Evidence map›Paper›PMID 26834214›Full record

ArticleThe Journal of rheumatology2016

Longitudinal Evaluation of Lipoprotein Variables in Systemic Lupus Erythematosus Reveals Adverse Changes with Disease Activity and Prednisone and More Favorable Profiles with Hydroxychloroquine Therapy.

Laura Durcan, Deborah A Winegar, Margery A Connelly, James D Otvos, Laurence S Magder, Michelle Petri

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of rheumatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 2 pooled it
9.0field-weighted citation impact, top 2% 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

39 citing papers in PubMed, 2 syntheses or guidelines pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  13. Atherosclerosis in Systemic Lupus Erythematosus.Current atherosclerosis reports · 2023
    Review
  14. Article
  15. Article
  16. Hydroxychloroquine in systemic lupus erythematosus: overview of current knowledge.Therapeutic advances in musculoskeletal disease · 2022
    Review
  17. Review
  18. Article
  19. Article
  20. 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

6 authors at 4 institutions in 1 country.

Laura DurcanFrom the Johns Hopkins University School of Medicine, Baltimore; Department of Epidemiology and Public Health, University of Maryland, College Park, Maryland; LipoScience, Laboratory Corporation of America Holdings, Raleigh, North Carolina, USA.L. Durcan, MD, Johns Hopkins University School of Medicine; D.A. Winegar, PhD, LipoScience, Laboratory Corporation of America Holdings; M.A. Connelly, PhD, MBA, LipoScience, Laboratory Corporation of America Holdings; J.D. Otvos, PhD, LipoScience, Laboratory Corporation of America Holdings; L.S. Magder, MPH, PhD, Department of Epidemiology and Public Health, University of Maryland; M. Petri, MD, MPH, Johns Hopkins University School of Medicine. laurajanedurcan@hotmail.com.
Deborah A WinegarFrom the Johns Hopkins University School of Medicine, Baltimore; Department of Epidemiology and Public Health, University of Maryland, College Park, Maryland; LipoScience, Laboratory Corporation of America Holdings, Raleigh, North Carolina, USA.L. Durcan, MD, Johns Hopkins University School of Medicine; D.A. Winegar, PhD, LipoScience, Laboratory Corporation of America Holdings; M.A. Connelly, PhD, MBA, LipoScience, Laboratory Corporation of America Holdings; J.D. Otvos, PhD, LipoScience, Laboratory Corporation of America Holdings; L.S. Magder, MPH, PhD, Department of Epidemiology and Public Health, University of Maryland; M. Petri, MD, MPH, Johns Hopkins University School of Medicine.
Margery A ConnellyFrom the Johns Hopkins University School of Medicine, Baltimore; Department of Epidemiology and Public Health, University of Maryland, College Park, Maryland; LipoScience, Laboratory Corporation of America Holdings, Raleigh, North Carolina, USA.L. Durcan, MD, Johns Hopkins University School of Medicine; D.A. Winegar, PhD, LipoScience, Laboratory Corporation of America Holdings; M.A. Connelly, PhD, MBA, LipoScience, Laboratory Corporation of America Holdings; J.D. Otvos, PhD, LipoScience, Laboratory Corporation of America Holdings; L.S. Magder, MPH, PhD, Department of Epidemiology and Public Health, University of Maryland; M. Petri, MD, MPH, Johns Hopkins University School of Medicine.
James D OtvosFrom the Johns Hopkins University School of Medicine, Baltimore; Department of Epidemiology and Public Health, University of Maryland, College Park, Maryland; LipoScience, Laboratory Corporation of America Holdings, Raleigh, North Carolina, USA.L. Durcan, MD, Johns Hopkins University School of Medicine; D.A. Winegar, PhD, LipoScience, Laboratory Corporation of America Holdings; M.A. Connelly, PhD, MBA, LipoScience, Laboratory Corporation of America Holdings; J.D. Otvos, PhD, LipoScience, Laboratory Corporation of America Holdings; L.S. Magder, MPH, PhD, Department of Epidemiology and Public Health, University of Maryland; M. Petri, MD, MPH, Johns Hopkins University School of Medicine.
Laurence S MagderFrom the Johns Hopkins University School of Medicine, Baltimore; Department of Epidemiology and Public Health, University of Maryland, College Park, Maryland; LipoScience, Laboratory Corporation of America Holdings, Raleigh, North Carolina, USA.L. Durcan, MD, Johns Hopkins University School of Medicine; D.A. Winegar, PhD, LipoScience, Laboratory Corporation of America Holdings; M.A. Connelly, PhD, MBA, LipoScience, Laboratory Corporation of America Holdings; J.D. Otvos, PhD, LipoScience, Laboratory Corporation of America Holdings; L.S. Magder, MPH, PhD, Department of Epidemiology and Public Health, University of Maryland; M. Petri, MD, MPH, Johns Hopkins University School of Medicine.
Michelle PetriFrom the Johns Hopkins University School of Medicine, Baltimore; Department of Epidemiology and Public Health, University of Maryland, College Park, Maryland; LipoScience, Laboratory Corporation of America Holdings, Raleigh, North Carolina, USA.L. Durcan, MD, Johns Hopkins University School of Medicine; D.A. Winegar, PhD, LipoScience, Laboratory Corporation of America Holdings; M.A. Connelly, PhD, MBA, LipoScience, Laboratory Corporation of America Holdings; J.D. Otvos, PhD, LipoScience, Laboratory Corporation of America Holdings; L.S. Magder, MPH, PhD, Department of Epidemiology and Public Health, University of Maryland; M. Petri, MD, MPH, Johns Hopkins University School of Medicine.
Johns Hopkins Medicine · USJohns Hopkins University · USLabCorp (United States) · USUniversity of Maryland, College Park · US

Funding

Lupus CohortR01AR043727 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI PETRI, MICHELLE A · 1997 to 2015
$8.2M
HOPKINS LUPUS COHORTR55AR043727 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI PETRI, MICHELLE A · 1996 to 1996
–
NIAMS NIH HHS AR 43727NIAMS NIH HHS R01 AR043727
6 · The paper itself

Abstract

objectiveSystemic lupus erythematosus (SLE) is associated with accelerated atherosclerotic cardiovascular disease. Patients with SLE have adverse lipoprotein variables, but little is known about how these change with treatment and disease activity. The nuclear magnetic resonance LipoProfile test contains a glycoprotein signal-termed GlycA, an inflammatory marker, which has not been evaluated in SLE. We assessed patients longitudinally to determine how lipoproteins and GlycA change with active SLE.

methodsSera from selected clinical visits of patients in the Hopkins Lupus Cohort were analyzed for lipoprotein and GlycA levels. Univariate and multivariate analyses were performed to evaluate lipoprotein variables and their relationship to ethnicity, disease activity, prednisone use, and hydroxychloroquine (HCQ) therapy.

resultsFifty-two patients were included over 229 visits. Adverse changes in lipoprotein variables with disease activity were demonstrated. For each point increase in the Systemic Lupus Erythematosus Disease Activity Index, there was a decrease in high-density lipoprotein (HDL) even after adjusting for corticosteroid use. Prednisone was associated with higher very low-density lipoprotein, low-density lipoprotein, HDL, and triglycerides. HCQ was associated with more favorable variables. GlycA levels were higher than in normal populations and increased with disease activity.

conclusionAdverse changes in lipoprotein profiles were associated with SLE activity and prednisone therapy. This gives insight into mechanisms of atherosclerosis in SLE. Favorable lipoprotein variables occurred in those taking HCQ. GlycA increased with disease activity and was higher than in healthy populations.

Indexed as

AdultAntirheumatic AgentsFemaleHumansHydroxychloroquineLipoproteinsLongitudinal StudiesLupus Erythematosus, SystemicMaleMiddle AgedPrednisoneSeverity of Illness IndexAntirheumatic AgentsHydroxychloroquineLipoproteinsPrednisoneDISEASE ACTIVITYDYSLIPIDEMIAGlycAHYDROXYCHLOROQUINENUCLEAR MAGNETIC RESONANCE LIPOPROTEIN PROFILESYSTEMIC LUPUS ERYTHEMATOSUS

Identifiers

PMID26834214
PMCPMC4818734
OpenAlexW2255510115

What OpenQuestion holds

Textmetadata
LicenceTDM
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.