%; P = 0.000 and P = 0.000, respectively). Logistic regression analysis of the rs1048990 (C/G) polymorphism showed that the odds ratio (OR) (adjusted for age, smoking, waist circumference, fasting plasma glucose, systolic blood pressure, HDL-C, triglyceride, and total cholesterol) was 3.93 (95% confidence interval [CI], 2.35-6.59; P = 0.000) for the G allele and 5.09 (95% CI, 2.71-9.57; P = 0.000) for CG and GG genotype when compared with the CC genotype. Logistic regression analysis of the rs2230087 (G/A) polymorphism showed that the adjusted OR was 5.70 (95% CI, 1.63-19.98; P = 0.007) for the A allele and 6.08 (95% CI, 1.66-22.29; P = 0.006) for GA and AA genotype when compared with the GG genotype. In multiple logistic regression analysis with T2DM as the independent Variable rs1048990 (C/G) and rs2230087 (G/A) polymorphisms were the predictor for T2DM. Conclusion: We suggest that the G allele of rs1048990 (C/G) polymorphism and the A allele of rs2230087 (G/A) polymorphism may be genetic risk factor to type 2 diabetes mellitus in Korean subjects.

 
 
 
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