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Studies on the creatine kinase MM isoforms of normal and Duchenne muscular dystrophic patients.

AbstractOBJECTIVE:
To study the changes of creatine kinase MM (CK-MM) isoforms in Duchenne muscular dystrophy (DMD) patients.
METHODS:
Serum samples from 49 DMD patients and 40 control subjects were collected for CK-MM isoforms measurement. CK-MM isoforms were separated within 30 minutes by electrophoresis on agarose gel with a discontinuous buffer system at constant current of 30 mA and low voltage of 200-300 V, then measured by fluorescence scanning.
RESULTS:
Significant differences of MM2/MM1 ratio were found between DMD patients and control subjects (P < 0.05) as well as among the three different age groups of DMD patients (P < 0.05).
CONCLUSIONS:
CK-MM isoforms may present useful information for the early diagnosis and evaluation of DMD and the ratio of MM2/MM1 can be considered as a specific indicator of the degree of seriousness for DMD patients.
AuthorsX Zhao, C Bi, Z Yang
JournalChinese medical journal (Chin Med J (Engl)) Vol. 111 Issue 1 Pg. 75-7 (Jan 1998) ISSN: 0366-6999 [Print] China
PMID10322660 (Publication Type: Journal Article)
Chemical References
  • Biomarkers
  • Isoenzymes
  • Creatine Kinase
Topics
  • Adolescent
  • Adult
  • Biomarkers
  • Child
  • Child, Preschool
  • Creatine Kinase (blood)
  • Electrophoresis, Agar Gel
  • Female
  • Humans
  • Isoenzymes
  • Male
  • Muscular Dystrophies (enzymology)

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