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1.
Article in Chinese | MEDLINE | ID: mdl-36878504

ABSTRACT

Objective: To investigate the efficacy of the first-day suspension method for improving the success rate of construction of nasopharyngeal carcinoma-patient derived organoids (NPC-PDO). Methods: The tumor samples of 14 nasopharyngeal carcinoma(NPC) patients, i.e.,13 males and 1 female, with a mean age of 43.0±12.0 years old, were collected from the Affiliated Tumor Hospital of Guangxi Medical University and the First Affiliated Hospital of Guangxi Medical University from January 2022 to July 2022. The tumor samples of 3 patients were digested into single cell suspension and divided into 2 groups, for comparing the efficacy of NPC-PDO construction by the direct inoculation method and the first-day suspension method. The remaining 11 patients were randomized to receive either the direct inoculation method or the first-day suspension method for NPC-PDO construction. The diameter and the number of spheres of NPC-PDO constructed by the two methods were compared by optical microscope; the 3D cell viability detection kit was used to compare the cell viability; the survival rates were compared by trypan blue staining; the success rates of the two construction methods were compared; the number of cases which could be successfully passaged for more than 5 generations and were consistent with the original tissue by pathological examination was counted; and the dynamic changes of cells in suspension overnight were observed by live cell workstation. The independent sample t-test was applied to compare the measurement data of the two groups, and the chi-square test was used to compare the classification data. Results: Compared with the direct inoculation, the diameter and the number of spheres of NPC-PDO constructed by the first-day suspension method were increased, with a higher cell activity, and the success rate of construction was obviously improved (80.0% vs 16.7%, χ2=4.41, P<0.05). In the suspension state, some of the cells aggregated and increased their ability to proliferate. Conclusion: The first-day suspension method can improve the success rate of NPC-PDO construction, especially for those whose original tumor sample size is small.


Subject(s)
Microscopy , Nasopharyngeal Neoplasms , Male , Humans , Female , Adult , Middle Aged , Nasopharyngeal Carcinoma , China , Organoids
2.
Eur Rev Med Pharmacol Sci ; 24(7): 3818-3828, 2020 04.
Article in English | MEDLINE | ID: mdl-32329858

ABSTRACT

OBJECTIVE: Methyltransferase-like 3 (Mettl3), one of "writers" for N6-methyladenosine RNA methylation is determined to participate in a variety of cell biological functions. However, the functions of Mettl3 on tumor growth of glioma remain unknown. Here, we conducted a research to explore the contribution of Mettl3 in the progression of glioma. PATIENTS AND METHODS: To detect the expression level of RNAs, quantitative Real Time-Polymerase Chain Reaction (qRT-PCR) was performed. To access the relative level of proteins, Western blot was conducted. The proliferative ability of glioma cells was detected by CCK-8 assay and colony formation assay. The migration and invasion of glioma cells were determined by wound healing assay and transwell invasion assay. RESULTS: The expression of Mettl3 was significantly downregulated in tumor tissues compared to the adjacent normal tissues. The downregulation of Mettl3 led to the enhancement of glioma cell proliferation, migration, and invasion in vitro, and promoted the tumor growth of glioma cells in vivo. In addition, further investigation confirmed that Mettl3 plays critical roles in the development of glioma by targeting PI3K/Akt pathway. CONCLUSIONS: Our study proves that Mettl3 plays a critical role in the proliferation, migration, and invasion of glioma cells by inactivating PI3K/Akt signaling pathway, providing a novel mechanism of glioma tumorigenesis and raising a new target for the treatment of glioma.


Subject(s)
Cell Movement , Glioma/metabolism , Methyltransferases/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Proto-Oncogene Proteins c-akt/metabolism , Cell Proliferation , Glioma/pathology , Humans , Methyltransferases/genetics , Signal Transduction , Tumor Cells, Cultured
3.
Eur Rev Med Pharmacol Sci ; 23(10): 4243-4253, 2019 May.
Article in English | MEDLINE | ID: mdl-31173296

ABSTRACT

OBJECTIVE: We investigated the effects of long non-coding RNA (lncRNA) H19 on glioma cell proliferation, invasion, migration, and apoptosis and the underlying mechanisms. PATIENTS AND METHODS: H19 expression in glioma tissues, para-carcinoma tissues, and glioma cell lines was analyzed by Real-time polymerase chain reaction (RT-PCR). After transfecting U251 and U87MG cells with siRNA-H19, cell proliferation was detected by the cell counting kit-8 (CCK8) assay. Invasion and migration were detected by a transwell assay; cell cycle distribution and apoptosis were measured by flow cytometry analysis; Dvl2, GSK-3ß, cyclin D1, and ß-catenin expressions were detected by RT-PCR and Western blotting. RESULTS: H19 expression in glioma tissues was higher than that in para-carcinoma tissues and associated with poor prognosis in glioma patients. Cell proliferation, invasion, and migration significantly decreased, the percentage of glioma cells in G0/G1 significantly increased, the percentage of glioma cells in the S phase significantly decreased, and apoptosis significantly increased in U251 and U87MG cells transfected with siRNA-H19 compared to those in the siRNA-NC group. Downregulation of H19 decreased DVL2, cyclin D1, and ß-catenin expression and increased GSK-3ß expression. The inhibitory effects of downregulation of H19 on glioma cell proliferation, invasion, and migration were reversed by SKL2001 via the activation of the Wnt/ß-catenin signal pathway, which was further enhanced by inhibition of the Wnt/ß-catenin signal pathway by XAV939. CONCLUSIONS: H19 was overexpressed in glioma tissues and glioma cell lines. Downregulation of H19 inhibited cell proliferation, invasion, and migration, arrested cell cycle progression in the G0/G1 phase, and induced cell apoptosis by restraining activation of the Wnt/ß-catenin signaling pathway in glioma cells. Therefore, H19 is a potential therapeutic target for glioma therapy.


Subject(s)
Brain Neoplasms/genetics , Brain Neoplasms/pathology , Glioma/genetics , Glioma/pathology , RNA, Long Noncoding/drug effects , RNA, Long Noncoding/genetics , Wnt Signaling Pathway/genetics , beta Catenin/genetics , Adult , Aged , Antineoplastic Agents/pharmacology , Apoptosis/genetics , Cell Count , Cell Line, Tumor , Cell Proliferation , Drug Delivery Systems , Female , Humans , Male , Middle Aged , Mitosis/genetics , Neoplasm Invasiveness/genetics , Prognosis , Transfection , Wnt Signaling Pathway/drug effects
4.
Bratisl Lek Listy ; 120(4): 316-319, 2019.
Article in English | MEDLINE | ID: mdl-31023056

ABSTRACT

OBJECTIVE: This study investigated the association between serum uric acid (sUA) and stroke risk in men with hypertriglyceridemia. METHODS: Between 2002 and 2012, male patients with pure hypertriglyceridemia and a triglyceride (TG) level ≥ 150 mg/dL were enrolled. Eligible patients were categorized into two groups according to their sUA levels (≥ and < 8 mg/dL). Clinical characteristics and comorbidities that are risk factors for stroke were recorded and compared between the groups. RESULTS: A total of 265 male patients (95 with sUA ≥ 8 mg/dL and 170 with sUA < 8 mg/dL) were enrolled. The incidence of ischemic type of stroke was significantly higher in patients with sUA ≥ 8 mg/dL (p = 0.038), particularly in the age range of 45-65 years. Multivariate Cox proportional analyses confirmed that age (p = 0.003) and UA (p = 0.019) were major predictive factors for stroke free (ischemic type of stroke) survival. CONCLUSION: Among men with hypertriglyceridemia, the incidence rate of ischemic type of stroke significantly increased with sUA levels ≥ 8 mg/dL, particularly in men aged 45 to 65 years. Hyperuricemia is considered a potential predictive factor for ischemic type of stroke and may indicate the need for preventive management in patients with hypertriglyceridemia (Tab. 3, Fig. 1, Ref. 28).


Subject(s)
Biomarkers , Hypertriglyceridemia , Hyperuricemia , Stroke , Uric Acid , Aged , Biomarkers/blood , Humans , Hypertriglyceridemia/complications , Male , Middle Aged , Predictive Value of Tests , Risk Factors , Stroke/diagnosis , Stroke/etiology , Uric Acid/blood
5.
Nutr Metab Cardiovasc Dis ; 27(11): 1008-1014, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28986076

ABSTRACT

BACKGROUND AND AIMS: Increased body fat relates to enhanced inflammatory cytokine production, which, in turn, activates the renin-angiotensin-aldosterone system and increases the risk of chronic kidney disease (CKD). Herein, we aimed to examine the association between obesity and the risk of CKD in a population-representative cohort in Taiwan. METHODS AND RESULTS: A multistage systematic sampling process was applied in the National Health Interview Survey (NHIS) 2000, 2005, and 2009. Participants were interviewed by a standardized face-to-face questionnaire to obtain information on their demographics, socioeconomic status, lifestyle factors, and body mass index (BMI). The BMI values were classified as follows: underweight (<18.5 kg/m2), normal (18.5-23.9 kg/m2), overweight (24-26.9 kg/m2), and obesity (≥27 kg/m2). The NHIS dataset was linked to National Health Insurance claims data to identify the incidence of CKD. Univariate and multivariate Cox proportional hazard models with competing risks were used to investigate the association between BMI and CKD incidence. We analyzed 45,012 subjects (mean age, 42.03 years; 50.09% males). During 374,254 person-years of follow-up, a total of 1913 new-onset CKD cases were identified. Kaplan-Meier curves comparing the four BMI groups revealed a significant difference (p < 0.01, log-rank test). After controlling for confounding factors, the relative risk of incident CKD was significantly higher in the obese group compared to the normal-weight group (adjusted hazard ratio = 1.32; 95% confidence interval: 1.17-1.49), with a significant linear trend (p < 0.01). CONCLUSION: Obesity was suggested as an independent risk factor for CKD. Further studies focusing on the effect of losing weight on CKD prevention are warranted.


Subject(s)
Obesity/epidemiology , Renal Insufficiency, Chronic/epidemiology , Adult , Body Mass Index , Cross-Sectional Studies , Female , Health Surveys , Humans , Incidence , Kaplan-Meier Estimate , Linear Models , Male , Multivariate Analysis , Obesity/diagnosis , Proportional Hazards Models , Renal Insufficiency, Chronic/diagnosis , Retrospective Studies , Risk Assessment , Risk Factors , Taiwan/epidemiology , Time Factors
6.
Int J Obes (Lond) ; 41(6): 971-975, 2017 06.
Article in English | MEDLINE | ID: mdl-28280271

ABSTRACT

BACKGROUND: Obesity affects immune function by increasing the number of T helper lymphocytes, which may reduce the risk of tuberculosis (TB) infection. However, the effect of obesity on TB development has not been extensively studied. This nationwide population-based cohort study investigated the effect of obesity on TB development in Taiwanese adults. METHODS: We included 46 028 adult participants (age ⩾18 years) from three rounds (2001, 2005 and 2009) of the Taiwan National Health Interview Survey. Obesity and overweight were defined as a body mass index (BMI) ⩾27 and 24-26.9 (kg/m2), respectively. Data on BMI and other covariates at baseline were collected by in-person interviews. Incident cases of active TB were identified from the National Health Insurance database. Multivariable logistic regression was used to estimate the associations of obesity and overweight with active TB, with adjustment for age, sex, smoking, alcohol consumption, socioeconomic status and other covariates. RESULTS: In total, 241 new cases of active TB occurred during the study period. Obesity (adjusted odds ratio [AOR], 0.43; 95% confident interval [CI], 0.28-0.67) and overweight (AOR, 0.67; 95% CI, 0.49-0.91) were associated with lower risk of incident TB, after adjusting for demographic characteristics and comorbidities. There was a linear dose-response relation of BMI with active TB incidence (AOR per unit change in BMI, 0.92; 95% CI, 0.88-0.95; P <0.001). CONCLUSION: Obesity and overweight are associated with lower risk of active TB. Future studies should investigate the underlying mechanisms and clinical and epidemiological consequences of these findings.


Subject(s)
Overweight/immunology , Thinness/immunology , Tuberculosis/immunology , Adult , Body Mass Index , CD4-CD8 Ratio , Comorbidity , Cross-Sectional Studies , Female , Health Surveys , Humans , Leptin/metabolism , Lymphocyte Activation , Male , Middle Aged , Overweight/epidemiology , Overweight/physiopathology , Risk Factors , T-Lymphocytes/immunology , Taiwan/epidemiology , Thinness/epidemiology , Thinness/physiopathology , Tuberculosis/epidemiology , Tuberculosis/physiopathology
7.
Blood Cancer J ; 4: e177, 2014 Jan 17.
Article in English | MEDLINE | ID: mdl-24442206

ABSTRACT

Recently, mutations of the additional sex comb-like 1 (ASXL1) gene were identified in patients with myelodysplastic syndrome (MDS), but the interaction of this mutation with other genetic alterations and its dynamic changes during disease progression remain to be determined. In this study, ASXL1 mutations were identified in 106 (22.7%) of the 466 patients with primary MDS based on the French-American-British (FAB) classification and 62 (17.1%) of the 362 patients based on the World Health Organization (WHO) classification. ASXL1 mutation was closely associated with trisomy 8 and mutations of RUNX1, EZH2, IDH, NRAS, JAK2, SETBP1 and SRSF2, but was negatively associated with SF3B1 mutation. Most ASXL1-mutated patients (85%) had concurrent other gene mutations at diagnosis. ASXL1 mutation was an independent poor prognostic factor for survival. Sequential studies showed that the original ASXL1 mutation remained unchanged at disease progression in all 32 ASXL1-mutated patients but were frequently accompanied with acquisition of mutations of other genes, including RUNX1, NRAS, KRAS, SF3B1, SETBP1 and chromosomal evolution. On the other side, among the 80 ASXL1-wild patients, only one acquired ASXL1 mutation at leukemia transformation. In conclusion, ASXL1 mutations in association with other genetic alterations may have a role in the development of MDS but contribute little to disease progression.

8.
AJNR Am J Neuroradiol ; 35(6): 1052-7, 2014 Jun.
Article in English | MEDLINE | ID: mdl-23639561

ABSTRACT

Different MR imaging patterns of cerebral fat embolism have been reported in the literature without a systematic review. Our goal was to describe the patterns, explore the relationship between disease course and the imaging patterns, and discuss the underlying mechanism. We reveal 5 distinctive MR imaging patterns: 1) scattered embolic ischemia occurring dominantly at the acute stage; 2) confluent symmetric cytotoxic edema located at the cerebral white matter, which mainly occurs at the subacute stage; 3) vasogenic edematous lesions also occurring at the subacute stage; 4) petechial hemorrhage, which persists from the acute to the chronic stage; and 5) chronic sequelae, occurring at late stage, including cerebral atrophy, demyelinating change, and sequelae of infarction or necrosis. Underlying mechanisms of these imaging patterns are further discussed. Recognition of the 5 evolving MR imaging patterns of cerebral fat embolism may result in adjustment of the appropriate management and improve the outcome.


Subject(s)
Embolism, Fat/epidemiology , Embolism, Fat/pathology , Intracranial Embolism/epidemiology , Intracranial Embolism/pathology , Magnetic Resonance Imaging/statistics & numerical data , Female , Humans , Male , Prevalence , Reproducibility of Results , Risk Assessment , Sensitivity and Specificity
9.
Leukemia ; 28(1): 50-8, 2014 Jan.
Article in English | MEDLINE | ID: mdl-23929217

ABSTRACT

Conventionally, acute myeloid leukemia (AML) patients are categorized into good-, intermediate- and poor-risk groups according to cytogenetic changes. However, patients with intermediate-risk cytogenetics represent a largely heterogeneous population regarding treatment response and clinical outcome. In this study, we integrated cytogenetics and molecular mutations in the analysis of 318 patients with de novo non-M3 AML who received standard chemotherapy. According to the mutation status of eight genes, including NPM1, CEBPA, IDH2, RUNX1, WT1, ASXL1, DNMT3A and FLT3, that had prognostic significance, 229 patients with intermediate-risk cytogenetics could be refinedly stratified into three groups with distinct prognosis (P<0.001); patients with good-risk genotypes had a favorable outcome (overall survival, OS, not reached) similar to those with good-risk cytogenetics, whereas those with poor-risk genotypes had an unfavorable prognosis (OS, 10 months) similar to those with poor-risk cytogenetics (OS, 13.5 months), and the remaining patients with other genotypes had an intermediate outcome (OS, 25 months). Integration of cytogenetic and molecular profiling could thus reduce the number of intermediate-risk AML patients from around three-fourth to one-fourth. In conclusion, integration of cytogenetic and molecular changes improves the prognostic stratification of AML patients, especially those with intermediate-risk cytogenetics, and may lead to better decision on therapeutic strategy.


Subject(s)
Chromosome Aberrations , Leukemia, Myeloid, Acute/genetics , Adolescent , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Mutation , Nucleophosmin , Risk Factors , Young Adult
10.
Int J Immunopathol Pharmacol ; 25(3): 741-50, 2012.
Article in English | MEDLINE | ID: mdl-23058024

ABSTRACT

Leukocyte adhesion to endothelium plays a critical initiating role in inflammation. Berberine, an anti-inflammatory natural compound, is known to attenuate lipopolysaccharide (LPS)-induced lung injury and improve survival of endotoxemic animals with mechanism not fully clarified. This study investigated the effects of berberine on the LPS-induced leukocyte-endothelial cell adhesion both in vivo and in vitro. We first established an animal model to observe the in vivo LPS-induced adhesion of leukocytes to the endothelium of venules in the lung tissue dose-dependently. Pretreatment of LPS-stimulated rats with berberine for 1 h reduced the leukocyte-endothelium adhesion and vascular cell adhesion molecule-1 (VCAM-1) expression in lung. Pretreatment of LPS-stimulated vascular endothelial cells with berberine also dose-dependently decreased the number of adhered THP-1 cells and VCAM-1 expression at both RNA and protein levels. Berberine was further confirmed to inhibit the nuclear translocation and DNA binding activity of LPS-activated nuclear factor-kappa B (NF-kappa B). These data demonstrated an additional molecular mechanism for the profound anti-inflammatory effect of berberine.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Berberine/pharmacology , Cell Adhesion/drug effects , Endothelial Cells/drug effects , Leukocytes/drug effects , Lipopolysaccharides/pharmacology , Lung/blood supply , Vascular Cell Adhesion Molecule-1/metabolism , Venules/drug effects , Active Transport, Cell Nucleus/drug effects , Animals , Binding Sites , Cells, Cultured , Coculture Techniques , DNA/metabolism , Dose-Response Relationship, Drug , Down-Regulation , Endothelial Cells/immunology , Human Umbilical Vein Endothelial Cells/drug effects , Human Umbilical Vein Endothelial Cells/immunology , Leukocytes/immunology , Male , NF-kappa B/metabolism , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley , Vascular Cell Adhesion Molecule-1/genetics , Venules/immunology
11.
Clin Genet ; 82(5): 460-5, 2012 Nov.
Article in English | MEDLINE | ID: mdl-21848650

ABSTRACT

This study explored the role of TCOF1 insertion mutations in Taiwanese patients with craniofacial anomalies. Twelve patients with single or multiple, asymmetrical congenital craniofacial anomalies were enrolled. Genomic DNA was prepared from leukocytes; the coding regions of TCOF1 were analyzed by polymerase chain reaction and direct sequencing. Clinical manifestations were correlated to the TCOF1 mutation. Six of 12 patients diagnosed with hemifacial microsomia exhibited a novel insertion mutation 4127 ins G (frameshift) in exon 24 in the TCOF1 gene. All six patients were diagnosed with anomalies on the left side. In addition, four of these six patients had hearing impairment; three had other major anomalies; and two had developmental delay. The insertion caused a frameshift, an early truncation, the loss of two putative nuclear localization signals (residues 1404-1420 and 1424-1440), and the loss of coiled coil domain (1406-1426) in treacle protein. These findings support the existence of two regulators of growth of the mandibular condyles.


Subject(s)
Facial Asymmetry/genetics , Mutagenesis, Insertional , Nuclear Proteins/genetics , Phosphoproteins/genetics , Adult , Child , Child, Preschool , Craniofacial Abnormalities/genetics , Craniofacial Abnormalities/pathology , Exons , Female , Frameshift Mutation , Genome, Human/genetics , Humans , Infant , Infant, Newborn , Male , Nuclear Localization Signals/genetics , Nuclear Proteins/metabolism , Phenotype , Phosphoproteins/metabolism , Polymorphism, Single Nucleotide , Sequence Analysis, DNA , Taiwan
12.
Interv Neuroradiol ; 17(1): 22-6, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21561555

ABSTRACT

Collateral networks between the external carotid artery and internal carotid arteries become crucial for cerebral perfusion after occlusion of internal carotid arteries. We report the first case of a patient who received percutaneous transluminal angioplasty and stenting in a collateral vessel between the external and internal carotid artery for treatment of radiation induced severe stenosis of the internal carotid artery in the context of a contralateral internal carotid artery occlusion.


Subject(s)
Angioplasty , Aorta, Thoracic/diagnostic imaging , Carotid Stenosis/therapy , Radiation Injuries/therapy , Stents , Carotid Artery, External/diagnostic imaging , Carotid Artery, Internal/diagnostic imaging , Carotid Stenosis/etiology , Cerebral Angiography , Collateral Circulation , Head and Neck Neoplasms/radiotherapy , Humans , Male , Middle Aged , Tomography, X-Ray Computed
13.
Interv Neuroradiol ; 16(4): 394-9, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21162769

ABSTRACT

Successful management of aneurysms of complex morphology depends primarily on adjunct use of balloons or stents. However, these two methods are technically demanding and have higher complication rates. As an alternative to these two techniques, we have used a catheter-assisted technique with a number of cases. It is simple, versatile, and less demanding technically. This technique should be considered as an alternative strategy in cases of wide-necked aneurysms.


Subject(s)
Catheterization/instrumentation , Catheterization/methods , Embolization, Therapeutic/instrumentation , Embolization, Therapeutic/methods , Intracranial Aneurysm/therapy , Adult , Aged , Cerebral Angiography , Female , Humans , Intracranial Aneurysm/diagnostic imaging , Male , Middle Aged
14.
Eur Respir J ; 36(4): 808-18, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20530035

ABSTRACT

An accumulating body of evidence incriminates Rho kinase (ROCK) in the pathogenesis of pulmonary hypertension (PH). The therapeutic efficacy of azaindole-1, a novel highly selective and orally active ROCK inhibitor, has not yet been investigated in PH. This study aimed to investigate the effects of azaindole-1 on 1) acute hypoxic pulmonary vasoconstriction (HPV), 2) proliferation of pulmonary arterial smooth muscle cells (PASMCs) and 3) animal models of PH. Azaindole-1 significantly inhibited HPV in isolated, ventilated and buffer-perfused murine lungs and proliferation of primary rat PASMCs in vitro. Azaindole-1 was administered orally from 21 to 35 days after monocrotaline (MCT) injection in rats and hypoxic exposure in mice. Azaindole-1 (10 and 30 mg per kg body weight per day in rats and mice, respectively) significantly improved haemodynamics and right ventricular hypertrophy. Moreover, the medial wall thickness and muscularisation of peripheral pulmonary arteries were ameliorated. Azaindole-1 treatment resulted in a decreased immunoreactivity for phospho-myosin phosphatase target subunit 1 and proliferating cell nuclear antigen in pulmonary vessels of MCT-injected rats, suggesting an impaired ROCK activity and reduced proliferating cells. Azaindole-1 provided therapeutic benefit in experimental PH, and this may be attributable to its potent vasorelaxant and antiproliferative effects. Azaindole-1 may offer a useful approach for treatment of PH.


Subject(s)
Azabicyclo Compounds/therapeutic use , Hypertension, Pulmonary/drug therapy , Indoles/therapeutic use , Animals , Cell Proliferation , Disease Models, Animal , Enzyme Inhibitors/pharmacology , Hemodynamics , Lung/pathology , Male , Mice , Rats , Rats, Sprague-Dawley , Telemetry/methods , Tetrazolium Salts/pharmacology , Thiazoles/pharmacology , Thymidine/chemistry , Treatment Outcome , rho-Associated Kinases/antagonists & inhibitors
15.
Clin Radiol ; 65(2): 109-17, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20103432

ABSTRACT

AIM: To assess the ability of coronary angiography performed using dual-source computed tomography (DSCT) to evaluate coronary artery disease (CAD) in a population with unselected heart rates and extensive coronary calcification. MATERIALS AND METHODS: Forty-four patients at intermediate to high risk for CAD underwent both DSCT coronary angiography and invasive coronary angiography (ICA) within 30 days. No beta blockers were administered prior to imaging. Image quality and quantitatively stenosis of all coronary segments with a diameter > or = 1.5mm were accessed. Patients were stratified according to mean heart rate (< 70 versus > or = 70 bpm) and heart rate variability (< 10 versus > or = 10 bpm). DSCT detection of coronary stenosis by segment, vessel, and patient characteristics were compared to the reference standard of ICA. RESULTS: Diagnostic accuracy for all patients was high regarding sensitivity (97%), positive predictive value (PPV, 84.2%), and negative predictive value (NPV, 83.3%) but low regarding specificity (45.5%) with a moderate interobserver agreement (Kappa = 0.50). The accuracy for vessel-based diagnosis was high regarding sensitivity (96.6%), specificity (80.8%), PPV (80.3%), and NPV (96.7%). The segment-based diagnostic results revealed a moderate interobserver agreement for image quality and sensitivity, specificity, PPV and NPV for all segments of 66.9, 97.8, 90.8, and 89.9%, respectively. CONCLUSION: DSCT coronary angiography has high diagnostic accuracy in assessing CAD among patients at intermediate to high risk without using heart rate-modulating premedication. DSCT is not superior to ICA for diagnosis of calcified segments.


Subject(s)
Calcinosis/diagnostic imaging , Coronary Angiography/methods , Coronary Stenosis/diagnostic imaging , Tomography, X-Ray Computed/methods , Aged , Electrocardiography , Epidemiologic Methods , Female , Heart Rate , Humans , Male , Middle Aged , Radiographic Image Interpretation, Computer-Assisted/methods
16.
Eur Respir J ; 31(3): 599-610, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18032446

ABSTRACT

Phosphodiesterase (PDE) inhibitors are currently under investigation for the therapy of pulmonary hypertension. The present study was designed to investigate chronic effects of oral pumafentrine, a mixed selective PDE-3/4 inhibitor, in monocrotaline (MCT)-induced pulmonary hypertension in rats. Treatment with pumafentrine (10 mg.kg(-1) daily) from week 4 to 6 after a single injection of MCT (60 mg.kg(-1)) partially reversed pulmonary hypertension and right heart hypertrophy in rats. In addition, small pulmonary arterial muscularisation, media hypertrophy and decrease in lumen area were largely reversed. Inhibition of smooth muscle proliferation under pumafentrine was demonstrated in vivo as was a pro-apoptotic effect of pumafentrine on vascular cells. Moreover, pumafentrine dose-dependently increased cyclic adenosine monophosphate levels and inhibited proliferation of cultured pulmonary arterial smooth muscle cells. In conclusion, oral pumafentrine partially reverses monocrotaline-induced pulmonary hypertension, lung vascular remodelling and right heart hypertrophy in rats.


Subject(s)
Hypertension, Pulmonary/drug therapy , Hypertrophy, Right Ventricular/drug therapy , Lung/drug effects , Muscle, Smooth, Vascular/drug effects , Myocytes, Smooth Muscle/drug effects , Naphthyridines/pharmacology , Phosphodiesterase Inhibitors/pharmacology , Animals , Cyclic Nucleotide Phosphodiesterases, Type 3/drug effects , Cyclic Nucleotide Phosphodiesterases, Type 4/drug effects , Disease Models, Animal , Hypertension, Pulmonary/chemically induced , Hypertension, Pulmonary/pathology , Hypertrophy, Right Ventricular/chemically induced , Lung/pathology , Male , Monocrotaline/administration & dosage , Phosphodiesterase 3 Inhibitors , Phosphodiesterase 4 Inhibitors , Rats
17.
Circulation ; 104(25): 3152-7, 2001 Dec 18.
Article in English | MEDLINE | ID: mdl-11748116

ABSTRACT

BACKGROUND: The myocardial sleeve of the superior vena cava (SVC) has been identified as a potential initiating focus in atrial fibrillation, but information on cell-to-cell linkage at this site is lacking. METHODS AND RESULTS: We examined the SVC in 8 dogs by immunoconfocal and electron microscopy. Cardiomyocytes outlined with vinculin and bearing striations positive for alpha-actinin are found in the proximal segment of the SVC. These cells, grouped in bundles of various orientations according to location, extend cephalically as far as 3 cm from the right atrium (RA)-SVC junction. Comparison between the junctional level and the level 2 cm distal shows that the myocardial layer in the latter is thinner and not as compact and is composed of longer cells (87.3+/-15.7 versus 71.6+/-14.4 micrometer, P<0.01). Gap junctions made of connexin43 (Cx43), Cx40, and Cx45 are aggregated mainly at the intercalated disks, and colocalization of connexins is a common feature throughout the myocardial sleeve. Areas of atypical expression exist, however, characterized by a center of abundant Cx43 labels surrounded by a periphery of scattered tiny Cx40-labeled spots. Although in the ventral subluminal compact myocardial layer, individual cells at both levels are surrounded by similar numbers of cells, the number of aggregation of labeled gap junctions at the distal level is less (2.3+/-0.6 versus 3.7+/-0.9, P<0.01). In addition, electron-microscopic examination demonstrates that the gap junctions at the distal level are smaller in size (0.37+/-0.30 versus 0.55+/-0.34 micrometer, P<0.01). CONCLUSIONS: The myocardial sleeve in the canine SVC is a heterogeneous structure, which could potentially form a substrate for heterogeneity of electrical coupling.


Subject(s)
Gap Junctions/metabolism , Myocardium/metabolism , Vena Cava, Superior/metabolism , Actinin/analysis , Animals , Connexin 43/analysis , Connexins/analysis , Dogs , Gap Junctions/ultrastructure , Heart/anatomy & histology , Immunohistochemistry , Microscopy, Confocal , Microscopy, Electron , Myocardium/ultrastructure , Vena Cava, Superior/ultrastructure , von Willebrand Factor/analysis , Gap Junction alpha-5 Protein
18.
Phys Rev E Stat Nonlin Soft Matter Phys ; 64(1 Pt 2): 015601, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11461324

ABSTRACT

The defect excitation and nonuniform melting of a two-dimensional Coulomb cluster with 300 charged particles (interacting with 1/r type force) in a uniform neutralizing background are studied numerically. Intrinsic defects exist around the outer circular shells surrounding the inner triangular lattice. They are the source regions for anisotropic particle thermal vibrations and then cyclic hoppings with the increasing temperature. It leads to the nonuniform melting associated with the thermal motion of intrinsic defects, and then the thermal excitation of dislocation pairs and disclinations. The intrinsic defect free center core has the highest melting temperature. It shows the sequential losses of translational and then orientational orders.

19.
J Clin Virol ; 17(2): 91-9, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10942089

ABSTRACT

BACKGROUND: An epidemic of enterovirus 71 (EV71) occurred in Taiwan from April to December of 1998, with two peaks, one in June and the other in October. Many enteroviruses were isolated in our laboratory from 258 cases during this outbreak. Approximately half of the enteroviruses isolated were EV71 and one fifth were coxsackievirus A16. OBJECTIVES: To analyze laboratory findings in the EV71 epidemic of 1998 in Taiwan, various EV71 specimens in different cell lines were examined. In addition, genetic analysis of 5' non-coding region (NCR) was performed to analyze the strain variation in this outbreak. RESULTS: The cytopathic effect induced by EV71 was observed 2-13 (mean of 4.5) days post-inoculation in Vero cells and 4-15 (mean of 6.6) days in green monkey kidney (GMK) cells inoculated with throat swabs. Of the total positive EV71 cases, virus was most frequently obtained from throat swabs (91.7%), less from stools (64.8%), and none from cerebral spinal fluid (CSF). Molecular analyses of EV71 by sequencing the 5' NCR of 34 strains obtained from different clinical categories and various geographic areas showed that their sequences differed (0-13 bp in 681 bp sequenced) by approximately 0-2%. The sequences of these isolates differed from EV71 prototype BrCr or MS strain by 17.5-19%, with the exception of two samples which exhibited nucleotide variation by only 8.9 and 8.2%, when compared to the MS strain. CONCLUSION: EV71 was most frequently isolated from throat swab specimens in Vero cells. The molecular analyses of the 5' NCR of EV71 revealed that most isolates from this epidemic belonged to a group of closely related clones and only two were in a different group which was clustered with the EV71 MS strain.


Subject(s)
Disease Outbreaks , Enterovirus Infections/epidemiology , Enterovirus/isolation & purification , Adolescent , Animals , Cell Line , Child , Child, Preschool , Chlorocebus aethiops/virology , Enterovirus/genetics , Enterovirus Infections/cerebrospinal fluid , Enterovirus Infections/mortality , Enterovirus Infections/virology , Feces/virology , Female , Humans , Infant , Infant, Newborn , Male , Pharynx/virology , Phylogeny , Polymorphism, Genetic , RNA, Untranslated/genetics , RNA, Viral/genetics , Rectum/virology , Seasons , Sequence Analysis, RNA , Taiwan/epidemiology , Vero Cells
20.
Arterioscler Thromb Vasc Biol ; 20(7): 1753-62, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10894813

ABSTRACT

Endothelial cells form gap junctions that, according to vessel type, may be composed of up to 3 types of connexin, connexin37, connexin40, and connexin43. Although changes in connexin expression have been linked to growth and injury in cultured endothelial cells, information on connexin expression in regenerating endothelium in situ is lacking. We investigated gap junction distribution and expression of all 3 endothelial connexins during healing in rat carotid artery after denudation injury. En face viewing of the vascular luminal surface by means of immunoconfocal microscopy was used to examine the spatial and temporal expression pattern of the endothelial connexins. Gap junction spots labeled by specific antisera against connexin37, connexin40, and connexin43 were quantified 7, 14, and 28 days after injury, and the relations among the connexins were examined by using colocalization analysis. Complementary electron microscopy was also conducted. After injury, the regenerating endothelium initially expressed small, sparse gap junctions, the numbers of which progressively increased to values equivalent to those of controls. Although connexin40 gap-junctional spot size and area returned to uninjured levels by 28 days after injury, connexin37 and connexin43 spot size and area exceeded those of the uninjured artery (P<0.05). Double-label analysis showed that even though colocalization of connexins to the same gap-junctional spot is a common feature, the extent of colocalization was time dependent (>80% in the intact artery at postinjury day 28 and <70% at postinjury days 7 and 14, P<0.01). We conclude that distinct alterations in expression of the 3 connexins are associated with regeneration of the arterial endothelium in situ, implying different intercellular communication requirements during the various phases of the healing process.


Subject(s)
Carotid Artery Injuries/metabolism , Connexins/biosynthesis , Endothelium, Vascular/metabolism , Gap Junctions/physiology , Animals , Antibodies , Connexin 43/analysis , Connexin 43/biosynthesis , Connexin 43/immunology , Connexins/analysis , Connexins/immunology , Endothelium, Vascular/chemistry , Endothelium, Vascular/ultrastructure , Gap Junctions/chemistry , Gap Junctions/ultrastructure , Male , Microscopy, Confocal , Microscopy, Electron , Muscle, Smooth, Vascular/chemistry , Muscle, Smooth, Vascular/metabolism , Rats , Rats, Sprague-Dawley , Wound Healing/physiology , Gap Junction alpha-5 Protein , Gap Junction alpha-4 Protein
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