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1.
J Eur Acad Dermatol Venereol ; 38(9): 1783-1790, 2024 Sep.
Article in English | MEDLINE | ID: mdl-38153843

ABSTRACT

BACKGROUND: Prediction of the response to a biological treatment in psoriasis patients would allow efficient treatment allocation. OBJECTIVE: To identify polymorphisms associated with secukinumab response in psoriasis patients in a daily practice setting. METHODS: We studied 180 SNPs in patients with moderate-to-severe plaque psoriasis recruited from 15 Spanish hospitals. Treatment effectiveness was evaluated by absolute PASI ≤3 and ≤1 at 6 and 12 months. Individuals were genotyped using a custom Taqman array. Multiple logistic regression models were generated. Sensitivity, specificity and area under the curve (AUC) were analysed. RESULTS: A total of 173 patients were studied at 6 months, (67% achieved absolute PASI ≤ 3 and 65% PASI ≤ 1) and 162 at 12 months (75% achieved absolute PASI ≤ 3 and 64% PASI ≤ 1). Multivariable analysis showed the association of different sets of SNPs with the response to secukinumab. The model of absolute PASI≤3 at 6 months showed best values of sensitivity and specificity. Four SNPs were associated with the capability of achieving absolute PASI ≤ 3 at 6 months. rs1801274 (FCGR2A), rs2431697 (miR-146a) and rs10484554 (HLCw6) were identified as risk factors for failure to achieve absolute PASI≤3, while rs1051738 (PDE4A) was protective. AUC including these genotypes, weight of patients and history of biological therapy was 0.88 (95% CI 0.83-0.94), with a sensitivity of 48.6% and specificity of 95.7% to discriminate between both phenotypes. CONCLUSION: We have identified a series of polymorphisms associated with the response to secukinumab capable of predicting the potential response/non-response to this drug in patients with plaque psoriasis.


Subject(s)
Antibodies, Monoclonal, Humanized , Polymorphism, Single Nucleotide , Psoriasis , Humans , Psoriasis/drug therapy , Psoriasis/genetics , Female , Male , Antibodies, Monoclonal, Humanized/therapeutic use , Middle Aged , Adult , Dermatologic Agents/therapeutic use , MicroRNAs/genetics , Severity of Illness Index , Treatment Outcome
2.
Actas Dermosifiliogr ; 115(1): T1-T9, 2024 Jan.
Article in English, Spanish | MEDLINE | ID: mdl-37923068

ABSTRACT

BACKGROUND AND OBJECTIVE: The treatment of psoriasis should not only focus on skin affectations but also weigh the parameters for health-related quality of life (HRQoL), thereby tackling the concept of cumulative life course impairment (CLCI) and treating the patient from a holistic perspective. The CRYSTAL study aimed to characterize psoriasis with real-word data from Spanish clinical practice in patients with moderate to severe disease who received continuous systemic treatment for at least 24 weeks by using the absolute Psoriasis Area and Severity Index (PASI) score and its correlation to HRQoL. MATERIAL AND METHODS: This was a non-interventional, cross-sectional study conducted in 30 centers in Spain, with 301 patients between the ages of 18 and 75 years. The study collected data regarding current treatment and absolute PASI and their relationship to HRQoL using the Dermatology Life Quality Index (DLQI), to activity impairment using the Work Productivity and Activity Impairment (WPAI) questionnaire, and to treatment satisfaction. RESULTS: The mean (SD) age was 50.5 (12.5) years, with a duration of disease of 14 (14.1) years. The mean (SD) absolute PASI reported was 2.3 (3.5), with 28.7% of patients presenting with PASI from >1 to ≤3 and 22.6% with PASI>3. Higher PASI scores were associated with higher DLQI (p<0.001) and WPAI scores and lower levels of treatment satisfaction (p<0.001). CONCLUSIONS: These data indicate that achieving lower absolute PASI values may correlate not only with better HRQoL but also with better work productivity and treatment satisfaction.


Subject(s)
Psoriasis , Quality of Life , Humans , Adolescent , Young Adult , Adult , Middle Aged , Aged , Spain/epidemiology , Cross-Sectional Studies , Psoriasis/complications , Psoriasis/drug therapy , Skin , Severity of Illness Index , Treatment Outcome
3.
Actas Dermosifiliogr ; 115(1): 1-9, 2024 Jan.
Article in English, Spanish | MEDLINE | ID: mdl-37429433

ABSTRACT

BACKGROUND AND OBJECTIVE: The treatment of psoriasis should not only focus on skin affectations but also weigh the parameters for health-related quality of life (HRQoL), thereby tackling the concept of cumulative life course impairment (CLCI) and treating the patient from a holistic perspective. The CRYSTAL study aimed to characterize psoriasis with real-word data from Spanish clinical practice in patients with moderate to severe disease who received continuous systemic treatment for at least 24 weeks by using the absolute Psoriasis Area and Severity Index (PASI) score and its correlation to HRQoL. MATERIAL AND METHODS: This was a non-interventional, cross-sectional study conducted in 30 centers in Spain, with 301 patients between the ages of 18 and 75 years. The study collected data regarding current treatment and absolute PASI and their relationship to HRQoL using the Dermatology Life Quality Index (DLQI), to activity impairment using the Work Productivity and Activity Impairment (WPAI) questionnaire, and to treatment satisfaction. RESULTS: The mean (SD) age was 50.5 (12.5) years, with a duration of disease of 14 (14.1) years. The mean (SD) absolute PASI reported was 2.3 (3.5), with 28.7% of patients presenting with PASI from >1 to ≤3 and 22.6% with PASI>3. Higher PASI scores were associated with higher DLQI (p<0.001) and WPAI scores and lower levels of treatment satisfaction (p<0.001). CONCLUSIONS: These data indicate that achieving lower absolute PASI values may correlate not only with better HRQoL but also with better work productivity and treatment satisfaction.


Subject(s)
Psoriasis , Quality of Life , Humans , Adolescent , Young Adult , Adult , Middle Aged , Aged , Spain/epidemiology , Cross-Sectional Studies , Psoriasis/complications , Psoriasis/drug therapy , Skin , Severity of Illness Index , Treatment Outcome
4.
Climacteric ; 25(2): 195-202, 2022 Apr.
Article in English | MEDLINE | ID: mdl-34323137

ABSTRACT

BACKGROUND: Dementia is a major public health problem. Estrogen is a regulator of the central nervous system and its deficit could be involved in cognitive decline in older women. OBJECTIVE: This study aimed to evaluate the association of bilateral oophorectomy, menopause hormone therapy (MHT) and other factors on mild cognitive impairment (MCI). METHOD: The case-control study included 941 otherwise healthy postmenopausal women aged 60 years and over from six Latin American countries. Personal and family data were recorded and MCI was assessed using the Montreal Cognitive Assessment test (MoCA). RESULTS: Average age, years of education and body mass index were 66.1 ± 5.8 years, 12.4 ± 5.0 years and 26.0 ± 4.3 kg/m2, respectively. A total of 30.2% had undergone bilateral oophorectomy and 40.3% had used MHT. A total of 232 women (24.7%) had MCI. The prevalence of MCI was higher in women with intact ovaries and non-MHT users as compared to MHT users (29.3% vs. 11.7% [odds ratio (OR) 0.32; 95% confidence interval (CI) 0.20-0.51]). Among oophorectomized women, MCI prevalence was higher among non-MHT users as compared to MHT users (45.2% vs. 12.8% [OR 0.18; 95% CI 0.10-0.32]). Logistic regression analysis determined that the variables associated with MCI were age >65 years (OR 1.69; 95% CI 1.20-2.38), parity (having >2 children; OR 1.69; 95% CI 1.21-2.37), bilateral oophorectomy (OR 1.56; 95% CI 1.09-2.24), hypertension (OR 1.41; 95% CI 1.01-1.96), being sexually active (OR 0.56; 95% CI 0.40-0.79), education >12 years (OR 0.46; 95% CI 0.32-0.65) and MHT use (OR 0.31; 95% CI 0.21-0.46). CONCLUSION: Age, parity, bilateral oophorectomy and hypertension are independent factors associated with MCI; contrary to this, higher educational level, maintaining sexual activity and using MHT are protective factors.


Subject(s)
Cognitive Dysfunction , Hypertension , Aged , Case-Control Studies , Child , Cognitive Dysfunction/epidemiology , Female , Hormone Replacement Therapy , Humans , Menopause , Middle Aged , Ovariectomy
5.
J Eur Acad Dermatol Venereol ; 34(12): 2821-2829, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32271966

ABSTRACT

BACKGROUND: Little has been published on the real-world effectiveness and safety of apremilast in psoriasis. OBJECTIVES: To evaluate the effectiveness, safety and drug survival of apremilast at 52 weeks in patients with moderate to severe plaque psoriasis or palmoplantar psoriasis in routine clinical practice. METHODS: Retrospective, multicentre study of adult patients with moderate to severe plaque psoriasis or palmoplantar psoriasis treated with apremilast from March 2016 to March 2018. RESULTS: We studied 292 patients with plaque psoriasis and 85 patients with palmoplantar psoriasis. The mean (SD) Psoriasis Area and Severity Index (PASI) score was 10.7 (7.0) at baseline and 3.0 (4.2) at 52 weeks. After 12 months of treatment, 73.6% of patients had a PASI score of 3 or less. In terms of relative improvement by week 52, 49.7% of patients achieved PASI-75 (≥75% reduction in PASI score) and 26.5% achieved PASI-90. The mean physician global assessment score for palmoplantar psoriasis fell from 4.2 (5.2) at baseline to 1.3 (1.3) at week 52. Overall drug survival after 1 year of treatment with apremilast was 54.9 %. The main reasons for treatment discontinuation were loss of efficacy (23.9%) and adverse events (15.9%). Almost half of the patients in our series (47%) experienced at least one adverse event. The most common events were gastrointestinal problems. CONCLUSIONS: Apremilast may be a suitable alternative for the treatment of moderate to severe psoriasis and palmoplantar psoriasis. Although the drug has a good safety profile, adverse gastrointestinal effects are common.


Subject(s)
Psoriasis , Thalidomide , Adult , Humans , Psoriasis/drug therapy , Retrospective Studies , Severity of Illness Index , Thalidomide/adverse effects , Thalidomide/analogs & derivatives , Treatment Outcome
6.
J Eur Acad Dermatol Venereol ; 33(3): 553-559, 2019 Mar.
Article in English | MEDLINE | ID: mdl-30317679

ABSTRACT

BACKGROUND: Ixekizumab (anti-IL17A) is effective as treatment for moderate-to-severe plaque psoriasis, but real-life data on effectiveness and safety are currently very limited. OBJECTIVE: To evaluate the efficacy and safety of ixekizumab in a cohort of real-life plaque psoriasis patients. METHODS: Retrospective chart review of 100 patients with moderate-to-severe plaque psoriasis treated with ixekizumab at seven Spanish dermatological centres. RESULTS: According to the as observed analysis, the percentage of patients achieving a 75% and 90% of reduction from the baseline score of Psoriasis Area and Severity Index (PASI) was 87.5%-50.0% at week 12-16; 88.3%-58.4% at week 24 and 82.9%-58.5% at week 52, respectively. The mean ± standard deviation (SD) score of PASI at baseline was 12.9 ± 9.2, and it declined rapidly after ixekizumab administration to 1.9 ± 4.0 (P < 0.001) at week 12-16 and was maintained at 1.7 ± 4.1 and 1.8 ± 2.9 at week 24 and 52, respectively. Ixekizumab response was not affected by clinical variables like body mass index, disease duration or the presence of psoriatic arthritis. However, the bio-naive group showed significantly higher PASI 75 response rate at week 12-16 compared to patients previously exposed to biologic agents (P = 0.037). Twenty-six (26%) patients experienced adverse events (AEs) during the follow-up period, being most of them of mild-to-moderate intensity. The most common AE was local reaction at the site of injection (14/26; 53.8%). At the end of the observational period, 15 (15%) patients discontinued ixekizumab treatment due to limited clinical improvement (n = 11), adverse events (n = 3) or lost to follow-up (n = 1) within a mean ± SD time of 6.0 ± 3.9 months. CONCLUSION: The present study illustrates the initial experience with ixekizumab in real-world clinical practice confirming its usefulness and safety in the management of plaque psoriasis patients.


Subject(s)
Antibodies, Monoclonal, Humanized/therapeutic use , Dermatologic Agents/therapeutic use , Psoriasis/drug therapy , Adult , Antibodies, Monoclonal, Humanized/adverse effects , Biological Products/therapeutic use , Dermatologic Agents/adverse effects , Female , Humans , Injection Site Reaction/etiology , Male , Middle Aged , Retreatment , Retrospective Studies , Severity of Illness Index
7.
Actas Dermosifiliogr ; 108(10): 924-930, 2017 Dec.
Article in English, Spanish | MEDLINE | ID: mdl-28803615

ABSTRACT

INTRODUCTION AND OBJECTIVES: The Early Arthritis for Psoriatic patients (EARP) questionnaire is a screening tool for psoriatic arthritis. The original Italian version has good measurement properties but the EARP required translation and adaptation for use in Spain. This article describes the cultural adaptation process as a step prior to validation. MATERIAL AND METHODS: We used the principles of good practice for the cross-cultural adaptation of patient-reported outcomes measurement established by the International Society Pharmacoeconomics and Outcome Research. The steps in this process were preparation, forward translation, reconciliation, back-translation and review, harmonization, cognitive debriefing and review, and proofreading. During preparation the developers of the original questionnaire were asked for their permission to adapt the EARP for use in Spain and to act as consultants during the process. RESULTS: The original questionnaire was translated into Spanish by native Spanish translators, who made slight changes that were approved by the questionnaire's developers. The Spanish version was then back-translated into Italian; that version was reviewed to confirm equivalence with the original Italian text. The reconciled Spanish EARP was then tested for comprehensibility and interpretation in a group of 35 patients. All the patients answered all items without making additional comments. CONCLUSION: This cultural adaptation of the EARP questionnaire for Spanish populations is the first step towards its later use in routine clinical practice. The application of a cross-cultural adaptation method ensured equivalence between the original and Spanish versions of the EARP. The Spanish questionnaire will be validated in a second stage.


Subject(s)
Arthritis, Psoriatic/diagnosis , Surveys and Questionnaires , Adult , Aged , Cultural Characteristics , Culturally Competent Care , Early Diagnosis , Educational Status , Female , Humans , Language , Male , Middle Aged , Spain , Translations
8.
Appl Environ Microbiol ; 82(10): 3092-9, 2016 05 15.
Article in English | MEDLINE | ID: mdl-27016572

ABSTRACT

UNLABELLED: Avian botulism kills thousands of waterbirds every year, including endangered species, but information about the differences between species in vulnerability to botulism outbreaks and the capacity to act as carriers of Clostridium botulinum is still poorly known. Here, we estimated the vulnerability to botulism of 11 waterbird species from Mediterranean wetlands by comparing the number of affected birds with the census of individuals at risk. The capacity of different species to act as carriers was studied by detecting the presence of the C. botulinum type C/D botulinum neurotoxin (BoNT) gene in fecal samples and prey items of waterbirds in the wild and by the serial sampling of cloacal swabs of birds affected by botulism. We found differences among species in their vulnerabilities to botulism, probably related to feeding habits, season of arrival, turnover, and, possibly, phylogenetic resilience. The globally endangered white-headed duck (Oxyura leucocephala) showed mortality rates in the studied outbreaks of 7% and 17% of the maximum census, which highlights botulism as a risk factor for the conservation of the species. Invasive water snails, such as Physa acuta, may be important drivers in botulism epidemiology, because 30% of samples tested positive for the BoNT gene during outbreaks. Finally, our results show that birds may excrete the pathogen for up to 7 days, and some individuals can do it for longer periods. Rails and ducks excreted C. botulinum more often and for longer times than gulls, which could be related to their digestive physiology (i.e., cecum development). IMPORTANCE: Botulism is an important cause of mortality in waterbirds, including some endangered species. The global climate change may have consequences in the ecology of wetlands that favor the occurrence of botulism outbreaks. Here, we offer some information to understand the ecology of this disease that can be useful to cope with these global changes in the future. We have found that some species (i.e., coots and dabbling ducks) are more vulnerable to botulism and have a more relevant role in the onset and amplification of the outbreaks than other species (i.e., flamingos and grebes). Feeding habits can explain these differences in part; in addition to the well-known role of necrophagous fly maggots, we found here that water snails are frequent carriers of Clostridium botulinum This is relevant, because these water snails can thrive in eutrophic and polluted wetlands, exacerbating other changes driven by climate change in wetlands.


Subject(s)
Bird Diseases/epidemiology , Botulism/veterinary , Carrier State/veterinary , Clostridium botulinum/isolation & purification , Disease Outbreaks , Disease Susceptibility , Animals , Bacterial Shedding , Birds , Botulinum Toxins/genetics , Botulism/epidemiology , Carrier State/epidemiology , Clostridium botulinum/classification , Clostridium botulinum/genetics , Feces/microbiology , Mediterranean Region/epidemiology , Snails/microbiology , Time Factors , Wetlands
9.
Actas Dermosifiliogr ; 107(3): 194-206, 2016 Apr.
Article in English, Spanish | MEDLINE | ID: mdl-26614486

ABSTRACT

Methotrexate (MTX) is the most frequently used conventional systemic drug in the treatment of psoriasis. Despite over 50years of experience in this setting, certain aspects of the use of this drug in clinical practice are still little standardized and poorly understood. For this reason, a group of 15 experts took part in a consensus development conference to achieve consensus on a series of recommendations on the use of MTX in psoriasis. The guidelines, which were developed on the basis of a systematic review of the literature, were validated by 2 rounds of voting and categorized by level of evidence and grade of recommendation. Before MTX can be used to treat moderate to severe psoriasis, the patient must be evaluated to assess the suitability of the treatment, including consideration of vaccination status and screening for tuberculosis and pregnancy. The recommended starting dose for a patient with no risk factors is 10 to 20mg/wk, the therapeutic dose for most patients is 15mg/wk, and the maximum dose is 20mg/wk. Most patients who respond to treatment will show improvement within 8weeks. Parenteral administration of MTX is desirable when there is a risk of erroroneous dosing, nonadherence, gastrointestinal intolerance, or inadequate response to the therapeutic dose taken orally. Noninvasive methods are preferred for monitoring hepatotoxicity. MTX is a good treatment option for patients with a history of cancer, but is not recommended in patients with chronic hepatitisB infection or individuals who are seropositive for human immunodeficiency virus.


Subject(s)
Methotrexate/therapeutic use , Psoriasis/drug therapy , Contraindications , HIV Infections , Hepatitis B, Chronic , Humans , Neoplasms , Practice Guidelines as Topic , Risk Factors
10.
Actas Dermosifiliogr ; 106 Suppl 1: 60-6, 2015 Nov.
Article in Spanish | MEDLINE | ID: mdl-26895940

ABSTRACT

Nail diseases are a diagnostic challenge and high-frequency ultrasound with colour Doppler is a simple and painless diagnostic test that can often be useful. Ultrasound allows real-time evaluation of the anatomical structures of the nail and its vascularisation. The present study reviews the literature on ultrasound findings in the normal nail and in inflammatory and tumoural disease.


Subject(s)
Nail Diseases/diagnostic imaging , Ultrasonography , Humans , Nail Diseases/therapy , Nails/diagnostic imaging
11.
Curr Biol ; 34(3): 615-622.e4, 2024 02 05.
Article in English | MEDLINE | ID: mdl-38199065

ABSTRACT

Convergent extension (CE) requires the coordinated action of the planar cell polarity (PCP) proteins1,2 and the actin cytoskeleton,3,4,5,6 but this relationship remains incompletely understood. For example, PCP signaling orients actomyosin contractions, yet actomyosin is also required for the polarized localization of PCP proteins.7,8 Moreover, the actin-regulating Septins play key roles in actin organization9 and are implicated in PCP and CE in frogs, mice, and fish5,6,10,11,12 but execute only a subset of PCP-dependent cell behaviors. Septin loss recapitulates the severe tissue-level CE defects seen after core PCP disruption yet leaves overt cell polarity intact.5 Together, these results highlight the general fact that cell movement requires coordinated action by distinct but integrated actin populations, such as lamella and lamellipodia in migrating cells13 or medial and junctional actin populations in cells engaged in apical constriction.14,15 In the context of Xenopus mesoderm CE, three such actin populations are important, a superficial meshwork known as the "node-and-cable" system,4,16,17,18 a contractile network at deep cell-cell junctions,6,19 and mediolaterally oriented actin-rich protrusions, which are present both superficially and deeply.4,19,20,21 Here, we exploited the amenability of the uniquely "two-dimensional" node and cable system to probe the relationship between PCP proteins, Septins, and the polarization of this actin network. We find that the PCP proteins Vangl2 and Prickle2 and Septins co-localize at nodes, and that the node and cable system displays a cryptic, PCP- and Septin-dependent anteroposterior (AP) polarity in its organization and dynamics.


Subject(s)
Actins , Septins , Mice , Animals , Septins/metabolism , Actins/metabolism , Actomyosin/metabolism , Actin Cytoskeleton/metabolism , Cell Movement/physiology , Cell Polarity/physiology , Membrane Proteins/metabolism , LIM Domain Proteins/metabolism
12.
Actas Dermosifiliogr ; 104(5): 400-8, 2013 Jun.
Article in English, Spanish | MEDLINE | ID: mdl-23669590

ABSTRACT

BACKGROUND: Although national guidelines on biologic agents for treating moderate to severe psoriasis in adults have been published in several countries, increased knowledge on the practical aspects of their implementation is required. OBJECTIVE: The objective of this study was to survey Spanish dermatologists to determine their expert opinions on practical aspects of psoriasis treatment with biologics. MATERIALS AND METHODS: An online survey was sent to 309 dermatologists who belong to the Spanish Psoriasis Group and/or the Spanish Academy of Dermatology and Venereology (AEDV). The questionnaire was designed specifically for the study and included items on various aspects of the treatment of psoriasis in clinical practice. Six coordinators in different geographic areas worked together to write the final expert report. RESULTS: The response rate was 97% (300 returned questionnaires). The biologics preferred, or considered to be the best option (median score 4 out of 4 points) by respondents, were infliximab for its short-term efficacy (74% of the respondents) and rapid onset of action (78%); ustekinumab for convenience of administration (73%); and etanercept because of its suitability for cyclic treatment (71%), safety in long-term use (72%), and the possibility of temporary interruption of treatment under certain circumstances (76%). Etanercept was assigned the highest evaluations for safety and expected survival time (scored 5 on each item by 49% and 33% of the respondents, respectively). Thirty percent of the respondents considered that clinical guidelines contain important information for therapeutic management of psoriasis. CONCLUSIONS: This study provides a unique perspective on the opinions of a large sample of dermatologists as regards current treatment of psoriasis with biologics in Spain.


Subject(s)
Attitude of Health Personnel , Biological Factors/therapeutic use , Dermatology , Practice Patterns, Physicians' , Psoriasis/drug therapy , Adult , Aged , Female , Humans , Male , Middle Aged , Severity of Illness Index , Spain , Surveys and Questionnaires
13.
Actas Dermosifiliogr ; 104(7): 598-616, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23891453

ABSTRACT

Phototherapy, classic systemic treatments (methotrexate, acitretin, and ciclosporin), and biologic agents (etanercept, infliximab, adalimumab, and ustekinumab) constitute a broad therapeutic arsenal that increases the likelihood of achieving control of severe and extensive disease in patients with psoriasis. Acitretin continues to be a very valuable tool in both monotherapy, in which it is combined with other systemic treatments (classic or biologic), and in sequential therapy. Thanks to its lack of a direct immunosuppressive effect and its ability to achieve a long-term response, acitretin has an important role in the treatment of psoriasis, although this has not always been acknowledged in relevant treatment guidelines. We present consensus guidelines for the use of acitretin in psoriasis drawn up by the Psoriasis Group of the Spanish Academy of Dermatology and Venereology. These guidelines provide a detailed account of acitretin, including pharmacological properties, indications and contraindications, adverse effects, and factors that should be taken into account to enhance the safe use of this drug. They also propose treatment strategies for use in routine clinical practice. The overall aim of these guidelines is to define the criteria for the use and management of acetretin in psoriasis.


Subject(s)
Acitretin/therapeutic use , Immunosuppressive Agents/therapeutic use , Psoriasis/drug therapy , Abnormalities, Drug-Induced/etiology , Acitretin/administration & dosage , Acitretin/adverse effects , Acitretin/pharmacokinetics , Biotransformation , Cardiovascular Diseases/complications , Comorbidity , Contraindications , Drug Administration Schedule , Drug Interactions , Female , Gene Expression Regulation/drug effects , Humans , Immunosuppressive Agents/administration & dosage , Immunosuppressive Agents/adverse effects , Immunosuppressive Agents/pharmacokinetics , Keratinocytes/drug effects , Keratinocytes/pathology , Metabolic Syndrome/complications , Pregnancy , Pregnancy Complications , Psoriasis/complications , Psoriasis/genetics , Receptors, Retinoic Acid/agonists , Risk Assessment , Tetracyclines/pharmacokinetics
14.
Actas Dermosifiliogr ; 104(8): 694-709, 2013 Oct.
Article in English | MEDLINE | ID: mdl-24018211

ABSTRACT

Biologic therapy is a well-established strategy for managing moderate and severe psoriasis. Nevertheless, the high cost of such therapy, the relatively short span of clinical experience with biologics, and the abundance of literature now available on these agents have made evidence-based and consensus-based clinical guidelines necessary. The ideal goal of psoriasis treatment is to achieve complete or nearly complete clearing of lesions and to maintain it over time. Failing that ideal, the goal would be to reduce involvement to localized lesions that can be controlled with topical therapy. Although current evidence allows us to directly or indirectly compare the efficacy or risk of primary or secondary failure of available biologics based on objective outcomes, clinical trial findings cannot be directly translated to routine practice. As a result, the prescribing physician must tailor the treatment regimen to the individual patient. This update of the clinical practice guidelines issued by the Spanish Academy of Dermatology and Venereology (AEDV) on biologic therapy for psoriasis incorporates information from the most recent publications on this topic.


Subject(s)
Biological Factors/therapeutic use , Evidence-Based Medicine , Psoriasis/drug therapy , Acitretin/therapeutic use , Adult , Age Factors , Arthritis, Psoriatic/drug therapy , Biological Factors/adverse effects , Biological Factors/economics , Child , Clinical Trials as Topic , Combined Modality Therapy , Cost-Benefit Analysis , Drug Substitution , Female , Humans , Immunosuppressive Agents/therapeutic use , Male , Meta-Analysis as Topic , Multicenter Studies as Topic , Photochemotherapy , Pregnancy , Pregnancy Complications/drug therapy , Severity of Illness Index , Sex Factors , Spain , Treatment Failure , Treatment Outcome
18.
Actas Dermosifiliogr ; 102(3): 175-86, 2011 Apr.
Article in Spanish | MEDLINE | ID: mdl-21310368

ABSTRACT

Novel treatment strategies and new information concerning the management of moderate to severe psoriasis justify a reassessment of the role of the classic therapies in this setting. This consensus statement evaluates narrowband UV-B therapy, which is currently considered the phototherapy option of choice in psoriasis because of its risk-to-benefit ratio. The role of excimer laser and photodynamic therapies are also discussed. These targeted therapies are still only available in a small number of centers in Spain and are used principally in the treatment of localized and recalcitrant forms of psoriasis. We discuss the efficacy and safety of phototherapy as well as treatment regimens, combination therapy, and clinical considerations relating to the characteristics of the patient or the disease.


Subject(s)
Lasers, Excimer/therapeutic use , Low-Level Light Therapy/methods , Photochemotherapy/methods , Psoriasis/therapy , Ultraviolet Therapy/methods , Acitretin/therapeutic use , Adrenal Cortex Hormones/administration & dosage , Adrenal Cortex Hormones/therapeutic use , Adult , Child , Clinical Trials as Topic , Combined Modality Therapy , Comorbidity , Contraindications , Erythema/etiology , Female , Humans , Lasers, Excimer/adverse effects , Low-Level Light Therapy/adverse effects , Neoplasms, Radiation-Induced/etiology , Neoplasms, Radiation-Induced/prevention & control , PUVA Therapy/adverse effects , PUVA Therapy/methods , Photochemotherapy/adverse effects , Pregnancy , Pregnancy Complications/radiotherapy , Psoriasis/drug therapy , Psoriasis/radiotherapy , Radiotherapy Dosage , Ultraviolet Therapy/adverse effects
19.
Biochemistry (Mosc) ; 75(4): 443-51, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20618133

ABSTRACT

A knockout mutant with a deletion in a quorum sensing system gene qseC was generated from the vaccine strain Francisella tularensis 15 by site-directed mutagenesis. The variant with the inactivated gene qseC differed from the parental strain in growth rate on solid nutrient medium but had the same growth dynamics in liquid nutrient medium. The mutation abolished almost completely the resistance of the vaccine strain to normal rabbit serum and its ability to survive in macrophages; in addition, the strain lost the residual virulence. A significant phenotypic alteration was observed in the lipopolysaccharide of F. tularensis. Particularly, the mutant strain synthesized no noticeable amount of the lipopolysaccharide with the high-molecular-mass O-polysaccharide, presumably as a result of impairing biosynthesis of the repeating unit, namely, a loss of the ability to incorporate a formyl group, an N-acyl substituent of 4-amino-4,6-dideoxy-D-glucose.


Subject(s)
Bacterial Proteins/genetics , Francisella tularensis/genetics , Lipopolysaccharides/chemistry , Quorum Sensing/genetics , Animals , Bacterial Vaccines/immunology , Francisella tularensis/immunology , Francisella tularensis/metabolism , Gene Knockout Techniques , Mutagenesis, Site-Directed , O Antigens/chemistry , Phenotype , Rabbits , Spectrometry, Mass, Electrospray Ionization , Virulence
20.
Actas Dermosifiliogr ; 101(2): 156-63, 2010 Mar.
Article in Spanish | MEDLINE | ID: mdl-20223158

ABSTRACT

BACKGROUND: Biologic therapies have been a major breakthrough in the treatment of psoriasis because they are more selective and have a better short-term and medium-term safety profile. There are reliable data to support both the efficacy and the safety of these drugs. However, it is always useful to report the clinical experience of dermatologists who are experts in the use of biologic agents to treat psoriasis, particularly with regard to their safety. MATERIAL AND METHODS: We present the results of a survey administered to the members of Spanish Psoriasis Group and based on a series of questions referring to the clinical safety of these agents. A total of 988 patients treated with efalizumab, infliximab, etanercept, and adalimumab were reported by 15 members of the group. RESULTS: There was a particularly high proportion of reactions (34%) to infliximab infusions. Blood test abnormalities were detected in 13.25% of patients and infections in 12.24%, with one case of pulmonary tuberculosis. Attention is drawn to the adverse effects profile of efalizumab: de novo arthritis in 5.8% and rebound in 20.9% of patients. CONCLUSION: The safety data provided by our study should be taken into account in view of the large number of patients recruited by dermatologists experienced in the use of this type of therapy.


Subject(s)
Antibodies, Monoclonal/adverse effects , Dermatologic Agents/adverse effects , Immunoglobulin G/adverse effects , Immunosuppressive Agents/adverse effects , Psoriasis/drug therapy , Adalimumab , Antibodies, Monoclonal/therapeutic use , Antibodies, Monoclonal, Humanized , Arthritis/chemically induced , Biological Products/adverse effects , Biological Products/therapeutic use , Cardiovascular Diseases/chemically induced , Dermatologic Agents/therapeutic use , Drug Eruptions/etiology , Dyspnea/chemically induced , Etanercept , Fever/chemically induced , Health Surveys , Humans , Immunocompromised Host , Immunoglobulin G/therapeutic use , Immunosuppressive Agents/therapeutic use , Infections/etiology , Infliximab , Nausea/chemically induced , Receptors, Tumor Necrosis Factor/therapeutic use , Spain/epidemiology , Tumor Necrosis Factor-alpha/antagonists & inhibitors
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