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Gender differences in serum CK-MB mass levels in healthy Braziliansubjects

机译:健康巴西受试者血清CK-MB质量水平的性别差异

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The creatine kinase-isoenzyme MB (CK-MB) mass assay is one of the laboratory tests used for the diagnosis of myocardial infarction. It is recommended, however, that reference limits should take gender and race into account. In the present study, we analyzed the plasma CK-MB mass and troponin levels of 244 healthy volunteers without a personal history of coronary artery disease and with no chronic diseases, muscular trauma or hypothyroidism, and not taking statins. The tests were performed with commercial kits, CK-MB mass turbo kit and Troponin I turbo kit, using the Immulite 1000 analyzer from Siemens Healthcare Diagnostic. The values were separated according to gender and showed significant differences by the Mann-Whitney test. Mean (± SD) CK-MB mass values were 2.55 ± 1.09 for women (N = 121; age = 41.20 ± 10.13 years) and 3.49 ± 1.41 ng/mL for men (N = 123; age = 38.16 ± 11.12 years). Gender-specific reference values at the 99th percentile level, according to the Medicalc statistical software, were 5.40 ng/mL for women and 7.13 ng/mL for men. The influence of race was not considered because of the high miscegenation of the Brazilian population. The CK-MB values obtained were higher than the 5.10 mg/mL proposed by the manufacturer of the laboratory kit. Therefore, decision limits should be related to population and gender in order to improve the specificity of this diagnostic tool, avoiding misclassification of patients
机译:肌酸激酶-同工酶MB(CK-MB)质量测定是用于诊断心肌梗塞的实验室检查之一。但是,建议参考限值应考虑性别和种族。在本研究中,我们分析了244位健康的志愿者的血浆CK-MB质量和肌钙蛋白水平,这些患者没有冠心病的个人病史,没有慢性疾病,肌肉外伤或甲状腺功能减退,并且未服用他汀类药物。使用Siemens Healthcare Diagnostic的Immulite 1000分析仪,使用商业套件,CK-MB质量涡轮套件和Troponin I涡轮套件进行了测试。这些值是根据性别分开的,并且通过Mann-Whitney检验显示出显着差异。女性(N = 121;年龄= 41.20±10.13岁)的平均(±SD)CK-MB质量值为2.55±1.09,男性(N = 123;年龄= 38.16±11.12岁)为3.49±1.41 ng / mL。根据Medicalc统计软件,在第99个百分点的性别特定参考值是女性为5.40 ng / mL,男性为7.13 ng / mL。由于巴西人口的高种族歧视,未考虑种族的影响。获得的CK-MB值高于实验室试剂盒制造商建议的5.10 mg / mL。因此,决策限制应与人群和性别相关,以提高该诊断工具的特异性,避免患者分类错误

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