Uric acid (UA) is produced in the liver as an end product of purine catabolism and approximately 1/3 of it is degraded in the gut and 2/3 is renally excreted. 1, 2 Increased serum uric acid (SUA) or hyperuricemia is clinically defined as SUA level ≥ 7 mg/dL in men and postmenopausal women and ≥ 6 mg/dL in premenopausal women. 3 Hyperuricemia has been linked with many clinical conditions. 4 It is known to play a critical role in the development of type-2 diabetes mellitus (T2DM) as well as in progression of its complications. 5, 6, 7 Hyperuricemia is an independent risk factor for kidney dysfunction in patients with DM. 8 The mechanisms of hyperuricemia-induced renal injury mainly include oxidative stress, endothelial dysfunction, renal fibrosis, and inflammation. 3 Recent studies have reported that hyperuricemia is associated with kidney damage independent of hypertension in diabetic patients. 9 On the other hand, higher levels of serum insulin may decrease uric acid clearance by the kidneys. 9 As a rule,  hyperinsulinemia is the basis of T2DM pathophysiology. 10. Therefore, diabetic patients are more prone to uric acid injury. It is also reported that hyperuricemia may positively influence urinary albumin excretion by decreasing glomerular filtration rate (GFR) and increases the risk of kidney failure. 11, 12 We know that albuminuria is an early marker for renal damage, and hence its measurement is important for the detection of diabetic kidney disease (DKD) or diabetic nephropathy (DN). This study was undertaken to determine the possible association of SUA with urinary albumin-creatinine ratio (ACR) in type-2 diabetic subjects.

Results of the present study is summarized in Table 1.

Both animal and human studies have suggested that hyperuricemia is strongly associated with renal damage in DM. 6, 13 The various mechanisms by which hyperuricemia initiates renal damage in diabetics are well recognized. 3, 6 One such mechanism is activation of renin angiotensin-aldosterone system (RAAS). In diabetes RAAS activation causes a range of pathological changes including vascular dysfunction, high intraglomerular pressure, inflammation, and so on, leading to cardiovascular and renal complications. 14 From table-1 it is clear that there is significant increase in mean ACR from group-1 → group-2 → group- 3 which is proportional to increase in SUA levels suggesting that increase in SUA is responsible for increased urinary albumin excretion. The increase in albumin excretion is may be due to decrease in GFR which in turn is due to increased SUA. 11 In the present study, a significant (p < 0.01) positive correlation was found between SUA and ACR. Our study is consistent with the studies of Fukui, et al. 8 where they have reported a positive correlation of serum uric acid and urinary albumin excretion in 343 men with T2DM. Another study has shown that SUA and microalbuminuria were significantly and positively correlated with nephropathy in type-2 diabetic patients. 15 Siu and colleagues 16 reported lowering serum uric acid level in patients with hyperuricemia was associated with regression of kidney disease. Fu et al. in a study on Chinese diabetic patients found that hyperuricemia was significantly associated with abnormal albuminuria in patients without diuretics or use of uricosuric agents or alcohol. 17 Since appearance of albuminuria is the first sign of kidney damage and onset of DN in patients with DM, measuring SUA in patients with T2DM and correcting the levels if there is hyperuricemia may prove to be beneficial for preventing the progression of T2DM to DN.

This study shows a positive correlation between SUA and urinary ACR ratio suggesting the importance of SUA levels as a predictor of albuminuria in type-2 diabetic subjects. The pathogenic role of hyperuricemia in renal injury, in increasing urinary albumin excretion rate and in progression of diabetes to its chronic complication, nephropathy, is worthy of further investigation. Also, we call for further research studies on use of SUA lowering drugs in various clinical conditions witnessing hyperuricemia.