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Metanephrine- Fractionated Plasma

Reproductive
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Report in 96Hrs

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At Home

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Fasting Required

Details

Catecholamine metabolites.

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Metanephrine - Fractionated Plasma Test Guide

  • Why is it done?
    • Measures plasma levels of free metanephrines (epinephrine and norepinephrine metabolites) to detect catecholamine-secreting tumors
    • Primary indication: Screening for pheochromocytoma and paraganglioma in patients with suspected catecholamine excess
    • Evaluates patients presenting with hypertension, palpitations, excessive sweating, headaches, or anxiety attacks
    • Used in genetic syndromes associated with pheochromocytoma (MEN2A, MEN2B, NF1, VHL)
    • Monitoring patients with known pheochromocytoma or paraganglioma after surgical treatment or during medical management
    • Typically performed in the supine position after 30 minutes of rest to obtain baseline values
  • Normal Range
    • Plasma Free Metanephrines (Reference Range):
    • Normetanephrine: 0.4-0.9 nmol/L (or <0.9 nmol/L) or <0.61-0.89 nmol/L depending on laboratory
    • Metanephrine: 0.1-0.3 nmol/L (or <0.3 nmol/L) or <0.10-0.31 nmol/L depending on laboratory
    • Total metanephrines: <1.2 nmol/L
    • Units: nmol/L (nanomoles per liter) or pg/mL (picograms per milliliter)
    • Interpretation:
    • Normal: Values within reference range suggest absence of pheochromocytoma (>99% sensitive when normal)
    • Elevated: Values above upper reference limit suggest possible catecholamine-secreting tumor; typically >1.4x upper reference limit is considered positive
    • Borderline: Results between upper limit of normal and 1.4x upper limit warrant repeat testing or further investigation
    • Reference ranges vary by laboratory method and patient position; always refer to specific laboratory reference values
  • Interpretation
    • Elevated Metanephrines:
    • Strongly suggestive of pheochromocytoma or paraganglioma, particularly if markedly elevated (>2x upper limit of normal)
    • Elevated normetanephrine suggests tumor secreting norepinephrine
    • Elevated metanephrine alone may indicate tumor secreting primarily epinephrine (adrenal origin)
    • Normal Results:
    • Effectively rules out pheochromocytoma with >99% sensitivity when properly collected and within normal range
    • Symptoms suggestive of pheochromocytoma with normal metanephrines suggest alternative diagnoses
    • Factors Affecting Results:
    • Patient position and stress level: Standing vs supine position affects values significantly
    • Medications: Decongestants, stimulants, tricyclic antidepressants, sympathomimetic agents can elevate results
    • Recent exercise, caffeine intake, nicotine, and emotional stress can cause false elevations
    • Acute illness, sleep apnea, and certain medical conditions may elevate metanephrines
    • Improper blood collection technique or sample handling can invalidate results
    • Clinical Significance:
    • This test is the gold standard initial screening for catecholamine-secreting tumors due to superior sensitivity
    • More sensitive than 24-hour urine metanephrines for detecting pheochromocytoma
    • Helps differentiate true pheochromocytoma from pseudo-pheochromocytoma or essential hypertension
  • Associated Organs
    • Primary Organs/Systems:
    • Adrenal medulla: Primary site of pheochromocytoma (80-90% of cases)
    • Sympathetic nervous system: Paraganglioma can occur along sympathetic chain
    • Cardiovascular system: Affected by excessive catecholamine secretion
    • Medical Conditions Associated with Abnormal Results:
    • Pheochromocytoma: Catecholamine-secreting tumor of adrenal medulla (90-95% malignant potential of 10%)
    • Paraganglioma: Extra-adrenal catecholamine-secreting tumor; higher malignancy rate (30-40%) than adrenal pheochromocytoma
    • Multiple Endocrine Neoplasia Type 2 (MEN2A and MEN2B): Genetic predisposition to pheochromocytoma
    • Neurofibromatosis Type 1 (NF1): Associated with increased pheochromocytoma risk
    • Von Hippel-Lindau Disease (VHL): High risk for pheochromocytoma development
    • Potential Complications of Untreated Abnormal Results:
    • Hypertensive crisis: Acute, severe elevation in blood pressure
    • Myocardial infarction: Due to catecholamine-induced increased cardiac demand
    • Arrhythmias: Life-threatening cardiac dysrhythmias from excessive catecholamines
    • Pulmonary edema: Secondary to hypertensive crisis
    • Stroke: Hypertension-related cerebrovascular event
    • Tumor metastasis: Malignant paragangliomas can spread systemically if not identified and treated
  • Follow-up Tests
    • Confirmatory Tests if Results Elevated:
    • 24-hour Urine Free Metanephrines and Catecholamines: Confirmation of plasma results
    • Clonidine Suppression Test: To distinguish true pheochromocytoma from secondary causes of elevated catecholamines
    • Imaging Studies:
    • CT Abdomen and Pelvis: Standard imaging to locate adrenal masses
    • MRI Abdomen: Alternative imaging, better for characterizing adrenal lesions
    • I-123 MIBG Scan: Functional imaging for pheochromocytoma and paraganglioma detection
    • PET-CT with 18F-FDG or 68Ga-DOTATATE: Enhanced detection for malignant paragangliomas and metastases
    • Complementary Laboratory Tests:
    • Plasma Catecholamines (Epinephrine, Norepinephrine): Direct measurement of catecholamine levels
    • Chromogranin A: Tumor marker, elevated in pheochromocytoma and paraganglioma
    • Blood Pressure Monitoring: 24-hour ambulatory BP monitoring or home BP log to assess hypertension
    • Electrocardiogram (ECG): To assess for catecholamine-induced cardiac effects
    • Genetic Testing:
    • SDHA, SDHB, SDHD, SDHAF2 gene testing: For familial paraganglioma syndrome
    • RET proto-oncogene testing: For MEN2 syndromes
    • NF1 gene testing: For neurofibromatosis type 1
    • Monitoring Frequency:
    • Post-surgical: Metanephrines typically checked at 1-2 weeks post-op, then periodically (every 3-6 months initially, then annually)
    • Genetic syndrome carriers: Annual or biennial screening recommended
    • Known malignancy: More frequent monitoring (quarterly to semi-annually) depending on treatment plan
  • Fasting Required?
    • Fasting Status: Fasting is NOT required for this test
    • Patient Preparation Requirements:
    • Rest in supine position (lying down) for 30 minutes before blood draw to obtain standardized baseline
    • Maintain calm environment: Minimize stress and anxiety which can artificially elevate catecholamine levels
    • Avoid caffeine for at least 12 hours before testing
    • Avoid nicotine/tobacco for at least 1 hour before testing
    • No vigorous exercise for 24 hours prior to test
    • Medications to Avoid or Discuss:
    • Decongestants (pseudoephedrine, phenylephrine): Can cause false elevation in metanephrines
    • Sympathomimetic agents: Amphetamines, methylphenidate, ephedrine should be avoided
    • Tricyclic antidepressants (amitriptyline, imipramine): May elevate results; discuss with ordering physician
    • Antihistamines (first generation): Can cause elevation; avoid 48 hours prior if possible
    • Cold and cough medications: Contain sympathomimetic agents; avoid 24 hours prior
    • Appetite suppressants: Can elevate metanephrines; coordinate with ordering physician
    • Note: Do NOT discontinue essential medications (antihypertensives) without physician approval; inform lab of all current medications
    • Dietary Considerations:
    • Avoid tyramine-rich foods 24 hours prior: Aged cheeses, cured meats, fermented foods, soy sauce, some Asian dishes
    • Light meals acceptable; normal eating pattern is encouraged unless otherwise instructed
    • Collection Procedure Notes:
    • Blood collected via peripheral vein puncture into tubes with specific anticoagulant (usually EDTA or heparin)
    • Sample must be placed on ice immediately after collection and transported rapidly to lab
    • Plasma must be separated within 15 minutes of collection to prevent in vitro catecholamine release
    • Proper handling is critical to avoid falsely elevated results

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