The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants - PubMed (original) (raw)
Review
The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants
Howard J Edenberg. Alcohol Res Health. 2007.
Abstract
The primary enzymes involved in alcohol metabolism are alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH). Both enzymes occur in several forms that are encoded by different genes; moreover, there are variants (i.e., alleles) of some of these genes that encode enzymes with different characteristics and which have different ethnic distributions. Which ADH or ALDH alleles a person carries influence his or her level of alcohol consumption and risk of alcoholism. Researchers to date primarily have studied coding variants in the ADH1 B, ADH1C, and ALDH2 genes that are associated with altered kinetic properties of the resulting enzymes. For example, certain ADH1B and ADH1C alleles encode particularly active ADH enzymes, resulting in more rapid conversion of alcohol (i.e., ethanol) to acetaldehyde; these alleles have a protective effect on the risk of alcoholism. A variant of the ALDH2 gene encodes an essentially inactive ALDH enzyme, resulting in acetaldehyde accumulation and a protective effect. It is becoming clear that noncoding variants in both ADH and ALDH genes also may influence alcohol metabolism and, consequently, alcoholism risk; the specific nature and effects of these variants still need further study.
Figures
Figure 1
Relative sizes and positions of the seven human alcohol dehydrogenase (ADH) genes on the long arm of chromosome 4 (i.e., chromosome 4q). They are shown in the direction in which the genes are transcribed (arrows), but this is opposite to their orientation on chromosome 4q (i.e., ADH5 is closest to the region where the chromosome arms are joined [i.e., the centromere]). The distances between the genes are indicated in kilobasepairs (kb).
Figure 2
Linkage disequilibrium (LD) among single-nucleotide polymorphisms (SNPs) in the alcohol dehydrogenase (ADH) genes. The positions of the genes are indicated at the top. SNPs in which particular combinations of alleles are commonly inherited together have a high LD, depicted in the figure as darker-shaded boxes at the intersections of the SNPs that are being compared. SNPs in which combinations of alleles essentially are random have a lower LD (indicated by lighter shades). SNPs within genes generally are in high LD with each other, whereas SNPs in different genes typically have a lower LD between them. One region of moderately high LD spans most of the genes except ADH7. At one site of the ADH7 gene, frequent rearrangement of the genetic information (i.e., recombination) has occurred so that SNPs upstream of that site are randomly associated with SNPs downstream of that site (as indicated by the area of mostly white boxes). SOURCE: Modified from Edenberg et al. 2006.
Similar articles
- Expression pattern, ethanol-metabolizing activities, and cellular localization of alcohol and aldehyde dehydrogenases in human large bowel: association of the functional polymorphisms of ADH and ALDH genes with hemorrhoids and colorectal cancer.
Chiang CP, Jao SW, Lee SP, Chen PC, Chung CC, Lee SL, Nieh S, Yin SJ. Chiang CP, et al. Alcohol. 2012 Feb;46(1):37-49. doi: 10.1016/j.alcohol.2011.08.004. Epub 2011 Sep 22. Alcohol. 2012. PMID: 21940137 - Effect of the allelic variants of aldehyde dehydrogenase ALDH2*2 and alcohol dehydrogenase ADH1B*2 on blood acetaldehyde concentrations.
Peng GS, Yin SJ. Peng GS, et al. Hum Genomics. 2009 Jan;3(2):121-7. doi: 10.1186/1479-7364-3-2-121. Hum Genomics. 2009. PMID: 19164089 Free PMC article. Review. - Overview of the role of alcohol dehydrogenase and aldehyde dehydrogenase and their variants in the genesis of alcohol-related pathology.
Crabb DW, Matsumoto M, Chang D, You M. Crabb DW, et al. Proc Nutr Soc. 2004 Feb;63(1):49-63. doi: 10.1079/pns2003327. Proc Nutr Soc. 2004. PMID: 15099407 Review. - Allelic variation at alcohol metabolism genes ( ADH1B, ADH1C, ALDH2) and alcohol dependence in an American Indian population.
Mulligan CJ, Robin RW, Osier MV, Sambuughin N, Goldfarb LG, Kittles RA, Hesselbrock D, Goldman D, Long JC. Mulligan CJ, et al. Hum Genet. 2003 Sep;113(4):325-36. doi: 10.1007/s00439-003-0971-z. Epub 2003 Jul 12. Hum Genet. 2003. PMID: 12884000 - Research on alcohol metabolism among Asians and its implications for understanding causes of alcoholism.
Suddendorf RF. Suddendorf RF. Public Health Rep. 1989 Nov-Dec;104(6):615-20. Public Health Rep. 1989. PMID: 2511595 Free PMC article.
Cited by
- Alcohol Dependence Genetics: Lessons Learned From Genome-Wide Association Studies (GWAS) and Post-GWAS Analyses.
Hart AB, Kranzler HR. Hart AB, et al. Alcohol Clin Exp Res. 2015 Aug;39(8):1312-27. doi: 10.1111/acer.12792. Epub 2015 Jun 25. Alcohol Clin Exp Res. 2015. PMID: 26110981 Free PMC article. Review. - The Role of Alcohol, LPS Toxicity, and ALDH2 in Dental Bony Defects.
Tsai HC, Chen CH, Mochly-Rosen D, Li YE, Chen MH. Tsai HC, et al. Biomolecules. 2021 Apr 28;11(5):651. doi: 10.3390/biom11050651. Biomolecules. 2021. PMID: 33925003 Free PMC article. - Genetic Variants of Alcohol Metabolizing Enzymes and Alcohol-Related Liver Cirrhosis Risk.
Ayuso P, García-Martín E, Cornejo-García JA, Agúndez JAG, Ladero JM. Ayuso P, et al. J Pers Med. 2021 May 13;11(5):409. doi: 10.3390/jpm11050409. J Pers Med. 2021. PMID: 34068303 Free PMC article. - Alcohol-metabolizing genes and alcohol phenotypes in an Israeli household sample.
Meyers JL, Shmulewitz D, Aharonovich E, Waxman R, Frisch A, Weizman A, Spivak B, Edenberg HJ, Gelernter J, Hasin DS. Meyers JL, et al. Alcohol Clin Exp Res. 2013 Nov;37(11):1872-81. doi: 10.1111/acer.12176. Epub 2013 Jul 29. Alcohol Clin Exp Res. 2013. PMID: 23895337 Free PMC article. - Alcohol Consumption and Cardiovascular Disease: A Narrative Review of Evolving Perspectives and Long-Term Implications.
Georgescu OS, Martin L, Târtea GC, Rotaru-Zavaleanu AD, Dinescu SN, Vasile RC, Gresita A, Gheorman V, Aldea M, Dinescu VC. Georgescu OS, et al. Life (Basel). 2024 Sep 9;14(9):1134. doi: 10.3390/life14091134. Life (Basel). 2024. PMID: 39337917 Free PMC article. Review.
References
- Birley AJ, Whitfield JB, Neale MC, et al. Genetic time-series analysis identifies a major QTL for in vivo alcohol metabolism not predicted by in vitro studies of structural protein polymorphism at the ADH1B or ADH1C loci. Behavioral Genetics. 2005;35(5):509–524. - PubMed
- Chen YC, Lu RB, Peng GS, et al. Alcohol metabolism and cardiovascular response in an alcoholic patient homozygous for the ALDH2*2 variant gene allele. Alcoholism: Clinical and Experimental Research. 1999b;23(12):1853–1860. - PubMed
- Chen HJ, Tian H, Edenberg HJ. Natural haplotypes in the regulatory sequences affect human alcohol dehydrogenase 1C (ADH1C) gene expression. Human Mutation. 2005;25(2):150–155. - PubMed
- Choi IG, Son HG, Yang BH, et al. Scanning of genetic effects of alcohol metabolism gene (ADH1B and ADH1C) polymorphisms on the risk of alcoholism. Human Mutation. 2005;26(3):224–234. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous