Evidence map›Paper›PMID 40491768›Full record

ArticleFrontiers in medicine2025

Comprehensive analysis of life quality of patients with vitiligo in Romania: insights from a multivariate approach.

László Fekete, Vladimir Bacârea, Gyula László Fekete, Júlia Edit Fekete, Béla Kovács

Abstract read
In one paragraph

Article in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. Article
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

5 authors.

László FeketeDoctoral School of Medicine and Pharmacy, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Târgu Mureș, Târgu Mureș, Romania.
Vladimir BacâreaDepartment M2, Research Methodology, George Emil Palade University of Medicine, Pharmacy, Science and Technology of Târgu Mureș, Târgu Mureş, Romania.
Gyula László FeketeDepartment M4, Dermatology, George Emil Palade University of Medicine, Pharmacy, Science and Technology of Târgu Mureș, Târgu Mureş, Romania.
Júlia Edit FeketeNational Institute of Public Health, Regional Center for Public Health, Târgu Mureş, Romania.
Béla KovácsDepartment F1, Biochemistry and Environmental Chemistry George Emil Palade University of Medicine, Pharmacy, Science and Technology of Târgu Mureș, Târgu Mureş, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Vitiligo is a rare skin disorder affecting approximately 2% of the world's population with significant impact on body image and subsequent psychosocial involvement in terms of self-esteem and quality of life. Our study focused on assessing these psychosocial aspects in Romanian vitiligo patients. Methods: Assessment of self-esteem and quality of life were evaluated by self-reported completion of the Rosenberg self-esteem and Dermatology Life Quality Index validated questionnaires. Sociodemographic data were also collected from the 114 respondents, including age, gender, residence, marital status, level of education and debut of vitiligo. Besides classical statistical evaluation, dimensionality reduction analysis techniques, such as principal component analysis and multiple correspondence analysis were employed to investigate in complexity the impact of various factors on the quality of life and self-esteem of patients with vitiligo. Results: Our findings suggest that age, marital status and disease duration were amongst the most important factors that affects the psychosocial well-being of patients with vitiligo. Elderly, married patients with long-established vitiligo scored better on the quality-of-life outcomes and higher on the self-esteem questionnaire compared to their younger, single and recently diagnosed peers with vitiligo. Conclusion: Our findings highlight the significant influence of sociodemographic factors on self-esteem and quality of life in vitiligo patients, emphasizing the need for further research and personalized support to address the psychosocial impact of the condition.

Indexed as

DLQImultivariate data analysispsychosocial burdenRomaniaRSEvitiligo

Identifiers

PMID40491768
PMCPMC12146156

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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.