280 research outputs found

    Lupus Anticoagulunt Associated with Transient Severe Factor X Deficiency: A Report of Two Patients Presenting with Major Bleeding Complications

    Get PDF
    Abstract Acquired factor X (FX) deficiency is rare, but has been reported in diverse disease states, including systemic amyloidosis and respiratory infections. FX deficiency associated with lupus anticoagulant (LA) and a bleeding diathesis has not been previously reported. We report two patients both of whom presented with a severe bleeding diathesis after a preceding respiratory infection due to isolated FX deficiency associated with a LA. The FX deficiency and LA were transient. We conclude that patients with LA may rarely present with severe acquired FX deficiency. This may be another mechanism whereby patients with antiphospholipid antibodies present with bleeding complications

    Prognostic models for surgical-site infection in gastrointestinal surgery: systematic review

    Get PDF
    BACKGROUND: Identification of patients at high risk of surgical-site infection may allow clinicians to target interventions and monitoring to minimize associated morbidity. The aim of this systematic review was to identify and evaluate prognostic tools for the prediction of surgical-site infection in gastrointestinal surgery.METHODS: This systematic review sought to identify original studies describing the development and validation of prognostic models for 30-day SSI after gastrointestinal surgery (PROSPERO: CRD42022311019). MEDLINE, Embase, Global Health, and IEEE Xplore were searched from 1 January 2000 to 24 February 2022. Studies were excluded if prognostic models included postoperative parameters or were procedure specific. A narrative synthesis was performed, with sample-size sufficiency, discriminative ability (area under the receiver operating characteristic curve), and prognostic accuracy compared.RESULTS: Of 2249 records reviewed, 23 eligible prognostic models were identified. A total of 13 (57 per cent) reported no internal validation and only 4 (17 per cent) had undergone external validation. Most identified operative contamination (57 per cent, 13 of 23) and duration (52 per cent, 12 of 23) as important predictors; however, there remained substantial heterogeneity in other predictors identified (range 2-28). All models demonstrated a high risk of bias due to the analytic approach, with overall low applicability to an undifferentiated gastrointestinal surgical population. Model discrimination was reported in most studies (83 per cent, 19 of 23); however, calibration (22 per cent, 5 of 23) and prognostic accuracy (17 per cent, 4 of 23) were infrequently assessed. Of externally validated models (of which there were four), none displayed 'good' discrimination (area under the receiver operating characteristic curve greater than or equal to 0.7).CONCLUSION: The risk of surgical-site infection after gastrointestinal surgery is insufficiently described by existing risk-prediction tools, which are not suitable for routine use. Novel risk-stratification tools are required to target perioperative interventions and mitigate modifiable risk factors.</p

    Case Report Monoclonal Gammopathy of Undetermined Significance (MGUS) in a Man with Fragile X-associated Tremor/Ataxia Syndrome

    Get PDF
    We report the clinical presentation and laboratory findings of a 69-year-old man with fragile X-associated tremor ataxia syndrome (FXTAS), a progressive neurodegenerative disorder, who was noted to have monoclonal gammopathy of undetermined significance (MGUS), a plasma cell proliferative disorder and a precursor disease of multiple myeloma. Both MGUS and FXTAS are associated with microRNA (miRNA) dysregulation. We speculate that individuals with FXTAS may be predisposed to MGUS and further studies are warranted regarding this association

    New class of inhibitors of amyloid-beta fibril formation. Implications for the mechanism of pathogenesis in Alzheimer's disease

    Get PDF
    The amyloid hypothesis suggests that the process of amyloid-beta protein (Abeta) fibrillogenesis is responsible for triggering a cascade of physiological events that contribute directly to the initiation and progression of Alzheimer's disease. Consequently, preventing this process might provide a viable therapeutic strategy for slowing and/or preventing the progression of this devastating disease. A promising strategy to achieve prevention of this disease is to discover compounds that inhibit Abeta polymerization and deposition. Herein, we describe a new class of small molecules that inhibit Abeta aggregation, which is based on the chemical structure of apomorphine. These molecules were found to interfere with Abeta1-40 fibrillization as determined by transmission electron microscopy, Thioflavin T fluorescence and velocity sedimentation analytical ultracentrifugation studies. Using electron microscopy, time-dependent studies demonstrate that apomorphine and its derivatives promote the oligomerization of Abeta but inhibit its fibrillization. Preliminary structural activity studies demonstrate that the 10,11-dihydroxy substitutions of the D-ring of apomorphine are required for the inhibitory effectiveness of these aporphines, and methylation of these hydroxyl groups reduces their inhibitory potency. The ability of these small molecules to inhibit Abeta amyloid fibril formation appears to be linked to their tendency to undergo rapid autoxidation, suggesting that autoxidation product(s) acts directly or indirectly on Abeta and inhibits its fibrillization. The inhibitory properties of the compounds presented suggest a new class of small molecules that could serve as a scaffold for the design of more efficient inhibitors of Abeta amyloidogenesis in vivo

    Drivers of leafcutter ant populations and their interā€trophic relationships in Amazonian forest islands

    Get PDF
    Under habitat loss and fragmentation, the intensity of local ecological processes involving species interactions changes pervasively, accelerating local species extinctions, and disrupting essential ecosystem functions. We addressed this issue by examining the direct population drivers of apex predators (five felid species), armadillo mesopredators, leafcutter ants (Atta sexdens and Atta cephalotes), and the indirect effects mediated by their inter-trophic relationships in a ~25-yr-old land-bridge island system formed by a hydroelectric dam in the Central Amazon. These trophic groups and pioneer tree abundance were surveyed across 34 variable-sized islands and three continuous forest sites. Leafcutter populations were characterized in relation to their occurrence, colony density, and proportion of inactive colonies, and for each leafcutter response, we considered the direct and/or indirect effects of forest area on each trophic group. Leafcutter occupancy was best explained by the direct model, colony density by either the direct or the indirect model, and proportion of inactive colonies by an indirect model via the effects of pioneer tree abundance. The direct forest area effects were positive for apex predators and leafcutter occupancy, but negative for armadillos and pioneer trees. Yet leafcutter colony density declined in increasingly larger forest areas. The absence or low abundance of apex predators on small islands released armadillo hyper-abundance, which contrary to expectation from top-down control, covaried positively with leafcutter colony density. Finally, the indirect model showed that leafcutter colonies were more active under higher pioneer tree abundances. That leafcutter density increases on smaller islands whenever present is likely attributed to the hyper-abundance of pioneer plants and canopy gaps. Although apex predators apparently suppressed armadillos, the remaining fraction of the food web seems to be controlled by bottom-up mechanisms most likely related the overall low foliage palatability typical of wet evergreen forests. Our findings can be used to inform the long-term viability of forest ecosystems affected by hydropower development in lowland Amazonia

    Topology of Type II REases revisited; structural classes and the common conserved core

    Get PDF
    Type II restriction endonucleases (REases) are deoxyribonucleases that cleave DNA sequences with remarkable specificity. Type II REases are highly divergent in sequence as well as in topology, i.e. the connectivity of secondary structure elements. A widely held assumption is that a structural core of five Ī²-strands flanked by two Ī±-helices is common to these enzymes. We introduce a systematic procedure to enumerate secondary structure elements in an unambiguous and reproducible way, and use it to analyze the currently available X-ray structures of Type II REases. Based on this analysis, we propose an alternative definition of the core, which we term the Ī±Ī²Ī±-core. The Ī±Ī²Ī±-core includes the most frequently observed secondary structure elements and is not a sandwich, as it consists of a five-strand Ī²-sheet and two Ī±-helices on the same face of the Ī²-sheet. We use the Ī±Ī²Ī±-core connectivity as a basis for grouping the Type II REases into distinct structural classes. In these new structural classes, the connectivity correlates with the angles between the secondary structure elements and with the cleavage patterns of the REases. We show that there exists a substructure of the Ī±Ī²Ī±-core, namely a common conserved core, ccc, defined here as one Ī±-helix and four Ī²-strands common to all Type II REase of known structure

    The need for multidisciplinarity in specialist training to optimize future patient care

    Get PDF
    Harmonious interactions between radiation, medical, interventional and surgical oncologists, as well as other members of multidisciplinary teams, are essential for the optimization of patient care in oncology. This multidisciplinary approach is particularly important in the current landscape, in which standard-of-care approaches to cancer treatment are evolving towards highly targeted treatments, precise image guidance and personalized cancer therapy. Herein, we highlight the importance of multidisciplinarity and interdisciplinarity at all levels of clinical oncology training. Potential deficits in the current career development pathways and suggested strategies to broaden clinical training and research are presented, with specific emphasis on the merits of trainee involvement in functional multidisciplinary teams. Finally, the importance of training in multidisciplinary research is discussed, with the expectation that this awareness will yield the most fertile ground for future discoveries. Our key message is for cancer professionals to fulfil their duty in ensuring that trainees appreciate the importance of multidisciplinary research and practice
    • ā€¦
    corecore