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1.
Access Microbiol ; 6(2)2024.
Artigo em Inglês | MEDLINE | ID: mdl-38482357

RESUMO

Severe acute respiratory syndrome (SARS) coronavirus 2 (SARS-CoV-2) is a novel human coronavirus that was identified in 2019. SARS-CoV-2 infection results in an acute, severe respiratory disease called coronavirus disease 2019 (COVID-19). The emergence and rapid spread of SARS-CoV-2 has led to a global public health crisis, which continues to affect populations across the globe. Real time reverse transcription polymerase chain reaction (rRT-PCR) is the reference standard test for COVID-19 diagnosis. Serological tests are valuable tools for serosurveillance programs and establishing correlates of protection from disease. This study evaluated the performance of one in-house enzyme linked immunosorbent assay (ELISA) utilizing the pre-fusion stabilized ectodomain of SARS-CoV-2 spike (S), two commercially available chemiluminescence assays Ortho VITROS Immunodiagnostic Products Anti-SARS-CoV-2 Total Reagent Pack and Abbott SARS-CoV-2 IgG assay and one commercially available Surrogate Virus Neutralization Test (sVNT), GenScript USA Inc., cPass SARS-CoV-2 Neutralization Antibody Detection Kit for the detection of SARS-CoV-2 specific antibodies. Using a panel of rRT-PCR confirmed COVID-19 patients' sera and a negative control group as a reference standard, all three immunoassays demonstrated high comparable positivity rates and low discordant rates. All three immunoassays were highly sensitive with estimated sensitivities ranging from 95.4-96.6 %. ROC curve analysis indicated that all three immunoassays had high diagnostic accuracies with area under the curve (AUC) values ranging from 0.9698 to 0.9807. High positive correlation was demonstrated among the conventional microneutralization test (MNT) titers and the sVNT inhibition percent values. Our study indicates that independent evaluations are necessary to optimize the overall utility and the interpretation of the results of serological tests. Overall, we demonstrate that all serological tests evaluated in this study are suitable for the detection of SARS-CoV-2 antibodies.

2.
Sci Rep ; 13(1): 630, 2023 Jan 12.
Artigo em Inglês | MEDLINE | ID: mdl-36635349

RESUMO

Despite advances in seismology and computing, the ability to image subsurface volcanic environments is poor, limiting our understanding of the overall workings of volcanic systems. This is related to substantive structural heterogeneities which strongly scatters seismic waves obscuring the ballistic arrivals normally used in seismology for wave velocity determination. Here we address this constraint by, using a deep learning approach, a Fourier neural operator (FNO), to model and invert seismic signals in volcanic settings. The FNO is trained using 40,000+ simulations of elastic wave propagation through complex volcano models, and includes the full scattered wavefield. Once trained, the forward network is used to predict elastic wave propagation and is shown to accurately reproduce the seismic wavefield. The FNO is also trained to predict heterogeneous velocity models given a limited set of input seismograms. It is shown to capture details of the complex velocity structure that lie far outside the ability of current methods available in volcano imagery.

3.
Sci Data ; 9(1): 220, 2022 05 19.
Artigo em Inglês | MEDLINE | ID: mdl-35589721

RESUMO

Induced seismicity is one of the main factors that reduces societal acceptance of deep geothermal energy exploitation activities, and felt earthquakes are the main reason for closure of geothermal projects. Implementing innovative tools for real-time monitoring and forecasting of induced seismicity was one of the aims of the recently completed COSEISMIQ project. Within this project, a temporary seismic network was deployed in the Hengill geothermal region in Iceland, the location of the nation's two largest geothermal power plants. In this paper, we release raw continuous seismic waveforms and seismicity catalogues collected and prepared during this project. This dataset is particularly valuable since a very dense network was deployed in a seismically active region where thousand of earthquakes occur every year. For this reason, the collected dataset can be used across a broad range of research topics in seismology ranging from the development and testing of new data analysis methods to induced seismicity and seismotectonics studies.

4.
J Womens Health (Larchmt) ; 31(3): 301-309, 2022 03.
Artigo em Inglês | MEDLINE | ID: mdl-35275742

RESUMO

Women and girls with bleeding disorders experience abnormal and excessive bleeding that can negatively impact their overall health and quality of life. In this report, we provide an overview of the biology, types, clinical care, and state of the science related to bleeding disorders in girls and women and describe Centers for Disease Control and Prevention (CDC) activities related to (1) surveillance of bleeding disorders in women; (2) scientific review, research, and collaboration to inform health care gaps in identifying and caring for women with bleeding disorders; and (3) development of health promotion and education programs to bring awareness about bleeding disorders to both women and girls in the population at large and various health care providers who care for women. Findings generated from surveillance and research activities inform the development of new public health programs aimed at improving diagnostic and health care services and empowering women with bleeding disorders with the knowledge they need to navigate a complex health care system with the need for specialty care services. Additional work is needed to improve provider awareness and understanding of the unique needs of women and girls with bleeding disorders to achieve appropriate care and treatment and ensure optimal outcomes and quality of life.


Assuntos
Transtornos da Coagulação Sanguínea , Qualidade de Vida , Centers for Disease Control and Prevention, U.S. , Feminino , Promoção da Saúde , Hemorragia , Humanos , Estados Unidos
5.
Sci Adv ; 7(39): eabh0894, 2021 Sep 24.
Artigo em Inglês | MEDLINE | ID: mdl-34559568

RESUMO

The propensity for dynamic earthquake triggering is thought to depend on the local stress state and amplitude of the stress perturbation. However, the nature of this dependency has not been confirmed within a single crustal volume. Here, we show that at Sierra Negra volcano, Galápagos Islands, the intensity of dynamically triggered earthquakes increased as inflation of a magma reservoir elevated the stress state. The perturbation of short-term seismicity within teleseismic surface waves also increased with peak dynamic strain. Following rapid coeruptive subsidence and reduction in stress and background seismicity rates, equivalent dynamic strains no longer triggered detectable seismicity. These findings offer direct constraints on the primary controls on dynamic triggering and suggest that the response to dynamic stresses may help constrain the evolution of volcanic unrest.

6.
Haemophilia ; 27(6): 1037-1044, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34480812

RESUMO

INTRODUCTION: Females may have haemophilia with the same factor VIII (FVIII) or factor IX (FIX) levels as affected males. Characterization of females with haemophilia would be useful for health care planning to meet their unique needs. Federally-funded haemophilia treatment centres (HTCs) in the United States contribute data on all individuals with bleeding disorders receiving care to the Population Profile (HTC PP) component of the Community Counts Public Health Surveillance of Bleeding Disorders project. AIMS: To estimate the number of females with haemophilia receiving care at HTCs in the United States and compare their characteristics with those of males with haemophilia. METHODS: HTC PP data collected on people receiving care at an HTC from January 2012 through September 2020 with haemophilia A and B were evaluated by sex for demographic and clinical characteristics. RESULTS: A factor level < 40% was reported for 23,196 males (97.8%) and 1667 females (47.6%) attending HTCs; 51 (.48%) severe, 79 (1.4%) moderate, and 1537 (17.9%) mild haemophilia patients were female. Females were older, more often White, and less often non-Hispanic than males. Females were less likely to have history of HIV or HCV infection, even among those with severe disease, but twice as likely to have infection status unknown. Females with mild haemophilia were more often uninsured than males. CONCLUSIONS: Females with severe or moderate haemophilia are uncommon, even in specialized care centres; however, almost one in five patients with mild haemophilia was female, indicating needs for specialized care based on factor level and history for affected females.


Assuntos
Hemofilia A , Hemofilia B , Hemostáticos , Feminino , Hemofilia A/complicações , Hemofilia A/epidemiologia , Hemofilia A/terapia , Hemofilia B/epidemiologia , Hemofilia B/terapia , Humanos , Masculino , Estados Unidos/epidemiologia
7.
Nat Commun ; 12(1): 2332, 2021 04 20.
Artigo em Inglês | MEDLINE | ID: mdl-33879800

RESUMO

Wind driven ocean wave-wave interactions produce continuous Earth vibrations at the seafloor called secondary microseisms. While the origin of associated Rayleigh waves is well understood, there is currently no quantified explanation for the existence of Love waves in the most energetic region of the microseism spectrum (3-10 s). Here, using terrestrial seismic arrays and 3D synthetic acoustic-elastic simulations combined with ocean wave hindcast data, we demonstrate that, observed from land, our general understanding of Rayleigh and Love wave microseism sources is significantly impacted by 3D propagation path effects. We show that while Rayleigh to Love wave conversions occur along the microseism path, Love waves predominantly originate from steep subsurface geological interfaces and bathymetry, directly below the ocean source that couples to the solid Earth. We conclude that, in contrast to Rayleigh waves, microseism Love waves observed on land do not directly relate to the ocean wave climate but are significantly modulated by continental margin morphologies, with a first order effect from sedimentary basins. Hence, they yield rich spatio-temporal information about ocean-land coupling in deep water.

8.
Nat Commun ; 12(1): 1397, 2021 03 02.
Artigo em Inglês | MEDLINE | ID: mdl-33654084

RESUMO

Recent large basaltic eruptions began after only minor surface uplift and seismicity, and resulted in caldera subsidence. In contrast, some eruptions at Galápagos Island volcanoes are preceded by prolonged, large amplitude uplift and elevated seismicity. These systems also display long-term intra-caldera uplift, or resurgence. However, a scarcity of observations has obscured the mechanisms underpinning such behaviour. Here we combine a unique multiparametric dataset to show how the 2018 eruption of Sierra Negra contributed to caldera resurgence. Magma supply to a shallow reservoir drove 6.5 m of pre-eruptive uplift and seismicity over thirteen years, including an Mw5.4 earthquake that triggered the eruption. Although co-eruptive magma withdrawal resulted in 8.5 m of subsidence, net uplift of the inner-caldera on a trapdoor fault resulted in 1.5 m of permanent resurgence. These observations reveal the importance of intra-caldera faulting in affecting resurgence, and the mechanisms of eruption in the absence of well-developed rift systems.

9.
Data Brief ; 34: 106673, 2021 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-33537366

RESUMO

This work describes the data used in the EPSL research article "Quantifying strong seismic propagation effects in the upper volcanic edifice using sensitivity kernels". The dataset is generated in order to investigate to what extent the seismic signals recorded on volcanoes are affected by near surface velocity structure. Data were calculated using the computational spectral elements scheme SPECFEM2D, where the wave propagation beneath Mount Etna volcano, Italy, was simulated in both homogeneous and heterogeneous models. The heterogeneous model comprises a low-velocity superficial structure (top several hundred meters) based on the previously published studies. Several different source mechanisms and locations were used in the simulations. The seismic wavefield was "recorded" by 15 surface receivers distributed along the surface of the volcano. The associated sensitivity kernels were also computed. These kernels highlight the region of the velocity model that affects the recorded seismogram within a desired time window. The text files describing the velocity models used in the simulations are also provided. The data may be of interest to volcano seismologists, as well as earthquake seismologists studying path effects and wave propagation through complex media.

10.
Haemophilia ; 27(2): e164-e179, 2021 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-33314404

RESUMO

Women and girls reported as "haemophilic females" may have complex genetic causes for their haemophilia phenotype. In addition, women and girls may have excessive bleeding requiring treatment simply because they are heterozygous for haemophilia alleles. While severe and moderate haemophilia are rare in females, 16% of patients with mild haemophilia A and almost one-quarter of those with mild haemophilia B seen in U.S. haemophilia treatment centres are women and girls. A phenotypic female with a low level of factor VIII or factor IX may be classified into one of the following categories of causality: homozygosity (two identical haemophilia alleles), compound heterozygosity (two different haemophilia alleles), hemizygosity (one haemophilia allele and no normal allele), heterozygosity (one haemophilia allele and one normal allele), genetic causes other than haemophilia and non-genetic causes. Studies required for classification may include coagulation parameters, F8 or F9 sequencing, F8 inversion testing, multiplex ligation-dependent probe amplification, karyotyping and X chromosome inactivation studies performed on the patient and parents. Women and girls who are homozygous, compound heterozygous or hemizygous clearly have haemophilia, as they do not have a normal allele. Heterozygous women and girls with factor levels below the haemostatic range also meet the definitions used for haemophilia treatment.


Assuntos
Hemofilia A , Hemofilia B , Fator IX/genética , Fator VIII/genética , Feminino , Hemofilia A/genética , Hemofilia B/genética , Heterozigoto , Humanos , Fenótipo
12.
MMWR Surveill Summ ; 69(5): 1-18, 2020 09 04.
Artigo em Inglês | MEDLINE | ID: mdl-32881847

RESUMO

PROBLEM/CONDITION: Hemophilia is an X-linked genetic disorder that primarily affects males and results in deficiencies in blood-clotting proteins. Hemophilia A is a deficiency in factor VIII, and hemophilia B is a deficiency in factor IX. Approximately one in 5,000 males are born with hemophilia, and hemophilia A is about four times as common as hemophilia B. Both disorders are characterized by spontaneous internal bleeding and excessive bleeding after injuries or surgery. Hemophilia can lead to repeated bleeding into the joints and associated chronic joint disease, neurologic damage, damage to other organ systems, and death. Although no precise national U.S. prevalence estimates for hemophilia exist because of the difficulty identifying cases among persons who receive care from various types of health care providers, two previous state-based studies estimated hemophilia prevalence at 13.4 and 19.4 per 100,000 males. In addition, these studies showed that 67% and 82% of persons with hemophilia received care in a federally funded hemophilia treatment center (HTC), and 86% and 94% of those with the most severe cases of hemophilia (i.e., those with the lowest levels of clotting factor activity in the circulating blood) received care in a federally funded HTC. As of January 2020, the United States had 144 HTCs. PERIOD COVERED: 1998-2019. DESCRIPTION OF THE SYSTEM: Surveillance for hemophilia, which is a complex, chronic condition, is challenging because of its low prevalence, the difficulty in ascertaining cases uniformly, and the challenges in routinely characterizing and tracking associated health complications. Over time, two systems involving many stakeholders have been used to conduct ongoing hemophilia surveillance. During 1998-2011, CDC and the HTCs collaborated to establish the Universal Data Collection (UDC) surveillance system. The purposes of the UDC surveillance system were to monitor human immunodeficiency virus (HIV) and bloodborne viral hepatitis in persons with hemophilia, thereby tracking blood safety, and to track the prevalence of and trends in complications associated with hemophilia. HTC staff collected clinical data and blood specimens from UDC participants and submitted them to CDC. CDC tested specimens for viral hepatitis and HIV. In 2011, the UDC surveillance system was replaced by a new hemophilia surveillance system called Community Counts. CDC and the HTCs established Community Counts to expand laboratory testing and the collection of clinical data to better identify and track emerging health issues in persons with hemophilia. RESULTS: This report is the first comprehensive summary of CDC's hemophilia surveillance program, which comprises both UDC and Community Counts. Data generated from these surveillance systems have been used in the development of public health and clinical guidelines and practices to improve the safety of U.S. blood products and either prevent hemophilia-related complications or identify complications early. Several factors have played a role in the effectiveness of the UDC and Community Counts systems, including 1) a stable data collection design that was developed and is continually reviewed in close partnership with HTC regional leaders and providers to ensure surveillance activities are focused on maximizing the scientific and clinical impact; 2) flexibility to respond to emerging health priorities through periodic updates to data collection elements and special studies; 3) high data quality for many clinical indicators and state-of-the-art laboratory testing methods for hemophilia treatment product inhibitors (developed and refined in part based on CDC research); 4) timely data and specimen collection and submission, laboratory specimen testing, analysis, and reporting; and 5) the largest and most representative sample of persons with hemophilia in the United States and one of the largest and most comprehensive data collection systems on hemophilia worldwide. INTERPRETATION: CDC has successfully developed, implemented, and maintained a surveillance system for hemophilia. The program can serve as an example of how to conduct surveillance for a complex chronic disease by involving stakeholders, improving and building new infrastructure, expanding data collection (e.g., new diagnostic assays), providing testing guidance, establishing a registry with specimen collection, and integrating laboratory findings in clinical practice for the individual patient. PUBLIC HEALTH ACTION: Hemophilia is associated with substantial lifelong morbidity, excess premature deaths, and extensive health care needs throughout life. Through monitoring data from Community Counts, CDC will continue to characterize the benefits and adverse events associated with existing or new hemophilia treatment products, thereby contributing to maximizing the health and longevity of persons with hemophilia.


Assuntos
Hemofilia A/epidemiologia , Vigilância da População/métodos , Adolescente , Adulto , Idoso , Centers for Disease Control and Prevention, U.S. , Criança , Pré-Escolar , Coleta de Dados , Feminino , Humanos , Lactente , Masculino , Pessoa de Meia-Idade , Avaliação de Programas e Projetos de Saúde , Características de Residência , Estados Unidos/epidemiologia , Adulto Jovem
13.
Ann Emerg Med ; 76(3S): S28-S36, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-32928459

RESUMO

STUDY OBJECTIVE: We provide an updated assessment of trends in sickle cell disease (SCD)-related mortality, a significant source of mortality in the United States among black persons, using 1979 to 2017 US mortality data. METHODS: SCD-related deaths were identified with International Classification of Diseases codes. Because SCD-related death is rare in other races, the analysis focused on black decedents. Age-specific and average annual SCD-related death rates were calculated. Causes of death codes were categorized into 20 groups relevant to SCD outcomes. SCD-related deaths were compared with non-SCD-related deaths after matching on race, sex, age group, and year of death. RESULTS: There were 25,665 SCD-related deaths reported among blacks in the United States from 1979 through 2017. During that period, the annual SCD-related death rate declined in children and increased in adults, and the median age at death increased from 28 to 43 years. Acute causes of death, such as infection and cerebrovascular complications, were more common in younger age groups. Chronic complications were more common in adults. SCD-related deaths were more likely to be related to acute cardiac, pulmonary, and cerebrovascular complications; acute infections; and chronic cardiac and pulmonary complications and renal disorders; and less likely to be related to drug overdose and chronic infections than non-SCD-related deaths. CONCLUSION: These data indicate SCD-related deaths are now more likely to be related to chronic complications of the disease than to acute complications. More research regarding prevention and treatment of chronic complications of SCD is necessary because persons with SCD are living longer.


Assuntos
Anemia Falciforme/mortalidade , Adolescente , Adulto , Fatores Etários , Anemia Falciforme/complicações , Doenças Cardiovasculares/etiologia , Doenças Cardiovasculares/mortalidade , Causas de Morte , Criança , Pré-Escolar , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fatores Sexuais , Estados Unidos/epidemiologia , Adulto Jovem
14.
Nat Commun ; 11(1): 3728, 2020 07 21.
Artigo em Inglês | MEDLINE | ID: mdl-32694505

RESUMO

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

15.
Nat Commun ; 11(1): 2504, 2020 05 19.
Artigo em Inglês | MEDLINE | ID: mdl-32427822

RESUMO

Glacier runoff and melt from volcanic and geothermal activity accumulates in glacier dammed lakes in glaciated areas around the world. These lakes eventually drain, creating hazardous subglacial floods that are usually only confirmed after they exit the glacier and reach local river systems, which can be many tens of kilometres from the flood source. Once in the river systems, they travel rapidly to populated areas. Such delayed detection represents a potentially lethal shortcoming in early-warning. Here we demonstrate how to advance early-warning potential through the analysis of four such floods in a glaciated region of Iceland. By comparing exceptional multidisciplinary hydrological, GPS and seismic ground vibration (tremor) data, we show that array analysis of seismic tremor can be used for early location and tracking of the subglacial flood front. Furthermore the timing and size of the impending flood can be estimated, prior to it entering the river system. Advanced warnings of between 20 to 34 hours are achieved for large (peak discharge of more than 3000 m3/s, accumulation time of ~ 5.25 years) to small floods (peak discharges from 210 to 380 m3/s, accumulation times of ~ 1.3 years) respectively.

16.
Transfus Med ; 30(3): 226-230, 2020 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-32131139

RESUMO

OBJECTIVE: In the multicentre Haemoglobinopathy Blood Surveillance Project, to evaluate the seroprevalence of parvovirus B19 and DNA viral load in sickle cell disease (SCD). BACKGROUND: Although the epidemiology of parvovirus B19 seropositivity in SCD has been well documented, there are few studies that have assessed possible persistent parvovirus DNAemia and associated risk factors including blood transfusion. METHODS: A qualitative analysis of parvovirus B19 serology using ELISA and quantitative parvovirus B19 DNA by RT-PCR was performed in patients with SCD. RESULTS: Of 322 patients, 113 (35%) were parvovirus IgG positive and 119 (37%) were IgM positive at enrolment. The prevalence of IgG positivity increased with age. 71/322 (22%) were parvovirus DNA positive at enrolment with a mean viral load of 15 227 ± 55 227 SD. (range 72-329 238 IU/mL). Patients who were positive for parvovirus B19 DNA received a significantly higher red blood cell transfusion volume in the prior year compared to patients who were negative (mean RBC volume = 8310 mL vs 5435 mL, respectively; P = .0073). Seventy-seven patients had follow-up testing approximately 1 year after enrolment and 11/28 (39%) patients had persistently positive IgM. CONCLUSION: Further studies are needed to better understand the natural history of parvovirus B19 infection in SCD especially in relation to RBC transfusion as a risk factor, as well as disease outcome and severity.


Assuntos
Anemia Falciforme , Anticorpos Antivirais/sangue , DNA Viral/sangue , Eritema Infeccioso , Imunoglobulina G/sangue , Imunoglobulina M/sangue , Parvovirus B19 Humano/metabolismo , Adolescente , Adulto , Anemia Falciforme/sangue , Anemia Falciforme/epidemiologia , Anemia Falciforme/terapia , Anemia Falciforme/virologia , Centers for Disease Control and Prevention, U.S. , Criança , Pré-Escolar , Eritema Infeccioso/sangue , Eritema Infeccioso/epidemiologia , Feminino , Humanos , Lactente , Recém-Nascido , Masculino , Fatores de Risco , Estados Unidos
18.
Birth Defects Res ; 111(20): 1618-1632, 2019 12 01.
Artigo em Inglês | MEDLINE | ID: mdl-31328417

RESUMO

BACKGROUND: The National Birth Defects Prevention Study (NBDPS) is a multisite, population-based, case-control study of genetic and nongenetic risk factors for major structural birth defects. Eligible women had a pregnancy affected by a birth defect or a liveborn child without a birth defect between 1997 and 2011. They were invited to complete a telephone interview to collect pregnancy exposure data and were mailed buccal cell collection kits to collect specimens from themselves, their child (if living), and their child's father. Over 23,000 families representing more than 30 major structural birth defects provided DNA specimens. METHODS: To evaluate their utility for exome sequencing (ES), specimens from 20 children with colonic atresia were studied. Evaluations were conducted on specimens collected using cytobrushes stored and transported in open versus closed packaging, on native genomic DNA (gDNA) versus whole genome amplified (WGA) products and on a library preparation protocol adapted to low amounts of DNA. RESULTS: The DNA extracted from brushes in open packaging yielded higher quality sequence data than DNA from brushes in closed packaging. Quality metrics of sequenced gDNA were consistently higher than metrics from corresponding WGA products and were consistently high when using a low input protocol. CONCLUSIONS: This proof-of-principle study established conditions under which ES can be applied to NBDPS specimens. Successful sequencing of exomes from well-characterized NBDPS families indicated that this unique collection can be used to investigate the roles of genetic variation and gene-environment interaction effects in birth defect etiologies, providing a valuable resource for birth defect researchers.


Assuntos
Anormalidades Congênitas/genética , Anormalidades Congênitas/prevenção & controle , Sequenciamento do Exoma , Interação Gene-Ambiente , Família , Humanos
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