Evidence map›Paper›PMID 31411331›Full record

ArticleRheumatology (Oxford, England)2020

Sudanese and Swedish patients with systemic lupus erythematosus: immunological and clinical comparisons.

Sahwa Elbagir, Amir I Elshafie, Elnour M Elagib, NasrEldeen A Mohammed, Mawahib I E Aledrissy, Azita Sohrabian, Musa A M Nur, Elisabet Svenungsson, Iva Gunnarsson, Johan Rönnelid

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Rheumatology (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

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  9. Rheumatic diseases in Africa.Nature reviews. Rheumatology · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Sahwa ElbagirDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Amir I ElshafieDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Elnour M ElagibRheumatology Unit, Military Hospital, Omdurman, Sudan.
NasrEldeen A MohammedFaculty of Medical Laboratory Sciences, Al Neelain University, Khartoum, Sudan.
Mawahib I E AledrissyRheumatology Unit, Alribat University Hospital, Khartoum, Sudan.
Azita SohrabianDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Musa A M NurRheumatology Unit, Alribat University Hospital, Khartoum, Sudan.
Elisabet SvenungssonDivision of Rheumatology, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Iva GunnarssonDivision of Rheumatology, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Johan RönnelidDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Uppsala University · SEKarolinska University Hospital · SEAl-Neelain University · SD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSLE is known to have an aggressive phenotype in black populations, but data from African cohorts are largely lacking. We therefore compared immunological and clinical profiles between Sudanese and Swedish patients using similar tools.

methodsConsecutive SLE patients from Sudan (n = 115) and Sweden (n = 340) and from 106 Sudanese and 318 Swedish age- and sex-matched controls were included. All patients fulfilled the 1982 ACR classification criteria for SLE. Ten ANA-associated specificities and C1q-binding immune complexes (CICs) were measured. Cut-offs were established based on Sudanese and Swedish controls, respectively. Disease activity was measured with a modified SLEDAI and organ damage with the SLICC Damage Index. In a nested case-control design, Swedish and Sudanese patients were matched for age and disease duration.

resultsFemales constituted 95.6% and 88.1% of Sudanese and Swedish patients, respectively (P = 0.02), with younger age at inclusion (33 vs 47.7 years; P < 0.0001) and shorter disease duration (5 vs 14 years; P < 0.0001) among Sudanese patients. Anti-Sm antibodies were more frequent in Sudanese patients, whereas anti-dsDNA, anti-histone and CICs were higher in Swedish patients. In the matched analyses, there was a trend for higher SLEDAI among Swedes. However, Sudanese patients had more damage, solely attributed to high frequencies of cranial/peripheral neuropathy and diabetes.

conclusionWhile anti-Sm is more common in Sudan than in Sweden, the opposite is found for anti-dsDNA. Sudanese patients had higher damage scores, mainly because of neuropathy and diabetes. Sudanese patients were younger, with a shorter SLE duration, possibly indicating a more severe disease course with impact on survival rates.

Indexed as

AdultAgedAge FactorsAntibodies, AntinuclearAutoantibodiesBlack PeopleCase-Control StudiesChi-Square DistributionCross-Sectional StudiesFemaleGenetic Predisposition to DiseaseHumansLupus Erythematosus, SystemicMaleMiddle AgedPrevalenceAntibodies, AntinuclearAutoantibodiesAfricaautoantibodiescomparative studySudanSwedensystemic lupus erythematosus

Identifiers

PMID31411331
PMCPMC7188463
OpenAlexW2968433005

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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.