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Platelet Counts and Genetic Polymorphisms of Alcohol Dehydrogenase-1B and Aldehyde Dehydrogenase-2 in Japanese Alcoholic Men.
Yokoyama, Akira; Yokoyama, Tetsuji; Mizukami, Takeshi; Matsui, Toshifumi; Kimura, Mitsuru; Matsushita, Sachio; Higuchi, Susumu; Maruyama, Katsuya.
Afiliación
  • Yokoyama A; National Hospital Organization Kurihama Medical and Addiction Center, Yokosuka, Kanagawa, Japan.
  • Yokoyama T; Department of Health Promotion, National Institute of Public Health, Wako, Saitama, Japan.
  • Mizukami T; National Hospital Organization Kurihama Medical and Addiction Center, Yokosuka, Kanagawa, Japan.
  • Matsui T; National Hospital Organization Kurihama Medical and Addiction Center, Yokosuka, Kanagawa, Japan.
  • Kimura M; Department of Geriatric Medicine, Kyorin University Hospital, Mitaka, Tokyo, Japan.
  • Matsushita S; National Hospital Organization Kurihama Medical and Addiction Center, Yokosuka, Kanagawa, Japan.
  • Higuchi S; National Hospital Organization Kurihama Medical and Addiction Center, Yokosuka, Kanagawa, Japan.
  • Maruyama K; National Hospital Organization Kurihama Medical and Addiction Center, Yokosuka, Kanagawa, Japan.
Alcohol Clin Exp Res ; 41(1): 171-178, 2017 01.
Article en En | MEDLINE | ID: mdl-27991683
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.

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.

RESULTS:

Thrombocytopenia (<15 × 104 /µl) was observed in 25.9% of the subjects upon admission. The platelet counts increased from 21.4 ± 0.3 × 104 /µl (mean ± SE) to 27.6 ± 0.3 × 104 /µl, and a rebound platelet increase of  ≥10 × 104 /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 × 104 /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 × 104 /µl, respectively). The ALDH2*1/*1 genotype was associated with a lower platelet count (-2.1 to -3.9 × 104 /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]).

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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 / 8_ODS3_consumo_sustancias_psicoactivas Problema de salud: 2_sustancias_psicoativas / 8_alcohol Asunto principal: Polimorfismo Genético / Alcohol Deshidrogenasa / Pueblo Asiatico / Alcoholismo / Aldehído Deshidrogenasa Mitocondrial Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Alcohol Clin Exp Res Año: 2017 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 / 8_ODS3_consumo_sustancias_psicoactivas Problema de salud: 2_sustancias_psicoativas / 8_alcohol Asunto principal: Polimorfismo Genético / Alcohol Deshidrogenasa / Pueblo Asiatico / Alcoholismo / Aldehído Deshidrogenasa Mitocondrial Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Alcohol Clin Exp Res Año: 2017 Tipo del documento: Article País de afiliación: Japón
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