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1.
BJOG ; 127(2): 139-146, 2020 01.
Article de Anglais | MEDLINE | ID: mdl-31597208

RÉSUMÉ

Community-wide high-throughput sequencing has transformed the study of the vaginal microbiome, and clinical applications are on the horizon. Here we outline the three main community sequencing methods: (1) amplicon sequencing, (2) shotgun metagenomic sequencing, and (3) metatranscriptomic sequencing. We discuss the advantages and limitations of community sequencing generally, and the unique strengths and weaknesses of each method. We briefly review the contributions of community sequencing to vaginal microbiome research and practice. We develop suggestions for critically interpreting research results and potential clinical applications based on community sequencing of the vaginal microbiome. TWEETABLE ABSTRACT: We review the advantages and limitations of amplicon sequencing, metagenomics, and metatranscriptomics methods for the study of the vaginal microbiome.


Sujet(s)
Microbiote/génétique , Vagin/microbiologie , Femelle , Humains , ARN ribosomique 16S , Reproductibilité des résultats , Analyse de séquence d'ADN
2.
Sci Rep ; 6: 19393, 2016 Jan 20.
Article de Anglais | MEDLINE | ID: mdl-26786552

RÉSUMÉ

Non-fibrillar soluble oligomeric forms of amyloid-ß peptide (oAß) and tau proteins are likely to play a major role in Alzheimer's disease (AD). The prevailing hypothesis on the disease etiopathogenesis is that oAß initiates tau pathology that slowly spreads throughout the medial temporal cortex and neocortices independently of Aß, eventually leading to memory loss. Here we show that a brief exposure to extracellular recombinant human tau oligomers (oTau), but not monomers, produces an impairment of long-term potentiation (LTP) and memory, independent of the presence of high oAß levels. The impairment is immediate as it raises as soon as 20 min after exposure to the oligomers. These effects are reproduced either by oTau extracted from AD human specimens, or naturally produced in mice overexpressing human tau. Finally, we found that oTau could also act in combination with oAß to produce these effects, as sub-toxic doses of the two peptides combined lead to LTP and memory impairment. These findings provide a novel view of the effects of tau and Aß on memory loss, offering new therapeutic opportunities in the therapy of AD and other neurodegenerative diseases associated with Aß and tau pathology.


Sujet(s)
Potentialisation à long terme , Mémoire , Agrégats de protéines , Agrégation pathologique de protéines , Multimérisation de protéines , Protéines tau/métabolisme , Maladie d'Alzheimer/métabolisme , Maladie d'Alzheimer/anatomopathologie , Maladie d'Alzheimer/psychologie , Peptides bêta-amyloïdes/métabolisme , Animaux , Modèles animaux de maladie humaine , Espace extracellulaire/métabolisme , Hippocampe/métabolisme , Hippocampe/anatomopathologie , Souris , Neurones/métabolisme , Protéines tau/composition chimique
3.
J Nucl Med ; 35(8): 1351-7, 1994 Aug.
Article de Anglais | MEDLINE | ID: mdl-8046493

RÉSUMÉ

UNLABELLED: Canine models of autologous PE and balloon occlusion of the pulmonary vasculature were used to evaluate radioaerosol deposition and to quantify radioaerosol clearance in the immediate postembolic period. METHODS: A total of 28 animals were anesthetized, intubated and studied (central balloon occlusion = 4, peripheral balloon occlusion = 7, autologous PE = 5, various control groups = 12). A gamma camera computer system was used to monitor the distribution and clearance rate of inhaled DTPA radioaerosol. The perfusion defect distribution was determined after the radioaerosol study using 99mTc-MAA. RESULTS: A new radioaerosol deposition defect was seen in 3 of 16 animals in a zone of acute vascular occlusion by a balloon (n = 2) or PE (n = 1). In addition, radioaerosol clearance rates were altered substantially. Peripheral vascular occlusion and PE caused radioaerosol clearance rates to accelerate significantly (control clearance half-time = 33.6 +/- 4.6 min, post-balloon occlusion = 19.0 +/- 8.3 min, post-PE = 12.4 +/_ 3.7 min, both p < 0.05). In only one case did these clearance rate changes create a visible abnormality in the aerosol images. CONCLUSIONS: The pulmonary deposition patterns and clearance rates of 99mTc-DTPA radioaerosol can be altered by acute vascular occlusion or PE. These findings should be considered when interpreting radioaerosol images in patients with suspected PE.


Sujet(s)
Poumon/imagerie diagnostique , Artère pulmonaire , Embolie pulmonaire/imagerie diagnostique , Pentétate de technétium (99mTc) , Aérosols , Animaux , Cathétérisme , Chiens , Scintigraphie , Agrégat d'albumine marquée au technétium (99mTc)
4.
Radiographics ; 13(6): 1337-48, 1993 Nov.
Article de Anglais | MEDLINE | ID: mdl-8290728

RÉSUMÉ

The x-ray spectrum is defined as the energy distribution of the radiation produced in an x-ray exposure. The x-ray spectrum has a major impact on image quality and radiation dose delivered to patients. The authors explored the effects of three key factors on x-ray spectra: generator type, peak tube potential, and filtration. Different generator types are characterized by the amount of ripple in the kilovoltage waveform. Those with high (100%) ripple such as single-phase units produce less penetrating radiation than units with low (4%) ripple such as three-phase, 12-pulse generators. As peak tube potential increases, the half-value layer increases nearly linearly; radiation output increases by approximately the square of the tube potential. Filtration materials with atomic numbers less than 42, such as aluminum, titanium, copper, and niobium, produce similar spectra, with only slight variations in efficiency. Although aluminum has the lowest efficiency, this may be compensated for by increasing milliampere seconds. Filtration in addition to the inherent filtration provided by the tube reduces both skin surface dose and average depth-dose, with the optimal amount being approximately 2-3 mm or less of aluminum-equivalent material.


Sujet(s)
Radiographie , Filtration , Humains , Dose de rayonnement , Radioprotection , Amélioration d'image radiographique , Radiographie/instrumentation , Radiométrie
8.
Surgery ; 104(3): 500-6, 1988 Sep.
Article de Anglais | MEDLINE | ID: mdl-3261895

RÉSUMÉ

The appropriate therapy for continued bleeding despite sclerotherapy remains controversial. This study evaluates a devascularization procedure performed without the risks of major surgery and general anesthesia. Fifty consecutive patients, each with an endoscopically proven variceal hemorrhage that was uncontrollable with sclerotherapy, were treated with minimally invasive devascularization. The procedure was performed in three stages. First, the portal pressure was sharply reduced by angiographic embolization of the midsplenic artery. Then the esophagogastric variceal network was thrombosed by means of a catheter introduced during laparotomy, which created a portoazygos disconnection. Finally, the left gastric and left gastroepiploic arteries were embolized, which completed devascularization of the proximal stomach. According to the Child classification, 16 patients were in class B and 34 were in class C. All Child's class B patients (16/16) and 71% (24/34) of Child's class C patients survived hospitalization. One-year survival was 94% (15/16) for Child's class B and 62% (21/34) for Child's class C patients. Rebleeding occurred in 63% (25/40) of the discharged patients but caused the death of only seven. In conclusion, the 20% initial hospital mortality for these difficult patients was significantly better than that reported for emergency surgery, and the rate of rebleeding was comparable to that seen with other nonshunting therapies.


Sujet(s)
Artères/chirurgie , Varices oesophagiennes et gastriques/chirurgie , Hémorragie gastro-intestinale/chirurgie , Solutions sclérosantes/usage thérapeutique , Embolisation thérapeutique , Varices oesophagiennes et gastriques/thérapie , Oesophage/vascularisation , Femelle , Études de suivi , Hémorragie gastro-intestinale/thérapie , Humains , Mâle , Adulte d'âge moyen , Rate/vascularisation , Estomac/vascularisation
19.
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