METHODS AND COMPOSITIONS RELATED TO ALCOHOL USE OR COMPLICATIONS THEREFROM
This document describes materials and methods for determining whether or not an individual will suffer from severe alcohol withdrawal syndrome or complications therefrom, or seizures related to alcohol withdrawal. This document also describes materials and methods for determining whether or not an individual presenting with myocardial infarction (MI) or acute coronary syndrome is suffering from heavy alcohol consumption (HAC) or alcohol use disorder (AUD).
1 . A method of determining whether or not an individual will suffer from severe alcohol withdrawal syndrome or complications therefrom, comprising the steps of:
determining the methylation status of CpG site cg07375256 in a biological sample from the individual;
wherein the methylation status of the at least one CpG dinucleotide identifies individuals that will suffer from severe alcohol withdrawal syndrome or complications therefrom.
2 . The method of claim 1 , wherein the complications from severe alcohol withdrawal syndrome comprise seizures.
3 . The method of claim 1 , wherein an increase in methylation at cg07375256 is indicative of an increased likelihood that the individual will suffer from severe alcohol withdrawal syndrome or complications therefrom.
4 . The method of claim 1 , wherein a decrease in methylation at cg07375256 is indicative of a reduced likelihood that the individual will suffer from severe alcohol withdrawal syndrome or complications therefrom.
5 . The method of claim 1 , wherein the determining step comprises methylation sensitive digital PCR (MSdPCR).
6 . The method of claim 1 , wherein the determining step comprises:
contacting DNA in the biological sample with bisulfite under alkaline conditions to produce bisulfite-treated DNA;
optionally, amplifying the bisulfite-treated DNA to produce amplified bisulfite-treated DNA;
contacting the bisulfite-treated DNA with at least one oligonucleotide that is complementary to a sequence comprising the at least one CpG dinucleotide; and
detecting the methylation status of the at least one CpG dinucleotide.
7 . The method of claim 1 , wherein the methylation status is determined using bisulfite treated DNA.
8 . The method of claim 1 , wherein the at least one oligonucleotide detects the CpG site in the methylated state.
9 . The method of claim 1 , wherein the at least one oligonucleotide detects the CpG site in the unmethylated state.
10 . The method of claim 1 , wherein the biological sample is selected from the group consisting of peripheral blood, lymphocytes, urine, saliva, and buccal cells.
11 . The method of claim 1 , further comprising assigning a number to the individual based on the Prediction of Alcohol Withdrawal Syndrome Scale (PAWSS).
12 . The method of claim 1 , further comprising treating the individual for severe alcohol withdrawal syndrome or complications therefrom.
13 . The method of claim 1 , further comprising not treating the individual for severe alcohol withdrawal syndrome or complications therefrom.
14 . A method of determining whether an individual presenting with myocardial infarction (MI) or acute coronary syndrome (ACS) is suffering from heavy alcohol consumption (HAC) or alcohol use disorder (AUD), comprising the steps of:
determining the alcohol T score (ATS) (i.e., average of 4 Zscores for cg02583484, cg04987734, cg09935388 and cg04583842) for the individual; and
determining the methylation status of CpG site cg07375256 in a biological sample from the individual
wherein the ATS and the methylation status of CpG site cg07375256 are indicative of whether an individual presenting with MI or ACS is suffering from HAC or AUD.
15 . The method of claim 14 , wherein the determining step comprises methylation sensitive digital PCR (MSdPCR).
16 . The method of claim 14 , wherein the determining step comprises:
contacting DNA in the biological sample with bisulfite under alkaline conditions to produce bisulfite-treated DNA;
optionally, amplifying the bisulfite-treated DNA to produce amplified bisulfite-treated DNA;
contacting the bisulfite-treated DNA with at least one oligonucleotide that is complementary to a sequence comprising the at least one CpG dinucleotide; and
detecting the methylation status of the at least one CpG dinucleotide.
17 . The method of claim 14 , wherein the methylation status is determined using bisulfite treated DNA.
18 . The method of claim 14 , wherein the at least one oligonucleotide detects the CpG site in the methylated state.
19 . The method of claim 14 , wherein the at least one oligonucleotide detects the CpG site in the unmethylated state.
20 . The method of claim 14 , wherein the biological sample is selected from the group consisting of peripheral blood, lymphocytes, urine, saliva, and buccal cells.
21 . The method of claim 14 , further comprising treating the individual for HAC, AUD, MI and/or ACS.