2,070 research outputs found

    The two-stage therapeutic effect of posture biofeedback training on back pain and the associated mechanism: A retrospective cohort study

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    Introduction: Back pain is an extremely common symptom experienced by people of all ages and the number one cause of disability worldwide.2 Poor posture has been identified as one of the factors leading to back pain. Digital biofeedback technology demonstrates the promising therapeutic ability in pain management through posture training. One common goal of such an approach is to increase users’ posture awareness with associated movement correction. However, we lack a deep understanding of the biofeedback therapeutic mechanisms and the temporal dynamics of efficacy.Objective: This study investigates the temporal dynamics of the biofeedback learning process and associated outcomes in daily life settings, testing the mechanism of the biofeedback-associated pain reduction.Methods: This retrospective real-world evidence study followed 981 users who used the UpRight posture biofeedback platform. Piecewise mixed models were used for modeling the two-stage trajectory of pain levels, perceived posture quality, and weekly training duration following an 8-week biofeedback training. Also, the mediation effect of perceived posture quality on the analgesic effect of training duration was tested using Monte Carlo simulations based on lagged effect mixed models.Results: The analysis revealed significant pain level reduction (p <.0001) and posture quality improvement (p <.0001) during the first 4 weeks of the training, maintaining similar pain levels and perceived posture quality during the next 4 weeks. In addition, weekly training duration demonstrated an increase during the first 3 weeks (p <.001) and decreased during the next 5 weeks (p <.001). Moreover, training duration predicted following-week perceived posture quality (p <.001) and in turn perceived posture quality predicted following-week pain (p <.001) (p = 0.30). Finally, perceived posture quality mediated the effect of weekly training duration on the pain levels in 2 weeks (p <.0001).Conclusion: Our findings provide a better understanding of the therapeutic dynamic during digital biofeedback intervention targeting pain, modeling the associated two-stage process. Moreover, the study sheds light on the biofeedback mechanism and may assist in developing a better therapeutic approach targeting perceived posture quality

    Infinite families of superintegrable systems separable in subgroup coordinates

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    A method is presented that makes it possible to embed a subgroup separable superintegrable system into an infinite family of systems that are integrable and exactly-solvable. It is shown that in two dimensional Euclidean or pseudo-Euclidean spaces the method also preserves superintegrability. Two infinite families of classical and quantum superintegrable systems are obtained in two-dimensional pseudo-Euclidean space whose classical trajectories and quantum eigenfunctions are investigated. In particular, the wave-functions are expressed in terms of Laguerre and generalized Bessel polynomials.Comment: 19 pages, 6 figure

    Superintegrable systems with spin and second-order integrals of motion

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    We investigate a quantum nonrelativistic system describing the interaction of two particles with spin 1/2 and spin 0, respectively. We assume that the Hamiltonian is rotationally invariant and parity conserving and identify all such systems which allow additional integrals of motion that are second order matrix polynomials in the momenta. These integrals are assumed to be scalars, pseudoscalars, vectors or axial vectors. Among the superintegrable systems obtained, we mention a generalization of the Coulomb potential with scalar potential V0=αr+328r2V_0=\frac{\alpha}{r}+\frac{3\hbar^2}{8r^2} and spin orbital one V1=2r2V_1=\frac{\hbar}{2r^2}.Comment: 32 page

    Superintegrable Systems with a Third Order Integrals of Motion

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    Two-dimensional superintegrable systems with one third order and one lower order integral of motion are reviewed. The fact that Hamiltonian systems with higher order integrals of motion are not the same in classical and quantum mechanics is stressed. New results on the use of classical and quantum third order integrals are presented in Section 5 and 6.Comment: To appear in J. Phys A: Mathematical and Theoretical (SPE QTS5

    Self-consistent field theory of polarized BEC: dispersion of collective excitation

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    We suggest the construction of a set of the quantum hydrodynamics equations for the Bose-Einstein condensate (BEC), where atoms have the electric dipole moment. The contribution of the dipole-dipole interactions (DDI) to the Euler equation is obtained. Quantum equations for the evolution of medium polarization are derived. Developing mathematical method allows to study effect of interactions on the evolution of polarization. The developing method can be applied to various physical systems in which dynamics is affected by the DDI. Derivation of Gross-Pitaevskii equation for polarized particles from the quantum hydrodynamics is described. We showed that the Gross-Pitaevskii equation appears at condition when all dipoles have the same direction which does not change in time. Comparison of the equation of the electric dipole evolution with the equation of the magnetization evolution is described. Dispersion of the collective excitations in the dipolar BEC, either affected or not affected by the uniform external electric field, is considered using our method. We show that the evolution of polarization in the BEC leads to the formation of a novel type of the collective excitations. Detailed description of the dispersion of collective excitations is presented. We also consider the process of wave generation in the polarized BEC by means of a monoenergetic beam of neutral polarized particles. We compute the possibilities of the generation of Bogoliubov and polarization modes by the dipole beam.Comment: 16 pages, 15 figures. arXiv admin note: substantial text overlap with arXiv:1106.082

    Expansion of the human μ-opioid receptor gene architecture: novel functional variants

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    The μ-opioid receptor (OPRM1) is the principal receptor target for both endogenous and exogenous opioid analgesics. There are substantial individual differences in human responses to painful stimuli and to opiate drugs that are attributed to genetic variations in OPRM1. In searching for new functional variants, we employed comparative genome analysis and obtained evidence for the existence of an expanded human OPRM1 gene locus with new promoters, alternative exons and regulatory elements. Examination of polymorphisms within the human OPRM1 gene locus identified strong association between single nucleotide polymorphism (SNP) rs563649 and individual variations in pain perception. SNP rs563649 is located within a structurally conserved internal ribosome entry site (IRES) in the 5′-UTR of a novel exon 13-containing OPRM1 isoforms (MOR-1K) and affects both mRNA levels and translation efficiency of these variants. Furthermore, rs563649 exhibits very strong linkage disequilibrium throughout the entire OPRM1 gene locus and thus affects the functional contribution of the corresponding haplotype that includes other functional OPRM1 SNPs. Our results provide evidence for an essential role for MOR-1K isoforms in nociceptive signaling and suggest that genetic variations in alternative OPRM1 isoforms may contribute to individual differences in opiate responses

    Neuropeptidomic Components Generated by Proteomic Functions in Secretory Vesicles for Cell–Cell Communication

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    Diverse neuropeptides participate in cell–cell communication to coordinate neuronal and endocrine regulation of physiological processes in health and disease. Neuropeptides are short peptides ranging in length from ~3 to 40 amino acid residues that are involved in biological functions of pain, stress, obesity, hypertension, mental disorders, cancer, and numerous health conditions. The unique neuropeptide sequences define their specific biological actions. Significantly, this review article discusses how the neuropeptide field is at the crest of expanding knowledge gained from mass-spectrometry-based neuropeptidomic studies, combined with proteomic analyses for understanding the biosynthesis of neuropeptidomes. The ongoing expansion in neuropeptide diversity lies in the unbiased and global mass-spectrometry-based approaches for identification and quantitation of peptides. Current mass spectrometry technology allows definition of neuropeptide amino acid sequence structures, profiling of multiple neuropeptides in normal and disease conditions, and quantitative peptide measures in biomarker applications to monitor therapeutic drug efficacies. Complementary proteomic studies of neuropeptide secretory vesicles provide valuable insight into the protein processes utilized for neuropeptide production, storage, and secretion. Furthermore, ongoing research in developing new computational tools will facilitate advancements in mass-spectrometry-based identification of small peptides. Knowledge of the entire repertoire of neuropeptides that regulate physiological systems will provide novel insight into regulatory mechanisms in health, disease, and therapeutics
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