Evidence map›Paper›PMID 37300599›Full record

ArticleJournal of gastroenterology2023

Hierarchical contribution of individual lifestyle factors and their interactions on adenomatous and serrated polyp risk.

Jihee Kim, Kirti Nath, Kurt Schmidlin, Helen Schaufelberger, Christiana Quattropani, Simone Vannini, Sandro Mossi, Miriam Thumshirn, Michael Manz, Lev Litichevskiy and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of gastroenterology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
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

11 citing papers in PubMed, 18 citations in OpenAlex.

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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

18 authors at 5 institutions in 2 countries.

Jihee Kim *Microbiology Department and Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, 3610 Hamilton Walk, Philadelphia, PA, 19104, USA.
Kirti Nath *Microbiology Department and Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, 3610 Hamilton Walk, Philadelphia, PA, 19104, USA.
Kurt SchmidlinInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
Helen SchaufelbergerClinica Luganese Moncucco, Lugano, Switzerland.
Christiana QuattropaniClinica Luganese Moncucco, Lugano, Switzerland.
Simone VanniniClinica Luganese Moncucco, Lugano, Switzerland.
Sandro MossiClinica Luganese Moncucco, Lugano, Switzerland.
Miriam ThumshirnClarunis, University Hospital of Basel, Basel, Switzerland.
Michael ManzClarunis, University Hospital of Basel, Basel, Switzerland.
Lev LitichevskiyMicrobiology Department and Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, 3610 Hamilton Walk, Philadelphia, PA, 19104, USA.
Jiaxin FanDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.
Oxana Dmitrieva-PosoccoMicrobiology Department and Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, 3610 Hamilton Walk, Philadelphia, PA, 19104, USA.
Mingyao LiDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.
Maayan LevyMicrobiology Department and Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, 3610 Hamilton Walk, Philadelphia, PA, 19104, USA.
Primo SchärDepartment of Biomedicine, Genome Plasticity Group, University of Basel, Basel, Switzerland.
Marcel ZwahlenInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
Christoph A Thaiss *Microbiology Department and Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, 3610 Hamilton Walk, Philadelphia, PA, 19104, USA. thaiss@pennmedicine.upenn.edu.
Kaspar Truninger *Department of Biomedicine, Genome Plasticity Group, University of Basel, Basel, Switzerland. k.truninger@hin.ch.ORCID http://orcid.org/0000-0002-6569-6059
University of Pennsylvania · USClinica Luganese Moncucco · CHUniversity Hospital of Basel · CHUniversity of Basel · CHUniversity of Bern · CH

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007170 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI BRASS, LAWRENCE F · 1985 to 2022
$54.0M
VIRAL VECTOR COREP30DK019525 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Patrick Seale · 1986 to 2026
$48.3M
Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI Trevor M Penning · 2006 to 2026
$35.3M
TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI REBECCA G WELLS · 1997 to 2026
$32.5M
Training Program in Computational GenomicsT32HG000046 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI JUNHYONG KIM, Mingyao Li · 1999 to 2026
$9.5M
Study Design and Data AnalysisP30AR069589 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Elizabeth Anne Grice · 2016 to 2026
$8.6M
Post-biotic interventions to ameliorate age-related inflammationDP2AG067511 · NIA · UNIVERSITY OF PENNSYLVANIA · PI LEVY, MAAYAN · 2019 to 2019
$2.4M
A conserved function of amyloid proteins in host-microbiome interactionsDP2AG067492 · NIA · UNIVERSITY OF PENNSYLVANIA · PI THAISS, CHRISTOPH ALEXANDER · 2019 to 2019
$2.4M
NHGRI NIH HHS T32 HG000046NIAMS NIH HHS P30 AR069589NIA NIH HHS DP2 AG067492NIA NIH HHS DP2 AG067511NIDDK NIH HHS P30 DK019525NIDDK NIH HHS P30 DK050306NIEHS NIH HHS P30 ES013508NIGMS NIH HHS T32 GM007170
6 · The paper itself

Abstract

backgroundIndividual colorectal polyp risk factors are well characterized; however, insights into their pathway-specific interactions are scarce. We aimed to identify the impact of individual risk factors and their joint effects on adenomatous (AP) and serrated polyp (SP) risk.

methodsWe collected information on 363 lifestyle and metabolic parameters from 1597 colonoscopy participants, resulting in over 521,000 data points. We used multivariate statistics and machine-learning approaches to assess associations of single variables and their interactions with AP and SP risk.

resultsIndividual factors and their interactions showed common and polyp subtype-specific effects. Abdominal obesity, high body mass index (BMI), metabolic syndrome, and red meat consumption globally increased polyp risk. Age, gender, and western diet associated with AP risk, while smoking was associated with SP risk. CRC family history was associated with advanced adenomas and diabetes with sessile serrated lesions. Regarding lifestyle factor interactions, no lifestyle or dietary adjustments mitigated the adverse smoking effect on SP risk, whereas its negative effect was exacerbated by alcohol in the conventional pathway. The adverse effect of red meat on SP risk was not ameliorated by any factor, but was further exacerbated by western diet along the conventional pathway. No modification of any factor reduced the negative impact of metabolic syndrome on AP risk, whereas increased fatless fish or meat substitutes' intake mitigated its effect on SP risk.

conclusionsIndividual risk factors and their interactions for polyp formation along the adenomatous and serrated pathways are strongly heterogeneous. Our findings may facilitate tailored lifestyle recommendations and contribute to a better understanding of how risk factor combinations impact colorectal carcinogenesis.

Indexed as

AdenomaAdenomatous PolypsColonic PolypsColorectal NeoplasmsMetabolic SyndromeColonoscopyHumansRisk FactorsAdenomatous polypsIndividual risk factorsRisk factor interactionsSerrated polyps

Identifiers

PMID37300599
PMCPMC10423128
OpenAlexW4380204103

What OpenQuestion 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 OpenQuestion graph.