Evidence map›Paper›PMID 34067715›Full record

ReviewJournal of cardiovascular development and disease2021

The Aging Vasculature: Glucose Tolerance, Hypoglycemia and the Role of the Serum Response Factor.

Hazel Aberdeen, Kaela Battles, Ariana Taylor, Jeranae Garner-Donald, Ana Davis-Wilson, Bryan T Rogers, Candice Cavalier, Emmanuel D Williams

Open access · goldAbstract readReview
In one paragraph

Review in Journal of cardiovascular development and disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
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

8 authors at 2 institutions in 1 country.

Hazel AberdeenDepartment of Biomedical Sciences, Baptist Health Sciences University, Memphis, TN 38103, USA.
Kaela BattlesDepartment of Biology and Chemistry, Southern University and A&M College, Baton Rouge, LA 70813, USA.
Ariana TaylorDepartment of Biology and Chemistry, Southern University and A&M College, Baton Rouge, LA 70813, USA.
Jeranae Garner-DonaldDepartment of Biology and Chemistry, Southern University and A&M College, Baton Rouge, LA 70813, USA.
Ana Davis-WilsonDepartment of Biology and Chemistry, Southern University and A&M College, Baton Rouge, LA 70813, USA.
Bryan T RogersDepartment of Biology and Chemistry, Southern University and A&M College, Baton Rouge, LA 70813, USA.
Candice CavalierDepartment of Biology and Chemistry, Southern University and A&M College, Baton Rouge, LA 70813, USA.
Emmanuel D WilliamsDepartment of Biology and Chemistry, Southern University and A&M College, Baton Rouge, LA 70813, USA.
Southern University and Agricultural and Mechanical College · USSouthwest Baptist University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The fastest growing demographic in the U.S. at the present time is those aged 65 years and older. Accompanying advancing age are a myriad of physiological changes in which reserve capacity is diminished and homeostatic control attenuates. One facet of homeostatic control lost with advancing age is glucose tolerance. Nowhere is this more accentuated than in the high proportion of older Americans who are diabetic. Coupled with advancing age, diabetes predisposes affected subjects to the onset and progression of cardiovascular disease (CVD). In the treatment of type 2 diabetes, hypoglycemic episodes are a frequent clinical manifestation, which often result in more severe pathological outcomes compared to those observed in cases of insulin resistance, including premature appearance of biomarkers of senescence. Unfortunately, molecular mechanisms of hypoglycemia remain unclear and the subject of much debate. In this review, the molecular basis of the aging vasculature (endothelium) and how glycemic flux drives the appearance of cardiovascular lesions and injury are discussed. Further, we review the potential role of the serum response factor (SRF) in driving glycemic flux-related cellular signaling through its association with various proteins.

Indexed as

agingglucosehearthypoglycemiaserum response factorvascular

Identifiers

PMID34067715
PMCPMC8156687
OpenAlexW3163789588

What Socratic 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 Socratic graph.