Evidence map›Paper›PMID 37064002›Full record

Article3 Biotech2023

Exploring the molecular underpinning of psoriasis and its associated comorbidities through network approach: cross talks of genes and pathways.

Saumya Choudhary, Noor Saba Khan, Rashi Verma, Pallavi Saxena, Harpreet Singh, Arun Kumar Jain, George Thomas, Dibyabhaba Pradhan, Neeraj Kumar

Abstract read
In one paragraph

Article in 3 Biotech, 2023. 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
–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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Impact of a dermatological rehabilitation program on cardiovascular risks of psoriasis patients.Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG · 2025
    Article
  5. 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

9 authors.

Saumya ChoudharyICMR-National Institute of Pathology, New Delhi, 110029 India.ORCID 0000-0002-6449-1094
Noor Saba Khan *ICMR-National Institute of Pathology, New Delhi, 110029 India.
Rashi Verma *ICMR-National Institute of Pathology, New Delhi, 110029 India.
Pallavi SaxenaICMR-National Institute of Pathology, New Delhi, 110029 India.
Harpreet SinghICMR-AIIMS Computational Genomics Centre (ISRM) Division, Indian Council of Medical Research, New Delhi, 110029 India.
Arun Kumar JainICMR-National Institute of Pathology, New Delhi, 110029 India.ORCID 0000-0001-8325-2892
George ThomasDepartment of Molecular and Cellular Engineering, Sam Higginbottom University of Agriculture, Technology and Sciences, Prayagraj (Allahabad), 211007 India.ORCID 0000-0001-5020-7454
Dibyabhaba PradhanICMR-AIIMS Computational Genomics Centre (ISRM) Division, Indian Council of Medical Research, New Delhi, 110029 India.ORCID 0000-0002-2459-5032
Neeraj KumarICMR-National Institute of Pathology, New Delhi, 110029 India.ORCID 0000-0002-3535-9019

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with psoriasis often complain of several linked disorders including autoimmune and cardiometabolic diseases. Understanding of molecular link between psoriasis and associated comorbidities would be of great interest at the point of patient care management. Integrative unbiased network approach, indicates significant unidirectional gene overlap between psoriasis and its associated comorbid condition including obesity (31 upregulated and 26 downregulated), ischemic stroke (14 upregulated and 2 downregulated), dyslipidaemia (5 upregulated, 5 downregulated), atherosclerosis (8 upregulated and 1 downregulated) and type II diabetes (5 upregulated, 5 downregulated). The analysis revealed substantial gene sharing among the different psoriasis-associated comorbidities. Molecular comorbidity index determining the strength of the interrelation between psoriasis and its comorbidities indicates prevalence of dyslipidaemia followed by type II diabetes among psoriasis patients. The Jaccard coefficient indices revealed psoriasis shared maximum number of biological pathways with dyslipidaemia followed by type 2 diabetes, ischemic stroke, obesity and atherosclerosis. Moreover, pathway annotation highlighted nearly 45 shared pathways amongst psoriasis and its comorbidities and a substantial number of shared pathways was found among multi-morbidities. Overall, the present study established conceivable link between psoriasis and comorbid diseases. The shared genes and overlapped pathways may be explored as a common productive target for psoriasis and its comorbid conditions. Supplementary Information: The online version contains supplementary material available at 10.1007/s13205-023-03533-y.

Indexed as

ComorbidityDiseasomeInteractomeNetwork analysisPsoriasis

Identifiers

PMID37064002
PMCPMC10102268

What OpenQuestion holds

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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.