<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rabinowitz JA</submitter><funding>national institute on drug abuse</funding><funding>national institute of mental health</funding><funding>NIDA NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>NHGRI NIH HHS</funding><pagination>e0266384</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8993003</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>This study examined whether polygenic risk scores (PRS) for lifetime cannabis and alcohol use were associated with misusing opioids, and whether sex differences existed in these relations in an urban, African-American sample.&lt;h4>Methods&lt;/h4>Data were drawn from three cohorts of participants (N = 1,103; 45% male) who were recruited in first grade as part of a series of elementary school-based, universal preventive intervention trials conducted in a Mid-Atlantic region of the U.S. In young adulthood, participants provided a DNA sample and reported on whether they had used heroin or misused prescription opioids in their lifetime. Three substance use PRS were computed based on prior GWAS: lifetime cannabis use from Pasman et al. (2018), heavy drinking indexed via maximum number of drinks from Gelernter et al. (2019), and alcohol consumption from Kranzler et al. (2019).&lt;h4>Results&lt;/h4>Higher PRS for lifetime cannabis use, greater heavy drinking, and greater alcohol consumption were associated with heightened risk for misusing opioids among the whole sample. Significant sex by PRS interactions were also observed such that higher PRS for heavy drinking and alcohol consumption were associated with a greater likelihood of opioid misuse among males, but not females.&lt;h4>Conclusion&lt;/h4>Our findings further elucidate the genetic contributions to misusing opioids by showing that the genetics of cannabis and alcohol consumption are associated with lifetime opioid misuse among young adults, though replication of our findings is needed.</pubmed_abstract><journal>PloS one</journal><pubmed_title>Positive associations between cannabis and alcohol use polygenic risk scores and phenotypic opioid misuse among African-Americans.</pubmed_title><pmcid>PMC8993003</pmcid><funding_grant_id>R01 DA044184</funding_grant_id><funding_grant_id>R01 MH057005</funding_grant_id><funding_grant_id>R01 MH042968</funding_grant_id><funding_grant_id>R01 DA044015</funding_grant_id><funding_grant_id>R01 MH 42968</funding_grant_id><funding_grant_id>P50 MH 38725</funding_grant_id><funding_grant_id>R01 HG010480</funding_grant_id><funding_grant_id>R01 DA004392</funding_grant_id><funding_grant_id>R01DA044184-02S1</funding_grant_id><funding_grant_id>DA11796 MH57005</funding_grant_id><funding_grant_id>R01 DA011796</funding_grant_id><funding_grant_id>R00 HG012223</funding_grant_id><funding_grant_id>DA 09897</funding_grant_id><funding_grant_id>K99 HG012223</funding_grant_id><funding_grant_id>R01 DA009897</funding_grant_id><funding_grant_id>DA 04392</funding_grant_id><pubmed_authors>Domingue B</pubmed_authors><pubmed_authors>Rabinowitz JA</pubmed_authors><pubmed_authors>Maher BS</pubmed_authors><pubmed_authors>Benke K</pubmed_authors><pubmed_authors>Renteria ME</pubmed_authors><pubmed_authors>Kertes D</pubmed_authors><pubmed_authors>Huhn AS</pubmed_authors><pubmed_authors>Kuo SI</pubmed_authors><pubmed_authors>Ialongo NS</pubmed_authors><pubmed_authors>Campos AI</pubmed_authors><pubmed_authors>Jin J</pubmed_authors><pubmed_authors>Reboussin BA</pubmed_authors><pubmed_authors>Uhl G</pubmed_authors><pubmed_authors>Thrul J</pubmed_authors><pubmed_authors>Troiani V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Positive associations between cannabis and alcohol use polygenic risk scores and phenotypic opioid misuse among African-Americans.</name><description>&lt;h4>Background&lt;/h4>This study examined whether polygenic risk scores (PRS) for lifetime cannabis and alcohol use were associated with misusing opioids, and whether sex differences existed in these relations in an urban, African-American sample.&lt;h4>Methods&lt;/h4>Data were drawn from three cohorts of participants (N = 1,103; 45% male) who were recruited in first grade as part of a series of elementary school-based, universal preventive intervention trials conducted in a Mid-Atlantic region of the U.S. In young adulthood, participants provided a DNA sample and reported on whether they had used heroin or misused prescription opioids in their lifetime. Three substance use PRS were computed based on prior GWAS: lifetime cannabis use from Pasman et al. (2018), heavy drinking indexed via maximum number of drinks from Gelernter et al. (2019), and alcohol consumption from Kranzler et al. (2019).&lt;h4>Results&lt;/h4>Higher PRS for lifetime cannabis use, greater heavy drinking, and greater alcohol consumption were associated with heightened risk for misusing opioids among the whole sample. Significant sex by PRS interactions were also observed such that higher PRS for heavy drinking and alcohol consumption were associated with a greater likelihood of opioid misuse among males, but not females.&lt;h4>Conclusion&lt;/h4>Our findings further elucidate the genetic contributions to misusing opioids by showing that the genetics of cannabis and alcohol consumption are associated with lifetime opioid misuse among young adults, though replication of our findings is needed.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-31T01:04:57.099Z</modification><creation>2025-04-04T11:31:32.337Z</creation></dates><accession>S-EPMC8993003</accession><cross_references><pubmed>35395044</pubmed><doi>10.1371/journal.pone.0266384</doi></cross_references></HashMap>