Evidence map›Paper›PMID 26752689›Full record

Trial reportAtherosclerosis2016

Specific cell-derived microvesicles: Linking endothelial function to carotid artery intima-media thickness in low cardiovascular risk menopausal women.

Virginia M Miller, Brian D Lahr, Kent R Bailey, Howard N Hodis, Sharon L Mulvagh, Muthuvel Jayachandran

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Atherosclerosis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Lessons from KEEPS: the Kronos Early Estrogen Prevention Study.Climacteric : the journal of the International Menopause Society · 2021
    Trial
  2. Trial
  3. Article
  4. Review
  5. Extracellular vesicles as tools and targets in therapy for diseases.Signal transduction and targeted therapy · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Extracellular Vesicles as Messengers in Atherosclerosis.Journal of cardiovascular translational research · 2020
    Review
  11. Article
  12. Risk factors of neurovascular ageing in women.Journal of neuroendocrinology · 2020
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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

6 authors at 3 institutions in 1 country.

Virginia M MillerDepartment of Surgery, Mayo Clinic, Rochester, MN 55905, USA; Department of Physiology & Biomedical Engineering, Mayo Clinic, Rochester, MN 55905, USA. Electronic address: miller.virginia@mayo.edu.
Brian D LahrDepartment of Health Sciences Research (Division of Biomedical Statistics and Informatics), Mayo Clinic, Rochester, MN 55905, USA.
Kent R BaileyDepartment of Health Sciences Research (Division of Biomedical Statistics and Informatics), Mayo Clinic, Rochester, MN 55905, USA; Department of Health Sciences Research (Division of Epidemiology), Mayo Clinic, Rochester, MN 55905, USA.
Howard N HodisAtherosclerosis Research Unit, University of Southern California, Los Angeles, CA 9033, USA.
Sharon L MulvaghDepartment of Internal Medicine (Division of Cardiovascular Diseases), Mayo Clinic, Rochester, MN 55905, USA.
Muthuvel JayachandranDepartment of Physiology & Biomedical Engineering, Mayo Clinic, Rochester, MN 55905, USA.
Mayo Clinic in Florida · USMayo Clinic in Arizona · USUniversity of Southern California · US

Funding

MAYO CLINIC CENTER FOR TRANSLATIONAL SCIENCE ACTIVITIESUL1RR024150 · NCRR · MAYO CLINIC ROCHESTER · PI RIZZA, ROBERT A. · 2006 to 2011
$66.4M
Wisconsin Alzheimer's Disease Research CenterP50AG033514 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI JOHNSON, STERLING C · 2009 to 2018
$16.2M
Mayo Clinic Interdisciplinary Women's Health Research ProgramK12HD065987 · NICHD · MAYO CLINIC ROCHESTER · PI KANTARCI, KEJAL · 2010 to 2023
$6.7M
Sex-specific Risk for Vascular Dysfunction and Cognitive DeclineP50AG044170 · NIA · MAYO CLINIC ROCHESTER · PI MILLER, VIRGINIA M · 2012 to 2017
$6.1M
Estrogen, Platelets, and ArtherosclerosisR01HL090639 · NHLBI · MAYO CLINIC ROCHESTER · PI BAILEY, KENT R, MILLER, VIRGINIA M · 2008 to 2012
$1.9M
NCRR NIH HHS UL1 RR024150NHLBI NIH HHS NIH HL90639NHLBI NIH HHS R01 HL090639NIA NIH HHS P50 AG033514NIA NIH HHS P50 AG044170NICHD NIH HHS HD65987NICHD NIH HHS K12 HD065987
6 · The paper itself

Abstract

backgroundDecreases in endothelial function measured by reactive hyperemic index (RHI) correlated with increases in carotid intima-media thickness (CIMT) in recently menopausal women with a low risk cardiovascular profile. Factors linking this association are unknown.

objectiveAssess, longitudinally, markers of platelet activation and cell-derived, blood-borne microvesicles (MV) in relationship to RHI and CIMT in asymptomatic, low risk menopausal women.

methodsRHI by digital pulse tonometry (n = 93), CIMT by ultrasound (n = 113), measures of platelet activation and specific cell-derived, blood-borne MV were evaluated in women throughout the Kronos Early Estrogen Prevention Study (KEEPS) at Mayo Clinic.

resultsCIMT, but not RHI, increased significantly over 4 years. The average change in CIMT correlated significantly with the average follow-up values of MV positive for common leukocyte antigen [CD45; ρ = 0.285 (P = 0.002)] and VCAM-1 [ρ = 0.270 (P = 0.0040)]. Using principal components analysis (PC) on the aggregate set of average follow-up measures, the first derived PC representing numbers of MV positive for markers of vascular endothelium, inflammatory cells (leukocyte and monocytes), pro-coagulant (tissue factor), and cell adhesion molecules (ICAM-1 and VCAM-1) associated with changes in RHI and CIMT. Changes in RHI associated with another PC defined by measures of platelet activation (dense granular ATP secretion, surface expression of P-selectin and fibrinogen receptors).

conclusionsMV derived from activated endothelial and inflammatory cells, and those expressing cell adhesion and pro-coagulant molecules may reflect early vascular dysfunction in low risk menopausal women. Assays of MV as non-conventional measures to assess cardiovascular risk in asymptomatic women remain to be developed.

Indexed as

Carotid Intima-Media ThicknessAdultBiomarkersBlood PlateletsCarotid ArteriesCarotid Artery DiseasesCell-Derived MicroparticlesDisease ProgressionEndothelium, VascularEstrogen Replacement TherapyFemaleHumansHyperemiaInflammation MediatorsLongitudinal StudiesManometryBiomarkersInflammation MediatorsAtherosclerosisInflammationKEEPSKronos Early Estrogen Prevention StudyLeukocytesMicroparticlesPlatelets

Identifiers

PMID26752689
PMCPMC4764461
OpenAlexW2220931894

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.