Literature DB >> 31650796

Serum Aminotransferase Level in Rhabdomyolysis according to Concurrent Liver Disease.

Kyeong Min Jo1, Nae-Yun Heo1, Seung Ha Park1, Young Soo Moon1, Tae Oh Kim1, Jongha Park1, Joon Hyuk Choi1, Yong Eun Park1, Jin Lee1.   

Abstract

BACKGROUND/AIMS: The serum aminotransferase level is usually elevated in rhabdomyolysis, and these enzymes originate from the skeletal muscle. On the other hand, there is limited data showing whether the degree of elevation of these enzymes differs according to the concurrent liver disease.
METHODS: Patients with rhabdomyolysis were selected when their serum creatinine kinase level was >1,000 U/L. They were categorized as the group with and without concurrent liver disease. The AST and ALT levels in both groups were compared. In addition, the aminotransferase level was compared between those with rhabdomyolysis and those with alcoholic liver disease.
RESULTS: Among the 165 patients with rhabdomyolysis, 19 had concurrent liver disease. The median peak AST was higher in the group with concurrent liver disease (332 U/L [interquartile range (IQR), 127-1,604] vs. 219 U/L [IQR, 115-504]). In addition, the median peak ALT was higher in the group with concurrent liver disease (107 U/L [IQR, 74-418] vs. 101 U/L [IQR, 56-218]). On the other hand, there was no significant difference in both enzymes between the two groups. The median peak AST level was significantly higher in those with rhabdomyolysis than in those with alcoholic liver disease (221 U/L [IQR, 118-553] vs. 103 U/L [IQR, 59-206]), but the median peak ALT was not significantly different (102 U/L [IQR, 58-222] vs. 51 U/L [IQR, 26-117]).
CONCLUSIONS: Rhabdomyolysis showed an elevated AST-dominant aminotransferase level, which is not different according to concurrent liver disease. Therefore, it is recommended that rhabdomyolysis be considered first in cases of elevated aminotransferase levels in patients with a suspicious skeletal muscle injury.

Entities:  

Keywords:  Alanine transaminase; Aspartate aminotransferases; Liver diseases; Rhabdomyolysis

Mesh:

Substances:

Year:  2019        PMID: 31650796     DOI: 10.4166/kjg.2019.74.4.205

Source DB:  PubMed          Journal:  Korean J Gastroenterol        ISSN: 1598-9992


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