Evidence map›Paper›PMID 28118525›Full record

ArticleArthritis care & research2017

Predictors of Reduced Health-Related Quality of Life in Adult Patients With Idiopathic Inflammatory Myopathies.

Michal Feldon, Payam Noroozi Farhadi, Hermine I Brunner, Lukasz Itert, Bob Goldberg, Abdullah Faiq, Jesse Wilkerson, Kathryn M Rose, Lisa G Rider, Frederick W Miller and 1 more

Abstract read
In one paragraph

Article in Arthritis care & research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
–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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  20. Idiopathic inflammatory myopathies.Nature reviews. Disease primers · 2021
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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

11 authors.

Michal FeldonCincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Payam Noroozi FarhadiNational Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, Maryland.
Hermine I BrunnerCincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Lukasz ItertCincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Bob GoldbergThe Myositis Association, Alexandria, Virginia.
Abdullah FaiqNational Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, Maryland.
Jesse WilkersonSocial and Scientific Systems, Durham, North Carolina.
Kathryn M RoseSocial and Scientific Systems, Durham, North Carolina.
Lisa G RiderNational Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, Maryland.
Frederick W MillerNational Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, Maryland.
Edward H GianniniCincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

Funding

Environmental/genetic Risk Factors and Pathogenesis of Autoimmune DiseaseZIAES101074 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI RIDER, LISA · 2009 to 2025
$34.6M
Assessment, Therapy and Prevention Of Autoimmune DiseaseZIAES101081 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI RIDER, LISA · 2009 to 2025
$17.6M
Pathogenesis And Genetic/environmental Risk Factors ForZ01ES101074 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI MILLER, FREDERICK · 2002 to 2008
$2.7M
CREATING A NATIONAL MYOSITIS PATIENT REGISTRYH75DP001743 · DP · MYOSITIS ASSOCIATION · PI GOLDBERG, BOB · 2008 to 2008
$167k
Intramural NIH HHS Z01 ES101074Intramural NIH HHS ZIA ES101081NCCDPHP CDC HHS H75 DP001743
6 · The paper itself

Abstract

objectiveExtensive studies on health-related quality of life (HRQoL) in idiopathic inflammatory myopathies (IIMs) are lacking. Our objective was to document HRQoL and to identify factors associated with a reduced HRQoL in patients with IIM.

methodsA total of 1,715 patients (median age 49.9 years, 70% female, 87% white) who met probable or definite Bohan and Peter criteria or Griggs criteria for myositis were included from the Myovision registry. HRQoL was ascertained using the Short Form 12 (SF-12) health survey questionnaire. HRQoL physical component summary (PCS) and mental component summary (MCS) scores in relation to different patient and disease characteristics were compared to scores from matched normative data from the US general population and rheumatoid arthritis (RA) patients. Bivariate and multiple linear regression analyses were performed to assess the association between HRQoL and patient and disease parameters.

resultsThe mean SF-12 summary scores were significantly lower in IIM patients than in the normative and RA populations. A diagnosis of inclusion body myositis, older age, patient-reported negative effect of disease on work, presence of another co-occurring autoimmune disease, polypharmacy, and IIM-associated lung disease and joint involvement were significantly associated with lower PCS scores. Lower MCS scores were associated with joint involvement and a negative effect of disease on work.

conclusionIn this large study of patient-reported outcomes in IIM, an association was found between multiple disease characteristics and reduced HRQoL, mostly in the physical domain. In the US, the HRQoL of IIM patients was found to be lower than that of the general population and RA patients.

Indexed as

Health StatusAdultCross-Sectional StudiesFemaleHealth SurveysHumansMaleMiddle AgedMyositisPredictive Value of TestsQuality of LifeRegistries

Identifiers

PMID28118525
PMCPMC5524619

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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.