Evidence map›Paper›PMID 3501348›Full record

ArticleClinical and experimental immunology1987

Family study of the major histocompatibility complex in HLA DR3 negative patients with systemic lupus erythematosus.

J R Batchelor, A H Fielder, M J Walport, J David, D K Lord, N Davey, I A Dodi, P Malasit, W Wanachiwanawin, R Bernstein

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 1987. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Genetic bases of autoimmune hepatitis.Digestive diseases and sciences · 2002
    Review
  6. Article
  7. Article
  8. Article
  9. Complement and glomerulonephritis--an update.Pediatric nephrology (Berlin, Germany) · 1993
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

10 authors at 1 institution in 1 country.

J R BatchelorDepartment of Immunology, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.
A H Fielder
M J Walport
J David
D K Lord
N Davey
I A Dodi
P Malasit
W Wanachiwanawin
R Bernstein
Hammersmith Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Susceptibility to systemic lupus erythematosus (SLE) is known to be governed by genes in the HLA region of the 6th chromosome. From previous studies it has not been possible to distinguish between the effects of null genes for the complement component C4 and HLA-DR3, because of the marked linkage disequilibrium between DR3 and a null allele of C4A (C4A QO) in caucasoid populations. We report here an immunogenetic study of 44 cases of SLE, selected because they were DR3 negative. Eighteen of the 30 Caucasoid cases (60%) had extended HLA haplotypes with a C4 null allele, compared with 22 of 60 (37%) of a control panel of 60 DR3 negative normal Caucasoid subjects. This difference is significant (chi 2 = 4.41; 0.05 greater than P greater than 0.01). Of 14 non-caucasoid patients analysed, 10 had a C4 null allele. It is concluded that the null alleles of the C4 A and B genes are themselves directly responsible for conferring susceptibility to SLE.

Indexed as

Major Histocompatibility ComplexAllelesDisease SusceptibilityHaplotypesHLA-D AntigensHLA-DR3 AntigenHLA-DR AntigensHumansLupus Erythematosus, SystemicWhite PeopleHLA-D AntigensHLA-DR3 AntigenHLA-DR Antigens

Identifiers

PMID3501348
PMCPMC1542102
OpenAlexW216931163

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.