Evidence map›Paper›PMID 29390428›Full record

ArticleMedicine2017

Clinical and serological features of systemic sclerosis in a multicenter African American cohort: Analysis of the genome research in African American scleroderma patients clinical database.

Nadia D Morgan, Ami A Shah, Maureen D Mayes, Robyn T Domsic, Thomas A Medsger, Virginia D Steen, John Varga, Mary Carns, Paula S Ramos, Richard M Silver and 19 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 2 pooled it
6.9field-weighted citation impact, top 2% 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

52 citing papers in PubMed, 2 syntheses or guidelines pooled it, 113 citations in OpenAlex.

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  17. [Fever in rheumatological diseases].Zeitschrift fur Rheumatologie · 2024
    Review
  18. Redox Pathogenesis in Rheumatic Diseases.ACR open rheumatology · 2024
    Review
  19. Observational
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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

29 authors at 18 institutions in 1 country.

Nadia D MorganDivision of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD Division of Rheumatology, University of Texas-McGovern Medical School, Houston, TX Division of Rheumatology, University of Pittsburgh, PA Division of Rheumatology, Georgetown University School of Medicine, Washington, DC Division of Rheumatology, Northwestern University, Feinberg School of Medicine, Chicago, IL Division of Rheumatology, Medical University of South Carolina, Charleston, SC Division of Rheumatology, University of Michigan, Ann Arbor, MI Division of Rheumatology, Robert Wood Johnson University, New Brunswick, NJ Division of Rheumatology, Hospital for Special Surgery, New York, NY Department of Rheumatology, Arthritis and Osteoporosis Consultants of the Carolinas, Charlotte, NC Division of Rheumatology, Tulane University School of Medicine, New Orleans, LA Division of Rheumatology, University of California San Francisco, CA Division of Rheumatology, University of Pennsylvania, Philadelphia, PA Division of Rheumatology, Boston University School of Medicine, Boston, MA Division of Rheumatology, George Washington University, Washington, DC Division of Rheumatology, Stanford University School of Medicine, Stanford, CA Division of Rheumatology, University of Chicago Pritzker School of Medicine, Chicago, IL Division of Rheumatology, New York University Langone Medical Center, New York, NY National Human Genome Research Institute National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, USA.
Ami A Shah
Maureen D Mayes
Robyn T Domsic
Thomas A Medsger
Virginia D Steen
John Varga
Mary Carns
Paula S Ramos
Richard M Silver
Elena Schiopu
Dinesh Khanna
Vivien Hsu
Jessica K Gordon
Heather Gladue
Lesley A Saketkoo
Lindsey A Criswell
Chris T Derk
Marcin A Trojanowski
Victoria K Shanmugam
Lorinda Chung
Antonia Valenzuela
Reem Jan
Avram Goldberg
Elaine F Remmers
Daniel L Kastner
Fredrick M Wigley
Pravitt Gourh
Francesco Boin
Georgetown University · USJohns Hopkins University · USMedical University of South Carolina · USNational Human Genome Research Institute · USNorthwestern University · USStanford University · USUniversity of California, San Francisco · USUniversity of Michigan–Ann Arbor · USUniversity of Pittsburgh · USBoston University · USGeorge Washington University · USHospital for Special Surgery · USJohnson University · USNational Institutes of Health · USNYU Langone Health · USTulane University · USUniversity of Chicago · USUniversity of Pennsylvania · US

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
Genetic Analysis of Complex Inflammatory DisordersZIAHG200371 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI KASTNER, DANIEL · 2011 to 2024
$18.8M
SOUTH CAROLINA CLINICAL & TRANSLATIONAL RESEARCH INSTITUTE (SCTR)UL1RR029882 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T. · 2009 to 2011
$10.1M
South Carolina Clinical & Translational Research Institute (SCTR)UL1TR000062 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T. · 2012 to 2014
$9.4M
Role of TGF-beta and CTGF Signaling Transgenic Mouse Models of SclerodermaP50AR054144 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI TAN, FILEMON K. · 2006 to 2010
$7.7M
Multidisciplinary Rheumatology Training ProgramT32AR048522 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI CLIFTON O BINGHAM, LIVIA A CASCIOLA-ROSEN · 2003 to 2026
$6.4M
Two-Stage Genome-Wide Association Study in Systemic SclerosisR01AR055258 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MAYES, MAUREEN MAUREEN · 2008 to 2012
$5.9M
Patient Resource CoreP60AR062755 · NIAMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI GILKESON, GARY S · 2012 to 2016
$5.8M
Outcomes Research in Rheumatic DiseasesK24AR063120 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KHANNA, DINESH · 2012 to 2022
$1.6M
Cancer, Autoantigens, and Scleroderma Investigating the ConnectionK23AR061439 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI SHAH, AMI AALOK · 2012 to 2016
$699k
SCLERODERMA FAMILY REGISTRY AND DNA REPOSITORY-264002251-264002251-264002251N01AR002251 · NIAMS · WAYNE STATE UNIVERSITY · PI MAYES, MAUREEN · 2000 to 2006
$659k
The role of natural selection in SLE risk among African-AmericansK01AR067280 · NIAMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAMOS, PAULA SOFIA · 2015 to 2018
$516k
NCATS NIH HHS UL1 TR000062NCATS NIH HHS UL1 TR001450NCRR NIH HHS UL1 RR029882NIAMS NIH HHS K01 AR067280NIAMS NIH HHS K23 AR061439NIAMS NIH HHS K24 AR063120NIAMS NIH HHS N01 AR002251NIAMS NIH HHS P50 AR054144NIAMS NIH HHS P60 AR062755NIAMS NIH HHS R01 AR055258NIAMS NIH HHS R03 AR065801NIAMS NIH HHS T32 AR048522
6 · The paper itself

Abstract

Racial differences exist in the severity of systemic sclerosis (SSc). To enhance our knowledge about SSc in African Americans, we established a comprehensive clinical database from the largest multicenter cohort of African American SSc patients assembled to date (the Genome Research in African American Scleroderma Patients (GRASP) cohort).African American SSc patients were enrolled retrospectively and prospectively over a 30-year period (1987-2016), from 18 academic centers throughout the United States. The cross-sectional prevalence of sociodemographic, clinical, and serological features was evaluated. Factors associated with clinically significant manifestations of SSc were assessed using multivariate logistic regression analyses.The study population included a total of 1009 African American SSc patients, comprised of 84% women. In total, 945 (94%) patients met the 2013 American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) classification criteria for SSc, with the remaining 64 (6%) meeting the 1980 ACR or CREST (calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, telangiectasia) criteria. While 43% were actively employed, 33% required disability support. The majority (57%) had the more severe diffuse subtype and a young age at symptom onset (39.1 ± 13.7 years), in marked contrast to that reported in cohorts of predominantly European ancestry. Also, 1 in 10 patients had a severe Medsger cardiac score of 4. Pulmonary fibrosis evident on computed tomography (CT) chest was present in 43% of patients and was significantly associated with anti-topoisomerase I positivity. 38% of patients with CT evidence of pulmonary fibrosis had a severe restrictive ventilator defect, forced vital capacity (FVC) ≤50% predicted. A significant association was noted between longer disease duration and higher odds of pulmonary hypertension, telangiectasia, and calcinosis. The prevalence of potentially fatal scleroderma renal crisis was 7%, 3.5 times higher than the 2% prevalence reported in the European League Against Rheumatism Scleroderma Trials and Research (EUSTAR) cohort.Our study emphasizes the unique and severe disease burden of SSc in African Americans compared to those of European ancestry.

Indexed as

AdultBlack or African AmericanChromosome MappingCohort StudiesCross-Sectional StudiesDatabases, FactualFemaleHumansMalePrevalenceProspective StudiesRetrospective StudiesScleroderma, SystemicSeverity of Illness IndexSocioeconomic FactorsUnited States

Identifiers

PMID29390428
PMCPMC5758130
OpenAlexW2781436519

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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.