Evidence map›Paper›PMID 39164739›Full record

ArticleLipids in health and disease2024

Association between remnant cholesterol and the risk of 4 site-specific cancers: evidence from a cross-sectional and Mendelian randomization study.

Mengjie Li, Qi Liu, Ming Shi, Manyi Fu, Guijuan He

Abstract read
In one paragraph

Article in Lipids in health and disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Cholesterol as a metabolic integrator of oncogenic signaling, immune evasion, and therapy resistance.Apoptosis : an international journal on programmed cell death · 2026
    Review
  3. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Mengjie Li *School of Nursing, Zhejiang Chinese Medical University, Hangzhou, China.
Qi Liu *First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China.
Ming ShiSchool of Nursing, Zhejiang Chinese Medical University, Hangzhou, China.
Manyi FuSchool of Nursing, Zhejiang Chinese Medical University, Hangzhou, China.
Guijuan HeSchool of Nursing, Zhejiang Chinese Medical University, Hangzhou, China. sheryhe@163.com.

Funding

Zhejiang Province Natural Science Foundation project LTGY23H250001
6 · The paper itself

Abstract

backgroundRecent studies have implicated remnant cholesterol (RC) in the etiology, progression, and prognosis of cancer. However, very few of them concentrated on the study of the precise relationship between serum RC levels and cancer risk, leaving this subject unexplored. Consequently, this study aims to investigate the association between serum RC levels and 4 site-specific cancers, employing a dual approach that combines observational and mendelian randomization (MR) analysis.

methodsBased on data from the National Health and Nutrition Examination Survey (NHANES) from 1999 to 2020, this study collected data from18,067 participants. To rule out confounders, this study utilized weighted multivariable logistic regression and assessed non-linear associations using restricted cubic spline (RCS) regression, followed by two-piecewise linear regression. Sensitivity analysis conducted in this study included subgroup analysis, multiple imputation, outlier removal, and propensity score matching. To strengthen causal inference, this study employed univariable and multivariable MR analysis. The robustness and reliability of the findings were estimated by the application of replication and meta-analysis.

resultsThe results of multivariable logistic regression analysis demonstrated a significant association between serum RC levels and breast cancer, showing that individuals in the higher logRC category had a higher risk of breast cancer compared to those in the lower category (Q3 vs. Q1: OR = 1.71, 95% CI: 1.01-2.88, P = 0.044). Weighted RCS revealed an inverted L-shape association between RC and the risk of breast cancer (P-nonlinear = 0.0386, P-overall = 0.010). Primary MR analysis provided evidence for an increased risk of breast (IVW: OR = 1.08, 95% CI: 1.03-1.12, P = 0.000951) and colorectal cancer (IVW: OR = 1.12, 95% CI: 1.00-1.24, P = 0.0476) associated with RC. However, the results of replication and meta-analysis did not support a significant causal association of RC with the risk of breast cancer (OR = 1.04, 95% CI: 0.95-1.13), lung cancer (OR = 0.95, 95% CI: 0.88-1.03), colorectal cancer (OR = 1.05, 95% CI: 0.92-1.19), and prostate cancer (OR = 1.01, 95% CI: 0.95-1.08).

conclusionAlthough a non-linear relationship was observed in the cross-sectional study between remnant cholesterol levels and breast cancer risk, MR analyses failed to provide any causal evidence.

Indexed as

CholesterolMendelian Randomization AnalysisAdultAgedBreast NeoplasmsColorectal NeoplasmsCross-Sectional StudiesFemaleHumansLipoproteinsLogistic ModelsLung NeoplasmsMaleMiddle AgedNeoplasmsNutrition SurveysCholesterolLipoproteinsremnant-like particle cholesterolTriglyceridesCancerMendelian randomizationNHANESRemnant cholesterol

Identifiers

PMID39164739
PMCPMC11334515

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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.