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Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

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258 IV. SPECIAL POPULATIONSdrug is associat<strong>ed</strong> with a mark<strong>ed</strong> increase in the probability <strong>of</strong> abusing otherclasses <strong>of</strong> drugs (Tsuang et al., 1998). One <strong>of</strong> the strongest pr<strong>ed</strong>ictors for presence<strong>of</strong> an SUD is the presence <strong>of</strong> another SUD (Bierut et al., 1998).Much <strong>of</strong> the evidence for the heritability <strong>of</strong> the general and specific vulnerabilityfor SUD is taken from studies <strong>of</strong> familial aggregation. Bierut and colleagues(1998) compar<strong>ed</strong> siblings <strong>of</strong> probands with alcohol dependence andthose <strong>of</strong> a control group for the presence <strong>of</strong> lifetime SUDs. Siblings <strong>of</strong> alcoholicprobands were not only more likely to have a lifetime alcohol use disorder, butthey also had an increas<strong>ed</strong> risk <strong>of</strong> cannabis, cocaine, and nicotine dependence.Fifty percent <strong>of</strong> the alcohol-dependent siblings <strong>of</strong> alcohol-dependent probandshad an additional diagnosis <strong>of</strong> cannabis and/or cocaine dependence. What iscompelling with respect to understanding the risk for multiple substanc<strong>ed</strong>ependence is that the siblings <strong>of</strong> cannabis-dependent probands had an increas<strong>ed</strong>risk <strong>of</strong> cannabis dependence, siblings <strong>of</strong> cocaine-dependent probandshad an increas<strong>ed</strong> risk for cocaine dependence, and siblings <strong>of</strong> habitual smokerswere at higher risk for nicotine dependence (Bierut et al., 1998). In anotherstudy, Tsuang and colleagues (1998) demonstrat<strong>ed</strong> that there is a general drugabuse vulnerability factor with genetic, family, and nonfamily environmentalcomponents that is shar<strong>ed</strong> across all drugs <strong>of</strong> abuse, in addition to genetic factorsthat appear to be unique for most classes <strong>of</strong> drug abuse. So although thereappear to be nongenetic general and specific factors for familial transmission <strong>of</strong>vulnerability to SUDs, multiple SUDs among probands render increas<strong>ed</strong> vulnerabilityto multiple SUDs in relatives, at least through both drug-specific andcommon genetic factors.NEUROPSYCHOLOGICAL IMPACTOF MULTIPLE SUBSTANCE USE DISORDERSAs compar<strong>ed</strong> with non-polysubstance-using drug abusers, those with multipleSUDs demonstrate the greatest degree <strong>of</strong> chronic neuropsychological impairmentand recover the least function with long-term abstinence (Beatty et al.,1997; M<strong>ed</strong>ina, Shear, Schafer, Armstrong, & Dyer, 2003). This may be due inpart to the increas<strong>ed</strong> cumulative exposure <strong>of</strong> the brain to drugs and alcohol:Multiple substance users tend to use as much <strong>of</strong> a particular substance (e.g.,alcohol or cocaine) as those who use only alcohol or cocaine (Selby & Azrin,1998). Selby and Azrin (1998) conduct<strong>ed</strong> a comprehensive neuropsychologicalbattery with 355 prison inmates classifi<strong>ed</strong> by DSM-IV criteria into four groups:those with alcohol use disorders, cocaine use disorders, multiple SUDs, and nohistory <strong>of</strong> SUD. The multiple SUDs and the alcohol groups demonstrat<strong>ed</strong> significantimpairment on most measures compar<strong>ed</strong> to the cocaine or no-druggroups, but the multiple SUDs group perform<strong>ed</strong> worse than the cocaine alone,alcohol alone or no SUD groups on measures <strong>of</strong> short-term memory, long-term

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