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Polygenic risk score for ulcerative colitis predicts immune checkpoint inhibitor-mediated colitis.

Authors :
Middha P
Thummalapalli R
Betti MJ
Yao L
Quandt Z
Balaratnam K
Bejan CA
Cardenas E
Falcon CJ
Faleck DM
Gubens MA
Huntsman S
Johnson DB
Kachuri L
Khan K
Li M
Lovly CM
Murray MH
Patel D
Werking K
Xu Y
Zhan LJ
Balko JM
Liu G
Aldrich MC
Schoenfeld AJ
Ziv E
Source :
Nature communications [Nat Commun] 2024 Mar 26; Vol. 15 (1), pp. 2568. Date of Electronic Publication: 2024 Mar 26.
Publication Year :
2024

Abstract

Immune checkpoint inhibitor-mediated colitis (IMC) is a common adverse event of treatment with immune checkpoint inhibitors (ICI). We hypothesize that genetic susceptibility to Crohn's disease (CD) and ulcerative colitis (UC) predisposes to IMC. In this study, we first develop a polygenic risk scores for CD (PRS <subscript>CD</subscript> ) and UC (PRS <subscript>UC</subscript> ) in cancer-free individuals and then test these PRSs on IMC in a cohort of 1316 patients with ICI-treated non-small cell lung cancer and perform a replication in 873 ICI-treated pan-cancer patients. In a meta-analysis, the PRS <subscript>UC</subscript> predicts all-grade IMC (OR <subscript>meta</subscript> =1.35 per standard deviation [SD], 95% CI = 1.12-1.64, P = 2×10 <superscript>-03</superscript> ) and severe IMC (OR <subscript>meta</subscript> =1.49 per SD, 95% CI = 1.18-1.88, P = 9×10 <superscript>-04</superscript> ). PRS <subscript>CD</subscript> is not associated with IMC. Furthermore, PRS <subscript>UC</subscript> predicts severe IMC among patients treated with combination ICIs (OR <subscript>meta</subscript> =2.20 per SD, 95% CI = 1.07-4.53, P = 0.03). Overall, PRS <subscript>UC</subscript> can identify patients receiving ICI at risk of developing IMC and may be useful to monitor patients and improve patient outcomes.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
15
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
38531883
Full Text :
https://doi.org/10.1038/s41467-023-44512-4