Evidence map›Paper›PMID 42319479›Full record

ArticleEuropean journal of nutrition2026

Glycemic index, glycemic load, and colorectal cancer risk stratified by insulin receptor expression: the Japan Public Health Center-based Prospective study.

Yuki Homma, Shiori Nakano, Kenshiro Nishihara, Taiki Yamaji, Atsushi Goto, Akihisa Hidaka, Taichi Shimazu, Aya Kuchiba, Masahiro Saito, Fumihito Kunishima and 6 more

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Article in European journal of nutrition, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Yuki HommaDivision of Epidemiology, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID http://orcid.org/0009-0002-4414-8739
Shiori NakanoDivision of Epidemiology, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID http://orcid.org/0000-0001-5762-850X
Kenshiro NishiharaDivision of Epidemiology, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID http://orcid.org/0009-0005-8096-900X
Taiki YamajiDivision of Epidemiology, National Cancer Center Institute for Cancer Control, Tokyo, Japan. tyamaji@ncc.go.jp.ORCID http://orcid.org/0000-0002-4799-8782
Atsushi GotoDivision of Epidemiology, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID http://orcid.org/0000-0003-0669-654X
Akihisa HidakaDivision of Epidemiology, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID http://orcid.org/0000-0002-1772-8159
Taichi ShimazuDivision of Behavioral Sciences, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID http://orcid.org/0000-0001-6000-9830
Aya KuchibaTeikyo University Graduate School of Public Health, Tokyo, Japan.ORCID http://orcid.org/0000-0002-6786-3527
Masahiro SaitoDepartment of Diagnostic Pathology, Hiraka General Hospital, Yokote, Japan.
Fumihito KunishimaDepartment of Diagnostic Pathology, Okinawa Prefecture Chubu Hospital, Uruma, Japan.ORCID http://orcid.org/0009-0001-6743-0158
Ryouji NakazaDepartment of Clinical Laboratory, Nakagami Hospital, Okinawa, Japan.
Ikuma KatoDivision of Pathology, Shizuoka Cancer Center, Shizuoka, Japan.
Norie SawadaDivision of Cohort Research, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID http://orcid.org/0000-0002-9936-1476
Manami InoueDivision of Cohort Research, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID http://orcid.org/0000-0003-1276-2398
Shoichiro TsuganeDivision of Cohort Research, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID http://orcid.org/0000-0003-4105-2774
Motoki IwasakiDivision of Epidemiology, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID http://orcid.org/0000-0003-3319-4131

Funding

Japan Agency for Medical Research and Development 19ck0106370h0003Japan Agency for Medical Research and Development JP19ck0106266Japan Agency for Medical Research and Development JP22ck0106551Ministry of Health, Labour, and Welfare of Japan Ministry of Health, Labour, and Welfare of JapanNational Cancer Center Research and Development Fund 2020-J-4National Cancer Center Research and Development Fund 2023-J-4National Cancer Center Research and Development Fund 23-A-31National Cancer Center Research and Development Fund 26-A-2National Cancer Center Research and Development Fund 29-A-4
6 · The paper itself

Abstract

purposeGlycemic index (GI) and glycemic load (GL) are markers for postprandial glucose level. Since insulin, a hormone secreted to control hyperglycemia, is likely to promote the progression of tumor cells, the association between GI/GL and risk of colorectal cancer (CRC) has been researched for decades but still remains controversial. This study investigated the association between GI/GL and CRC risk, considering subtypes based on insulin receptor beta (IRβ) expression.

methodsIn a large-scale, population-based prospective cohort study involving 18,537 Japanese participants, a total of 415 CRC cases were evaluated for IRβ expression using immunohistochemistry. GI and GL were calculated using a validated food frequency questionnaire. The Cox proportional hazards model was used to assess the hazard ratios (HRs) and 95% confidence intervals (CIs) of the risk of CRC and its specific subtypes. Additionally, we conducted sensitivity analyses to confirm the robustness of the results.

resultsNo significant associations were observed between dietary GI, GL and overall CRC risk. Further, no significant associations were detected in IRβ-stratified analyses. The heterogeneities in the associations by IRβ status were also not statistically significant. (GI: p for heterogeneity 0.83 for men and 0.96 for women; GL: p for heterogeneity 0.84 for men and 0.60 for women) Sensitivity analyses yielded robust results.

conclusionsThis study did not observe a significant association between GI/GL and overall CRC or IRβ-defined subtypes. These results, particularly those from the assessment of IRβ status, do not support a possible association between GI/GL and CRC development.

Indexed as

Colorectal NeoplasmsGlycemic IndexGlycemic LoadReceptor, InsulinAdultAgedBlood GlucoseFemaleHumansJapanMaleMiddle AgedProportional Hazards ModelsProspective StudiesRisk FactorsBlood GlucoseReceptor, InsulinColorectal cancerGlycemic indexGlycemic loadHeterogeneityInsulin receptor

Identifiers

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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.