Evidence map›Paper›PMID 32187205›Full record

ArticlePloS one2020

Frailty, markers of immune activation and oxidative stress in HIV infected elderly.

Susana Álvarez, Fátima Brañas, Matilde Sánchez-Conde, Santiago Moreno, Juan Carlos López-Bernaldo de Quirós, Mª Ángeles Muñoz-Fernández

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
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  12. Host Risk Factors for Tuberculosis.Infectious disorders drug targets · 2025
    Review
  13. Immune aging and infectious diseases.Chinese medical journal · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Effects of immune exhaustion and senescence of innate immunity in autoimmune disorders.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Review
  19. Article
  20. 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 4 institutions in 1 country.

Susana ÁlvarezLaboratorio Inmuno-Biología Molecular (LIBM), Immunology Section, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Fátima BrañasGeriatrics Department, Hospital Universitario Infanta Leonor, Madrid, Spain.
Matilde Sánchez-CondeInfectious Diseases Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Santiago MorenoInfectious Diseases Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Juan Carlos López-Bernaldo de QuirósInstituto de Investigación Sanitaria Gregorio Marañón (IISGM), Madrid, Spain.
Mª Ángeles Muñoz-FernándezLaboratorio Inmuno-Biología Molecular (LIBM), Immunology Section, Hospital General Universitario Gregorio Marañón, Madrid, Spain.ORCID 0000-0002-0813-4500
Hospital General Universitario Gregorio Marañón · ESHospital Universitario Infanta Leonor · ESHospital Universitario Ramón y Cajal · ESInstituto Ramón y Cajal de Investigación Sanitaria · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

People living with HIV-1 experience an accelerated aging due to the persistent and chronic activation of the immune system. This phenomenon conduces to immune exhaustion and precipitate immunosenescence. In general, frailty is defined as a syndrome of physiological degeneration in the elderly. Circulating naïve and memory T cells were studied by flow cytometry in non-frail and frail HIV-1-infected groups. Thymopoiesis, cell activation, senescence and cell proliferation were analyzed by CD31, HLA-DR/CD38, CD28/CD57 and Ki-67 expression, respectively. Plasma levels of sCD14 and MDA were measured by ELISA. Frail infected individuals showed a reduced number of memory T cells, both CD4+ and CD8+ populations. Activated CD3+CD4+HLA-DR+ T cells were lower in frail individuals, and directly correlated with CD3+CD8+HLA-DR+ and CD8M cells. Senescent CD8+CD28-CD57+ cells were reduced in frail HIV-1 infected individuals and inversely correlated with CD8RTE, CD8N and CD3+CD4+HLA-DR+. Higher plasma levels of sCD14 and MDA were found in HIV-1 infected frail individuals. Our data show association among frailty, markers of immune activation and oxidative stress. Understanding the immune mechanisms underlying frailty status in HIV-1 population is of high relevance not only for the prediction of continuing longevity but also for the identification of potential strategies for the elderly.

Indexed as

ImmunosenescenceAgedAgingBiomarkersCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell SeparationCross-Sectional StudiesEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryFrailtyGeriatric AssessmentHIV-1HIV InfectionsHumansBiomarkers

Identifiers

PMID32187205
PMCPMC7080240
OpenAlexW3011328744

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.