Evidence map›Paper›PMID 31897958›Full record

ArticleClinical rheumatology2020

Systemic lupus erythematosus in the setting of HIV-1 infection: a longitudinal analysis.

Benjamin S Naovarat, John D Reveille, Gloria A Salazar, Francis M Williams, Binh Y Nguyen

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Systemic Lupus Erythematosus Risk: The Role of Environmental Factors.Rheumatic diseases clinics of North America · 2022
    Review
  4. 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

5 authors.

Benjamin S NaovaratDivision of Rheumatology, The University of Texas-McGovern Medical School, 6431 Fannin, MSB 5.270, Houston, TX, 77030, USA.
John D ReveilleDivision of Rheumatology, The University of Texas-McGovern Medical School, 6431 Fannin, MSB 5.270, Houston, TX, 77030, USA. john.d.reveille@uth.tmc.edu.ORCID http://orcid.org/0000-0001-5950-0913
Gloria A SalazarDivision of Rheumatology, The University of Texas-McGovern Medical School, 6431 Fannin, MSB 5.270, Houston, TX, 77030, USA.
Francis M WilliamsDivision of Rheumatology, The University of Texas-McGovern Medical School, 6431 Fannin, MSB 5.270, Houston, TX, 77030, USA.
Binh Y NguyenDivision of Rheumatology, The University of Texas-McGovern Medical School, 6431 Fannin, MSB 5.270, Houston, TX, 77030, USA.

Funding

The Department of Health and Human Services Ryan White Title I Grant 6H12HA000390
6 · The paper itself

Abstract

Patients with concomitant HIV-1 infection and systemic lupus erythematosus (SLE) followed longitudinally at an HIV outpatient clinic from 1994 to 2019 were examined. Patients met 1982 and 1997 ACR classification criteria for SLE at the Thomas Street clinic from 1994 to 2019. Clinical and demographic comparisons were made with a non HIV-SLE patient cohort, the Lupus in Minorities Studies, Nature versus Nurture (LUMINA) study. Twenty-two patients with concomitant HIV-1 infection and SLE were identified, including 18 females, 3 males, and 1 male to female transgender. Overall, 81.8% of SLE-HIV patients were African-American compared to 55.3% of the 5856 patients seen at the HIV clinic from 2016 to 2017 (p = 0.02, OR = 3.6). There were 12 patients that developed HIV-1 in the setting of SLE and 10 patients that developed SLE in the setting HIV-1. This demographic distribution was significant when compared with the 1604 unique patients in the HIV rheumatology clinic from 1994 to 2019 (p = 0.03, OR = 5.9) and also significant when compared with the 5856 patients attending the county HIV clinic overall in 2016-2017 (p = 0.008, OR = 7.2). When comparing with the non-HIV SLE cohort, anti-dsDNA antibodies were noted less frequently in all HIV-SLE patients (p = 0.0002) including all sub-cohorts of our patients. Skin/mucosal involvement (p = 0.0003) and cytopenias (p = 0.0001) occurred less frequently in the patients that were diagnosed with HIV after their SLE diagnosis compared to non-HIV SLE patients. In a large county HIV clinic setting, the prevalence of SLE was significantly higher in African American women. Anti-dsDNA antibodies were less frequent in HIV-1 positive SLE patients.Key Points• This paper presents clinical and laboratory data on the largest cohort of SLE patients with HIV-1 infection reported to date.• The prevalence of SLE in a large outpatient HIV-1 clinic was larger than reported in HIV negative population studies.• The prevalence of SLE was particularly high in black HIV-1 infected women.• Skin/mucosal involvement and anti-ds DNA antibodies were less common in patients with HIV-1 and SLE compared to patients with SLE without SLE>.

Indexed as

AdultAmbulatory CareAntibodies, AntinuclearBlack or African AmericanDNAFemaleHIV-1HIV InfectionsHumansLongitudinal StudiesLupus Erythematosus, SystemicMaleMiddle AgedPrevalenceWhite PeopleAntibodies, AntinuclearDNAHAARTHIV-1LupusOutcome

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Registered trials

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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.