Evidence map›Paper›PMID 37108492›Full record

ReviewInternational journal of molecular sciences2023

Pharmacogenomics on the Treatment Response in Patients with Psoriasis: An Updated Review.

Ching-Ya Wang, Chuang-Wei Wang, Chun-Bing Chen, Wei-Ti Chen, Ya-Ching Chang, Rosaline Chung-Yee Hui, Wen-Hung Chung

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.6field-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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Medicina (Kaunas, Lithuania) · 2026
    Observational
  3. Genetic Association Study ofLife (Basel, Switzerland) · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Genes · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. 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

7 authors at 1 institution in 2 countries.

Ching-Ya WangDepartment of Dermatology, Chang Gung Memorial Hospital, Linkou Branch, Taoyuan 333, Taiwan.ORCID 0000-0003-1118-0900
Chuang-Wei WangDepartment of Dermatology, Chang Gung Memorial Hospital, Linkou Branch, Taoyuan 333, Taiwan.ORCID 0000-0002-7921-4129
Chun-Bing ChenDepartment of Dermatology, Chang Gung Memorial Hospital, Linkou Branch, Taoyuan 333, Taiwan.ORCID 0000-0002-7378-4235
Wei-Ti ChenDepartment of Dermatology, Chang Gung Memorial Hospital, Linkou Branch, Taoyuan 333, Taiwan.ORCID 0000-0002-1929-4008
Ya-Ching ChangDepartment of Dermatology, Chang Gung Memorial Hospital, Linkou Branch, Taoyuan 333, Taiwan.ORCID 0000-0003-4937-7557
Rosaline Chung-Yee HuiCollege of Medicine, Chang Gung University, Taoyuan 333, Taiwan.
Wen-Hung ChungDepartment of Dermatology, Chang Gung Memorial Hospital, Linkou Branch, Taoyuan 333, Taiwan.
Chang Gung University · TW

Funding

Chang Gung Memorial Hospital CORPG3M0221-2 and CORPG2M0031National Science and Technology Council, Taiwan NSTC 111-2326-B-182A-003-, 111-2314-B-182A-113-MY3
6 · The paper itself

Abstract

The efficacy and the safety of psoriasis medications have been proved in trials, but unideal responses and side effects are noted in clinical practice. Genetic predisposition is known to contribute to the pathogenesis of psoriasis. Hence, pharmacogenomics gives the hint of predictive treatment response individually. This review highlights the current pharmacogenetic and pharmacogenomic studies of medical therapy in psoriasis. HLA-Cw*06 status remains the most promising predictive treatment response in certain drugs. Numerous genetic variants (such as ABC transporter, DNMT3b, MTHFR, ANKLE1, IL-12B, IL-23R, MALT1, CDKAL1, IL17RA, IL1B, LY96, TLR2, etc.) are also found to be associated with treatment response for methotrexate, cyclosporin, acitretin, anti-TNF, anti-IL-12/23, anti-IL-17, anti-PDE4 agents, and topical therapy. Due to the high throughput sequencing technologies and the dramatic increase in sequencing cost, pharmacogenomic tests prior to treatment by whole exome sequencing or whole genome sequencing may be applied in clinical in the future. Further investigations are necessary to manifest potential genetic markers for psoriasis treatments.

Indexed as

PharmacogeneticsPsoriasisAcitretinEndonucleasesHumansMethotrexateTumor Necrosis Factor InhibitorsAcitretinEndonucleasesMethotrexateTumor Necrosis Factor Inhibitorsadverse effectdrugpharmacogeneticspharmacogenomicspolymorphismspsoriasistreatment responsewhole genome sequencing

Identifiers

PMID37108492
PMCPMC10138383
OpenAlexW4366088419

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.