Evidence map›Paper›PMID 39775081›Full record

ArticleArchives of dermatological research2025

Biologic therapy for psoriasis is associated with the development of metabolic dysfunction-associated steatotic liver disease (MASLD). A study on the association of cardiometabolic conditions with psoriasis treatment.

Gwyneth Armijo-Borjon, Alessandra Irais Miranda-Aguirre, Arnulfo Garza-Silva, Iván Francisco Fernández-Chau, Miguel Ángel Sanz-Sánchez, Arnulfo González-Cantú, Maria Elena Romero-Ibarguengoitia

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Article in Archives of dermatological research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

7 authors.

Gwyneth Armijo-BorjonResearch Department, Hospital Clínica Nova de Monterrey, San Nicolás de los Garza, Nuevo León, México.ORCID http://orcid.org/0009-0005-7163-3125
Alessandra Irais Miranda-AguirreResearch Department, Hospital Clínica Nova de Monterrey, San Nicolás de los Garza, Nuevo León, México.ORCID http://orcid.org/0000-0002-8171-6013
Arnulfo Garza-SilvaResearch Department, Hospital Clínica Nova de Monterrey, San Nicolás de los Garza, Nuevo León, México.ORCID http://orcid.org/0000-0002-2200-1958
Iván Francisco Fernández-ChauResearch Department, Hospital Clínica Nova de Monterrey, San Nicolás de los Garza, Nuevo León, México.ORCID http://orcid.org/0009-0007-4423-2814
Miguel Ángel Sanz-SánchezResearch Department, Hospital Clínica Nova de Monterrey, San Nicolás de los Garza, Nuevo León, México.
Arnulfo González-CantúResearch Department, Hospital Clínica Nova de Monterrey, San Nicolás de los Garza, Nuevo León, México.ORCID http://orcid.org/0000-0003-0103-0079
Maria Elena Romero-IbarguengoitiaResearch Department, Hospital Clínica Nova de Monterrey, San Nicolás de los Garza, Nuevo León, México. MROMEROI@novaservicios.com.mx.ORCID http://orcid.org/0000-0002-2572-4043

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPsoriasis requires a comprehensive assessment of concomitant diseases to make better therapeutic decisions. This study examined the differences in the onset and progression of associated cardiometabolic comorbidities in psoriasis patients based on their treatments.

methodsA retrospective longitudinal study was conducted on patients aged over 13 years with psoriasis seen at a Northern Mexican Hospital between 2012 and 2023. Patients were categorized into three groups according on the type of treatment received: topical, systemic, and biologic. A logistic regression analysis was performed to identify predictors of comorbidity development.

results197 patients were included; 52.8% were women, with a mean (SD) age of 54.45 (16.91) years, divided into topical [n = 90 (45.7%)], systemic [n = 57 (29.1%)], and biologic [n = 50 (25.5%)] groups, metabolic dysfunction-associated steatotic liver disease (MASLD) was significantly more prevalent in the biologic group [22 (44%)], p < 0.001. The logistic regression showed that type 2 diabetes mellitus, biological treatments (OR = 5.798, p = 0.001), and body mass index (OR = 1.144, p = 0.002), predicted the development of MASLD with a Nagelkerke's R

conclusionsPsoriasis patients using biological therapies have a greater predisposition to MASLD. These patients should receive a comprehensive approach to identify metabolic conditions, and screening tests for MASLD are recommended.

Indexed as

PsoriasisAdultAgedBiological ProductsBiological TherapyBody Mass IndexComorbidityDiabetes Mellitus, Type 2Fatty LiverFemaleHumansLongitudinal StudiesMaleMexicoMiddle AgedPrevalenceBiological ProductsComorbidityMetabolic-associated fatty liver diseasePsoriasisSeverityTreatment

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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 Socratic graph.