Evidence map›Paper›PMID 36765646›Full record

ArticleCancers2023

Autoimmune and Metabolic Diseases and the Risk of Early-Onset Colorectal Cancer, a Nationwide Nested Case-Control Study.

Erik Lundqvist, Ida Hed Myrberg, Sol Erika Boman, Deborah Saraste, Caroline E Weibull, Kalle Landerholm, Staffan Haapaniemi, Anna Martling, Pär Myrelid, Caroline Nordenvall

Abstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
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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

10 authors.

Erik LundqvistDepartment of Biomedical and Clinical Sciences, Linköping University, 58183 Linköping, Sweden.ORCID 0000-0001-5312-1023
Ida Hed MyrbergDepartment of Medicine, Division of Clinical Epidemiology, Karolinska University Hospital, Karolinska Institutet, 17177 Stockholm, Sweden.ORCID 0000-0002-8297-2238
Sol Erika BomanDepartment of Medicine, Division of Clinical Epidemiology, Karolinska University Hospital, Karolinska Institutet, 17177 Stockholm, Sweden.
Deborah SarasteDepartment of Surgery, Södersjukhuset, 11883 Stockholm, Sweden.
Caroline E WeibullDepartment of Medicine, Division of Clinical Epidemiology, Karolinska University Hospital, Karolinska Institutet, 17177 Stockholm, Sweden.
Kalle LanderholmDepartment of Biomedical and Clinical Sciences, Linköping University, 58183 Linköping, Sweden.
Staffan HaapaniemiDepartment of Biomedical and Clinical Sciences, Linköping University, 58183 Linköping, Sweden.
Anna MartlingDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Division of Coloproctology, Center for Digestive Diseases, Karolinska University Hospital, 17177 Stockholm, Sweden.
Pär MyrelidDepartment of Biomedical and Clinical Sciences, Linköping University, 58183 Linköping, Sweden.ORCID 0000-0001-7518-9213
Caroline NordenvallDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Division of Coloproctology, Center for Digestive Diseases, Karolinska University Hospital, 17177 Stockholm, Sweden.ORCID 0000-0002-5112-8894

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Incidence of early-onset (<50 years) colorectal cancer (EOCRC) is increasing in developed countries. The aim was to investigate autoimmune and metabolic conditions as risk factors for EOCRC. In a nationwide nested case-control study, we included all EOCRC cases in Sweden diagnosed during 2007-2016, together with controls, matched for birth year, sex, and county. Information on exposure of autoimmune or metabolic disease was collected from the National Patient Register and Prescribed Drugs Registry. Hazard ratios (HR) as measures of the association between EOCRC and the exposures were estimated using conditional logistic regression. In total, 2626 EOCRC patients and 15,756 controls were included. A history of metabolic disease nearly doubled the incidence hazard of EOCRC (HR 1.82, 95% CI 1.66-1.99). A sixfold increased incidence hazard of EOCRC (HR 5.98, 95% CI 4.78-7.48) was seen in those with inflammatory bowel disease (IBD), but the risk increment decreased in presence of concomitant metabolic disease (HR 3.65, 95% CI 2.57-5.19). Non-IBD autoimmune disease was not statistically significantly associated with EOCRC. IBD and metabolic disease are risk factors for EOCRC and should be considered in screening guidelines.

Indexed as

autoimmune diseasediabetes mellitusearly-onset colorectal cancerhyperlipidemiahypertensioninflammatory bowel diseasemetabolic diseaseobesityrisk factors

Identifiers

PMID36765646
PMCPMC9913656

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.