USE OF BIOMARKERS FOR DETECTION OF EXCESSIVE ALCOHOL USE
Methods of diagnosing excessive alcohol use are disclosed herein. More particularly, the present disclosure is directed to methods of diagnosing excessive alcohol use by identifying expression levels of various serum biomarkers. In some embodiments, expression levels of these biomarkers are affected by alcohol use even up to 30 days after consumption of alcohol.
1 . A method for diagnosing excessive alcohol use in a subject, the method comprising:
obtaining a sample from a subject suspected of excessive alcohol use;
contacting the sample with an agent that specifically binds to a biomarker selected from the group consisting of AT-Rich Interactive Domain-Containing Protein 4B (ARID4B), phosphatidylcholine-sterol acyltransferase (LCAT), hepatocyte growth factor-like protein (MST1), ADP-ribosylation factor 6 (ARL6), sCD14, sCD163, and neopterin, and combinations thereof, to form a complex between the agent and biomarker;
detecting the complex to determine an expression level of the biomarker in the sample; and
diagnosing excessive alcohol use in the subject if the expression level of the biomarker is increased as compared to the expression level of the biomarker in a reference sample.
2 . The method of claim 1 , wherein the sample is selected from the group consisting of serum, plasma, whole blood and urine.
3 . The method of claim 1 , wherein the biomarker is AT-Rich Interactive Domain-Containing Protein 4B (ARID4B).
4 . The method of claim 1 , wherein the biomarker is ADP-ribosylation factor 6 (ARL6).
5 . The method of claim 1 , wherein the biomarkers are AT-Rich Interactive Domain-Containing Protein 4B (ARID4B), phosphatidylcholine-sterol acyltransferase (LCAT), hepatocyte growth factor-like protein (MST1), and ADP-ribosylation factor 6 (ARL6).
6 . The method of claim 1 , wherein the biomarkers are sCD14 and sCD163.
7 . The method of claim 1 , wherein the agent is selected from an antibody, a ligand, and combinations thereof.
8 . The method of claim 1 further comprising completing a self-administered questionnaire by the subject at risk for excessive alcohol use.
9 . A method for diagnosing excessive alcohol use in a subject, the method comprising:
obtaining a sample from a subject suspected of excessive alcohol use;
analyzing the sample by liquid chromatography/mass spectrometry to determine a concentration of a biomarker selected from the group consisting of AT-Rich Interactive Domain-Containing Protein 4B (ARID4B), phosphatidylcholine-sterol acyltransferase (LCAT), hepatocyte growth factor-like protein (MST1), ADP-ribosylation factor 6 (ARL6), sCD14, sCD163, and neopterin, and combinations thereof; and
diagnosing excessive alcohol use in the subject if the concentration level of the biomarker is increased as compared to the concentration of the biomarker in a reference sample.
10 . The method of claim 9 , wherein the sample is selected from the group consisting of serum, plasma, whole blood and urine.
11 . The method of claim 9 , wherein the biomarker is AT-Rich Interactive Domain-Containing Protein 4B (ARID4B).
12 . The method of claim 9 , wherein the biomarker is ADP-ribosylation factor 6 (ARL6).
13 . The method of claim 9 , wherein the biomarkers are AT-Rich Interactive Domain-Containing Protein 4B (ARID4B), phosphatidylcholine-sterol acyltransferase (LCAT), hepatocyte growth factor-like protein (MST1), and ADP-ribosylation factor 6 (ARL6).
14 . The method of claim 9 , wherein the biomarkers are sCD14 and sCD163.
15 . The method of claim 9 further comprising completing a self-administered questionnaire by the subject at risk for excessive alcohol use.
16 . A method for diagnosing excessive alcohol use in a subject, the method comprising:
obtaining a sample from a subject suspected of excessive alcohol use;
contacting the sample with an agent that specifically binds to sCD40, to form a complex between the agent and sCD40;
detecting the complex to determine an expression level of sCD40 in the sample; and
diagnosing excessive alcohol use in the subject if the expression level of the sCD40 is decreased as compared to the expression level of the sCD40 in a reference sample.
17 . The method of claim 16 , wherein the agent is selected from an antibody, a ligand, and combinations thereof.
18 . The method of claim 1 further comprising completing a self-administered questionnaire by the subject at risk for excessive alcohol use.
19 . A biomarker panel for diagnosing excessive alcohol use, the biomarker panel comprising at least two biomarkers selected from the group consisting of AT-rich interactive domain-containing protein 4B (ARID4B), ETS domain-containing transcription factor ERF (ERF), actin-like protein 6A (ACTL6A), IgG (immunoglobulin lambda), phosphatidylcholine-sterol acyltransferase (LCAT), intercellular adhesion molecule 2 (ICAM2), hepatocyte growth factor-like protein (MST1), and ADP-ribosylation factor 6 (ARL6), sCD14, sCD163, and sCD40.
20 . The biomarker panel of claim 19 , wherein the biomarkers are AT-Rich Interactive Domain-Containing Protein 4B (ARID4B), phosphatidylcholine-sterol acyltransferase (LCAT), hepatocyte growth factor-like protein (MST1), and ADP-ribosylation factor 6 (ARL6).