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1.
Phys Rev Lett ; 122(18): 181601, 2019 May 10.
Artigo em Inglês | MEDLINE | ID: mdl-31144902

RESUMO

We find new and compelling evidence for the metastability of supersymmetry-breaking states in holographic backgrounds whose consistency has been the source of ongoing disagreements in the literature. As a concrete example, we analyze anti-D3 branes at the tip of the Klebanov-Strassler throat. Using the blackfold formalism we examine how temperature affects the conjectured metastable state and determine whether and how the existing extremal results generalize when going beyond extremality. In the extremal limit we exactly recover the results of Kachru, Pearson, and Verlinde, in a regime of parameter space that was previously inaccessible. Away from extremality we uncover a metastable black Neveu-Schwarz five-brane (NS5) state that disappears near a geometric transition where black anti-D3 branes and black NS5 branes become indistinguishable. This is remarkably consistent with complementary earlier results based on the analysis of regularity conditions of backreacted solutions. We therefore provide highly nontrivial evidence for the metastability of antibranes in noncompact throat geometries since we find a consistent picture over different regimes in parameter space.

2.
Int J Immunogenet ; 44(1): 27-31, 2017 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-28032448

RESUMO

This study shows, for the first time, high-resolution allele frequencies of HLA-DQA1 loci in Madeira Island (Portugal) and allows us to better understand and refine present knowledge on DQB1 variation, with the identification of several alleles not previously reported in this population. Estimates on haplotype profile, involving HLA-A, HLA-B, HLA-DRB1, HLA-DQA1 and HLA-DQB1, are also reported.


Assuntos
Frequência do Gene , Variação Genética , Cadeias alfa de HLA-DQ/genética , Cadeias beta de HLA-DQ/genética , Haplótipos , Alelos , Feminino , Expressão Gênica , Antígenos HLA-A/genética , Antígenos HLA-A/imunologia , Antígenos HLA-B/genética , Antígenos HLA-B/imunologia , Cadeias alfa de HLA-DQ/imunologia , Cadeias beta de HLA-DQ/imunologia , Cadeias HLA-DRB1/genética , Cadeias HLA-DRB1/imunologia , Humanos , Masculino , Portugal
3.
Int J Immunogenet ; 44(6): 305-313, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-28834219

RESUMO

This study confirms for Madeira Island (Portugal) population the Type 1 Diabetes (T1D) susceptible and protective Human leucocyte antigens (HLA) markers previously reported in other populations and adds some local specificities. Among the strongest T1D HLA associations, stands out, as susceptible, the alleles DRB1*04:05 (OR = 7.3), DQB1*03:02 (OR = 6.1) and DQA1*03:03 (OR = 4.5), as well as the haplotypes DRB1*04:05-DQA1*03:03-DQB1*03:02 (OR = 100.9) and DRB1*04:04-DQA1*03:01-DQB1*03:02 (OR = 22.1), and DQB1*06:02 (OR = 0.07) and DRB1*15:01-DQA1*01:02-DQB1*06:02 (OR = 0.04) as protective. HLA-DQA1 positive for Arginine at position 52 (Arg52) (OR = 15.2) and HLA-DQB1 negative for Aspartic acid at the position 57 (Asp57) (OR = 9.0) alleles appear to be important genetic markers for T1D susceptibility, with higher odds ratio values than any single allele and than most of the haplotypes. Genotypes generated by the association of markers Arg52 DQA1 positive and Asp57 DQB1 negative increase T1D susceptibility much more than one would expected by a simple additive effect of those markers separately (OR = 26.9). This study also confirms an increased risk for DRB1*04/DRB1*03 heterozygote genotypes (OR = 16.8) and also a DRB1*04-DQA1*03:01-DQB1*03:02 haplotype susceptibility dependent on the DRB1*04 allele (DRB1*04:01, OR = 7.9; DRB1*04:02, OR = 3.2; DRB1*04:04, OR = 22.1).


Assuntos
Alelos , Diabetes Mellitus Tipo 1/genética , Haplótipos/genética , Antígenos de Histocompatibilidade Classe II/genética , Feminino , Humanos , Ilhas , Desequilíbrio de Ligação/genética , Masculino , Portugal
4.
Eur Radiol ; 26(12): 4268-4276, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27384609

RESUMO

OBJECTIVES: To propose national diagnostic reference levels (DRLs) for interventional radiology and to evaluate the impact of the procedural complexity on patient doses. METHODS: Eight interventional radiology units from Spanish hospitals were involved in this project. The participants agreed to undergo common quality control procedures for X-ray systems. Kerma area product (KAP) was collected from a sample of 1,649 procedures. A consensus document established the criteria to evaluate the complexity of seven types of procedures. DRLs were set as the 3rd quartile of KAP values. RESULTS: The KAP (3rd quartile) in Gy cm2 for the procedures included in the survey were: lower extremity arteriography (n = 784) 78; renal arteriography (n = 37) 107; transjugular hepatic biopsies (THB) (n = 30) 45; biliary drainage (BD) (n = 314) 30; uterine fibroid embolization (UFE) (n = 56) 214; colon endoprostheses (CE) (n = 31) 169; hepatic chemoembolization (HC) (n = 269) 303; femoropopliteal revascularization (FR) (n = 62) 119; and iliac stent (n = 66) 170. The complexity involved the increases in the following KAP factors from simple to complex procedures: THB x4; BD x13; UFE x3; CE x3; HC x5; FR x5 and IS x4. CONCLUSIONS: The evaluation of the procedure complexity in patient doses will allow the proper use of DRLs for the optimization of interventional radiology. KEY POINTS: • National DRLs for interventional procedures have been proposed given level of complexity • For clinical audits, the level of complexity should be taken into account. • An evaluation of the complexity levels of the procedure should be made.


Assuntos
Angiografia/métodos , Angiografia/normas , Controle de Qualidade , Radiologia Intervencionista/métodos , Radiologia Intervencionista/normas , Feminino , Humanos , Doses de Radiação , Valores de Referência , Espanha , Inquéritos e Questionários
5.
Mycologia ; 104(5): 1121-32, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22495444

RESUMO

Thirty-five corticioid collections from the Canary Islands and Azores Archipelago were examined morphologically and subjected to molecular phylogenetic analysis. These specimens, almost all collected on endemic and/or xerophilic vegetation, were similar in morphological and ecological characteristics to Hypochnicium prosopidis from the Sonoran Desert (Arizona, USA) and Hyphoderma amoenum. Thirty-seven new ITS nrDNA sequences from these specimens, including the nomenclatural type of the above-mentioned species, were obtained and aligned with homologous sequences from GenBank. These collections were distributed in two strongly supported monophyletic clades. However, similar patterns of morphological variability shared by specimens included in both clades and their differences with related species suggest that they should be described as a single new species. Therefore Hyphoderma macaronesicum is proposed. Studies will be required to test, in a more robust multilocus genealogical framework, whether these populations constitute two cryptic species or whether they are the same taxon. The position of Hypochnicium prosopidis in the resolved tree and its morphological characters suggest that it should be included in Hyphoderma and the new combination Hyphoderma prosopidis is proposed.


Assuntos
Fungos/classificação , Fungos/genética , Polyporales/classificação , Arizona , Açores , Sequência de Bases , DNA Fúngico/genética , DNA Ribossômico/genética , Fungos/isolamento & purificação , Dados de Sequência Molecular , Filogenia , Polyporales/genética , Polyporales/isolamento & purificação , Polyporales/ultraestrutura , Análise de Sequência de DNA/métodos , Espanha
6.
Nat Cell Biol ; 2(9): 661-5, 2000 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10980708

RESUMO

The nucleus is known to be compartmentalized into units of function, but the processes leading to the spatial organization of chromosomes and nuclear compartments are not yet well defined. Here we report direct quantitative analysis of the global structural perturbations of interphase chromosome and interchromosome domain distribution caused by infection with herpes simplex virus-1 (HSV-1). Our results show that the peripheral displacement of host chromosomes that correlates with expansion of the viral replication compartment (VRC) is coupled to a twofold increase in nuclear volume. Live cell dynamic measurements suggest that viral compartment formation is driven by the functional activity of viral components and underscore the significance of spatial regulation of nuclear activities.


Assuntos
Núcleo Celular/virologia , Cromatina/virologia , Herpesvirus Humano 1/fisiologia , Núcleo Celular/ultraestrutura , Células HeLa , Histonas/genética , Histonas/ultraestrutura , Humanos , Microscopia Confocal , Microscopia de Fluorescência
7.
Acta Ortop Mex ; 35(1): 85-91, 2021.
Artigo em Espanhol | MEDLINE | ID: mdl-34480446

RESUMO

The purpose of this review is to provide an overview of current literature on the diagnosis and treatment of sacroiliac pain. Designation as a source of lower back pain has been controversial; However, as knowledge about the joint increases, its role as a generator of chronic pain has become better elucidated. The literature states that sacroiliac joint is the cause of pain in up to 30% of patients. Clinically, diagnosing sacroiliac pain can be difficult to assess; However, pain semiology, patient posture/movement and manual testing are useful for making the presumptive diagnosis of sacroiliac dysfunction. The most effective diagnostic test is image-guided injection of anesthetic solutions into the joint, which is considered positive if there is at least 75% acute symptom relief. Treatment begins with physiotherapy and/or intra-articular infiltration of steroids. If these fails, a possible option is radiofrequency (rizotomy) denervation of the joint. If this does not provide adequate relief, surgery may be considered, in the form of fusion; various work supports favorable outcomes in selected patients.


El propósito de esta revisión es proporcionar una visión general de la literatura actual sobre el diagnóstico y tratamiento del dolor sacroilíaco. La designación como fuente de dolor lumbar ha sido controvertida; sin embargo, a medida que aumenta el conocimiento sobre la articulación, su papel como generador de dolor crónico se ha dilucidado mejor. La literatura afirma que la articulación sacroilíaca es la causa de dolor en hasta 30% de los pacientes. Clínicamente, el diagnóstico de dolor sacroilíaco puede ser difícil de evaluar; sin embargo, la semiología del dolor, la postura/movimiento del paciente y las pruebas manuales son útiles para hacer el diagnóstico presuntivo de disfunción sacroilíaca. La prueba diagnóstica más efectiva es la inyección guiada por imagen de soluciones anestésicas en la articulación, que se considera positiva si hay al menos 75% de alivio de los síntomas de forma aguda. El tratamiento comienza con fisioterapia y/o infiltración intraarticular de esteroides. Si éstos fallan, una posible opción es la denervación por radiofrecuencia (rizotomía) de la articulación. Si esto no proporciona un alivio adecuado, se puede considerar la intervención quirúrgica en forma de fusión; diversos trabajos respaldan los resultados favorables en pacientes seleccionados.


Assuntos
Dor Lombar , Articulação Sacroilíaca , Humanos , Injeções Intra-Articulares , Dor Lombar/diagnóstico , Dor Lombar/etiologia , Dor Lombar/terapia , Articulação Sacroilíaca/diagnóstico por imagem
8.
J Food Prot ; 72(9): 1941-7, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19777898

RESUMO

This study analyzed the content of gamma-emitting radionuclides in fish farmed on the island of Tenerife (Canary Islands, Spain). The fish species included in this study were sea bass, gilthead bream, and rainbow trout. The first two species are produced in offshore enclosures, while the third is produced in a freshwater fish farm. All measurements were performed using two high-purity germanium gamma-ray detectors. The content of gamma-emitting radionuclides in the fodder used to feed the different species of farmed fish studied was also determined. The following nuclides were often detected in the analyzed samples: 137Cs, 40K, 235U, 228Ac, 214Bi, 208Tl, 212Pb, and 214Pb. As a complement to this analysis, 210Po concentrations in two fish samples were determined by alpha spectrometry. The nuclide presenting the highest concentration was, as expected, the naturally occurring 40K, with an average concentration of 0.13 +/- 0.01 Bq/g (wet weight) (Bq/gww) in gilthead bream and sea bass and 0.12 +/- 0.01 Bq/gww in rainbow trout. The 235U concentrations determined in the same fish species were 0.6 +/- 0.5, 0.8 +/- 0.7, and 1.6 +/- 1.0 mBq/gww, respectively. This nuclide is seldom reported in fish samples. The concentrations of 137Cs (the only artificial nuclide determined in this study) in gilthead bream and sea bass were 0.026 +/- 0.006 and 0.044 +/- 0.01 mBq/gww, respectively. In addition to the radiometric analysis, the contribution of the analyzed nuclides to the effective dose from the mean daily intake of the fish was calculated. The calculated contribution, in terms of dose per person, produced by intake of the analyzed fish was 0.8 microSv/year. This value does not represent a significant risk to the local population.


Assuntos
Contaminação de Alimentos/análise , Radioisótopos/análise , Radiometria/métodos , Alimentos Marinhos/análise , Poluentes Químicos da Água/análise , Animais , Bass , Monitoramento Ambiental , Pesqueiros , Humanos , Oncorhynchus mykiss , Dourada , Espanha , Especificidade da Espécie
9.
Neuromuscul Disord ; 29(7): 517-524, 2019 07.
Artigo em Inglês | MEDLINE | ID: mdl-31201046

RESUMO

Spinal muscular atrophy (SMA) is an autosomal recessive disease caused by homozygous deletions or loss-of-function mutations in SMN1, which result in a degeneration of motor neurons in the spinal cord and brain stem. Even without a randomized placebo-controlled trial, salbutamol has been offered to patients with SMA in the neuromuscular clinics of most of hospitals for many years. We describe the response to salbutamol in 48 patients with SMA type II who were not taking any other medication. We investigate the changes over an eighteen-month period in motor functional scales and we analyze side effects and subjective response to treatment. Our results suggest that oral administration of salbutamol might be helpful in the maintenance of motor function in patients with SMA type II. An apparent beneficial effect was observed in functional scales of children under the age of 6, especially during the first 6 months of therapy. The majority of patients of all ages referred some kind of subjective positive effect associated with therapy intake. Salbutamol seemed safe and was well tolerated without serious side effects.


Assuntos
Agonistas Adrenérgicos beta/efeitos adversos , Agonistas Adrenérgicos beta/uso terapêutico , Albuterol/efeitos adversos , Albuterol/uso terapêutico , Atrofias Musculares Espinais da Infância/tratamento farmacológico , Adolescente , Idade de Início , Criança , Pré-Escolar , Feminino , Hospitalização/estatística & dados numéricos , Humanos , Lactente , Estudos Longitudinais , Masculino , Movimento , Procedimentos Ortopédicos/estatística & dados numéricos , Estudos Prospectivos , Escoliose/etiologia , Atrofias Musculares Espinais da Infância/fisiopatologia , Resultado do Tratamento , Adulto Jovem
10.
Tissue Antigens ; 72(6): 593-8, 2008 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19000146

RESUMO

Human leukocyte antigen (HLA)-A locus polymorphisms were examined at high-resolution level, using sequence-based typing, in the four most representative Guinea-Bissau (Northwest Africa) ethnic groups: Balanta, Bijagós, Fula and Papel. Despite the Fula group having significant differences when compared with the other three ethnic groups, all four groups most likely received a genetic input from non sub-Saharans. The Bijagós and Papel groups showed similarities to neighboring populations from Mali and Senegal. The Balanta, despite their oral tradition of an East Africa origin, show affinities to Cameroon populations, highly influenced by Bantu migrations. These results are congruent with historical sources and other genetic studies that support the finding that the Guinea-Bissau genetic pool was influenced by several migrations from North Africa, Sahara and East Africa.


Assuntos
Etnicidade/genética , Antígenos HLA-A/genética , Alelos , Frequência do Gene , Guiné-Bissau , Humanos , Masculino , Filogenia , Polimorfismo Genético
11.
Ann Rheum Dis ; 67(9): 1305-9, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18063673

RESUMO

OBJECTIVES: The aim of the current study was to determine the contribution of interleukin (IL)1 gene cluster polymorphisms previously implicated in susceptibility for ankylosing spondylitis (AS) to AS susceptibility in different populations worldwide. METHODS: Nine polymorphisms in the IL1 gene cluster members IL1A (rs2856836, rs17561 and rs1894399), IL1B (rs16944), IL1F10 (rs3811058) and IL1RN (rs419598, the IL1RA VNTR, rs315952 and rs315951) were genotyped in 2675 AS cases and 2592 healthy controls recruited in 12 different centres in 10 countries. Association of variants with AS was tested by Mantel-Haenszel random effects analysis. RESULTS: Strong association was observed with three single nucleotide polymorphisms (SNPs) in the IL1A gene (rs2856836, rs17561, rs1894399, p = 0.0036, 0.000019 and 0.0003, respectively). There was no evidence of significant heterogeneity of effects between centres, and no evidence of non-combinability of findings. The population attributable risk fraction of these variants in Caucasians is estimated at 4-6%. CONCLUSIONS: This study confirms that IL1A is associated with susceptibility to AS. Association of the other IL1 gene complex members could not be excluded in specific populations. Prospective meta-analysis is a useful tool in confirmation studies of genes associated with complex genetic disorders such as AS, providing sufficiently large sample sizes to produce robust findings often not achieved in smaller individual cohorts.


Assuntos
Interleucina-1/genética , Polimorfismo de Nucleotídeo Único , Espondilite Anquilosante/genética , Frequência do Gene , Predisposição Genética para Doença , Genótipo , Humanos , Interleucina-1alfa/genética , Família Multigênica , Estudos Prospectivos , Espondilite Anquilosante/imunologia
12.
Int Endod J ; 41(11): 997-1004, 2008 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19133089

RESUMO

AIM: To present two cases of external root resorption and in so doing highlight rarer causative factors as well as the difficulties in classifying root resorption. SUMMARY: Root resorption in the permanent dentition is usually pathological. Local factors are the most frequent causes of resorption, most commonly excessive pressure and inflammation. However, many systemic abnormalities have been implicated in the resorption process. Resorption is often an incidental finding during routine examination. Otherwise, late in the disease process, tooth mobility or infection may arise. A rarer form of root resorption is external apical root resorption which may or may not be linked to systemic disease. In most cases, no causative factors are found. At present there is no curative treatment for external apical root resorption. The current management for these patients is symptomatic, minimal intervention and long-term monitoring. KEY LEARNING POINTS: * Apical resorption may be associated with a systemic disease or of an idiopathic origin. It may also occur in association with orthodontic treatment or with pathoses such as tumours, cysts, etc. * In the absence of signs or symptoms of pulpal and/or periapical disease, endodontic treatment is not indicated. * Long-term monitoring of affected patients is essential.


Assuntos
Reabsorção da Raiz/etiologia , Ápice Dentário/patologia , Materiais Dentários , Calcificações da Polpa Dentária/etiologia , Cavidade Pulpar/diagnóstico por imagem , Síndrome de Ehlers-Danlos/complicações , Seguimentos , Gengivite/complicações , Humanos , Masculino , Polietilenos , Radiografia , Reabsorção da Raiz/diagnóstico , Reabsorção da Raiz/terapia , Contenções , Raiz Dentária/diagnóstico por imagem , Adulto Jovem
13.
Mycologia ; 100(4): 673-6, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18833760

RESUMO

Gloeodontia xerophila sp. nov. is described and illustrated from material collected on dead xerophyte debris in the Canary Islands. This species is characterized by the odontioid hymenophore with short aculei, up to 2 mm long, dimitic hyphal system and amyloid, subglobose and verrucose spores, 4-5 x 3-4 microm. The new taxon is compared with other species in the genus and a key to the species of Gloeodontia is provided.


Assuntos
Magnoliopsida/microbiologia , Polyporales/isolamento & purificação , Oceano Atlântico , Polyporales/química , Polyporales/classificação , Polyporales/citologia , Esporos Fúngicos/química , Esporos Fúngicos/citologia
14.
Semergen ; 44(7): 492-499, 2018 Oct.
Artigo em Espanhol | MEDLINE | ID: mdl-29453018

RESUMO

Acute rhinosinusitis is an important health problem. Even though its frequency is not well documented in our country?, the economic burden it bears is not insignificant as it notably alters the quality of life of affected patients. Its diagnosis is generally clinical in nature, with further studies reserved only for the differential diagnoses of complications or tumour-like processes. The most frequent causes are viral infections, although Streptococcus pneumoniae and Haemophilus influenzae are the most commonly isolated bacterial agents. Although complications are uncommon nowadays, they can be serious when they occur, and commonly include orbital infections, closely followed in frequency by intracranial and bone infections. Treatment should consist of symptomatic measures, like saline rinses and antibiotics in cases of bacterial origin.


Assuntos
Atenção Primária à Saúde , Rinite/terapia , Sinusite/terapia , Doença Aguda , Antibacterianos/uso terapêutico , Infecções Bacterianas/microbiologia , Infecções Bacterianas/terapia , Humanos , Qualidade de Vida , Rinite/microbiologia , Sinusite/microbiologia
15.
Semergen ; 44(5): 355-363, 2018.
Artigo em Espanhol | MEDLINE | ID: mdl-28882733

RESUMO

BACKGROUND: Primary Care is the fundamental axis of our health system and obliges us to be consistent with our prescriptions. The non-steroidal anti-inflammatory drugs (NSAIDs) have been associated with increased cardiovascular risk and increased risk of all causes of death, as well as acute myocardial infarction (AMI) in patients with a previous myocardial infarction. Pain and cardiac patient management are 2 basic pillars in our daily activity, and we must know the limitations of NSAIDs in patients with established cardiovascular risk. OBJECTIVES: We present a review of the scientific literature with primary interest in the role of NSAIDs and cardiovascular risk. The objective is to determine the relationship between the consumption of different NSAIDs and the fatal and non-fatal events among patients with known coronary disease. METHOD: This is a review of the scientific literature with primary interest in the role of NSAIDs and cardiovascular risk. The literature review was conducted in PubMed search engines like Tripdatabase and with certain keywords. Of the 15 original papers found, 9 did not correspond completely to the central focus, so the approach was decided from 6 original articles from the past 5 years, which address the central focus of increased cardiovascular risk found (fatal and non-fatal events) in patients with prior cardiovascular disease or AMI being prescribed NSAIDs for any reason. The risk of fatal/non-fatal events in each of the studies is expressed by the odds ratio (OR)/hazard ratio (HR), defined as the probability of an event occurring. RESULTS: A moderate risk was observed for ibuprofen. It increases the risk of acute coronary syndrome after 5 years of cardiovascular event, especially in the 2nd year (OR 1.63; 95% CI 1.42-1.87). It also increases the risk of stroke (HR 1.23; 95% IC 1.10-1.38). Cyclo-oxygenase-2 inhibitors were the third risk group, after nabumetone and diclofenac. Celecoxib increases risk from the 14th day of treatment (HR 2.3; 95% CI 1.79-3.02), having an OR of 1.47 (95% CI 1.05-2.07) for new AMI. Rofecoxib shows a risk of fatal cardiovascular events, even at low doses, and after 7 days of treatment (HR 2.5; 95% CI 1.91-3.46), with an OR of 2.30 (95% CI 1.76-2.99) for new AMI. Naproxen had a lower risk of cardiovascular death and new cardiovascular events, but no significant results except for treatment longer than 90 days (HR 1.55; 95% CI 1.10-2.17), with increased gastrointestinal bleeding and associated comorbidity during the first year of treatment (HR 1.44; 95% CI 1.07-1.94). Ketorolac is seen as the drug of greatest risk for new AMI: Oral treatment (OR 3.91; 95% CI 2.02-7.58). The review highlights the cardio-protective factor of certain drugs, such as antiplatelet agents and statins in patients, with NSAIDs use. For example, in patients with greater comorbidity, differences were observed in the OR, with antiplatelet agents consumption giving an OR of 1.37 (95% CI 0.68-2.74), compared to the non-consumption, OR 1.79 (95% CI 1.16-2.78). CONCLUSIONS: The consumption of various NSAIDs and their relationship to increased risk of fatal and non-fatal acute coronary syndrome is classified by years. Consumption increases the risk regardless of the time elapsed in relation to those that did not take them, with the figures remaining virtually stable for five years. Diclofenac and cyclooxygenase-2 inhibitors (especially Rofecoxib) showed an increased risk, unlike naproxen, which had a lower risk. However, naproxen, and because of its greater capacity to generate gastrointestinal bleeding, increased for this reason, fatal events and comorbidity in these patients. Despite this, it still has the best cardiovascular safety profile.


Assuntos
Síndrome Coronariana Aguda/epidemiologia , Anti-Inflamatórios não Esteroides/efeitos adversos , Infarto do Miocárdio/epidemiologia , Síndrome Coronariana Aguda/etiologia , Síndrome Coronariana Aguda/mortalidade , Anti-Inflamatórios não Esteroides/administração & dosagem , Doença das Coronárias/epidemiologia , Doença das Coronárias/mortalidade , Humanos , Infarto do Miocárdio/etiologia , Infarto do Miocárdio/mortalidade , Fatores de Risco , Fatores de Tempo
16.
Fungal Syst Evol ; 2: 57-68, 2018 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-32467888

RESUMO

This article re-evaluates the taxonomy of Hyphoderma macaronesicum based on various strategies, including the cohesion species recognition method through haplotype networks, multilocus genetic analyses using the genealogical concordance phylogenetic concept, as well as species tree reconstruction. The following loci were examined: the internal transcribed spacers of nuclear ribosomal DNA (ITS nrDNA), the intergenic spacers of nuclear ribosomal DNA (IGS nrDNA), two fragments of the protein-coding RNA polymerase II subunit 2 (RPB2), and two fragments of the translation elongation factor 1-α (EF1-α). Our results indicate that the name H. macaronesicum includes at least two separate species, one of which is newly described as Hyphoderma paramacaronesicum. The two species are readily distinguished based on the various loci analysed, namely ITS, IGS, RPB2 and EF1-α.

17.
Arch Intern Med ; 141(4): 520-1, 1981 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-7212897

RESUMO

A 27-year-old, full-term pregnant woman with progressive systemic sclerosis (PSS) came to the hospital with marked proteinuria and edema. Two days later, she gave birth to a normal baby. After delivery and during the next 48 hours, renal failure developed. A renal biopsy specimen disclosed findings characteristic of PSS, and immunofluorescence studies displayed nonspecific deposits of fibrinogen and complement. The patient's general condition deteriorated, with development of pericarditis and pulmonary failure; after several peritoneal dialysis treatments, a peritoneal infection developed, and the patient died of Gram-negative sepsis. The association of PSS and nephrotic syndrome is unusual.


Assuntos
Injúria Renal Aguda/etiologia , Síndrome Nefrótica/complicações , Complicações na Gravidez , Transtornos Puerperais/etiologia , Escleroderma Sistêmico/complicações , Injúria Renal Aguda/patologia , Adulto , Feminino , Humanos , Recém-Nascido , Rim/patologia , Síndrome Nefrótica/patologia , Gravidez , Escleroderma Sistêmico/patologia
18.
Med Phys ; 42(8): 4933-40, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-26233219

RESUMO

PURPOSE: In clinical practice, specific air kerma strength (SK) value is used in treatment planning system (TPS) permanent brachytherapy implant calculations with (125)I and (103)Pd sources; in fact, commercial TPS provide only one SK input value for all implanted sources and the certified shipment average is typically used. However, the value for SK is dispersed: this dispersion is not only due to the manufacturing process and variation between different source batches but also due to the classification of sources into different classes according to their SK values. The purpose of this work is to examine the impact of SK dispersion on typical implant parameters that are used to evaluate the dose volume histogram (DVH) for both planning target volume (PTV) and organs at risk (OARs). METHODS: The authors have developed a new algorithm to compute dose distributions with different SK values for each source. Three different prostate volumes (20, 30, and 40 cm(3)) were considered and two typical commercial sources of different radionuclides were used. Using a conventional TPS, clinically accepted calculations were made for (125)I sources; for the palladium, typical implants were simulated. To assess the many different possible SK values for each source belonging to a class, the authors assigned an SK value to each source in a randomized process 1000 times for each source and volume. All the dose distributions generated for each set of simulations were assessed through the DVH distributions comparing with dose distributions obtained using a uniform SK value for all the implanted sources. The authors analyzed several dose coverage (V100 and D90) and overdosage parameters for prostate and PTV and also the limiting and overdosage parameters for OARs, urethra and rectum. RESULTS: The parameters analyzed followed a Gaussian distribution for the entire set of computed dosimetries. PTV and prostate V100 and D90 variations ranged between 0.2% and 1.78% for both sources. Variations for the overdosage parameters V150 and V200 compared to dose coverage parameters were observed and, in general, variations were larger for parameters related to (125)I sources than (103)Pd sources. For OAR dosimetry, variations with respect to the reference D0.1cm(3) were observed for rectum values, ranging from 2% to 3%, compared with urethra values, which ranged from 1% to 2%. CONCLUSIONS: Dose coverage for prostate and PTV was practically unaffected by SK dispersion, as was the maximum dose deposited in the urethra due to the implant technique geometry. However, the authors observed larger variations for the PTV V150, rectum V100, and rectum D0.1cm(3) values. The variations in rectum parameters were caused by the specific location of sources with SK value that differed from the average in the vicinity. Finally, on comparing the two sources, variations were larger for (125)I than for (103)Pd. This is because for (103)Pd, a greater number of sources were used to obtain a valid dose distribution than for (125)I, resulting in a lower variation for each SK value for each source (because the variations become averaged out statistically speaking).


Assuntos
Algoritmos , Braquiterapia/métodos , Neoplasias da Próstata/radioterapia , Radiometria/métodos , Humanos , Radioisótopos do Iodo/administração & dosagem , Masculino , Modelos Biológicos , Órgãos em Risco , Paládio/administração & dosagem , Próstata/patologia , Próstata/efeitos da radiação , Neoplasias da Próstata/patologia , Radioisótopos/administração & dosagem , Dosagem Radioterapêutica , Planejamento da Radioterapia Assistida por Computador/métodos , Reto/efeitos da radiação , Uretra/efeitos da radiação
19.
J Bone Miner Res ; 18(9): 1664-73, 2003 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-12968676

RESUMO

UNLABELLED: More severe vertebral fractures have more personal impact. In the European Prospective Osteoporosis Study, more severe vertebral collapse was predictable from prior fracture characteristics. Subjects with bi-concave or crush fractures at baseline had a 2-fold increase in incident fracture size and thus increased risk of a disabling future fracture. INTRODUCTION: According to Euler's buckling theory, loss of horizontal trabeculae in vertebrae increases the risk of fracture and suggests that the extent of vertebral collapse will be increased in proportion. We tested the hypothesis that the characteristics of a baseline deformity would influence the size of a subsequent deformity. METHODS: In 207 subjects participating in the European Prospective Osteoporosis Study who suffered an incident spine fracture in a previously normal vertebra, we estimated loss of volume (fracture size) from plane film images of all vertebral bodies that were classified as having a new fracture. The sum of the three vertebral heights (anterior, mid-body, and posterior) obtained at follow-up was subtracted from the sum of the same measures at baseline. Each of the summed height loss for vertebrae with a McCloskey-Kanis deformity on the second film was expressed as a percentage. RESULTS AND CONCLUSIONS: In univariate models, the numbers of baseline deformities and the clinical category of the most severe baseline deformity were each significantly associated with the size of the most severe incident fracture and with the cumulated sum of all vertebral height losses. In multivariate modeling, age and the clinical category of the baseline deformity (crush > bi-concave > uni-concave > wedge) were the strongest determinants of both more severe and cumulative height loss. Baseline biconcave and crush fractures were associated at follow-up with new fractures that were approximately twice as large as those seen with other types of deformity or who previously had undeformed spines. In conclusion, the characteristics of a baseline vertebral deformity determines statistically the magnitude of vertebral body volume lost when a subsequent fracture occurs. Because severity of fracture and number of fractures are determinants of impact, the results should improve prediction of the future personal impact of osteoporosis once a baseline prevalent deformity has been identified.


Assuntos
Fraturas da Coluna Vertebral/etiologia , Fraturas da Coluna Vertebral/patologia , Coluna Vertebral/patologia , Idoso , Idoso de 80 Anos ou mais , Densidade Óssea , Europa (Continente) , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Osteoporose/complicações , Osteoporose/metabolismo , Osteoporose Pós-Menopausa/complicações , Osteoporose Pós-Menopausa/metabolismo , Prognóstico , Estudos Prospectivos , Fraturas da Coluna Vertebral/metabolismo , Coluna Vertebral/metabolismo
20.
J Bone Miner Res ; 17(4): 716-24, 2002 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11918229

RESUMO

Vertebral fracture is one of the major adverse clinical consequences of osteoporosis; however, there are few data concerning the incidence of vertebral fracture in population samples of men and women. The aim of this study was to determine the incidence of vertebral fracture in European men and women. A total of 14,011 men and women aged 50 years and over were recruited from population-based registers in 29 European centers and had an interviewer-administered questionnaire and lateral spinal radiographs performed. The response rate for participation in the study was approximately 50%. Repeat spinal radiographs were performed a mean of 3.8 years following the baseline film. All films were evaluated morphometrically. The definition of a morphometric fracture was a vertebra in which there was evidence of a 20% (+4 mm) or more reduction in anterior, middle, or posterior vertebral height between films--plus the additional requirement that a vertebra satisfy criteria for a prevalent deformity (using the McCloskey-Kanis method) in the follow-up film. There were 3174 men, mean age 63.1 years, and 3,614 women, mean age 62.2 years, with paired duplicate spinal radiographs (48% of those originally recruited to the baseline survey). The age standardized incidence of morphometric fracture was 10.7/1,000 person years (pyr) in women and 5.7/1,000 pyr in men. The age-standardized incidence of vertebral fracture as assessed qualitatively by the radiologist was broadly similar-12.1/1,000 pyr and 6.8/1,000 pyr, respectively. The incidence increased markedly with age in both men and women. There was some evidence of geographic variation in fracture occurrence; rates were higher in Sweden than elsewhere in Europe. This is the first large population-based study to ascertain the incidence of vertebral fracture in men and women over 50 years of age across Europe. The data confirm the frequent occurrence of the disorder in men as well as in women and the rise in incidence with age.


Assuntos
Osteoporose/epidemiologia , Fraturas da Coluna Vertebral/epidemiologia , Distribuição por Idade , Idoso , Comorbidade , Europa (Continente)/epidemiologia , Feminino , Humanos , Incidência , Masculino , Pessoa de Meia-Idade , Prevalência , Estudos Prospectivos , Distribuição por Sexo
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