Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 32
Filtrar
Más filtros

País/Región como asunto
Tipo del documento
Intervalo de año de publicación
1.
Cardiol Young ; 31(3): 464-467, 2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-33228820

RESUMEN

Anthracycline-related cardiomyopathy is of concern in children treated for acute myeloid leukemia (AML). Risk is dose-dependent, increasing with higher doses. We aim to highlight the risk of early-onset cardiotoxicity with low-cumulative anthracycline dose in a young Omani boy with AML. We conclude in the presence of other known risk factors for cardiac dysfunction, there is probably no risk-free anthracycline dose.


Asunto(s)
Cardiomiopatías , Leucemia Mieloide Aguda , Antraciclinas/efectos adversos , Antibióticos Antineoplásicos/efectos adversos , Cardiotoxicidad/etiología , Niño , Humanos , Leucemia Mieloide Aguda/tratamiento farmacológico , Masculino
2.
Am J Med Genet A ; 179(7): 1235-1240, 2019 07.
Artículo en Inglés | MEDLINE | ID: mdl-31074094

RESUMEN

Cardiomyopathies are clinically heterogeneous disorders and are the leading cause of cardiovascular morbidity and mortality. Different etiologies have a significant impact on prognosis. Recently, novel biallelic loss-of-function pathogenic variants in alpha-kinase 3 (ALPK3) were implicated in causing early-onset pediatric cardiomyopathy (cardiomyopathy, familial hypertrophic 27; OMIM 618052). To date, eight patients, all presented during early childhood, were reported with biallelic ALPK3 pathogenic variants. We describe the molecular and clinical phenotype characterization of familial cardiomyopathy on one family with six affected individuals. We identified homozygosity for an ALPK3 deleterious sequence variant (NM_020778.4:c.639G>A:p.Trp213*) in all the affected individuals. They presented with either dilated cardiomyopathy that progressed to hypertrophic cardiomyopathy (HCM) or HCM with left ventricular noncompaction. The age of presentation in our cohort extends between infancy to the fourth decade. The phenotypic severity decreases with the progression of age.


Asunto(s)
Cardiomiopatía Dilatada/genética , Cardiomiopatía Hipertrófica/genética , Proteínas Musculares/genética , Mutación , Fenotipo , Proteínas Quinasas/genética , Adulto , Edad de Inicio , Secuencia de Bases , Cardiomiopatía Dilatada/diagnóstico , Cardiomiopatía Dilatada/enzimología , Cardiomiopatía Dilatada/fisiopatología , Cardiomiopatía Hipertrófica/diagnóstico , Cardiomiopatía Hipertrófica/enzimología , Cardiomiopatía Hipertrófica/fisiopatología , Niño , Preescolar , Consanguinidad , Femenino , Expresión Génica , Homocigoto , Humanos , Lactante , Masculino , Proteínas Musculares/metabolismo , Linaje , Proteínas Quinasas/metabolismo , Secuenciación del Exoma
3.
J Prosthodont ; 28(5): 483-487, 2019 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-30997930

RESUMEN

Full-arch implant-supported restorations using a metal-acrylic resin design have had a high success rate but are also associated with frequent technical complications including framework misfit due to casting errors, debonding of denture teeth, and fracture of the acrylic from the metal framework. This clinical report describes a case of maxillary and mandibular full-arch implant-supported rehabilitation associated with technical and biological complications and use of digital technology for fabricating monolithic restorations. The use of a bio-functional try-in and its subsequent use as a conversion prosthesis for fabricating a master cast is described. The use of the patient's existing metal bar to fabricate a retread type prosthesis is also described along with using digital technology for fabricating a new metal bar and a monolithic type of restoration. The integration of digital and conventional workflows to obtain an increased level of accuracy and simplicity is also discussed.


Asunto(s)
Diseño de Prótesis Dental , Prótesis Dental de Soporte Implantado , Resinas Acrílicas , Dentaduras , Humanos , Flujo de Trabajo
4.
Cardiol Young ; 28(1): 155-158, 2018 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-28847319

RESUMEN

Premature ventricular contractions are a rare side effect of filgrastim, reported mainly in elderly men. Here we report the case of a 9-year-old child with thalassaemia who developed frequent premature ventricular contractions after three doses of filgrastim were given for deferiprone-induced agranulocytosis. The arrhythmia resolved 3 weeks after discontinuation of filgrastim. Children treated with filgrastim should be carefully monitored for potentially serious arrhythmia.


Asunto(s)
Agranulocitosis/inducido químicamente , Filgrastim/efectos adversos , Piridonas/efectos adversos , Talasemia/tratamiento farmacológico , Complejos Prematuros Ventriculares/diagnóstico , Niño , Deferiprona , Electrocardiografía Ambulatoria , Humanos , Masculino , Complejos Prematuros Ventriculares/inducido químicamente
5.
Hum Mutat ; 38(6): 692-703, 2017 06.
Artículo en Inglés | MEDLINE | ID: mdl-28247525

RESUMEN

COX5A is a nuclear-encoded subunit of mitochondrial respiratory chain complex IV (cytochrome c oxidase). We present patients with a homozygous pathogenic variant in the COX5A gene. Clinical details of two affected siblings suffering from early-onset pulmonary arterial hypertension, lactic acidemia, failure to thrive, and isolated complex IV deficiency are presented. We show that the variant lies within the evolutionarily conserved COX5A/COX4 interface domain, suggesting that it alters the interaction between these two subunits during complex IV biogenesis. In patient skin fibroblasts, the enzymatic activity and protein levels of complex IV and several of its subunits are reduced. Lentiviral complementation rescues complex IV deficiency. The monomeric COX1 assembly intermediate accumulates demonstrating a function of COX5A in complex IV biogenesis. A potential therapeutic lead is demonstrated by showing that copper supplementation leads to partial rescue of complex IV deficiency in patient fibroblasts.


Asunto(s)
Acidosis Láctica/genética , Ciclooxigenasa 1/genética , Grupo Citocromo c/genética , Insuficiencia de Crecimiento/genética , Hipertensión Pulmonar/genética , Acidosis Láctica/patología , Núcleo Celular/genética , Ciclooxigenasa 1/química , Grupo Citocromo c/química , Deficiencia de Citocromo-c Oxidasa , Complejo IV de Transporte de Electrones , Insuficiencia de Crecimiento/patología , Fibroblastos , Predisposición Genética a la Enfermedad , Homocigoto , Humanos , Hipertensión Pulmonar/patología , Mitocondrias/genética , Mutación , Subunidades de Proteína/genética
6.
Chembiochem ; 17(7): 620-9, 2016 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-26762569

RESUMEN

Despite extensive research into triosephosphate isomerases (TIMs), there exists a gap in understanding of the remarkable conjunction between catalytic loop-6 (residues 166-176) movement and the conformational flip of Glu165 (catalytic base) upon substrate binding that primes the active site for efficient catalysis. The overwhelming occurrence of serine at position 96 (98% of the 6277 unique TIM sequences), spatially proximal to E165 and the loop-6 residues, raises questions about its role in catalysis. Notably, Plasmodium falciparum TIM has an extremely rare residue--phenylalanine--at this position whereas, curiously, the mutant F96S was catalytically defective. We have obtained insights into the influence of residue 96 on the loop-6 conformational flip and E165 positioning by combining kinetic and structural studies on the PfTIM F96 mutants F96Y, F96A, F96S/S73A, and F96S/L167V with sequence conservation analysis and comparative analysis of the available apo and holo structures of the enzyme from diverse organisms.


Asunto(s)
Dominio Catalítico , Plasmodium falciparum/enzimología , Plasmodium falciparum/genética , Triosa-Fosfato Isomerasa/genética , Triosa-Fosfato Isomerasa/metabolismo , Secuencia de Aminoácidos , Catálisis , Secuencia Conservada , Variación Genética , Mutación , Conformación Proteica , Estructura Terciaria de Proteína , Triosa-Fosfato Isomerasa/química
7.
Lancet Oncol ; 16(7): e352-61, 2015 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-26149887

RESUMEN

Cancers of the breast, uterine cervix, and lip or oral cavity are three of the most common malignancies in India. Together, they account for about 34% of more than 1 million individuals diagnosed with cancer in India each year. At each of these cancer sites, tumours are detectable at early stages when they are most likely to be cured with standard treatment protocols. Recognising the key role that effective early detection and screening programmes could have in reducing the cancer burden, the Indian Institute for Cytology and Preventive Oncology, in collaboration with the US National Cancer Institute Center for Global Health, held a workshop to summarise feasible options and relevant evidence for screening and early detection of common cancers in India. The evidence-based recommendations provided in this Review are intended to act as a guide for policy makers, clinicians, and public health practitioners who are developing and implementing strategies in cancer control for the three most common cancers in India.


Asunto(s)
Neoplasias de la Mama/epidemiología , Detección Precoz del Cáncer/normas , Neoplasias de la Boca/epidemiología , Guías de Práctica Clínica como Asunto , Neoplasias del Cuello Uterino/epidemiología , Neoplasias de la Mama/prevención & control , Países en Desarrollo , Medicina Basada en la Evidencia , Femenino , Humanos , India/epidemiología , Labio/patología , Masculino , Neoplasias de la Boca/prevención & control , Prevalencia , Medición de Riesgo , Neoplasias del Cuello Uterino/prevención & control
8.
Sultan Qaboos Univ Med J ; 24(2): 283-287, 2024 May.
Artículo en Inglés | MEDLINE | ID: mdl-38828243

RESUMEN

Restrictive cardiomyopathy is one of the rarest forms of cardiomyopathies in paediatric patients characterised by impaired myocardial relaxation or compliance with restricted ventricular filling, leading to a reduced diastolic volume with a preserved systolic function. We report 2 cases-a 5-year-old boy who presented with abdominal distension and palpitation with family history of similar complaints but no definite genetic diagnosis as yet and a 5-year-old girl who presented with chronic cough and shortness of breath. Both cases were diagnosed in a tertiary care hospital in Muscat, Oman, in 2019 and are managed supportively with regular outpatient follow-up. This is the first series of reported cases of paediatric restrictive cardiomyopathy from Oman.


Asunto(s)
Cardiomiopatía Restrictiva , Humanos , Cardiomiopatía Restrictiva/diagnóstico , Preescolar , Masculino , Femenino , Omán , Ecocardiografía/métodos
9.
Sci Rep ; 13(1): 4740, 2023 03 23.
Artículo en Inglés | MEDLINE | ID: mdl-36959347

RESUMEN

Acoustic signal analysis has been employed in various medical devices. However, studies involving cough sound analysis to screen the potential pulmonary tuberculosis (PTB) suspects are very few. The main objective of this cross-sectional validation study was to develop and validate the Swaasa AI platform to screen and prioritize at risk patients for PTB based on the signature cough sound as well as symptomatic information provided by the subjects. The voluntary cough sound data was collected at Andhra Medical College-India. An Algorithm based on multimodal convolutional neural network architecture and feedforward artificial neural network (tabular features) was built and validated on a total of 567 subjects, comprising 278 positive and 289 negative PTB cases. The output from these two models was combined to detect the likely presence (positive cases) of PTB. In the clinical validation phase, the AI-model was found to be 86.82% accurate in detecting the likely presence of PTB with 90.36% sensitivity and 84.67% specificity. The pilot testing of model was conducted at a peripheral health care centre, RHC Simhachalam-India on 65 presumptive PTB cases. Out of which, 15 subjects truly turned out to be PTB positive with a positive predictive value of 75%. The validation results obtained from the model are quite encouraging. This platform has the potential to fulfil the unmet need of a cost-effective PTB screening method. It works remotely, presents instantaneous results, and does not require a highly trained operator. Therefore, it could be implemented in various inaccessible, resource-poor parts of the world.


Asunto(s)
Mycobacterium tuberculosis , Tuberculosis Pulmonar , Humanos , Estudios Transversales , Tos/diagnóstico , Esputo , Tuberculosis Pulmonar/diagnóstico , Inteligencia Artificial
10.
Sci Rep ; 13(1): 18284, 2023 10 25.
Artículo en Inglés | MEDLINE | ID: mdl-37880351

RESUMEN

The Advent of Artificial Intelligence (AI) has led to the use of auditory data for detecting various diseases, including COVID-19. SARS-CoV-2 infection has claimed more than six million lives to date and therefore, needs a robust screening technique to control the disease spread. In the present study we created and validated the Swaasa AI platform, which uses the signature cough sound and symptoms presented by patients to screen and prioritize COVID-19 patients. We collected cough data from 234 COVID-19 suspects to validate our Convolutional Neural Network (CNN) architecture and Feedforward Artificial Neural Network (FFANN) (tabular features) based algorithm. The final output from both models was combined to predict the likelihood of having the disease. During the clinical validation phase, our model showed a 75.54% accuracy rate in detecting the likely presence of COVID-19, with 95.45% sensitivity and 73.46% specificity. We conducted pilot testing on 183 presumptive COVID subjects, of which 58 were truly COVID-19 positive, resulting in a Positive Predictive Value of 70.73%. Due to the high cost and technical expertise required for currently available rapid screening methods, there is a need for a cost-effective and remote monitoring tool that can serve as a preliminary screening method for potential COVID-19 subjects. Therefore, Swaasa would be highly beneficial in detecting the disease and could have a significant impact in reducing its spread.


Asunto(s)
Inteligencia Artificial , COVID-19 , Humanos , Estudios Transversales , Tos/diagnóstico , COVID-19/diagnóstico , SARS-CoV-2
11.
J Indian Prosthodont Soc ; 12(3): 191-7, 2012 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-23997471

RESUMEN

Prosthodontic management of occlusal wear problems is a demanding task on the part of the prosthodontist. Various factors such as vertical dimension of occlusion, centric relation, occlusal contact pattern, esthetics and phonetics need to be considered simultaneously for both anterior and posterior teeth during occlusal rehabilitation. This may be further complicated by existing restorations, pulpal exposure, missing teeth and tooth sensitivity. Different philosophies have been documented for rehabilitation of such cases and the choice of the treatment plan depends on the skill and experience of the clinician. This case report gives an overview of the different philosophies used for rehabilitation of such cases and a report which utilises Hobo's twin stage technique for the same.

12.
Cureus ; 14(7): e26526, 2022 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-35936150

RESUMEN

Libman-Sacks endocarditis (LSE) is an uncommon disorder that might be confused with infective endocarditis. It is one of the systemic lupus erythematosus (SLE) manifestations that could present with heart failure. We report a 12-year-old girl who presented with a history of shortness of breath, joint pain for four weeks, and fever for about one week. On examination, she was pale, edematous, and febrile. Her cardiac exam revealed a pan-systolic murmur of mitral regurgitation, harsh, grade 3/6 best heard at the apex. She was diagnosed with systemic lupus erythematosus with lupus nephritis and carditis. Her echocardiography revealed severe mitral regurgitation with nodular thickening of the valve in keeping with a diagnosis of LSE. After appropriate management of her underlying disorder using immunosuppressive, we saw a dramatic clinical improvement and her heart failure symptoms resolved. This case proves that SLE can have significant cardiac involvement and a proper evaluation would help in overall management and prognosis.

13.
Acta Biomed ; 93(2): e2022022, 2022 05 11.
Artículo en Inglés | MEDLINE | ID: mdl-35546036

RESUMEN

BACKGROUND AND AIM OF THE WORK: Cardiac complications occur in patients with non-transfusion dependent thalassemia (NTDT). The study aimed to evaluate transfusion effect on systolic and diastolic cardiac function in young NTDT patients.  Methods:  Study design: Cohort study. Seventeen regularly-transfused patients with NTDT (12.5±5.3 years; group 1) and 15 none/minimally transfused patients (13.2±4.8 years; group 2) were followed up for 5 years and compared as regards their clinical parameters, echocardiographic and Tissue-Doppler-Imaging. RESULTS: Group 2 patients had significantly higher peak late-diastolic velocity of the left-ventricular-inflow Doppler (Am). Mitral-valve A-wave duration/pulmonary-veins, A-wave duration-ratio and pulmonary-vein S/D velocities-ratio were larger in group 2 as well (p = < 0.01). The diameters of right and left outflow-tract were larger with a higher cardiac-index in patients of group 2. Systolic-function was similar in the 2 studied groups. CONCLUSION: Diastolic function assessment revealed indicators of an abnormal relaxation of left-ventricle in non-transfused patients, which suggests a diastolic dysfunction. An increase in the diameter of the outflow-tract is likely attributed to high cardiac-output status in non-transfused NTDT patients as they have a higher cardiac index. Early start of regular transfusion for NTDT patients might prevent serious long-term cardiac complications.


Asunto(s)
Ecocardiografía Doppler , Talasemia , Niño , Estudios de Cohortes , Diástole , Ecocardiografía , Humanos , Talasemia/complicaciones , Talasemia/terapia , Función Ventricular Izquierda
14.
Sultan Qaboos Univ Med J ; 21(2): e324-e326, 2021 May.
Artículo en Inglés | MEDLINE | ID: mdl-34221485

RESUMEN

Cor triatriatum sinistrum (CTS) is a rare congenital cardiac anomaly characterised by an abnormal septum within the left atrium impairing blood flow to the left ventricle. We report the case of a two-month-old male infant who presented with symptoms of heart failure since the age of two weeks. He was admitted to a local hospital and was managed with antibiotics because of the impression of pneumonia. Due to persistent unresolved tachypnoea and tachycardia, he was referred to Sultan Qaboos University Hospital, Muscat, Oman, in 2019 for cardiac evaluation which confirmed a diagnosis of isolated CTS with severe stenosis and pulmonary hypertension. He underwent an urgent surgical excision of the membrane with uneventful recovery.


Asunto(s)
Corazón Triatrial , Corazón Triatrial/complicaciones , Corazón Triatrial/diagnóstico , Corazón Triatrial/cirugía , Femenino , Atrios Cardíacos/fisiopatología , Humanos , Lactante , Masculino , Omán , Embarazo , Enfermedades Raras
15.
Food Nutr Bull ; 29(4): 249-54, 2008 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-19227049

RESUMEN

BACKGROUND: Recent research has highlighted the influence of maternal factors on the health of the offspring. Intrauterine experiences may program metabolic, cardiovascular, and psychiatric disorders. We have shown that maternal vitamin B12 status affects adiposity and insulin resistance in the child. Vitamin B12 is important for brain development and function. OBJECTIVE: We investigated the relationship between maternal plasma vitamin B12 status during pregnancy and the child's cognitive function at 9 years of age. METHODS: We studied children born in the Pune Maternal Nutrition Study. Two groups of children were selected on the basis of maternal plasma vitamin B12 concentration at 28 weeks of gestation: group 1 (n = 49) included children of mothers with low plasma vitamin B12 (lowest decile, < 77 pM) and group 2 (n = 59) children of mothers with high plasma vitamin B12 (highest decile, > 224 pM). RESULTS: Children from group 1 performed more slowly than those from group 2 on the Color Trail A test (sustained attention, 182 vs. 159 seconds; p < .05) and the Digit Span Backward test (short-term memory, p < .05), after appropriate adjustment for confounders. There were no differences between group 1 and group 2 on other tests of cognitive function (intelligence, visual agnosia). CONCLUSIONS: Maternal vitamin B12 status in pregnancy influences cognitive function in offspring.


Asunto(s)
Atención/fisiología , Cognición/fisiología , Fenómenos Fisiologicos Nutricionales Maternos/fisiología , Memoria a Corto Plazo/fisiología , Estado Nutricional , Vitamina B 12/sangre , Adulto , Análisis de Varianza , Atención/efectos de los fármacos , Encéfalo/efectos de los fármacos , Encéfalo/crecimiento & desarrollo , Niño , Femenino , Edad Gestacional , Humanos , India , Masculino , Memoria a Corto Plazo/efectos de los fármacos , Embarazo/sangre , Efectos Tardíos de la Exposición Prenatal , Vitamina B 12/administración & dosificación
17.
Int J Comput Assist Radiol Surg ; 12(4): 529-538, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-28028655

RESUMEN

OBJECTIVE: The aim of this study is to assess the performance of a computer-aided semi-automated algorithm we have adapted for the purpose of segmenting malignant pleural mesothelioma (MPM) on CT. METHODS: Forty-five CT scans were collected from 15 patients (M:F [Formula: see text] 10:5, mean age 62.8 years) in a multi-centre clinical drug trial. A computer-aided random walk-based algorithm was applied to segment the tumour; the results were then compared to radiologist-drawn contours and correlated with measurements made using the MPM-adapted Response Evaluation Criteria in Solid Tumour (modified RECIST). RESULTS: A mean accuracy (Sørensen-Dice index) of 0.825 (95% CI [0.758, 0.892]) was achieved. Compared to a median measurement time of 68.1 min (range [40.2, 102.4]) for manual delineation, the median running time of our algorithm was 23.1 min (range [10.9, 37.0]). A linear correlation (Pearson's correlation coefficient: 0.6392, [Formula: see text]) was established between the changes in modified RECIST and computed tumour volume. CONCLUSION: Volumetric tumour segmentation offers a potential solution to the challenges in quantifying MPM. Computer-assisted methods such as the one presented in this study facilitate this in an accurate and time-efficient manner and provide additional morphological information about the tumour's evolution over time.


Asunto(s)
Procesamiento de Imagen Asistido por Computador/métodos , Neoplasias Pulmonares/diagnóstico por imagen , Mesotelioma/diagnóstico por imagen , Neoplasias Pleurales/diagnóstico por imagen , Tomografía Computarizada por Rayos X/métodos , Anciano , Algoritmos , Femenino , Humanos , Masculino , Mesotelioma Maligno , Persona de Mediana Edad , Carga Tumoral
18.
Comput Med Imaging Graph ; 55: 124-132, 2017 01.
Artículo en Inglés | MEDLINE | ID: mdl-27634547

RESUMEN

Neovascularization (NV) is a characteristic of the onset of sight-threatening stage of DR, called proliferative DR (PDR). Identification of PDR requires modeling of these unregulated ill-formed vessels, and other associated signs of PDR. We present an approach that models the micro-pattern of local variations (using texture based analysis) and quantifies structural changes in vessel patterns in localized patches, to arrive at a score of neovascularity. The distribution of patch-level confidence scores is collated into an image-level decision of presence or absence of PDR. Evaluated on a dataset of 779 images combining public data and clinical data from local hospitals, the patch-level neovascularity prediction has a sensitivity of 92.4% at 92.6% specificity. For image-level PDR identification our method is shown to achieve sensitivity of 83.3% at a high specificity operating point of 96.1% specificity, and specificity of 83% at high sensitivity operating point of 92.2% sensitivity. Our approach could have potential application in DR grading where it can localize NVE regions and identify PDR images for immediate intervention.


Asunto(s)
Retinopatía Diabética/diagnóstico por imagen , Fondo de Ojo , Interpretación de Imagen Asistida por Computador/métodos , Neovascularización Patológica/diagnóstico por imagen , Humanos , Sensibilidad y Especificidad
19.
Front Microbiol ; 8: 463, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28377757

RESUMEN

The present study shows the existence of two specific sub-populations of Mycobacterium smegmatis and Mycobacterium tuberculosis cells differing in size and density, in the mid-log phase (MLP) cultures, with significant differential susceptibility to antibiotic, oxidative, and nitrite stress. One of these sub-populations (~10% of the total population), contained short-sized cells (SCs) generated through highly-deviated asymmetric cell division (ACD) of normal/long-sized mother cells and symmetric cell divisions (SCD) of short-sized mother cells. The other sub-population (~90% of the total population) contained normal/long-sized cells (NCs). The SCs were acid-fast stainable and heat-susceptible, and contained high density of membrane vesicles (MVs, known to be lipid-rich) on their surface, while the NCs possessed negligible density of MVs on the surface, as revealed by scanning and transmission electron microscopy. Percoll density gradient fractionation of MLP cultures showed the SCs-enriched fraction (SCF) at lower density (probably indicating lipid-richness) and the NCs-enriched fraction (NCF) at higher density of percoll fractions. While live cell imaging showed that the SCs and the NCs could grow and divide to form colony on agarose pads, the SCF, and NCF cells could independently regenerate MLP populations in liquid and solid media, indicating their full genomic content and population regeneration potential. CFU based assays showed the SCF cells to be significantly more susceptible than NCF cells to a range of concentrations of rifampicin and isoniazid (antibiotic stress), H2O2 (oxidative stress),and acidified NaNO2 (nitrite stress). Live cell imaging showed significantly higher susceptibility of the SCs of SC-NC sister daughter cell pairs, formed from highly-deviated ACD of normal/long-sized mother cells, to rifampicin and H2O2, as compared to the sister daughter NCs, irrespective of their comparable growth rates. The SC-SC sister daughter cell pairs, formed from the SCDs of short-sized mother cells and having comparable growth rates, always showed comparable stress-susceptibility. These observations and the presence of M. tuberculosis SCs and NCs in pulmonary tuberculosis patients' sputum earlier reported by us imply a physiological role for the SCs and the NCs under the stress conditions. The plausible reasons for the higher stress susceptibility of SCs and lower stress susceptibility of NCs are discussed.

20.
Annu Int Conf IEEE Eng Med Biol Soc ; 2015: 4330-3, 2015 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-26737253

RESUMEN

Diabetic macular edema (DME) is one of the vision-impairing manifestations of Diabetic Retinopathy (DR). Early detection and treatment of DME can prevent permanent vision loss in people suffering from DR. However, the clinical detection through biomicroscopy is time-consuming. In this paper, a computer-assisted grading method has been proposed to determine the DME severity based on the spatial distribution of exudative lesions around macula. The region around macula is classified into zonal levels and severity of the DME is graded based on the presence of exudative lesions in each zone. The proposed method has been evaluated on diverse public and local databases, and produced the sensitivity of 89.54% for 9.1 false positive per image (FPPI) for exudate detection and 98.8% accuracy for DME grading.


Asunto(s)
Edema Macular , Retinopatía Diabética , Exudados y Transudados , Fondo de Ojo , Humanos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA