Serum enzymes in the neonatal period. Diagnostic aid in muscle pathology

Biology of the Neonate
|January 1, 1975
PubMed

Insights

Serum enzyme levels in newborns were established to aid in early disease detection. Creatine phosphokinase (CPK) normalizes by 10 days, enabling early diagnosis of muscular dystrophy.

Area of Science:

  • Neonatal Medicine
  • Biochemistry
  • Pediatric Diagnostics

Background:

  • Establishing normal serum enzyme reference ranges in neonates is crucial for accurate clinical interpretation.
  • Variations in enzyme levels can indicate underlying physiological immaturity or disease states.

Purpose of the Study:

  • To define normal serum enzyme standards for term and preterm infants during the neonatal period.
  • To assess the utility of these standards for early diagnosis of specific conditions, such as muscular dystrophy.

Main Methods:

  • Measurement of serum enzyme levels including creatine phosphokinase (CPK), lactate dehydrogenase (LDH), diphosphofructoaldolase (ALD), glutamic-oxalacetic transaminase (SGOT), and glutamic pyruvic transaminase (SGPT).
  • Analysis of enzyme levels in relation to precise days of the neonatal period for both term and preterm infants.

Main Results:

  • Creatine phosphokinase (CPK) levels reached adult standards by 10 days of life, suggesting potential for early muscular dystrophy diagnosis.
  • Lactate dehydrogenase (LDH) and diphosphofructoaldolase (ALD) remained elevated at 10 days.
  • Lower SGOT and SGPT levels in preterm infants were observed, likely due to immature enzyme synthesis.

Conclusions:

  • Neonatal serum enzyme profiles, particularly CPK, can serve as early indicators for conditions like Duchenne muscular dystrophy.
  • Enzyme levels like LDH and ALD show a different developmental trajectory in neonates.
  • Preterm infants exhibit distinct enzyme patterns, highlighting the impact of physiological immaturity on enzyme synthesis.

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