<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Middha P</submitter><funding>NCATS NIH HHS</funding><funding>NICHD NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NHGRI NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>Immune checkpoint inhibitors (ICIs) are a remarkable advancement in cancer therapeutics; however, a substantial proportion of patients develop severe immune-related adverse events (irAEs). Understanding and predicting irAEs is a key to advancing precision immuno-oncology. Immune checkpoint inhibitor-mediated colitis (IMC) is a significant complication from ICI and can have life-threatening consequences. Based on clinical presentation, IMC mimics inflammatory bowel disease, however the link is poorly understood. We hypothesized that genetic susceptibility to Crohn's disease (CD) and ulcerative colitis (UC) may predispose to IMC. We developed and validated polygenic risk scores for CD (PRS&lt;sub>CD&lt;/sub>) and UC (PRS&lt;sub>UC&lt;/sub>) in cancer-free individuals and assessed the role of each of the</pubmed_abstract><journal>medRxiv : the preprint server for health sciences</journal><pagination>2023.05.15.23289680</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10246037</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Polygenic risk score for ulcerative colitis predicts immune checkpoint inhibitor-mediated colitis.</pubmed_title><pmcid>PMC10246037</pmcid><funding_grant_id>T32 CA009207</funding_grant_id><funding_grant_id>UL1 TR002243</funding_grant_id><funding_grant_id>UG1 CA233259</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>U01 HG004798</funding_grant_id><funding_grant_id>RC2 GM092618</funding_grant_id><funding_grant_id>U01 HG006378</funding_grant_id><funding_grant_id>S10 OD017985</funding_grant_id><funding_grant_id>R01 CA251758</funding_grant_id><funding_grant_id>UL1 TR000445</funding_grant_id><funding_grant_id>R01 NS032830</funding_grant_id><funding_grant_id>P30 CA068485</funding_grant_id><funding_grant_id>UL1 RR024975</funding_grant_id><funding_grant_id>P50 GM115305</funding_grant_id><funding_grant_id>U01 CA253560</funding_grant_id><funding_grant_id>K24 CA169004</funding_grant_id><funding_grant_id>P01 CA129243</funding_grant_id><funding_grant_id>S10 RR025141</funding_grant_id><funding_grant_id>R01 HD074711</funding_grant_id><funding_grant_id>R01 CA227466</funding_grant_id><funding_grant_id>U19 HL065962</funding_grant_id><pubmed_authors>Quandt Z</pubmed_authors><pubmed_authors>Huntsman S</pubmed_authors><pubmed_authors>Cardenas E</pubmed_authors><pubmed_authors>Patel D</pubmed_authors><pubmed_authors>Ziv E</pubmed_authors><pubmed_authors>Faleck DM</pubmed_authors><pubmed_authors>Falcon CJ</pubmed_authors><pubmed_authors>Aldrich MC</pubmed_authors><pubmed_authors>Thummalapalli R</pubmed_authors><pubmed_authors>Kachuri L</pubmed_authors><pubmed_authors>Middha P</pubmed_authors><pubmed_authors>Balaratnam K</pubmed_authors><pubmed_authors>Balko JM</pubmed_authors><pubmed_authors>Yao L</pubmed_authors><pubmed_authors>Bejan CA</pubmed_authors><pubmed_authors>Murray MH</pubmed_authors><pubmed_authors>Johnson DB</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Betti MJ</pubmed_authors><pubmed_authors>Zhan LJ</pubmed_authors><pubmed_authors>Werking K</pubmed_authors><pubmed_authors>Schoenfeld AJ</pubmed_authors><pubmed_authors>Khan K</pubmed_authors><pubmed_authors>Princess Margaret Lung Group</pubmed_authors><pubmed_authors>Lovly CM</pubmed_authors><pubmed_authors>Gubens MA</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors><pubmed_authors>Liu G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Polygenic risk score for ulcerative colitis predicts immune checkpoint inhibitor-mediated colitis.</name><description>Immune checkpoint inhibitors (ICIs) are a remarkable advancement in cancer therapeutics; however, a substantial proportion of patients develop severe immune-related adverse events (irAEs). Understanding and predicting irAEs is a key to advancing precision immuno-oncology. Immune checkpoint inhibitor-mediated colitis (IMC) is a significant complication from ICI and can have life-threatening consequences. Based on clinical presentation, IMC mimics inflammatory bowel disease, however the link is poorly understood. We hypothesized that genetic susceptibility to Crohn's disease (CD) and ulcerative colitis (UC) may predispose to IMC. We developed and validated polygenic risk scores for CD (PRS&lt;sub>CD&lt;/sub>) and UC (PRS&lt;sub>UC&lt;/sub>) in cancer-free individuals and assessed the role of each of the</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Sep</publication><modification>2025-04-19T05:38:35.347Z</modification><creation>2025-04-19T05:38:35.347Z</creation></dates><accession>S-EPMC10246037</accession><cross_references><pubmed>37292751</pubmed><doi>10.1101/2023.05.15.23289680</doi></cross_references></HashMap>