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Platelet Counts and Genetic Polymorphisms of Alcohol Dehydrogenase-1B and Aldehyde Dehydrogenase-2 in Japanese Alcoholic Men.

Authors :
Yokoyama A
Yokoyama T
Mizukami T
Matsui T
Kimura M
Matsushita S
Higuchi S
Maruyama K
Source :
Alcoholism, clinical and experimental research [Alcohol Clin Exp Res] 2017 Jan; Vol. 41 (1), pp. 171-178. Date of Electronic Publication: 2016 Dec 19.
Publication Year :
2017

Abstract

Background: Thrombocytopenia during intoxication, rebound thrombocytosis during 1 to 3 weeks of abstinence, and subsequent normalization of the platelet count are common in alcoholics.<br />Methods: We evaluated 989 Japanese alcoholic men to identify the effects of genetic polymorphisms of alcohol dehydrogenase-1B (ADH1B; rs1229984) and aldehyde dehydrogenase-2 (ALDH2; rs671) on platelet counts during an 8-week in-hospital abstinence period.<br />Results: Thrombocytopenia (<15 × 10 <superscript>4</superscript> /μl) was observed in 25.9% of the subjects upon admission. The platelet counts increased from 21.4 ± 0.3 × 10 <superscript>4</superscript> /μl (mean ± SE) to 27.6 ± 0.3 × 10 <superscript>4</superscript> /μl, and a rebound platelet increase of  ≥10 × 10 <superscript>4</superscript> /μl was observed in 28.6% of the patients during the first 2 weeks after admission. By 4 weeks, the mean platelet counts had returned to intermediate levels and remained stable thereafter. The reversible suppression and rebound increase in the platelet counts were more prominent in the slow-metabolizing ADH1B*1/*1 group than in the fast-metabolizing ADH1B*2 group. Throughout the 8 weeks, the mean platelet counts of the active ALDH2*1/*1 group were consistently lower than those in the inactive ALDH2*1/*2 group. Cirrhosis was a strong determinant of a lower platelet count. After adjustments for nongenetic factors including cirrhosis, multiple linear regression analyses showed that the ADH1B*1/*1 genotype was associated with a lower platelet count (partial regression coefficient = -1.3 × 10 <superscript>4</superscript> /μl) on the admission day, but subsequently had a positive effect on the platelet count at 1 and 2 weeks after admission (+1.5 and +3.8 × 10 <superscript>4</superscript> /μl, respectively). The ALDH2*1/*1 genotype was associated with a lower platelet count (-2.1 to -3.9 × 10 <superscript>4</superscript> /μl) consistently throughout the 8 weeks. Multiple logistic regression analyses showed that the ADH1B*1/*1 genotype increased the risk of thrombocytopenia upon admission (odds ratio [95% confidence interval] = 1.61 [1.14 to 2.27]) and of a rebound platelet increase during the first 2 weeks (3.86 [2.79 to 5.34]). The ALDH2*1/*1 genotype increased the risk of thrombocytopenia upon admission (1.73 [1.06 to 2.82]).<br />Conclusions: In alcoholics, the ADH1B*1/*1 genotype increased the risk of thrombocytopenia upon admission and of a rebound platelet increase 2 weeks thereafter, while the ALDH2*1/*1 genotype was associated with lower platelet counts throughout the 8-week hospital stay.<br /> (Copyright © 2016 by the Research Society on Alcoholism.)

Details

Language :
English
ISSN :
1530-0277
Volume :
41
Issue :
1
Database :
MEDLINE
Journal :
Alcoholism, clinical and experimental research
Publication Type :
Academic Journal
Accession number :
27991683
Full Text :
https://doi.org/10.1111/acer.13283