Evidence map›Paper›PMID 27651918›Full record

ReviewLupus science & medicine2016

I too, am America: a review of research on systemic lupus erythematosus in African-Americans.

Edith M Williams, Larisa Bruner, Alyssa Adkins, Caroline Vrana, Ayaba Logan, Diane Kamen, James C Oates

Abstract readReview
In one paragraph

Review in Lupus science & medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–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

30 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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.

Edith M WilliamsDivision of Rheumatology, Department of Public Health Sciences, Medicine, MUSC Center for Health Disparities Research, Medical University of South Carolina , Charleston, South Carolina , USA.
Larisa BrunerArnold School of Public Health, University of South Carolina , Columbia, South Carolina , USA.
Alyssa AdkinsUniversity of South Carolina , Columbia, South Carolina , USA.
Caroline VranaDepartment of Public Health Sciences , Medical University of South Carolina , Charleston, South Carolina , USA.
Ayaba LoganThe Department of Public Health and Programs in Nurse Anesthesia , Liaison for College of Nursing, Medical University of South Carolina Library , Charleston, South Carolina , USA.
Diane KamenDepartment of Rheumatology and Immunology , Medical University of South Carolina , Charleston, South Carolina , USA.
James C OatesDepartment of Medicine, Division of Rheumatology, Medical University of South Carolina , Charleston, South Carolina , USA.

Funding

Intervention to Improve Quality of Life for African-American Lupus Patients (IQAN)K01AR060026 · NIAMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI WILLIAMS, EDITH MARIE · 2012 to 2015
$448k
NIAMS NIH HHS K01 AR060026
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is a multi-organ autoimmune disorder that can cause significant morbidity and mortality. A large body of evidence has shown that African-Americans experience the disease more severely than other racial-ethnic groups. Relevant literature for the years 2000 to August 2015 were obtained from systematic searches of PubMed, Scopus, and the EBSCOHost platform that includes MEDLINE, CINAHL, etc. to evaluate research focused on SLE in African-Americans. Thirty-six of the 1502 articles were classified according to their level of evidence. The systematic review of the literature reported a wide range of adverse outcomes in African-American SLE patients and risk factors observed in other mono and multi-ethnic investigations. Studies limited to African-Americans with SLE identified novel methods for more precise ascertainment of risk and observed novel findings that hadn't been previously reported in African-Americans with SLE. Both environmental and genetic studies included in this review have highlighted unique African-American populations in an attempt to isolate risk attributable to African ancestry and observed increased genetic influence on overall disease in this cohort. The review also revealed emerging research in areas of quality of life, race-tailored interventions, and self-management. This review reemphasizes the importance of additional studies to better elucidate the natural history of SLE in African-Americans and optimize therapeutic strategies for those who are identified as being at high risk.

Indexed as

Autoimmune DiseasesEpidemiologySystemic Lupus Erythematosus

Identifiers

PMID27651918
PMCPMC5013381

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.