Schöniger-Hekele Maximilian, Ramskogler Katrin, Hartl Doris, Lesch Otto M, Müller Christian
Klinische Abteilung Gastroenterologie und Hepatologie, Universitätsklinik für Innere Medizin IV, University of Vienna, Austria.
Wien Med Wochenschr. 2006 Apr;156(7-8):216-22. doi: 10.1007/s10354-005-0238-5.
Biological markers for chronic alcohol consumption like MCV or gammaGT or carbohydrate deficient transferrin (CDT) are useful, but far from being perfect. In patients with liver disease a reliable marker for chronic alcohol consumption as the underlying etiology is highly needed. Recently, a new ELISA based version of the carbohydrate-deficient-transferrin (CDT-TRISIALO (-)) assay has been developed, which measures asialo-, monosialo- and disialo transferrin, but excludes trisialo- transferrin; that modification suggests higher sensitivity and specificity in detecting recent alcohol consumption in patients.
The study goal was to evaluate the sensitivity, specificity, positive and negative predicitive value of this new carbohydrate-deficient-transferrin assay (CDT-TRISIALO (-)) in a group of patients with liver disease and to compare the results with that of the established CDT assay (CDT-TRISIALO (+)).
Our study population consisted of 110 consecutive patients (male: n = 80 [72.7 %], female: n = 30 [27.3 %]) with liver disease of the following etiologies: chronic alcohol consumption (n = 51 [46.4 %]; Out of them 30 alcohol abusing patients were assessed by cage = 1 and 21 alcohol dependent patients were assessed by cage = 2, chronic viral hepatitis (n = 33 [30.0 %]) including 25 [22.7 %] patients with chronic hepatitis C infection and 8 [7.3 %] patients with chronic hepatitis B infection), haemochromatosis (n = 4 [3.6 %]), mechanical cholestasis (n = 17 [15.5 %]) and other liver diseases (n = 5 [4.6 %] including autoimmune hepatitis (n = 2) and primary biliary cirrhosis (n = 3)). 27.3 % of our patients (n = 30) had no liver cirrhosis whereas the majority (72.7 %, n = 80) had liver cirrhosis.
In our population of liver disease patients the CDT-TRISIALO (-) assay had a sensitivity of 72.7 % and specificity of 58.1 % for recent alcohol consumption at the published cutoff level of 2.6 %. The positive predictive value was 34.0 % and the negative predictive value was 87.8 %. Sensitivity and specificity of the CDT-TRISIALO (+) assay at the recommended cutoff level of 4.7 % were similar, 77.3 % and 49.3 %, respectively. The positive and negative predictive values were 30.9 % and 88.1 %. CDTTRISIALO (+) and CDT-TRISIALO (-) levels increased significantly with higher Child-Pugh stages.
The newly developed carbohydrate deficient transferrin test (CDT-TRISIALO (-)) is of no advantage as compared to the established assay (CDT-TRISIALO (+)) when used in a patient population with liver disease. In that population, normal CDT-TRISIALO (-) helps to exclude recent alcohol consumption; this results from the high negative predictive value of a normal CDT-TRISIALO (-).
诸如平均红细胞体积(MCV)、γ-谷氨酰转肽酶(gammaGT)或缺糖转铁蛋白(CDT)等慢性酒精摄入的生物学标志物是有用的,但远非完美。对于患有肝病的患者,非常需要一种可靠的标志物来确定慢性酒精摄入是否为潜在病因。最近,已开发出一种基于酶联免疫吸附测定(ELISA)的缺糖转铁蛋白(CDT-TRISIALO (-))检测方法,该方法可检测去唾液酸转铁蛋白、单唾液酸转铁蛋白和双唾液酸转铁蛋白,但不包括三唾液酸转铁蛋白;这种改进表明在检测患者近期酒精摄入方面具有更高的敏感性和特异性。
本研究的目的是评估这种新的缺糖转铁蛋白检测方法(CDT-TRISIALO (-))在一组肝病患者中的敏感性、特异性、阳性预测值和阴性预测值,并将结果与已确立的CDT检测方法(CDT-TRISIALO (+))进行比较。
我们的研究人群包括110例连续的肝病患者(男性:n = 80 [72.7%],女性:n = 30 [27.3%]),病因如下:慢性酒精摄入(n = 51 [46.4%];其中30例酒精滥用患者通过CAGE问卷评分为1,21例酒精依赖患者通过CAGE问卷评分为2),慢性病毒性肝炎(n = 33 [30.0%]),包括25例[22.7%]慢性丙型肝炎感染患者和8例[7.3%]慢性乙型肝炎感染患者),血色素沉着症(n = 4 [3.6%]),机械性胆汁淤积(n = 17 [15.5%])和其他肝病(n = 5 [4.6%],包括自身免疫性肝炎(n = 2)和原发性胆汁性肝硬化(n = 3))。我们的患者中有27.3%(n = 30)没有肝硬化,而大多数(72.7%,n = 80)有肝硬化。
在我们的肝病患者群体中,CDT-TRISIALO (-)检测方法在已公布的2.6%的临界值水平下,对近期酒精摄入的敏感性为72.7%,特异性为58.1%。阳性预测值为34.0%,阴性预测值为87.8%。CDT-TRISIALO (+)检测方法在推荐的4.7%的临界值水平下的敏感性和特异性分别为77.3%和49.3%,阳性和阴性预测值分别为30.9%和88.1%。CDT-TRISIALO (+)和CDT-TRISIALO (-)水平随着Child-Pugh分期的升高而显著增加。
在肝病患者群体中使用时,新开发的缺糖转铁蛋白检测方法(CDT-TRISIALO (-))与已确立的检测方法(CDT-TRISIALO (+))相比没有优势。在该群体中,正常的CDT-TRISIALO (-)有助于排除近期酒精摄入;这是由于正常的CDT-TRISIALO (-)具有较高的阴性预测值。