Evidence map›Paper›PMID 30374313›Full record

ArticleFrontiers in physiology2018

Coronary Microvascular Remodeling in Type 2 Diabetes: Synonymous With Early Aging?

Patricia E McCallinhart, Ian L Sunyecz, Aaron J Trask

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Sex differences in vascular aging and impact of GPER deletion.American journal of physiology. Heart and circulatory physiology · 2022
    Article
  6. Review
  7. Guidelines for the measurement of vascular function and structure in isolated arteries and veins.American journal of physiology. Heart and circulatory physiology · 2021
    Review
  8. Coronary microvascular adaptations distal to epicardial artery stenosis.American journal of physiology. Heart and circulatory physiology · 2021
    Review
  9. Article
  10. Coronary remodeling and biomechanics: Are we going with the flow in 2020?American journal of physiology. Heart and circulatory physiology · 2021
    Review
  11. Review
  12. Reduced stiffness and augmented traction force in type 2 diabetic coronary microvascular smooth muscle.American journal of physiology. Heart and circulatory physiology · 2020
    Article
  13. 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

3 authors at 2 institutions in 1 country.

Patricia E McCallinhartCenter for Cardiovascular Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH, United States.
Ian L SunyeczCenter for Cardiovascular Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH, United States.
Aaron J TraskCenter for Cardiovascular Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH, United States.
Nationwide Children's Hospital · USThe Ohio State University · US

Funding

Differential Macro- and Micro-Vascular Remodeling in Type 2 Diabetes and Metabolic SyndromeR00HL116769 · NHLBI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI TRASK, AARON J · 2016 to 2018
$747k
Asylum Research MFP-3D-BIO Atomic Force MicroscopeS10OD023438 · OD · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI TRASK, AARON J · 2017 to 2017
$316k
NHLBI NIH HHS R00 HL116769NIH HHS S10 OD023438
6 · The paper itself

Abstract

Type 2 diabetes mellitus (T2DM) is suggested to cause an "early vascular aging" phenomenon that is associated with vascular dysfunction, remodeling, and adverse alterations in vascular stiffness. Given that both T2DM and aging are prominent risk factors for cardiovascular disease, the aim of this study was to test the hypothesis that coronary resistance microvessel (CRM) remodeling and impairments in flow occur in the compound setting of T2DM and aging. Normal heterozygous Db/db controls and homozygous db/db mice were aged to 16 (young) or 36 (aged) weeks for all experiments and passive pressure myography and echocardiography were used to assess vascular mechanics, and structure. CRM wall thickness was significantly increased at each pressure in aged control mice compared to young control mice (9.4 ± 0.6 vs. 6.8 ± 0.2 μm, respectively,

Indexed as

agingcoronary remodelingmicrocirculationtype 2 diabetesvascular remodelingvascular stiffness

Identifiers

PMID30374313
PMCPMC6196247
OpenAlexW2894244694

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.