Evidence map›Paper›PMID 39744067›Full record

ArticleFrontiers in genetics2024

Assessing the causal relationships between circulating metabolic biomarkers and breast cancer by using mendelian randomization.

Bowen Wang, Yue Ling, Hui Zhang, Ming Yang

Abstract read
In one paragraph

Article in Frontiers in genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Bowen WangDepartment of Breast Surgery, General Surgery Center, First Hospital of Jilin University, Changchun, Jilin, China.
Yue LingDepartment of Ophthalmology, The Second Hospital of Jilin University, Changchun, Jilin, China.
Hui ZhangDepartment of Breast Surgery, General Surgery Center, First Hospital of Jilin University, Changchun, Jilin, China.
Ming YangDepartment of Breast Surgery, General Surgery Center, First Hospital of Jilin University, Changchun, Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Previous studies have established a causal relationship between metabolites and breast cancer (BC), but the underlying mechanisms remain unclear. Thus, we aimed to investigate the genetic relationship between metabolites and BC, including its subtypes, using Mendelian randomization (MR) analysis. Methods: Utilizing the latest and most comprehensive summary statistics from genome-wide association studies we conducted an Mendelian randomization study. Data on 233 metabolites, used as exposure variables, were obtained from a study involving 136,016 participants. BC data, used as outcome variables, were sourced from a study comprising 122,977 cases and 105,974 controls. We used the inverse-variance weighted method as the primary approach, along with three supplementary methods, to assess the causal relationship. We also used Cochran's Q test to detect heterogeneity and MR-Egger regression to examine the presence of horizontal pleiotropy. Results: Upon analyzing 233 metabolites across 11 classes in relation to BC, we found six classes of metabolites (fatty acids glycerides and phospholipids, lipoprotein subclasses, lipids, apolipoproteins, and lipoprotein particle size) associated with overall BC. Five classes of metabolites (fatty acids glycerides and phospholipids, lipoprotein subclasses, lipids, and lipoprotein particle size) were related to estrogen receptor (ER) + BC, and eight classes of metabolites (fatty acids, amino acids, glycerides and phospholipids, lipoprotein subclasses, lipids, apolipoproteins, glycolysis-related metabolites, and lipoprotein particle size) were linked to ER- BC. Conclusion: Our study demonstrates a genetic causal relationship between most metabolites and BC, confirming the link between these factors. This research provides a significant foundation for the prevention and treatment of BC.

Indexed as

breast cancercirculating metabolic biomarkerslipidslipoproteinmendelian randomizationmetabolite

Identifiers

PMID39744067
PMCPMC11688392

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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.