Evidence map›Paper›PMID 32998388›Full record

ReviewInternational journal of molecular sciences2020

New Insights for BPIFB4 in Cardiovascular Therapy.

Marta Dossena, Anna Ferrario, Valentina Lopardo, Elena Ciaglia, Annibale Alessandro Puca

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. BPIFB4 Circulating Levels and Its Prognostic Relevance in COVID-19.The journals of gerontology. Series A, Biological sciences and medical sciences · 2021
    Article
  5. Article
  6. Adaptive Immune Responses in Human Atherosclerosis.International journal of molecular sciences · 2020
    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

5 authors at 2 institutions in 1 country.

Marta DossenaCardiovascular Research Unit, IRCCS MultiMedica, 20138 Milan, Italy.
Anna FerrarioCardiovascular Research Unit, IRCCS MultiMedica, 20138 Milan, Italy.
Valentina LopardoDepartment of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Via Salvatore Allende, 84081 Baronissi, Italy.
Elena CiagliaDepartment of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Via Salvatore Allende, 84081 Baronissi, Italy.
Annibale Alessandro PucaCardiovascular Research Unit, IRCCS MultiMedica, 20138 Milan, Italy.ORCID 0000-0002-0347-1460
University of Salerno · ITMultiMedica · IT

Funding

Fondazione Umberto Veronesi FUV 2019 cod.2198Italian Ministry of Health Ricerca Finalizzata RF-2016-02364864
6 · The paper itself

Abstract

Aging is the most relevant risk factor for cardiovascular diseases which are the main cause of mortality in industrialized countries. In this context, there is a progressive loss of cardiovascular homeostasis that translates in illness and death. The study of long living individuals (LLIs), which show compression of morbidity toward the end of their life, is a valuable approach to find the key to delay aging and postpone associate cardiovascular events. A contribution to the age-related decline of cardiovascular system (CVS) comes from the immune system; indeed, it is dysfunctional during aging, a process described as immunosenescence and comprises the combination of several processes overpowering both innate and adaptative immune system. We have recently discovered a longevity-associated variant (LAV) in bactericidal/permeability-increasing fold-containing family B member 4 (BPIFB4), which is a secreted protein able to enhance endothelial function through endothelial nitric oxide synthase (eNOS) activation and capable to protect from hypertension, atherosclerosis, diabetic cardiopathy, frailty, and inflammaging. Here, we sum up the state of the art of the mechanisms involved in the main pathological processes related to CVD (atherosclerosis, aging, diabetic cardiopathy, and frailty) and shed light on the therapeutic effects of LAV-BPIFB4 in these contexts.

Indexed as

Adaptive ImmunityAge FactorsAnimalsAtherosclerosisDiabetic CardiomyopathiesFrailtyGene Expression Regulation, DevelopmentalGenetic TherapyHumansHypertensionImmunity, InnateImmunosenescenceIntercellular Signaling Peptides and ProteinsLongevityMiceNitric Oxide Synthase Type IIIBPIFB4 protein, humanIntercellular Signaling Peptides and ProteinsNitric Oxide Synthase Type IIINOS3 protein, humanPhosphoproteinsProtein IsoformsagingBPIFB4cardiovascular disease

Identifiers

PMID32998388
PMCPMC7583974
OpenAlexW3088324448

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.