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(Management of DNA banks: ethical concerns)
Moutel G., De Montgolfier S., Corviole K., Gaillard M., Durlach V., Leutenegger M., Adnet J.-J., Hervé C.
Presse médicale (Paris, France : 1983) 28, 3 (1999) 135-9 - http://www.hal.inserm.fr/inserm-00118855
(10026722)
[Management of DNA banks: ethical concerns]
Grégoire Moutel1, Sandrine De Montgolfier1, Karine Corviole2, Martine Gaillard1, Vincent Durlach, Marc Leutenegger3, Jean-Jacques Adnet4, Christian Hervé1
1 :  Laboratoire d'Ethique Médicale, de Droit de la Santé et de Santé Publique
http://www.ethique.inserm.fr
Université Paris V - Paris Descartes
156 rue de Vaugirard Paris 75015
France
2 :  Institut Jean Godinot
CRLCC Jean Godinot
Rue du Général Koenig 51100 Reims
France
3 :  Clinique médicale
Hôpital Robert Debré – CHU Reims
Rue du Général Koenig 51100 Reims
France
4 :  Laboratoire d'histologie, cytologie, biologie cellulaire et moléculaire Pol Bouin
CHU Reims – Université de Reims - Champagne Ardenne
Rue Cognacq Jay 51100 Reims
France
With the creation of DNA banks, short and long-term studies can be conducted on the DNA of many individuals using stored cells and tissues. These studies allow an analysis of the pathophysiological impact of genetics and help define individual markers predictive of risk. Genome analysis is thus an important advance in medical science, providing essential information for establishing appropriate measures to slow disease development, limit severity or improve safe recovery. The use of genetic results may however have an adverse effect in certain situations if the genetic information collected were deviated from its purely medical purpose under the influence of social, occupational or economic factors. The aim of our study was to analyse the ethical challenges linked to the implementation of DNA banks in France, particularly to see how to maintain the concept of individual protection in biomedical research within the patient-physician relationship in the current context of legal and administrative regulations in France. In this study, we discuss a set of criteria which should be systematically evaluated in information collection and consent procedures prior to blood or tissue procurement for DNA bank purposes.
Sciences du Vivant/Ethique
Français
0755-4982

Articles dans des revues avec comité de lecture
Presse médicale (Paris, France : 1983)
non spécifiée
23/01/1999
28
3
135-9

Biothèques – Banques d'ADN – Ethique – Information – Relation médecin-malade – Evaluation – Biobanks – DNA banking – Ethical concerns – Patient relationship
Biological Specimen Banks – DNA – English Abstract – Ethics – Medical – Gene Library – Humans – Physician-Patient Relations – Tissue and Organ Procurement
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