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1.
Niger J Clin Pract ; 27(2): 188-193, 2024 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-38409146

RESUMEN

BACKGROUND: Congenital diseases are still an important medical, social, and economic problem all over the world. In North Cyprus, in addition to other reasons, early prenatal diagnostic measures are undertaken to prevent births with thalassemia major, a locally widespread genetic disease. AIM: This study aims to evaluate the results of prenatal invasive diagnostic tests performed in a private obstetrics clinic in Northern Cyprus and show the diagnosis process of thalassemia and chromosomal anomalies. MATERIALS AND METHODS: This study is a retrospective, descriptive study. Chorionic villus sampling (CVS) results and the amniocentesis tests performed between 1990 and 2022 are evaluated. Thalassemia and chromosome analysis of samples obtained by CVS and amniocentesis tests were performed. To diagnose alpha or beta thalassemia and sickle cell, 239 CVS was performed. And to diagnose chromosomal anomalies, 396 CVS and amniocentesis were performed. RESULTS: The mean age of the 480 pregnant women included in the study was 31.12 years (18-46) and 30% of them were older than 34 years. The most common indications for invasive prenatal diagnostic test (IPDT) were; mother/father thalassemia minor/major, advanced maternal age, high risk of ultrasonography erase findings, and the noninvasive screening test. The result of IPDT detected 7.3% chromosomal anomaly and 69.5% thalassemia and sickle cell anemia. Of the 239 CVS performed to diagnose alpha or beta thalasemia and sickle cell, 23.4% beta major, 42.3% beta minor, and 2.1% alpha minor were diagnosed. Of the 396 CVS and amniocentesis performed to diagnose chromosomal anormalies; 2.8% of Down syndrome and 4.54% of other chromosomal anomalies were diagnosed. CONCLUSION: IPDT is important in correctly diagnosing fetal anomalies at the prenatal stage to help families decide at the right time.


Asunto(s)
Anemia de Células Falciformes , Trastornos de los Cromosomas , Talasemia , Embarazo , Femenino , Humanos , Adolescente , Adulto Joven , Adulto , Persona de Mediana Edad , Estudios Retrospectivos , Chipre , Diagnóstico Prenatal/métodos , Muestra de la Vellosidad Coriónica , Aberraciones Cromosómicas , Pruebas Diagnósticas de Rutina
2.
Niger J Clin Pract ; 24(3): 362-368, 2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-33723110

RESUMEN

BACKGROUND: Pulmonary rehabilitation (PR) is a core component of the management of patients with chronic obstructive pulmonary disease (COPD). Although several types of PR programs are implemented for patients with COPD on the basis of patient preferences or clinical protocols, the clinical efficiencies of these programs may vary, with each program having its own unique purpose, procedures, benefits, challenges, and effectiveness. AIM: The aim of this study was to compare the effects of self-management and hospital-based PR programs in COPD patients. MATERIALS AND METHODS: This study was prospective intervention research. Fifty-eight patients with stable COPD were randomly allocated to a hospital-based outpatient group and a self-management group before commencement of a 12-week PR program. Before and after the PR program, all patients were evaluated using the 6-min walk test, Modified Borg Scale, St. George's Respiratory Questionnaire, State-Trait Anxiety Inventory, and Standardized Mini-Mental Test. RESULTS: Pulmonary functions, dyspnea, quality of life, and 6MWT distance were significantly improvement the hospital-based PR than self-management PR (P < 0.05). Moreover, cognitive function significantly improved after the PR program in both groups with no significant intergroup difference (P > 0.05). CONCLUSIONS: Our findings suggest that PR is useful for to improvement functional capacity, quality of life, cognitive function and anxiety, in patients with COPD. A hospital-based PR is more effective than a self-management PR program.


Asunto(s)
Enfermedad Pulmonar Obstructiva Crónica , Automanejo , Hospitales , Humanos , Estudios Prospectivos , Calidad de Vida , Encuestas y Cuestionarios , Resultado del Tratamiento
3.
Zebrafish ; 17(5): 305-318, 2020 10.
Artículo en Inglés | MEDLINE | ID: mdl-32931381

RESUMEN

Rapidly accumulating literature has proven feasibility of the zebrafish xenograft models in cancer research. Nevertheless, online databases for searching the current zebrafish xenograft literature are in great demand. Herein, we have developed a manually curated database, called ZenoFishDb v1.1 (https://konulab.shinyapps.io/zenofishdb), based on R Shiny platform aiming to provide searchable information on ever increasing collection of zebrafish studies for cancer cell line transplantation and patient-derived xenografts (PDXs). ZenoFishDb v1.1 user interface contains four modules: DataTable, Visualization, PDX Details, and PDX Charts. The DataTable and Visualization pages represent xenograft study details, including injected cell lines, PDX injections, molecular modifications of cell lines, zebrafish strains, as well as technical aspects of the xenotransplantation procedures in table, bar, and/or pie chart formats. The PDX Details module provides comprehensive information on the patient details in table format and can be searched and visualized. Overall, ZenoFishDb v1.1 enables researchers to effectively search, list, and visualize different technical and biological attributes of zebrafish xenotransplantation studies particularly focusing on the new trends that make use of reporters, RNA interference, overexpression, or mutant gene constructs of transplanted cancer cells, stem cells, and PDXs, as well as distinguished host modifications.


Asunto(s)
Bases de Datos Factuales , Trasplante Heterólogo , Pez Cebra/cirugía , Animales , Bases de Datos Factuales/estadística & datos numéricos
4.
Neural Netw ; 116: 279-287, 2019 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-31125914

RESUMEN

Convolutional neural networks with strong representation ability of deep structures have ever increasing popularity in many research areas. The main difference of Convolutional Neural Networks with respect to existing similar artificial neural networks is the inclusion of the convolutional part. This inclusion directly increases the performance of artificial neural networks. This fact has led to the development of many different convolutional models and techniques. In this work, a novel convolution technique named as Differential Convolution and updated error back-propagation algorithm is proposed. The proposed technique aims to transfer feature maps containing directional activation differences to the next layer. This implementation takes the idea of how convolved features change on the feature map into consideration. In a sense, this process adapts the mathematical differentiation operation into the convolutional process. Proposed improved back propagation algorithm also considers neighborhood activation errors. This property increases the classification performance without changing the number of filters. Four different experiment sets were performed to observe the performance and the adaptability of the differential convolution technique. In the first experiment set utilization of the differential convolution on a traditional convolutional neural network structure made a performance boost up to 55.29% for the test accuracy. In the second experiment set differential convolution adaptation raised the top1 and top5 test accuracies of AlexNet by 5.3% and 4.75% on ImageNet dataset. In the third experiment set differential convolution utilized model outperformed all compared convolutional structures. In the fourth experiment set, the Differential VGGNet model obtained by adapting proposed differential convolution technique performed 93.58% and 75.06% accuracy values for CIFAR10 and CIFAR100 datasets, respectively. The accuracy values of the Differential NIN model containing differential convolution operation were 92.44% and 72.65% for the same datasets. In these experiment sets, it was observed that the differential convolution technique outperformed both traditional convolution and other compared convolution techniques. In addition, easy adaptation of the proposed technique to different convolutional structures and its efficiency demonstrate that popular deep learning models may be improved with differential convolution.


Asunto(s)
Aprendizaje Profundo , Redes Neurales de la Computación , Reconocimiento de Normas Patrones Automatizadas/métodos , Aprendizaje Profundo/tendencias , Humanos , Reconocimiento de Normas Patrones Automatizadas/tendencias
5.
Sci Rep ; 8(1): 1570, 2018 01 25.
Artículo en Inglés | MEDLINE | ID: mdl-29371671

RESUMEN

Acetylcholinesterase (AChE), an enzyme responsible for degradation of acetylcholine, has been identified as a prognostic marker in liver cancer. Although in vivo Ache tumorigenicity assays in mouse are present, no established liver cancer xenograft model in zebrafish using an ache mutant background exists. Herein, we developed an embryonic zebrafish xenograft model using epithelial (Hep3B) and mesenchymal (SKHep1) liver cancer cell lines in wild-type and ache sb55 sibling mutant larvae after characterization of cholinesterase expression and activity in cell lines and zebrafish larvae. The comparison of fluorescent signal reflecting tumor size at 3-days post-injection (dpi) revealed an enhanced tumorigenic potential and a reduced migration capacity in cancer cells injected into homozygous ache sb55 mutants when compared with the wild-type. Increased tumor load was confirmed using an ALU based tumor DNA quantification method modified for use in genotyped xenotransplanted zebrafish embryos. Confocal microscopy using the Huh7 cells stably expressing GFP helped identify the distribution of tumor cells in larvae. Our results imply that acetylcholine accumulation in the microenvironment directly or indirectly supports tumor growth in liver cancer. Use of this model system for drug screening studies holds potential in discovering new cholinergic targets for treatment of liver cancers.


Asunto(s)
Acetilcolinesterasa/deficiencia , Línea Celular Tumoral , Modelos Animales de Enfermedad , Xenoinjertos , Neoplasias Hepáticas/patología , Pez Cebra , Animales , Trasplante de Neoplasias
6.
J Endocrinol Invest ; 41(3): 293-298, 2018 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-28770447

RESUMEN

BACKGROUND: Elastase-1 is a proteolytic enzyme secreted by pancreatic acinar cells, and measurements of the concentration this enzyme are used to evaluate pancreatic exocrine function. We aimed to determine whether pancreatic exocrine function declines due to chronic hypercalcemia by measuring fecal elastase levels. METHODS: 75 patients with primary hyperparathyroidism (18 men and 47 women) and 30 healthy subjects (11 men and 19 women) participated in this study. Renal function tests, lipid parameters, bone mineral density, and serum calcium, phosphorus, vitamin D, parathormone, glucose, and thyroid stimulating hormone levels as well as fecal elastase concentrations, were determined in these patients and controls. RESULTS: The mean fecal elastase level was 335.3 ± 181.4 µg/g in the PHPT group and 317.4 ± 157.3 µg/g in the control group. There was no significant difference in fecal elastase levels between the two groups (p = 0.5). CONCLUSIONS: Chronic hypercalcemia in primary hyperparathyroidism did not decrease the fecal elastase level, which is an indirect indicator of chronic pancreatitis; therefore, chronic hypercalcemia in PHPT may not cause chronic pancreatitis.


Asunto(s)
Insuficiencia Pancreática Exocrina/etiología , Heces/enzimología , Hipercalcemia/complicaciones , Hiperparatiroidismo Primario/fisiopatología , Elastasa Pancreática/metabolismo , Pancreatitis Crónica/etiología , Adulto , Anciano , Anciano de 80 o más Años , Biomarcadores/análisis , Estudios de Casos y Controles , Insuficiencia Pancreática Exocrina/enzimología , Femenino , Estudios de Seguimiento , Humanos , Hipercalcemia/metabolismo , Masculino , Persona de Mediana Edad , Pancreatitis Crónica/enzimología , Pronóstico
7.
Eur Rev Med Pharmacol Sci ; 21(19): 4391-4397, 2017 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-29077155

RESUMEN

OBJECTIVE: We aimed to determine the efficacy of troponin I, D-dimer, and lactate levels and right ventricular diameter (RVD)/left ventricular diameter (LVD) ratio on pulmonary computed tomography angiography (PCTA) in the risk classification of patients who were diagnosed with acute pulmonary embolism (APE) in Emergency Department (ED). PATIENTS AND METHODS: Patients who were diagnosed as having APE by PCTA in ED were included in this retrospective study. Patients were grouped as high-risk (undergoing cardiopulmonary resuscitation or given thrombolytic therapy), moderate-risk (with non-high-risk and positive ECO findings) and low risk (others). Troponin I, D-dimer, and lactate levels of patients were determined. RVD, RVD/LVD ratio, and interventricular septum deviation were calculated from PCTA images. RESULTS: A total of 121 patients were included (35 high, 36 moderate, 50 low risk). Lactate was different in the high-risk group from the other groups, whereas there was no difference between the moderate and low-risk groups. Troponin I levels were not different between the high-risk and moderate-risk groups. There were statistically significant differences between the high, moderate, and low-risk groups in terms of mean RVD/LVD ratios. ROC analyses performed in order to define high-risk group revealed a cut-off value of > 2.3 (AUC = 0.848, sensitivity = 70%, specificity = 90%, + Likelihood ratio (LR) = 7, -LR = 0.33, 95% CI = 0.752-0.943) for lactate and > 1.40 (AUC = 0.695 sensitivity = 71%, specificity = 80%, + LR = 3.6, -LR = 0.36, 95% CI = 0.668-0.822) for RVD/LVD ratio. CONCLUSIONS: Lactate levels and RVD/LVD ratio were shown to be useful in distinguishing high-risk patients from other patient groups. Troponin I is important in terms of showing cardiac involvement, but it is inadequate in distinguishing between high and moderate-risk patients. Lactate, troponin I, and RVD/LVD ratio may be used together for a more accurate separation of patients with high, intermediate and low-risk.


Asunto(s)
Servicio de Urgencia en Hospital , Embolia Pulmonar/diagnóstico , Troponina I/metabolismo , Adulto , Anciano , Anciano de 80 o más Años , Biomarcadores/metabolismo , Femenino , Humanos , Masculino , Persona de Mediana Edad , Curva ROC , Estudios Retrospectivos , Factores de Riesgo , Sensibilidad y Especificidad , Disfunción Ventricular Derecha/fisiopatología
8.
Clin Exp Obstet Gynecol ; 42(5): 586-9, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26524803

RESUMEN

PURPOSE: Subcutaneous edema detected sonographically in the forms of nuchal edema, cystic hygroma (CH), or non-immune hydrops (NIH) may be a sign of chromosomal abnormalities. The aim of this study was to investigate the chromosome abnormality incidence in fetuses with nuchal edema, CH, or NIH. MATERIALS AND METHODS: The authors performed cytogenetic analysis of 218 singleton fetuses with ultrasound diagnosis of subcutaneous edema in the forms of nuchal edema in the first and second trimesters. RESULTS: Chromosomal abnormality rates were 30.4, 10.4, 36.8, 34.1, and 60% in the nuchal translucency (NT), nuchal fold thickness (NF), CH, NIH, and CH with NIH groups, respectively. In 71 cases with detected chromosomal abnormalities, 37%, 44%, 15%, and 4% of the pathologic karyotypes were identified as monosomy X, trisomy 21, trisomy 18, and trisomy 13, respectively. CONCLUSIONS: This study confirms that subcutaneous edema detected sonographically, in the forms of nuchal edema, CH, or NIH, is a significant indicator of abnormal karyotype and deserves further investigation.


Asunto(s)
Aberraciones Cromosómicas , Hidropesía Fetal/diagnóstico por imagen , Linfangioma Quístico/diagnóstico por imagen , Medida de Translucencia Nucal , Adolescente , Adulto , Femenino , Edad Gestacional , Humanos , Cariotipificación , Masculino , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Embarazo , Segundo Trimestre del Embarazo , Ultrasonografía Prenatal , Adulto Joven
9.
Clin Exp Obstet Gynecol ; 42(3): 327-30, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26152003

RESUMEN

The authors' aim was to detect the associated anomalies and their effect on the management of the fetuses with omphalocele and gastroschisis. Between the period of 2007-2013, the data of fetuses with abdominal wall defects were analyzed. Chromosomal abnormalities and associated morphologic anomalies diagnosed by ultrasonography and autopsy were evaluated. Of the. 61 fetuses, ten (20.4%) omphalocele cases and nine (75%) gastroschisis cases were isolated. Chromosomal abnormalities were found in seven fetuses with omphalocele cases. All fetuses with abnormal karyotypes had multiple additional anomalies. Termination rate was 65.3% for omphalocele group versus none in the gastroschisis group. To give better counseling about the prognosis and outcome of the fetuses with abdominal wall defects, detection of additional anomalies as well as type of the defect are essential tools even if the karyotype is normal.


Asunto(s)
Anomalías Múltiples/diagnóstico por imagen , Aberraciones Cromosómicas/estadística & datos numéricos , Trastornos de los Cromosomas/genética , Gastrosquisis/diagnóstico por imagen , Hernia Umbilical/diagnóstico por imagen , Adulto , Trastornos de los Cromosomas/epidemiología , Femenino , Feto , Gastrosquisis/epidemiología , Gastrosquisis/genética , Hernia Umbilical/epidemiología , Hernia Umbilical/genética , Humanos , Cariotipo , Cariotipificación , Masculino , Embarazo , Pronóstico , Estudios Retrospectivos , Centros de Atención Terciaria , Ultrasonografía Prenatal , Adulto Joven
11.
Clin Microbiol Infect ; 20(11): O847-53, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-24831227

RESUMEN

This study reviewed the clinical, laboratory, therapeutic and prognostic data on genitourinary involvement of brucellosis in this largest case series reported. This multicentre study pooled adult patients with genitourinary brucellar involvement from 34 centres treated between 2000 and 2013. Diagnosis of the disease was established by conventional methods. Overall 390 patients with genitourinary brucellosis (352 male, 90.2%) were pooled. In male patients, the most frequent involved site was the scrotal area (n=327, 83.8%), as epididymo-orchitis (n=204, 58%), orchitis (n=112, 31.8%) and epididymitis (n=11, 3.1%). In female patients, pyelonephritis (n=33/38, 86.8%) was significantly higher than in male patients (n=11/352, 3.1%; p<0.0001). The mean blood leukocyte count was 7530±3115/mm3. Routine laboratory analysis revealed mild to moderate increases for erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP). The mean treatment duration and length of hospital stay were significantly higher when there were additional brucellar foci (p<0.05). Surgical operations including orchiectomy and abscess drainage were performed in nine (2.3%) patients. Therapeutic failure was detected in six (1.5%), relapse occurred in four (1%), and persistent infertility related to brucellosis occurred in one patient. A localized scrotal infection in men or pyelonephritis in women in the absence of leucocytosis and with mild to moderate increases in inflammatory markers should signal the possibility of brucellar genitourinary disease.


Asunto(s)
Brucelosis/tratamiento farmacológico , Brucelosis/patología , Enfermedades Urogenitales Femeninas/tratamiento farmacológico , Enfermedades Urogenitales Femeninas/patología , Enfermedades Urogenitales Masculinas/tratamiento farmacológico , Enfermedades Urogenitales Masculinas/patología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Brucelosis/diagnóstico , Femenino , Enfermedades Urogenitales Femeninas/diagnóstico , Humanos , Masculino , Enfermedades Urogenitales Masculinas/diagnóstico , Persona de Mediana Edad , Pronóstico , Estudios Retrospectivos , Adulto Joven
12.
J Obstet Gynaecol ; 34(7): 571-5, 2014 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-24867317

RESUMEN

The aim of our study was to evaluate the incidences and chromosomal abnormality detection rates of various indications for genetic amniocentesis. We retrospectively analysed 6,142 amniocentesis cases performed in a single centre between January 2007 and April 2013. We assessed the indications for prenatal diagnosis, fetal karyotypes, maternal ages, fetal ultrasound findings and maternal serum screening results. The most common indication for genetic amniocentesis was an abnormal maternal serum-screening test (36.6%), followed by advanced maternal age (28%), advanced maternal age and an abnormal maternal serum screening test (14.9%) and abnormal ultrasound findings (11.2%). The highest positive predictive values obtained from the indications included abnormal ultrasound findings and abnormal maternal serum screening test (12.9%) and advanced maternal age (12.2%). Although advanced maternal age and abnormal maternal serum screening tests were the most common indicators, their association with abnormal ultrasound findings should be identified to increase the efficacy of genetic amniocentesis.


Asunto(s)
Amniocentesis/estadística & datos numéricos , Aberraciones Cromosómicas/estadística & datos numéricos , Femenino , Humanos , Embarazo , Estudios Retrospectivos , Turquía
13.
Br J Surg ; 99(10): 1365-73, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-22961514

RESUMEN

BACKGROUND: Preliminary experience has suggested that preperitoneal mesh positioning causes less chronic pain than Lichtenstein's technique for inguinal hernia repair. Therefore, a randomized clinical trial was conducted with the aim of evaluating the incidence of postoperative chronic pain after transinguinal preperitoneal (TIPP) mesh repair versus Lichtenstein's technique. METHODS: Patients with a primary unilateral inguinal hernia were randomized to either TIPP or Lichtenstein's repair in two training hospitals. The primary outcome was the number of patients with chronic pain after surgery. Secondary outcomes were adverse events. Follow-up was scheduled after 14 days, 3 months and 1 year. Patients and outcome assessors were blinded. RESULTS: A total of 302 patients were randomized to TIPP (143) or Lichtenstein (159) repair. Baseline characteristics were comparable in the two groups. Some 98.0 per cent of the patients were included in the analysis (141 in the TIPP group and 155 in the Lichtenstein group). Significantly fewer patients in the TIPP group had continuous chronic pain 1 year after surgery: five patients (3.5 per cent) versus 20 patients (12.9 per cent) in the Lichtenstein group (P = 0.004). An additional 12 patients (8.5 per cent) in the TIPP group and 60 (38.7 per cent) in the Lichtenstein group experienced pain during activity (P = 0.001). There were two patients with recurrence in the TIPP group and four in the Lichtenstein group, but no significant differences were found in other severe adverse events between the groups. CONCLUSION: Fewer patients had continuous chronic pain at 1 year after the TIPP mesh inguinal hernia repair compared with Lichtenstein's repair.


Asunto(s)
Hernia Inguinal/cirugía , Herniorrafia/efectos adversos , Dolor Postoperatorio/etiología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Dolor Crónico , Método Doble Ciego , Femenino , Humanos , Masculino , Persona de Mediana Edad , Tempo Operativo , Grupo de Atención al Paciente , Resultado del Tratamiento , Adulto Joven
14.
J Cardiovasc Surg (Torino) ; 53(4): 419-26, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22854521

RESUMEN

AIM: The aim of this paper was to evaluate short-term outcome of the use of endoanchors to secure the primary migrated endograft and additional extender cuffs to the aortic wall in patients with previous failed endovascular aortic aneurysm repair. METHODS: Consecutive patients who needed proximal repair of a primary failed endograft due to migration (with or without type IA endoleaks) were treated with endoanchors, with or without additional extender cuffs. Data of this group were prospectively gathered in vascular referral centers that were early adopters of the endoanchor technique. Preprocedural and periprocedural data were prospectively gathered and retrospectively analyzed. Follow-up after endoanchor placement consisted of regular hospital visits, with computed tomography or duplex scanning at 1, 6, and 12 months. RESULTS: From July 2010 to May 2011, 11 patients (8 men), mean age 77 years (range, 59-88 years), were treated with endoanchors for a failed primary endograft (2 Excluder endografts, 1 AneuRx endograft, and 8 Talent endografts) due to distal migration of the main body, with or without type IA endoleak. Revision consisted of using endoanchors to secure the body of the primary endograft to the aortic wall to avoid persistent migration. Most patients had additional proximal extender cuffs with suprarenal fixation, which were secured with endoanchors to the aortic wall and in some patients also to the primary endograft. A median of 6 endoanchors were implanted. All endoanchors were positioned correctly but one. One endoanchor dislodged but was successfully retrieved using an endovascular snare. During a mean follow-up of 10 months (range, 3-18 months) no endoanchor-related complications or renewed migration of the endografts occurred. Two patients underwent repeat intervention due to persistent type IA endoleak during follow-up. CONCLUSION: The use of endoanchors to secure migrated endografts to the aortic wall is safe and feasible and might help to overcome persistent migration of primary failed endografts. In combination with the use of sole extender cuffs the majority of proximal EVAR failures can be solved.


Asunto(s)
Aneurisma de la Aorta Abdominal/cirugía , Implantación de Prótesis Vascular/instrumentación , Prótesis Vascular , Endofuga/cirugía , Procedimientos Endovasculares/instrumentación , Migración de Cuerpo Extraño/cirugía , Stents , Anciano , Anciano de 80 o más Años , Aortografía/métodos , Implantación de Prótesis Vascular/efectos adversos , Endofuga/diagnóstico , Endofuga/etiología , Procedimientos Endovasculares/efectos adversos , Europa (Continente) , Femenino , Migración de Cuerpo Extraño/diagnóstico , Migración de Cuerpo Extraño/etiología , Humanos , Masculino , Persona de Mediana Edad , Diseño de Prótesis , Reoperación , Estudios Retrospectivos , Factores de Tiempo , Tomografía Computarizada por Rayos X , Resultado del Tratamiento , Ultrasonografía Doppler Dúplex
15.
Exp Mol Pathol ; 89(2): 182-9, 2010 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-20515682

RESUMEN

Smad-interacting protein 1 (SIP1, also known as ZEB2) represses the transcription of E-cadherin and mediates epithelial-mesenchymal transition in development and tumor metastasis. Due to the lack of human SIP1-specific antibodies, its expression in human tumor tissues has not been studied in detail by immunohistochemistry. Hence, we generated two anti-SIP1 monoclonal antibodies, clones 1C6 and 6E5, with IgG1 and IgG2a isotypes, respectively. The specificity of these antibodies was shown by Western blotting studies using siRNA mediated downregulation of SIP1 and ZEB1 in a human osteosarcoma cell line. In the same context, we also compared them with 5 commercially available SIP1 antibodies. Antibody specificity was further verified in an inducible cell line system by immunofluorescence. By using both antibodies, we evaluated the tissue expression of SIP1 in paraffin-embedded tissue microarrays consisting of 22 normal and 101 tumoral tissues of kidney, colon, stomach, lung, esophagus, uterus, rectum, breast and liver. Interestingly, SIP1 predominantly displayed a cytoplasmic expression, while the nuclear localization of SIP1 was observed in only 6 cases. Strong expression of SIP1 was found in distal tubules of kidney, glandular epithelial cells of stomach and hepatocytes, implicating a co-expression of SIP1 and E-cadherin. Squamous epithelium of the esophagus and surface epithelium of colon and rectum were stained with moderate to weak intensity. Normal uterus, breast and lung tissues remained completely negative. By comparison with their normal tissues, we observed SIP1 overexpression in cancers of the kidney, breast, lung and uterus. However, SIP1 expression was found to be downregulated in tumors from colon, rectum, esophagus, liver and stomach tissues. Finally we did nuclear/cytoplasmic fractionation in 3 carcinoma cell lines and detected SIP1 in both fractions, nucleus being the dominant one. To our best knowledge, this is the first comprehensive immunohistochemical study of the expression of SIP1 in a series of human cancers. Our finding that SIP1 is not exclusively localized to nucleus suggests that the subcellular localization of SIP1 is regulated in normal and tumor tissues. These novel monoclonal antibodies may help elucidate the role of SIP1 in tumor development.


Asunto(s)
Anticuerpos Monoclonales , Citoplasma/metabolismo , Proteínas de Homeodominio/análisis , Inmunohistoquímica , Neoplasias/metabolismo , Proteínas Represoras/análisis , Animales , Especificidad de Anticuerpos/inmunología , Cadherinas/genética , Cadherinas/inmunología , Cadherinas/metabolismo , Línea Celular , Citoplasma/inmunología , Epitelio/inmunología , Epitelio/metabolismo , Femenino , Técnica del Anticuerpo Fluorescente , Proteínas de Homeodominio/inmunología , Humanos , Ratones , Ratones Endogámicos BALB C , Neoplasias/inmunología , Proteínas Represoras/inmunología , Caja Homeótica 2 de Unión a E-Box con Dedos de Zinc
16.
Genet Couns ; 21(4): 381-4, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-21290967

RESUMEN

Here, we describe a stillborn fetus who had lower mesodermal defects sequence associated with craniorachischisis, anencephaly, bilateral pulmonary hypoplasia.


Asunto(s)
Anomalías Múltiples , Mesodermo/anomalías , Defectos del Tubo Neural , Mortinato , Anencefalia , Femenino , Humanos , Pulmón/anomalías
17.
Zoonoses Public Health ; 56(2): 65-70, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18705658

RESUMEN

An outbreak of trichinellosis occurred in Izmir, Turkey, between January and March 2004. The outbreak was caused by the consumption of raw meat balls made of beef deceptively mixed with pork infected with Trichinella britovi. A total of 1098 people who had consumed this food either in 14 restaurants or from the street vendors located in three different neighbourhoods, consulted six different healthcare centres with a wide range of clinical signs and symptoms. Of them, 418 (38.1%) patients fulfilled the criteria for the diagnosis of acute trichinellosis. The most commonly observed signs and symptoms were myalgia (89.2%), arthralgia (69.9%) and eyelid (67%) and facial oedema (65.8%). High levels of creatinine kinase (69.3%) and lactate dehydrogenase (93.8%) with leucocytosis (>10 000/mm(3), 58.9%) and eosinophilia (>1000/mm(3), 60.5%) were the most prominent laboratory findings. All, but 13 of these patients were treated with mebendazole or albendazole. Based on the physicians' assessments of disease severity, 78 (19%) patients were additionally given prednisolone in whom a significantly more rapid recovery of clinical signs and symptoms (e.g. fever, myalgia, facial and eyelid oedema) was observed, with a rapid improvement in leucocytosis, eosinophilia and muscle enzymes, compared with those, who had not received corticosteroids (P < 0.05). Beef illegally mixed with pork of unknown origin, by a wholesale butcher who had sold this product to restaurants and street vendors at a lower price than the prevailing market price of beef, was the cause of this large-scale outbreak in a country with a predominantly Muslim population.


Asunto(s)
Antihelmínticos/uso terapéutico , Contaminación de Alimentos/análisis , Trichinella/aislamiento & purificación , Triquinelosis/epidemiología , Triquinelosis/transmisión , Corticoesteroides/uso terapéutico , Animales , Bovinos , Brotes de Enfermedades/veterinaria , Inspección de Alimentos , Parasitología de Alimentos , Humanos , Productos de la Carne/parasitología , Salud Pública , Porcinos , Resultado del Tratamiento , Triquinelosis/tratamiento farmacológico , Triquinelosis/patología , Turquía/epidemiología
18.
Eur J Contracept Reprod Health Care ; 13(3): 238-42, 2008 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-18609340

RESUMEN

OBJECTIVE: To determine whether the use of the subdermal contraceptive implant releasing etonogestrel (Implanon) affects serum hormonal and biochemical indices. METHODS: Seventy women with a mean age of 28.5+/-3.4 years were enrolled into this prospective observational study. After placement of an Implanon rod, they were followed-up for three years. Baseline and end-of-study values of serum low-density lipoprotein (LDL), high-density lipoprotein (HDL), cholesterol, triglycerides, fasting glucose, blood urea nitrogen (BUN), creatinine, SGOT, SGPT, follicle stimulating hormone (FSH), luteinizing hormone (LH), oestradiol, free 3,5,3'-tri-iodothyronine (fT3), free thyroxine (fT4), thyroid stimulating hormone (TSH), and prolactine (PRL) were compared using Student's t-test. RESULTS: There was no failure of contraception during the three year period. No statistically significant differences were observed between the initial and final levels of fasting blood glucose, BUN, SGOT, SGPT, LDL, HDL, E2, FSH, LH, fT3, fT4 and TSH (p>0.05), but the increase in PRL, cholesterol and triglycerides, and the decrease in creatinine levels at the end of three years were statistically significant (p<0.05) although the values were still within normal ranges. CONCLUSION: Our findings confirm data from the literature according to which Implanon does not affect meaningfully reproductive hormonal parameters, thyroid function, hepatic and renal functions, and glucose metabolism. However, further studies are needed to elucidate lipid metabolism changes.


Asunto(s)
Anticonceptivos Femeninos/farmacología , Creatinina/sangre , Desogestrel/farmacología , Hormonas/sangre , Lípidos/sangre , Adulto , Alanina Transaminasa/sangre , Aspartato Aminotransferasas/sangre , Análisis Químico de la Sangre , Glucemia/análisis , Implantes de Medicamentos , Estradiol/sangre , Femenino , Estudios de Seguimiento , Gonadotropinas Hipofisarias/sangre , Humanos , Pruebas de Función Renal , Hormonas Tiroideas/sangre , Turquía
19.
Int J Gynecol Cancer ; 18(2): 223-7, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-17511800

RESUMEN

The objective of this study is to evaluate the cardiac safety of pegylated liposomal doxorubicin (PLD) reaching or exceeding a cumulative dose of 550 mg/m(2) in patients with recurrent ovarian and peritoneal cancer. A total of 14 patients (11 ovarian cancer, 3 primary peritoneal cancer) who received PLD in our center between February 2004 and October 2006 met inclusion criteria of the study. PLD was administered at doses of 30 mg/m(2) together with carboplatin or 50 mg/m(2) as a single agent every 3-6 weeks. Left ventricular ejection fraction (LVEF) estimations performed by M Mode ultrasound (General Electric Vivid-3, Milwaukee, Wisconsin) and clinical cardiac status were used to detect PLD-related cardiotoxicity. The median cumulative dose of PLD was 685.5 mg/m(2) (range 552-1015 mg/m(2)) and the median number of PLD courses was 9.5 (range 7-17). One patient had also been previously treated with conventional doxorubicin. LVEF scans were obtained on 10 of the 14 patients at the beginning of the therapy and on all patients at the end of therapy. No clinical evidence (symptoms or physical findings) of cardiac dysfunction had been observed in these patients either during active treatment or follow-up period. Despite small number of patients and lack of control group, our study suggests that the cumulative doses in excess of 550 mg/m(2) of PLD seem to not carry a significant risk of cardiomyopathy as judged by LVEF and clinical follow-up.


Asunto(s)
Antineoplásicos/uso terapéutico , Doxorrubicina/análogos & derivados , Cardiopatías/inducido químicamente , Neoplasias Ováricas/tratamiento farmacológico , Neoplasias Peritoneales/tratamiento farmacológico , Polietilenglicoles/uso terapéutico , Adulto , Anciano , Antineoplásicos/efectos adversos , Relación Dosis-Respuesta a Droga , Doxorrubicina/efectos adversos , Doxorrubicina/uso terapéutico , Ecocardiografía , Femenino , Cardiopatías/diagnóstico por imagen , Humanos , Persona de Mediana Edad , Recurrencia Local de Neoplasia , Polietilenglicoles/efectos adversos
20.
Gynecol Oncol ; 108(1): 154-9, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-17945337

RESUMEN

OBJECTIVE: The aim of this study was to evaluate the usefulness of integrated 2-[18F] fluoro-2-deoxy-D-glucose positron emission tomography/computed tomography (PET/CT) for the detection of para-aortic nodal status and to test whether PET/CT change management strategy in locally advanced cervical cancer (LACC) patients with negative conventional CT findings. MATERIALS AND METHODS: Sixteen locally advanced (FIGO stage IIB-IVA) cervical squamous cancer patients with negative conventional CT findings were eligible to enter this prospective study. All patients underwent firstly PET/CT scans then extraperitoneal surgical exploration for para-aortic lymphadenectomy. Based on histopathologic confirmation, the accuracy, sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of the PET/CT for para-aortic lymph node metastasis were estimated. RESULTS: The median age was 48.7 (range 42-67). The accuracy, sensitivity, specificity, PPV and NPV of the PET/CT were 75%, 50%, 83.3%, 50% and 83.3%, respectively. The treatment was modified in four of sixteen (25%) patients; four patients received EFRT in combination with cisplatin chemotherapy instead of standard pelvic field radiotherapy in combination with cisplatin chemotherapy. CONCLUSION: Our results, despite our study group is small, suggest that PET/CT is an effective imaging technique in the evaluation of LACC with negative CT findings. It may help planning the management especially selecting radiation field. However, larger controlled studies are needed to recommend PET/CT as an alternative to pre-treatment surgical staging.


Asunto(s)
Fluorodesoxiglucosa F18 , Ganglios Linfáticos/diagnóstico por imagen , Recurrencia Local de Neoplasia/diagnóstico por imagen , Radiofármacos , Neoplasias del Cuello Uterino/diagnóstico por imagen , Adulto , Anciano , Anciano de 80 o más Años , Antígeno Ca-125/sangre , Femenino , Humanos , Metástasis Linfática , Persona de Mediana Edad , Recurrencia Local de Neoplasia/sangre , Recurrencia Local de Neoplasia/patología , Estadificación de Neoplasias , Tomografía de Emisión de Positrones , Estudios Prospectivos , Tomografía Computarizada por Rayos X , Neoplasias del Cuello Uterino/sangre , Neoplasias del Cuello Uterino/patología
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