Evidence map›Paper›PMID 40328654›Full record

ArticleBMJ open2025

Cohort profile: the Swedish Inception Cohort in inflammatory bowel disease (SIC-IBD).

Benita Salomon, Olle Grännö, Daniel Bergemalm, Hans Strid, Adam Carstens, Henrik Hjortswang, Maria Ling Lundström, Jóhann P Hreinsson, Sven Almer, Francesca Bresso and 18 more

Abstract read
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed.

  1. Article
  2. Article
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

28 authors.

Benita Salomon *School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID http://orcid.org/0009-0002-8951-9839
Olle Grännö *Department of Laboratory Medicine, Clinical Microbiology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Daniel BergemalmDepartment of Gastroenterology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Hans StridCentre for Digestive Health, Department of Gastroenterology, Dermatovenereology and Rheumatology, Karolinska University Hospital, Stockholm, Sweden.
Adam CarstensDepartment of Internal Medicine, Ersta Hospital, Stockholm, Sweden.
Henrik HjortswangDepartment of Gastroenterology, County Council of Östergötland, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Maria Ling LundströmDepartment of Medical Sciences, Gastroenterology Research Group, Uppsala University, Uppsala, Sweden.
Jóhann P HreinssonDepartment of Molecular and Clinical Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Sven AlmerCentre for Digestive Health, Department of Gastroenterology, Dermatovenereology and Rheumatology, Karolinska University Hospital, Stockholm, Sweden.
Francesca BressoCentre for Digestive Health, Department of Gastroenterology, Dermatovenereology and Rheumatology, Karolinska University Hospital, Stockholm, Sweden.
Carl ErikssonDepartment of Gastroenterology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Olof GripDepartment of Gastroenterology, Skåne University Hospital, Malmö/Lund, Sweden.
André BlombergDepartment of Medicine, Geriatrics and Emergency Medicine, Sahlgrenska University Hospital, Östra Hospital, Gothenburg, Sweden.
Jan MarsalDepartment of Gastroenterology, Skåne University Hospital, Malmö/Lund, Sweden.
Niloofar NikaeinSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID http://orcid.org/0000-0002-5253-2768
Shoaib BakhtyarSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Carl Mårten LindqvistSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Elisabeth Hultgren HörnquistSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID http://orcid.org/0000-0001-5460-8888
Maria K MagnussonDepartment of Microbiology and Immunology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Åsa V KeitaDepartment of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
Mauro D'AmatoDepartment of Medicine and Surgery, LUM University, Casamassima, Italy.
Dirk RepsilberSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Lena ÖhmanDepartment of Microbiology and Immunology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Johan D SöderholmDepartment of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
Marie CarlsonDepartment of Medical Sciences, Gastroenterology Research Group, Uppsala University, Uppsala, Sweden.
Charlotte R H HedinCentre for Digestive Health, Department of Gastroenterology, Dermatovenereology and Rheumatology, Karolinska University Hospital, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-4921-8516
Robert KruseSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Jonas HalfvarsonDepartment of Gastroenterology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden jonas.halfvarsson@regionorebrolan.se.ORCID http://orcid.org/0000-0003-0122-7234

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThere is a need for diagnostic and prognostic biosignatures to improve long-term outcomes in inflammatory bowel disease (IBD). Here, we describe the establishment of the Swedish Inception Cohort in IBD (SIC-IBD) and demonstrate its potential for the identification of such signatures.

participantsPatients aged ≥18 years with gastrointestinal symptoms who were referred to the gastroenterology unit due to suspected IBD at eight Swedish hospitals between November 2011 and March 2021 were eligible for inclusion. FINDINGS TO DATE: In total, 367 patients with IBD (Crohn's disease, n=142; ulcerative colitis, n=201; IBD-unclassified, n=24) and 168 symptomatic controls were included. In addition, 59 healthy controls without gastrointestinal symptoms were recruited as a second control group. Biospecimens and clinical data were collected at inclusion and in patients with IBD also during follow-up to 10 years. Levels of faecal calprotectin and high-sensitivity C-reactive protein were higher in patients with IBD compared with symptomatic controls and healthy controls. Preliminary results highlight the potential of serum protein signatures and autoantibodies, as well as results from faecal markers, to differentiate between IBD and symptomatic controls in the cohort. During the first year of follow-up, 37% (53/142) of the patients with Crohn's disease, 24% (48/201) with ulcerative colitis and 4% (1/24) with IBD-U experienced an aggressive disease course. FUTURE PLANS: We have established an inception cohort enabling ongoing initiatives to collect and generate clinical data and multi-omics datasets. The cohort will allow analyses for translation into candidate biosignatures to support clinical decision-making in IBD. Additionally, the data will provide insights into mechanisms of disease pathogenesis.

Indexed as

Colitis, UlcerativeCrohn DiseaseInflammatory Bowel DiseasesAdultAutoantibodiesBiomarkersCase-Control StudiesCohort StudiesC-Reactive ProteinFecesFemaleHumansLeukocyte L1 Antigen ComplexMaleMiddle AgedSwedenAutoantibodiesBiomarkersC-Reactive ProteinLeukocyte L1 Antigen ComplexGASTROENTEROLOGYInflammatory bowel diseasePrognosis

Identifiers

PMID40328654
PMCPMC12056626

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.