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Hyper-CK-emia in pediatric celiac disease: prevalence and clinical importance
Mukadder Ayse Selimoglu1, Vildan Ertekin, Sevin Altinkaynak
1Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Faculty of Medicine, Inonu University, Malatya, Turkey. ayseselimoglu@hotmail.com
Insights
Hyper-creatine phosphokinase (CK) elevation (HCK) is common in children with celiac disease (CD), similar to hyper-transaminasemia (HT). This suggests HCK may indicate muscle involvement rather than liver injury in pediatric CD.
Area of Science:
- Pediatric Gastroenterology
- Clinical Biochemistry
- Autoimmune Diseases
Background:
- Hyper-transaminasemia (HT) is a known indicator of celiac disease (CD).
- Hyper-creatine phosphokinase (CK)-emia (HCK) is less recognized in CD.
- Myopathy has been associated with CD in previous reports.
Purpose of the Study:
- To investigate serum CK levels in children diagnosed with CD.
- To determine the prevalence of HCK in pediatric CD patients.
- To explore the relationship between CK levels and other biochemical markers in CD.
Main Methods:
- Included 126 newly diagnosed children with CD.
- Measured serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), and CK levels.
- Analyzed correlations between CK, AST, ALT, hemoglobin, and cholesterol.
Main Results:
- Elevated AST, ALT, and CK were found in 51.6%, 35.7%, and 39.7% of patients, respectively.
- Isolated HCK was observed in 7.1% of children.
- CK levels positively correlated with AST and ALT, and inversely with hemoglobin and cholesterol.
Conclusions:
- This study is the first to report elevated serum CK levels in children with CD.
- HCK is as prevalent as HT in pediatric CD.
- Elevated transaminases in CD may stem from myopathy, not solely liver injury.
Abstract:
Hyper-transaminasemia (HT) is a well-known laboratory sign of celiac disease (CD); however, hyper-creatine phosphokinase (CK)-emia (HCK) is not so familiar. As there are reported cases of myopathy associated CD in the literature, we aimed to investigate serum CK levels of children with CD. Newly diagnosed 126 children were included. Serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), and CK levels were determined. Mean age was 8.7+/-4.4 years (11 mo to 18 y). Of patients, 77 (61.1%) had classic form, 49 (38.9%) had atypical form. Elevated levels of AST, ALT, and CK, respectively, were found in 65 (51.6%), 45 (35.7%), and 50 (39.7%) patients. Isolated HCK was detected in 9 (7.1%) patients. AST, ALT, and CK were all elevated in 29 (23.0%) children. Mean serum AST, ALT, and CK levels were found as 56.1+/-53.7 U/L (11 to 403), 44.7+/-44.0 U/L (7 to 290), and 258.0+/-686.5 U/L (36 to 5956), respectively. In 95 (75.4%) children, AST/ALT value was greater than 1, and in 19 (15.1%) it was greater than 2. We found positive correlations with the level of CK and AST, and ALT (P=0.01). CK level was inversely correlated with hemoglobin and cholesterol levels (P=0.013 and 0.007). In conclusion, this is the first study, which determined elevated serum levels of CK in CD and demonstrated that HCK is as common as HT in children with CD. We emphasize that HT seen in CD is not necessarily a sign of liver injury, but may also be due to myopathy.
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