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1.
Biomark Med ; 18(8): 373-383, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-39041842

RESUMEN

Aim: This retrospective clinical study was designed to examine the predictive value of thromboelastography (TEG) combined with coagulation function for venous thromboembolism (VTE) in hospitalized patients with cancer. Materials & methods: Among 215 patients admitted between May 2020 and January 2022, 39 (18.14%) were diagnosed with VTE during hospitalization. Results: Significant differences were found in D-dimer, ATIII and TEG parameters (maximum amplitude and coagulation index) between VTE-positive and VTE-negative patients (p < 0.05). Multivariate analysis revealed tumor node metastasis stage, concomitant infection, smoking history and D-dimer as independently associated with VTE. The constructed model and D-dimer areas under the curve were 0.809 and 0.764, respectively. Conclusion: TEG parameters were not significantly predictive indicators for VTE, with D-dimer remaining a key predictor.


[Box: see text].


Asunto(s)
Productos de Degradación de Fibrina-Fibrinógeno , Neoplasias , Tromboelastografía , Tromboembolia Venosa , Humanos , Tromboembolia Venosa/sangre , Tromboembolia Venosa/etiología , Tromboembolia Venosa/diagnóstico , Masculino , Femenino , Persona de Mediana Edad , Neoplasias/complicaciones , Neoplasias/sangre , Estudios Retrospectivos , Anciano , Productos de Degradación de Fibrina-Fibrinógeno/metabolismo , Productos de Degradación de Fibrina-Fibrinógeno/análisis , Factores de Riesgo , Factores de Coagulación Sanguínea/metabolismo , Factores de Coagulación Sanguínea/análisis , Adulto
2.
Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-981731

RESUMEN

OBJECTIVE@#To explore the relationship between spinous process deviation and lumbar disc herniation in young patients.@*METHODS@#From March 2015 to January 2022, 30 treated young (under the age of 30) patients with lumbar disc herniation were included as the young group. In addition 30 middle-aged patients (quinquagenarian group) with lumbar disc herniation and 30 patients with non-degenerative spinal diseases (young non-degenerative group) were selected as control groups. The angle of the spinous process deviation was measured on CT and statistically analyzed by various groups. All the data were measured twice and the average value was taken and recorded.@*RESULTS@#The average angle of spinous process deviation in the degenerative lumbar vertebra of young patients were (3.89±3.77) degrees, similar to the (3.72±2.98) degrees of quinquagenarian patients(P=0.851). The average angle of s spinous process deviation young non-degenerative group were (2.20±2.28) degrees, significantly less than young group(P=0.040). The spinous process deviation angle of the superior vertebral of the degenerative lumbar in the young group was (4.10±3.44) degrees, which similar to the (3.47±2.87) degrees in the quinquagenarian group (P=0.447). A total of 19 young patients had the opposite deviation direction of the spinous process of the degenerative lumbar vertebra and upper vertebra, while only 7 quinquagenarian patients had this condition(P=0.02). The type of lumbar disc herniation in young patients had no significant relationship with the direction of spinous process deflection of the degenerative or upper lumbar vertebra (P>0.05).@*CONCLUSION@#Spinous process deviation is a risk factor of young lumbar disc herniation patients. If the deviation directions of adjacent lumbar spinous processes are opposite, it will increase the incidence of lumbar disc herniation in young patients. There was no significant correlation between the type of disc herniation and the deviation direction of the spinous process of the degenerative or upper lumbar vertebra. People with such anatomical variation can strengthen the stability of spine and prevent lumbar disc herniation through reasonable exercise.


Asunto(s)
Persona de Mediana Edad , Humanos , Desplazamiento del Disco Intervertebral/complicaciones , Cuerpo Vertebral , Enfermedades de la Columna Vertebral , Fusión Vertebral/efectos adversos , Vértebras Lumbares/diagnóstico por imagen , Degeneración del Disco Intervertebral/etiología
3.
Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-818372

RESUMEN

Objective The relationship between calcified nanoparticles (CNPs) and the formation of urinary stones is drawing increasing attention and the specific mechanisms involved. This study aims to investigate the mechanisms of the formation of kidney stone caused by CNPs. Methods A total of 48 rats were randomly and equally divided into a CNPs group (each rat was injected with 2 mL CNPs through the tail vein to establish a rat kidney stone model of CNPs), and a control group (injected the same amount of sterile isotonic saline instead of CNPs). We compared the expression levels of autophagy-related proteins, such as Beclin-1 and LC-3, the formation of autophagosomes and calcium salt crystals in renal tissues at time points of 3h, 6h, 12h, 24h, 1w, 2w, 4w and 8w in two groups. Results The relative expression levels and positive cells of Beclin-1 and LC-3 in CNPs group at 3h,6h,12h,24h, 1w, 2w, 4w, 8w were significantly higher than those in the control group (P< 0.05), and reached the highest value at 24 (P< 0.05). The number of autophagosomes at 24h, 1w, 2w, 4w, and 8w in the CNPs group ((2.83±0.32), (3.00±0.26), (3.70±0.44), (3.90±0.98), (4.70±0.51)/HP, respectively) were significantly higher than those in the control group (0.73±0.15)/HP (P <0.05). The scores of calcium salt crystals in the CNPs group at 2w, 4w, and 8w significantly increased compared to the control group (P <0.05). The calcium salt crystal formation score ((0.92 ± 0.98) points) was positively correlated with the expression intensities of Beclin-1 and LC-3 ((6.78 ± 4.25), (2.61 ± 2.57), respectively) (r = 0.843, 0.628, P <0.05), which was positively correlated with the number of autophagosomes (2.53 ± 1.41) (r = 0.923, P <0.001). Conclusion CNPs may damage renal tubular epithelial cells, and induce immediate autophagic activity, also increase expression of autophagy-related proteins and autophagosome formation, which will promote the formation and aggregation of calcium salt crystals in renal tubules to some extent.

4.
Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-295522

RESUMEN

<p><b>OBJECTIVE</b>To investigate the correlation between RARbeta gene promoter methylation and P53 gene mutations in non-small cell lung cancer (NSCLC).</p><p><b>METHODS</b>Promoter methylation of RARbeta and P53 mutations of exons 5 through 9 in 198 resected primary NSCLC tissues were determined by methylation-specific PCR and direct sequencing.</p><p><b>RESULTS</b>RARbeta gene promoter methylation and P53 mutation were detected in 58.1% and 36.4% of tumors, respectively. Both were higher in males than in females and in smokers than in nonsmokers. A higher prevalence of RARbeta promoter methylation was found in patients with advanced stage tumors than those with TNM stage I. P53 gene mutations were more frequent in squamous cell carcinoma and adeno-squamous carcinoma than adenocarcinoma. All such differences were statistically significant (P< 0.05). Frequencies of P53 mutations, including G:C>T:A mutations, transversions and missense mutations were significantly higher in tumors with RARbeta methylation than in those without (P< 0.05). A significantly higher prevalence of RARbeta methylation was found in tumors with only G:C>T:A mutation in P53 gene than those without P53 mutations (P< 0.05). This difference (OR=3.737, 95%CI: 1.414-9.873) was still statistically significant (P< 0.05) in smokers (OR=4.020, 95%CI: 1.263-12.800), squamous cell carcinomas (OR=5.480, 95%CI: 1.400-21.446) or patients with advanced tumors (OR=3.446, 95%CI: 1.054-11.267) after adjusting for age and sex.</p><p><b>CONCLUSION</b>RARbeta methylation is associated with G:C>T:A mutations in P53 gene in NSCLC.</p>


Asunto(s)
Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Secuencia de Bases , Carcinoma de Pulmón de Células no Pequeñas , Genética , Patología , Metilación de ADN , Genes p53 , Predisposición Genética a la Enfermedad , Neoplasias Pulmonares , Genética , Patología , Datos de Secuencia Molecular , Mutación , Regiones Promotoras Genéticas , Receptores de Ácido Retinoico , Genética
5.
Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-295540

RESUMEN

<p><b>OBJECTIVE</b>To investigate the effect of CYP1A1 and GSTM1 genetic polymorphisms and BPDE-DNA adducts on lung tumorigenesis.</p><p><b>METHODS</b>The case control study has included 200 cases of lung cancer and 200 controls. DNA was extracted from blood samples of all subjects. The genotype of both CYP1A1 and GSTM1 were detected with PCR-based restriction fragment length polymorphisms (PCR-RELP). BPDE-DNA adducts were detected with competitive ELISA.</p><p><b>RESULTS</b>CYP1A1 mutant genotype and GSTM1 null genotype with smoke has increased the risk of lung cancer, with OR being 2.406(1.321-4.382), 2.755(1.470-5.163), respectively. The level of BPDE-DNA adducts in patients was greater than control, and the adduct level in ever smokers was higher than never smokers, the difference was statistically significant (P= 0.0252). GSTM1 null genotype individuals with BPDE-DNA level higher than 5 adducts/10(8) nucleotide have increased risk of lung cancer (OR= 1.988, 95%CI: 1.011-3.912). Compared with never smokers with CYP1A1 wild genotype, smokers with CYP1A1 mutation genotype had an increased risk of forming a higher level of DNA adducts (P= 0.0459). Smokers with GSTM1 null genotype formed more DNA adducts compared with never smokers with GSTM1 functional genotype (OR = 2.432, 95% CI: 1.072-4.517).</p><p><b>CONCLUSION</b>GSTM1 null genotype with higher level DNA adducts may increase the risk of lung cancer. DNA adducts form easier in smokers with CYP1A1 mutation genotype and GSTM1 null genotype, which in turn may influence lung tumorigenesis.</p>


Asunto(s)
Femenino , Humanos , Masculino , Persona de Mediana Edad , 7,8-Dihidro-7,8-dihidroxibenzo(a)pireno 9,10-óxido , Carcinógenos , Estudios de Casos y Controles , Citocromo P-450 CYP1A1 , Genética , Aductos de ADN , Genética , Genotipo , Glutatión Transferasa , Genética , Neoplasias Pulmonares , Genética , Polimorfismo Genético
6.
Chinese Journal of Neuromedicine ; (12): 989-992, 2011.
Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-1033372

RESUMEN

Objective To explore the establishment of animal models of incomplete spinal cord ischemic injury to provide ideal carriers for researching the pathogenesis of incomplete spinal cord ischemic injury.Methods Twenty-four New Zealand rabbits were randomly divided into a control group (n=8) and 2 experimental groups (n=16); control group only underwent sham-operation without inducing spinal cord injury to exclude the influences of anesthesia and surgery on motor evoked potential (MEP); in the experimental groups,spinal cord ischemia injury models were established by the methods of selective ligation of segmental spinal artery from cranio-caudal direction.Baseline MEP after anesthetization were recorded,and the MEP 30 min,2 and 7 d after vascular ligation were noted.Motor function was assessed after narcotic conscious,and 2 and 7 d after vascular ligation.The specimens 7 d after ligation were taken for HE staining.Results The amplitude of MEP in the experimental group having 3 lumbar artery ligation 30 minutes after ligation was significantly different as compared with that in the control group (P<0.05); no significant differences on the amplitude of MEP were noted between these 2 groups 2 and 7 d after ligation (P>0.05).Significant differences on the amplitude of MEP were noted between control group and experimental group having 4 lumbar artery ligation 30 min,and 2 and 7 d after ligation (P<0.05).The latency of all these rabbits showed no significant difference 30 min,and 2 and 7 d after ligation (P>0.05).The amplitude changes of MEP were accorded with the results of motor function scale.Conclusion Reversible incomplete spinal cord ischemia animal models can be established after 3 lumbar artery ligation; irreversible incomplete spinal cord ischemia animal models can be established after 4 lumbar artery ligation.

7.
Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-234325

RESUMEN

<p><b>OBJECTIVE</b>To investigate the effects of promoter methylation of p16, death-associated protein kinase (DAPK) and retinoic acid receptor-beta (RAR beta) genes on clinical data in non-small cell lung cancers, and to study the effect of smoking on the risk of gene methylation.</p><p><b>METHODS</b>The promoter methylation of p16, DAPK and RAR beta genes in 200 primary non-small cell lung cancers and the corresponding nonmalignant lung tissues were determined by methylation-specific PCR.</p><p><b>RESULTS</b>Methylation in the tumor tissues was detected in 51.0% for p16, 60.0% for DAPK, and 58.0% for RAR beta gene, with significant differences (P < 0.05) when compared with those in the corresponding nonmalignant tissues(12.5%, 11.5% and 15.0%) respectively. p16 gene methylation in tumor tissue was associated with age significantly in unconditional logistic regression analysis (P < 0.01) and histologic type (P < 0.05). DAPK gene methylation in tumor tissue was associated significantly with age (P < 0.05), gender (P < 0.05) and clinical type (P < 0.05). RAR beta gene methylation in tumor tissue was associated with clinical type (P < 0.05) and tumor stage (P < 0.05) significantly. The interaction odds ratio (OR) for the gene-gene interaction in tumor tissue between p16 and DAPK was 1.987 (95%CI:1.055-3.743). The results of the gene-smoking analyses revealed that a relationship existed between cigarette smoking and p16 gene methylation (OR = 3.139, 95%CI: 1.046-9.419), the OR for the relationship of DAPK gene methylation and cigarette smoking was 3.585(95%CI: 1.270-10.123) in tumor tissue. The RAR beta gene methylation did not differ based on the smoking status of patients in tumor tissue.</p><p><b>CONCLUSION</b>The p16, DAPK and RAR beta genes methylation are strongly associated with clinical data of non-small cell lung cancer, and methylation of p16 and DAPK genes are associated with tobacco smoking.</p>


Asunto(s)
Proteínas Reguladoras de la Apoptosis , Genética , Proteínas Quinasas Dependientes de Calcio-Calmodulina , Genética , Carcinoma de Pulmón de Células no Pequeñas , Genética , Patología , Metilación de ADN , Proteínas Quinasas Asociadas a Muerte Celular , Genes p16 , Modelos Logísticos , Neoplasias Pulmonares , Genética , Patología , Estadificación de Neoplasias , Regiones Promotoras Genéticas , Receptores de Ácido Retinoico , Genética , Fumar
8.
Chinese Journal of Neuromedicine ; (12): 475-479, 2010.
Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-1032987

RESUMEN

Objective To provide the theoretical basis for the application of cortical somatosensory evoked potential (CSEP) in monitoring the function of the spinal cord to prevent postoperative neurological dysfunction. Methods Thirty-three New Zealand rabbits were randomly divided into 6 groups: 8 were chosen as control group to eliminate the influence of anesthesia and surgery on the evoked potential; the other 25 were assigned to 5 sub-experimental groups (n=5) according to the artery number being ligatured in the left renal arteries and the spinal arteries. Baseline evoked potential in each group was noted immediately after anesthesia; the CSEP were recorded at different time points (before vascular ligation, 30 min and 2 d after vascular ligation). Motor functions were assessed after narcotic conscious and 2 d after vascular ligation. The specimens were taken for HE staining. Results The latency was not sensitive to spinal cord ischemia and no significant difference of that was found between the experimental groups and the control group (P>0.05); except that, the changes of theamplitudes were very complex and the specificity of motor function was decreased. The amplitude reduced and then gradually restored in the 2, 3 and 4 levels of ligation. The changes of amplitude could indicate the degree of pathological damage in the spinal cord and its motor function. Conclusion Complex amplitude of somatosensory evoked potential can be found in the acute phase of ischemia in the spinal cord. Specificity of motor function is poor resulting from its signal averaging process. Motor evoked potential monitoring in the operation should also be added in the detection of the spinal cord.

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