| No Liquor Sales | ||
|  National Institute on Alcohol Abuse and Alcoholism No. 
        18 PH 357 July 1992 
        The Genetics of Alcoholism 
        The idea that alcoholism runs in families is an 
        ancient one. In recent decades, science has advanced this idea from the 
        status of folk-observation to systematic investigation (1-3). In the 1970s, 
        studies documented that alcoholism does run in families (4,5). But does 
        alcoholism run in families because a child learns to become an alcoholic 
        from parents and the home environment, or because a child inherits genes 
        that create an underlying predisposition for alcoholism? Or both? The 
        studies did not resolve these questions. 
        	Why do we do genetic research? The discovery of a 
        specific genetic effect on the development of alcoholism would be beneficial 
        for at least three reasons. First, it would lead to the identification 
        of some people at risk, who could act to avoid developing alcohol-related 
        problems (6,7). Second, it may help us to understand the role of environmental 
        factors that are critical in the development of alcoholism (8). Third, 
        it may lead to better treatments, based on new understandings of the physiological 
        mechanisms of alcoholism (9-11). 
        	Although investigations of the inheritance of a vulnerability 
        to alcoholism are discussed here, a separate and distinct issue, not 
        addressed here, is the possibility that a vulnerability to organ damage 
        by alcohol is under some genetic control (12). 
        	Researchers investigate possible genetic components 
        of alcoholism by studying populations and families as well as genetic, 
        biochemical, and neurobehavioral markers and characteristics (13,14). 
        Two major methods of investigating the inheritance of alcoholism are studies 
        of twins and of adoptees (15). Twin studies compare the incidence of alcoholism 
        in identical twins with the incidence of alcoholism in fraternal twins 
        (16,17). If there is a genetic component in the risk for alcoholism, then 
        identical twins, who have identical genes, would be expected to exhibit 
        similar histories of developing alcoholism (or not developing alcoholism). 
        Fraternal twins, who are genetically different individuals born at the 
        same time, would be more likely to differ in their tendencies to develop 
        alcoholism. In general, researchers using the twin method have found these 
        expectations to be true. 
        	For example, Pickens and co-workers (18) studied 
        169 same-sex pairs of twins, both males and females, at least one of which 
        had sought treatment for alcoholism. The researchers found greater concordance 
        of alcohol dependence in identical twins than in fraternal twins. They 
        also found greater concordance of alcohol abuse (defined by DSM-III--Diagnostic 
        and Statistical Manual of Mental Disorders, Third Edition, of the 
        American Psychiatric Association) in identical male twins but not in identical 
        female twins. Other twin studies have produced more detailed information; 
        for example, Partanen and co-workers (19), in studying 902 male Finnish 
        twins, found that less severe drinking patterns were less heritable, and 
        more severe drinking patterns were more heritable. 
        	Among the difficulties in designing twin studies 
        is accounting for unequal environmental conditions. Early studies assumed 
        that the environments of two fraternal twins were as similar to each other 
        as were the environments of two identical twins. Later studies showed 
        that the environments of identical twins are more alike than are the environments 
        of fraternal twins, and recent twin studies have taken this difference 
        into account (14). The results of twin studies are useful and have suggested 
        the possibility of a genetic component in inheritance (20); however, because 
        focuses of the studies have varied, the results are difficult to interpret. 
         009;Adoption studies may employ a number of techniques. 
        One is to compare the histories of children of alcoholics who are adopted 
        by nonalcoholics and grow up in a nondrinking environment with the histories 
        of children of nonalcoholics similarly raised in a nondrinking environment 
        (21-23). If genetic factors play a role, then the adopted children of 
        alcoholics should preferentially develop alcoholism as adults. 
        	Problems in designing and interpreting adoption studies 
        result from, among other things, the lack of detailed data on parents 
        who give up children for adoption, and environmental biases (as in the 
        predominance of a certain type of adopting family) (24). 
        	In a pioneering study of adopted Danish children, 
        Goodwin and co-workers found some evidence for the expected trends (4,21). 
        Cloninger and co-workers subsequently performed a series of much larger 
        studies of adoptees, which also revealed these trends (8,25). 
        	Cloninger and co-workers (23) hypothesized that so-called 
        type II alcoholics--characterized as having an early onset of drinking 
        problems, usually being male, and displaying personality disorders such 
        as antisocial behavior--had a more heritable form of alcoholism (26). 
        However, other researchers have argued that the scenario of inheritance 
        is more complex, and what is inherited is a mix of personality traits, 
        such as those related to antisocial behavior, rather than alcoholism itself 
        (27). Genes might play a direct role in the development of alcoholism, 
        as in affecting the body's metabolism of alcohol; or they might play a 
        less direct role, influencing a person's temperament or personality in 
        such a way that the person becomes vulnerable to alcoholism. 
        	Different models for the way in which alcoholism 
        runs in families have been suggested by a limited number of family studies. 
        Interpretation of these studies has been complicated by the likelihood 
        that alcoholism is a heterogeneous condition, that is, a collection of 
        different conditions that look similar, but whose mechanisms and modes 
        of inheritance may differ. Additional studies are needed to sort out the 
        mechanisms of transmission (28,29). 
        	Population and family studies such as those cited 
        above attempt to establish the presence of a broad genetic influence on 
        alcoholism. To investigate specific genes, researchers have employed genetic 
        marker studies. If specific human genes are related to alcoholism, then 
        genes lying close to them on the same chromosome--and the traits they 
        determine--may be inherited at the same time that the risk of alcoholism 
        is inherited. This phenomenon is called linkage. An assortment of genes 
        hypothesized to be linked to alcoholism has been examined (30), but none 
        has passed a rigorous test for linkage (31). 
        	Still being studied is a marker referred to as the 
        dopamine D2 receptor, which Blum and co-workers (32) found to be present 
        more often in alcoholics than in nonalcoholics (also see 33). In animal 
        studies, the dopamine D2 receptor had been associated with brain functions 
        relating to reward, reinforcement, and motivation. However, a number of 
        researchers have been unable to duplicate the results of Blum's study 
        (34,35). Some researchers believe dopamine D2 might modulate the severity 
        of alcoholism, rather than serve as a primary cause. The dopamine D2 association 
        continues to be interesting, but it does not seem to be transmitted in 
        families in such a way that it is responsible for alcoholism; its role, 
        if any, has yet to be determined (36). 
        	To search the human genome for specific genes related 
        to alcoholism, researchers employ two experimental techniques. The first, 
        the candidate gene approach, involves hypothesizing that particular genes 
        are related to the physiology of alcoholism and then individually testing 
        these genes for linkage (37). The second approach, scanning of the human 
        genome, involves characterizing, piece by piece, the entire length of 
        DNA and finding ge nes that relate to alcoholism, without proposing candidate 
        genes. 
        	Additionally, researchers use animal models to study 
        the genetics of alcoholism. These models have several advantages over 
        human subjects. Using animals, researchers can study larger numbers and 
        more generations of subjects, can arrange informative matings, can better 
        manipulate the environment, and can make measurements that would not be 
        possible on humans. The main limitation of using animals to study alcoholism 
        is that there is no animal model of alcoholism that encompasses the whole 
        spectrum of alcoholic behaviors in humans. 
        	Researchers nevertheless have studied alcohol-related 
        behaviors in animals that are believed to resemble aspects of human alcoholism. 
        These include consumption of and preference for alcohol, sedation induced 
        by alcohol, locomotor activation by alcohol (thought by some investigators 
        to model the euphoric effects of alcohol in humans), motor discoordination 
        and hypothermia induced by alcohol, withdrawal from alcohol, and tolerance 
        to various effects of alcohol (38). Researchers have succeeded in breeding 
        lines of rodents with high or low measures of most of these traits; this 
        success demonstrates that the traits are substantially genetically determined 
        in rodents. 
        	Researchers, using animals, have yet to identify 
        a single gene responsible for any alcohol-related behavior. They have 
        established that all of the above-mentioned traits are determined by multiple 
        genes, and that the individual traits are, for the most part, determined 
        independently of each other. One useful distinction revealed by studies 
        using animals is that genes determining the tendency to become tolerant 
        to certain effects of alcohol are different from genes determining the 
        severity of withdrawal symptoms (even though in a clinical setting these 
        reactions are often seen together) (38). Using the powerful genetic methods 
        available in animals, investigators are beginning to map genes responsible 
        for some of the animals' alcohol-related behaviors. The recent development 
        of a scheme that makes it possible to predict the location on the human 
        genome of a similar gene mapped in a mouse will provide an additional 
        source of candidate genes for linkage studies in humans (39). This approach 
        also will help to distinguish those animal behaviors now under study that 
        will be most valuable for understanding human alcohol-related behavior. 
        The Genetics of Alcoholism--A Commentary by  Progress has been made in understanding genetic 
        vulnerability to alcoholism. We know, for instance, that more than one 
        gene is likely to be responsible for this vulnerability. We now must determine 
        what these genes are and whether they are specific for alcohol or define 
        something more general, such as differences in temperament or personality 
        that increase an individual's vulnerability to alcoholism. We must also 
        determine how genes and the environment interact to influence vulnerability 
        to alcoholism. Based on our current understanding, it is probable that 
        environmental influences will be at least as important, and possibly more 
        important, than genetic influences. Success in uncovering the genes involved 
        in a vulnerability to alcoholism will help us to recognize the potential 
        for alcoholism in high-risk individuals, to intervene at an early stage, 
        and to develop new treatments for alcohol-related problems. This is a 
        productive area of research that will continue to yield important answers 
        to the basic questions of what causes alcoholism and how we can prevent 
        and treat it. 
        References 
        (1) Roe, A. The adult adjustment of children of 
        alcoholic parents raised in foster homes. Quarterly Journal of Studies 
        on Alcohol 5:378-393, 1944. (2) Goodwin, D.W. The genetics 
        of alcoholism: A state of the art review. Alcohol Health & Research 
        World 2(3):2-12, 1978. (3) Goldman, D., & Linnoila, M. 
        Genetic approaches to alcoholism. Progress in Neuro-Psychopharmacology 
        and Biological Psychiatry 10:237-242, 1986. (4) Goodwin, D.W.; 
        Schulsinger, F.; Moller, N.; Hermansen, L.; Winokur, G.; & Guze, S.B. 
        Drinking problems in adopted and nonadopted sons of alcoholics. Archives 
        of General Psychiatry 31:164-169, 1974. (5) Cotton, N.S. The 
        familial incidence of alcoholism: A review. Journal of Studies on Alcohol 
        40:89-116, 1979. (6) Goodwin, D.W. Biological factors in alcohol 
        use and abuse: Implications for recognizing and preventing alcohol problems 
        in adolescence. International Review of Psychiatry 1:41-49, 1989. 
        (7) Goodwin, D.W. Genetic determinants of reinforcement from alcohol. 
        In: Cox, W.M., ed. Why People Drink: Parameters of Alcohol as a Reinforcer. 
        New York: Gardner Press, 1990. pp. 37-50. (8) Cloninger, C.R.; 
        Bohman, M.; & Sigvardsson, S. Inheritance of alcohol abuse: Cross-fostering 
        analysis of adopted men. Archives of General Psychiatry 36:861-868, 
        1981. (9) Begleiter, H., & Porjesz, B. Potential biological 
        markers in individuals at high risk for developing alcoholism. Alcoholism: 
        Clinical and Experimental Research 12:488-493, 1988. (10) Goedde, 
        H.W., & Agarwal, D.P., eds. Alcoholism: Biomedical and Genetic 
        Aspects. New York: Pergamon Press, 1989. (11) Crabbe, J.C., & 
        Harris, R.A., eds. The Genetic Basis of Alcohol and Drug Actions. 
        New York: Plenum Press, 1991. (12) Annoni, G.; Weiner, F.R.; Colombo, 
        M.; Czaja, M.J.; & Zern, M.A. Albumin and collagen gene regulation 
        in alcohol- and virus-induced human liver disease. Gastroenterology 
        98:197-202, 1990. (13) Cloninger, C.R., & Begleiter, H., 
        eds. Genetics and Biology of Alcoholism: Banbury Report 33. New 
        York: Cold Spring Harbor Laboratory Press, 1990. (14) McGue, M. 
        "Genes, Environment, and the Etiology of Alcoholism." Paper presented 
        at the Working Group on the Development of Alcohol-Related Problems in 
        High-Risk Youth conference, Washington, DC, Nov. 14-16, 1991. (15) 
        Pickens, R.W., & Svikis, D.S. Genetic influences in human substance 
        abuse. Journal of Addictive Diseases 10:205-214, 1991. (16) 
        Hrubec, Z., & Omenn, G.S. Evidence of genetic predisposition to 
        alcoholic cirrhosis and psychosis: Twin concordances for alcoholism and 
        its biological endpoints by zygosity among male veterans. Alcoholism: 
        Clinical and Experimental Research 5:207-212, 1981. (17) Pickens, 
        R.W., & Svikis, D.S. The twin method in the study of vulnerability 
        to drug abuse. In: Pickens, R.W., and Svikis, D.S., eds. Biological 
        Vulnerability to Drug Abuse. National Institute on Drug Abuse Research 
        Monograph Series No. 89. DHHS Pub. No. (ADM)88-1590. Washington, DC: Supt. 
        of Docs., U.S. Govt. Print. Off., 1988. pp. 41-51. (18) Pickens, R.W.; 
        Svikis, D.S.; McGue, M.; Lykken, D.T.; Heston, L.L.; & Clayton, P.J. 
        Heterogeneity in the inheritance of alcoholism. Archives of General 
        Psychiatry 48:19-28, 1991. (19) Partanen, J.; Bruun, K.; & 
        Markkanen, T. Inheritance of Drinking Behavior. Helsinki: Finnish 
        Foundation for Alcohol Studies, 1966. (20) Kendler, K.S.; Heath, 
        A.C.; Neale, M.C.; Kessler, R.C.; & Eaves, L.J. A population-based 
        twin study of alcoholism in women. Journal of the American Medical 
        Association 268(14): 1877-1882, 1992. (21) Goodwin, D.W.; Schulsinger, 
        F.; Hermansen, L.; Guze, S.B.; & Winokur, G. Alcohol problems in adoptees 
        raised apart from alcoholic biological parents. Archives of General 
        Psychiatry 28:238-243, 1973. (22) Cadoret, R.J.; Cain, C.A.; 
        & Grove, W.M. Development of alcoholism in adoptees raised apart from 
        alcoholic biologic relatives. Archives of General Psychiatry 37:561-563, 
        1980. (23) Cloninger, C.R.; Bohman, M.; Sigvardsson, S.; & 
        von-Knorring, A.L. Psychopathology in adopted-out children of alco holics: 
        The Stockholm adoption study. In: Galanter, M., ed. Recent Developments 
        in Alcoholism. Vol. 3. New York: Plenum Press, 1985. pp. 37-51. (24) 
        Searles, J.S. The role of genetics in the pathogenesis of alcoholism. 
        Journal of Abnormal Psychology 97(2):153-167, 1988. (25) Bohman, 
        M.; Sigvardsson, S.; & Cloninger, C.R. Maternal inheritance of 
        alcohol abuse: Cross-fostering analysis of adopted women. Archives 
        of General Psychiatry 38:965-969, 1981. (26) Cloninger, C.R. 
        Neurogenetic adaptive mechanisms in alcoholism. Science 236:410-416, 
        1987. (27) Schuckit, M.A. Biological vulnerability to alcoholism. 
        Journal of Consulting and Clinical Psychology 55(3):301-309, 1987. 
        (28) Hill, S.Y. Absence of paternal sociopathy in the etiology 
        of severe alcoholism: Is there a type III alcoholism? Journal of Studies 
        on Alcohol 53:161-169, 1992. (29) Gilligan, S.B.; Reich, T.; 
        & Cloninger, C.R. Etiologic heterogeneity in alcoholism. Genetic 
        Epidemiology 4:395-414, 1987. (30) Cook, C.C., & Gurling, 
        H.M. Candidate genes and favored loci for alcoholism. In: Cloninger, C.R., 
        and Begleiter, H., eds. Genetics and Biology of Alcoholism: Banbury 
        Report 33. New York: Cold Spring Harbor Laboratory Press, 1990. pp. 
        227-236. (31) Goldman, D. Molecular markers for linkage of genetic 
        loci contributing to alcoholism. In: Galanter, M., ed. Recent Developments 
        in Alcoholism. Vol. 6. New York: Plenum Press, 1988. pp. 333-349. 
        (32) Blum, K.; Noble, E.P.; Sheridan, P.J.; Montgomery, A.; Ritchie, 
        T.; Jagadeeswaran, P.; Nogami, H.; Briggs, A.H.; & Cohn, J.B. Allelic 
        association of human dopamine D2 receptor gene in alcoholism. Journal 
        of the American Medical Association 263(15):2055-2060, 1990. (33) 
        Comings, D.E.; Comings, B.G.; Muhleman, D.; Dietz, G.; Shahbahrami, 
        B.; Tast, D.; Knell, E.; Kocsis, P.; Baumgarten, R.; Kovacs, B.W.; Levy, 
        D.L.; Smith, M.; Borison, R.L.; Evans, D.D.; Klein, D.N.; MacMurray, J.; 
        Tosk, J.M.; Sverd, J.; Gysin, R.; & Flanagan, S.D. The dopamine D2 
        receptor locus as a modifying gene in neuropsychiatric disorders. Journal 
        of the American Medical Association 266(13):1793-1800, 1991. (34) 
        Bolos, A.M.; Dean, M.; Lucas-Derse, S.; Ramsburg, M.; Brown, G.L.; 
        & Goldman, D. Population and pedigree studies reveal a lack of association 
        between the dopamine D2 receptor gene and alcoholism. Journal of the 
        American Medical Association 264:3156-3160, 1990. (35) Turner, 
        E.; Ewing, J.; Shilling, P.; Smith, T.L.; Irwin, M.; Schuckit, M.; 
        & Kelsoe, J.R. Lack of association between an RFLP near the D2 dopamine 
        receptor gene and severe alcoholism. Biological Psychiatry 31:285-290, 
        1992. (36) Karp, R.W. D2 or not D2? Alcoholism: Clinical and 
        Experimental Research 16:786-787, 1992. (37) Goldman, D., & 
        Haber, R. Genetic variation in serotonin and ALDH underlying alcoholism. 
        In: Cloninger, C.R., and Begleiter, H., eds. Genetics and Biology of 
        Alcoholism: Banbury Report 33. New York: Cold Spring Harbor Laboratory 
        Press, 1990. pp. 237-252. (38) Phillips, T.J., & Crabbe, J.C. 
        Behavioral studies of genetic differences in alcohol action. In: Crabbe, 
        J.C., and Harris, R.A., eds. The Genetic Basis of Alcohol and Drug 
        Actions. New York: Plenum Press, 1991. pp. 25-104. (39) Nadeau, 
        J.H. Linkage and Synteny Homologies Between Mouse and Man. 
        Bar Harbor, ME: Jackson Laboratory, 1990. 
        All material contained in the Alcohol Alert is in the public 
        domain and may be used or reproduced without permission from NIAAA. Citation 
        of the source is appreciated. 
        Copies of the Alcohol Alert are available free of charge 
        from the Scientific Communications Branch, Office of Scientific Affairs, 
        NIAAA, Willco Building, Suite 409, 6000 Executive Boulevard, Bethesda, 
        MD 20892-7003. Telephone: 301-443-3860. 
   
 | ||