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1.
Public Health Genomics ; 19(5): 269-75, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27553645

RESUMO

BACKGROUND: The practice of biorepository-based genetics research raises questions related to what ethical obligations researchers have to their participants. It is important to explore and include the thoughts of current biorepository participants as we move forward with this type of research. METHODS: Thirty participants (17 cancer patients, 7 cancer-free controls, and 6 relatives) were drawn from the Northwest Cancer Genetics Registry and participated in qualitative interviews lasting between 45 and 90 min. Topics explored in this study include which types of genetic test results participants of large biorepositories expect and would like to receive from research analyzing their samples, as well as thoughts on best practice for conducting this type of research. RESULTS: Cancer cases, controls, and first-degree relatives have differing views on what results they would like to receive from biorepository-based research. Participants across all groups attempted to balance the costs and benefits of returning individual research results. DISCUSSION: In the wake of precision medicine, it is important to describe the range of ways participants in large biorepositories both think and talk about the utilization of their specimens for genetics research.


Assuntos
Acesso à Informação , Pesquisa em Genética/ética , Testes Genéticos/ética , Neoplasias , Medicina de Precisão , Acesso à Informação/ética , Acesso à Informação/psicologia , Adulto , Análise Custo-Benefício , Feminino , Humanos , Masculino , Neoplasias/genética , Neoplasias/psicologia , Medicina de Precisão/economia , Medicina de Precisão/métodos , Medicina de Precisão/psicologia , Pesquisa Qualitativa , Revelação da Verdade/ética
2.
Stud Health Technol Inform ; 150: 836-40, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19745430

RESUMO

The aim of this paper was to assess relationship between possible endemic nephropathy (EN) markers visually by the CoPlot methodology, and to illustrate this promising data analysis approach. From 912 screened persons in 3 Croatian endemic villages, 25 persons were diagnosed as confirmed EN patients, 371 as non-EN, and the remainder were classified as suspected of having EN, or at risk. Data on 25 confirmed EN patients were matched with appropriate non-EN examinees. All records with missing data were excluded, resulting in 35 subjects with complete data on the 13 key EN variables for CoPlot mapping. CoPlot solution met the accepted goodness of fit measure thresholds. Result showed relationship between EN markers, identifying some nearly duplicated variables, and possible outliers needing some subsequent analysis.


Assuntos
Nefropatia dos Bálcãs/diagnóstico , Apresentação de Dados , Vigilância da População/métodos , Nefropatia dos Bálcãs/epidemiologia , Nefropatia dos Bálcãs/fisiopatologia , Biomarcadores , Croácia/epidemiologia , Diagnóstico Diferencial , Humanos , Programas de Rastreamento , Análise Multivariada
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