Evidence map›Paper›PMID 21378287›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2011

Identification and molecular analysis of glycosaminoglycans in cutaneous lupus erythematosus and dermatomyositis.

Laura M Chang, Prateesh Maheshwari, Sheila Werth, Lana Schaffer, Steven R Head, Carrie Kovarik, Victoria P Werth

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Cutaneous mucinosis of infancy: a rare case of joint involvement.Pediatric rheumatology online journal · 2021
    Article
  5. Article
  6. Article
  7. Pathophysiology of cutaneous lupus erythematosus.Arthritis research & therapy · 2015
    Review
  8. Article
  9. Article
  10. Identification of specific chondroitin sulfate species in cutaneous autoimmune disease.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2011
    Article
  11. Article
  12. 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

7 authors at 3 institutions in 1 country.

Laura M ChangPhiladelphia VA Medical Center, Philadelphia, Pennsylvania, USA.
Prateesh Maheshwari
Sheila Werth
Lana Schaffer
Steven R Head
Carrie Kovarik
Victoria P Werth
University of Pennsylvania · USJoint Center for Structural Genomics · USPhiladelphia VA Medical Center · US

Funding

Structural Basis of Immune Recognition of Glycosylated AntigensU54GM062116 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SASISEKHARAN, RAM · 2001 to 2010
$80.3M
Penn Dermatology Research Training ProgramT32AR007465 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Elizabeth Anne Grice, David Joel Margolis · 1986 to 2026
$9.0M
PATIENT-ORIENTED RESEARCH IN SKIN AUTOMMUNE DISEASEK24AR002207 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI WERTH, VICTORIA P · 2001 to 2012
$1.3M
NIAMS NIH HHS K24 AR002207NIAMS NIH HHS K24-AR 02207NIAMS NIH HHS T32 AR007465NIAMS NIH HHS T32-AR007465-25NIGMS NIH HHS GM-62116NIGMS NIH HHS U54 GM062116
6 · The paper itself

Abstract

Glycosaminoglycans (GAGs), also known histologically as dermal mucin, accumulate in several inflammatory skin conditions. Because different GAG species have distinct immunologic effects, the authors examined two GAGs, hyaluronan (HA) and chondroitin sulfate (CS), using specific stains in cutaneous lupus erythematosus (CLE) and dermatomyositis (DM). In the dermis of one CLE subtype, tumid LE (TLE), they found only increased HA, but both HA and CS were significantly elevated in another CLE subtype, discoid LE (DLE). DM lesional dermis accumulated mainly CS but not HA. The authors then used glycomic gene expression microarrays to assess the expression of HA- and CS-related genes in CLE skin. Real-time quantitative PCR confirmed significantly increased expression of HAS2, CHSY1, and C4ST1 in the combined groups of CLE lesions (n = 8) compared to healthy controls (n = 4). Thus, the increase in HA in CLE presumably results from upregulation of HAS2, whereas CHSY1 and C4ST1 appear to contribute to increased CS. Based on their known immunomodulatory effects in other systems, HA and CS may thus participate in the pathophysiology of these inflammatory skin conditions.

Indexed as

Case-Control StudiesCD3 ComplexChondroitin SulfatesDermatomyositisDermisHumansHyaluronic AcidLupus Erythematosus, CutaneousOligonucleotide Array Sequence AnalysisReverse Transcriptase Polymerase Chain ReactionT-LymphocytesCD3 ComplexChondroitin SulfatesHyaluronic Acid

Identifiers

PMID21378287
PMCPMC3201158
OpenAlexW2055396296

What OpenQuestion holds

Textmetadata
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.