Evidence map›Paper›PMID 22674006›Full record

ReviewNature medicine2012

Taming lupus-a new understanding of pathogenesis is leading to clinical advances.

Zheng Liu, Anne Davidson

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Nature medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04468438 (Role of Estrogen in the Flarring up of Lupus Nepheritis), which is not on this map. Cited by 216 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
216citing papers in PubMed, 1 pooled it
29.2field-weighted citation impact, top 1% 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.

NCT04468438 unknown statusnot on this mapstarted 2020, after this paper: background citation

Role of Estrogen in the Flarring up of Lupus Nepheritis

TypeobservationalSponsorAssiut UniversityRan2020 to 2021Enrolled100ConditionsActivity of Lupus NepheritisArmsserum estrogen and urinary albumin creatinine ratio
3 · Its place in the literature

Who cites it

216 citing papers in PubMed, 1 synthesis or guideline pooled it, 422 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Aberrant METTL1-mediated tRNA mNature communications · 2024
    Article
  17. Review
  18. Review
  19. Biomarkers for systemic lupus erythematosus: A scoping review.Immunity, inflammation and disease · 2024
    Article
  20. Skin Aging and the Upcoming Role of Ferroptosis in Geroscience.International journal of molecular sciences · 2024
    Review

156 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Zheng LiuCenter for Autoimmunity and Musculoskeletal Diseases, Feinstein Institute for Medical Research, Manhasset, New York, USA.
Anne Davidson
Feinstein Institute for Medical Research · US

Funding

Targeting renal inflammatory pathways of SLE nephritis in mouse and manR01DK085241 · NIDDK · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI DAVIDSON, ANNE · 2010 to 2013
$2.2M
Regulation of the anti-phospholipid response in SLER01AI083901 · NIAID · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI DAVIDSON, ANNE · 2010 to 2014
$2.2M
Functional significance of an ITGAM polymorphism in SLER21AR057930 · NIAMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI DAVIDSON, ANNE · 2010 to 2011
$402k
NIAID NIH HHS R01 AI083901NIAMS NIH HHS R21 AR057930NIDDK NIH HHS R01 DK085241NIDDK NIH HHS R01 DK085241-01
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is an autoimmune disease that is characterized by the loss of tolerance to nuclear self antigens, the production of pathogenic autoantibodies and damage to multiple organ systems. Over the years, patients with SLE have been managed largely with empiric immunosuppressive therapies, which are associated with substantial toxicities and do not always provide adequate control of the disease. The development of targeted therapies that specifically address disease pathogenesis or progression has lagged, largely because of the complex and heterogeneous nature of the disease, as well as difficulties in designing uniform outcome measures for clinical trials. Recent advances that could improve the treatment of SLE include the identification of genetic variations that influence the risk of developing the disease, an enhanced understanding of innate and adaptive immune activation and regulation of tolerance, dissection of immune cell activation and inflammatory pathways and elucidation of mechanisms and markers of tissue damage. These discoveries, together with improvements in clinical trial design, form a platform from which to launch the development of a new generation of lupus therapies.

Indexed as

Adaptive ImmunityBlood-Brain BarrierFemaleGenetic Predisposition to DiseaseHumansImmunity, InnateLupus Erythematosus, SystemicMaleSex CharacteristicsToll-Like ReceptorsToll-Like Receptors

Identifiers

PMID22674006
PMCPMC3607103
OpenAlexW1978259263

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.