Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2010 Jun;34(6):946-54.
doi: 10.1111/j.1530-0277.2010.01169.x. Epub 2010 Apr 5.

Future prospects for biomarkers of alcohol consumption and alcohol-induced disorders

Affiliations

Future prospects for biomarkers of alcohol consumption and alcohol-induced disorders

Willard M Freeman et al. Alcohol Clin Exp Res. 2010 Jun.

Abstract

The lack of reliable measures of alcohol intake is a major obstacle to the diagnosis, treatment, and research of alcohol abuse and alcoholism. Successful development of a biomarker that allows for accurate assessment of alcohol intake and drinking patterns would not only be a major advance in clinical care but also a valuable research tool. A number of advances have been made in testing the validity of proposed biomarkers as well as in identifying potential new biomarkers through systems biology approaches. This commentary will examine the definition of a biomarker of heavy drinking, the types of potential biomarkers, the steps in biomarker development, the current state of biomarker development, and critical obstacles for the field. The challenges in developing biomarkers for alcohol treatment and research are similar to those found in other fields. However, the alcohol research field must reach a competitive level of rigor and organization. We recommend that NIAAA consider taking a leadership role in organizing investigators in the field and providing a common set of clinical specimens for biomarker validation studies.

PubMed Disclaimer

Figures

Figure 1
Figure 1. Metrics for assessing biomarker performance
Unlike traditional statistics that examine differences between populations, diagnostics are intended to be informative of the individual patient. Sensitivity, specificity, positive predictive value, negative predictive value, and accuracy measures can be used to summarize a biomarker’s ability to correct classify subjects. In this example, the ability to classify heavy alcohol drinking and non-heavy alcohol drinking (abstainers or light drinkers) is portrayed. Sensitivity and specificity are the most commonly used measures, and, in this case, they respectively give the percentage of alcohol abusing and non-alcohol abusing subjects correctly identified.
Figure 2
Figure 2. Steps in developing biomarkers of alcohol-related disorders
As described in the text, development of a clinical biomarker requires multiple steps/stages of development. Successful completion of each of these steps results in a validated biomarker that is both sensitive and specific.
Figure 3
Figure 3. Biomarker development and use
Through the process of biomarker development steadily increasing numbers of samples are examined. With successful completion of each stage the confidence, the likelihood that a biomarker will be clinically useful, increases.

Similar articles

Cited by

References

    1. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders DSM-IV-TR. American Psychiatric Association; 2000.
    1. Anderson L, Hunter CL. Quantitative mass spectrometric multiple reaction monitoring assays for major plasma proteins. Mol Cell Proteomics. 2006;5:573–588. - PubMed
    1. Anton RF, Lieber C, Tabakoff B. Carbohydrate-deficient transferrin and gamma-glutamyltransferase for the detection and monitoring of alcohol use: results from a multisite study. Alcohol Clin Exp Res. 2002;26:1215–1222. - PubMed
    1. Baker M. In biomarkers we trust? Nat Biotechnol. 2005;23:297–304. - PubMed
    1. Bateman RJ, Munsell LY, Morris JC, Swarm R, Yarasheski KE, Holtzman DM. Human amyloid-beta synthesis and clearance rates as measured in cerebrospinal fluid in vivo. Nat Med. 2006;12:856–861. - PMC - PubMed

Publication types

MeSH terms