Evidence map›Paper›PMID 24336757›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2014

Lipoprotein-associated phospholipase A2, a novel cardiovascular inflammatory marker, in HIV-infected patients.

Alexandra Mangili, Raabia Ahmad, Robert L Wolfert, Jeffrey Kuvin, Joseph F Polak, Richard H Karas, Christine A Wanke

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
3.2field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Alexandra MangiliNutrition Infection Unit, Tufts University School of Medicine.
Raabia Ahmad
Robert L Wolfert
Jeffrey Kuvin
Joseph F Polak
Richard H Karas
Christine A Wanke
Tufts University · USDiazyme (United States) · USTufts Medical Center · US

Funding

PROTEASE INHIBITOR RELATED DYSLIPIDEMIAR01HL065947 · NHLBI · TUFTS UNIVERSITY BOSTON · PI WANKE, CHRISTINE A · 2000 to 2011
$5.5M
Genetic Analysis of HIV ComplicationsK23AI071872 · NIAID · TUFTS MEDICAL CENTER · PI MANGILI, ALEXANDRA · 2006 to 2010
$613k
NHLBI NIH HHS R01 HL065947NHLBI NIH HHS R01HL065947NIAID NIH HHS K23 AI071872
6 · The paper itself

Abstract

backgroundLipoprotein-associated phospholipase A2 (Lp-PLA2) is an emerging biomarker of cardiovascular disease. This study was conducted to describe the distribution of Lp-PLA2 in a cohort of human immunodeficiency virus (HIV)-infected adults and to determine associations between Lp-PLA2, cardiometabolic risk factors, and subclinical atherosclerosis in this population.

methodsLp-PLA2 was assessed in 341 (25% women, 52% white, 74% on highly active antiretroviral therapy [HAART]) participants of a cohort with detailed characterization of atherogenic risk factors, including surrogate markers of carotid and coronary atherosclerosis.

resultsMean Lp-PLA2 mass was 313 ± 105 ng/mL and activity 173 ± 49 nmol/minute/mL. Seventy-five percent of participants had abnormal Lp-PLA2. Those in the highest Framingham Risk Score tertile had significantly higher Lp-PLA2 activity. Participants with abnormal carotid intima-media thickness (cIMT) had higher Lp-PLA2 mass and activity. Those with coronary artery calcium (CAC) scores >100 had significantly higher Lp-PLA2 mass than those with lower or nondetectable calcium. Those on HAART and protease inhibitor (PI)-based treatment had significantly higher Lp-PLA2 mass and activity than those who were treatment-naive or not on PIs. In multivariate regression, HAART and PI use were positively associated with Lp-PLA2 activity and mass after adjusting for age, race, sex, low-density and high-density lipoprotein cholesterol levels, triglyceride level, and smoking. Adding Lp-PLA2 activity tertiles to the model improved the predictive value for abnormal common cIMT, but not internal cIMT or CAC score.

conclusionsLp-PLA2 is highly abnormal in HIV-infected patients and is associated with several cardiovascular and HIV treatment-specific risk factors. Lp-PLA2 may be used as an additional and more vascular specific biomarker for cardiovascular risk stratification in HIV-positive patients.

Indexed as

1-Alkyl-2-acetylglycerophosphocholine EsteraseAdultAntiretroviral Therapy, Highly ActiveBiomarkersCarotid Artery DiseasesCarotid Intima-Media ThicknessCohort StudiesCoronary Artery DiseaseC-Reactive ProteinFemaleHIV InfectionsHumansMaleMiddle Aged1-Alkyl-2-acetylglycerophosphocholine EsteraseBiomarkersC-Reactive ProteinPLA2G7 protein, humanatherosclerosiscardiovascularHIVinflammationLpPLA2

Identifiers

PMID24336757
PMCPMC3935500
OpenAlexW2153777696

What OpenQuestion holds

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Registered trials

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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.