Evidence map›Paper›PMID 35953237›Full record

ArticleLupus science & medicine2022

Depression, stigma and social isolation: the psychosocial trifecta of primary chronic cutaneous lupus erythematosus, a cross-sectional and path analysis.

Cristina Drenkard, Kristina A Theis, Timothy T Daugherty, Charles G Helmick, Charmayne Dunlop-Thomas, Gaobin Bao, Laura Aspey, Tené T Lewis, S Sam Lim

Open access · goldAbstract read
In one paragraph

Article in Lupus science & medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

5 citing papers in PubMed, 19 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Cristina DrenkardDepartment of Medicine/Rheumatology, Emory University School of Medicine, Atlanta, Georgia, USA CDRENKA@emory.edu.ORCID 0000-0002-6832-7291
Kristina A TheisDivision of Population Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Timothy T DaughertyDepartment of Medicine, Washington University in St Louis, St Louis, Missouri, USA.
Charles G HelmickDivision of Population Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Charmayne Dunlop-ThomasDepartment of Medicine/Rheumatology, Emory University School of Medicine, Atlanta, Georgia, USA.
Gaobin BaoDepartment of Medicine/Rheumatology, Emory University School of Medicine, Atlanta, Georgia, USA.
Laura AspeyDepartment Medicine/Dermatology, Emory University School of Medicine, Atlanta, Georgia, USA.
Tené T LewisDepartment of Epidemiology, Emory University School of Public Health, Atlanta, Georgia, USA.
S Sam LimDepartment of Medicine/Rheumatology, Emory University School of Medicine, Atlanta, Georgia, USA.ORCID 0000-0003-2361-0787
Emory University · USCenters for Disease Control and Prevention · USWashington University in St. Louis · US

Funding

The Georgians Organized Against Lupus (GOAL) Cohort: Advancing Health DisparitiesU01DP005119 · DP · EMORY UNIVERSITY · PI DRENKARD, CRISTINA MARTA, LIM, SUNG SAM · 2014 to 2018
$4.8M
Psychosocial Factors and Lupus Disease Progression Among African American WomenR01AR065493 · NIAMS · UNIV OF MARYLAND, COLLEGE PARK · PI CHAE, H. DAVID, LIM, SUNG SAM · 2014 to 2022
$4.2M
Social Stressors and Atherosclerosis in African-American Women with LupusR01AR070898 · NIAMS · EMORY UNIVERSITY · PI LEWIS, TENÉ T · 2016 to 2020
$3.3M
The Georgians Organized Against Lupus (GOAL) Cohort: Addressing Health Disparities in Lupus through Social Determinants of HealthU01DP006488 · DP · EMORY UNIVERSITY · PI DRENKARD, CRISTINA MARTA, LIM, SUNG SAM · 2019 to 2021
$2.6M
A widespread self-management education program to reduce health disparities in African American women with systemic lupus erythematosusR01MD010455 · NIMHD · EMORY UNIVERSITY · PI DRENKARD, CRISTINA MARTA · 2016 to 2020
$1.9M
ACL HHS U01DP005119NCCDPHP CDC HHS U01 DP005119NCCDPHP CDC HHS U01 DP006488NIAMS NIH HHS R01 AR065493NIAMS NIH HHS R01 AR070898NIMHD NIH HHS R01 MD010455
6 · The paper itself

Abstract

objectiveDepression is common in individuals with chronic cutaneous lupus erythematosus (CCLE). However, how CCLE may impact patients' psychological well-being is poorly understood, particularly among disproportionally affected populations. We examined the relationships between depression and psychosocial factors in a cohort of predominantly Black patients with primary CCLE (CCLE without systemic manifestations).

methodsCross-sectional assessment of individuals with dermatologist-validated diagnosis of primary CCLE. NIH-PROMIS short-forms were used to measure depression, disease-related stigma, social isolation and emotional support. Linear regression analyses (ɑ=0.05) were used to test an a priori conceptual model of the relationship between stigma and depression and the effect of social isolation and emotional support on that association.

resultsAmong 121 participants (87.6% women; 85.1% Black), 37 (30.6%) reported moderate to severe depression. Distributions of examined variables divided equally among those which did (eg, work status, stigma (more), social isolation (more), emotional support (less)) and did not (eg, age, sex, race, marital status) significantly differ by depression. Stigma was significantly associated with depression (b=0.77; 95% CI0.65 to 0.90), whereas social isolation was associated with both stigma (b=0.85; 95% CI 0.72 to 0.97) and depression (b=0.70; 95% CI0.58 to 0.92). After controlling for confounders, stigma remained associated with depression (b=0.44; 95% CI0.23 to 0.66) but lost significance (b=0.12; 95% CI -0.14 to 0.39) when social isolation (b=0.40; 95% CI 0.19 to 0.62) was added to the model. Social isolation explained 72% of the total effect of stigma on depression. Emotional support was inversely associated with depression in the univariate analysis; however, no buffer effect was found when it was added to the multivariate model.

conclusionOur findings emphasise the psychosocial challenges faced by individuals living with primary CCLE. The path analysis suggests that stigmatisation and social isolation might lead to depressive symptoms. Early clinical identification of social isolation and public education demystifying CCLE could help reduce depression in patients with CCLE.

Indexed as

Lupus Erythematosus, DiscoidLupus Erythematosus, SystemicCross-Sectional StudiesDepressionFemaleHumansMaleSocial IsolationAutoimmune DiseasesEpidemiologyOutcome Assessment, Health CareQuality of LIfe

Identifiers

PMID35953237
PMCPMC9379542
OpenAlexW4291923499

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.