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1.
Rheumatol Int ; 42(4): 651-657, 2022 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-35152321

RESUMEN

The association between psoriatic arthritis (PsA) and psoriasis is well known, but some have suggested that other musculoskeletal (MSK) conditions might also be more common in patients with skin psoriasis compared with the general population. The aim of our study was to describe the prevalence of a large panel of MSK conditions, in consecutive patients with psoriasis according to skin phenotype. This was a cross-sectional study. We consecutively included 148 patients, consulting for their skin psoriasis, in the dermatology department of a tertiary hospital, Hospital Cochin in Paris, France. After the scheduled consultation with a dermatologist, a rheumatologist conducted a dedicated face-to-face interview to collected data, included demographics, comorbidities, information about the psoriasis, the MSK conditions and their treatments. Of the 148 patients, 122 (82%) had at least one MSK condition. The most common condition was mechanical back pain, present in 98 (66%) patients. Nineteen (13%) patients had spondyloarthritis (SpA), of which 95% had PsA. For all MSK conditions, the dominant psoriasis phenotype was psoriasis vulgaris. The prevalence of the other phenotypes of psoriasis differed by disease. In SpA patients, the three predominant psoriasis phenotypes were: psoriasis vulgaris (82%), scalp involvement (76%) and inverse psoriasis (65%). For all MSK diseases, the prevalence was higher than expected in the general population. Our data suggest that skin psoriasis is associated with different MSK diseases, and not only PsA.


Asunto(s)
Artritis Psoriásica , Enfermedades Musculoesqueléticas , Psoriasis , Artritis Psoriásica/diagnóstico , Artritis Psoriásica/epidemiología , Estudios Transversales , Humanos , Enfermedades Musculoesqueléticas/diagnóstico , Enfermedades Musculoesqueléticas/epidemiología , Prevalencia , Psoriasis/epidemiología
2.
Acta Derm Venereol ; 100(18): adv00316, 2020 11 04.
Artículo en Inglés | MEDLINE | ID: mdl-33111960

RESUMEN

Anti-interleukin-17 agents have recently been developed for the treatment of psoriasis. This study evaluated the tolerance and effectiveness of anti-interleukin-17 agents for psoriasis in elderly patients in daily practice. A multicentre, retrospective study was performed, involving psoriatic patients aged ≥65 years who had received an anti-interleukin-17 agent, including secukinumab, ixekizumab or brodalumab. A total of 114 patients were included: 72 received secukinumab, 35 ixekizumab, and 7 brodalumab. Treatment was stopped in 32 patients (28.9%), because of relapses in 14 patients (41.2%), primary failures in 11 patients (32.4%), or adverse events in 7 patients (20.6%). The 3 most frequently reported adverse events were injection site reactions (n = 4), oral candidiasis (n = 3), and influenza-like illness (n = 3). Regarding effectiveness, 80 patients (70%) reached a Physician Global Assessment score of 0/1, 6 months after treatment initiation. In conclusion, anti-interleukin-17 therapy appears to be an effective and safe therapeutic option for psoriasis treatment in patients aged ≥ 65 years.


Asunto(s)
Anticuerpos Monoclonales , Psoriasis , Anciano , Anticuerpos Monoclonales/efectos adversos , Humanos , Inmunoterapia , Psoriasis/diagnóstico , Psoriasis/tratamiento farmacológico , Estudios Retrospectivos , Resultado del Tratamiento
3.
Rev Prat ; 68(9): 966-971, 2018 Nov.
Artículo en Francés | MEDLINE | ID: mdl-30869350

RESUMEN

Clinical evaluation of a psoriatic patient. Psoriasis is a frequent and burdening inflammatory dermatosis. It affects the quality of life of patients in a deep and sustained way, even if the disease is not very extensive. As we now have an array of very effective treatments, it is important to be able to evaluate the objective and subjective severity of the dermatosis, in order to choose the optimal therapeutic goal for each patient. Of course, an associated psoriasis arthritis must be sought because it will influence the choice of treatment. There is a growing body of evidence suggesting a link between psoriasis and a number of comorbidities such as metabolic syndrome, diabetes, increased cardiovascular risk, depression, etc. In order for the patient to be fully taken care of, these risks must be detected and prevented.


Évaluation clinique d'un patient atteint de psoriasis. Le psoriasis est une dermatose inflammatoire fréquente et affichante. Elle grève la qualité de vie des patients de façon durable et profonde, même si l'atteinte n'est pas très étendue. À l'heure où nous disposons de nombreux traitements très efficaces, il est important de savoir évaluer la sévérité objective et ressentie d'un psoriasis, pour décider au mieux de l'objectif thérapeutique à atteindre pour un patient donné. Bien entendu, la présence ou non d'une atteinte rhumatologique doit être recherchée car elle influence le choix du traitement. De plus en plus de travaux évoquent un lien entre le psoriasis et un certain nombre de comorbidités comme le syndrome métabolique, le diabète, un risque cardiovasculaire accru, la dépression… Afin que le patient soit pris en charge dans sa globalité ces facteurs de risque doivent être dépistés et prévenus.


Asunto(s)
Artritis Psoriásica , Síndrome Metabólico , Psoriasis , Comorbilidad , Humanos , Calidad de Vida
4.
Eur J Immunol ; 41(9): 2596-605, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21688259

RESUMEN

The ontogenic relationship between pro-inflammatory populations of interleukin-17 (IL-17A)- and/or IL-22-producing T cells and other T-cell subsets is currently unclear in humans. To appreciate T helper cell-lineage commitment, we combined cytokine production profiles of in vitro expanded T-cell clones with T-cell receptor (TCR) clonotypic signatures. Moreover, ex vivo cytokine production profiles at the single-cell level were analyzed using an original approach based on the hierarchical cluster analysis of multiparametric flow cytometry data. These combined approaches enabled the delineation of distinct functional T-cell subsets, including Th1, Th2, Tr1, Th17 cells and a highly polyfunctional IL-22-producing T-cell population. Cluster analysis highlighted that the IL-22-producing T-cell population should be considered independently from the Th17 and Th1 subsets, although it was more closely related to the former. In parallel, we observed extensive TCRαß sharing across all five subsets defined. The strategy described here allows the objective definition of cellular subsets and an unbiased insight into their similarities. Together, our results underscore the ontogenic plasticity of CD4(+) T-cell progenitors, which can adopt a differentiation profile irrespective of antigen specificity.


Asunto(s)
Interleucina-17/metabolismo , Interleucinas/metabolismo , Subgrupos de Linfocitos T/metabolismo , Células TH1/metabolismo , Células Th2/metabolismo , Antígenos de Diferenciación/metabolismo , Diferenciación Celular , Linaje de la Célula , Separación Celular , Células Clonales , Citometría de Flujo , Humanos , Inmunofenotipificación/métodos , Receptores de Antígenos de Linfocitos T/metabolismo , Especificidad del Receptor de Antígeno de Linfocitos T , Subgrupos de Linfocitos T/citología , Subgrupos de Linfocitos T/inmunología , Células TH1/citología , Células TH1/inmunología , Células Th2/citología , Células Th2/inmunología , Interleucina-22
5.
Rev Prat ; 54(1): 56-9, 2004 Jan 15.
Artículo en Francés | MEDLINE | ID: mdl-15049602

RESUMEN

Even though systemic immunomodulating or immunosuppressive therapies have shown efficacy in patients with psoriasis, their usage remains restricted to patients with severe, refractory forms of the disease. Indeed, the risk/benefit balance should be cautiously taken into account before prescribing such drugs. Nevertheless, risks inherent to their usage are limited by a careful knowledge of prescription rules and by a monitoring of side effects.


Asunto(s)
Adyuvantes Inmunológicos/efectos adversos , Adyuvantes Inmunológicos/uso terapéutico , Inmunosupresores/efectos adversos , Inmunosupresores/uso terapéutico , Psoriasis/tratamiento farmacológico , Humanos , Psoriasis/inmunología , Índice de Severidad de la Enfermedad
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