Evidence map›Paper›PMID 24821613›Full record

ArticleArthritis care & research2014

Association of health-related quality of life in childhood-onset systemic lupus erythematosus with ethnicity: results from a multiethnic multicenter Canadian cohort.

Deborah M Levy, Christine A Peschken, Lori B Tucker, Gaëlle Chédeville, Adam M Huber, Janet E Pope, Canadian Network for Improved Outcomes in SLE (CaNIOS) 1000 Faces Investigators, Earl D Silverman

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in Arthritis care & research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03802188 (Hydroxychloroquine Exposure in Systemic Lupus Erythematosus), which is not on this map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 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.

NCT03802188 unknown statusnot on this mapstarted 2018, after this paper: background citation

Hydroxychloroquine Exposure in Systemic Lupus Erythematosus (SLE)

TypeobservationalSponsorMcGill University Health Centre/Research Institute of the McGill University Health CentreRan2018 to 2025Enrolled3,700ConditionsSystemic Lupus Erythematosus
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Physical pain among Indigenous Peoples in Canada: a scoping review.Canadian journal of anaesthesia = Journal canadien d'anesthesie · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. 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

8 authors.

Deborah M LevyHospital for Sick Children and University of Toronto, Toronto, Ontario, Canada.
Christine A Peschken
Lori B Tucker
Gaëlle Chédeville
Adam M Huber
Janet E Pope
Canadian Network for Improved Outcomes in SLE (CaNIOS) 1000 Faces Investigators
Earl D Silverman

Funding

Neurocognitive Function in Childhood-Onset SLE (cSLE)K23AR053202 · NIAMS · HOSPITAL FOR SICK CHLDRN (TORONTO) · PI LEVY, DEBORAH M · 2007 to 2011
$649k
NIAMS NIH HHS K23 AR053202NIAMS NIH HHS K23-AR-053202
6 · The paper itself

Abstract

objectiveTo evaluate the influence of ethnicity on self-reported health-related quality of life (HRQOL) in the Canadian childhood-onset systemic lupus erythematosus (cSLE) population.

methodsPatients with cSLE at 4 pediatric centers were consecutively enrolled. Sociodemographics and multiple disease activity measures were collected. The Child Health Questionnaire (CHQ) was administered and analyzed by ethnicity.

resultsWe enrolled 213 cSLE patients, and complete data from 196 patients with the following ethnicities were analyzed: white (33%), Asian (32%), South Asian (16%), African American (11%), Latino/Hispanic (5%), and Aboriginal (4%). Compared to healthy children, cSLE patients rated their HRQOL significantly more poorly in 9 of 10 individual domains, and in 4 of 10 domains when compared to a cohort of juvenile arthritis patients. Within the cSLE cohort, CHQ scores were lower in 5 of 10 domains in white patients versus nonwhite ethnicities (P < 0.05 for each). Physical summary scores were lower for white patients compared to the other ethnicities aggregated together (mean ± SD 46.0 ± 11.9 versus 50.4 ± 10.1; P = 0.009); however, psychosocial summary scores were similar among the groups (mean ± SD 40.5 ± 14.6 versus 42.8 ± 12.7; P = 0.26). Disease activity measures, including the Systemic Lupus Erythematosus Disease Activity Index 2000, the Systemic Lupus Activity Measure, Revised, and physician global visual analog scale, were similar across ethnicities. However, patient-reported Systemic Lupus Erythematosus Activity Questionnaire symptom scores were greater in patients of white ethnicity compared to those of Asian ethnicity (mean ± SD 8.2 ± 5.8 versus 4.5 ± 4.7; P = 0.004).

conclusionThe self- and parent-reported health status of Canadian cSLE patients differed across ethnicities, with white patients reporting lower HRQOL despite similar and overall low disease activity.

Indexed as

Quality of LifeAdolescentAge of OnsetCanadaChildEthnicityFemaleHealth StatusHealth SurveysHumansLupus Erythematosus, SystemicMaleRacial GroupsSeverity of Illness Index

Identifiers

PMID24821613
PMCPMC4229486

What OpenQuestion holds

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Registered trials

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.