Bergström Jonas P, Helander Anders
Department of Clinical Neuroscience, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
Clin Chim Acta. 2008 Mar;389(1-2):164-6. doi: 10.1016/j.cca.2007.11.020. Epub 2007 Dec 4.
Carbohydrate-deficient transferrin (CDT) is an alcohol biomarker used for detection and follow-up of excessive alcohol consumption. This HPLC study evaluated some clinical conditions and medications previously suggested to interfere with and cause non-alcohol related elevations of CDT.
Serum samples were collected from patients with end-stage liver disease (n=50), type 2 diabetes mellitus (n=46), cystic fibrosis (n=24), an elevated C-reactive protein level (CRP>100 mg/L; n=15), and from patients taking enzyme inducing or non-enzyme inducing antiepileptic drugs (n=43). Subjects with known or suspected alcohol-related problems were excluded. A sensitive and specific HPLC candidate CDT reference method was used to determine the relative amount of disialotransferrin to total transferrin.
Of the 178 samples, 9 (5%) had a %disialotransferrin level > or =1.8% (>97.5th percentile) and were considered CDT positive. The highest frequency of elevated results was found in patients with end-stage liver disease (12%, n=6), including 3 with hemochromatosis, 1 with hepatitis C, 1 with autoimmune hepatitis and 1 with unspecified liver disease and cirrhosis. The other elevated %disialotransferrin results were from 2 patients taking enzyme-inducing antiepileptic drugs and 1 with type 2 diabetes. Five of 8 examined %disialotransferrin positive samples were also positive for ethyl glucuronide (EtG).
This HPLC study found an overall low frequency of elevated %disialotransferrin levels in the clinical conditions and medications examined. Previous reports of frequent false-positive CDT results thus seem to be connected with the analytical methodology used rather than representing true clinical or pharmacological interferences.
缺糖转铁蛋白(CDT)是一种用于检测和跟踪过量饮酒情况的酒精生物标志物。本高效液相色谱(HPLC)研究评估了一些先前提示会干扰并导致非酒精相关性CDT升高的临床状况和药物。
收集了终末期肝病患者(n = 50)、2型糖尿病患者(n = 46)、囊性纤维化患者(n = 24)、C反应蛋白水平升高(CRP>100 mg/L;n = 15)的患者以及服用酶诱导或非酶诱导抗癫痫药物的患者(n = 43)的血清样本。排除已知或疑似与酒精相关问题的受试者。采用一种灵敏且特异的HPLC候选CDT参考方法来测定双唾液酸转铁蛋白与总转铁蛋白的相对含量。
在178份样本中,9份(5%)的双唾液酸转铁蛋白百分比水平≥1.8%(>第97.5百分位数),被视为CDT阳性。终末期肝病患者中结果升高的频率最高(12%,n = 6),其中包括3例血色素沉着症患者、1例丙型肝炎患者、1例自身免疫性肝炎患者以及1例病因不明的肝病和肝硬化患者。其他双唾液酸转铁蛋白百分比升高的结果来自2例服用酶诱导抗癫痫药物的患者和1例2型糖尿病患者。在8份检测的双唾液酸转铁蛋白阳性样本中,有5份的葡萄糖醛酸乙酯(EtG)也呈阳性。
本HPLC研究发现,在所检测的临床状况和药物中,双唾液酸转铁蛋白百分比水平升高的总体频率较低。因此,先前关于CDT结果频繁出现假阳性的报道似乎与所使用的分析方法有关,而非代表真正的临床或药理学干扰。