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1.
Diagnosis (Berl) ; 6(3): 307-309, 2019 08 27.
Article in English | MEDLINE | ID: mdl-30412465

ABSTRACT

The isoenzyme creatine kinase muscle/brain (CK-MB) still plays an important role for the differential diagnosis of CK elevations and the clarification of their origin from heart or skeletal muscle. Therefore, it is necessary to know the diagnostic pitfalls in interpreting CK-MB results. We demonstrate a case of macro-CK type 2 in a 75-year-old patient with metastatic castration-resistant prostate cancer and its identification by isoenzyme electrophoresis, which can be typical for cancer diseases.


Subject(s)
Antineoplastic Agents/therapeutic use , Creatine Kinase/blood , Docetaxel/therapeutic use , Electrophoresis, Agar Gel , Prostatic Neoplasms, Castration-Resistant/drug therapy , Acute Kidney Injury/therapy , Aged , Diagnosis, Differential , Humans , Isoenzymes , Male
2.
Epilepsia ; 44(5): 708-11, 2003 May.
Article in English | MEDLINE | ID: mdl-12752471

ABSTRACT

PURPOSE: To investigate a possible relation between antiepileptic drugs (AEDs) and the fatty acid composition of membranes. METHODS: Fatty acid (FA) composition of erythrocytes was studied in children with epilepsy receiving AED monotherapy. Children taking valproate (VPA, n = 28), carbamazepine (CBZ, n = 17), or phenobarbitone (PB, n = 14) were compared with healthy controls (n = 25). FAs were measured by capillary-gas chromatography (GC-FID). RESULTS: Significant changes (p < 0.05) in the FA composition of membranes were found. In children treated with VPA, C13:0 was decreased (8.2 +/- 2% vs. 10.7 +/- 4% in controls) and C14:0 increased (1.4 +/- 0.5% vs.1 +/- 0.5% in controls). C17:0 again was reduced (9.9 +/- 4% vs. 13.2 +/- 6% in controls), whereas the long-chained acids were enhanced: C18:2n-6 (6 +/- 2.4% vs. 3.9 +/- 2.5% in controls), and C20:4n-6 (1.9 +/- 1.7% vs. 1.4 +/- 0.5% in controls). The nonidentified FAs also increased with VPA therapy: 2.5 +/- 0.8% versus 1.7 +/- 0.9% in controls. Children treated with CBZ showed only minimal changes of FA composition: C13:0 was decreased compared with controls (8 +/- 2% vs. 10.7 +/- 4%). No changes were seen in patients taking PB. The mean corpuscular volume (MCV) showed important differences between the study groups: MCV was 84.7 +/- 6.0 fl during VPA therapy (p < 0.001) and 85.7 +/- 4.1 fl with CBZ (p < 0.001). During PB, the MCV increased to 82.87 +/- 3.29 fl compared with controls (78.73 +/- 4.92 fl; p < 0.01). CONCLUSIONS: VPA therapy is associated with changes of the FA composition of membranes, which is not the case with PB therapy. The implications of this finding remain to be established.


Subject(s)
Anticonvulsants/therapeutic use , Carbamazepine/therapeutic use , Epilepsy/drug therapy , Erythrocyte Membrane/drug effects , Fatty Acids/blood , Phenobarbital/therapeutic use , Valproic Acid/therapeutic use , Adolescent , Child , Child, Preschool , Epilepsy/blood , Female , Humans , Infant , Male , Reference Values
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