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Why This Matters

Identifying people at very early, preclinical stages of Crohn’s disease could allow enrollment in prevention trials and earlier intervention. Faecal calprotectin may help select higher‑risk first‑degree relatives for further evaluation.

Who Should Pay Attention

First‑degree relatives of Crohn’s patients, clinicians doing IBD screening or prevention research, pediatric gastroenterology teams, and researchers designing prevention trials.

Study Snapshot

Story typeResearch paper
Evidence typeResearch paper
Source depthJournal abstract

What To Know

The researchers screened FDRs aged 6–38 with faecal calprotectin; persistent elevation (>70 µg/g on at least two tests) triggered panenteric video capsule endoscopy or ileocolonoscopy.

About 19% of those screened had persistently elevated calprotectin; among evaluated participants, some had endoscopic findings compatible with presymptomatic Crohn’s disease and others had non‑specific mucosal changes or probable histological inflammation despite normal mucosa.

Higher calprotectin (>225 µg/g) was strongly predictive of presymptomatic disease in this cohort. The authors propose that calprotectin can help identify at‑risk individuals for prevention trials.

Keep In Mind

Findings are based on the study abstract (panenteric capsule/endoscopy and colonoscopy used after persistent calprotectin elevation). The predictive cutpoint (>225 µg/g) and prevalence estimates are cohort‑specific and need replication; the study does not provide results of any prevention intervention.

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.
PublicationGut
AuthorsDan Turner, Sarah Kenigsberg, Gili Focht +14 more
InstitutionInstitute of Pediatric Gastroenterology, Shaare Zedek Medical Center, Jerusalem, Jerusalem District, Israel turnerd@szmc.org.il.
Study typeJournal article
Indexed viaPubMed
Source typeResearch paper
PublishedOct 7, 2026, 12:00 AM
Content availableJournal abstract

Conflict statement: Competing interests: DT, SK, HH, WE, LP, YA-F, AMG, IA-B, OL, GF, WT and KC declare no conflicts in relation to the content of this study. KJ: Advisory board (AbbVie, McKesson Canada, Janssen, Viatris, Celltrion; CSL Behring Canada); Speaker’s bureau (AbbVie). JT: Research support from AbbVie and Johnson & Johnson; has received advisory board/speaker fees from Eli Lilly, AbbVie, Johnson & Johnson, Pfizer, Sandoz and Tillots Pharma. RP: Consultant for Abbott, AbbVie, Abbivax, Alimentiv, Amgen, AnaptysBio, AstraZeneca, Biogen, Boehringer Ingelheim, Bristol-Myers Squibb, Celgene, Celltrion, Cosmos Pharmaceuticals, Eisai, Elan, Eli Lilly, Ferring, Galapagos, Inviva, Fresenius Kabi, Genentech, Gilead Sciences, Glaxo-Smith Kline, JAMP Bio, Janssen, Merck, Mirador, Novartis, Oppilan Pharma, Odyssey, Organon, Pandion Pharma, Pendopharm, Pfizer, Progenity, Prometheus Biosciences, Protagonist Therapeutics, Roche, Sandoz, Sanofi, Satisfai Health, Shire, Sublimity Therapeutics, Spyre Therapeutics, Takeda Pharmaceuticals, Teva, Tillots, Trellus, Union Biopharma, Viatris, Ventyx, UCB; Speaker’s fees for AbbVie, Amgen, Arena Pharmaceuticals, Bristol-Myers Squibb, Celgene, Eli Lilly, Ferring, Fresenius Kabi, Gilead Sciences, Janssen, Merck, Organon, Pfizer, Roche, Sandoz, Shire, Takeda Pharmaceuticals; Advisory Boards for AbbVie, Alimentiv (formerly Robarts), Amgen, Arena Pharmaceuticals, AstraZeneca, Biogen, Boehringer Ingelheim, Bristol-Myers Squibb, Celgene, Eli Lilly, Ferring, Fresenius Kabi, Genentech, Gilead Sciences, Glaxo-Smith Kline, JAMP Bio, Janssen, Merck, Mylan, Novartis, Oppilan Pharma, Organon, Pandion Pharma, Pfizer, Progenity, Protagonist Therapeutics, Roche, Sandoz, Sanofi, Sublimity Therapeutics, Takeda Pharmaceuticals, Ventyx.

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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