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1.
Surg Endosc ; 36(2): 1456-1465, 2022 02.
Artigo em Inglês | MEDLINE | ID: mdl-34085095

RESUMO

BACKGROUND: The oncologic efficacy of laparoscopic versus open surgery for advanced distal gastric cancer (ADGC) beyond 3 years after surgery remain obscure. METHODS: A total of 1256 patients with ADGC at two teaching institutions in China from April 2007 to December 2014 were enrolled. The general data of the two groups were identified to enable rigorous estimation of propensity scores. Restricted mean survival time (RMST) and Landmark analysis was used to compare survival. RESULTS: After matching 461 patients each in the open distal gastrectomy (ODG) and laparoscopic distal gastrectomy (LDG) groups, they were included into analysis. The 3- and 5-year overall survival (OS) and disease-free survival were comparable in two groups. RMST-stratified analysis showed that the 3-year RMST of ODG group was similar to that of LDG group in patients with cT4a (- 1.38 years, p = 0.163) or with cT4a and tumor size > 5 cm, whereas the 5-year RMST had significant differences between groups in cT4a patients(- 8.36 years, P = 0.005) or cT4a and tumor size > 5 cm patients(4.67 years, P = 0.042). In patients with cT4a and tumors > 5 cm, the number of peritoneal recurrences was significantly fewer in the ODG group than in the LDG group (4 vs. 17, P = 0.033), and the peritoneal recurrence time and multiple-site recurrence time were both later in the ODG group. CONCLUSION: By reducing recurrence, ODG achieves a better survival for GC patients with serous infiltration and tumors larger than 5 cm beyond 3 years after surgery. The present findings can serve as a reference for surgical options and the setting of follow-up time point for clinical studies.


Assuntos
Laparoscopia , Neoplasias Gástricas , Gastrectomia , Humanos , Excisão de Linfonodo , Pontuação de Propensão , Estudos Retrospectivos , Neoplasias Gástricas/patologia , Resultado do Tratamento
2.
Sensors (Basel) ; 19(16)2019 Aug 11.
Artigo em Inglês | MEDLINE | ID: mdl-31405244

RESUMO

The intelligent inspection of power lines and other difficult-to-access structures and facilities has been greatly enhanced by the use of Unmanned Aerial Vehicles (UAVs), which allow inspection in a safe, efficient, and high-quality fashion. This paper analyzes the characteristics of a scene containing power equipment and the operation mode of UAVs. A low-cost virtual scene is created, and a training sample for the power-line components is generated quickly. Taking a vibration-damper as the main object, an assembled detector based on geometrical constraint (ADGC) is proposed and is used to analyze the virtual dataset. The geometric positional relationship is used as the constraint, and the Faster R-CNN, Deformable Part Model (DPM), and Haar cascade classifiers are combined, which allows the features of different classifiers, such as contour, shape, and texture to be fully used. By combining the characteristics of virtual data and real data using UAV images, the power components are detected by the ADGC. The result produced by the detector with relatively good performance can help expand the training set and achieve a better detection model. Moreover, this method can be smoothly transferred to other power-line facilities and other power-line scenarios.

3.
Alzheimers Dement ; 12(2): 121-129, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26449541

RESUMO

INTRODUCTION: Ebbert et al. reported gene-gene interactions between rs11136000-rs670139 (CLU-MS4A4E) and rs3865444-rs670139 (CD33-MS4A4E). We evaluate these interactions in the largest data set for an epistasis study. METHODS: We tested interactions using 3837 cases and 4145 controls from Alzheimer's Disease Genetics Consortium using meta-analyses and permutation analyses. We repeated meta-analyses stratified by apolipoprotein E (APOE) ε4 status, estimated combined odds ratio (OR) and population attributable fraction (cPAF), and explored causal variants. RESULTS: Results support the CLU-MS4A4E interaction and a dominant effect. An association between CLU-MS4A4E and APOE ε4 negative status exists. The estimated synergy factor, OR, and cPAF for rs11136000-rs670139 are 2.23, 2.45, and 8.0, respectively. We identified potential causal variants. DISCUSSION: We replicated the CLU-MS4A4E interaction in a large case-control series and observed APOE ε4 and possible dominant effect. The CLU-MS4A4E OR is higher than any Alzheimer's disease locus except APOE ε4, APP, and TREM2. We estimated an 8% decrease in Alzheimer's disease incidence without CLU-MS4A4E risk alleles and identified potential causal variants.


Assuntos
Doença de Alzheimer/genética , Apolipoproteína E4/genética , Clusterina/genética , Epistasia Genética , Proteínas de Membrana/genética , Lectina 3 Semelhante a Ig de Ligação ao Ácido Siálico/genética , Alelos , Feminino , Predisposição Genética para Doença , Variação Genética , Estudo de Associação Genômica Ampla/métodos , Humanos , Masculino , Fatores de Risco
4.
Neurobiol Aging ; 74: 135-146, 2019 02.
Artigo em Inglês | MEDLINE | ID: mdl-30448613

RESUMO

The International Genomics of Alzheimer's Project (IGAP) is a consortium for characterizing the genetic landscape of Alzheimer's disease (AD). The identified and/or confirmed 19 single-nucleotide polymorphisms (SNPs) associated with AD are located on non-coding DNA regions, and their functional impacts on AD are as yet poorly understood. We evaluated the roles of the IGAP SNPs by integrating data from many resources, based on whether the IGAP SNP was (1) a proxy for a coding SNP or (2) associated with altered mRNA transcript levels. For (1), we confirmed that 12 AD-associated coding common SNPs and five nonsynonymous rare variants are in linkage disequilibrium with the IGAP SNPs. For (2), the IGAP SNPs in CELF1 and MS4A6A were associated with expression of their neighboring genes, MYBPC3 and MS4A6A, respectively, in blood. The IGAP SNP in DSG2 was an expression quantitative trait loci (eQTL) for DLGAP1 and NETO1 in the human frontal cortex. The IGAP SNPs in ABCA7, CD2AP, and CD33 each acted as eQTL for AD-associated genes in brain. Our approach for identifying proxies and examining eQTL highlighted potentially impactful, novel gene regulatory phenomena pertinent to the AD phenotype.


Assuntos
Doença de Alzheimer/genética , Estudos de Associação Genética , Polimorfismo de Nucleotídeo Único/genética , Idoso , Idoso de 80 Anos ou mais , Proteínas CELF1/genética , Proteínas de Transporte/genética , Desmogleína 2/genética , Feminino , Humanos , Desequilíbrio de Ligação/genética , Masculino , Proteínas de Membrana/genética , Locos de Características Quantitativas/genética , RNA Mensageiro/genética , RNA não Traduzido/genética , Receptores de N-Metil-D-Aspartato , Proteínas Associadas SAP90-PSD95/genética , Transcrição Gênica/genética
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