Evidence map›Paper›PMID 33821395›Full record

ReviewInflammation2021

Understanding Accelerated Atherosclerosis in Systemic Lupus Erythematosus: Toward Better Treatment and Prevention.

Allison B Reiss, Benna Jacob, Saba Ahmed, Steven E Carsons, Joshua DeLeon

Abstract readReview
PubMed Publisher
In one paragraph

Review in Inflammation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  13. Biologics : targets & therapy · 2024
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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.

Allison B ReissDepartment of Medicine and Biomedical Research Institute, NYU Long Island School of Medicine, 101 Mineola Boulevard, Mineola, NY, 11501, USA. Allison.Reiss@NYULangone.org.ORCID http://orcid.org/0000-0002-4478-2441
Benna JacobDepartment of Medicine and Biomedical Research Institute, NYU Long Island School of Medicine, 101 Mineola Boulevard, Mineola, NY, 11501, USA.
Saba AhmedDepartment of Medicine and Biomedical Research Institute, NYU Long Island School of Medicine, 101 Mineola Boulevard, Mineola, NY, 11501, USA.
Steven E CarsonsDepartment of Medicine and Biomedical Research Institute, NYU Long Island School of Medicine, 101 Mineola Boulevard, Mineola, NY, 11501, USA.
Joshua DeLeonDepartment of Medicine and Biomedical Research Institute, NYU Long Island School of Medicine, 101 Mineola Boulevard, Mineola, NY, 11501, USA.
Biomedical Research Institute · USNew York College of Traditional Chinese Medicine · US

Funding

CSRD VA 1
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) carries a significant risk of cardiovascular disease (CVD). The prevalence of premature CVD is especially noteworthy because it occurs in premenopausal women with SLE who would otherwise have very low rates of CVD. While traditional risk factors likely play a role in development of CVD in the setting of SLE, they do not fully explain the excess risk. The pathogenesis of CVD in SLE is not fully understood, but the inflammatory nature of SLE is believed to be a key factor in accelerating atherosclerosis. Systemic inflammation may lead to an abnormal lipid profile with elevated triglycerides, total cholesterol, and low-density lipoprotein cholesterol and dysfunctional high-density lipoprotein cholesterol. Additionally, the inflammatory milieu of SLE plasma promotes endothelial dysfunction and vascular injury, early steps in the progression of atherosclerotic CVD. Despite the overall headway that has been achieved in treating lupus, innovative therapeutics specifically targeting the progression of atherosclerosis within the lupus population are currently lacking. However, there have been advancements in the development of promising modalities for diagnosis of subclinical atherosclerosis and detection of high CVD risk patients. Due to the significant impact of CVD on morbidity and mortality, research addressing prevention and treatment of CVD in SLE needs to be prioritized. This review explores the intricate interplay of SLE-specific properties that contribute to atherosclerosis and CVD within this population, as well as screening methods and possible therapies.

Indexed as

Adrenal Cortex HormonesAtherosclerosisAutoantibodiesBiomarkersCardiovascular DiseasesCell- and Tissue-Based TherapyHumansHydroxymethylglutaryl-CoA Reductase InhibitorsInflammation MediatorsLupus Erythematosus, SystemicRisk FactorsSex FactorsAdrenal Cortex HormonesAutoantibodiesBiomarkersHydroxymethylglutaryl-CoA Reductase InhibitorsInflammation Mediatorsatherosclerosiscardiovascular diseasehyperlipidemiainflammationrisk factorssystemic lupus erythematosus

Identifiers

PMID33821395
OpenAlexW3140249128

What OpenQuestion holds

Texttitle and abstract
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.