Archives of Neurology · 1970 · 57 citations · 19 references
MedicineBiochemistryPhysiologyCellular MetabolismEnzymologyNeuromuscular DisordersElectrolyte DisordersEnzyme DeficienciesMuscle DisordersMuscle PathologyMuscle WeaknessMuscular DystrophyEnzymesMuscle Enzyme DisordersMuscle Enzyme TestingSerum BiomarkersSerum Creatine Kinase AssessmentSerum Enzyme Activity MeasurementSerum Enzyme AssaysSkeletal Myopathy
THE MEASUREMENT of serum enzyme activities, particularly those of creatine phosphokinase (CPK), aldolase, and glutamic oxaloacetic transaminase (SGOT), is an important adjunct in the diagnosis of primary muscle disease.<sup>1-4</sup>Elevations have been found in patients with muscular dystrophy and polymyositis,<sup>5-7</sup>whereas patients with neurogenic atrophy generally have had normal levels.<sup>8</sup> Altered potassium metabolism has long been associated with muscle dysfunction,<sup>9</sup>but only a few references have appeared linking hypokalemia, myopathy, and serum enzyme elevation.<sup>10-12</sup>Three patients with hypokalemia and severe muscle weakness were studied; all had marked alterations in their serum enzymes, particularly CPK. <h3>Methods</h3> Creatine phosphokinase determinations were done using the method of Nielsen and Ludvigsen.<sup>13</sup>The normal range is 0μU to 18μU per milliliter. Glutamic oxaloacetic transaminase determinations were performed using a modification of the method of Henry and co-workers.<sup>14</sup>The normal values are in the range of
19
Richard J. Henry, Neil Chiamori, Orville J. Golub et al. · American Journal of Clinical Pathology · 1960 · 690 citations
High Creatine Phosphokinase Activity of Sera with Progressive Muscular Dystrophy
Setsuro Ebashi, Y Toyokura, Hironao Momoi et al. · The Journal of Biochemistry · 1959 · 169 citations
The consequences of potassium depletion
L. G. Welt, William Hollander, William B. Blythe · Journal of Chronic Diseases · 1960 · 120 citations
Medicine, Physiology, Soil Sciences +12