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1.
Breast Cancer Res Treat ; 171(2): 435-442, 2018 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-29808287

RESUMEN

PURPOSE: In 2013, Angelina Jolie disclosed in the New York Times (NYT) that she had undergone risk-reducing bilateral mastectomy (RRBM) after learning that she was a BRCA1 mutation carrier. We examined the rates of BRCA testing and RRBM from 1997 to 2016, and quantified trends before and after the Jolie op-ed. METHODS: This observational study of insurance claims data representative of the commercially-insured US population (Truven MarketScan® database) measured BRCA testing and RRBM rates among females ≥ 18 years. Censoring events were breast cancer or ovarian cancer diagnosis, last follow-up date (September 2016), or death. Interrupted time series analyses were used to quantify trends before and after the op-ed. RESULTS: Angelina Jolie's NYT op-ed led to a statistically significant increase in the uptake of genetic testing and in RRBM among women without previous diagnosis of breast or ovarian cancer in the US population, and in women who did not undergo testing for BRCA (P < 0.0001 for both). The rate (slope) of RRBM among women who were previously tested for BRCA (P = 0.70) was unchanged. After excluding women with in-situ tumors, the editorial's effect became less pronounced, suggesting that high-risk women with in-situ breast cancers were most influenced by Jolie's announcement. CONCLUSION: The Angelina Effect-a term coined by Time magazine to describe the rise in internet searches related to breast cancer genetics and counseling-represents a long-lasting impact of celebrity on public health awareness as significant increases in genetic testing and mastectomy rates were observed and sustained in subsequent years.


Asunto(s)
Neoplasias de la Mama/epidemiología , Mastectomía Profiláctica/estadística & datos numéricos , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Neoplasias de la Mama/diagnóstico , Neoplasias de la Mama/etiología , Neoplasias de la Mama/cirugía , Bases de Datos Factuales , Femenino , Genes BRCA1 , Pruebas Genéticas/estadística & datos numéricos , Heterocigoto , Humanos , Incidencia , Persona de Mediana Edad , Mutación , Vigilancia en Salud Pública , Estados Unidos/epidemiología , Adulto Joven
2.
PLoS One ; 10(10): e0140611, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26509706

RESUMEN

OBJECTIVE: To evaluate trends and identify predictors of treatment initiation of oral anti-diabetic drugs (OAD) in youth. PATIENTS AND METHODS: We identified a select population of children, ages 8-18 years, with at least 13 months of continuous health plan coverage within the years 2001-2012 in a large US commercial insurance claims database. New use of an OAD was defined as the first claim for an outpatient dispensing following a 12-month wash out period. Treatment incidence was estimated monthly over the study period, and stratified by age, gender, geographic region, and provider specialty. RESULTS: The median size of the source population during the study period was 2.2 million children. A total of 13,824 initiators (mean monthly incidence of 4.6 (95% CI = 3.6, 5.5) per 100,000 youths) were identified. Initiators were more likely to be females, age 15-18, from the southern region, and have visited a family practitioner (versus a general pediatrician) prior to initiation. Time trends demonstrate a 43% increase in initiation from 2002-2012, with a gradual decrease starting from early 2008. CONCLUSION: Incidence of filled OAD medications in youth increased over time, especially for patients treated by family practitioners. Additional research is needed into factors influencing prescribing by family practitioners and pediatricians.


Asunto(s)
Diabetes Mellitus Tipo 2/tratamiento farmacológico , Hipoglucemiantes/administración & dosificación , Hipoglucemiantes/uso terapéutico , Administración Oral , Adolescente , Distribución por Edad , Niño , Diabetes Mellitus Tipo 2/epidemiología , Femenino , Humanos , Incidencia , Seguro de Salud , Masculino
3.
Am J Clin Nutr ; 91(6): 1621-6, 2010 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-20427729

RESUMEN

BACKGROUND: Vitamin D has been added to calcium-fortified orange juice. It is unknown whether vitamin D is as bioavailable from orange juice as it is from supplements. OBJECTIVES: The objective was to compare the bioavailability of vitamin D(2) and vitamin D(3) from orange juice with that from vitamin D(2) and vitamin D(3) supplements. A secondary aim was to determine which form of vitamin D is more bioavailable in orange juice. DESIGN: A randomized, placebo-controlled, double-blind study was conducted in healthy adults aged 18-84 y (15-20/group) who received 1000 IU vitamin D(3), 1000 IU vitamin D(2), or placebo in orange juice or capsule for 11 wk at the end of winter. RESULTS: A total of 64% of subjects began the study deficient in vitamin D (ie, 25-hydroxyvitamin D [25(OH)D]) concentrations <20 ng/mL). Analysis of the area under the curve showed no significant difference in serum 25(OH)D between subjects who consumed vitamin D-fortified orange juice and those who consumed vitamin D supplements (P = 0.084). No significant difference in serum 25(OH)D(3) was observed between subjects who consumed vitamin D(3)-fortified orange juice and vitamin D(3) capsules (P > 0.1). Similarly, no significant difference in serum 25(OH)D(2) was observed between subjects who consumed vitamin D(2)-fortified orange juice and vitamin D(2) capsules (P > 0.1). No significant overall difference in parathyroid hormone concentrations was observed between the groups (P = 0.82). CONCLUSION: Vitamin D(2) and vitamin D(3) are equally bioavailable in orange juice and capsules.


Asunto(s)
Bebidas , Colecalciferol/administración & dosificación , Citrus sinensis , Ergocalciferoles/administración & dosificación , Alimentos Fortificados , Frutas , Deficiencia de Vitamina D/dietoterapia , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Disponibilidad Biológica , Calcio/sangre , Colecalciferol/sangre , Colecalciferol/farmacocinética , Suplementos Dietéticos , Método Doble Ciego , Ergocalciferoles/sangre , Ergocalciferoles/farmacocinética , Femenino , Humanos , Persona de Mediana Edad , Hormona Paratiroidea/sangre , Deficiencia de Vitamina D/sangre , Deficiencia de Vitamina D/metabolismo , Adulto Joven
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