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Patient Info
Creatine Kinase (CK): Unexpectedly High
2
Asymptomatic high CK: General
More common in males than females
May occur at all ages
If high CK persists after rest: Evaluation usually includes
EMG
Muscle biopsy
High CK with few, no, or atypical symptoms: Causes
Endocrine
Hypothyroid
Hypoparathyroid
Exercise
4
Acute
Producing
Muscle Hypertrophy
Muscle Trauma: Injections (esp phenothiazines); Psychosis; Falls
CK time course after injury
Onset of rise: < 12 hours
Peak values: 1 to 3 days
Decline: 3 to 5 days
Half life: 36 to 48 hours
Failure to decrease: Ongoing muscle injury
EMG
Rarely elevates a normal CK to abnormal levels
Peak CK: 1x to 1.5x baseline in 6 hours
Return to baseline: 48 hours
Myopathies (asymptomatic)
Dystrophy
Dystrophinopathy
Limb-Girdle MD (LGMD):
1C
;
2A
;
2B
;
2P
Metabolic
Glycogen Storage Disorders
CPT2 deficiency
AMPDA deficiency
Other hereditary myopathy
Central core
Danon
Distal
Malignant Hyperthermia
Mitochondrial disease
MLIP
Myofibrillar myopathy
Myopathy with tubular aggregates
Myotonia:
Congenita
;
DM2
Rippling muscle syndromes
Acquired disorders
Inflammatory
Drug toxicity
Denervation
5
Motor neuron diseases
Small fiber polyneuropathies
Not: Sensory-Motor polyneuropathies
Newborns
3
May be high with vaginal delivery or C-section
Range: 265 to 3100
Idiopathic
Hereditary Idiopathic
Other Idiopathic: 50% to 80% of HyperCKemia
Normal muscle: 30%
Non-specific muscle abnormalities: 30%
Creatine Kinase (CK): Low or Normal
1
Muscle disease
Muscle mass: Reduced
Disuse:
Type 2 fiber atrophy
End-stage muscle
Corticosteroid related
Treatment:
Myosin-loss
myopathy
Cushing disease
SLONM
Immune
Common pattern:
CK Normal with Aldolase High
Dermatomyositis, childhood type
: Some patients
IMPP
syndromes
Graft vs Host
(GvHD) myopathy
Perimyositis
Sarcoid
&
Granulomatous myopathies
Systemic disorders
Hyperthyroidism
Multiorgan failure
Rheumatic diseases: Active inflammation
Rheumatoid arthritis
Systemic lupus erythematosis
Spondyloarthropathies
Fasciitis
Rule out:
NMJ disorders
See:
Creatine kinase (CK) very high
Return to Myopathy & NMJ Index
References
1. Clin Rheumatol 2000;19:296-300
2. J Neurol 2002;249:305-311
3.
Neurosciences (Riyadh) 2022;27:263-269
4.
Am J Case Rep 2022;23:e937084
5.
Muscle Nerve 2013;48:252-255
,
Sci Rep 2024;14:13816
6/17/2024