Evidence map›Paper›PMID 41737997›Full record

ArticlePsoriasis (Auckland, N.Z.)2026

The Psoriatic Disease Assessment Index (PSODAI) Score to Evaluate Systemic Involvement of Psoriasis.

Yanhua Liang, Baoqing Deng, Epipode Ntawuyamara, Hervé Bachelez, Fuxi Wang, Hao Zhang, Zhenying Zhang, Zhengfeng Li, Lin Dang, Yajie Wang and 13 more

Abstract read
In one paragraph

Article in Psoriasis (Auckland, N.Z.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

23 authors.

Yanhua LiangDepartment of Dermatology, Cosmetology and Venereology, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangdong, People's Republic of China.ORCID 0000-0001-8315-1661
Baoqing DengDepartment of Dermatology, Shenzhen Baoan Center for Chronic Disease Control, Shenzhen, People's Republic of China.
Epipode NtawuyamaraDepartment of Dermatology and Venereology, University Teaching Hospital of Kamenge, University of Burundi, Bujumbura, Burundi.
Hervé BachelezDepartment of Dermatology, Hôpital Saint-Louis, APHP & INSERM U1183, Imagine Institute for Human Genetic Diseases, Paris Cité University, Paris, France.
Fuxi WangDepartment of Dermatology, The Second People's Hospital of Shenzhen, Shenzhen, Guangdong, People's Republic of China.
Hao ZhangDepartment of Dermatology, Shenzhen Center for Chronic Disease Control, Shenzhen Institute of Dermatology, Shenzhen, Guangdong, People's Republic of China.
Zhenying ZhangDepartment of Dermatology, the University of Hong Kong-Shenzhen Hospital, Shenzhen, Guangdong, People's Republic of China.
Zhengfeng LiDepartment of Dermatology, the University of Hong Kong-Shenzhen Hospital, Shenzhen, Guangdong, People's Republic of China.
Lin DangDepartment of Dermatology, Longgang Central Hospital, Shenzhen, Guangdong, People's Republic of China.
Yajie WangDepartment of Dermatology, Cosmetology and Venereology, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangdong, People's Republic of China.
Xianbiao ZouDepartment of Dermatovenerology & Medical Cosmetology, South China Hospital, Medical School, Shenzhen University, Shenzhen, People's Republic of China.
Li WangDepartment of Dermatology, Shenzhen Hospital Beijing University of Chinese Medicine, Shenzhen, People's Republic of China.
Dejian DuanDepartment of Dermatology, Shenzhen Bao'an Chinese Medicine Hospital, Guangzhou University of Chinese Medicine, Shenzhen, People's Republic of China.
Hongxiang ChenDepartment of Dermatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Shenzhen, Guangdong, People's Republic of China.
Wenjun ZhengDepartment of Dermatology and Venereology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Hui HuangDepartment of Cardiology, The Eighth Affiliated Hospital of Sun Yat-Sen University, Shenzhen, People's Republic of China.
Min ZhangDepartment of Respiratory, The Second People's Hospital of Shenzhen, Shenzhen, Guangdong, People's Republic of China.
Qingxian CaiNational Clinical Research Center for Infectious Diseases, The Third People's Hospital of Shenzhen, The Second Affiliated Hospital of Southern University of Science and Technology, Shenzhen, Guangdong, People's Republic of China.
Ye ChenDepartment of Gastroenterology, Integrative Clinical Microecology Center, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangdong, People's Republic of China.
Yingli ZhangShenzhen Mental Health Center, Shenzhen Kangning Hospital, Shenzhen, Guangdong, People's Republic of China.
Zeyuan LuDepartment of Endocrinology, The Eighth Affiliated Hospital of Sun Yat-sen University, Shenzhen, People's Republic of China.
Yalin RenDepartment of Ophthalmology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, People's Republic of China.
Jinxian HuangDepartment of Medicine, Division of Rheumatology, The University of Hong Kong-Shenzhen Hospital, ShenzheN, Guangdong, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: To the best of our knowledge, no validated scoring instrument currently exists that comprehensively evaluates both cutaneous manifestations and systemic comorbidities of psoriasis. This multicenter study aimed to develop and validate a novel multidimensional scoring system addressing this clinical gap. Methods: Under the guidance of the Shenzhen Psoriasis Academy, we conducted seven expert meetings to analyze existing evidence from PubMed, Wanfang, and CNKI databases. Through iterative Delphi consensus processes involving 26 specialists across 10 disciplines, we established the Psoriasis Disease Assessment Index (PSODAI). This 60-point composite instrument evaluates cutaneous involvement and nine key organ/system comorbidities. An accompanying online calculator (http://www.psodai.com.cn/) was developed for clinical implementation. Validation involved 254 psoriasis patients from six tertiary centers, with comparative analyses against PASI and DLQI metrics. Results: The PSODAI framework stratifies disease severity as mild (0-20), moderate (21-40), and severe (41-60). Comparative analysis revealed comparable proportions of moderate-to-severe cases between PSODAI and conventional tools (PASI/DLQI) (p>0.05). Notably, 11 patients (4.3%) classified as severe by PASI were re-categorized as mild through PSODAI's systemic evaluation, primarily due to limited extracutaneous manifestations. Conclusion: As the first comorbidity-integrated assessment tool, PSODAI enables cross-specialty collaboration for holistic patient management. Its clinical adoption may facilitate timely comorbidity detection and preventive interventions. Further multicenter validation is warranted to confirm these preliminary findings.

Indexed as

comorbidityconsensusdisease severitypsoriasissystemic scoring

Identifiers

PMID41737997
PMCPMC12927750

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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.