930 research outputs found

    Barriers for Individuals with Prediabetes from Enrolling in the YMCA’s Diabetes Prevention Program

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    Introduction: This qualitative research study examined barriers to enrollment in YMCA of Greater Seattle’s Diabetes Prevention Program (DPP) and how to improve the enrollment and referral process. Methodology: This was a quality improvement project that used qualitative methods in the research design. Semi-structured interviews and open-ended questionnaires were used to explore barriers in enrollment and to improve the referral and enrollment process from the perspective of participants with prediabetes referred to the DPP, YMCA staff who facilitate the DPP, and primary care providers who referred participant to the DPP. Results: A total of 10 interviews were conducted with the participants between the ages of 32-78 (P1-P10) who declined enrollment to the DPP. The cohort of participants were African heritage (n=6) , Asian (n=1) and White (n=3). There were a total of 8 women and two men. Five main themes resulted from the thematic analysis: 1) cost, 2) gap in communication, 3) time constraint, 4) adequate knowledge, and 5) program format. Three YMCA staff and one provider expressed similar barriers based on their perspectives. In addition, the referral process can be improved through a more thorough explanation of the DPP to eligible participants and reducing or covering the DPP cost. Conclusion: Better referral management, shared decision-making, and financial assistance seem to be the underpinning elements for the success of the participants’ enrollment into the DPP

    Thermosensitive chitosan/poly(N-isopropyl acrylamide) nanoparticles embedded in aniline pentamer/silk fibroin/polyacrylamide as an electroactive injectable hydrogel for healing critical-sized calvarial bone defect in aging rat model

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    Thermosensitive nanoparticles with phase transition abilities have been considered as suitable materials in biomedical fields, especially drug delivery systems. Moreover, electroactive injectable hydrogels supporting bone regeneration of the elderly will highly be desired in bone tissue engineering applications. Herein, thermosensitive nanoparticles were fabricated using chitosan/poly(N-isopropyl acrylamide) for simvastatin acid delivery. The nanoparticles were incorporated into electroactive injectable hydrogels based on aniline pentamer/silk fibroin/polyacrylamide containing vitamin C. The nanoparticles had thermosensitive properties as simvastatin acid had higher release rates at 37 than 23 °C without significant burst release. The hydrogels also revealed an appropriate gelation time, stable mechanical and rheological characteristics, high water absorbency, and proper biodegradability. In vitro studies indicated that the hydrogel was biocompatible and nontoxic, especially those containing drugs. Implantation of the hydrogels containing both simvastatin acid and vitamin C into the critical calvarial bone defect of the aged rat also demonstrated significant enhancement of bone healing after 4 and 8 weeks post-implantation. We found that the electroactive injectable hydrogels containing thermosensitive nanoparticles exhibited great potential for treating bone defects in the elderly ratsThis work has financially supported National Institute for Medical Research Development (NIMAD) Grant No. 972340. SCK has been the European Research Area Chair of the European Commission and the European Union Framework Programme for Research and Innovation Horizon 2020 (n◦ 668983 — FoReCaST and PTDC/BTM-ORG/28168/2017 of FCT, Portugal supported SCK

    Large-scale expansions of Friedreich's ataxia GAA•TTC repeats in an experimental human system: role of DNA replication and prevention by LNA-DNA oligonucleotides and PNA oligomers

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    Friedreich's ataxia (FRDA) is caused by expansions of GAA•TTC repeats in the first intron of the human FXN gene that occur during both intergenerational transmissions and in somatic cells. Here we describe an experimental system to analyze large-scale repeat expansions in cultured human cells. It employs a shuttle plasmid that can replicate from the SV40 origin in human cells or be stably maintained in S. cerevisiae utilizing ARS4-CEN6. It also contains a selectable cassette allowing us to detect repeat expansions that accumulated in human cells upon plasmid transformation into yeast. We indeed observed massive expansions of GAA•TTC repeats, making it the first genetically tractable experimental system to study large-scale repeat expansions in human cells. Further, GAA•TTC repeats stall replication fork progression, while the frequency of repeat expansions appears to depend on proteins implicated in replication fork stalling, reversal, and restart. Locked nucleic acid (LNA)-DNA mixmer oligonucleotides and peptide nucleic acid (PNA) oligomers, which interfere with triplex formation at GAA•TTC repeats in vitro, prevented the expansion of these repeats in human cells. We hypothesize, therefore, that triplex formation by GAA•TTC repeats stall replication fork progression, ultimately leading to repeat expansions during replication fork restart

    Transmission of Îą-synucleinopathy from olfactory structures deep into the temporal lobe

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    Supplemental files to the publication Transmission of Îą-synucleinopathy from olfactory structures deep into the temporal lobe : Supplemental information (PDF): Materials and methods, tables, and supplemental figures S1-S8 (all supplemental figures are mentioned in the main text). Two mp4 movie files showing perinuclear localization of pSer129 signal (red) around NeuN+ nuclei (green). One movie shows a rotating cell and in the other video, the red pSer129 signal is peeled away to reveal the underlying green NeuN+ nucleus. Four high resolution figures (TIFF files)
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