324 research outputs found

    Association Between Periodontitis and Blood Pressure Highlighted in Systemically Healthy Individuals: Results From a Nested Case-Control Study

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    Recent evidence suggests hypertension and periodontitis are closely linked but limited data is available on the nature of the association. We aimed to investigate the relationship between periodontitis and mean arterial blood pressure in a sample of otherwise systemically healthy individuals. A case-control study including 250 cases (participants with periodontitis) and 250 controls (without periodontitis) was designed from a register of clinical trials conducted between 2000 and 2018 in a university setting. Cases were age, sex, and body mass index balanced with controls. Linear, logistic regression, and mediation models were planned to test the association between various periodontal measures and arterial blood pressure. We further investigated the role of systemic inflammation assessed by hs-CRP (high-sensitivity C-reactive protein) and white cell counts. Cases presented with 3.36 mm Hg (95% CI, 0.91-5.82, P=0.007) higher mean systolic blood pressure and 2.16 mm Hg (95% CI, 0.24-4.08, P=0.027) higher diastolic blood pressure than controls. Diagnosis of periodontitis was associated with mean systolic blood pressure (β=3.46±1.25, P=0.005) and greater odds of systolic blood pressure ≥140 mm Hg (odds ratio, 2.3 [95% CI, 1.15-4.60], P=0.018) independent of common cardiovascular risk factors. Similar findings were observed when continuous measures of periodontal status were modeled against systolic blood pressure. Measures of systemic inflammation although elevated in periodontitis were not found to be mediators of the association between periodontitis and arterial blood pressure values. Periodontitis is linked to higher systolic blood pressure in otherwise healthy individuals. Promotion of periodontal and systemic health strategies in the dental and medical setting could help reduce the burden of hypertension and its complications

    Impact of the treatment of periodontitis on systemic health and quality of life: A systematic review

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    AIM: To investigate the effect of treatment of periodontitis on systemic health outcomes, pregnancy complications, and associated quality of life. MATERIALS AND METHODS: Systematic electronic searches were conducted to identify randomized controlled trials with minimum 6-month follow-up and reporting on the outcomes of interest. Qualitative and quantitative analyses were performed as deemed suitable. RESULTS: Meta-analyses confirmed reductions of high-sensitivity C-reactive protein (hs-CRP) [0.56 mg/L, 95% confidence interval (CI) (−0.88, −0.25), p < .001]; interleukin (IL)-6 [0.48 pg/ml, 95% CI (−0.88, −0.08), p = .020], and plasma glucose [1.33 mmol/l, 95% CI (−2.41, −0.24), p = .016], and increase of flow-mediated dilation (FMD) [0.31%, 95% CI (0.07, 0.55), p = .012] and diastolic blood pressure [0.29 mmHg, 95% CI (0.10, 0.49), p = .003] 6 months after the treatment of periodontitis. A significant effect on preterm deliveries (<37 weeks) was observed [0.77 risk ratio, 95% CI (0.60, 0.98), p = .036]. Limited evidence was reported on quality-of-life (QoL) outcomes in the included studies. CONCLUSIONS: Treatment of periodontitis results in systemic health improvements including improvement in cardiometabolic risk, reduction in systemic inflammation and the occurrence of preterm deliveries. Further research is however warranted to confirm whether these changes are sustained over time. Further, appropriate QoL outcomes should be included in the study designs of future clinical trials

    Astrophysical S17(0) factor extraction from breakup of 8B on 58Ni at energies near the Coulomb barrier

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    We have performed continuum-discretized coupled channels (CDCC) calculations of the breakup of 8B on 58Ni and direct proton transfer for the 8B+58Ni system at laboratory energies of 20-28.4 MeV. The influence of the 7Be core-target optical potential (OP) on the breakup cross section was investigated. Elastic scattering angular distributions for the 7Be+58Ni and 8B+58Ni systems at five different energies around the Coulomb barrier were studied, and a reasonable energy-independent OP for each system was obtained. Using these OPs and two different 7Be-p relative motion wave functions, and summing breakup and direct proton transfer contributions, we were able to fit the experimental cross section at a 8B laboratory energy of 25.75 MeV. We calculated the excitation function for the 7Be emission in the 8B+58Ni reaction, where 7Be products were measured at the forward angle θlab=45° in the energy interval Elab=20-28.4 MeV. In view of the peripheral character of the B8 breakup reaction at near-barrier energies, we could extract the asymptotic normalization coefficient for the 7Be-p system, which was found to be CBe-p,p3/22=0.543±0.027 fm-1. Finally, the astrophysical S17(0) factor was found to be S17(0)=20.8±1.1 eV b.Ministerio de Ciencia e Innovación FPA2006-13807-c02-01Programa Consolider-Ingenio 2010 CSD2007-0004

    The Rad50 coiled-coil domain is indispensable for Mre11 complex functions

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    The Mre11 complex (Mre11, Rad50 and Xrs2 in Saccharomyces cerevisiae) influences diverse functions in the DNA damage response. The complex comprises the globular DNA-binding domain and the Rad50 hook domain, which are linked by a long and extended Rad50 coiled-coil domain. In this study, we constructed rad50 alleles encoding truncations of the coiled-coil domain to determine which Mre11 complex functions required the full length of the coils. These mutations abolished telomere maintenance and meiotic double-strand break (DSB) formation, and severely impaired homologous recombination, indicating a requirement for long-range action. Nonhomologous end joining, which is probably mediated by the globular domain of the Mre11 complex, was also severely impaired by alteration of the coiled-coil and hook domains, providing the first evidence of their influence on this process. These data show that functions of Mre11 complex are integrated by the coiled coils of Rad50.Swiss National Science Foundation and Eugen and Elisabeth Schellenberg Foundation GM56888, PBZH33-112756, PA0033-117484Ministerio de Ciencia e Innovación BFU2006-05260, 2010 CSD2007-01

    Algoritmo de control anticipatorio assisted-as-needed para neurorrehabilitación funcional de extremidad superior

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    Los dispositivos robóticos se están convirtiendo en una alternativa muy extendida a las terapias de neurorrehabilitación funcional tradicionales al ofrecer una práctica más intensiva sin incrementar el tiempo empleado en la supervisión por parte de los terapeutas especialistas. Por ello, este trabajo de investigación propone un algoritmo de control anticipatorio que, bajo el paradigma 'assisted-as-needed', proporcione a una ortesis robótica las capacidades de actuación necesarias para comportarse tal y como lo haría un terapeuta que proporciona una sesión de terapia manual. Dicho algoritmo de control ha sido validado mediante un simulador robótico obteniéndose resultados que demuestran su eficacia

    Electrónica de Potencia y Créditos ECTS: Experiencia Piloto y Material Docente Empleado

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    En esta comunicación se presenta por una parte la adaptación de la asignatura Electrónica de Potencia a créditos ECTS, realizado en la Escuela Politécnica Superior de Jaén dentro de la Experiencia Piloto Andaluza y por otra, un trabajo realizado en el Departamento de Ingeniería Electrónica de la Universidad de Jaén, sobre ésta materia, con el que se pretende potenciar la docencia de la misma; trabajo realizado sobre las diferentes unidades didácticas, en formato electrónico interactivo, incorporando hipertexto, gráficos, enlaces a sitios Web y problemas propuestos con sus correspondientes enlaces a las herramientas de simulación como Mathcad y Pspice

    Depth sensors-based upper limb motion capture system for functional neurorehabilitation

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    Versatile and accurate motion capture systems, with the required properties to be integrated within both clinical and domiciliary environments, would represent a significant advance in following the progress of the patients as well as in allowing the incorporation of new data exploitation and analysis methods to enhance the functional neurorehabilitation therapeutic processes. Besides, these systems would permit the later development of new applications focused on the automatization of the therapeutic tasks in order to increase the therapist/patient ratio, thus decreasing the costs [1]. However, current motion capture systems are not still ready to work within uncontrolled environments

    Backscattering measurement of 6He on 209Bi: Critical interaction distance

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    An elastic backscattering experiment has been performed at energies below the Coulomb barrier to investigate static and dynamic effects in the interaction of 6He with 209Bi. The measured cross sections are presented in terms of the dσ/dσRuth ratio, as a function of the distance of closest approach on a Rutherford trajectory. The data are compared with a three-body CDCC calculation and good agreement is observed. In addition, the critical distance of interaction was extracted. A larger value was obtained for the exotic 6He nucleus as compared with the weakly bound 6Li and 9Be nuclei and the tightly bound 4He, 12C, and 16O nuclei.Ministerio de Economía y Competitividad FIS2013-41994-P FIS2014-53448-C2-1-

    Positron Emission Tomography-Computed Tomography and Magnetic Resonance Imaging Assessments in a Mouse Model of Implant-Related Bone and Joint Staphylococcus aureus Infection.

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    Osteomyelitis is an infection of the bone, associated with an inflammatory process. Imaging plays an important role in establishing the diagnosis and the most appropriate patient management. However, data are lacking regarding the use of preclinical molecular imaging techniques to assess osteomyelitis progression in experimental models. This study aimed to compare structural and molecular imaging to assess disease progression in a mouse model of implant-related bone and joint infections caused by Staphylococcus aureus. In SWISS mice, the right femur was implanted with a resorbable filament impregnated with S. aureus (infected group, n = 10) or sterile culture medium (uninfected group, n = 6). Eight animals (5 infected, 3 uninfected) were analyzed with magnetic resonance imaging (MRI) at 1, 2, and 3 weeks postintervention, and 8 mice were analyzed with [18F]fluorodeoxyglucose (FDG)-positron emission tomography (PET)-computed tomography (CT) at 48 h and at 1, 2, and 3 weeks postintervention. In infected animals, CT showed bone lesion progression, mainly in the distal epiphysis, although some uninfected animals presented evident bone sequestra at 3 weeks. MRI showed a lesion in the articular area that persisted for 3 weeks in infected animals. This lesion was smaller and less evident in the uninfected group. At 48 h postintervention, FDG-PET showed higher joint uptake in the infected group than in the uninfected group (P = 0.025). Over time, the difference between groups increased. These results indicate that FDG-PET imaging was much more sensitive than MRI and CT for differentiating between infection and inflammation at early stages. FDG-PET clearly distinguished between infection and postsurgical bone healing (in uninfected animals) from 48 h to 3 weeks after implantation. IMPORTANCE Our results encourage future investigations on the utility of the model for testing different therapeutic procedures for osteomyelitis.We thank Yolanda Sierra, Alexandra de Francisco, and María de la Jara Felipe, from the Imaging Laboratory for Small Animals of the Instituto de Investigación Sanitaria, Gregorio Marañón, for their excellent work with animal preparation and imaging protocols. Additionally, we thank Daniel Calle, from the Advanced Imaging Unit of CNIC, for his help in imaging postprocessing. This study was partially supported by the Instituto de Salud Carlos III (grants PI20/ 01632 and PT20/00044), cofunded by the European Regional Development Fund (ERDF), A way to make Europe. This work was also supported by the Diagnosis and Treatment Follow-up of Severe Staphylococcal Infections with Anti-Staphylococcal Antibodies and Immune-PET project of the Grant Fundación BBVA a Equipos de Investigación Científica 2018, by the Fundación Ramón Areces, and by Comunidad de Madrid (S2022/BMD-7403 RENIM-CM). The CNIC is supported by the Instituto de Salud Carlos III (ISCIII), the Ministerio de Ciencia e Innovación (MCIN), and the Pro CNIC Foundation, and it is a Severo Ochoa Center of Excellence (grant CEX2020-001041-S, funded by MICIN/AEI/10.13039/501100011033).S

    Neuroprotective fragment C of tetanus toxin modulates IL-6 in an ALS mouse model

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    Neuroinflammation plays a significant role in amyotrophic lateral sclerosis (ALS) pathology, leading to the development of therapies targeting inflammation in recent years. Our group has studied the tetanus toxin C-terminal fragment (TTC) as a therapeutic molecule, showing neuroprotective properties in the SOD1G93A mouse model. However, it is unknown whether TTC could have some effect on inflammation. The objective of this study was to assess the effect of TTC on the regulation of inflammatory mediators to elucidate its potential role in modulating inflammation occurring in ALS. After TTC treatment in SOD1G93A mice, levels of eotaxin-1, interleukin (IL)-2, IL-6 and macrophage inflammatory protein (MIP)-1 alpha (ff) and galectin-1 were analyzed by immunoassays in plasma samples, whilst protein expression of caspase-1, IL-1β, IL-6 and NOD-, LRR- and pyrin domain-containing protein 3 (NLRP3) was measured in the spinal cord, extensor digitorum longus (EDL) muscle and soleus (SOL) muscle. The results showed reduced levels of IL-6 in spinal cord, EDL and SOL in treated SOD1G93A mice. In addition, TTC showed a different role in the modulation of NLRP3 and caspase-1 depending on the tissue analyzed. In conclusion, our results suggest that TTC could have a potential anti-inflammatory effect by reducing IL-6 levels in tissues drastically affected by the disease. However, further research is needed to study more in depth the anti-inflammatory effect of TTC in ALS
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