How is chronic kidney disease (CKD) defined and staged?

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Last updated: February 7, 2026View editorial policy

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Definition of Chronic Kidney Disease

Chronic kidney disease is defined as either kidney damage or decreased kidney function (GFR <60 mL/min/1.73 m²) persisting for 3 months or more, regardless of the underlying cause. 1, 2, 3

Core Diagnostic Components

CKD diagnosis relies on three essential elements that must be present: 1

  • Structural/Anatomical Component: Markers of kidney damage, most importantly albuminuria 1
  • Functional Component: Based on glomerular filtration rate measurement 1
  • Temporal Component: Abnormalities must persist for at least 3 months 1, 2

Markers of Kidney Damage

Persistent proteinuria serves as the principal marker of kidney damage, even when GFR remains normal. 1, 2

Specific diagnostic thresholds include: 1, 2

  • Albumin-creatinine ratio >30 mg/g in spot urine samples
  • Sex-specific cutpoints: >17 mg/g in men and >25 mg/g in women

Additional markers of kidney damage beyond proteinuria: 1

  • Abnormalities in urine sediment
  • Abnormalities in blood and urine chemistry measurements
  • Abnormal findings on imaging studies

GFR Thresholds and Interpretation

GFR <60 mL/min/1.73 m² represents loss of half or more of normal adult kidney function and marks the threshold where complications of CKD increase substantially. 1

Key GFR reference values: 1

  • Normal GFR in young adults: approximately 120-130 mL/min/1.73 m²
  • GFR declines with age as part of normal aging
  • However, decreased GFR in elderly patients remains an independent predictor of adverse outcomes including death and cardiovascular disease 1

The definition of CKD applies uniformly regardless of patient age, despite age-related GFR decline. 1

CKD Staging System

CKD is classified into five stages based on GFR level, independent of the underlying cause: 1, 2

Stage GFR (mL/min/1.73 m²) Description
1 ≥90 Kidney damage with normal or increased GFR
2 60-89 Kidney damage with mild decrease in GFR
3 30-59 Moderate decrease in GFR
4 15-29 Severe decrease in GFR
5 <15 Kidney failure

Critical staging caveat: Stages 1 and 2 require documented evidence of kidney damage (such as albuminuria) in addition to the GFR level—GFR alone does not define early-stage CKD. 1, 2

Modern Risk Stratification

The KDIGO classification system provides more comprehensive risk stratification by combining: 3

  • GFR categories (G1-G5): ranging from normal/high (≥90 mL/min/1.73 m²) to kidney failure (<15 mL/min/1.73 m²)
  • Albuminuria categories (A1-A3): from normal (<30 mg/g) to severely increased (≥300 mg/g)

Both urine albumin measurement and GFR assessment should be used together to test people at risk for CKD. 3

Clinical Implications for Outcomes

The definition prioritizes early detection because: 1

  • Decreased GFR associates with multiple complications: hypertension, anemia, malnutrition, bone disease, neuropathy, and decreased quality of life
  • These complications can be prevented or ameliorated by treatment at earlier stages
  • Treatment can slow progression to kidney failure
  • Cardiovascular disease events are more common than kidney failure in CKD patients 1
  • CKD patients should be considered in the highest risk group for subsequent cardiovascular events 1

Common pitfall: Do not dismiss mildly reduced GFR as "normal aging" without considering it represents true CKD requiring medication dose adjustments and increased cardiovascular risk monitoring. 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Diagnostic Indications of Chronic Kidney Disease

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Chronic Kidney Disease Definition and Classification

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.

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