Evidence map›Paper›PMID 40995592›Full record

ArticleFrontiers in endocrinology2025

Atherogenic ApoB-dyslipidemia, atherosclerotic cardiovascular disease, cardiac dysfunction and remodeling in high-risk young women with and without polycystic ovary syndrome: A pilot study.

Xiaoying Wu, Mich Wilke, Jesse Batara, Spencer Proctor, Melanie Cree, Mahua Ghosh, Paolo Raggi, Jonathon Windram, Harald Becher, Donna Vine

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
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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

10 authors.

Xiaoying WuPCOS Together Laboratory, University of Alberta, Edmonton, AB, Canada.
Mich WilkePCOS Together Laboratory, University of Alberta, Edmonton, AB, Canada.
Jesse BataraWomen and Children's Research Institute, Edmonton, AB, Canada.
Spencer ProctorMetabolic and Cardiovascular Disease Laboratory, University of Alberta, Edmonton, AB, Canada.
Melanie CreeDivision of Pediatric Endocrinology, Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Mahua GhoshDivision Endocrinology and Metabolism, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.
Paolo RaggiDivision Cardiology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.
Jonathon WindramDivision Cardiology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.
Harald BecherDivision Cardiology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.
Donna VinePCOS Together Laboratory, University of Alberta, Edmonton, AB, Canada.

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI BRYAN C BERGMAN · 1995 to 2026
$32.6M
NIDDK NIH HHS P30 DK048520
6 · The paper itself

Abstract

Introduction: Polycystic ovary syndrome (PCOS) is associated with increased cardiometabolic risk in young women of reproductive age. There are limited studies on atherogenic dyslipidemia, inclusive of triglycerides (TG), Apolipoprotein (apo) B-lipoproteins and remnant-cholesterol (C), atherosclerotic cardiovascular disease (ACVD), cardiac function and remodeling in young women with and without PCOS. The aim of this pilot study was to investigate the relationship of atherogenic dyslipidemia and other cardiometabolic risk factors with ACVD, cardiac function-remodeling in high-risk young overweight-obese PCOS women compared to non-PCOS and healthy-weight controls. Methods: Women with and without PCOS (non-PCOS control) aged 18 - 45 years who were overweight and obese (>25kg/m Results: PCOS (n=48) and non-PCOS control overweight-obese age-BMI matched groups (n=19) were shown to have significantly higher fasting and non-fasting lipids including TG, remnant-C, total ApoB and ApoB48, compared to healthy-weight non-PCOS controls (n=10). PCOS and non-PCOS control overweight-obese groups had significantly higher SBP, DBP, cIMT and evidence of cardiac dysfunction and remodeling, with reduced Mitral E/A ratio, intraventricular (IV) relaxation time and increased Left ventricle (LV) end diastolic and systolic diameter, LV posterior wall thickness and IV septal thickness, compared to healthy-weight non-PCOS controls. Individuals with PCOS had significantly higher fasting plasma TG and remnant-C compared to the non-PCOS overweight-obese control group. The PCOS group tended to have 25% higher carotid plaque height, although this was not significant, compared to the non-PCOS overweight-obese control group. DBP, HOMA-IR and ApoB predicted 40% of the variability in cIMT and ApoB was shown to predict 14% of the variability in carotid plaque height, independent of age and BMI. A 1mg/ml increase in ApoB was associated with a 0.041mm increase in cIMT and a 0.75mm increase in carotid plaque height in all young women. Discussion: Our pilot results supports the potential of apoB-dyslipidemia, cIMT, carotid plaque height and left ventricular diastolic dysfunction and remodeling to be used in screening for CVD risk in high-risk populations such as overweight-obese women with and without PCOS. ApoB may be useful to predict atherosclerotic vascular burden and progression of cIMT and carotid plaque, and could be used to develop a female specific algorithm for ACVD risk in high-risk young women with and without PCOS.

Indexed as

Apolipoproteins BAtherosclerosisCardiovascular DiseasesDyslipidemiasPolycystic Ovary SyndromeVentricular RemodelingAdolescentAdultApolipoprotein B-100Carotid Intima-Media ThicknessCase-Control StudiesFemaleHumansMiddle AgedObesityPilot ProjectsAPOB protein, humanApolipoprotein B-100Apolipoproteins BApoB-lipoproteinsatherogenic dyslipidemiaatherosclerosiscardiac functioncardiac remodelingPCOSplaqueremnant-cholesterol

Identifiers

PMID40995592
PMCPMC12454106

What OpenQuestion holds

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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.