What does an estimated glomerular filtration rate (eGFR) of 58, indicating stage 3a chronic kidney disease (CKD), imply for my diagnosis and management, given the reference range for normal eGFR is typically above 60?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: December 15, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Understanding Your eGFR of 58 and CKD Stage 3a Diagnosis

With an eGFR of 58 mL/min/1.73 m², you do have stage 3a CKD, but this diagnosis requires confirmation with additional testing—specifically cystatin C measurement—because creatinine-based eGFR alone can be misleading, and approximately 23% of patients in your situation actually have normal kidney function when properly tested. 1, 2

Why the Confusion About CKD Stages Makes Sense

Your confusion is completely justified. Here's the critical distinction that resolves the apparent contradiction:

  • CKD Stage 1 (eGFR ≥90) and Stage 2 (eGFR 60-89) require evidence of kidney damage (such as albuminuria, blood in urine, or structural abnormalities) to be diagnosed as CKD. 3
  • An eGFR above 60 without kidney damage is simply normal—not CKD Stage 1 or 2. 3
  • Stage 3a (eGFR 45-59) is diagnosed by the reduced eGFR alone, regardless of other markers of damage. 3

This means an eGFR of 70 in someone without proteinuria or other kidney damage is normal, not "CKD Stage 2." The staging system only applies when kidney disease is actually present. 3

The Critical Problem: Creatinine-Based eGFR Can Be Wrong

Your provider should order a cystatin C test immediately to confirm whether you truly have CKD. 3, 1, 2 Here's why this matters:

  • Creatinine is produced by muscle breakdown, so your muscle mass directly affects the result independent of actual kidney function. 1, 4
  • Research shows that when cystatin C is measured in patients with creatinine-based eGFR of 45-59 (like your 58), approximately one-third have cystatin C-based eGFR ≥60, meaning they don't actually have CKD. 3, 2
  • The KDIGO guidelines specifically recommend measuring cystatin C in adults with creatinine-based eGFR 45-59 mL/min/1.73 m² who lack other markers of kidney damage (like protein in urine) to confirm the CKD diagnosis. 3, 1

What You Need to Do Next

Request these specific tests from your provider: 1, 2

  1. Serum cystatin C measurement (in addition to your routine creatinine)
  2. Urine albumin-to-creatinine ratio (UACR) to check for protein in your urine
  3. Urinalysis to check for blood or other abnormalities

The laboratory should calculate three eGFR values using the 2012 CKD-EPI equations: 1

  • eGFR based on creatinine alone (eGFRcreat)
  • eGFR based on cystatin C alone (eGFRcys)
  • eGFR based on both combined (eGFRcreat-cys)

Interpreting Your Results

If your cystatin C-based eGFR comes back ≥60 mL/min/1.73 m²: 2

  • You do NOT have CKD
  • Your declining creatinine-based eGFR likely reflects factors other than true kidney disease (such as changes in muscle mass, diet, or medications)
  • No CKD-specific treatment or monitoring is needed beyond standard preventive care

If your cystatin C-based eGFR is also <60 mL/min/1.73 m²: 2

  • Stage 3a CKD is confirmed
  • The combined creatinine-cystatin C equation (eGFRcreat-cys) should guide all clinical decisions, as it's 94.9% accurate compared to measured GFR. 1, 4
  • You need CKD-specific management (see below)

If CKD Is Confirmed: What Changes

A confirmed CKD diagnosis triggers specific management that significantly slows progression: 5

  • Blood pressure control: Target <130/80 mmHg if you have proteinuria. 3
  • ACE inhibitors or ARBs are preferred if you have hypertension and any degree of albuminuria (UACR ≥30 mg/g) or eGFR <60. 3
  • Annual monitoring of eGFR and UACR at minimum. 3
  • Protein intake should be approximately 0.8 g/kg/day. 3
  • Avoid nephrotoxic medications (NSAIDs, certain antibiotics) when possible. 3

Research shows that patients with a recorded CKD diagnosis have significantly reduced eGFR decline (from 3.20 mL/min/year before diagnosis to 0.74 mL/min/year after diagnosis) due to appropriate management. 5 Conversely, delayed diagnosis increases risk of progression to kidney failure by 63% per year of delay. 5

Common Pitfalls to Avoid

  • Don't assume a single creatinine-based eGFR of 58 definitively means you have CKD—demand confirmatory testing with cystatin C. 3, 1, 2
  • Don't confuse "normal eGFR range" with "CKD staging"—an eGFR of 70 without kidney damage is normal, not CKD Stage 2. 3
  • If you have variable muscle mass (weight loss, malnutrition, extreme exercise, or muscle-wasting conditions), creatinine-based eGFR is particularly unreliable, making cystatin C testing even more critical. 1, 4

Insurance and Cost Considerations

Cystatin C testing is increasingly covered by insurance when ordered with appropriate clinical justification (such as stage 3a CKD with borderline eGFR), as it has been incorporated into major KDIGO guidelines since 2012 with strengthened recommendations in 2024. 4 The cost is higher than routine creatinine testing but is considered affordable and clinically necessary for accurate diagnosis in your situation. 2

References

Guideline

Estimating Kidney Function using eGFR

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Cystatin C Testing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Cystatin C Testing for Accurate Kidney Function Assessment in Stage 3a CKD

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.