X. Pares et al., GENETIC-POLYMORPHISM OF LIVER ALCOHOL-DEHYDROGENASE IN SPANISH SUBJECTS - SIGNIFICANCE OF ALCOHOL-CONSUMPTION AND LIVER-DISEASE, Alcohol and alcoholism, 29(6), 1994, pp. 701-705
Class I alcohol dehydrogenase (ADH) phenotypes have been studied by st
arch gel electrophoresis and activity analysis in liver tissue obtaine
d at necropsy from 61 non-alcoholic subjects with normal liver (contro
ls), and in biopsies from 60 chronic alcoholics with liver disease and
from 24 subjects with non-alcoholic liver disease. Twenty-three per c
ent of controls exhibited the ADH(2)(2-1) phenotype, which represents
the highest frequency for atypical ADH found in a Caucasian population
. Both alcoholic and non-alcoholic patients with liver disease showed
a lower frequency of the atypical phenotype (6.6% and 8.8%, respective
ly). No differences in the ADH(2) locus were detected among groups of
patients with different severity of alcoholic and non-alcoholic liver
disease. The allele frequencies of the ADH(3) locus for the controls (
ADH(3)(I) = 0.63, ADH(3)(2) = 0.37) are common to those of other Cauca
sian populations. Similar ADH(3) allele frequencies were observed in p
atients with alcoholic and non-alcoholic liver disease. Discrepancies
between the various phenotyping and genotyping studies now known for s
everal populations suggest that local differences may exist in the dis
tribution of the ADH polymorphism in even geographically close regions
, and that the effect of ADH polymorphism on vulnerability towards alc
ohol may not be identical in different populations.