Evidence map›Paper›PMID 25384789›Full record

ReviewThe Journal of physiology2016

Microvascular perfusion heterogeneity contributes to peripheral vascular disease in metabolic syndrome.

Jefferson C Frisbee, Adam G Goodwill, Stephanie J Frisbee, Joshua T Butcher, Fan Wu, Paul D Chantler

Open access · greenAbstract readReview
In one paragraph

Review in The Journal of physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Antioxidants (Basel, Switzerland) · 2023
    Article
  4. Review
  5. Advances in translational imaging of the microcirculation.Microcirculation (New York, N.Y. : 1994) · 2021
    Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Cardiovascular consequences of metabolic syndrome.Translational research : the journal of laboratory and clinical medicine · 2017
    Review
  15. Article
  16. Article
  17. The endothelial glycocalyx promotes homogenous blood flow distribution within the microvasculature.American journal of physiology. Heart and circulatory physiology · 2016
    Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Jefferson C FrisbeeDepartment of Physiology and Pharmacology, West Virginia University Health Sciences Center, Morgantown, WV, USA.
Adam G GoodwillDepartment of Physiology and Pharmacology, West Virginia University Health Sciences Center, Morgantown, WV, USA.
Stephanie J FrisbeeCenter for Cardiovascular and Respiratory Sciences, West Virginia University Health Sciences Center, Morgantown, WV, USA.
Joshua T ButcherDepartment of Physiology and Pharmacology, West Virginia University Health Sciences Center, Morgantown, WV, USA.
Fan WuNovartis Institutes for BioMedical Research, Drug Metabolism and Pharmacokinetics, East Hanover, NJ, USA.
Paul D ChantlerCenter for Cardiovascular and Respiratory Sciences, West Virginia University Health Sciences Center, Morgantown, WV, USA.
West Virginia University · US

Funding

Translation CoreP30DK097512 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Carmella Evans-Molina · 2015 to 2026
$17.4M
NIDDK NIH HHS P30 DK097512
6 · The paper itself

Abstract

A major challenge facing public health is the increased incidence and prevalence of the metabolic syndrome, a clinical condition characterized by excess adiposity, impaired glycaemic control, dyslipidaemia and moderate hypertension. The greatest concern for this syndrome is the profound increase in risk for development of peripheral vascular disease (PVD) in afflicted persons. However, ongoing studies suggest that reductions in bulk blood flow to skeletal muscle may not be the primary contributor to the premature muscle fatigue that is a hallmark of PVD. Compelling evidence has been provided suggesting that an increasingly spatially heterogeneous and temporally stable distribution of blood flow at successive arteriolar bifurcations in metabolic syndrome creates an environment where a large number of the pre-capillary arterioles have low perfusion, low haematocrit, and are increasingly confined to this state, with limited ability to adapt perfusion in response to a challenged environment. Single pharmacological interventions are unable to significantly restore function owing to a divergence in their spatial effectiveness, although combined therapeutic approaches to correct adrenergic dysfunction, elevated oxidant stress and increased thromboxane A2 improve perfusion-based outcomes. Integrated, multi-target therapeutic interventions designed to restore healthy network function and flexibility may provide for superior outcomes in subjects with metabolic syndrome-associated PVD.

Indexed as

AnimalsHumansMetabolic SyndromeMicrocirculationMuscle, SkeletalPeripheral Vascular DiseasesThromboxanesThromboxanes

Identifiers

PMID25384789
PMCPMC4933102
OpenAlexW1597398005

What OpenQuestion holds

Textmetadata
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.