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1.
Artif Intell Med ; 142: 102573, 2023 08.
Artículo en Inglés | MEDLINE | ID: mdl-37316096

RESUMEN

Medical information extraction consists of a group of natural language processing (NLP) tasks, which collaboratively convert clinical text to pre-defined structured formats. This is a critical step to exploit electronic medical records (EMRs). Given the recent thriving NLP technologies, model implementation and performance seem no longer an obstacle, whereas the bottleneck locates on a high-quality annotated corpus and the whole engineering workflow. This study presents an engineering framework consisting of three tasks, i.e., medical entity recognition, relation extraction and attribute extraction. Within this framework, the whole workflow is demonstrated from EMR data collection through model performance evaluation. Our annotation scheme is designed to be comprehensive and compatible between the multiple tasks. With the EMRs from a general hospital in Ningbo, China, and the manual annotation by experienced physicians, our corpus is of large scale and high quality. Built upon this Chinese clinical corpus, the medical information extraction system show performance that approaches human annotation. The annotation scheme, (a subset of) the annotated corpus, and the code are all publicly released, to facilitate further research.


Asunto(s)
Registros Electrónicos de Salud , Médicos , Humanos , China , Almacenamiento y Recuperación de la Información , Procesamiento de Lenguaje Natural
2.
Oxid Med Cell Longev ; 2021: 4728714, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34336093

RESUMEN

BACKGROUND: Mitochondrial NADH dehydrogenase subunit 2 (MT-ND2) m. 5178C>A gene mutation has protective effects against various diseases, but the molecular mechanism is still unclear. In previous study, we found a heteroplasmy level of MT-ND2 m. 5178C>A mutation in normotensive controls. Peripheral blood samples were obtained from essential hypertension individuals carrying the mutation and healthy controls without gene mutation to establish immortalized lymphocyte lines. To investigate the effect of the MT-ND2 m. 5178C>A gene mutation, comparative analyses of the two group cell lines were performed, including measurements of cell proliferation, viability, ATP synthesis, mitochondrial oxidative stress, and oxidative phosphorylation. RESULTS: The cell proliferation rate and viability of the MT-ND2 m. 5178C>A mutant lymphocyte line were higher than those of the control group. Mitochondrial functions of the MT-ND2 m. 5178C>A mutant lymphocyte were increased, including increased ATP synthesis, decreased ROS production, increased mitochondrial membrane potential and Bcl-2 gene transcription and protein translation, decreased Caspase 3/7 activity, and decreased early apoptosis and late apoptosis. The oxygen consumption rate (OCR) of the mutant lymphocyte line was higher than that of the control group, including basal OCR, ATP-linked OCR, maximal OCR, proton leak OCR, and reserve OCR, and there was no significant difference in nonmitochondrial OCR. The activity of Mitochondrial Complex I of the mutant group was increased than that of the control group. CONCLUSIONS: The MT-ND2 m. 5178C>A mutation is a protective mutation that may be related to improvement of mitochondrial functions and decrease in apoptosis.


Asunto(s)
Mitocondrias/enzimología , Mitocondrias/genética , Mutación , NADH Deshidrogenasa/genética , Adenosina Trifosfato/biosíntesis , Apoptosis/fisiología , Estudios de Casos y Controles , Hipertensión Esencial/genética , Hipertensión Esencial/patología , Femenino , Humanos , Masculino , Potencial de la Membrana Mitocondrial , Persona de Mediana Edad , Mitocondrias/patología , Especies Reactivas de Oxígeno/metabolismo
3.
BMC Cardiovasc Disord ; 20(1): 497, 2020 11 25.
Artículo en Inglés | MEDLINE | ID: mdl-33238890

RESUMEN

BACKGROUND: Systematic investigation and analysis of cardiovascular health status (CVHS) of Chinese women is rare. This study aimed to assess CVHS and atherosclerotic cardiovascular disease (ASCVD) burden in the Chinese women physicians (CWP) and community-based non-physician cohort (NPC). METHODS: In this prospective, multicenter, observational study, CVHS using the American Heart Association (AHA) defined 7 metrics (such as smoking and fasting glucose) and ASCVD risk factors including hypertension, hyperlipidemia and type-2 diabetes were evaluated in CWP compared with NPC. RESULTS: Of 5832 CWP with a mean age of 44 ± 7 years, only 1.2% achieved the ideal CVHS and 90.1% showed at least 1 of the 7 AHA CVHS metrics at a poor level. Total CVHS score was significantly decreased and ASCVD risk burden was increased in postmenopausal subjects in CWP although ideal CVHS was not significantly influenced by menopause. Compared to 2596 NPC, fewer CWP had ≥ 2 risk factors (8% vs. 27%, P < 0.001); CWP scored significantly higher on healthy factors, a composite of total cholesterol, blood pressure, fasting glucose (P < 0.001), but, poorly on healthy behaviors (P < 0.001), specifically in the physical activity component; CWP also showed significantly higher levels of awareness and rates of treatment for hypertension and hyperlipidemia, but, not for type-2 diabetes. CONCLUSION: Chinese women's cardiovascular health is far from ideal and risk intervention is sub-optimal. Women physicians had lower ASCVD burden, scored higher in healthy factors, but, took part in less physical activity than the non-physician cohort. These results call for population-specific early and improved risk intervention.


Asunto(s)
Aterosclerosis/epidemiología , Estado de Salud , Médicos Mujeres , Salud de la Mujer , Mujeres Trabajadoras , Adulto , Aterosclerosis/diagnóstico , Aterosclerosis/prevención & control , China/epidemiología , Diabetes Mellitus Tipo 2/epidemiología , Diabetes Mellitus Tipo 2/terapia , Dislipidemias/epidemiología , Dislipidemias/terapia , Estilo de Vida Saludable , Factores de Riesgo de Enfermedad Cardiaca , Humanos , Hipertensión/epidemiología , Hipertensión/terapia , Masculino , Menopausia , Persona de Mediana Edad , Servicios Preventivos de Salud , Estudios Prospectivos , Factores Protectores , Medición de Riesgo , Conducta de Reducción del Riesgo , Factores Sexuales
4.
Eur J Pharmacol ; 865: 172622, 2019 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-31618620

RESUMEN

Mitochondrial DNA mutations promote hypertensive renal dysfunction, but the molecular mechanism remains unclear. This study compared renal damage between spontaneously hypertensive rats (SHR) and SHR with mitochondrial transfer (t)RNA mutations. To investigate the role of mitochondrial outer membrane voltage-dependent anion channel 1 (VDAC1) in the process of tRNA-promoting mitochondrial dysfunction, we treated HK-2 cells with H2O2, cyclosporine (CsA), or atractylodin (Atr) to observe the association between VDAC1 and mitochondrial function. Intriguingly, the mitochondrial structure of SHR carrying tRNA mutations was obviously disordered, and reactive oxygen species production and VDAC1 and Bax expression and binding were increased, which was associated with marked renal dysfunction. The expression of VDAC1 and Bax was also up-regulated in HK-2 cells by H2O2 treatment. However, CsA and Atr had no significant effect on the expression of VDAC1 and Bax. H2O2 caused mitochondrial membrane potential collapse, while CsA could increase the mitochondrial membrane potential and Atr had the opposite effect. Treatment with H2O2 significantly decreased ATP synthesis, which was improved by intervention with Atr. H2O2 also decreased the maximum oxygen consumption rate, while CsA and Atr had no significant effect. We found that H2O2 promoted the colocalization of VDAC1 and Bax, which was partially inhibited by intervention with CsA or Atr. In conclusion, we found that tRNA mutations promoted hypertensive renal insufficiency. Increased reactive oxygen species was an important associated mechanism, which inhibited mitochondrial function by affecting VDAC1 expression and function.


Asunto(s)
Riñón/fisiopatología , Membranas Mitocondriales/metabolismo , Mutación , ARN de Transferencia/genética , Canal Aniónico 1 Dependiente del Voltaje/metabolismo , Adenosina Trifosfato/biosíntesis , Animales , Presión Sanguínea , Línea Celular , Regulación de la Expresión Génica , Potencial de la Membrana Mitocondrial , Oxígeno/metabolismo , Transporte de Proteínas , Ratas , Ratas Endogámicas SHR , Especies Reactivas de Oxígeno/metabolismo , Proteína X Asociada a bcl-2/metabolismo
5.
PeerJ ; 7: e6804, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31086741

RESUMEN

BACKGROUND: The incidences of premature coronary heart disease present a rising trend worldwide. The possible risk factors that may predict the incidence of repeat percutaneous coronary intervention (PCI) in premature acute coronary syndrome (ACS) remains unclear. METHODS: A total of 203 patients ≤45 years with ACS from Chinese PLA General Hospital who have undergone angiography twice were included in this report. Data were collected from medical records of patients during hospitalization. Baseline characteristics which have significant differences in the univariate analysis were enrolled into the multiple logistic regression analysis. According to the odds ratio (OR) of these variables, different values were assigned to build a risk model to predict the possible risk of the premature ACS patients undergoing repeat PCI. RESULTS: Of the 203 young patients, 88 patients (43.3%) underwent repeat PCI. The intermit time (OR 1.002, (95% CI [1.001-1.002])), diastolic blood pressure of second procedure (OR 0.967, (95% CI [0.938-0.996])), stent diameter (OR 0.352, (95% CI [0.148-0.840])), HbA1C of the first procedure (OR 1.835, (95% CI [1.358-2.479])), and Troponin T of the second procedure (OR 1.24, (95% CI [0.981-1.489])) were significantly associated with the incidence of repeat PCI in patients with premature ACS. An aggregate score between 0 and 6 was calculated based on these cutpoints. CONCLUSION: For young patients with premature ACS, risk of undergoing repeat PCI was high. HbA1C was a significant, independent predictor for the incidence of repeat revascularization, and weighed more than traditional lipid profile. The glucose metabolism and disorders in patients with premature ACS should be routinely screened.

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