Albuminuria Deforolimus was assessed using random urine sample. For bivariate analysis using chi square

and multivariate analysis using regression logistic method. Results: The characteristic data of type 2 diabetes mellitus patients in Indonesia showed majority were female (65,5%), suffered type 2 diabetes mellitus more than 5 years (68,6%), with poor glucose control (76%). The prevalence of hypertension, dyslipidemia and overweight in type 2 diabetes melitus patients were 81,3%, 78,1% and 81,3% respectively. Albuminuria was found in 61 patients (63,5%). The prevalence of vitamin D 25(OH)D deficiency in patients with type 2 diabetes mellitus was 49% with a median value 16,35 ng / mL (4,2–41,4 ng /mL). There was no significant correlation between vitamin D deficiency with the severity of albuminuria (OR 0,887; 95% CI 0,335 to 2,296). Confounding factors such as poor blood glucose control and overweight strongly influenced the association between vitamin D deficiency

with the incidence Target Selective Inhibitor Library cell line of albuminuria in patients with type 2 diabetes mellitus. Conclusion: The results of this study have not been able to show an association between vitamin D deficiency with the severity of albuminuria in patients with type 2 diabetes mellitus. GOJASENI PONGSATHORN, PHAOPHA ANGKANA, CHAILIMPAMONTREE WORAWON, CHITTINANDANA ANUTRA Bhumibol Adulyadej Hospital, Directorate of Medical Services, Royal Thai Air Force Introduction: Microalbuminuria is often regarded as a marker of endothelial dysfunction and associated with an increase risk of cardiovascular and kidney disease. For non-diabetic patients, however, prognostic value of microalbuminuria for predicting kidney disease progression is still debated. Gemcitabine Methods: A prospective cohort study was performed at out-patients departments of Bhumibol Adulyadej hospital, Royal Thai Air Force. In the period of 2006–2007, a total of 559 non-diabetic hypertensive patients (283 males, 276 females), aged 58.0 ± 11.6 years were participated in albuminuria

screening program. Albuminuria thresholds were evaluated and defined using albumin-creatinine ratio (ACR). Renal function of the patients was subsequently obtained in the year 2013. The risks of developing CKD stage 3 were also examined prospectively in subgroup (n = 483) with baseline GFR ≥ 60 ml/min/1.73 m2. Results: During baseline screening program, normoalbuminuria (ACR < 30 mg/g) and microalbuminuria (ACR 30–300 mg/g) was found in 80.4% and 19.6% respectively. Baseline GFR by CKD-EPI formula was not statistically different between both groups (79.65 ± 16.25 vs 79.91 ± 18.98 ml/min/1.73 m2, p = 0.939). Subsequent clinical data at follow-up was available for analysis in 435 patients (72.6%). During a median follow-up period of 72 months (maximum 88 months), GFR numerically decreased more in patients who had baseline microalbuminuria compared with normoalbuminuria group but the difference was not statistically significant (delta GFR – 6.18 ± 18.09 vs – 2.03 ± 15.38 ml/min/1.73 m2, p = 0.632).