Usefulness of indirect alcohol biomarkers for predicting recidivism of drunk-driving among previously convicted drunk-driving offenders: results from the recidivism of alcohol-impaired driving (ROAD) study

Addiction. 2014 Jan;109(1):71-8. doi: 10.1111/add.12372. Epub 2013 Nov 20.

Abstract

Aim: In several European countries, drivers under the influence (DUI), suspected of chronic alcohol abuse are referred for medical and psychological examination. This study (the ROAD study, or Recidivism Of Alcohol-impaired Driving) investigated the usefulness of indirect alcohol biomarkers for predicting drunk-driving recidivism in previously convicted drunk-driving offenders.

Design, setting, participants and measurements: The ROAD study is a prospective study (2009-13) that was performed on 517 randomly selected drivers in Belgium. They were convicted for drunk-driving for which their licence was confiscated. The initial post-arrest blood samples were collected and analysed for percentage carbohydrate-deficient transferrin (%CDT), transaminsase activities [alanine amino transferase (ALT), aspartate amino transferase (AST)], gamma-glutamyltransferase (γGT) and red cell mean corpuscular volume (MCV). The observation time for each driver was 3 years and dynamic.

Findings: A logistic regression analysis revealed that ln(%CDT) (P < 0.001), ln(γGT) (P < 0.01) and ln(ALT) (P < 0.05) were the best biochemical predictors of recidivism of drunk-driving. The ROAD index (which includes ln(%CDT), ln(γGT), -ln(ALT) and the sex of the driver) was calculated and had a significantly higher area under the receiver operator characteristic curve (0.71) than the individual biomarkers for drunk-driving recidivism. Drivers with a high risk of recidivating (ROAD index ≥ 25%; third tertile) could be distinguished from drivers with an intermediate risk (16% ≤ ROAD index < 25%; second tertile; P < 0.001) and a low recidivism risk (ROAD index < 16%; first tertile; P < 0.05).

Conclusions: Of all routinely used indirect alcohol markers, percentage of carbohydrate-deficient transferrin is the major predictor of recidivism of drunk-driving. The association with gamma-glutamyltransferase, alanine amino transferase and the sex of the driver could have additional value for identifying drunk-drivers at intermediate risk of recidivism. Non-specific indirect alcohol markers, such as alanine amino transferase, gamma-glutamyltransferase, aspartate amino transferase and red cell mean corpuscular volume have minimal added value to % carbohydrate-deficient transferrin for distinguishing drunk drivers with a low or high risk of recidivism.

Keywords: Alcoholism; carbohydrate‐deficient transferrin; driver's licence; drunk‐driving; liver disease; logistic regression; transferrin.

MeSH terms

  • Adult
  • Alanine Transaminase / metabolism*
  • Alcohol Drinking / blood
  • Alcohol Drinking / epidemiology
  • Alcohol Drinking / metabolism*
  • Aspartate Aminotransferases / metabolism*
  • Automobile Driving / legislation & jurisprudence*
  • Automobile Driving / statistics & numerical data
  • Belgium
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Criminals / statistics & numerical data*
  • Erythrocyte Indices*
  • Female
  • Humans
  • Licensure
  • Logistic Models
  • Male
  • Middle Aged
  • Prospective Studies
  • Risk Assessment
  • Transferrin / metabolism*
  • gamma-Glutamyltransferase / metabolism*

Substances

  • Biomarkers
  • Transferrin
  • gamma-Glutamyltransferase
  • Aspartate Aminotransferases
  • Alanine Transaminase