A 22-Year Follow-Up (Range 16 to 23) of Original Subjects with Baseline Alcohol Use Disorders from the Collaborative Study on Genetics of Alcoholism.
- Authors
- Schuckit, Marc A; Smith, Tom L; Danko, George; Kramer, John; Bucholz, Kathleen K; McCutcheon, Vivia; Chan, Grace; Kuperman, Samuel; Hesselbrock, Victor; Dick, Danielle M; Hesselbrock, Michie; Porjesz, Bernice; Edenberg, Howard J; Nureberger, John I; Gregg, Marcy; Schoen, Lara; Kawamura, Mari; Mendoza, Lee Anne
- Year
- 2018
- Journal
- Alcoholism, clinical and experimental research
- PMID
- 29975427
- DOI
- 10.1111/acer.13810
- PMCID
- PMC6120781
BACKGROUND: Recent reports indicate higher-than-expected problematic drinking in older populations. However, few data describe how to predict which older individuals are most likely to demonstrate alcohol-related problems, including those with earlier alcohol use disorders (AUDs). These analyses evaluate predictors of alcohol outcomes in individuals with earlier AUDs in the Collaborative Study on Genetics of Alcoholism (COGA). METHODS: Original COGA participants with baseline AUDs at about age 40 were interviewed 13 to 26 years later and placed into clinically derived outcome categories. Chi-square and analysis of variance evaluated baseline differences across 4 outcome groups, with significant items entered into binary logistic regression backwards elimination analyses predicting outcomes. RESULTS: Low-Risk Drinkers (N = 100) at follow-up were predicted by baseline higher levels of response to alcohol (high LRs), lower histories of alcohol treatment, experience with fewer types of illicit drugs, and were more likely to have been widowed. At follow-up, Problem Drinkers (N = 192) differed from High-Risk Drinkers (N = 93) who denied multiple alcohol problems by exhibiting baseline lower LRs, higher Sensation Seeking, and a higher proportion who were widowed. Abstinent (N = 278) outcomes were predicted by a history of higher baseline AUD treatments, higher alcohol problems, lower usual drinks, as well as older age and European American heritage. Thirty-four subjects (4.9%) could not be classified and were not included in these analyses. CONCLUSIONS: These results generated from AUD individuals from both treatment and nontreatment settings reinforce low probabilities of recent Low-Risk Drinking in individuals with AUDs, but also suggest many individuals with AUDs demonstrate good outcomes 2 decades later.
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| The collaborative study on the genetics of alcoholism: Sample and clinical data. | Dick DM et al. | — | 2023 | → |
| Associations between Suicidal Thoughts and Behaviors and Genetic Liability for Cognitive Performance, Depression, and Risk-Taking in a High-Risk Sample. | Johnson EC et al. | — | 2021 | → |
| Polygenic contributions to alcohol use and alcohol use disorders across population-based and clinically ascertained samples. | Johnson EC et al. | — | 2021 | → |
| Getting to the Heart of Low Sensitivity to Alcohol: Context Moderates Low Cardiovascular Response to Alcohol in Persons With a Family History of Alcohol Use Disorder. | Bates ME et al. | — | 2020 | → |
| A Pilot Follow-Up Study of Older Alcohol-Dependent COGA Adults. | Chan G et al. | — | 2019 | → |
| [Effect of clinical characteristics on relapse of alcohol dependence: a prospective cohort study]. | Zhu R et al. | — | 2019 | → |
| Predictors of Increases in Alcohol Problems and Alcohol Use Disorders in Offspring in the San Diego Prospective Study. | Schuckit MA et al. | — | 2019 | → |
| Prevalence and Correlates of Past-Year Recovery From DSM-5 Alcohol Use Disorder: Results From National Epidemiologic Survey on Alcohol and Related Conditions-III. | Fan AZ et al. | — | 2019 | → |
| The Genetic Relationship Between Alcohol Consumption and Aspects of Problem Drinking in an Ascertained Sample. | Johnson EC et al. | — | 2019 | → |
| Erratum. | — | — | 2018 | → |