Consensus statement on genetic research in dementia

M.G. Olde Rikkert; V van der; A. Burns; W. Dekkers; P. Robert; N. Sartorius; J. Selmes; G. Stoppe; M. Vernooij-Dassen; G. Waldemar

Consensus statement on genetic research in dementia

M.G. Olde Rikkert, V van der, A. Burns, W. Dekkers, P. Robert, N. Sartorius, J. Selmes, G. Stoppe, M. Vernooij-Dassen, G. Waldemar

12 Citations (Scopus)

Abstract

In this article, the authors describe how the European Dementia Consensus Network developed a consensus on research ethics in dementia, taking into account the questions posed by the era of genetic research and its new research methods. The consensus process started with a Delphi procedure to analyze relevant stakeholders' positions by describing their statements on the possibilities and limitations of research into genetic determinants of Alzheimer disease and to describe and analyze the moral desirability of genetic research on Alzheimer disease. The conclusions drawn from the Delphi procedure fuelled the development of the consensus statement, which is presented in this paper. The consensus statement aims to stimulate ethically acceptable research in the field of dementia and the protection of vulnerable elderly patients with dementia from application of inadequate research methods or designs
Udgivelsesdato: 2008/6

Original language	English
Journal	American Journal of Alzheimers Disease & Other Dementias
Volume	23
Issue number	3
Pages (from-to)	262-266
Number of pages	4
ISSN	1533-3175
Publication status	Published - 2008

Cite this

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title = "Consensus statement on genetic research in dementia",

abstract = "In this article, the authors describe how the European Dementia Consensus Network developed a consensus on research ethics in dementia, taking into account the questions posed by the era of genetic research and its new research methods. The consensus process started with a Delphi procedure to analyze relevant stakeholders' positions by describing their statements on the possibilities and limitations of research into genetic determinants of Alzheimer disease and to describe and analyze the moral desirability of genetic research on Alzheimer disease. The conclusions drawn from the Delphi procedure fuelled the development of the consensus statement, which is presented in this paper. The consensus statement aims to stimulate ethically acceptable research in the field of dementia and the protection of vulnerable elderly patients with dementia from application of inadequate research methods or designs Udgivelsesdato: 2008/6",

author = "Rikkert, {M.G. Olde} and der, {V van} and A. Burns and W. Dekkers and P. Robert and N. Sartorius and J. Selmes and G. Stoppe and M. Vernooij-Dassen and G. Waldemar",

year = "2008",

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journal = "American Journal of Alzheimer's Disease and other Dementias",

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T1 - Consensus statement on genetic research in dementia

AU - Rikkert, M.G. Olde

AU - der, V van

AU - Burns, A.

AU - Dekkers, W.

AU - Robert, P.

AU - Sartorius, N.

AU - Selmes, J.

AU - Stoppe, G.

AU - Vernooij-Dassen, M.

AU - Waldemar, G.

PY - 2008

Y1 - 2008

N2 - In this article, the authors describe how the European Dementia Consensus Network developed a consensus on research ethics in dementia, taking into account the questions posed by the era of genetic research and its new research methods. The consensus process started with a Delphi procedure to analyze relevant stakeholders' positions by describing their statements on the possibilities and limitations of research into genetic determinants of Alzheimer disease and to describe and analyze the moral desirability of genetic research on Alzheimer disease. The conclusions drawn from the Delphi procedure fuelled the development of the consensus statement, which is presented in this paper. The consensus statement aims to stimulate ethically acceptable research in the field of dementia and the protection of vulnerable elderly patients with dementia from application of inadequate research methods or designs Udgivelsesdato: 2008/6

AB - In this article, the authors describe how the European Dementia Consensus Network developed a consensus on research ethics in dementia, taking into account the questions posed by the era of genetic research and its new research methods. The consensus process started with a Delphi procedure to analyze relevant stakeholders' positions by describing their statements on the possibilities and limitations of research into genetic determinants of Alzheimer disease and to describe and analyze the moral desirability of genetic research on Alzheimer disease. The conclusions drawn from the Delphi procedure fuelled the development of the consensus statement, which is presented in this paper. The consensus statement aims to stimulate ethically acceptable research in the field of dementia and the protection of vulnerable elderly patients with dementia from application of inadequate research methods or designs Udgivelsesdato: 2008/6

M3 - Journal article

SN - 1533-3175

VL - 23

SP - 262

EP - 266

JO - American Journal of Alzheimer's Disease and other Dementias

JF - American Journal of Alzheimer's Disease and other Dementias

IS - 3

ER -