Evidence map›Paper›PMID 38221717›Full record

Observational studyArthritis care & research2024

A Prospective Observational Study of Disease Severity and Mortality in Hispanic American Patients With Systemic Sclerosis.

Bochra Jandali, Marka Lyons, Julio Charles, Meng Zhang, Samuel Theodore, Claudia Pedroza, Maureen D Mayes, Shervin Assassi

Abstract readComparative StudyObservational Study
In one paragraph

Observational study in Arthritis care & research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

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

8 authors.

Bochra JandaliMcGovern Medical School at the University of Texas Health Science Center at Houston.ORCID 0000-0002-2954-6344
Marka LyonsMcGovern Medical School at the University of Texas Health Science Center at Houston.
Julio CharlesMcGovern Medical School at the University of Texas Health Science Center at Houston.
Meng ZhangMcGovern Medical School at the University of Texas Health Science Center at Houston.
Samuel TheodoreMcGovern Medical School at the University of Texas Health Science Center at Houston.
Claudia PedrozaMcGovern Medical School at the University of Texas Health Science Center at Houston.
Maureen D MayesMcGovern Medical School at the University of Texas Health Science Center at Houston.ORCID 0000-0001-5070-2535
Shervin AssassiMcGovern Medical School at the University of Texas Health Science Center at Houston.ORCID 0000-0002-8059-9978

Funding

CFlm25 mediated alternative polyadenylation regulates fibrosis in systemic sclerosisR01AR073284 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ASSASSI, SHERVIN, MILLS, TINGTING WENG · 2019 to 2023
$1.7M
Interferon Regulatory Factor 7 Links Interferon Pathway Activation to the Exaggerates Fibrotic Response in Systemic SclerosisR01AR081280 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Shervin Assassi, Minghua Wu · 2023 to 2026
$1.1M
Role of Interferon Regulatory Factor 7 in Systemic Sclerosis PathogenesisR56AR078211 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ASSASSI, SHERVIN, WU, MINGHUA · 2021 to 2021
$346k
Department of Defense W81XWH-22-1-0162NIAMS NIH HHS R01 AR073284NIAMS NIH HHS R01AR073284NIAMS NIH HHS R01 AR081280NIAMS NIH HHS R01AR081280NIAMS NIH HHS R56 AR078211NIAMS NIH HHS R56AR078211NIH
6 · The paper itself

Abstract

objectiveTo characterize disease manifestations in Hispanic American patients with systemic sclerosis (SSc) in comparison with non-Hispanic White and Black patients.

methodsLongitudinal clinical characteristics were collected prospectively in the Genetics versus Environment in Scleroderma Outcome Study cohort. All patients fulfilled the classification criteria for SSc and had a disease duration less than five years at enrollment.

resultsA cohort of 427 patients, consisting of 124 Hispanic, 220 non-Hispanic White, and 83 non-Hispanic Black participants were examined. At enrollment, Hispanic patients were significantly younger but had longer disease duration, higher frequency of U1-RNP positivity as well as concurrent systemic lupus erythematosus (SLE) diagnosis, and lower income and educational levels in comparison to non-Hispanic White patients. Compared with non-Hispanic Black patients, Hispanic patients had more frequently limited cutaneous involvement and anticentromere antibodies. In the longitudinal analysis, Hispanic patients had significantly lower forced vital capacity percents predicted (point estimate, -9.3%; P < 0.001) than non-Hispanic White but not Black patients. Hispanic patients had similar longitudinal modified Rodnan Skin Scores like non-Hispanic White patients but lower measurements than non-Hispanic Black patients (point estimate, -3.2; P = 0.029). Hispanic patients had significantly higher serially obtained perceived functional disability scores than White patients (point estimate, 0.29; P < 0.001). Hispanic patients also had higher mortality rates than White Americans even after adjustment for age, gender, and socioeconomic statuses.

conclusionHispanic patients have higher likelihood of having U1-RNP positivity and SLE overlap, more severe restrictive lung disease, as well as higher rate of mortality than non-Hispanic White patients.

Indexed as

Hispanic or LatinoScleroderma, SystemicSeverity of Illness IndexAdultAgedBlack or African AmericanFemaleHumansLongitudinal StudiesMaleMiddle AgedProspective StudiesWhite People

Identifiers

PMID38221717
PMCPMC11132947

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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.