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1.
Cureus ; 15(9): e45339, 2023 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-37849589

RESUMEN

Acute fulminant cerebral edema (AFCE) is a recently identified encephalitis type associated with significant morbimortality. Described as rare, limited data exists on its early detection and treatment. This paper describes a case of AFCE that progressed to unresponsive intracranial hypertension. A previously healthy four-year-old boy presented with fever, myalgias, and neurological symptoms. Diagnostic assessments showed cerebrospinal fluid abnormalities, and despite medical interventions, his condition deteriorated rapidly and developed severe cerebral edema and herniation within 24 hours. A decompressive craniectomy was attempted to decrease intracranial pressure, without success. This case emphasizes the urgency of early AFCE recognition and effective management strategies given its severe prognosis, aiming to improve understanding and spur further research.

2.
Int Immunopharmacol ; 121: 110454, 2023 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-37301124

RESUMEN

Lycopene is a natural compound with one of the highest antioxidant activities. Its consumption is associated with lower risks in lung cancer and chronic obstructive pulmonary disease, for example. Experimentally, a murine model demonstrated the ingestion of lycopene, which reduced the damage in lungs caused by cigarette smoke. Since lycopene is highly hydrophobic, its formulations in supplements and preparations for laboratory assays are based on oils, additionally, bioavailavility is low. We developed a lycopene layered double hydroxide (Lyc-LDH) composite, which is capable of transporting lycopene aqueous media. Our objective was to evaluate the cytotoxicity of Lyc-LDH and the intra-cellular production of reactive oxygen species (ROS) in J774A.1 cells. Also, in vivo assays were conducted with 50 male C57BL/6 mice intranasally treated with Lyc-LDH 10 mg/kg (LG10), Lyc-LDH 25 mg/kg (LG25) and Lyc-LDH 50 mg/kg (LG50) during five days compared against a vehicle (VG) and control (CG) group. The blood, bronchoalveolar lavage fluid (BALF) and lung tissue were analyzed. The results revealed that Lyc-LDH composite attenuated intracellular ROS production stimulated with lipopolysacharide. In BALF, the highest doses of Lyc-LDH (LG25 and LG50) promoted influx of macrophages, lymphocytes, neutrophils and eosinophils compared to CG and VG. Also, LG50 increased the levels of IL-6 and IL-13, and promoted the redox imbalance in the pulmonary tissue. On the contrary, low concentrations did not produce significative effects. In conclusion, our results suggest that intranasal administration of high concentrations of Lyc-LDH induces inflammation as well as redox status changes in the lungs of healthy mice, however, results with low concentrations open a promising way to study LDH composites as vehicles for intranasal administration of antioxidant coadjuvants.


Asunto(s)
Antioxidantes , Estrés Oxidativo , Ratones , Masculino , Animales , Licopeno/farmacología , Antioxidantes/farmacología , Especies Reactivas de Oxígeno , Ratones Endogámicos C57BL , Pulmón/metabolismo , Hidróxidos/farmacología
3.
Porto Biomed J ; 8(3): e219, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37383526

RESUMEN

Background: The coronavirus disease 2019 (COVID-19) was classified as a pandemic in March 2020 by the World Health Organization. The Pfizer-BioNTech COVID-19 vaccine was the first to be authorized in the European Union, based on data from phase 1, 2, and 3 clinical trials of limited duration. Concerns have been raised regarding the vaccine's safety profile. Some of the adverse drug reactions (ADRs) associated with vaccines may not have been identified during clinical trials. This study aimed to identify ADRs associated with the Pfizer-BioNTech vaccine in health care professionals at a Portuguese tertiary university hospital. Methods: The data used in this analysis consist of ADRs reported through a spontaneous notification system from vaccines administered between December 27, 2020, and January 31, 2021. ADRs were categorized according to the MedDRA terminology. Results: A total of 8,605 Pfizer-BioNTech vaccines were administered to 4568 health care professionals. ADRs were reported among 520 of the vaccines, with an incidence of 13.56% in women and 5.31% in men. The mean age of the population reporting ADRs was 41.52 years, with a standard deviation of 9.83 years. The most frequent ADRs were myalgia (n = 274), headache (n = 199), pyrexia (n = 164), injection site pain (n = 160), fatigue (n = 84), nausea (n = 81), chills (n = 65), lymphadenopathy (n = 64), and arthralgia (n = 53). Hypersensitivity reactions occurred in 15 health care professionals, with no anaphylactic reactions observed. A total of four Important Medical Events were observed, which consisted of two cases of syncope, one case of sudden hearing loss, and one case of transverse myelitis. Conclusion: The vaccine was well-tolerated among the study participants. Reactogenicity was greater after the second dose. The incidence of ADRs was higher in women and individuals aged between 40 to 49 years. Systemic adverse reactions were most frequently reported. Systematic monitoring of ADRs of COVID-19 vaccines in real-life context is essential for a more robust establishment of its safety profile.

4.
J Headache Pain ; 24(1): 78, 2023 Jun 29.
Artículo en Inglés | MEDLINE | ID: mdl-37380951

RESUMEN

Migraine is a common and complex neurological disease potentially caused by a polygenic interaction of multiple gene variants. Many genes associated with migraine are involved in pathways controlling the synaptic function and neurotransmitters release. However, the molecular mechanisms underpinning migraine need to be further explored.Recent studies raised the possibility that migraine may arise from the effect of regulatory non-coding variants. In this study, we explored the effect of candidate non-coding variants potentially associated with migraine and predicted to lie within regulatory elements: VAMP2_rs1150, SNAP25_rs2327264, and STX1A_rs6951030. The involvement of these genes, which are constituents of the SNARE complex involved in membrane fusion and neurotransmitter release, underscores their significance in migraine pathogenesis. Our reporter gene assays confirmed the impact of at least two of these non-coding variants. VAMP2 and SNAP25 risk alleles were associated with a decrease and increase in gene expression, respectively, while STX1A risk allele showed a tendency to reduce luciferase activity in neuronal-like cells. Therefore, the VAMP2_rs1150 and SNAP25_rs2327264 non-coding variants affect gene expression, which may have implications in migraine susceptibility. Based on previous in silico analysis, it is plausible that these variants influence the binding of regulators, such as transcription factors and micro-RNAs. Still, further studies exploring these mechanisms would be important to shed light on the association between SNAREs dysregulation and migraine susceptibility.


Asunto(s)
Trastornos Migrañosos , Proteína 2 de Membrana Asociada a Vesículas , Humanos , Proteína 2 de Membrana Asociada a Vesículas/genética , Fusión de Membrana , Alelos , Trastornos Migrañosos/genética , Expresión Génica , Proteína 25 Asociada a Sinaptosomas/genética
5.
Rev. Bras. Odontol. Leg. RBOL ; 10(1): 30-38, 2023-06-26.
Artículo en Portugués | LILACS-Express | LILACS | ID: biblio-1525532

RESUMEN

Nesta pesquisa avaliou-se o plano de ensino de 25 faculdades do Brasil, sendo 5 faculdades por região para melhor representatividade do país. Um instrumento de coleta de dados foi construído para extração das informações necessárias, a saber: ementa e referências bibliográficas. Os dados obtidos por esta pesquisa foram tabulados em planilhas utilizando o programa Microsoft Office Excel. Inicialmente, cada frase das ementas foi transcrita para uma entrada de linha da planilha e forma associadas a 10 categorias de sentido. Foram transpostas para uma ementa provisória e proposta uma versão de ementa final. Já as referências bibliográficas foram descritas em linhas das planilhas, individualmente, e após a inclusão de todas foi feito um ranqueamento por frequência de citação. Em termos quantitativos esta pesquisa evidenciou que, as componentes curriculares de Odontologia Legal, abordam mais frequentemente em suas ementas os conteúdos relacionados às Ciências Forenses e ao Direito, sendo estas duas categorias responsáveis por 51,4% (121) das frases das ementas avaliadas e, Jorge Paulete Vanrell, é o autor mais frequentemente referenciado (80%) com sua obra Odontologia Legal e Antropologia Forense


In this research, the teaching plan of 25 colleges in Brazil was evaluated, with 5 colleges per region for better representation of the country. A data collection instrument was built to extract the necessary information, namely: menu and bibliographic references. The data obtained by this research were tabulated in spreadsheets using the Microsoft Office Excel program. Initially, each sentence of the menus was transcribed into a line entry in the spreadsheet and was associated with 10 categories of meaning. They were transposed to a provisional menu and a version of the final menu was proposed. The bibliographic references were described in lines of the spreadsheets, individually, and after the inclusion of all, a ranking was performed by citation frequency. In quantitative terms, this research showed that the Forensic Dentistry disciplines more frequently address content related to Forensic Sciences and Law in their menus, these two categories being responsible for 51.4% (121) of the sentences of the evaluated menus and, Jorge Paulete Vanrell is the author most frequently referenced (80%) with his work Odontologia Legal e Antropologia Forense

6.
Clin Genet ; 104(4): 479-485, 2023 10.
Artículo en Inglés | MEDLINE | ID: mdl-37243399

RESUMEN

Familial hemiplegic migraine (FHM) is a rare autosomal-dominant form of migraine with aura. Three disease-causing genes have been identified for FHM: CACNA1A, ATP1A2 and SCN1A. However, not all families are linked to one of these three genes.PRRT2 variants were also commonly associated with HM symptoms; therefore, PRRT2 is hypothesized as the fourth gene causing FHM. PRRT2 plays an important role in neuronal migration, spinogenesis, and synapse mechanisms during development and calcium-dependent neurotransmitter release. We performed exome sequencing to unravel the genetic cause of migraine in one family, and a novel PRRT2 variant (c.938C > T;p.Ala313Val) was identified with further functional studies to confirm its pathogenicity. PRRT2-A313V reduced protein stability, led to protein premature degradation by the proteasome and altered the subcellular localization of PRRT2 from the plasma membrane (PM) to the cytoplasm. We identified and characterized for the first time in a Portuguese patient, a novel heterozygous missense variant in PRRT2 associated with HM symptoms. We suggest that PRRT2 should be included in the diagnosis of HM.


Asunto(s)
Trastornos Migrañosos , Migraña con Aura , Humanos , Hemiplejía , Proteínas de la Membrana/genética , Trastornos Migrañosos/genética , Migraña con Aura/diagnóstico , Migraña con Aura/genética , Mutación , Mutación Missense/genética , Proteínas del Tejido Nervioso/genética , Linaje , Portugal
7.
Inflamm Res ; 72(3): 475-491, 2023 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-36617343

RESUMEN

BACKGROUND: Cysteinyl leukotrienes (CysLT) are potent inflammation-promoting mediators, but remain scarcely explored in COVID-19. We evaluated urinary CysLT (U-CysLT) relationship with disease severity and their usefulness for prognostication in hospitalized COVID-19 patients. The impact on U-CysLT of veno-venous extracorporeal membrane oxygenation (VV-ECMO) and of comorbidities such as hypertension and obesity was also assessed. METHODS: Blood and spot urine were collected in "severe" (n = 26), "critically ill" (n = 17) and "critically ill on VV-ECMO" (n = 17) patients with COVID-19 at days 1-2 (admission), 3-4, 5-8 and weekly thereafter, and in controls (n = 23) at a single time point. U-CysLT were measured by ELISA. Routine markers, prognostic scores and outcomes were also evaluated. RESULTS: U-CysLT did not differ between groups at admission, but significantly increased along hospitalization only in critical groups, being markedly higher in VV-ECMO patients, especially in hypertensives. U-CysLT values during the first week were positively associated with ICU and total hospital length of stay in critical groups and showed acceptable area under curve (AUC) for prediction of 30-day mortality (AUC: 0.734, p = 0.001) among all patients. CONCLUSIONS: U-CysLT increase during hospitalization in critical COVID-19 patients, especially in hypertensives on VV-ECMO. U-CysLT association with severe outcomes suggests their usefulness for prognostication and as therapeutic targets.


Asunto(s)
COVID-19 , Humanos , COVID-19/terapia , Leucotrienos , Biomarcadores , Cisteína , Estudios Retrospectivos
8.
Artículo en Inglés | MEDLINE | ID: mdl-35805650

RESUMEN

Temporomandibular disorders (TMD) and headache are complex. This study aims to assess the association between TMD, headache, and psychological dimensions such as psychological inflexibility and pain acceptance. The sample consisted of 120 participants following a non-probabilistic convenience sampling strategy through a direct invitation to the patients attending our facilities and their relatives (n = 61 diagnosed with headache, n = 34 diagnosed with TMD-headache, n = 25 control group). Diagnostic Criteria for Temporomandibular Disorders (DC-TMD), International Classification of Headache Disorders (ICHD-3 beta version), Chronic Pain Acceptance Questionnaire (CPAQ-8), and Psychological Inflexibility in Pain Scale (PIPS) were used as assessment tools. One-way ANOVA, multiple regression analysis (MRA), and the Johnson-Neyman approach were run by IBM SPSS, version 27 (IBM® Company, Chicago, IL, USA). The significance level was 0.05. One third of our sample presented with headache with TMD. Females were predominant. Males with headache, no systemic disease, less pain severity but higher frequency, living longer with the disease and having sensitive changes, showed higher pain acceptance. When headache occurs with TMD, women with higher education, no headache family history, less pain, and no motor changes showed higher pain acceptance. Patients with both conditions are more liable to have chronic pain and pain inflexibility. Pain intensity and willingness explain 50% of the psychological inflexibility in the headache group. In our sample, individuals suffering from both conditions show greater pain inflexibility, implicating more vivid suffering experiences, leading to altered daily decisions and actions. However, further studies are needed to highlight this possible association.


Asunto(s)
Dolor Crónico , Trastornos de la Articulación Temporomandibular , Dolor Facial , Femenino , Cefalea/epidemiología , Cefalea/etiología , Humanos , Masculino , Dimensión del Dolor , Encuestas y Cuestionarios , Trastornos de la Articulación Temporomandibular/complicaciones , Trastornos de la Articulación Temporomandibular/epidemiología
9.
Brain Sci ; 12(5)2022 Apr 21.
Artículo en Inglés | MEDLINE | ID: mdl-35624913

RESUMEN

Migraine is a complex neurovascular disorder affecting one billion people worldwide, mainly females. It is characterized by attacks of moderate to severe headache pain, with associated symptoms. Receptor activity modifying protein (RAMP1) is part of the Calcitonin Gene-Related Peptide (CGRP) receptor, a pharmacological target for migraine. Epigenetic processes, such as DNA methylation, play a role in clinical presentation of various diseases. DNA methylation occurs mostly in the gene promoter and can control gene expression. We investigated the methylation state of the RAMP1 promoter in 104 female blood DNA samples: 54 migraineurs and 50 controls. We treated DNA with sodium bisulfite and performed PCR, Sanger Sequencing, and Epigenetic Sequencing Methylation (ESME) software analysis. We identified 51 CpG dinucleotides, and 5 showed methylation variability. Migraineurs had a higher number of individuals with all five CpG methylated when compared to controls (26% vs. 16%), although non-significant (p = 0.216). We also found that CpG -284 bp, related to the transcription start site (TSS), showed higher methylation levels in cases (p = 0.011). This CpG may potentially play a role in migraine, affecting RAMP1 transcription or receptor malfunctioning and/or altered CGRP binding. We hope to confirm this finding in a larger cohort and establish an epigenetic biomarker to predict female migraine risk.

10.
Rev. ABENO ; 22(2): 1617, jan. 2022. graf, ilus
Artículo en Portugués | BBO - Odontología | ID: biblio-1373697

RESUMEN

As implicações éticas do uso de redes sociais por profissionais da saúde têm ocupado espaço na agenda da Bioética quando se considera os direitos do paciente e o risco de exposição de sua imagem. Este estudo buscou conhecer a percepção de estudantesde Odontologia sobre a exposição da imagem de pacientes em redes sociais. Trata-se de estudo observacional transversal, quantitativo, com aplicação de questionário a estudantes de um curso de Odontologia. Os dados foram tabulados e analisados por meio de estatísticas descritivas. A taxa de resposta foi de 73,5% (n=247), todos utilizando redes sociais e 33,1% (n=82) declararam já ter realizado fotografia de paciente na clínica de ensino. Muitos estudantes ainda não têm clareza sobre as questões éticas que envolvem a divulgação de imagem de pacientes em rede social. Isso revela a importância de se ater a esse tópico nos cursos brasileiros de graduação em Odontologia (AU).


The ethical implications of social networks use by health professionals have occupied space on the Bioethics' agenda, when considering the rights of patients and the risk of exposing their image. This study aimed to understand the perception of dentistry students about the exposure of patients image in social networks. This is a cross-sectional, quantitative, observational study, with the application of a questionnaire to students of a Dentistry course. It was used the descriptive statistics for tabulating and analyzing the data. The response rate was 73.5% (n=247), all using social networks, and 33.1% (n=82) reported having already taken a patient photograph at the training clinic. Many students are still unclear about the ethical issues surrounding the dissemination of patient images on social media. The ethical implications of social networks use by health professionals haveoccupied space on the Bioethics' agenda, when considering the rights of patients and the risk of exposing their image (AU).


Asunto(s)
Humanos , Masculino , Adolescente , Adulto , Persona de Mediana Edad , Estudiantes de Odontología , Actitud del Personal de Salud , Confidencialidad/ética , Ética Odontológica/educación , Redes Sociales en Línea , Percepción/ética , Bioética/educación , Estudios Transversales/métodos , Encuestas y Cuestionarios , Fotografía
11.
Hum Genet ; 141(1): 1-14, 2022 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-34686893

RESUMEN

Migraine is a common and complex neurologic disorder that affects approximately 15-18% of the general population. Although the cause of migraine is unknown, some genetic studies have focused on unravelling rare and common variants underlying the pathophysiological mechanisms of this disorder. This review covers the advances in the last decade on migraine genetics, throughout the history of genetic methodologies used, including recent application of next-generation sequencing techniques. A thorough review of the literature interweaves the genomic and transcriptomic factors that will allow a better understanding of the mechanisms underlying migraine pathophysiology, concluding with the clinical utility landscape of genetic information and future consideration to creating a new frontier toward advancing the field of personalized medicine.


Asunto(s)
Predisposición Genética a la Enfermedad , Genómica , Trastornos Migrañosos/genética , Trastornos Migrañosos/fisiopatología , Transcriptoma , Biomarcadores , Variación Genética , Estudio de Asociación del Genoma Completo , Humanos , Medicina de Precisión
12.
Rev. biol. trop ; 69(2)jun. 2021.
Artículo en Español | LILACS, SaludCR | ID: biblio-1387632

RESUMEN

Resumen Introducción: El banco de semillas en el suelo es uno de los indicadores ecológicos más importantes para la evaluación y monitoreo de recuperación de ecosistemas degradados. Así mismo, actualmente indicadores ecológicos de restauración son usados en áreas afectadas por la ruptura de la represa de relaves de Fundão en Mariana, Minas Gerais, Brasil. Objetivo: En este estudio se evaluó la variación de la riqueza, composición de especies, densidad y parámetros fitosociológicos del banco de semillas en dos profundidades de relaves mineros en Mariana, municipio de Mariana, Minas Gerais, Brasil. Métodos: Se recolectaron 15 muestras por nivel de profundidad, en la capa superior (Profundidad1, P1 = 0-2.5 cm) y capa inferior (Profundidad2, P2 = 2.5-5.0 cm) del relave de minería para examinar el banco de semillas viable, que luego se colocó en un invernadero para la germinación. Posteriormente se contaron e identificaron semanalmente todos los individuos de cada especie durante un período de seis meses. Resultados: Se demostró que existe un banco de semillas en las capas superficiales de relaves mineros acumulados en las áreas afectadas de Mariana, con una marcada diferencia entre profundidades en términos de riqueza de especies y densidad de individuos. Se observó una mayor riqueza y número de individuos en P1, (1 165 semillas germinadas), pertenecientes a 18 familias y 47 especies, en comparación a P2 (197 individuos), pertenecientes a 12 familias y 23 especies. El banco de semillas de la capa P1 está influenciado por la lluvia de semillas del bosque cercano. Por otro lado, el banco de semillas de P2, puede ser característico de los relaves mineros. Conclusiones: El banco de semillas estudiado puede tener efectos positivos sobre la recuperación en el área de estudio, debido a la alta proporción de especies nativas, pioneras y anemocóricas típicas de etapas iniciales de sucesión secundaria.


Abstract Introduction: The soil seed bank is one of the most important ecological indicators for evaluating and monitoring the resilience of degraded ecosystems. Likewise, ecological restoration indicators are currently used in areas affected by the rupture of the Fundão tailings dam in Mariana, Minas Gerais, Brazil. Objective: To evaluate the seed bank at two depths of areas affected by mining tailings, Mariana municipality, Minas Gerais, Brazil. Methods: 15 samples (40 × 40 cm) were collected per level of depth, in the upper layer (Depth1, P1 = 0-2.5 cm), and lower layer (Depth2, P2 = 2.5-5.0 cm) of the mining tailings to survey the viable seed bank, which was later placed in a greenhouse for germination and seedling identification. The samples were placed in plastic trays to germinate in the nursery, then counted and identified weekly for six months. Results: The results showed that there is a seed bank in the surface layers of accumulated mining tailings in the affected areas of Mariana, with a marked difference between depths in terms of species richness and density of individuals. Higher species richness and number of individuals were observed in P1, (1 165 germinated seeds), belonging to 18 families and 47 species, in comparison to P2 (197 individuals), belonging to 12 families and 23 species. Probably the seed bank of layer P1 is influenced by the rain of seeds from the nearby forest. On the other hand, the P2 seed bank can be characteristic of mining tailings. Conclusions: Seed bank patterns can have positive effects on forest resilience at the local-scale, due to the high proportion of native, pioneer and anemochorical species of early successional stages.


Asunto(s)
Banco de Semillas/tendencias , Minería , Regeneración , Brasil , Dispersión de Semillas
13.
An Acad Bras Cienc ; 93(1): e20201209, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33886703

RESUMEN

The restoration methods applied on the areas affected by the Fundão tailings dam collapse have a high priority in Mariana region. We evaluated the effect of different restoration methods and site preparation techniques, depth and seasonality on penetration resistance of tailings, and how these predictors affect tree aboveground biomass in areas affected by the Fundão dam collapse in Mariana, Brazil. No significant differences in penetration resistance and aboveground biomass between treatments were observed, but significant differences were observed between seasonal periods. The main univariate model explained the significant effects of depth and seasonality, mainly by a negatively wet effect on penetration resistance. According to the best models (univariate and multivariate) were those that had depth as a predictor. This study showed how penetration resistance can be an indicator to select the best period for restoration process in areas affected by the collapse of the Fundão dam, but no limit to the aboveground biomass recovery on tailing.


Asunto(s)
Minería , Colapso de la Estructura , Biomasa , Brasil , Monitoreo del Ambiente , Bosques
14.
Pharmacol Res ; 160: 105075, 2020 10.
Artículo en Inglés | MEDLINE | ID: mdl-32653651

RESUMEN

Nowadays, non-biological treatments remain valuable approaches among the therapeutic armamentarium of inflammatory bowel disease (IBD). Mesalamine is the core treatment of mild­to­moderate ulcerative colitis (UC) and corticosteroids are crucial for the induction of remission of moderate­to­severe flares in both UC and Crohn's disease (CD). Even approaches as cyclosporine, tacrolimus, azathioprine, methotrexate, and surgery still have a nuclear position as strategies to induce and/or maintain remission in IBD. Due to their particularities and to the accumulated evidence, each of these strategies conquered peculiar roles in the overall IBD strategy, all of them contributing to better outcomes. This review emphasizes the particular roles that non-biological treatments gained over time: recent mesalamine formulations to increase adhesion rates, higher doses of 5-ASA for high-risk patients, MMX technology to improve drug release and attain higher bowel concentrations, cyclosporine as a bridge to vedolizumab, tacrolimus as a potential alternative to thiopurines or infliximab, azathioprine in combination therapy with infliximab and dubious in monotherapy, and surgery as a mean to a "better end".


Asunto(s)
Antiinflamatorios/uso terapéutico , Colitis Ulcerosa/tratamiento farmacológico , Enfermedad de Crohn/tratamiento farmacológico , Fármacos Gastrointestinales/uso terapéutico , Corticoesteroides/uso terapéutico , Antiinflamatorios/efectos adversos , Colitis Ulcerosa/diagnóstico , Colitis Ulcerosa/inmunología , Enfermedad de Crohn/diagnóstico , Enfermedad de Crohn/inmunología , Ciclosporina/uso terapéutico , Procedimientos Quirúrgicos del Sistema Digestivo , Fármacos Gastrointestinales/efectos adversos , Humanos , Mesalamina/uso terapéutico , Metotrexato/uso terapéutico , Tacrolimus/uso terapéutico , Resultado del Tratamiento
15.
Pharmacol Res Perspect ; 8(3): e00601, 2020 06.
Artículo en Inglés | MEDLINE | ID: mdl-32476298

RESUMEN

Recently, the gut microbiome has become an important field of interest. Indeed, the microbiome has been associated to numerous drug interactions and it is thought to influence the efficacy of pharmacologic treatments. Although statins are widely prescribed medications, there remains considerable variability in its therapeutic response. In this context, we aimed to investigate how statins modulate the gut microbiome and, reversely, how can the microbiome influence the course of anti-hypercholesterolemic treatment. We conducted a systematic review by searching four online databases, in accordance with PRISMA guidelines. Studies addressing gut microbiome changes following statin treatment and those assessing statins' response and associating it with patients' microbiome were included. Due to the limited number of results, we decided to include studies enrolling both humans and animals. We summarized information from three human and seven animal studies and aimed to assess the influence of gut microbiome composition on statin response (Outcome 1) and to evaluate the impact of statin treatment on the gut microbiome (Outcome 2). An association between a certain microbiome composition that promoted the lipid-lowering effect of statins was found. However, what kind of microorganisms and how they can exert this effect remains uncertain. Furthermore, statins might have a role in the modulation of the gut microbiome, but then again, it is still unknown whether this change is directly caused by the drug or another metabolic mechanism. Even though gut microbiota may have several potential therapeutic implications, its use as a personalized predictive biomarker requires further studies.


Asunto(s)
Microbioma Gastrointestinal/efectos de los fármacos , Inhibidores de Hidroximetilglutaril-CoA Reductasas/farmacología , Hipercolesterolemia/tratamiento farmacológico , Animales , Humanos , Hipercolesterolemia/microbiología , Lípidos/sangre
17.
Orphanet J Rare Dis ; 14(1): 164, 2019 07 05.
Artículo en Inglés | MEDLINE | ID: mdl-31277718

RESUMEN

BACKGROUND: High resolution genome-wide copy number analysis, routinely used in clinical diagnosis for several years, retrieves new and extremely rare copy number variations (CNVs) that provide novel candidate genes contributing to disease etiology. The aim of this work was to identify novel genetic causes of neurodevelopmental disease, inferred from CNVs detected by array comparative hybridization (aCGH), in a cohort of 325 Portuguese patients with intellectual disability (ID). RESULTS: We have detected CNVs in 30.1% of the patients, of which 5.2% corresponded to novel likely pathogenic CNVs. For these 11 rare CNVs (which encompass novel ID candidate genes), we identified those most likely to be relevant, and established genotype-phenotype correlations based on detailed clinical assessment. In the case of duplications, we performed expression analysis to assess the impact of the rearrangement. Interestingly, these novel candidate genes belong to known ID-related pathways. Within the 8% of patients with CNVs in known pathogenic loci, the majority had a clinical presentation fitting the phenotype(s) described in the literature, with a few interesting exceptions that are discussed. CONCLUSIONS: Identification of such rare CNVs (some of which reported for the first time in ID patients/families) contributes to our understanding of the etiology of ID and for the ever-improving diagnosis of this group of patients.


Asunto(s)
Discapacidad Intelectual/genética , Aberraciones Cromosómicas , Hibridación Genómica Comparativa , Variaciones en el Número de Copia de ADN/genética , Femenino , Estudios de Asociación Genética , Genómica , N-Metiltransferasa de Histona-Lisina/genética , Humanos , Masculino , Linaje , Fenotipo
19.
Sci Total Environ ; 676: 746-755, 2019 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-31054418

RESUMEN

Understanding the levels and drivers of contamination in top predators is important for their conservation and eventual use as sentinels in environmental monitoring. Therefore, metals and trace elements were analyzed in feathers of Bonelli's eagles (Aquila fasciata) from southern Portugal in 2007-2013, where they are believed to be exposed to a wide range of contamination sources such as agricultural land uses, urban areas, active and abandoned mines and a coal-fired power plant. We focused on concentrations of aluminum (Al), arsenic (As), copper (Cu), chromium (Cr), mercury (Hg), lead (Pb), selenium (Se) and zinc (Zn), as these contaminants are potentially associated with those sources and are known to pose a risk for terrestrial vertebrates. Stable isotope values of nitrogen (δ15N: 15N/14N), carbon (δ13C: 13C/12C) and sulphur (δ34S: 34S/32S) were used as dietary proxies to control for potential effects of prey composition on the contamination pattern. The spatial distribution of potential contamination sources was quantified using geographic information systems. Concentrations of Hg in the southern part of the study area were above a reported toxicity threshold for raptors, particularly in territories closer to a coal-fired power plant at Sines, showing that contamination persisted after a previous assessment conducted in the 1990s. Hg and Se levels were positively correlated with δ15N, which indicates biomagnification. Concentrations of As, Cr, Cu, Pb and Zn were generally low and unrelated to mining- or industrial activities, indicating low environmental background concentrations. Al was found at higher concentrations in the southernmost areas of Portugal, but this pattern might be related to external soil contamination on feathers. Overall, this study indicates that, among all elements studied, Hg seems to be the most important contaminant for Bonelli's eagles in southern Portugal, likely due to the power plant emissions and biomagnification of Hg in terrestrial food webs.


Asunto(s)
Monitoreo del Ambiente , Contaminantes Ambientales/metabolismo , Falconiformes/metabolismo , Cadena Alimentaria , Animales , Exposición Dietética/estadística & datos numéricos , Contaminantes Ambientales/análisis , Plumas/química , Portugal , Rapaces , Oligoelementos/análisis
20.
Ann Clin Transl Neurol ; 6(4): 748-754, 2019 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-31019999

RESUMEN

OBJECTIVES: Transthyretin (TTR) familial amyloid polyneuropathy (FAP) (OMIM 176300) shows a variable age-at-onset (AO), including within families. We hypothesized that variants in C1QA and C1QC genes, might also act as genetic modifiers of AO in TTR-FAP Val30Met Portuguese patients. METHODS: We analyzed DNA samples of 267 patients (117 families). To search for variants, all exons and flanking regions were genotyped by automated sequencing. We used generalized estimating equations (GEEs) to take into account the non-independency of AO among relatives. Intensive in silico analyses were performed, using various software to assess miRNAs target sites, splicing sites, transcription factor binding sites alterations, and gene-gene interactions. RESULTS: Two variants for C1QA gene, GA genotype of rs201693493 (P < 0.001) and CT genotype of rs149050968 (P < 0.001), were significantly associated with later AO. In silico analysis demonstrated, that rs201693493 may alter splicing activity. Regarding C1QC, we found three statistically significant results: GA genotype of rs2935537 (P = 0.003), GA genotype of rs201241346 (P < 0.001) and GA genotype of rs200952686 (P < 0.001). The first two were associated with earlier AO, whereas the third was associated with later-onset. INTERPRETATION: C1QA was associated with later onset, whereas C1QC may have a double role: variants may confer earlier or later AO. As found in a study in Cyprus, we confirmed the role of complement C1Q genes (and thus of inflammation) as modulator of AO in Portuguese patients with TTR-FAP Val30Met.


Asunto(s)
Neuropatías Amiloides Familiares/metabolismo , Glicoproteínas de Membrana/genética , Prealbúmina/genética , Receptores de Complemento/genética , Adulto , Edad de Inicio , Anciano , Amiloide/genética , Amiloide/metabolismo , Neuropatías Amiloides Familiares/complicaciones , Neuropatías Amiloides Familiares/diagnóstico , Femenino , Genotipo , Humanos , Masculino , Persona de Mediana Edad , Mutación/genética , Polimorfismo de Nucleótido Simple/genética
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