CARBOHYDRATE-DEFICIENT TRANSFERRIN AS A MARKER OF ALCOHOL-ABUSE - RELATIONSHIP TO ALCOHOL-CONSUMPTION, SEVERITY OF LIVER-DISEASE, AND FIBROGENESIS

被引:40
作者
NIEMELA, O
SORVAJARVI, K
BLAKE, JE
ISRAEL, Y
机构
[1] HELSINKI UNIV, DEPT CLIN CHEM, HELSINKI, FINLAND
[2] ADDICT RES FDN, TORONTO, ON M5S 2S1, CANADA
关键词
CARBOHYDRATE-DEFICIENT TRANSFERRIN; COLLAGEN MARKERS; ETHANOL METABOLISM;
D O I
10.1111/j.1530-0277.1995.tb01601.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Carbohydrate-deficient transferrin (CDT) measurements have been widely examined as a marker of excessive alcohol consumption, yet the information on the sensitivity of this method has remained controversial. In addition, little is known of the relationship of this marker and the severity of alcoholic liver disease (ALD). To clarify these issues, we analyzed serum samples from 373 alcohol abusers, including 200 problem drinkers with no apparent liver pathology, 173 patients with clinical or morphological evidence of ALD, and 42 healthy controls. CDT was analyzed by anion-exchange chromatography followed by radioimmunoassay. At a specificity of 100%, the sensitivity of CDT was 36% in problem drinkers reporting a mean of 710 +/- 80 (mean +/- 2SE) g of ethanol/week, as compared with the sensitivities of 44% and 35% for gamma-glutamyltranspeptidase (GGT) and mean corpuscular volume (MCV), respectively. In a subgroup of problem drinkers (n = 51) with the highest ethanol intakes (1160 +/- 180 g of ethanol/week) and severe dependence, the sensitivity of CDT increased to 64%, compared with 55% for GGT and 39% for MCV. In ALD, the CDT values were significantly higher than in the alcoholics with nonliver pathology. However, when such patients were classified according to the clinical, laboratory, and morphological severity of liver disease, CDT was found to be primarily elevated in those with the early stage of ALD, such that there was a significant negative correlation between CDT and the combined morphological index of disease severity (r(s) = -0.315, p < 0.05). ALD markers of fibrogenesis were elevated more frequently than CDT, showing significant positive correlations with the indices of disease severity. Current data indicates that, although CDT concentration correlates with the amount of alcohol consumed, it lacks diagnostic sensitivity in alcohol abusers consuming <100 g of alcohol per day, thus hampering its use as a screen for consumption in community samples, The finding that CDT is increased in an early phase of ALD may prove to be of diagnostic value.
引用
收藏
页码:1203 / 1208
页数:6
相关论文
共 47 条
[31]  
ROSMAN AS, 1994, CLIN CHEM, V40, P1641
[32]   INFLUENCE OF CARBOHYDRATES ON THE ANTIGENIC STRUCTURE OF GONADOTROPINS - DISTINCTION OF AGONISTS AND ANTAGONISTS [J].
SAIRAM, MR ;
LINGGEN, J ;
SAIRAM, J ;
BHARGAVI, GN .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1990, 68 (05) :889-893
[33]   PATTERN OF ALCOHOL-USE ASSOCIATED WITH SELF-IDENTIFIED PROBLEM DRINKING [J].
SANCHEZCRAIG, M ;
ISRAEL, Y .
AMERICAN JOURNAL OF PUBLIC HEALTH, 1985, 75 (02) :178-180
[34]   CDT BY ANION-EXCHANGE CHROMATOGRAPHY FOLLOWED BY RIA AS A MARKER OF HEAVY DRINKING AMONG MEN [J].
SILLANAUKEE, P ;
SEPPA, K ;
LOF, K ;
KOIVULA, T .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1993, 17 (02) :230-233
[35]   COMPARISON OF DIFFERENT METHODS FOR DETECTING CARBOHYDRATE-DEFICIENT TRANSFERRIN [J].
SILLANAUKEE, P ;
LOF, K ;
HARLIN, A ;
MARTENSSON, O ;
BRANDT, R ;
SEPPA, K .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1994, 18 (05) :1150-1155
[36]   CARBOHYDRATE-COMPOSITION OF SERUM TRANSFERRIN IN ALCOHOLIC PATIENTS [J].
STIBLER, H ;
BORG, S .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1986, 10 (01) :61-64
[37]   CARBOHYDRATE-DEFICIENT TRANSFERRIN IN SERUM IN PATIENTS WITH LIVER-DISEASES [J].
STIBLER, H ;
HULTCRANTZ, R .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1987, 11 (05) :468-473
[38]   MICRO ANION-EXCHANGE CHROMATOGRAPHY OF CARBOHYDRATE-DEFICIENT TRANSFERRIN IN SERUM IN RELATION TO ALCOHOL-CONSUMPTION (SWEDISH PATENT 8400587-5) [J].
STIBLER, H ;
BORG, S ;
JOUSTRA, M .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1986, 10 (05) :535-544
[39]  
STIBLER H, 1991, CLIN CHEM, V37, P2029
[40]  
STIBLER H, 1989, ALCOHOL ALCOHOLISM, V24, P388