Strengthening the reporting of genetic risk prediction studies: the GRIPS statement

被引:12
作者
Janssens, A. Cecile J. W. [1 ]
Ioannidis, John P. A. [2 ,3 ,4 ,5 ,6 ,7 ]
van Duijn, Cornelia M. [1 ]
Little, Julian [8 ]
Khoury, Muin J. [9 ]
机构
[1] Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands
[2] Univ Ioannina, Sch Med, Dept Hyg & Epidemiol, GR-45110 Ioannina, Greece
[3] Fdn Res & Technol, Biomed Res Inst, Ioannina, Greece
[4] Tufts Univ, Sch Med, Dept Med, Boston, MA 02111 USA
[5] Tufts Med Ctr, Inst Clin Res & Hlth Policy Studies, Ctr Genet Epidemiol & Modeling, Boston, MA USA
[6] Tufts Med Ctr, Inst Clin Res & Hlth Policy Studies, Tufts CTSI, Boston, MA USA
[7] Stanford Univ, Sch Med, Stanford Prevent Res Ctr, Stanford, CA 94305 USA
[8] Univ Ottawa, Dept Epidemiol & Community Med, Ottawa, ON, Canada
[9] Ctr Dis Control & Prevent, Off Publ Hlth Genom, Atlanta, GA USA
基金
美国国家卫生研究院;
关键词
Genetic; Risk prediction; Methodology; Guidelines; Reporting; MARKER; EPIDEMIOLOGY; ASSOCIATION; CURVE;
D O I
10.1007/s10654-011-9552-y
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The rapid and continuing progress in gene discovery for complex diseases is fueling interest in the potential application of genetic risk models for clinical and public health practice. The number of studies assessing the predictive ability is steadily increasing, but the quality and completeness of reporting varies. A multidisciplinary workshop sponsored by the Human Genome Epidemiology Network developed a checklist of 25 items recommended for strengthening the reporting of Genetic RIsk Prediction Studies (GRIPS), building on the principles established by prior reporting guidelines. These recommendations aim to enhance the transparency of study reporting, and thereby to improve the synthesis and application of information from multiple studies that might differ in design, conduct, or analysis. A detailed Explanation and Elaboration document is published.
引用
收藏
页码:255 / 259
页数:5
相关论文
共 24 条
[1]   The revised CONSORT statement for reporting randomized trials: Explanation and elaboration [J].
Altman, DG ;
Schulz, KF ;
Moher, D ;
Egger, M ;
Davidoff, F ;
Elbourne, D ;
Gotzsche, PC ;
Lang, T .
ANNALS OF INTERNAL MEDICINE, 2001, 134 (08) :663-694
[2]   Towards complete and accurate reporting of studies of diagnostic accuracy: The STARD initiative [J].
Bossuyt, PM ;
Reitsma, JB ;
Bruns, DE ;
Gatsonis, CA ;
Glasziou, PP ;
Irwig, LM ;
Lijmer, JG ;
Moher, D ;
Rennie, D ;
de Vet, HCW .
CLINICAL CHEMISTRY, 2003, 49 (01) :1-6
[3]   Towards complete and accurate reporting of studies of diagnostic accuracy: The STARD initiative [J].
Bossuyt, PM ;
Reitsma, JB ;
Bruns, DE ;
Gatsonis, CA ;
Glasziou, PP ;
Irwig, LM ;
Lijmer, JG ;
Moher, D ;
Rennie, D ;
de Vet, HCW .
ANNALS OF INTERNAL MEDICINE, 2003, 138 (01) :40-44
[4]   Use and misuse of the receiver operating characteristic curve in risk prediction [J].
Cook, Nancy R. .
CIRCULATION, 2007, 115 (07) :928-935
[5]   Cancer risk prediction models: A workshop on development, evaluation, and application [J].
Freedman, AN ;
Seminara, D ;
Gail, MH ;
Hartge, P ;
Colditz, GA ;
Ballard-Barbash, R ;
Pfeiffer, RM .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (10) :715-723
[6]  
Hlatky Mark A, 2009, Circulation, V119, P2408, DOI 10.1161/CIRCULATIONAHA.109.192278
[7]   Assessment of Improved Prediction Beyond Traditional Risk Factors When Does a Difference Make a Difference? [J].
Janssens, A. Cecile J. W. ;
Khoury, Muin J. .
CIRCULATION-CARDIOVASCULAR GENETICS, 2010, 3 (01) :3-5
[8]   Genome-based prediction of common diseases: methodological considerations for future research [J].
Janssens, A. Cecile J. W. ;
van Duijn, Cornelia M. .
GENOME MEDICINE, 2009, 1
[9]  
Khoury MJ, 1998, AM J EPIDEMIOL, V148, P1
[10]   The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention? [J].
Khoury, Muin J. ;
Gwinn, Marta ;
Yoon, Paula W. ;
Dowling, Nicole ;
Moore, Cynthia A. ;
Bradley, Linda .
GENETICS IN MEDICINE, 2007, 9 (10) :665-674