Abstract
Originalsprog | Engelsk |
---|---|
Tidsskrift | Alcoholism: Clinical and Experimental Research |
Vol/bind | 19 |
Udgave nummer | 2 |
Sider (fra-til) | 457-61 |
Antal sider | 4 |
ISSN | 0145-6008 |
Status | Udgivet - 1995 |
Bibliografisk note
Keywords: Alcoholism; Biological Markers; Cross-Sectional Studies; Denmark; Female; Humans; Incidence; Male; Mass Screening; Predictive Value of Tests; Sampling Studies; Transferrin; Urban PopulationCitationsformater
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Carbohydrate-deficient transferrin--a valid marker of alcoholism in population studies? Results from the Copenhagen City Heart Study. / Grønbaek, M; Becker, U; Henriksen, Jens Henrik Sahl.
I: Alcoholism: Clinical and Experimental Research, Bind 19, Nr. 2, 1995, s. 457-61.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
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TY - JOUR
T1 - Carbohydrate-deficient transferrin--a valid marker of alcoholism in population studies? Results from the Copenhagen City Heart Study
AU - Grønbaek, M
AU - Becker, U
AU - Henriksen, Jens Henrik Sahl
N1 - Keywords: Alcoholism; Biological Markers; Cross-Sectional Studies; Denmark; Female; Humans; Incidence; Male; Mass Screening; Predictive Value of Tests; Sampling Studies; Transferrin; Urban Population
PY - 1995
Y1 - 1995
N2 - Carbohydrate-deficient transferrin (CDT) was analyzed by a modified radioimmunoassay test in a random population sample of 400 individuals, and results were compared with reported alcohol intake derived from a structured questionnaire. Among the 180 men, the test was found to be acceptable with respect to detecting harmful alcohol intake (> 35 beverages/week) and alcohol intake above the recommended level (21 beverages/week), although the positive predictive values were low. Among the 220 women, the test was invalid with low predictive values. CDT was compared with other known markers of high alcohol intake, and it was observed that CDT had higher sensitivity and specificity than AST and short Michigan Alcoholism Screening Test (sMAST) in men, whereas the positive and negative predictive values were low in all tests. A combination of CDT and AST proved to be a better marker of both harmful alcohol intake and alcohol intake above the recommended level than the other markers. Neither CDT, AST, CDT/AST, nor sMAST proved to be useful as markers of alcohol intake in women. There were no differences between the values for pre- and postmenopausal women. These results from a population survey indicate that CDT is a marker of alcohol intake among men, although not ideal, but CDT cannot be used in the screening of harmful alcohol intake in women.
AB - Carbohydrate-deficient transferrin (CDT) was analyzed by a modified radioimmunoassay test in a random population sample of 400 individuals, and results were compared with reported alcohol intake derived from a structured questionnaire. Among the 180 men, the test was found to be acceptable with respect to detecting harmful alcohol intake (> 35 beverages/week) and alcohol intake above the recommended level (21 beverages/week), although the positive predictive values were low. Among the 220 women, the test was invalid with low predictive values. CDT was compared with other known markers of high alcohol intake, and it was observed that CDT had higher sensitivity and specificity than AST and short Michigan Alcoholism Screening Test (sMAST) in men, whereas the positive and negative predictive values were low in all tests. A combination of CDT and AST proved to be a better marker of both harmful alcohol intake and alcohol intake above the recommended level than the other markers. Neither CDT, AST, CDT/AST, nor sMAST proved to be useful as markers of alcohol intake in women. There were no differences between the values for pre- and postmenopausal women. These results from a population survey indicate that CDT is a marker of alcohol intake among men, although not ideal, but CDT cannot be used in the screening of harmful alcohol intake in women.
M3 - Journal article
C2 - 7625582
VL - 19
SP - 457
EP - 461
JO - Alcoholism: Clinical and Experimental Research
JF - Alcoholism: Clinical and Experimental Research
SN - 0145-6008
IS - 2
ER -