Evidence map›Paper›PMID 38706738›Full record

ArticleEJIFCC2024

Optimization of the Diagnostic Capacity of Traditional Biomarkers in Muscle Damage and Its Use in the Diagnosis of Dermatomyositis and Polymyositis.

Sara Sanchez Asis, María Cristina Gómez Cobo, David Ramos Chavarino, Beatriz García García, Isabel Llompart Albern, José Antonio Delgado Rodríguez

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Article in EJIFCC, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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6 authors.

Sara Sanchez AsisDepartment of Laboratory Medicine, Hospital Universitari Son Espases, Palma, Spain.
María Cristina Gómez CoboDepartment of Laboratory Medicine, Hospital Universitari Son Espases, Palma, Spain.
David Ramos ChavarinoDepartment of Laboratory Medicine, Hospital Universitari Son Espases, Palma, Spain.
Beatriz García GarcíaDepartment of Laboratory Medicine, Hospital Universitari Son Espases, Palma, Spain.
Isabel Llompart AlbernDepartment of Laboratory Medicine, Hospital Universitari Son Espases, Palma, Spain.
José Antonio Delgado RodríguezDepartment of Laboratory Medicine, Hospital Universitari Son Espases, Palma, Spain.

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No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND-

aimCreatine kinase (CK) and aldolase are markers traditionally used in the study of muscle damage (MD). As CK determination is more specific to muscle damage, the demand for both determinations in routine laboratory tests would entail an extra cost.

methodsRetrospective observational study conducted between 2019-2020. CK and aldolase concentrations from 218 patients were studied.ROC curves were analyzed for CK and aldolase for muscle damage detection. Cut-off values were selected for both strategies. Specifity of CK and aldolase for dermatomyositis or polymyositis diagnosis in our population was studied using the McNemar's test.

resultsThe area under the ROC curve (AUC) for total CK was 0.716 (95%CI: 0.651-0.775), for CK in males it was 0.703 (95%CI: 0.592-0.799), and for CK in females was 0.719 (95%CI: 0.636-0.793). For aldolase, AUC was 0.505 (95%CI: 0.437-0.573). Optimized cut-off points for each determination were: 112 U/L for CK in men, with a sensitivity of 73.9% (95%CI: 51.6-89.8) and a specificity of 49.2% (95%CI: 35.9-62.5); 88 U/L for CK in women, with a sensitivity of 75.0% (95%CI: 57.8-87.9) and specificity of 50.5% (95%CI: 40.4-60.6); and 5.6 U/L for aldolase, with a sensitivity of 61.0% (95%CI: 53.2-68.8) and a specificity of 38.8% (95%CI: 26.5-52.6).Regarding the individuals diagnosed with dermatomyositis or polymyositis, 66.7% and 44.4% of them were correctly classified as pathological by CK and aldolase results, respectively. McNemar's test did not reveal significant differences.

conclusionThe determination of CK offers a better diagnostic performance of MD and, in addition, does not present significant differences regarding the determination of aldolase in cases of polymyositis and dermatomyositis. Therefore, the single determination of CK would be sufficient for MD screening.

Indexed as

aldolasecreatine kinasedermatomyositismuscle damagepolymyositis

Identifiers

PMID38706738
PMCPMC11063786

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