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Myoglobin


Definition


  • Myoglobin is the primary oxygen-carrying protein of muscle tissues found only in skeletal and cardiac muscle. It is a small-sized molecule that is rapidly released from damaged tissue and is not protein bound and rapidly excreted in urine. Plasma half-life is 9 minutes. It is linked in a reversible manner with oxygen, playing an important part in cellular aerobic metabolism.
  • Normal range (may be wide): 6 " “90 ng/mL.
    • Male: 28 " “72 ng/mL
    • Female: 25 " “58 ng/mL

Use


  • A cardiac biomarker, myoglobin is the one of the earliest markers for myocardial necrosis.
  • Myoglobin levels start to rise within 2 " “3 hours of myocardial infarction, reach their highest levels within 8 " “12 hours, and generally fall back to normal within 1 day.
  • A negative myoglobin result effectively rules out a heart attack, but a positive result must be confirmed by testing for troponin or another biomarker.
  • Sensitivity is >95% within 6 hours of onset of symptoms.
  • Myoglobin may precede release of CK-MB by 2 " “5 hours.

Interpretation


  • Within 1 " “3 hours in >85% of patients with AMI, myoglobin peaks in about 8 " “12 hours (may peak within 1 hour) to about 10 times the upper reference limit and becomes normal in about 24 " “36 hours or less; reperfusion causes a peak 4 " “6 hours earlier.
  • It is also increased in
    • Renal failure (high levels of urine myoglobin indicate an increased risk of kidney damage.)
    • Shock
    • Open heart surgery
    • Carriers of progressive muscular dystrophy
    • Extensive trauma
    • Myocarditis
    • Acute infectious diseases
      • Seizure
      • Toxin exposure: cocaine, narcotics, sea snake venom
      • Malignant hypertension

Limitations


  • With high-sensitivity troponins and 99% sensitivity cutoffs now currently used in MI diagnosis, myoglobin has been replaced by troponin as the preferred cardiac biomarker. Exceptions may be in rapid ACS protocols if local laboratory point-of-care troponin is unreliable. Nevertheless, myoglobin should not be the solitary biomarker used for diagnosis.
  • Increased values may occur with skeletal muscle damage, exhaustive exercise, or heavy alcohol abuse.
  • The myoglobin test displays a low specificity for AMI. Myoglobin may come from either heart or skeletal muscle, so an increase in serum myoglobin is not specific for damage to the heart.
  • Blood samples should be drawn every 2 " “3 hours for the first several hours after experiencing chest pain (myoglobin may be released in multiple short bursts) for accurate measurements.
  • Values are usually much higher in patients with uremia and muscle trauma compared to AMI.
  • Myoglobin should not be used for the diagnosis of MI but may be useful in conjunction with other biomarkers for prognosis postrevascularization.

Suggested Readings


1deLemos ‚  JA, Morrow ‚  DA, Gibson ‚  CM The prognostic value of serum myoglobin in patients with non-ST-segment elevation acute coronary syndromes: Results from the TIMI 11B and TACTICS-TIMI 18 studies. JACC.  2002;40:238. 2Ordway ‚  GA, Garry ‚  DJ. Myoglobin: An essential hemoprotein in striated muscle. J Exp Biol.  2004;207:3441 " “3446.
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