Evidence map›Paper›PMID 42845231›Full record

ArticleAllergy, asthma & immunology research2026

Genome-Wide Risk Assessment and Clinical Prediction of Iodinated Contrast Media-Induced Anaphylaxis.

Soo Jie Chung, Eunsoon Shin, Yong-Seok Kim, So-Hee Lee, Sun-Sin Kim, Sun Young Paik, Heung-Woo Park, Sae-Hoon Kim, Sungwon Jeon, Jong Bhak and 2 more

Abstract read
In one paragraph

Article in Allergy, asthma & immunology research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Soo Jie Chung *Department of Pulmonology and Allergy, Hallym University Dongtan Sacred Heart Hospital, Hwaseong, Korea.ORCID https://orcid.org/0000-0002-7717-1188
Eunsoon Shin *JS Link, Inc., Seoul, Korea.ORCID https://orcid.org/0000-0001-8408-2696
Yong-Seok KimJS Link, Inc., Seoul, Korea.ORCID https://orcid.org/0000-0001-8795-236X
So-Hee LeeDepartment of Internal Medicine, Seoul National University Hospital Healthcare System Gangnam Center, Seoul, Korea.ORCID https://orcid.org/0000-0003-0932-7256
Sun-Sin KimDepartment of Internal Medicine, Seoul National University Hospital Healthcare System Gangnam Center, Seoul, Korea.ORCID https://orcid.org/0000-0002-0664-3256
Sun Young PaikDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.ORCID https://orcid.org/0000-0002-9411-7714
Heung-Woo ParkDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.ORCID https://orcid.org/0000-0002-6970-3228
Sae-Hoon KimDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.ORCID https://orcid.org/0000-0002-2572-5302
Sungwon JeonAgingLab Inc., Ulsan, Korea.ORCID https://orcid.org/0000-0002-2729-9087
Jong BhakAgingLab Inc., Ulsan, Korea.ORCID https://orcid.org/0000-0002-4228-1299
Hye-Ryun KangDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.ORCID https://orcid.org/0000-0002-2317-4201
Yoon-Seok ChangDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.ORCID https://orcid.org/0000-0003-3157-0447

Funding

Ministry of Food and Drug Safety 20182MFDS445Seoul National University Bundang Hospital 14-2020-0024
6 · The paper itself

Abstract

purposeIodinated contrast media (ICM) are widely used in diagnostic imaging, but may trigger immediate hypersensitivity reactions, including anaphylaxis. Although human leukocyte antigen (HLA) associations have been proposed, genome-wide evidence remains limited. To identify genetic risk variants associated with ICM-induced anaphylaxis and evaluate their clinical utility.

methodsWe conducted a genome-wide association study (GWAS) in 91 Korean patients with confirmed ICM-induced anaphylaxis (discovery, n = 67; replication, n = 24) and 1,565 controls. Genotyping used a Korean-specific single nucleotide polymorphism (SNP) array. Significant variants were replicated. HLA alleles were imputed in the combined dataset. Linkage disequilibrium (LD) among significant loci was analyzed. Cumulative genetic burden was assessed by summing risk alleles per individual. A Least Absolute Shrinkage and Selection Operator-based prediction model incorporated genetic and clinical variables.

resultsNineteen SNPs reached genome-wide significance and were replicated, including rs2229629 in

conclusionsThis first GWAS of ICM-induced anaphylaxis identifies susceptibility loci across metabolic, immune, and neuroimmune pathways.

Indexed as

anaphylaxisarea under the curveContrast mediagenome-wide association studyHLA alleleshuman leukocyte antigenhypersensitivity reactionsingle nucleotide polymorphism

Identifiers

PMID42845231
PMCPMC13655407

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.