Completed Pregnancy, Children & Inherited Conditions Mental Health

Excessive drinking and alcohol related harms in Adulthood: ALSPAC at 24

In plain English

AI plain-English summary

Over 1 in 3 young adults in the UK drink excessively, and liver disease deaths have quadrupled in 40 years. This project uses the world’s most intensively followed birth cohort—ALSPAC (Children of the 90s)—to measure alcohol-related harms in 5,000 people aged 24/25. It addresses a critical gap: whether early binge drinking in adolescence directly causes liver damage, depression, cognitive problems, and persistent antisocial behaviour in young adulthood, or whether other factors like genetics or childhood conduct problems are the real drivers. The team will use genetic markers of alcohol consumption and sophisticated statistics to untangle cause from correlation. If successful, the findings will give clinicians and policymakers hard evidence on which drinking patterns are most dangerous and which young people are most at risk. This could sharpen public health messaging, target interventions at high-risk adolescents before harm sets in, and reduce the burden on the NHS from alcohol-related liver disease, injury, and mental health crises. The data will also be made available to other researchers, accelerating work on a problem that quietly strains healthcare systems and damages lives across the UK.

View original technical description
Reducing harm caused by alcohol is a key public health and policy priority. Liver disease deaths have increases over 4-fold in last 40 years. Over 1 in 3 young adults, both women and men, aged 20-24 drink excessively. These adverse patterns of drinking can originate in adolescence - with 50% of adolescents reporting binge drinking by aged 16. Several key alcohol related harms emerge in young adulthood, while others may persist into adulthood because of continued excessive drinking. The evidence on the relationship between patterns of excessive drinking and these key harms, especially how important early onset excessive drinking in adolescence is, needs to be strengthened. We aim to provide evidence on the proportion of young people who show signs of liver fibrosis/damage and the risk conferred by different patterns of alcohol use; the risk of poor cognitive and emotional processing associated with binge drinking; whether harmful alcohol use leads to depression in young adults; whether excessive alcohol use prevents people "maturing" out of antisocial behaviour; and amount of injury in young people associated with adverse patterns of alcohol use. In addition, harmful alcohol use or alcohol dependence also emerges in young adulthood. Further evidence is required on the relative contribution of different pathways to alcohol dependence. We plan to focus on three key pathways: the role of early behavioural or conduct problems; the impact of depressed mood and anxiety in early life and adolescence; and the potential effect of physiological response to alcohol (assessed in terms of the average amount of alcohol it takes to elicit an effect). Longitudinal data - which measures alcohol use over time, and social, environmental factors before and during alcohol use - are required to assess both of these issues - the influence of types of alcohol consumption on harm in young adulthood and pathways to problem alcohol use in young adulthood. The ALSPAC birth cohort (Children of the 90s) is the most extensively followed birth cohort in the world with detailed biological and behavioural data from before birth to late adolescence and early adulthood. We propose to take the unique opportunity provided by ALSPAC to measure alcohol related harms and outcomes in 5000 young people aged 24/25. Testing the robustness and strength of the association between alcohol and harm or the importance of different pathways to alcohol dependence will be important. Two key problems are confounding (where an association maybe explained by another factor) and missing data (which is higher in people from lower socio-economic groups with the greater early behavioural problems). We will utilize a range of sophisticated statistical techniques that seek to address these problems, including the use where possible of genetic markers of alcohol consumption (which are unrelated to other factors) and can strengthen evidence on causation. We are a multi-disciplinary team including leading experts in methodology, alcohol and related harms. The evidence we gather and data we collect will be beneficial to other academics working in the field, and critically to public and patient groups, clinicians and policy-makers with an interest in preventing alcohol related harm.

View the original record at the funder ↗

Researchers

A Brennan (Co-Investigator)Anne Lingford Hughes (Co-Investigator)Anthony David (Co-Investigator)Barbara Maughan (Co-Investigator)Colin Drummond (Co-Investigator)Debbie Lawlor (Co-Investigator)Derek Jones (Co-Investigator)Eileen Kaner (Co-Investigator)George Davey Smith (Co-Investigator)Glyn Lewis (Co-Investigator)Gunter Schumann (Co-Investigator)John Macleod (Co-Investigator)Jon Heron (Co-Investigator)Kate Tilling (Co-Investigator)Kenneth Kendler (Co-Investigator)Luisa Zuccolo (Co-Investigator)Marcus Munafo (Co-Investigator)Matt Field (Co-Investigator)Matthew Hickman (Principal Investigator)Michael Lynskey (Co-Investigator)Nick Sheron (Co-Investigator)Petra Sylvia Meier (Co-Investigator)Sarah Lewis (Co-Investigator)

Related Research

Grants with similar aims, by meaning.

Investigation of short and longer term health outcomes of adolescents who misuse alcohol using linked UK primary and secondary care databases
Alcohol Harms: The relationship between alcohol consumption and cardiovascular risk - A life-course perspective
ALSPAC and Adolescent Substance Use Trajectories: Consolidation of a UK research resource
An investigation of the multimorbidity of mental disorders and alcohol attributable conditions
Developing Pathways for older adults who are also drinking at increased-risk levels (Older adults Alcohol Pathway (OAP))

Original classification

Research Grant

Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.