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1.
Transl Psychiatry ; 14(1): 246, 2024 Jun 08.
Article in English | MEDLINE | ID: mdl-38851761

ABSTRACT

Acute COVID-19 infection can be followed by diverse clinical manifestations referred to as Post Acute Sequelae of SARS-CoV2 Infection (PASC). Studies have shown an increased risk of being diagnosed with new-onset psychiatric disease following a diagnosis of acute COVID-19. However, it was unclear whether non-psychiatric PASC-associated manifestations (PASC-AMs) are associated with an increased risk of new-onset psychiatric disease following COVID-19. A retrospective electronic health record (EHR) cohort study of 2,391,006 individuals with acute COVID-19 was performed to evaluate whether non-psychiatric PASC-AMs are associated with new-onset psychiatric disease. Data were obtained from the National COVID Cohort Collaborative (N3C), which has EHR data from 76 clinical organizations. EHR codes were mapped to 151 non-psychiatric PASC-AMs recorded 28-120 days following SARS-CoV-2 diagnosis and before diagnosis of new-onset psychiatric disease. Association of newly diagnosed psychiatric disease with age, sex, race, pre-existing comorbidities, and PASC-AMs in seven categories was assessed by logistic regression. There were significant associations between a diagnosis of any psychiatric disease and five categories of PASC-AMs with odds ratios highest for neurological, cardiovascular, and constitutional PASC-AMs with odds ratios of 1.31, 1.29, and 1.23 respectively. Secondary analysis revealed that the proportions of 50 individual clinical features significantly differed between patients diagnosed with different psychiatric diseases. Our study provides evidence for association between non-psychiatric PASC-AMs and the incidence of newly diagnosed psychiatric disease. Significant associations were found for features related to multiple organ systems. This information could prove useful in understanding risk stratification for new-onset psychiatric disease following COVID-19. Prospective studies are needed to corroborate these findings.


Subject(s)
COVID-19 , Mental Disorders , SARS-CoV-2 , Humans , COVID-19/psychology , COVID-19/complications , COVID-19/epidemiology , Male , Female , Mental Disorders/epidemiology , Middle Aged , Adult , Retrospective Studies , Aged , Phenotype , Post-Acute COVID-19 Syndrome , Comorbidity , Electronic Health Records , Young Adult , Risk Factors , Adolescent
2.
Nat Commun ; 15(1): 4774, 2024 Jun 11.
Article in English | MEDLINE | ID: mdl-38862473

ABSTRACT

Mounting ambitions and capabilities for public and private, non-government sector crewed space exploration bring with them an increasingly diverse set of space travelers, raising new and nontrivial ethical, legal, and medical policy and practice concerns which are still relatively underexplored. In this piece, we lay out several pressing issues related to ethical considerations for selecting space travelers and conducting human subject research on them, especially in the context of non-governmental and commercial/private space operations.


Subject(s)
Space Flight , Humans , Space Flight/ethics , Astronauts
3.
J Med Chem ; 67(11): 8708-8729, 2024 Jun 13.
Article in English | MEDLINE | ID: mdl-38748820

ABSTRACT

The lack of selective and safe in vivo IRE1α tool molecules has limited the evaluation of IRE1α as a viable target to treat multiple myeloma. Focus on improving the physicochemical properties of a literature compound by decreasing lipophilicity, molecular weight, and basicity allowed the discovery of a novel series with a favorable in vitro safety profile and good oral exposure. These efforts culminated in the identification of a potent and selective in vivo tool compound, G-5758, that was well tolerated following multiday oral administration of doses up to 500 mg/kg. G-5758 demonstrated comparable pharmacodynamic effects to induced IRE1 knockdown as measured by XBP1s levels in a multiple myeloma model (KMS-11).


Subject(s)
Endoribonucleases , Multiple Myeloma , Protein Serine-Threonine Kinases , Multiple Myeloma/drug therapy , Multiple Myeloma/pathology , Protein Serine-Threonine Kinases/antagonists & inhibitors , Protein Serine-Threonine Kinases/metabolism , Humans , Administration, Oral , Endoribonucleases/antagonists & inhibitors , Endoribonucleases/metabolism , Animals , Drug Discovery , Mice , Cell Line, Tumor , Structure-Activity Relationship , Antineoplastic Agents/pharmacology , Antineoplastic Agents/chemistry , Antineoplastic Agents/therapeutic use , Rats , Protein Kinase Inhibitors/pharmacology , Protein Kinase Inhibitors/chemistry , Protein Kinase Inhibitors/therapeutic use , Protein Kinase Inhibitors/pharmacokinetics , Gene Knockdown Techniques , X-Box Binding Protein 1/metabolism , X-Box Binding Protein 1/genetics
5.
Radiol Technol ; 95(5): 376-381, 2024 May.
Article in English | MEDLINE | ID: mdl-38719562
6.
Nat Immunol ; 25(5): 834-846, 2024 May.
Article in English | MEDLINE | ID: mdl-38561495

ABSTRACT

Cancer remains one of the leading causes of mortality worldwide, leading to increased interest in utilizing immunotherapy strategies for better cancer treatments. In the past decade, CD103+ T cells have been associated with better clinical prognosis in patients with cancer. However, the specific immune mechanisms contributing toward CD103-mediated protective immunity remain unclear. Here, we show an unexpected and transient CD61 expression, which is paired with CD103 at the synaptic microclusters of T cells. CD61 colocalization with the T cell antigen receptor further modulates downstream T cell antigen receptor signaling, improving antitumor cytotoxicity and promoting physiological control of tumor growth. Clinically, the presence of CD61+ tumor-infiltrating T lymphocytes is associated with improved clinical outcomes, mediated through enhanced effector functions and phenotype with limited evidence of cellular exhaustion. In conclusion, this study identified an unconventional and transient CD61 expression and pairing with CD103 on human immune cells, which potentiates a new target for immune-based cellular therapies.


Subject(s)
Antigens, CD , Apyrase , Integrin alpha Chains , Receptors, Antigen, T-Cell , Signal Transduction , Animals , Humans , Mice , Antigens, CD/metabolism , Antigens, CD/immunology , Cell Line, Tumor , Cytotoxicity, Immunologic , Integrin alpha Chains/metabolism , Lymphocytes, Tumor-Infiltrating/immunology , Lymphocytes, Tumor-Infiltrating/metabolism , Neoplasms/immunology , Neoplasms/therapy , Receptors, Antigen, T-Cell/metabolism , Receptors, Antigen, T-Cell/immunology , Signal Transduction/immunology , T-Lymphocytes, Cytotoxic/immunology
7.
Plant Cell Physiol ; 65(6): 1065-1079, 2024 Jun 27.
Article in English | MEDLINE | ID: mdl-38501734

ABSTRACT

Grass xylan consists of a linear chain of ß-1,4-linked xylosyl residues that often form domains substituted only with either arabinofuranose (Araf) or glucuronic acid (GlcA)/methylglucuronic acid (MeGlcA) residues, and it lacks the unique reducing end tetrasaccharide sequence found in dicot xylan. The mechanism of how grass xylan backbone elongation is initiated and how its distinctive substitution pattern is determined remains elusive. Here, we performed biochemical characterization of rice xylan biosynthetic enzymes, including xylan synthases, glucuronyltransferases and methyltransferases. Activity assays of rice xylan synthases demonstrated that they required short xylooligomers as acceptors for their activities. While rice xylan glucuronyltransferases effectively glucuronidated unsubstituted xylohexaose acceptors, they transferred little GlcA residues onto (Araf)-substituted xylohexaoses and rice xylan 3-O-arabinosyltransferase could not arabinosylate GlcA-substituted xylohexaoses, indicating that their intrinsic biochemical properties may contribute to the distinctive substitution patterns of rice xylan. In addition, we found that rice xylan methyltransferase exhibited a low substrate binding affinity, which may explain the partial GlcA methylation in rice xylan. Furthermore, immunolocalization of xylan in xylem cells of both rice and Arabidopsis showed that it was deposited together with cellulose in secondary walls without forming xylan-rich nanodomains. Together, our findings provide new insights into the biochemical mechanisms underlying xylan backbone elongation and substitutions in grass species.


Subject(s)
Oryza , Plant Proteins , Xylans , Xylans/metabolism , Oryza/genetics , Oryza/enzymology , Oryza/metabolism , Plant Proteins/metabolism , Plant Proteins/genetics , Pentosyltransferases/metabolism , Pentosyltransferases/genetics , Methyltransferases/metabolism , Methyltransferases/genetics , Xylem/metabolism , Arabidopsis/enzymology , Arabidopsis/genetics , Arabidopsis/metabolism , Glucuronosyltransferase/metabolism , Glucuronosyltransferase/genetics
8.
Radiol Technol ; 95(4): 263-270, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38519139

ABSTRACT

PURPOSE: To assess the patient gonadal shielding practices of radiologic technologists in the state of California. METHODS: A survey invitation was sent via email to registered radiologic technologists in California to collect data to determine whether there were significant associations between gonadal shielding practices and various categorical variables, including patient sex, patient age, body part, availability of gonadal shielding protocols, availability of gonadal shields, and supervisor encouragement. RESULTS: There was a significant association between gonadal shielding protocol availability and supervisor encouragement of using gonadal shielding (P = .005) and between gonadal shielding availability and supervisor encouragement of using gonadal shielding (P < .001). Contrary to other studies in the literature, there was a significant difference between patient sex and the likelihood of gonadal shielding use, with participants indicating that they shield girls and women more often than they shield boys and men (P < .001). DISCUSSION: There was a sex-based difference in the frequency of gonadal shielding usage among the sample in this study. Also, supervisors providing accessible protocols and encouraging gonadal shielding can increase technologists' use of gonadal shielding. CONCLUSION: Gonadal shielding is the current Code of Federal Regulations standard, although most professional and scientific organizations support discontinuing shielding during abdominal and pelvic radiography examinations. Shielding of these areas is more likely to occur with the availability of gonadal shielding, supervisory encouragement, protocols mandating shielding, and state regulations.


Subject(s)
Radiation Protection , Male , Humans , Female , Radiography , Radiation Protection/methods , California , Protective Devices , Radiation Dosage
9.
J Endocr Soc ; 8(3): bvae006, 2024 Jan 16.
Article in English | MEDLINE | ID: mdl-38328479

ABSTRACT

Hyperparathyroidism jaw-tumor syndrome is an autosomal dominant disorder caused by mutations in the CDC73/HRPT2 tumor suppressor gene, encoding parafibromin, and manifesting benign or malignant parathyroid tumors, ossifying jaw fibromas, uterine tumors, and kidney lesions. Sporadic parathyroid carcinomas also frequently exhibit inactivating CDC73 mutations and loss of parafibromin. To study the role of CDC73 in parathyroid cell proliferation in vivo, we generated mice with a parathyroid-specific deletion of Cdc73. Homozygous knockout mice on a mixed B6/129/CD1 background had decreased serum calcium and PTH and smaller parathyroid glands compared with heterozygous or wild-type littermates, whereas homozygous Cdc73-null mice on other backgrounds exhibited no abnormalities in parathyroid gland function or development. No hypercalcemia or parathyroid hypercellularity was observed in mice of any background examined at any age. Thus, although postnatally acquired complete loss of CDC73 causes parathyroid cell proliferation and hyperparathyroidism, such as seen in human hyperparathyroidism jaw-tumor syndrome, our results suggest that earlier, developmentally imposed complete loss of Cdc73 can cause a primary defect in parathyroid gland structure/function in a strain-dependent manner. This striking disparity in parathyroid phenotype related to genetic background offers a unique opportunity in an in vivo model system to precisely dissect and identify the responsible molecular mechanisms.

10.
Eur J Hum Genet ; 32(1): 10-20, 2024 Jan.
Article in English | MEDLINE | ID: mdl-37938797

ABSTRACT

COVID-19, the disease caused by SARS-CoV-2, has caused significant morbidity and mortality worldwide. The betacoronavirus continues to evolve with global health implications as we race to learn more to curb its transmission, evolution, and sequelae. The focus of this review, the second of a three-part series, is on the biological effects of the SARS-CoV-2 virus on post-acute disease in the context of tissue and organ adaptations and damage. We highlight the current knowledge and describe how virological, animal, and clinical studies have shed light on the mechanisms driving the varied clinical diagnoses and observations of COVID-19 patients. Moreover, we describe how investigations into SARS-CoV-2 effects have informed the understanding of viral pathogenesis and provide innovative pathways for future research on the mechanisms of viral diseases.


Subject(s)
COVID-19 , Animals , Humans , SARS-CoV-2
11.
Behav Brain Sci ; 46: e239, 2023 10 02.
Article in English | MEDLINE | ID: mdl-37779285

ABSTRACT

Communication barriers long-associated with ideographs, including combinatorial grapholinguistic complexity, computational encoding-decoding complexity, and technological rendering and deployment, become trivialized through advancements in interoperable smart mobile digital devices. Such technologies impart unprecedented extended-reality user hazards only mitigated by unprecedented colloquial and bureaucratic societal norms. Digital age norms thus influence natural ideographic language origins and evolution in ways novel to human history.


Subject(s)
Communication , Language , Humans , Technology
12.
Behav Brain Sci ; 46: e330, 2023 10 10.
Article in English | MEDLINE | ID: mdl-37813404

ABSTRACT

Microbes perfect social interactions with intuitive logics and goal-directed reciprocity. These multilevel, cognition-resembling adaptations in Dictyostelid cellular molds enable individual-to-group viability through public/private bacterial farming and dynamic marketspaces. Like humans and animals, Dictyostelid livestock-ownership depends on environmental sensing, cooperation, and competition. Moreover, social-norm policing of cosmopolitan colonies coordinates farmer decisions, phenotypes, and ownership identities with bacteria herding, privatization, and consumption.


Subject(s)
Ownership , Privatization , Animals , Humans , Cognition
13.
Radiol Technol ; 95(1): 26-35, 2023 09.
Article in English | MEDLINE | ID: mdl-37709517

ABSTRACT

PURPOSE: To provide an overview of trauma-informed care, including the neurobiology of trauma, interventions to reduce retraumatizing patients who have experienced trauma, and implications of trauma-informed care in medical imaging and radiation therapy. METHODS: A comprehensive search of electronic databases related to the purpose of this project resulted in the collection of 12 peer-reviewed journal articles. Two conference papers, 1 behavioral science textbook, 1 trauma neurobiology textbook, 1 professional conference presentation, and 1 governmental report also were reviewed to complement the journal articles. A thematic analysis was performed to identify commonalities among the selected sources. RESULTS: Four themes identified in the literature included definitions of trauma-informed care, neurobiology of trauma, pillars of trauma-informed care for intervention, and implications in medical imaging and radiation therapy. DISCUSSION: A trauma-informed health care professional realizes the prevalence of trauma, recognizes the signs and symptoms of trauma, responds by integrating knowledge about trauma into practice, and actively resists retraumatizing the patient (ie, avoids creating an environment that inadvertently reminds patients of their traumatic experiences and causes them to experience emotional and biological stress). The pillars of trauma-informed care include safety, trustworthiness or transparency, peer support, collaboration, empowerment, and responsiveness or cultural considerations. Delivery of health care often involves assessment and interventions in locations on the patient's body where trauma has previously occurred, increasing the probability of retraumatization and manifestation of signs and symptoms of trauma. Radiologic technologists and radiation therapists should be trauma-informed when they are interacting with and caring for patients to reduce retraumatization. A hypothetical case study also is presented to show how radiologic technologists can use the pillars of trauma-informed care in the clinic. CONCLUSION: Because many aspects of care, including routine care in medical imaging and radiation therapy, can be an unintentional reminder of a traumatic experience, health care professionals should be trauma-informed when they are interacting with and caring for patients.


Subject(s)
Allied Health Personnel , Diagnostic Imaging , Humans , Radiography , Emotions , Health Personnel
16.
Radiol Technol ; 94(5): 326-331, 2023 05.
Article in English | MEDLINE | ID: mdl-37253548

ABSTRACT

PURPOSE: To analyze peer-reviewed articles in the American Society of Radiologic Technologists (ASRT) scholarly journals, Radiologic Technology and Radiation Therapist, and identify types of research and collaborative efforts among top producers. METHODS: A retrospective analysis was conducted by searching the Radiologic Technology and Radiation Therapist archives on the ASRT website to evaluate peer-reviewed articles from 2011 to 2021. A Microsoft Excel spreadsheet was created to document the types of research being published in the ASRT journals, as well as the number of authors for each peer-reviewed article, education levels of authors, collaborative efforts of top producers of scholarship, and mean authorship index of top producers. RESULTS: During this 11-year period, 217 peer-reviewed articles were published in the ASRT journals with most being original research studies (152, 70.0%). Most of the articles were written by 2 authors (68, 31.3%) or 4 or more authors (65, 30.0%). Of the 635 total authors, most held a doctoral degree (247, 38.9%) or a master's degree (212, 33.4%). Five top producers of research were identified as having published 5 or more peer-reviewed articles, and their mean authorship index was 95.5. Four top producers routinely collaborated on research articles. DISCUSSION: Initiatives, such as mentorships, to promote continued publication of original research studies and increase standalone literature reviews and case studies specific to the ASRT journals might be warranted. Medical imaging and radiation therapy educators can capitalize on collaboration by mentoring undergraduate and graduate students in various research opportunities to prepare future scholars in the profession. Further, medical imaging and radiation therapy authors should consider rotating author responsibilities on a collaborative team. Because the ASRT is the premier professional association for the medical imaging and radiation therapy community, authors should consider publishing in their 2 journals to advance and add to the profession's body of knowledge. CONCLUSION: Research articles in the ASRT journals demonstrate high collaborative authorship efforts. This study provides a foundation for future research to improve advancement of knowledge in the medical imaging and radiation therapy profession.


Subject(s)
Periodicals as Topic , Publishing , Humans , United States , Retrospective Studies , Societies , Authorship
17.
Cell Stem Cell ; 30(5): 722-740.e11, 2023 05 04.
Article in English | MEDLINE | ID: mdl-37146586

ABSTRACT

Understanding clonal evolution and cancer development requires experimental approaches for characterizing the consequences of somatic mutations on gene regulation. However, no methods currently exist that efficiently link high-content chromatin accessibility with high-confidence genotyping in single cells. To address this, we developed Genotyping with the Assay for Transposase-Accessible Chromatin (GTAC), enabling accurate mutation detection at multiple amplified loci, coupled with robust chromatin accessibility readout. We applied GTAC to primary acute myeloid leukemia, obtaining high-quality chromatin accessibility profiles and clonal identities for multiple mutations in 88% of cells. We traced chromatin variation throughout clonal evolution, showing the restriction of different clones to distinct differentiation stages. Furthermore, we identified switches in transcription factor motif accessibility associated with a specific combination of driver mutations, which biased transformed progenitors toward a leukemia stem cell-like chromatin state. GTAC is a powerful tool to study clonal heterogeneity across a wide spectrum of pre-malignant and neoplastic conditions.


Subject(s)
Chromatin , Leukemia, Myeloid, Acute , Humans , Transposases/genetics , Transposases/metabolism , Genotype , Genomics , Gene Expression Regulation
18.
Cell Rep ; 42(5): 112470, 2023 05 30.
Article in English | MEDLINE | ID: mdl-37141092

ABSTRACT

Most existing studies characterizing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-specific T cell responses are peptide based. This does not allow evaluation of whether tested peptides are processed and presented canonically. In this study, we use recombinant vaccinia virus (rVACV)-mediated expression of SARS-CoV-2 spike protein and SARS-CoV-2 infection of angiotensin-converting enzyme (ACE)-2-transduced B cell lines to evaluate overall T cell responses in a small cohort of recovered COVID-19 patients and uninfected donors vaccinated with ChAdOx1 nCoV-19. We show that rVACV expression of SARS-CoV-2 antigen can be used as an alternative to SARS-CoV-2 infection to evaluate T cell responses to naturally processed spike antigens. In addition, the rVACV system can be used to evaluate the cross-reactivity of memory T cells to variants of concern (VOCs) and to identify epitope escape mutants. Finally, our data show that both natural infection and vaccination could induce multi-functional T cell responses with overall T cell responses remaining despite the identification of escape mutations.


Subject(s)
COVID-19 , SARS-CoV-2 , Humans , ChAdOx1 nCoV-19 , Vaccination , Antibodies, Viral
19.
Nat Commun ; 14(1): 2311, 2023 04 21.
Article in English | MEDLINE | ID: mdl-37085475

ABSTRACT

As renewed interest in human space-exploration intensifies, a coherent and modernized strategy for mission design and planning has become increasingly crucial. Biotechnology has emerged as a promising approach to increase resilience, flexibility, and efficiency of missions, by virtue of its ability to effectively utilize in situ resources and reclaim resources from waste streams. Here we outline four primary mission-classes on Moon and Mars that drive a staged and accretive biomanufacturing strategy. Each class requires a unique approach to integrate biomanufacturing into the existing mission-architecture and so faces unique challenges in technology development. These challenges stem directly from the resources available in a given mission-class-the degree to which feedstocks are derived from cargo and in situ resources-and the degree to which loop-closure is necessary. As mission duration and distance from Earth increase, the benefits of specialized, sustainable biomanufacturing processes also increase. Consequentially, we define specific design-scenarios and quantify the usefulness of in-space biomanufacturing, to guide techno-economics of space-missions. Especially materials emerged as a potentially pivotal target for biomanufacturing with large impact on up-mass cost. Subsequently, we outline the processes needed for development, testing, and deployment of requisite technologies. As space-related technology development often does, these advancements are likely to have profound implications for the creation of a resilient circular bioeconomy on Earth.


Subject(s)
Mars , Space Flight , Humans , Moon , Biotechnology
20.
Med Dosim ; 48(3): 161-164, 2023.
Article in English | MEDLINE | ID: mdl-37062599

ABSTRACT

In response to the coronavirus disease 2019 (COVID-19) pandemic, many cancer centers and clinics deployed remote work options for their employees. Due to the rapid response needed during this crisis, little to no feedback was obtained from dosimetrists. This study aimed to assess the productivity level and job satisfaction of medical dosimetrists in response to changes in working conditions due to the COVID-19 pandemic. With the assistance from the medical dosimetrists certification board (MDCB), critical data was gathered via an original instrument conducted and distributed by The University of Texas MD Anderson Cancer Center-School of Health Professions to all current practicing certified medical dosimetrists registered with the MDCB. Data were collected using Qualtrics and analyzed with IBM's SPSS. Most (326, 77.7%) participants indicated they transitioned to a version of remote work due to COVID-19. Almost half of the participants (208, 49.5%) reported increased job satisfaction due to the option to work remotely. The participants reported being extremely satisfied with the individual (247, 58.8%) and department (201, 47.9%) productivity levels even after implementing remote work options. Most participants (225, 53.6%), independent of age and years of experience, would prefer to stay in a hybrid role even after COVID-19 abates. These findings suggest that most dosimetrists prefer to perform their job remotely or asynchronously. A one size fits all job model design may make it difficult for organizations to attract, retain, and grow top dosimetrists. Industry leaders and employers may benefit by embracing this change as dosimetrists may value work-set-up flexibility over other employer-based benefits. Further research is needed to assess the unintended consequences of remote work environments in this profession.

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