Definition matters: assessment of tolerance to the effects of alcohol in a prospective cohort study of emerging adults.


Journal

Addiction (Abingdon, England)
ISSN: 1360-0443
Titre abrégé: Addiction
Pays: England
ID NLM: 9304118

Informations de publication

Date de publication:
11 2022
Historique:
received: 23 12 2021
accepted: 12 06 2022
pubmed: 7 7 2022
medline: 5 10 2022
entrez: 6 7 2022
Statut: ppublish

Résumé

Tolerance to the effects of alcohol is an important element in the diagnosis of alcohol use disorders (AUD); however, there is ongoing debate about its utility in the diagnosis AUD in adolescents and young adults. This study aimed to refine the assessment of tolerance in young adults by testing different definitions of tolerance and their associations with longitudinal AUD outcomes. Prospective cohort study. Australia. A contemporary cohort of emerging adults across Australia (n = 565, mean age = 18.9, range = 18-21 at baseline). Clinician-administered Structured Clinical Interview for DSM-IV Research Version (SCID-IV-RV) assessed for AUD criteria across five interviews, at 6-month intervals over 2.5 years. Tolerance definitions were operationalized using survey-type response (yes/no), clinician judgement (SCID-IV-RV), different initial drinking quantity and percentage increase thresholds and average heavy consumption metrics. AUD persistence was operationalized by the number of times AUD was present across the 2.5-year study period (n = 491), and new-onset AUD was operationalized as any new incidence of AUD during the follow-up period (n = 461). The (i) SCID-IV-RV clinician judgement [odds ratio (OR) = 2.50, P = 0.005], (ii) an initial drinking quantity threshold of four to five drinks and 50% minimum increase (OR = 2.48, P = 0.007) and (iii) 50% increase only (OR = 2.40, P = 0.005) were the tolerance definitions more strongly associated with any new onset of AUD throughout the four follow-up time-points than other definitions. However, these definitions were not associated with persistent AUD (Ps > 0.05). Average heavy consumption definitions of tolerance were most strongly associated with persistent AUD (OR = 6.66, P = 0.001; OR = 4.65, P = 0.004) but not associated with new-onset AUD (Ps > 0.05). Initial drink and percentage change thresholds appear to improve the efficacy of change-based tolerance as an indicator for new-onset alcohol use disorder diagnosis in self-report surveys of young adults. When predicting persistent alcohol use disorder, average heavy consumption-based indicators appear to be a better way to measure tolerance than self-reported change-based definitions.

Sections du résumé

BACKGROUND AND AIMS
Tolerance to the effects of alcohol is an important element in the diagnosis of alcohol use disorders (AUD); however, there is ongoing debate about its utility in the diagnosis AUD in adolescents and young adults. This study aimed to refine the assessment of tolerance in young adults by testing different definitions of tolerance and their associations with longitudinal AUD outcomes.
DESIGN
Prospective cohort study.
SETTINGS
Australia.
PARTICIPANTS
A contemporary cohort of emerging adults across Australia (n = 565, mean age = 18.9, range = 18-21 at baseline).
MEASUREMENTS
Clinician-administered Structured Clinical Interview for DSM-IV Research Version (SCID-IV-RV) assessed for AUD criteria across five interviews, at 6-month intervals over 2.5 years. Tolerance definitions were operationalized using survey-type response (yes/no), clinician judgement (SCID-IV-RV), different initial drinking quantity and percentage increase thresholds and average heavy consumption metrics. AUD persistence was operationalized by the number of times AUD was present across the 2.5-year study period (n = 491), and new-onset AUD was operationalized as any new incidence of AUD during the follow-up period (n = 461).
FINDINGS
The (i) SCID-IV-RV clinician judgement [odds ratio (OR) = 2.50, P = 0.005], (ii) an initial drinking quantity threshold of four to five drinks and 50% minimum increase (OR = 2.48, P = 0.007) and (iii) 50% increase only (OR = 2.40, P = 0.005) were the tolerance definitions more strongly associated with any new onset of AUD throughout the four follow-up time-points than other definitions. However, these definitions were not associated with persistent AUD (Ps > 0.05). Average heavy consumption definitions of tolerance were most strongly associated with persistent AUD (OR = 6.66, P = 0.001; OR = 4.65, P = 0.004) but not associated with new-onset AUD (Ps > 0.05).
CONCLUSIONS
Initial drink and percentage change thresholds appear to improve the efficacy of change-based tolerance as an indicator for new-onset alcohol use disorder diagnosis in self-report surveys of young adults. When predicting persistent alcohol use disorder, average heavy consumption-based indicators appear to be a better way to measure tolerance than self-reported change-based definitions.

Identifiants

pubmed: 35792050
doi: 10.1111/add.15991
pmc: PMC9796318
doi:

Substances chimiques

Ethanol 3K9958V90M

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2955-2964

Informations de copyright

© 2022 The Authors. Addiction published by John Wiley & Sons Ltd on behalf of Society for the Study of Addiction.

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Auteurs

Siobhan M O'Dean (SM)

The Matilda Centre for Research in Mental Health and Substance Use, University of Sydney, Sydney, Australia.

Louise Mewton (L)

Centre for Healthy Brain Ageing, University of New South Wales, Sydney, NSW, Australia.

Tammy Chung (T)

Department of Psychiatry, Rutgers, The State University of New Jersey, Institute for Health, Healthcare Policy and Aging Research, New Jersey, USA.

Peter Clay (P)

The Matilda Centre for Research in Mental Health and Substance Use, University of Sydney, Sydney, Australia.

Philip J Clare (PJ)

Prevention Research Collaboration, University of Sydney, Sydney, Australia.
National Drug and Alcohol Research Centre, UNSW, Sydney, Australia.

Raimondo Bruno (R)

National Drug and Alcohol Research Centre, UNSW, Sydney, Australia.
School of Psychological Sciences, University of Tasmania, Hobart, TAS, Australia.

Wing See Yuen (WS)

National Drug and Alcohol Research Centre, UNSW, Sydney, Australia.

Nyanda McBride (N)

National Drug Research Institute and enAble Institute, Curtin University, Perth, Australia.

Wendy Swift (W)

AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.

Ashling Isik (A)

The Matilda Centre for Research in Mental Health and Substance Use, University of Sydney, Sydney, Australia.

Emily Upton (E)

National Drug and Alcohol Research Centre, UNSW, Sydney, Australia.

Joel Tibbetts (J)

The Matilda Centre for Research in Mental Health and Substance Use, University of Sydney, Sydney, Australia.

Phoebe Johnson (P)

The Matilda Centre for Research in Mental Health and Substance Use, University of Sydney, Sydney, Australia.

Kypros Kypri (K)

School of Medicine and Public Health, University of Newcastle, NSW, Australia.

Tim Slade (T)

The Matilda Centre for Research in Mental Health and Substance Use, University of Sydney, Sydney, Australia.

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