2021
DOI: 10.1186/s13075-021-02545-4
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Clinical, laboratory, and genetic markers for the development or presence of psoriatic arthritis in psoriasis patients: a systematic review

Abstract: Twenty to thirty percent of psoriasis (Pso) patients will develop psoriatic arthritis (PsA). Detection of Pso patients that are (at risk for) developing PsA is essential to prevent structural damage. We conducted a systematic search of five bibliographic databases, up to May 2020. We searched for studies assessing markers (clinical, laboratory, genetic) associated with the development or presence of PsA in Pso patients. Study selection and quality assessment of the included studies was performed, followed by a… Show more

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Cited by 28 publications
(31 citation statements)
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References 136 publications
(255 reference statements)
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“…Recent consensus guidelines for managing psoriasis recommend using questionnaires to screen for the presence of PsA, and Salaff et al (176) developed a self-administered questionnaire, called Simple Psoriatic Arthritis Screening (SiPAS), which screens psoriasis patients for signs and symptoms of PsA with compared high sensibility and specificity. In a systematic review, 259 possible markers associated with the development or presence of PsA in patients with psoriasis were identified in 119 studies (177). Laboratory markers related to inflammation and bone metabolism showed a strong association (not prediction) of PsA in psoriasis, however only C-X-C motif ligand 10 reached a strong level of evidence for a positive predictive value (177), but whether these indicators are clinically useful remains to be further investigated.…”
Section: Psamentioning
confidence: 99%
See 1 more Smart Citation
“…Recent consensus guidelines for managing psoriasis recommend using questionnaires to screen for the presence of PsA, and Salaff et al (176) developed a self-administered questionnaire, called Simple Psoriatic Arthritis Screening (SiPAS), which screens psoriasis patients for signs and symptoms of PsA with compared high sensibility and specificity. In a systematic review, 259 possible markers associated with the development or presence of PsA in patients with psoriasis were identified in 119 studies (177). Laboratory markers related to inflammation and bone metabolism showed a strong association (not prediction) of PsA in psoriasis, however only C-X-C motif ligand 10 reached a strong level of evidence for a positive predictive value (177), but whether these indicators are clinically useful remains to be further investigated.…”
Section: Psamentioning
confidence: 99%
“…In a systematic review, 259 possible markers associated with the development or presence of PsA in patients with psoriasis were identified in 119 studies (177). Laboratory markers related to inflammation and bone metabolism showed a strong association (not prediction) of PsA in psoriasis, however only C-X-C motif ligand 10 reached a strong level of evidence for a positive predictive value (177), but whether these indicators are clinically useful remains to be further investigated.…”
Section: Psamentioning
confidence: 99%
“…It has been postulated that the initiation of PsA occurs after triggering by environmental factors in gut, entheses, or skin in patients who are genetically more susceptible to development of this disease (37). The genetics of PsA have been reviewed in detail (38)(39)(40)(41). In short, both HLA and non-HLA coding genes are associated with PsA.…”
Section: Initiation Of Psoriatic Arthritismentioning
confidence: 99%
“…In the non-HLA coding groups genes are related to innate immunity, cytokines (TNF, IFN, and IL-23/17) and antigen processing and presentation (38). However, genes that are specifically associated with development of PsA in PsO patients remain scarce (39). Two HLA-B27 haplotypes (C * 01 and C * 02, respectively) (42,43) and IL13 gene polymorphism were suggested to be independent associated with PsA development in PsO patients (44,45).…”
Section: Initiation Of Psoriatic Arthritismentioning
confidence: 99%
“…The top 25 most common DEGs in the suprabasal keratinocytes between GSE151177 and GSE162183 both included IL36G , a keratinocyte-derived cytokine known as an important factor in psoriasis pathogenesis ( Figures 3C, D ). The increased presence of IL-36 in was mainly seen in the suprabasal layer of psoriatic epidermis ( Figure 3E , Supplementary Figure 3E ) As strong IL-23R expression is detected in psoriatic epidermis ( 13 ), we presumed that IL-23 might be associated with IL-36 production. We used HaCaT and JurkaT cell lines to check the possible association between IL-23 and IL-36 γ.…”
Section: Resultsmentioning
confidence: 87%