Evidence map›Paper›PMID 38409583›Full record

ArticleScientific reports2024

Spatial heterogeneity of peri-tumoural lipid composition in postmenopausal patients with oestrogen receptor positive breast cancer.

Sai Man Cheung, Kwok-Shing Chan, Wenshu Zhou, Ehab Husain, Tanja Gagliardi, Yazan Masannat, Jiabao He

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Sai Man Cheung *School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK. g.cheung@abdn.ac.uk.
Kwok-Shing Chan *School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK.
Wenshu ZhouSchool of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK.
Ehab HusainDepartment of Pathology, Aberdeen Royal Infirmary, Aberdeen, UK.
Tanja GagliardiSchool of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK.
Yazan MasannatSchool of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK.
Jiabao HeSchool of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK. jiabao.he@newcastle.ac.uk.
University of Aberdeen · GBAberdeen Royal Infirmary · GBAthinoula A. Martinos Center for Biomedical Imaging · USNewcastle University · GB

Funding

Cancer Research UK 28312Cancer Research UK C68628/A28312
6 · The paper itself

Abstract

Deregulation of lipid composition in adipose tissue adjacent to breast tumour is observed in ex vivo and animal models. Novel non-invasive magnetic resonance imaging (MRI) allows rapid lipid mapping of the human whole breast. We set out to elucidate the spatial heterogeneity of peri-tumoural lipid composition in postmenopausal patients with oestrogen receptor positive (ER +) breast cancer. Thirteen participants (mean age, 62 ± [SD] 6 years) with ER + breast cancer and 13 age-matched postmenopausal healthy controls were scanned on MRI. The number of double bonds in triglycerides was computed from MRI images to derive lipid composition maps of monounsaturated, polyunsaturated, and saturated fatty acids (MUFA, PUFA, SFA). The spatial heterogeneity measures (mean, median, skewness, entropy and kurtosis) of lipid composition in the peri-tumoural region and the whole breast of participants and in the whole breast of controls were computed. The Ki-67 proliferative activity marker and CD163 antibody on tumour-associated macrophages were assessed histologically. Mann Whitney U or Wilcoxon tests and Spearman's coefficients were used to assess group differences and correlations, respectively. For comparison against the whole breast in participants, peri-tumoural MUFA had a lower mean (median (IQR), 0.40 (0.02), p < .001), lower median (0.42 (0.02), p < .001), a negative skewness with lower magnitude (- 1.65 (0.77), p = .001), higher entropy (4.35 (0.64), p = .007) and lower kurtosis (5.13 (3.99), p = .001). Peri-tumoural PUFA had a lower mean (p < .001), lower median (p < .001), a positive skewness with higher magnitude (p = .005) and lower entropy (p = .002). Peri-tumoural SFA had a higher mean (p < .001), higher median (p < .001), a positive skewness with lower magnitude (p < .001) and lower entropy (p = .012). For comparison against the whole breast in controls, peri-tumoural MUFA had a negative skewness with lower magnitude (p = .01) and lower kurtosis (p = .009), however there was no difference in PUFA or SFA. CD163 moderately correlated with peri-tumoural MUFA skewness (r

Indexed as

Breast NeoplasmsAnimalsFatty AcidsFatty Acids, MonounsaturatedFemaleHumansMiddle AgedPostmenopauseReceptors, EstrogenFatty AcidsFatty Acids, MonounsaturatedReceptors, EstrogenBreast cancerHeterogeneityInflammationLipid compositionOestrogen receptor

Identifiers

PMID38409583
PMCPMC10897464
OpenAlexW4392169810

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.