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Comprehensive Metabolic Panel (CMP-14) with eGFR Blood Test

An advanced 14-biomarker metabolic analysis plus eGFR to thoroughly evaluate kidney filtration, hepatic insulin sensitivity, glucose dynamics, and electrolyte/fluid balance.

At a glance

Price Starting from

$8.00USD

Test price · additional fees may apply

Sample
Blood (Serum)
Typical turnaround
1 - 2 days
Before your appointment

Your options, side by side

Compare retailer prices.

Find a listing that fits your needs. Review the details, then order with the retailer.

12 listings

12 matches · USD

Jason Health

Comprehensive Metabolic Panel

Listed price $8.00
Fees & listing detailsRecorded Mar 10, 2026
Additional listing fee
$0.00
Blood draw
Not provided
Service
$18.00
Requisition
Not provided

Listed prices exclude any extra charges shown here. Confirm the final total and collection requirements with the retailer.

This observation is older than 7 days.

New century Labs

Comprehensive Metabolic Panel

Listed price $15.00
Fees & listing detailsRecorded Mar 10, 2026
Additional listing fee
$0.00
Blood draw
Not provided
Service
Not provided
Requisition
$12.00

Listed prices exclude any extra charges shown here. Confirm the final total and collection requirements with the retailer.

This observation is older than 7 days.

Grass Roots Labs

CMP - Comprehensive Metabolic Panel w/ eGFR

Listed price $18.89
Fees & listing detailsRecorded Mar 10, 2026
Additional listing fee
$0.00
Blood draw
$4.00
Service
Not provided
Requisition
$6.00

Listed prices exclude any extra charges shown here. Confirm the final total and collection requirements with the retailer.

This observation is older than 7 days.

Discountedlabs

CMP Panel - Comprehensive Metabolic Panel

Listed price $19.00
Fees & listing detailsRecorded Mar 10, 2026
Additional listing fee
$0.00
Blood draw
$8.00
Service
Not provided
Requisition
Not provided

Listed prices exclude any extra charges shown here. Confirm the final total and collection requirements with the retailer.

This observation is older than 7 days.

Ulta Lab test

Comprehensive Metabolic Panel Test - CMP Most Popular

Listed price $22.95
Fees & listing detailsRecorded Mar 10, 2026
Additional listing fee
$0.00
Blood draw
$12.95
Service
Not provided
Requisition
Not provided

Listed prices exclude any extra charges shown here. Confirm the final total and collection requirements with the retailer.

This observation is older than 7 days.

Prices shown are listed test prices, not checkout totals. Expand a listing for supplied fees and its observation date. Check included measurements, collection requirements, and the performing lab before ordering.

Understand before you decide

The test, explained.

Overview

The Comprehensive Metabolic Panel (CMP-14) with eGFR is far more than a routine physical checklist; it is a profound biochemical snapshot of your cellular health.

While traditionally viewed as a simple screen for organ damage, modern clinical practice utilizes the CMP-14 to detect the earliest whispers of metabolic dysfunction. By analyzing the interplay between your fasting glucose, liver enzymes, and kidney filtration rates, this panel provides a roadmap for optimizing your metabolism through targeted lifestyle and dietary interventions before overt disease develops.

About this test

Clinical Interpretation of Your CMP-14

1. Glucose & Insulin Dynamics
  • Fasting Glucose (70–99 mg/dL): Glucose does not exist in a vacuum; it is tightly coupled with the hormone insulin. Fasting glucose is actually a lagging indicator of metabolic health—by the time your fasting glucose begins to rise into the 90s, compensatory hyperinsulinemia (insulin resistance) has often been developing for years. Modulating this through lifestyle choices—such as utilizing post-meal muscle contraction to act as a glucose sink, or employing specific supplements to enhance insulin sensitivity—directly impacts this baseline by clearing glucose from the bloodstream without requiring massive pancreatic insulin spikes.

2. Hepatic (Liver) Function & The Enzyme Ratio

Your liver is the primary site of glucose storage (glycogen) and fat metabolism. The enzymes here tell a complex story about ectopic fat storage.

  • ALT & AST (Alanine & Aspartate Aminotransferase): ALT is primarily localized in the liver, while AST is also found in skeletal and cardiac muscle. A temporary spike in AST can simply reflect a heavy resistance training session. However, chronic elevations—even within the "high normal" range—are heavily correlated with hepatic insulin resistance and non-alcoholic fatty liver disease (NAFLD).

  • The AST/ALT Ratio: In clinical research as of 2025, this ratio has emerged as a powerhouse biomarker. An altered AST/ALT ratio is now recognized as a non-invasive predictor of metabolic syndrome, indicating impaired fasting glucose and a higher triglyceride-glucose (TyG) index long before diabetes is formally diagnosed.

  • Albumin & Total Protein: These are synthesized by the liver. Albumin is a primary carrier protein for hormones, fatty acids, and exogenous supplements in the bloodstream. Optimal levels indicate robust hepatic synthesis and adequate amino acid availability.

3. Kidney Function & Microvascular Health

The kidneys filter roughly 150 quarts of blood daily. They are highly sensitive to microvascular damage from chronically elevated blood sugar and high blood pressure.

  • Creatinine (0.6–1.3 mg/dL): A metabolic byproduct of creatine phosphate in muscle tissue. If you carry a high amount of lean muscle mass or consume a high-protein diet, your baseline will naturally run higher. It is a critical variable in calculating your filtration rate.

  • BUN (Blood Urea Nitrogen): Reflects protein breakdown. While kidney dysfunction raises BUN, an isolated high BUN often simply reflects transient dehydration or a protein-heavy meal prior to the fast.

  • eGFR (Estimated Glomerular Filtration Rate): This calculates how efficiently your kidney's glomeruli are clearing waste. Recent data ties a declining eGFR not just to primary kidney disease, but as a systemic indicator of metabolic syndrome and chronic low-grade inflammation.

4. Electrolytes & Cellular Voltage
  • Sodium, Potassium, Chloride, and Carbon Dioxide: These are the electrical conductors of your body. They dictate the resting membrane potential of your cells, control action potentials for muscle contractions, and regulate the delicate acid-base (pH) balance of the blood. Potassium, in particular, is vital for driving glucose into the cell alongside insulin.

When to discuss this test

You should prioritize this comprehensive evaluation when:

  • You are actively biohacking or utilizing dietary interventions (like low-carb, fasting, or specific botanical supplements) and want objective data on your metabolic adaptation.
  • You are monitoring the reversal of impaired fasting glucose or prediabetes.
  • You want to assess the impact of your exercise and muscle mass on your baseline metabolic rate and kidney filtration.

Who may benefit

This panel is an absolute necessity for anyone moving away from reactive medicine and toward proactive health optimization. It is highly beneficial for individuals tracking insulin resistance, athletes monitoring their recovery and renal load, and those assessing their cardiovascular and hepatic risk profiles.

How this test is used

  • Insulin Resistance and Early-Stage Metabolic Syndrome
  • Hepatic Steatosis (Fatty Liver Disease)
  • Chronic Kidney Disease (CKD) and Diabetic Nephropathy
  • Systemic Electrolyte and Acid-Base Imbalances

Before your appointment

Plan your visit.

Fasting
Required · 10 hours
Collection timing
Morning collection preferred

How to prepare

  • Strict Fasting: Fast for a minimum of 10-12 hours. Do not consume any food or caloric beverages. Even black coffee can sometimes trigger an acute cortisol response in sensitive individuals, which may temporarily elevate fasting glucose via hepatic gluconeogenesis.
  • Hydration is Mandatory: Drink plenty of plain water. Dehydration concentrates the blood, leading to falsely elevated BUN, albumin, and sodium levels.
  • Exercise Caution: Avoid intense, muscle-damaging workouts (like heavy lifting or eccentric training) for 24-48 hours prior, as this can artificially spike AST and Creatinine levels, mimicking liver or kidney stress.

Important considerations

Context is Everything: Never interpret a single marker in isolation. For example, a mathematically low eGFR driven by a high creatinine might not mean kidney failure if you are a heavily muscled athlete. Similarly, minor shifts in liver enzymes must be correlated with your training intensity and supplement intake. Always evaluate these biomarkers as an interconnected web.

Follow the instructions from your retailer and clinician. Information on this page is educational and does not replace individual medical advice.

See what to expect

Sample reports & resources.

Published examples and supporting files for this test.

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For a closer look

Sources & further reading.

Further reading

2025–2026 Clinical Breakthroughs:

  • AST/ALT Ratio & Normoglycemia Reversion: A major 2025 retrospective cohort study published in Frontiers in Endocrinology demonstrated that the AST/ALT ratio is an independent predictor of reversing impaired fasting glucose (IFG). Tracking this ratio is now considered a vital tool for predicting whether lifestyle interventions will successfully return an individual to normoglycemia.
  • Triglyceride-Glucose (TyG) Index Correlation: 2025 research in the journal Taylor & Francis established a robust link between the TyG index (a modern marker of insulin resistance) and elevated ALT and AST levels. This confirms that even "normal" high-end liver enzymes are often masking underlying hepatic insulin resistance and early metabolic syndrome.
  • Heavy Metals & Diabetic Kidney Disease (DKD): Recent findings (late 2025, NIH/PMC) have identified that the AST/ALT ratio acts as a crucial mediator between environmental heavy metal exposure and the acceleration of diabetic kidney disease, bridging the gap between liver dysfunction, oxidative stress, and renal failure.

Sources