16 research outputs found

    Why Does Drinking Alcohol Affect Risk-Seeking Behavior? A Test of the Need for Cognitive Closure Hypothesis

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    Research suggests that the drinking environment can affect dynamic processes involved in group decision making. The current study evaluated the need for cognitive closure (NFCC) as a mechanism underlying previously observed effects of alcohol dosage-set (i.e., beliefs persons have about the content of their beverages) on risk-seeking behavior. Five-hundred-four social drinkers (261 female) were assembled into 168 three-person groups and randomly assigned to one of three beverage conditions: alcohol, placebo, and no-alcohol control. Following beverage consumption, groups were asked to choose between two options of equal expected value, one of which offered a greater yet less certain (i.e., “riskier”) outcome. Groups were given 150-sec to make a decision and were required to reach consensus. Group discussion was video-recorded, and behavioral measures of NFCC were systematically coded by three independent raters. Results did not support NFCC as a mechanism explaining the earlier finding; however, results suggested that the decision making task used here may not have offered a sensitive test of NFCC. Though methodological limitations were detected, supplemental analyses indicate that dosage-set affected group decision making prior to observable deliberation, and that groups valued affiliation more than they valued specific decision making outcomes regardless of which beverage was consumed or which decision was initially endorsed. These findings raise new questions regarding the effects of implicit cognitions and normative influence on decisions made in drinking contexts

    DRD4 Polymorphism Moderates the Effect of Alcohol Consumption on Social Bonding

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    Development of interpersonal relationships is a fundamental human motivation, and behaviors facilitating social bonding are prized. Some individuals experience enhanced reward from alcohol in social contexts and may be at heightened risk for developing and maintaining problematic drinking. We employed a 3 (group beverage condition) ×2 (genotype) design (N = 422) to test the moderating influence of the dopamine D4 receptor gene (DRD4 VNTR) polymorphism on the effects of alcohol on social bonding. A significant gene x environment interaction showed that carriers of at least one copy of the 7-repeat allele reported higher social bonding in the alcohol, relative to placebo or control conditions, whereas alcohol did not affect ratings of 7-absent allele carriers. Carriers of the 7-repeat allele were especially sensitive to alcohol's effects on social bonding. These data converge with other recent gene-environment interaction findings implicating the DRD4 polymorphism in the development of alcohol use disorders, and results suggest a specific pathway by which social factors may increase risk for problematic drinking among 7-repeat carriers. More generally, our findings highlight the potential utility of employing transdisciplinary methods that integrate genetic methodologies, social psychology, and addiction theory to improve theories of alcohol use and abuse

    TITLE PAGE WHY DOES DRINKING ALCOHOL AFFECT RISK-SEEKING BEHAVIOR? A TEST OF THE NEED FOR COGNITIVE CLOSURE HYPOTHESIS ABSTRACT WHY DOES DRINKING ALCOHOL AFFECT RISK-SEEKING BEHAVIOR? A TEST OF THE NEED FOR COGNITIVE CLOSURE HYPOTHESIS

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    Research suggests that the drinking environment can affect dynamic processes involved in group decision making. The current study evaluated the need for cognitive closure (NFCC) as a mechanism underlying previously observed effects of alcohol dosage-set (i.e., beliefs persons have about the content of their beverages) on risk-seeking behavior. Five-hundred-four social drinkers (261 female) were assembled into 168 three-person groups and randomly assigned to one of three beverage conditions: alcohol, placebo, and no-alcohol control. Following beverage consumption, groups were asked to choose between two options of equal expected value, one of which offered a greater yet less certain (i.e., "riskier") outcome. Groups were given 150-sec to make a decision and were required to reach consensus. Group discussion was video-recorded, and behavioral measures of NFCC were systematically coded by three independent raters. Results did not support NFCC as a mechanism explaining the earlier finding; however, results suggested that the decision making task used here may not have offered a sensitive test of NFCC. Though methodological limitations were detected, supplemental analyses indicate that dosage-set affected group decision making prior to observable deliberation, and that groups valued affiliation more than they valued specific decision making outcomes regardless of which beverage was consumed or which decision was initially endorsed. These findings raise new questions regarding the effects of implicit cognitions and normative influence on decisions made in drinking contexts

    Experiencing cigarette craving with a friend: A shared reality analysis.

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    DRD4 polymorphism moderates the effect of alcohol consumption on social bonding.

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    <p>Development of interpersonal relationships is a fundamental human motivation, and behaviors facilitating social bonding are prized. Some individuals experience enhanced reward from alcohol in social contexts and may be at heightened risk for developing and maintaining problematic drinking. We employed a 3 (group beverage condition) Ă—2 (genotype) design (N = 422) to test the moderating influence of the dopamine D4 receptor gene (DRD4 VNTR) polymorphism on the effects of alcohol on social bonding. A significant gene x environment interaction showed that carriers of at least one copy of the 7-repeat allele reported higher social bonding in the alcohol, relative to placebo or control conditions, whereas alcohol did not affect ratings of 7-absent allele carriers. Carriers of the 7-repeat allele were especially sensitive to alcohol's effects on social bonding. These data converge with other recent gene-environment interaction findings implicating the DRD4 polymorphism in the development of alcohol use disorders, and results suggest a specific pathway by which social factors may increase risk for problematic drinking among 7-repeat carriers. More generally, our findings highlight the potential utility of employing transdisciplinary methods that integrate genetic methodologies, social psychology, and addiction theory to improve theories of alcohol use and abuse.</p
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