Key result
Urinary ACE2 to creatinine levels were significantly increased in type 2 diabetic patients compared to healthy controls, and this augmentation was markedly attenuated by RAS inhibitors.
Why the study?
Are urinary ACE2 levels increased in type 2 diabetic patients, and does RAS inhibitor treatment affect its excretion?
Cross-Sectional (n=166)
Are urinary ACE2 levels increased in type 2 diabetic patients, and does RAS inhibitor treatment affect its excretion?
Urinary ACE2 is elevated in type 2 diabetes regardless of albuminuria, correlates with metabolic control, and is suppressed by RAS inhibitors, suggesting its potential as a biomarker for metabolic status and therapeutic response.
Urinary ACE2 may mark metabolic status in type 2 diabetes; hypothesis-generating for its role as a therapeutic biomarker.
BACKGROUND/AIMS: Angiotensin converting enzyme 2 (ACE2) is highly expressed in the kidney and recognized to be renoprotective by degrading Angiotensin II to Angiotensin (1-7) in diabetic nephropathy. However, little is known about the role of urinary ACE2 (UACE2) in diabetes. The present study was performed to evaluate UACE2 levels in type 2 diabetic patients with various degrees of albuminuria and its associations with metabolic parameters. The effect of RAS inhibitors on UACE2 excretion was also assessed. METHODS: A total of 132 type 2 diabetic patients with different degrees of albuminuria and 34 healthy volunteers were studied. UACE2 levels and activity were measured. RESULTS: Compared to healthy controls, UACE2 to creatinine (UACE2/Cr) levels were significantly increased in both albuminuric and non-albuminuric diabetic patients. UACE2/Cr levels were much higher in hypertensive diabetic patients compared with their normotensive counterparts and treatment with RAS inhibitors markedly attenuated the augmentation. Furthermore, UACE2/Cr was positively correlated with fasting blood glucose, hemoglobin A1C (HbA1C), triglyceride, and total cholesterol. In multiple regression analysis, UACE2/Cr was independently predicted by HbA1C and RAS inhibitors treatment. CONCLUSIONS: UACE2 increased in type 2 diabetic patients with various degrees of albuminuria and RAS inhibitors suppresses UACE2 excretion. UACE2 might potentially function as a marker for monitoring the metabolic status and therapeutic response of RAS inhibitors in diabetes.
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Liang et al. (2015) conducted a cross-sectional in Type 2 Diabetic Mellitus (n=166). Type 2 Diabetes Mellitus vs. Healthy volunteers was evaluated on Urinary ACE2 to creatinine (UACE2/Cr) levels. Urinary ACE2 to creatinine levels were significantly increased in type 2 diabetic patients compared to healthy controls, and this augmentation was markedly attenuated by RAS inhibitors.
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