What is Grade II Chronic Kidney Disease (CKD)?

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What is Grade II Chronic Kidney Disease (CKD)?

Grade II (Stage 2) CKD is defined as mildly decreased kidney function with a GFR of 60-89 mL/min/1.73 m² PLUS evidence of kidney damage (such as albuminuria ≥30 mg/g, structural abnormalities, or other markers of kidney damage) persisting for at least 3 months. 1

Critical Diagnostic Requirements

The GFR value alone is insufficient to diagnose Stage 2 CKD - you must document kidney damage in addition to the mildly decreased GFR. 2, 3 This is a common diagnostic pitfall that leads to overdiagnosis.

Evidence of kidney damage includes:

  • Albuminuria with UACR ≥30 mg/g (most common marker) 1
  • Structural abnormalities on imaging (reduced kidney size, cortical thinning) 2
  • Hematuria, pyuria, or urinary casts suggesting glomerulonephritis 4
  • Pathological findings on kidney biopsy 1

Chronicity must be confirmed by demonstrating abnormalities persist for at least 3 months through repeat measurements or review of historical data. 1, 3 A single abnormal eGFR could represent acute kidney injury rather than CKD. 2

Risk Stratification

The modern KDIGO classification uses a combined approach (CGA system) incorporating:

  • Cause of kidney disease 1, 3
  • GFR category (G2 = 60-89 mL/min/1.73 m²) 1, 3
  • Albuminuria category 1

For Stage 2 CKD specifically:

  • Low risk: GFR 60-89 with UACR <30 mg/g 1
  • Moderate risk: GFR 60-89 with UACR 30-300 mg/g 1
  • High risk: GFR 60-89 with UACR >300 mg/g 1

Clinical Significance

Stage 2 CKD represents early kidney disease where intervention can prevent progression. 5 At this stage:

  • Kidney function is only mildly reduced (60-89 mL/min/1.73 m² represents approximately 50-70% of normal young adult GFR) 1
  • Most patients are asymptomatic 5, 6
  • Cardiovascular risk is elevated 5-10 times compared to the general population 4
  • The disease is potentially reversible or stabilizable with appropriate management 2

Common Causes

The most frequent etiologies include:

  • Diabetes (20-40% of CKD cases) 4, 5
  • Hypertension 4, 5
  • Glomerulonephritis 4
  • Nephrotoxin exposure (NSAIDs, heavy metals) 4

Management Priorities

Blood pressure control is paramount, targeting <130/80 mmHg for all CKD patients. 2 For patients with albuminuria:

  • UACR 30-299 mg/g with hypertension: Initiate ACE inhibitor or ARB 2
  • UACR ≥300 mg/g: ACE inhibitor or ARB strongly recommended regardless of blood pressure 2

SGLT2 inhibitors should be initiated for cardiorenal protection if UACR ≥200 mg/g, regardless of diabetes status. 2 Consider even with lower albuminuria if heart failure or high cardiovascular risk is present. 2

Statin therapy is indicated for cardiovascular risk reduction in all CKD patients. 4, 2

Monitoring Frequency

  • Low risk (UACR <30 mg/g): Monitor eGFR and UACR annually 2, 3
  • Moderate risk (UACR 30-300 mg/g): Monitor every 6 months 4
  • High risk (UACR >300 mg/g): Monitor every 3-4 months 4

Critical Pitfalls to Avoid

Never diagnose Stage 2 CKD based on eGFR alone - this is the most common error and leads to inappropriate labeling of patients. 2, 3 Always confirm kidney damage through albuminuria testing or other markers.

Do not rely on serum creatinine alone - always calculate eGFR using validated equations (CKD-EPI 2021 is preferred). 4, 3

Do not skip albuminuria testing - eGFR and UACR provide independent prognostic information for cardiovascular events, CKD progression, and mortality. 4

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of CKD Stage 2

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Chronic Kidney Disease Staging and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Chronic Kidney Disease Causes and Risk Factors

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Kidney Disease: Chronic Kidney Disease.

FP essentials, 2021

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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