Evidence map›Paper›PMID 29912900›Full record

ArticlePloS one2018

HLA Class III: A susceptibility region to systemic lupus erythematosus in Tunisian population.

Hend Hachicha, Nadia Mahfoudh, Hajer Fourati, Nesrine Elloumi, Sameh Marzouk, Sawsan Feki, Raouia Fakhfakh, Faten Frikha, Abir Ayadi, Amira Maatoug and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

16 authors at 3 institutions in 1 country.

Hend HachichaImmunology Department, Habib Bourguiba University Hospital, Sfax, Tunisia.ORCID 0000-0002-5819-2899
Nadia MahfoudhHistocompatibility Department, Hedi Chaker University Hospital, Sfax, Tunisia.
Hajer FouratiUR12SP14, Habib Bourguiba University Hospital, Sfax, Tunisia.
Nesrine ElloumiUR12SP14, Habib Bourguiba University Hospital, Sfax, Tunisia.
Sameh MarzoukInternal Medicine Department, Hedi Chaker University Hospital of Sfax, Sfax, Tunisia.
Sawsan FekiImmunology Department, Habib Bourguiba University Hospital, Sfax, Tunisia.
Raouia FakhfakhUR12SP14, Habib Bourguiba University Hospital, Sfax, Tunisia.
Faten FrikhaInternal Medicine Department, Hedi Chaker University Hospital of Sfax, Sfax, Tunisia.
Abir AyadiUR12SP14, Habib Bourguiba University Hospital, Sfax, Tunisia.
Amira MaatougUR12SP14, Habib Bourguiba University Hospital, Sfax, Tunisia.
Lilia GaddourHistocompatibility Department, Hedi Chaker University Hospital, Sfax, Tunisia.
Feiza HakimHistocompatibility Department, Hedi Chaker University Hospital, Sfax, Tunisia.
Zouheir BahloulInternal Medicine Department, Hedi Chaker University Hospital of Sfax, Sfax, Tunisia.
Hafedh MakniHistocompatibility Department, Hedi Chaker University Hospital, Sfax, Tunisia.
Hatem MasmoudiImmunology Department, Habib Bourguiba University Hospital, Sfax, Tunisia.
Arwa KammounHistocompatibility Department, Hedi Chaker University Hospital, Sfax, Tunisia.
Hopital Universitaire Hedi Chaker · TNHopital Universitaire Habib Bourguiba · TNUniversity of Sfax · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesShort tandem repeats (STR) are usually used as informative polymorphic markers for genetic mapping and for disease susceptibility analysis. The involvement of these microsatellite markers localized in the MHC region was reported in many auto-immune diseases. In this study we analyzed for the first time eight polymorphisms of microsatellite loci at the HLA region: D6S291, D6S273, TNFa, b and c, MICA, D6S265 and D6S276, in Tunisian systemic lupus erythematosus (SLE) patients. MATERIALS AND

methodsWe performed a case control study in which the microsatellite loci were amplified using specific primers labeled with NED, VIC, PET or 6-FAM and analyzed using GeneScan software 3.7. For the statistical analysis, we used SPSS software and we performed a sub-haplotype scoring test using the haplo.stats software developed in the R language.

resultsWe found that two mean associated regions existed; the most statistically significant encompassed the 3 TNF markers (p = 0.0003, OR = 19.34); the latter covered the DR region. In fact, when scoring haplotypes in 3 marker- sliding windows, the p value increased as we moved away from the TNF region and decreased again when we approached the DRB1 locus. We also established for the first time the negative association between alleles of D6S291 and SLE. The majority of clinical and serological correlations were noted with TNF alleles.

conclusionOur results confirm the association between TNF and DRB1 polymorphisms and SLE. The association between alleles of D6S291 and SLE needs however to be verified by the analysis of other markers beyond this region.

Indexed as

AdolescentAdultAgedAged, 80 and overAllelesCase-Control StudiesFemaleGenetic Predisposition to DiseaseHLA AntigensHumansLupus Erythematosus, SystemicMaleMicrosatellite RepeatsMiddle AgedPolymorphism, GeneticTunisiaHLA Antigens

Identifiers

PMID29912900
PMCPMC6005577
OpenAlexW2809139942

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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.