Evidence map›Paper›PMID 19591781›Full record

ReviewBest practice & research. Clinical rheumatology2009

The search for lupus biomarkers.

Chau-Ching Liu, Joseph M Ahearn

Abstract readReview
In one paragraph

Review in Best practice & research. Clinical rheumatology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

46 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Platelet distribution width as a novel indicator of disease activity in systemic lupus erythematosus.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Multivariate strategy for the sample selection and integration of multi-batch data in metabolomics.Metabolomics : Official journal of the Metabolomic Society · 2017
    Article
  20. Serum TWEAK as a biomarker for disease activity of systemic lupus erythematosus.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2016
    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

2 authors.

Chau-Ching LiuLupus Center of Excellence, University of Pittsburgh Schools of Health Sciences, 3500 Terrace Street, Pittsburgh, PA 15261, USA. liu5@pitt.edu
Joseph M Ahearn

Funding

Erythrocytes as Time Capsules of Disease Activity in Systemic Lupus ErythematosusR01HL074335 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI AHEARN, JOSEPH M. · 2003 to 2007
$1.5M
Lymphocyte-Bound Complement Activation Products: Clues to SLE PathogenesisR01AI077591 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LIU, CHAU-CHING · 2008 to 2011
$1.2M
NHLBI NIH HHS R01 HL074335NIAID NIH HHS R01 AI077591
6 · The paper itself

Abstract

Few biomarkers for systemic lupus erythematosus (SLE) have been validated and employed for making clinical decisions. The lack of reliable, specific biomarkers for SLE hampers the proper clinical management of patients with SLE and impedes the development of new lupus therapeutics. This void has led to renewed enthusiasm for identifying biomarkers that precisely and specifically reflect the pathophysiological and clinical changes of SLE. Several laboratory markers have shown early promise as biomarkers for lupus susceptibility, diagnosis and monitoring. These include polymorphisms and copy-number variations of complement C4 and Fcgamma receptor genes (disease susceptibility), cell-bound complement C4d (diagnosis and/or disease activity), CD27(high) plasma cells (disease activity), 'interferon signature' (disease activity) and anti-C1q and anti-NMDA (disease activity and organ involvement). Although these and other promising candidate biomarkers have been identified, they still need to be validated through rigorous, large-scale multicentre studies. This article briefly reviews the historical aspects of lupus biomarkers and summarises current efforts to advance the field.

Indexed as

Genetic Predisposition to DiseaseBiomarkersHumansLupus Erythematosus, SystemicPolymorphism, Single NucleotideSeverity of Illness IndexBiomarkers

Identifiers

PMID19591781
PMCPMC2727983

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.