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1.
Cancer ; 125(10): 1693-1700, 2019 05 15.
Artículo en Inglés | MEDLINE | ID: mdl-30695113

RESUMEN

BACKGROUND: Prostate cancer racial disparities in mortality outcomes are the largest in all of oncology, and less aggressive treatment received by African American (AA) patients versus white patients is likely a contributing factor. However, the reasons underlying the differences in treatment are unclear. METHODS: This study examined a prospective, population-based cohort of 1170 men with newly diagnosed nonmetastatic prostate cancer enrolled from 2011 to 2013 before treatment throughout North Carolina. By phone survey, each participant was asked to rate the aggressiveness of his cancer, and his response was compared to the actual diagnosis based on a medical record review. Participants were also asked to rate the importance of 10 factors for their treatment decision-making process. RESULTS: Among AA and white patients with low-risk cancer (according to National Comprehensive Cancer Network guidelines), 78% to 80% perceived their cancers to be "not very aggressive." However, among high-risk patients, 54% of AA patients considered their cancers to be "not very aggressive," whereas 24% of white patients did (P < .001). Although both AA and white patients indicated that a cure was a very important decision-making factor, AAs were significantly more likely to consider cost, treatment time, and recovery time as very important. In a multivariable analysis, perceived cancer aggressiveness and cure as the most important factor were significantly associated with receiving any aggressive treatment and were associated with surgery (vs radiation). After adjustments for these factors and sociodemographic factors, race was not significantly associated with the treatment received. CONCLUSIONS: Racial differences in perceived cancer aggressiveness and factors important in treatment decision making provide novel insights into reasons for the known racial disparities in prostate cancer as well as potential targets for interventions to reduce these disparities.


Asunto(s)
Negro o Afroamericano/estadística & datos numéricos , Toma de Decisiones Clínicas , Detección Precoz del Cáncer , Neoplasias de la Próstata/etnología , Neoplasias de la Próstata/terapia , Población Blanca/estadística & datos numéricos , Anciano , Estudios de Cohortes , Bases de Datos Factuales , Disparidades en Atención de Salud , Humanos , Modelos Logísticos , Masculino , Persona de Mediana Edad , Análisis Multivariante , Invasividad Neoplásica/patología , Estadificación de Neoplasias , North Carolina , Neoplasias de la Próstata/diagnóstico , Estudios Retrospectivos
2.
Heredity (Edinb) ; 102(3): 218-25, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18971954

RESUMEN

Populations of anatomically archaic (Neandertal) and early modern (Cro-Magnoid) humans are jointly documented in the European fossil record, in the period between 40 000 and 25 000 years BP, but the large differences between their cultures, morphologies and DNAs suggest that the two groups were not close relatives. However, it is still unclear whether any genealogical continuity between them can be ruled out. Here, we simulated a broad range of demographic scenarios by means of a serial coalescence algorithm in which Neandertals, Cro-Magnoids and modern Europeans were either part of the same mitochondrial genealogy or of two separate genealogies. Mutation rates, population sizes, population structure and demographic growth rates varied across simulations. All models in which anatomically modern (that is, Cro-Magnoid and current) Europeans belong to a distinct genealogy performed better than any model in which the three groups were assigned to the same mitochondrial genealogy. The maximum admissible level of gene flow between Neandertals and the ancestors of current Europeans is 0.001% per generation, one order of magnitude lower than estimated in previous studies not considering genetic data on Cro-Magnoid people.


Asunto(s)
Genealogía y Heráldica , Hominidae/genética , Población Blanca/genética , Animales , Evolución Biológica , Simulación por Computador , ADN Mitocondrial/genética , Fósiles , Flujo Génico , Genética de Población/historia , Historia Antigua , Humanos , Modelos Genéticos , Paleontología , Población Blanca/historia
3.
Environ Technol ; 28(2): 225-34, 2007 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-17396417

RESUMEN

A study in the Etueffont landfill, located in Belfort (France), was conducted to evaluate the performance of combining natural lagooning and use of two sand filters for treating leachates through the coupling estimation of several abiotic and biotic parameters. Two gravel filters were installed in the upstream of the first basin which communicates with the remaing 2, 3 and 4 basins. The distribution of physical-chemical (T, pH, Eh, EC, O2, SM, SO4(2-), Cl-, Zn, Fe, Mg, Ni, Al, As, Ba, Cu, Sn, Zn, BOD, COD, KN, NH4+, NO2+ ,TP, AOX: absorbable organic halides, VFA: volatile fatty acids, and atrazine) and biological (bacteria, protozoa, phytoplankton) parameters was assessed in the leachate entering in basin 1, and downstream of the filters. The results showed slight variations in the physical-chemical composition of the leachate between 1999 and 2000, most likely ascribed to the maturation of the landfill but a very significant removal of SM (suspended matter) by the sand filters. This, applied to the majority of the studied parameters. Thus, the sand filter treatment of the leachates combined with natural lagooning was efficient in the improvement of water clarification.


Asunto(s)
Eliminación de Residuos , Dióxido de Silicio , Eliminación de Residuos Líquidos/métodos , Contaminantes del Agua/aislamiento & purificación , Purificación del Agua/métodos , Animales , Atrazina/análisis , Bacterias/aislamiento & purificación , Recuento de Colonia Microbiana , Eucariontes/aislamiento & purificación , Ácidos Grasos Volátiles/análisis , Filtración , Herbicidas/análisis , Metales/análisis , Nitrógeno/análisis , Fósforo/análisis , Fitoplancton/aislamiento & purificación
4.
J Am Coll Cardiol ; 33(3): 876-82, 1999 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-10080493

RESUMEN

OBJECTIVES: The purpose of this study was to assess the effects of L-arginine and N(G)-nitro-L-arginine methyl ester (L-NAME) on neointimal hyperplasia and vascular remodeling after balloon angioplasty in the hypercholesterolemic rabbit. BACKGROUND: Restenosis after balloon angioplasty is a consequence of both neointimal hyperplasia and vessel remodeling. Nitric oxide inhibits neointimal hyperplasia, but its effect on vessel remodeling is unknown. METHODS: Six weeks after induction of bilateral iliac atherosclerosis, 48 rabbits underwent successful angioplasty in 75 vessels. Eight rabbits (acute group) were sacrificed immediately after angioplasty. The remaining animals received either placebo (chronic control group), or a diet supplemented with either L-arginine (1.5 g/kg/day), or L-NAME (15 mg/kg/day) for 4 weeks after angioplasty. RESULTS: The intimal area was significantly greater in the chronic control group compared to the acute group (2.60+/-1.03 mm2 vs. 1.35+/-0.62 mm2). This increase in intimal area was lower in the L-arginine group (1.79+/-0.61 mm2), and greater in the L-NAME group (3.23+/-0.92 mm2). The area circumscribed by the internal elastic lamina (IEL) increased significantly in the control group compared to the acute group (from 2.52+/-0.66 to 3.33+/-0.85 mm2); a more marked increase occurred in the L-NAME group (3.90+/-0.85 mm2). By contrast, IEL area was unchanged in the L-arginine group (2.41+/-0.62 mm2). As a result, there was no significant difference in lumen area after 4 weeks in the chronic groups (control: 0.74+/-0.38 mm2; L-arginine: 0.50+/-0.43 mm2; L-NAME: 0.48+/-0.42 mm2). CONCLUSIONS: Our results demonstrate that L-arginine inhibits whereas L-NAME stimulates neointimal hyperplasia after experimental balloon angioplasty in the hypercholesterolemic rabbit. However, the lack of vessel enlargement in the L-arginine group resulted in a similar final lumen size in the L-NAME and L-arginine groups.


Asunto(s)
Arteriosclerosis/terapia , Hipercolesterolemia/complicaciones , Óxido Nítrico/fisiología , Trombosis/terapia , Túnica Íntima/patología , Angiografía , Angioplastia de Balón/efectos adversos , Animales , Arginina/uso terapéutico , Arteriosclerosis/complicaciones , Arteriosclerosis/patología , Modelos Animales de Enfermedad , Inhibidores Enzimáticos/uso terapéutico , Estudios de Seguimiento , Hipercolesterolemia/sangre , Hipercolesterolemia/patología , Hiperplasia/tratamiento farmacológico , Hiperplasia/metabolismo , Hiperplasia/patología , Arteria Ilíaca/diagnóstico por imagen , Masculino , NG-Nitroarginina Metil Éster/uso terapéutico , Conejos , Prevención Secundaria , Trombosis/etiología , Trombosis/patología , Túnica Íntima/efectos de los fármacos , Túnica Íntima/metabolismo
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