RESUMEN
OBJECTIVES: To determine the incremental diagnostic yield of exome sequencing (ES) after negative chromosomal microarray analysis (CMA) in cases of prenatally diagnosed agenesis of the corpus callosum (ACC) and to identify the associated genes and variants. METHODS: A systematic search was performed to identify relevant studies published up until June 2022 using four databases: PubMed, SCOPUS, Web of Science and The Cochrane Library. Studies in English reporting on the diagnostic yield of ES following negative CMA in prenatally diagnosed partial or complete ACC were included. Authors of cohort studies were contacted for individual participant data and extended cohorts were provided for two of them. The increase in diagnostic yield with ES for pathogenic/likely pathogenic (P/LP) variants was assessed in all cases of ACC, isolated ACC, ACC with other cranial anomalies and ACC with extracranial anomalies. To identify all reported genetic variants, the systematic review included all ACC cases; however, for the meta-analysis, only studies with ≥ three ACC cases were included. Meta-analysis of proportions was employed using a random-effects model. Quality assessment of the included studies was performed using modified Standards for Reporting of Diagnostic Accuracy criteria. RESULTS: A total of 28 studies, encompassing 288 prenatally diagnosed ACC cases that underwent ES following negative CMA, met the inclusion criteria of the systematic review. We classified 116 genetic variants in 83 genes associated with prenatal ACC with a full phenotypic description. There were 15 studies, encompassing 268 cases, that reported on ≥ three ACC cases and were included in the meta-analysis. Of all the included cases, 43% had a P/LP variant on ES. The highest yield was for ACC with extracranial anomalies (55% (95% CI, 35-73%)), followed by ACC with other cranial anomalies (43% (95% CI, 30-57%)) and isolated ACC (32% (95% CI, 18-51%)). CONCLUSIONS: ES demonstrated an incremental diagnostic yield in cases of prenatally diagnosed ACC following negative CMA. While the greatest diagnostic yield was observed in ACC with extracranial anomalies and ACC with other central nervous system anomalies, ES should also be considered in cases of isolated ACC. © 2023 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.
Asunto(s)
Agenesia del Cuerpo Calloso , Secuenciación del Exoma , Femenino , Humanos , Embarazo , Agenesia del Cuerpo Calloso/diagnóstico por imagen , Agenesia del Cuerpo Calloso/genética , Cuerpo CallosoRESUMEN
OBJECTIVE: Vaccination against SARS-CoV-2 is essential to mitigate the personal, social and global impact of the coronavirus disease (COVID-19) as we move from a pandemic to an endemic phase. Vaccines are now required that offer broad, long-lasting immunological protection from infection in addition to protection from severe illness and hospitalisation. Here we present a review of the evidence base for a new COVID-19 vaccine, PHH-1V (Bimervax®; HIPRA HUMAN HEALTH S.L.U), and the results of an expert consensus. METHODS: The expert committee consisted of Spanish experts in medicine, family medicine, paediatrics, immunology, microbiology, nursing, and veterinary medicine. Consensus was achieved using a 4-phase process consisting of a face-to-face meeting during which the scientific evidence base was reviewed, an online questionnaire to elicit opinions on the value of PHH-1V, a second face-to-face update meeting to discuss the evolution of the epidemiological situation, vaccine programmes and the scientific evidence for PHH-1V and a final face-to-face meeting at which consensus was achieved. RESULTS: The experts agreed that PHH-1V constitutes a valuable novel vaccine for the development of vaccination programmes aimed towards protecting the population from SARS-CoV-2 infection and disease. Consensus was based on evidence of broad-spectrum efficacy against established and emerging SARS-CoV-2 variants, a potent immunological response, and a good safety profile. The physicochemical properties of the PHH-1V formulation facilitate handling and storage appropriate for global uptake. CONCLUSIONS: The physicochemical properties, formulation, immunogenicity and low reactogenic profile of PHH-1V confirm the appropriateness of this new COVID-19 vaccine.
Asunto(s)
COVID-19 , Vacunas , Humanos , Niño , Vacunas contra la COVID-19 , COVID-19/prevención & control , SARS-CoV-2 , VacunaciónRESUMEN
Most of the complications and deaths related to seasonal flu occur in the elderly population (≥65 years) with comorbidities, and the influenza vaccine is the most effective way to prevent them. Immunization is less effective in older adults due to immunosenescence. MF59-adjuvanted vaccines, designed to improve the magnitude, persistence and amplitude of the immune response in elderly people, have been used in clinical practice since 1997 in their trivalent formulation and, since 2020, in their tetravalent formulation. Data from various studies show that these vaccines are not only safe for all age groups, with a reactogenicity profile similar to that of the conventional vaccine, but also that they are especially effective in boosting the immune response in the population aged 65 or over by increasing antibody titers after vaccination and significantly reducing the risk of hospital admission. Adjuvanted vaccines have been shown to provide cross-protection against heterologous strains and to be as effective as the high-dose vaccine in the population aged 65 or over. In this review, the scientific evidence on the efficacy and effectiveness of the MF59-adjuvanted vaccine in real clinical practice in people ≥65 years of age is analyzed through a narrative and descriptive review of the literature with data from clinical trials, observational studies and systematic reviews or meta-analysis.
Asunto(s)
Vacunas contra la Influenza , Gripe Humana , Anciano , Humanos , Adyuvantes Inmunológicos , Anticuerpos Antivirales , Gripe Humana/tratamiento farmacológico , Polisorbatos , EscualenoRESUMEN
La espasticidad es un fenómeno complejo de expresión clínica extremadamente variable, un proceso dinámico y evolutivo que puede condicionar la funcionalidad y tratamiento del paciente. La recomendación actual de tratamiento temprano persigue evitar su progresión y complicaciones, e implica un planteamiento individualizado basado en un amplio abanico de medidas farmacológicas y no farmacológicas. Esta guía resulta de un foro de especialistas expertos que afrontaron algunas incertezas frecuentes en el proceso de valoración y planteamiento terapéutico como la idoneidad de iniciar tratamiento, consideraciones para iniciar, continuar y cesar el tratamiento con toxina botulínica, tratamientos adyuvantes, el dolor o el seguimiento del paciente espástico. El resultado es un algoritmo de decisión para el abordaje terapéutico de la espasticidad. Tanto el avance científico como el intercambio de experiencia clínica en el que se basa esta guía puede apoyar la toma de decisiones sobre algunas áreas de penumbra que encontramos en la práctica clínica diaria.(AU)
Spasticity is a complex phenomenon of extremely variable clinical expression, a dynamic and evolutionary process that can condition the activity and treatment of the patient. The current recommendation for early treatment aims to avoid progression and complications, and involves an individualized approach based on a wide range of pharmacological and non-pharmacological measures. This guide results from a forum of expert specialists who faced some frequent uncertainties in the assessment process and therapeutic approach of the spastic patient such as the suitability of initiating treatment, considerations for initiating, continuing and ceasing treatment with botulinum toxin, adjuvant treatments, pain or follow-up. The result is one algorithm of decision for the therapeutic approach of spasticity. Both scientific progress and the exchange of clinical experience on which this guide is based, can support decision-making on some areas of gloom that we find in daily practice.(AU)
Asunto(s)
Espasticidad Muscular , Toxinas Botulínicas Tipo A , Terapéutica , Algoritmos , Dolor , Manejo del Dolor , Ondas de Radio , Bloqueo Nervioso , Medicina Física y RehabilitaciónRESUMEN
Spasticity is a complex phenomenon of extremely variable clinical expression, a dynamic and evolutionary process that can condition the activity and treatment of the patient. The current recommendation for early treatment aims to avoid progression and complications, and involves an individualized approach based on a wide range of pharmacological and non-pharmacological measures. This guide results from a forum of expert specialists who faced some frequent uncertainties in the assessment process and therapeutic approach of the spastic patient such as the suitability of initiating treatment, considerations for initiating, continuing and ceasing treatment with botulinum toxin, adjuvant treatments, pain or follow-up. The result is one algorithm of decision for the therapeutic approach of spasticity. Both scientific progress and the exchange of clinical experience on which this guide is based, can support decision-making on some areas of gloom that we find in daily practice.
Asunto(s)
Toxinas Botulínicas Tipo A , Espasticidad Muscular , Algoritmos , Toxinas Botulínicas Tipo A/uso terapéutico , Consenso , Humanos , Espasticidad Muscular/tratamiento farmacológico , Dolor , Guías de Práctica Clínica como AsuntoRESUMEN
Chronic thromboembolic pulmonary hypertension (CTEPH) and pulmonary arterial hypertension (PAH) are two forms of pulmonary hypertension (PH) characterized by obstructive vasculopathy. Endothelial dysfunction along with metabolic changes towards increased glycolysis are important in PAH pathophysiology. Less is known about such abnormalities in endothelial cells (ECs) from CTEPH patients. This study provides a systematic metabolic comparison of ECs derived from CTEPH and PAH patients. Metabolic gene expression was studied using qPCR in cultured CTEPH-EC and PAH-EC. Western blot analyses were done for HK2, LDHA, PDHA1, PDK and G6PD. Basal viability of CTEPH-EC and PAH-EC with the incubation with metabolic inhibitors was measured using colorimetric viability assays. Human pulmonary artery endothelial cells (HPAEC) were used as healthy controls. Whereas PAH-EC showed significant higher mRNA levels of GLUT1, HK2, LDHA, PDHA1 and GLUD1 metabolic enzymes compared to HPAEC, CTEPH-EC did not. Oxidative phosphorylation associated proteins had an increased expression in PAH-EC compared to CTEPH-EC and HPAEC. PAH-EC, CTEPH-EC and HPAEC presented similar HOXD macrovascular gene expression. Metabolic inhibitors showed a dose-dependent reduction in viability in all three groups, predominantly in PAH-EC. A different metabolic profile is present in CTEPH-EC compared to PAH-EC and suggests differences in molecular mechanisms important in the disease pathology and treatment.
Asunto(s)
Células Endoteliales/metabolismo , Hipertensión Arterial Pulmonar/genética , Hipertensión Arterial Pulmonar/metabolismo , Embolia Pulmonar/genética , Embolia Pulmonar/metabolismo , Adulto , Anciano , Células Cultivadas , Enfermedad Crónica , Femenino , Expresión Génica , Glutamato Deshidrogenasa/genética , Glutamato Deshidrogenasa/metabolismo , Glucólisis/genética , Hexoquinasa/genética , Hexoquinasa/metabolismo , Humanos , L-Lactato Deshidrogenasa/genética , L-Lactato Deshidrogenasa/metabolismo , Masculino , Persona de Mediana Edad , Fosforilación Oxidativa , Arteria Pulmonar/citología , Piruvato Deshidrogenasa (Lipoamida)/genética , Piruvato Deshidrogenasa (Lipoamida)/metabolismoRESUMEN
Objetivos Existe una relación entre la práctica habitual de un instrumento y la aparición de trastornos musculoesqueléticos. El síntoma más destacado de estos trastornos es el dolor, de manera que puede establecerse la existencia de dolor ligado a la interpretación musical como un problema ocupacional específico. La Comunidad Valenciana es una región con una tradición musical reconocida, en la que no se conoce suficientemente el impacto que tiene sobre la salud el desempeño musical. El objetivo de esta investigación ha sido definir la frecuencia del dolor de origen musculoesquelético en los estudiantes de música de nuestro medio y estudiar su localización regional en función del tipo de instrumento. Materiales y método Se han incluido en el estudio aquellos estudiantes de música que están cursando Grado Medio o Superior en conservatorios de la Comunidad Valenciana. Las variables se han recogido por medio de un cuestionario de salud que han cumplimentado los estudiantes. Para determinar la intensidad del dolor se han calculado las medias de la EVA y de las puntuaciones de dolor de los cuestionarios SRS-22 y CAVIDRA, validados para la población española. Se ha realizado un estudio de localización segmentaria del dolor en los diferentes grupos de instrumento. Resultados En el presente estudio se recogieron 268 encuestas, de las cuales 222 cumplían criterios de inclusión. El 68% de los encuestados declaraba haber desarrollado en algún momento molestias o dolor ligado a la interpretación musical. El sistema más frecuentemente afectado fue el musculoesquelético. Los síntomas relacionados con tocar más frecuentemente referidos fueron dolor, tensión muscular, contractura y fatiga. Conclusiones El 68% de los músicos presentan algún tipo de dolor ligado a la interpretación musical en algún momento de su carrera. El estudio de la topografía del dolor relacionada con el instrumento ofrece datos interesantes para definir estrategias de prevención (AU)
Objectives There is a relationship between routinely playing an instrument and musculoskeletal disorders. The most important of these disorders is pain. Therefore, playing-related musculoskeletal disorders can be established as a specific occupational problem. The Valencian Community is a region with a well-known musical tradition, in which the health impact of playing an instrument has not been sufficiently identified. The aim of this study was to define the frequency of musculoskeletal pain in music students in our environment and to identify its localization according to the instrument played. Materials and method This study included music students in the intermediate or advanced levels of the conservatoires of the Valencian Community. The variables were gathered through a health questionnaire completed by the students. To determine pain intensity, we calculated the mean VAS scores and the pain scores of the SRS-22 and CAVIDRA questionnaires, which have been validated for the Spanish population. Segmental pain localization was studied in the different groups of instruments. Results A total of 268 questionnaires were gathered, of which 222 met the inclusion criteria. Playing-related pain or discomfort was reported by 68% of respondents. The most frequently affected system was the musculoskeletal system. The most frequently-reported playing-related symptoms were pain, muscular tension, spasm and fatigue. Conclusions A total of 68% of the musicians in this study reported some type of playing-related pain at some time during their studies. Study of the topography of instrument-related pain provides useful data for the design of prevention strategies (AU)
Asunto(s)
Humanos , Masculino , Femenino , Niño , Adolescente , Adulto Joven , Adulto , Persona de Mediana Edad , Anciano , Dolor Musculoesquelético/epidemiología , Dolor Musculoesquelético/etiología , Música , Enfermedades Profesionales/epidemiología , Enfermedades Profesionales/etiología , Encuestas y Cuestionarios , Estudios Transversales , EstudiantesRESUMEN
OBJECTIVES: There is a relationship between routinely playing an instrument and musculoskeletal disorders. The most important of these disorders is pain. Therefore, playing-related musculoskeletal disorders can be established as a specific occupational problem. The Valencian Community is a region with a well-known musical tradition, in which the health impact of playing an instrument has not been sufficiently identified. The aim of this study was to define the frequency of musculoskeletal pain in music students in our environment and to identify its localization according to the instrument played. MATERIALS AND METHOD: This study included music students in the intermediate or advanced levels of the conservatoires of the Valencian Community. The variables were gathered through a health questionnaire completed by the students. To determine pain intensity, we calculated the mean VAS scores and the pain scores of the SRS-22 and CAVIDRA questionnaires, which have been validated for the Spanish population. Segmental pain localization was studied in the different groups of instruments. RESULTS: A total of 268 questionnaires were gathered, of which 222 met the inclusion criteria. Playing-related pain or discomfort was reported by 68% of respondents. The most frequently affected system was the musculoskeletal system. The most frequently-reported playing-related symptoms were pain, muscular tension, spasm and fatigue. CONCLUSIONS: A total of 68% of the musicians in this study reported some type of playing-related pain at some time during their studies. Study of the topography of instrument-related pain provides useful data for the design of prevention strategies.
Asunto(s)
Dolor Musculoesquelético , Música , Enfermedades Profesionales , Humanos , Dolor Musculoesquelético/epidemiología , Dolor Musculoesquelético/etiología , Enfermedades Profesionales/epidemiología , Enfermedades Profesionales/etiología , Estudiantes , Encuestas y CuestionariosRESUMEN
INTRODUCTION: There are few atopic dermatitis (AD) incidence cohort studies in young adults, the etiology of this disease remains obscure, and AD risk factors in adults are not well understood. The objective of this study was to estimate AD ten-year incidence and prevalence in a cohort of adolescent aged 14-16 at inception in Castellon province in Valencia Region, Spain and describe related risk factors. MATERIAL AND METHODS: From 2002 to 2012, a population-based prospective cohort study was carried out. Questionnaires from the International Study of Asthma and Allergies in Childhood (ISAAC) were used with an additional questionnaire for related factors completed by participants and their parents, respectively, in 2002. In 2012 the same questionnaires were completed by the participants' through a telephone interview, and incidence and prevalence of AD were estimated. Directed acyclic graphs, Poisson regression and inverse probability weighted regression adjustment were used. RESULTS: The participation rate was 79.5% (1435/1805) with AD lifetime prevalence of 34.9% and AD incidence of 13.5 per 1000 person years. Females presented higher prevalence and incidence than males. After adjustment significant risk factors were being female, history of asthma or allergic rhinitis, family history of AD, history of respiratory infections, history of bronchitis, history of pneumonia, history of sinusitis, and birthplace outside Castellon province. The highest AD population attributable risks were female, 30.3%, and history of respiratory infections 15.3%. Differences with AD childhood risk factors were found. CONCLUSIONS: AD incidence in our cohort was high and several risks factors were related to AD
No disponible
Asunto(s)
Humanos , Masculino , Femenino , Adolescente , Adulto Joven , Adulto , Dermatitis Atópica/epidemiología , Dermatitis Atópica/etiología , Estudios Prospectivos , Factores de Riesgo , Incidencia , Encuestas y Cuestionarios , Distribución por Sexo , Distribución de Poisson , Medición de Riesgo , España/epidemiologíaRESUMEN
INTRODUCTION: There are few atopic dermatitis (AD) incidence cohort studies in young adults, the etiology of this disease remains obscure, and AD risk factors in adults are not well understood. The objective of this study was to estimate AD ten-year incidence and prevalence in a cohort of adolescent aged 14-16 at inception in Castellon province in Valencia Region, Spain and describe related risk factors. MATERIAL AND METHODS: From 2002 to 2012, a population-based prospective cohort study was carried out. Questionnaires from the International Study of Asthma and Allergies in Childhood (ISAAC) were used with an additional questionnaire for related factors completed by participants and their parents, respectively, in 2002. In 2012 the same questionnaires were completed by the participants' through a telephone interview, and incidence and prevalence of AD were estimated. Directed acyclic graphs, Poisson regression and inverse probability weighted regression adjustment were used. RESULTS: The participation rate was 79.5% (1435/1805) with AD lifetime prevalence of 34.9% and AD incidence of 13.5 per 1000 person years. Females presented higher prevalence and incidence than males. After adjustment significant risk factors were being female, history of asthma or allergic rhinitis, family history of AD, history of respiratory infections, history of bronchitis, history of pneumonia, history of sinusitis, and birthplace outside Castellon province. The highest AD population attributable risks were female, 30.3%, and history of respiratory infections 15.3%. Differences with AD childhood risk factors were found. CONCLUSIONS: AD incidence in our cohort was high and several risks factors were related to AD.
Asunto(s)
Dermatitis Atópica/epidemiología , Infecciones del Sistema Respiratorio/epidemiología , Adolescente , Adulto , Niño , Femenino , Humanos , Incidencia , Masculino , Anamnesis/estadística & datos numéricos , Prevalencia , Estudios Prospectivos , Factores de Riesgo , Factores Sexuales , España/epidemiología , Encuestas y Cuestionarios/estadística & datos numéricos , Adulto JovenRESUMEN
Antecedentes y objetivo: Previamente se había iniciado el proceso metodológico para la validación transcultural al idioma español de la escala Hair Specific Skindex-29 (HSS-29), que mide el impacto de la alopecia androgénica femenina sobre la calidad de vida relacionada con la salud (CVRS). Para finalizar el proceso, el objetivo del estudio fue completar la validación a través de la determinación de su sensibilidad al cambio y su correlación con una escala generalista de CVRS (SF-12). Material y método: Se establecieron dos visitas, una basal y otra tras 6meses de tratamiento con suplemento alimenticio con actividad inhibidora de la enzima 5-alfa reductasa. En cada visita, investigadores y pacientes valoraron la gravedad de la alopecia mediante la escala Sinclair, el estado de la apariencia del cabello, y se administraron las escalas HSS-29 y SF-12. Resultados: Participaron 983 mujeres con alopecia androgénica. La media de puntuación en la escala HSS-29 cambió de 27,5 ± 18,7 en la visita basal a 19,3 ± 15,7 en la de seguimiento, y sus dimensiones funcional, emocional y sintomática también cambiaron significativamente. Tanto las diferencias entre basal y seguimiento en el índice HSS-29 global como en cada una de sus dimensiones se correlacionaron significativamente con las diferencias encontradas en las dimensiones de SF-12. Los coeficientes de correlación de Pearson oscilaron entre -0,1 y -0,4, y en todos los casos el grado de significación fue p < 0,001. Conclusiones: La versión en español de la escala HSS-29 posee sensibilidad, es decir, detecta cambios relacionados con la calidad de vida cuando las condiciones objetivas varían. Igualmente, se observó una correlación entre las escalas HSS-29 y SF-12
Background and objective: Work has already been done on validating the cross-cultural adaptation of the Hair-Specific Skindex-29 questionnaire (HSS-29) into Spanish. This questionnaire measures the impact of female-pattern hair loss on health-related quality of life (HRQoL). The aim of this study was to complete the validation process by testing the questionnaire's sensitivity to change and assessing its correlation with the generic 12-item Short-Form Health Survey (SF-12). Material and method: Patients who started treatment with a nutritional supplement that blocks the activity of 5-alpha-reductase were seen in two visits: a baseline visit and a follow-up visit at 6months. At each visit, hair loss severity was assessed by both investigators and patients via the Sinclair scale, evaluation of hair condition, and administration of HSS-29 and SF-12. Results: In total, 983 women with female-pattern hair loss participated in the study. The mean HSS-29 score decreased from 25.7 ± 18.7 at baseline to 19.3 ± 15.7 at follow-up and significant changes were also observed in the functioning, emotions, and symptoms domains. Changes in overall and subscale HSS-29 scores from baseline to follow-up were all significantly correlated with changes in SF-12 subscale scores. The Pearson correlation coefficients ranged from -0.1 to -0.4 and were all significant at P <.001. Conclusions: The Spanish version of HSS-29 is sensitive to change, as it detected changes in objective measurements of HRQoL. Correlations between HSS-29 and SF-12 scores were also observed
Asunto(s)
Humanos , Femenino , Adulto , Persona de Mediana Edad , Comparación Transcultural , Alopecia/diagnóstico , Calidad de Vida , Suplementos Dietéticos , Psicometría , Encuestas y Cuestionarios , Análisis de Datos , Escalas de Valoración Psiquiátrica BreveRESUMEN
BACKGROUND AND OBJECTIVE: Work has already been done on validating the cross-cultural adaptation of the Hair-Specific Skindex-29 questionnaire (HSS-29) into Spanish. This questionnaire measures the impact of female-pattern hair loss on health-related quality of life (HRQoL). The aim of this study was to complete the validation process by testing the questionnaire's sensitivity to change and assessing its correlation with the generic 12-item Short-Form Health Survey (SF-12). MATERIAL AND METHOD: Patients who started treatment with a nutritional supplement that blocks the activity of 5-alpha-reductase were seen in two visits: a baseline visit and a follow-up visit at 6months. At each visit, hair loss severity was assessed by both investigators and patients via the Sinclair scale, evaluation of hair condition, and administration of HSS-29 and SF-12. RESULTS: In total, 983 women with female-pattern hair loss participated in the study. The mean HSS-29 score decreased from 25.7±18.7 at baseline to 19.3±15.7 at follow-up and significant changes were also observed in the functioning, emotions, and symptoms domains. Changes in overall and subscale HSS-29 scores from baseline to follow-up were all significantly correlated with changes in SF-12 subscale scores. The Pearson correlation coefficients ranged from -0.1 to -0.4 and were all significant at P<.001. CONCLUSIONS: The Spanish version of HSS-29 is sensitive to change, as it detected changes in objective measurements of HRQoL. Correlations between HSS-29 and SF-12 scores were also observed.
Asunto(s)
Alopecia/psicología , Comparación Transcultural , Lenguaje , Calidad de Vida , Traducciones , 3-Oxo-5-alfa-Esteroide 4-Deshidrogenasa , Adolescente , Adulto , Anciano , Alopecia/diagnóstico , Alopecia/enzimología , Femenino , Encuestas Epidemiológicas , Humanos , Persona de Mediana Edad , Sensibilidad y Especificidad , Factores de Tiempo , Adulto JovenRESUMEN
Pharmacological inhibition of the sonic hedgehog (SHH) pathway can be beneficial against certain cancers but detrimental in others. Adamantinomatous craniopharyngioma (ACP) is a relevant pituitary tumour, affecting children and adults, that is associated with high morbidity and increased mortality in long-term follow-up. We have previously demonstrated overactivation of the SHH pathway in both human and mouse ACP. Here, we show that this activation is ligand dependent and induced by the expression of SHH protein in a small proportion of tumour cells. We investigate the functional relevance of SHH signalling in ACP through MRI-guided preclinical studies using an ACP mouse model. Treatment with vismodegib, a clinically approved SHH pathway inhibitor, results in a significant reduction in median survival due to premature development of highly proliferative and vascularised undifferentiated tumours. Reinforcing the mouse data, SHH pathway inhibition in human ACP leads to a significant increase in tumour cell proliferation both ex vivo, in explant cultures, and in vivo, in a patient-derived xenograft model. Together, our results demonstrate a protumourigenic effect of vismodegib-mediated SHH pathway inhibition in ACP.
Asunto(s)
Craneofaringioma/fisiopatología , Proteínas Hedgehog/antagonistas & inhibidores , Adolescente , Animales , Proliferación Celular , Niño , Preescolar , Modelos Animales de Enfermedad , Humanos , Masculino , Ratones , Neoplasias Hipofisarias , Transducción de SeñalRESUMEN
PURPOSE: Pilocytic astrocytoma is the most common childhood brain tumor, characterized by constitutive MAPK activation. MAPK signaling induces oncogene-induced senescence (OIS), which may cause unpredictable growth behavior of pilocytic astrocytomas. The senescence-associated secretory phenotype (SASP) has been shown to regulate OIS, but its role in pilocytic astrocytoma remains unknown.Experimental Design: The patient-derived pilocytic astrocytoma cell culture model, DKFZ-BT66, was used to demonstrate presence of the SASP and analyze its impact on OIS in pilocytic astrocytoma. The model allows for doxycycline-inducible switching between proliferation and OIS. Both states were studied using gene expression profiling (GEP), Western blot, ELISA, and cell viability testing. Primary pilocytic astrocytoma tumors were analyzed by GEP and multiplex assay. RESULTS: SASP factors were upregulated in primary human and murine pilocytic astrocytoma and during OIS in DKFZ-BT66 cells. Conditioned medium induced growth arrest of proliferating pilocytic astrocytoma cells. The SASP factors IL1B and IL6 were upregulated in primary pilocytic astrocytoma, and both pathways were regulated during OIS in DKFZ-BT66. Stimulation with rIL1B but not rIL6 reduced growth of DKFZ-BT66 cells and induced the SASP. Anti-inflammatory treatment with dexamethasone induced regrowth of senescent cells and inhibited the SASP. Senescent DKFZ-BT66 cells responded to senolytic BCL2 inhibitors. High IL1B and SASP expression in pilocytic astrocytoma tumors was associated with favorable progression-free survival. CONCLUSIONS: We provide evidence for the SASP regulating OIS in pediatric pilocytic astrocytoma, with IL1B as a relevant mediator. SASP expression could enable prediction of progression in patients with pilocytic astrocytoma. Further investigation of the SASP driving the unpredictable growth of pilocytic astrocytomas, and its possible therapeutic application, is warranted.
Asunto(s)
Astrocitoma/patología , Neoplasias Encefálicas/patología , Senescencia Celular , Interleucina-1beta/metabolismo , Animales , Astrocitoma/mortalidad , Astrocitoma/cirugía , Neoplasias Encefálicas/mortalidad , Neoplasias Encefálicas/cirugía , Proliferación Celular , Niño , Medios de Cultivo Condicionados/metabolismo , Conjuntos de Datos como Asunto , Modelos Animales de Enfermedad , Femenino , Perfilación de la Expresión Génica , Humanos , Masculino , Ratones , Cultivo Primario de Células , Pronóstico , Supervivencia sin Progresión , Células Tumorales CultivadasRESUMEN
In many of the alpine watersheds of Sierra Nevada (Southern Spain) exists an ancient network of dug canals that collect, transport and facilitate the recharge the snowmelt in the underlying aquifer during the spring season. This practice, known as careos, in the lower part of the watersheds supply drinking water as spring discharge during the dry season. To study how this managed recharge technique modifies the natural response of these basins this work focuses on characterizing the hydrological behavior of one of the sites, the Berchules watershed. The mechanisms for mineralization of groundwater are based on geochemical processes such as evapo-concentration in the soil layer and silicate mineral weathering due to dissolved CO2 originated from both soil biogenic processes and the atmosphere. Groundwater presents a main hydrogeochemical calciummagnesium-bicarbonate type facies, which is associated to groundwater flowing through the upper weathered silicates and quickly drained through springs located in the uplands and in the intermediate altitude catchment zone. Additionally, in the lower part of the basin some springs discharge mineralized groundwater with a sodium-calcium-bicarbonate composition associated to regional groundwater flow. In natural conditions, this hydrogeological system behaves as a sloping aquifer, occurring recharge between 1400 and 2500â¯mâ¯a.s.l. The springs discharge groundwater with an isotopic content and temperature in coherence with the local rainfall isotopic and thermal atmospheric altitudinal lines. Nevertheless, once the careo recharge begins the affected springs reveal the fingerprint of the concentrated recharge system by blurring the fingerprint of both the isotopic and thermal altitudinal dependence in the springs discharge. This validates the previous conceptual model and supports average recharge values of 141⯱â¯140â¯mm/yr and total average water resources of 181⯱â¯111â¯mm/yr which include a 40% increase in the study period due to the effect of the acequias de careo.
RESUMEN
Objectives: To analyse lipid changes and tolerability in a cohort of HIV-infected patients who switched their antiretroviral regimens to rilpivirine/emtricitabine/tenofovir (RPV/FTC/TDF) in a real-world setting. Methods: PRO-STR is a 48 week prospective observational post-authorization study in 25 hospitals. Patients with a viral load <1000 copies/mL, receiving at least 12 months of combination ART (cART), with constant posology for at least the prior 3 months, were categorized according to previous treatment [NNRTI or ritonavir-boosted PI (PI/r)]. Analytical tests were performed at the baseline visit, between week 16 and week 32, and at week 48. Results: A total of 303 patients were included (mean age 46.6 years; male 74.0%; previous treatment 74.7% NNRTI and 25.3% PI/r). Both groups exhibited significantly reduced lipid profiles, except for HDL cholesterol, for which a non-significant increase was observed. [NNRTI patients: total cholesterol (baseline: 195.5â±â38.4 mg/dL; week 48: 171.0â±â35.5 mg/dL), total cholesterol/HDL ratio (baseline: 4.2â±â1.2; week 48: 4.0â±â1.2), HDL (baseline: 49.1â±â12.0 mg/dL; week 48: 49.2â±â45.8 mg/dL), LDL (baseline: 119.2â±â30.2 mg/dL; week 48: 114.2â±â110.7 mg/dL), and triglycerides (baseline: 136.6â±â86.8 mg/dL; week 48: 113.4â±â67.8 mg/dL); PI/r patients: total cholesterol (baseline: 203.2â±â48.8 mg/dL; week 48: 173.4â±â36.9 mg/dL), total cholesterol/HDL ratio (baseline: 4.7â±â1.6; week 48: 4.0â±â1.2), HDL (baseline: 46.4â±â12.5 mg/dL; week 48: 52.1â±â54.4 mg/dL), LDL (baseline: 127.0â±â36.3 mg/dL; week 48: 111.4â±â35.8 mg/dL), and triglycerides (baseline: 167.6â±â107.7 mg/dL; week 48: 122.7â±â72.1 mg/dL)]. The most common intolerances were neuropsychiatric in the NNRTI patients and gastrointestinal and metabolic in the PI/r patients, and these intolerances were significantly reduced in both groups at week 48 [NNRTI: neuropsychiatric (baseline: 81.3%; week 48: 0.0%); PI/r: gastrointestinal (baseline: 48.7%; week 48: 0.0%) and metabolic (baseline: 42.1%; week 48: 0.0%)]. Conclusions: RPV/FTC/TDF improved the lipid profiles and reduced the intolerances after switching from NNRTI or PI-based regimens, in a cohort of HIV-infected patients.