Rubén Queiro, Paula Alvarez, Norma Calleja, Ignacio Braña, Stefanie Burger, Estefanía Pardo, Marta Loredo, Sara Alonso, Valentina Chiminazzo, Mercedes Alperi
{"title":"银屑病关节炎的表型可能根据皮肤或关节域是否首先出现或两者是否同时出现而有所不同。","authors":"Rubén Queiro, Paula Alvarez, Norma Calleja, Ignacio Braña, Stefanie Burger, Estefanía Pardo, Marta Loredo, Sara Alonso, Valentina Chiminazzo, Mercedes Alperi","doi":"10.55563/clinexprheumatol/8gl4ja","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>We aimed to analyse psoriatic arthritis (PsA) features based on psoriasis-arthritis lag times: simultaneous (S), psoriasis first (PF), arthritis first (AF).</p><p><strong>Methods: </strong>We carried out an inception cohort study involving 340 PsA patients. Phenotypic differences between patients were analysed based on the three disease latency models identified in the study. A post-hoc correction of significant p-values was applied by the Benjamini-Hochberg method.</p><p><strong>Results: </strong>Forty-five (13.2%) patients had S onset, 97 (28.5%) manifested AF, while in 198 (58.2%) psoriasis appeared first. Lag times were markedly different between PF (16.3 ±12.4 years) and AF (5.4 ±2.8 years) groups, p<0.001. The AF group presented less frequently the classic arthritogenic psoriasis pattern: nail (18.8%, p<0.001), scalp (28.1%, p=0.001), folds (10.9%, p=0.009), and ≥3 psoriasis body areas (18.8%, p<0.001), but showed more psoriasis family history (67.6%, p=0.001) and a milder overall joint phenotype. The S group associated a worse cardiometabolic profile and developed more dactylitis (44%, p=0.012) during follow-up. The PF group was younger at psoriasis onset (p<0.001), had more extensive psoriasis (p<0.001), and higher frequency of HLA-Cw6 positivity (43.2%). Within the PF group, patients with axial onset [median 19.0 years (IQR: 10.5-25.5)] had a longer psoriasis-arthritis latency compared to other onset forms [median 14.0 years (IQR: 5-24)].</p><p><strong>Conclusions: </strong>In this study, substantial phenotypic differences were identified based on the three PsA lag time models. In addition, the classic pattern of arthritogenic psoriasis did not prevail in the same way between these groups, which was novel.</p>","PeriodicalId":10274,"journal":{"name":"Clinical and experimental rheumatology","volume":" ","pages":"889-896"},"PeriodicalIF":3.4000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Psoriatic arthritis phenotype may vary depending on whether the skin or joint domain appears first or whether both appear simultaneously.\",\"authors\":\"Rubén Queiro, Paula Alvarez, Norma Calleja, Ignacio Braña, Stefanie Burger, Estefanía Pardo, Marta Loredo, Sara Alonso, Valentina Chiminazzo, Mercedes Alperi\",\"doi\":\"10.55563/clinexprheumatol/8gl4ja\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>We aimed to analyse psoriatic arthritis (PsA) features based on psoriasis-arthritis lag times: simultaneous (S), psoriasis first (PF), arthritis first (AF).</p><p><strong>Methods: </strong>We carried out an inception cohort study involving 340 PsA patients. Phenotypic differences between patients were analysed based on the three disease latency models identified in the study. A post-hoc correction of significant p-values was applied by the Benjamini-Hochberg method.</p><p><strong>Results: </strong>Forty-five (13.2%) patients had S onset, 97 (28.5%) manifested AF, while in 198 (58.2%) psoriasis appeared first. Lag times were markedly different between PF (16.3 ±12.4 years) and AF (5.4 ±2.8 years) groups, p<0.001. The AF group presented less frequently the classic arthritogenic psoriasis pattern: nail (18.8%, p<0.001), scalp (28.1%, p=0.001), folds (10.9%, p=0.009), and ≥3 psoriasis body areas (18.8%, p<0.001), but showed more psoriasis family history (67.6%, p=0.001) and a milder overall joint phenotype. The S group associated a worse cardiometabolic profile and developed more dactylitis (44%, p=0.012) during follow-up. The PF group was younger at psoriasis onset (p<0.001), had more extensive psoriasis (p<0.001), and higher frequency of HLA-Cw6 positivity (43.2%). Within the PF group, patients with axial onset [median 19.0 years (IQR: 10.5-25.5)] had a longer psoriasis-arthritis latency compared to other onset forms [median 14.0 years (IQR: 5-24)].</p><p><strong>Conclusions: </strong>In this study, substantial phenotypic differences were identified based on the three PsA lag time models. In addition, the classic pattern of arthritogenic psoriasis did not prevail in the same way between these groups, which was novel.</p>\",\"PeriodicalId\":10274,\"journal\":{\"name\":\"Clinical and experimental rheumatology\",\"volume\":\" \",\"pages\":\"889-896\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical and experimental rheumatology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.55563/clinexprheumatol/8gl4ja\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/5 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"RHEUMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and experimental rheumatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.55563/clinexprheumatol/8gl4ja","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/5 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
Psoriatic arthritis phenotype may vary depending on whether the skin or joint domain appears first or whether both appear simultaneously.
Objectives: We aimed to analyse psoriatic arthritis (PsA) features based on psoriasis-arthritis lag times: simultaneous (S), psoriasis first (PF), arthritis first (AF).
Methods: We carried out an inception cohort study involving 340 PsA patients. Phenotypic differences between patients were analysed based on the three disease latency models identified in the study. A post-hoc correction of significant p-values was applied by the Benjamini-Hochberg method.
Results: Forty-five (13.2%) patients had S onset, 97 (28.5%) manifested AF, while in 198 (58.2%) psoriasis appeared first. Lag times were markedly different between PF (16.3 ±12.4 years) and AF (5.4 ±2.8 years) groups, p<0.001. The AF group presented less frequently the classic arthritogenic psoriasis pattern: nail (18.8%, p<0.001), scalp (28.1%, p=0.001), folds (10.9%, p=0.009), and ≥3 psoriasis body areas (18.8%, p<0.001), but showed more psoriasis family history (67.6%, p=0.001) and a milder overall joint phenotype. The S group associated a worse cardiometabolic profile and developed more dactylitis (44%, p=0.012) during follow-up. The PF group was younger at psoriasis onset (p<0.001), had more extensive psoriasis (p<0.001), and higher frequency of HLA-Cw6 positivity (43.2%). Within the PF group, patients with axial onset [median 19.0 years (IQR: 10.5-25.5)] had a longer psoriasis-arthritis latency compared to other onset forms [median 14.0 years (IQR: 5-24)].
Conclusions: In this study, substantial phenotypic differences were identified based on the three PsA lag time models. In addition, the classic pattern of arthritogenic psoriasis did not prevail in the same way between these groups, which was novel.
期刊介绍:
Clinical and Experimental Rheumatology is a bi-monthly international peer-reviewed journal which has been covering all clinical, experimental and translational aspects of musculoskeletal, arthritic and connective tissue diseases since 1983.