Evidence map›Paper›PMID 36644561›Full record

ArticleAtherosclerosis plus2022

Atherosclerosis severity in patients with familial hypercholesterolemia: The role of T and B lymphocytes.

Waleria T Fonzar, Francisco A Fonseca, Henrique A Fonseca, Tuany P Silva, Alfredo A Rodrigues, Daniela Teixeira, Mayari E Ishimura, Maria E Coste, Carolina N França, Henrique T Bianco and 8 more

Open access · goldAbstract read
In one paragraph

Article in Atherosclerosis plus, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. 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

18 authors at 4 institutions in 1 country.

Waleria T FonzarDepartment of Medicine, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Francisco A FonsecaDepartment of Medicine, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Henrique A FonsecaDepartment of Medicine, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Tuany P SilvaDepartment of Medicine, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Alfredo A RodriguesDepartment of Medicine, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Daniela TeixeiraDepartment of Microbiology, Immunology and Parasitology, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Mayari E IshimuraDepartment of Microbiology, Immunology and Parasitology, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Maria E CosteDepartment of Medicine, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Carolina N FrançaDepartment of Medicine, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Henrique T BiancoDepartment of Medicine, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Magnus GidlundDepartment of Immunology, Universidade de São Paulo, São Paulo, SP, Brazil.
Rafael L MoraisDepartment of Biophysics, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Clarissa A BittencourtDepartment of Biophysics, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Carlos A FonzarDepartment of Medicine, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Viviane A Sant'AnnaDepartment of Medicine, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Ieda L MaugeriDepartment of Microbiology, Immunology and Parasitology, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Joao B PesqueroDepartment of Biophysics, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Maria C IzarDepartment of Medicine, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Universidade Federal de São Paulo · BRHospital Israelita Albert Einstein · BRUniversidade de Santo Amaro · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aims: Familial hypercholesterolemia (FH) is characterized by lifelong exposure to high LDL-c concentrations and premature atherosclerotic cardiovascular disease; nevertheless, disease severity can be heterogeneous.We aimed at evaluating if the immune-inflammatory system could modulate atherosclerosis burden in FH. Methods: From a cohort of subjects with confirmed FH (Dutch Lipid Clinic Network and genotype), 92 patients receiving high-intensity lipid-lowering therapy (statin ± ezetimibe) were included. The extension and severity of coronary atherosclerosis was assessed by standardized reporting systems (CAD-RADS) for coronary computed tomography angiography (CCTA) and coronary artery calcium (CAC) scores. Lipids, apolipoproteins, Results: In univariate analysis CAC correlated with age, systolic blood pressure, TCD4+ cells, and titers of IgM Conclusions: In subjects with FH, under high-intensity lipid-lowering therapy, age and CD4+T cells were associated to atherosclerosis burden.

Indexed as

Apolipoprotein B-D peptideCD4+T cellsCoronary computed tomography angiographyFamilial hypercholesterolemiaImmune system

Identifiers

PMID36644561
PMCPMC9833267
OpenAlexW4220701628

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.