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OBJECTIVES: With aging of the HIV-positive population, cardiovascular disease (CVD) increasingly contributes to morbidity and mortality. We investigated CVD-related and other causes of death (CODs) and factors associated with CVD in a multi-country Asian HIV-positive cohort. METHODS: Patient data from 2003-2017 were obtained from the Therapeutics, Research, Education and AIDS Training in Asia (TREAT Asia) HIV Observational Database (TAHOD). We included patients on antiretroviral therapy (ART) with > 1 day of follow-up. Cumulative incidences were plotted for CVD-related, AIDS-related, non-AIDS-related, and unknown CODs, and any CVD (i.e. fatal and nonfatal). Competing risk regression was used to assess risk factors of any CVD. RESULTS: Of 8069 patients with a median follow-up of 7.3 years [interquartile range (IQR) 4.4-10.7 years], 378 patients died [incidence rate (IR) 6.2 per 1000 person-years (PY)], and this total included 22 CVD-related deaths (IR 0.36 per 1000 PY). Factors significantly associated with any CVD event (IR 2.2 per 1000 PY) were older age [sub-hazard ratio (sHR) 2.21; 95% confidence interval (CI) 1.36-3.58 for age 41-50 years; sHR 5.52; 95% CI 3.43-8.91 for ≥ 51 years, compared with < 40 years], high blood pressure (sHR 1.62; 95% CI 1.04-2.52), high total cholesterol (sHR 1.89; 95% CI 1.27-2.82), high triglycerides (sHR 1.55; 95% CI 1.02-2.37) and high body mass index (BMI) (sHR 1.66; 95% CI 1.12-2.46). CVD crude IRs were lower in the later ART initiation period and in lower middle- and upper middle-income countries. CONCLUSIONS: The development of fatal and nonfatal CVD events in our cohort was associated with older age, and treatable risk factors such as high blood pressure, triglycerides, total cholesterol and BMI. Lower CVD event rates in middle-income countries may indicate under-diagnosis of CVD in Asian-Pacific resource-limited settings.
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Antirretrovirales/uso terapéutico , Enfermedades Cardiovasculares/epidemiología , Infecciones por VIH/tratamiento farmacológico , Adulto , Asia/epidemiología , Enfermedades Cardiovasculares/mortalidad , Causas de Muerte , Femenino , Infecciones por VIH/complicaciones , Humanos , Incidencia , Masculino , Persona de Mediana Edad , Medición de Riesgo , Factores de RiesgoRESUMEN
ETV6-NTRK3 (EN), a chimeric tyrosine kinase generated by t(12;15) translocations, is a dominantly acting oncoprotein in diverse tumor types. We previously showed that insulin-like growth factor 1 receptor (IGF1R) is essential for EN-mediated oncogenesis and that insulin receptor substrate 1 (IRS1) is constitutively tyrosine phosphorylated and bound by EN in transformed cells. Given that IRS1 is also an adapter for IGF1R, we hypothesized that IRS1 might localize EN to IGF1R at the membrane to activate phosphatidylinositol 3-kinase (PI3K)-Akt, which is critical for EN oncogenesis. In this study, we examined EN/IRS1/IGF1R complexes in detail. We find that both IRS1 and kinase active IGF1R are required for EN transformation, that tyrosine phosphorylated IRS1 is present in high molecular weight complexes with EN and IGF1R, and that EN colocalizes with IGF1R at the plasma membrane. Both IGF1R kinase activity and an intact cytoplasmic Y950 residue, the IRS1-docking site of IGF1R, are required, confirming the importance of the IGF1R/IRS1 interaction for EN oncogenesis. The dual specificity IGF1R and insulin receptor (INSR) inhibitor, BMS-536924, blocks EN transformation activity, cell survival and its interaction with IRS proteins, and induces a striking shift of EN proteins to smaller sized molecular complexes. We conclude that a tripartite complex of EN, IRS1 and IGF1R localizes EN to the membrane and that this is essential for EN-mediated transformation. These findings provide an explanation for the observed IGF1R dependency of EN transformation. Blocking IGF1R kinase activity may, therefore, provide a tractable therapeutic strategy for the many tumor types driven by the EN oncoprotein.
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Membrana Celular/metabolismo , Transformación Celular Neoplásica , Proteínas Sustrato del Receptor de Insulina/fisiología , Proteínas de Fusión Oncogénica/fisiología , Receptor IGF Tipo 1/fisiología , Animales , Interleucina-3/farmacología , Ratones , FosforilaciónRESUMEN
This study surveyed the frequency of autoantibodies among un-affected first-degree relatives (FDRs) of Filipino systemic lupus erythematosus (SLE) patients compared with healthy un-related Filipino controls. The sensitivity, specificity and predictive value of the autoantibodies for SLE diagnosis were also assessed in this Filipino cohort. Filipino patients included in the University of Santo Tomas (UST) Lupus Database and un-affected FDRs were recruited. Healthy controls included those with no known personal or family history of autoimmune disease. The following autoantibodies were tested in all subjects: anti-nuclear antibody (ANA), anti-dsDNA, anti-Ro/SSA, anti-chromatin, anti-thyroid microsome, and anti-cardiolipin antibodies. Participants included 232 SLE patients, 546 FDRs, and 221 healthy controls. Median age of patients was 27 (range 8-66) years with median disease duration of 27.5 (range 1-292) months. Median age of FDRs was 42.0 (range 5-87) years. Compared with healthy controls, there were significantly more FDRs with positive ANA at titers 1 : 40 to 1 : 160 (p < 0.001) and 1 : 320 (p = 0.003), anti-Ro/SSA (4.94% versus 0.45%, p = 0.003), and anti-dsDNA ≥ 5.0 IU/ml (4.58% versus 1.36%, p = 0.031). ANA titer ≥1 : 160, anti-dsDNA, anti-Ro/SSA and anti-chromatin had the highest predictive value for SLE diagnosis. These findings reinforce the role of genetic influence in SLE risk among Filipinos, with a significant proportion of un-affected FDRs of SLE patients testing positive for autoantibodies compared with healthy Filipino controls. A longitudinal observational study in this same cohort will determine which proportion of these un-affected FDRs will evolve into clinical SLE disease in the future.
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Autoanticuerpos/sangre , Lupus Eritematoso Sistémico/genética , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Autoanticuerpos/genética , Biomarcadores/sangre , Estudios de Casos y Controles , Niño , Preescolar , Composición Familiar , Femenino , Humanos , Lupus Eritematoso Sistémico/epidemiología , Lupus Eritematoso Sistémico/inmunología , Masculino , Persona de Mediana Edad , Filipinas/epidemiología , Valor Predictivo de las Pruebas , Adulto JovenRESUMEN
BACKGROUND: There is a need to assess neurobehavioral performance of children in developing countries using standardized developmental tools. METHODS: The Griffiths Mental Development Scales was evaluated in the Philippines by comparing the performance of 742 Filipino children longitudinally at 6, 12 and 24 months old to those of their British counterparts. RESULTS: The mean general and subquotient scores of Filipino children were all within average for age. Comparison with British children showed that except for performance subscales, Filipino children had significantly higher developmental subquotients at 6 months old. As the Filipino infants grew older, their developmental subquotients in all subscales were significantly lower, except for personal and social skills at 24 months old. The genetic predisposition as evidenced by modest maternal scores on the Wechsler Intelligence Scales and lack of familiarity with test materials are factors that may influence the developmental patterns of Filipino children. CONCLUSION: Although the performance of the Filipino children in the Griffiths test were within average with age, their performance on developmental subquotients at later ages of 12 and 24 months were significantly lower than British children and may have been influenced by differences in ethnicity, cultural traditions and limited environmental resources.
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Desarrollo Infantil , Discapacidades del Desarrollo/diagnóstico , Pruebas Neuropsicológicas , Preescolar , Comparación Transcultural , Países en Desarrollo , Femenino , Humanos , Lactante , Masculino , Filipinas , Desempeño Psicomotor , Reproducibilidad de los Resultados , Reino UnidoRESUMEN
In brain-imaging research, we are often interested in making quantitative claims about effects across subjects. Given that most imaging data consist of tens to thousands of spatially correlated time series, inter-subject comparisons are typically accomplished with simple combinations of inter-subject data, for example methods relying on group means. Further, these data are frequently taken from reduced channel subsets defined either a priori using anatomical considerations, or functionally using p-value thresholding to choose cluster boundaries. While such methods are effective for data reduction, means are sensitive to outliers, and current methods for subset selection can be somewhat arbitrary. Here, we introduce a novel "partial-ranking" approach to test for inter-subject agreement at the channel level. This non-parametric method effectively tests whether channel concordance is present across subjects, how many channels are necessary for maximum concordance, and which channels are responsible for this agreement. We validate the method on two previously published and two simulated EEG data sets.
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Algoritmos , Encéfalo/anatomía & histología , Encéfalo/fisiología , Electroencefalografía/estadística & datos numéricos , Procesamiento de Imagen Asistido por Computador/estadística & datos numéricos , Análisis de Varianza , Mapeo Encefálico , Simulación por Computador , Humanos , Modelos AnatómicosRESUMEN
While magnetoencephalography (MEG) is widely used to identify spatial locations of brain activations associated with various tasks, classification of single trials in stimulus-locked experiments remains an open subject. Very significant single-trial classification results have been published using electroencephalogram (EEG) data, but in the MEG case, the weakness of the magnetic fields originating from the relevant sources relative to external noise, and the high dimensionality of the data are difficult obstacles to overcome. We present here very significant MEG single-trial mean classification rates of words. The number of words classified varied from seven to nine and both visual and auditory modalities were studied. These results were obtained by using a variety of blind sources separation methods: spatial principal components analysis (PCA), Infomax independent components analysis (Infomax ICA) and second-order blind identification (SOBI). The sources obtained were classified using two methods, linear discriminant classification (LDC) and v-support vector machine (v-SVM). The data used here, auditory and visual presentations of words, presented nontrivial classification problems, but with Infomax ICA associated with LDC we obtained high classification rates. Our best single-trial mean classification rate was 60.1% for classification of 900 single trials of nine auditory words. On two-class problems rates were as high as 97.5%.