Cure8

Why This Matters

Genetic factors play a key role in some IBD cases and could help match patients to targeted treatments. Current genetic tests can miss important causes, so broader or different testing approaches may be needed to find treatable genetic contributors.

Who Should Pay Attention

Clinicians caring for IBD patients (adult and pediatric), geneticists and immunologists, researchers in IBD genetics and microbiome, and patients or families with early-onset, atypical, or treatment-refractory IBD.

Study Snapshot

Story typeResearch paper
Evidence typeResearch paper
Source depthJournal abstract

What To Know

This article abstract reviews the genetic architecture of IBD (monogenic, oligogenic, polygenic), discusses limitations of standard genetic screening (including mosaicism and regulatory variants), and argues for immunogenetic pathway–based classification to guide precision therapeutics.

The summary below is grounded in the source-provided abstract (structured content depth: abstract).

Keep In Mind

This classification is based on the article abstract; it is not a full-text review. The authors emphasize that negative genetic screens do not rule out genetic causes because newer mechanisms (mosaicism, regulatory variants) may be undetected by routine tests. Implementing pathway-based genetic evaluation may require specialized testing and interpretation.

Source Details

Review the original publication for the complete reporting, methods, and context.

Read Original Source
Research paper Evidence type derived from source or registry metadata.
PublicationGastroenterology clinics of North America
AuthorsO'Donnell JEM, Zeef DH, Gopan A +1 more
Study typeIm, review, journal article
Indexed viaEurope PMC
Source typeResearch paper
PublishedSep 16, 2026, 12:00 AM
Content availableJournal abstract

This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.

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