Management and Monitoring Strategies for Abnormal Albumin Creatinine Ratio (ACR)
For patients with an abnormal Albumin Creatinine Ratio (ACR), management should include regular monitoring of ACR and eGFR at least annually, with frequency increased based on severity, alongside targeted interventions to reduce cardiovascular and kidney disease progression risk. 1
Understanding ACR and Its Significance
- ACR is the preferred method for evaluating albuminuria over total protein measurements, as it more accurately predicts kidney and cardiovascular risks and has greater sensitivity for detecting clinically important albuminuria 1
- The term "microalbuminuria" is no longer recommended; instead, albuminuria should be categorized as A1 (<30 mg/g), A2 (30-300 mg/g), or A3 (>300 mg/g) 1
- Increased albuminuria at any level of GFR is associated with higher risk for adverse outcomes, with risk increasing as a continuum 1
- ACR demonstrates high within-individual variability (coefficient of variation 48.8%), which may affect interpretation of results 2
Monitoring Frequency
- All patients with abnormal ACR should be assessed at least annually for both ACR and eGFR 1
- Monitoring frequency should increase based on:
- For albuminuria monitoring, a doubling of ACR on subsequent testing exceeds expected variability and warrants evaluation 1
- Consider multiple urine collections for more accurate monitoring of changes over time, especially when making treatment decisions 2
Management Strategies Based on ACR Category
For ACR 30-299 mg/g (A2 category):
- Blood Pressure Management:
For ACR ≥300 mg/g (A3 category):
- Blood Pressure Management:
For All Patients with Abnormal ACR:
Glycemic Control:
Lifestyle Modifications:
Risk Assessment and Referral Criteria
- Use validated risk prediction tools to assess progression risk 1
- Consider referral to nephrology when:
Special Considerations
- When initiating hemodynamically active therapies (ACE inhibitors, ARBs, SGLT2 inhibitors), eGFR reductions >30% exceed expected variability and warrant evaluation 1
- For patients with diabetes, ACR should be assessed annually if type 1 diabetes duration is ≥5 years and in all patients with type 2 diabetes 1
- Point-of-care testing for ACR may facilitate access to earlier diagnosis and care, especially in rural or remote locations 1, 3
Common Pitfalls and Caveats
- ACR has high biological variability (>20%) between measurements; confirm abnormal results with 2-3 specimens collected over 3-6 months 1
- Several factors can transiently elevate ACR independently of kidney damage: exercise within 24h, infection, fever, heart failure, marked hyperglycemia, menstruation, and marked hypertension 1
- Urine dipstick tests have poor sensitivity (43.6%) and high false-discovery rates for detecting ACR ≥30 mg/g, making ACR measurement preferable for accurate risk assessment 4
- ACR variability may be higher in females and those with moderately increased albuminuria, while it may be lower in patients with reduced eGFR or those on SGLT2 inhibitors or RAS blockers 2