Alcohol Dehydrogenase‐1B Genotype (rs1229984) is a Strong Determinant of the Relationship Between Body Weight and Alcohol Intake in Japanese Alcoholic Men. (15th February 2013)
- Record Type:
- Journal Article
- Title:
- Alcohol Dehydrogenase‐1B Genotype (rs1229984) is a Strong Determinant of the Relationship Between Body Weight and Alcohol Intake in Japanese Alcoholic Men. (15th February 2013)
- Main Title:
- Alcohol Dehydrogenase‐1B Genotype (rs1229984) is a Strong Determinant of the Relationship Between Body Weight and Alcohol Intake in Japanese Alcoholic Men
- Authors:
- Yokoyama, Akira
Yokoyama, Tetsuji
Matsui, Toshifumi
Mizukami, Takeshi
Matsushita, Sachio
Higuchi, Susumu
Maruyama, Katsuya - Abstract:
- <abstract abstract-type="main" id="acer12069-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="acer12069-sec-0001" sec-type="section"> <title>Background</title> <p>The calories in alcoholic beverages consumed by alcoholics are a major energy source and a strong modifier of their body weight. Genetic polymorphisms of alcohol dehydrogenase‐1B (ADH1B) and aldehyde dehydrogenase‐2 (ALDH2) affect susceptibility to alcoholism and may affect body weight via gene‐associated differences in fuel utilization in alcoholics.</p> </sec> <sec id="acer12069-sec-0002" sec-type="section"> <title>Methods</title> <p>We evaluated associations between ADH1B/ALDH2 genotypes and the body weight and body mass index (BMI) of 1, 301 Japanese alcoholic men at the time of their first visit to an addiction center.</p> </sec> <sec id="acer12069-sec-0003" sec-type="section"> <title>Results</title> <p>Median (25th to 75th) caloric intake in the form of alcoholic beverages was 864 (588 to 1, 176) kcal/d. Age‐adjusted caloric intake did not differ according to ADH1B/ALDH2 genotypes. The body weight and BMI values showed that the <italic>ADH1B*2/*2</italic> and <italic>*1/*2</italic> carriers (<italic>n</italic> = 939) were significantly leaner than the <italic>ADH1B*1/*1</italic> carriers (<italic>n</italic> = 362) irrespective of age, drinking, smoking, and dietary habits. The age‐adjusted body weight values of the <italic>ADH1B*2/*2</italic>, <italic> ADH1B*1/*2</italic>, and<abstract abstract-type="main" id="acer12069-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="acer12069-sec-0001" sec-type="section"> <title>Background</title> <p>The calories in alcoholic beverages consumed by alcoholics are a major energy source and a strong modifier of their body weight. Genetic polymorphisms of alcohol dehydrogenase‐1B (ADH1B) and aldehyde dehydrogenase‐2 (ALDH2) affect susceptibility to alcoholism and may affect body weight via gene‐associated differences in fuel utilization in alcoholics.</p> </sec> <sec id="acer12069-sec-0002" sec-type="section"> <title>Methods</title> <p>We evaluated associations between ADH1B/ALDH2 genotypes and the body weight and body mass index (BMI) of 1, 301 Japanese alcoholic men at the time of their first visit to an addiction center.</p> </sec> <sec id="acer12069-sec-0003" sec-type="section"> <title>Results</title> <p>Median (25th to 75th) caloric intake in the form of alcoholic beverages was 864 (588 to 1, 176) kcal/d. Age‐adjusted caloric intake did not differ according to ADH1B/ALDH2 genotypes. The body weight and BMI values showed that the <italic>ADH1B*2/*2</italic> and <italic>*1/*2</italic> carriers (<italic>n</italic> = 939) were significantly leaner than the <italic>ADH1B*1/*1</italic> carriers (<italic>n</italic> = 362) irrespective of age, drinking, smoking, and dietary habits. The age‐adjusted body weight values of the <italic>ADH1B*2/*2</italic>, <italic> ADH1B*1/*2</italic>, and <italic>ADH1B*1/*1</italic> carriers were 58.4 ± 0.4, 58.7 ± 0.5, and 63.6 ± 0.5 kg, respectively (<italic>ADH1B*2</italic> vs. <italic>ADH1B*1/*1</italic> carriers, <italic>p</italic> &lt; 0.0001), and the corresponding BMI values were 21.0 ± 0.1, 21.0 ± 0.1, and 22.9 ± 0.2 kg/m<sup>2</sup>, respectively (<italic>ADH1B*2</italic> vs. <italic>ADH1B*1/*1</italic> carriers, <italic>p</italic> &lt; 0.0001). No effects of inactive ALDH2 on body weight or BMI were observed. A multivariate analysis showed that BMI decreased by 0.35 per 10‐year increase in age, by 1.73 in the presence of the <italic>ADH1B*2</italic> allele, by 1.55 when the preferred beverage was whiskey, and by 0.19 per +10 cigarettes/d and that it increased by 0.10 per +22 g ethanol (EtOH)/d and by 0.41 per increase in category of frequency of milk intake (every day, occasionally, rarely, and never). The increase in BMI as alcohol consumption increased was significantly smaller in the <italic>ADH1B*2</italic> group than in the <italic>ADH1B*1/*1</italic> group (<italic>p</italic> = 0.002).</p> </sec> <sec id="acer12069-sec-0004" sec-type="section"> <title>Conclusions</title> <p>ADH1B genotype was a strong determinant of body weight in the alcoholics. The more rapid EtOH elimination associated with the <italic>ADH1B*2</italic> allele may result in less efficient utilization of EtOH as an energy source in alcoholics.</p> </sec> </abstract> … (more)
- Is Part Of:
- Alcoholism. Volume 37:Number 7(2013:Jul.)
- Journal:
- Alcoholism
- Issue:
- Volume 37:Number 7(2013:Jul.)
- Issue Display:
- Volume 37, Issue 7 (2013)
- Year:
- 2013
- Volume:
- 37
- Issue:
- 7
- Issue Sort Value:
- 2013-0037-0007-0000
- Page Start:
- 1123
- Page End:
- 1132
- Publication Date:
- 2013-02-15
- Subjects:
- Alcoholism -- Periodicals
Alcoholism -- Periodicals
Alcoolisme
Electronic journals
Périodique électronique (Descripteur de forme)
Ressource Internet (Descripteur de forme)
616.861005 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=0145-6008;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1530-0277 ↗
http://www.alcoholism-cer.com/ ↗
http://www.blackwell-synergy.com/loi/acer ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/acer.12069 ↗
- Languages:
- English
- ISSNs:
- 0145-6008
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 0786.789300
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