Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration

被引：12

作者：

Janssens, A. Cecile J. W. ^{[1
]}

Ioannidis, John P. A. ^{[2
,3
,4
,5
,6
,7
]}

Bedrosian, Sara ^{[8
]}

Boffetta, Paolo ^{[9
,10
]}

Dolan, Siobhan M. ^{[11
]}

Dowling, Nicole ^{[8
]}

Fortier, Isabel ^{[12
]}

Freedman, Andrew N. ^{[13
]}

Grimshaw, Jeremy M. ^{[14
,15
]}

Gulcher, Jeffrey ^{[16
]}

Gwinn, Marta ^{[8
]}

Hlatky, Mark A. ^{[17
]}

Janes, Holly ^{[18
,19
]}

Kraft, Peter ^{[20
]}

Melillo, Stephanie ^{[8
]}

O'Donnell, Christopher J. ^{[21
,22
,23
]}

Pencina, Michael J. ^{[24
,25
]}

Ransohoff, David ^{[26
]}

Schully, Sheri D. ^{[13
]}

Seminara, Daniela ^{[13
]}

Winn, Deborah M. ^{[13
]}

Wright, Caroline F. ^{[27
]}

van Duijn, Cornelia M. ^{[1
]}

Little, Julian ^{[28
]}

Khoury, Muin J. ^{[8
]}

机构：

[1] Erasmus MC, Dept Epidemiol, POB 2040, NL-3000 CA 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, Ctr Genet Epidemiol & Modeling, Inst Clin Res & Hlth Policy Studies, Boston, MA USA

[6] Tufts Med Ctr, Tufts CTSI, Inst Clin Res & Hlth Policy Studies, Boston, MA USA

[7] Stanford Univ, Sch Med, Stanford Prevent Res Ctr, Stanford, CA 94305 USA

[8] Ctr Dis Control & Prevent, Off Publ Hlth Genom, Atlanta, GA USA

[9] Mt Sinai Sch Med, Tisch Canc Inst, New York, NY USA

[10] Int Prevent Res Inst, Lyon, France

[11] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USA

[12] Publ Populat Project Genom P3G, Montreal, PQ, Canada

[13] NCI, Div Canc Control & Populat Sci, NIH, Bethesda, MD 20892 USA

[14] Ottawa Hosp Res Inst, Clin Epidemiol Program, Ottawa, ON, Canada

[15] Univ Ottawa, Dept Med, Ottawa, ON, Canada

[16] DeCODE Genet, Reykjavik, Iceland

[17] Stanford Univ, Dept Hlth Res & Policy, Palo Alto, CA 94304 USA

[18] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Inst, Seattle, WA 98104 USA

[19] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA

[20] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA

[21] NHLBI, Framingham, MA USA

[22] NHLBIs Framingham Heart Study, Framingham, MA USA

[23] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Cardiol, Boston, MA USA

[24] Boston Univ, Dept Biostat, Boston, MA 02215 USA

[25] Harvard Clin Res Inst, Boston, MA USA

[26] Univ N Carolina, Sch Med, Chapel Hill, NC USA

[27] PHG Fdn, Cambridge, England

[28] Univ Ottawa, Dept Epidemiol & Community Med, Ottawa, ON, Canada

来源：

EUROPEAN JOURNAL OF EPIDEMIOLOGY | 2011年 / 26卷 / 04期

基金：

美国国家卫生研究院;

关键词：

Genetic; Risk prediction; Methodology; Guidelines; Reporting; GENOME-WIDE ASSOCIATION; HEART-DISEASE RISK; COMMON DISEASES; DIAGNOSTIC-ACCURACY; CARDIOVASCULAR RISK; CONTROLLED-TRIALS; CANCER-RISK; POLYMORPHISMS; POPULATION; VARIANTS;

D O I：

10.1007/s10654-011-9551-z

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 fuelling 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 they vary widely in completeness of reporting and apparent quality. Transparent reporting of the strengths and weaknesses of these studies is important to facilitate the accumulation of evidence on genetic risk prediction. 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, quality and completeness of study reporting, and thereby to improve the synthesis and application of information from multiple studies that might differ in design, conduct or analysis.

引用

页码：313 / 337

页数：25

共 91 条

[41] STrengthening the REporting of Genetic Association Studies (STREGA) - An Extension of the STROBE Statement [J].

Little, Julian ;

Higgins, Julian P. T. ;

Ioannidis, John P. A. ;

Moher, David ;

Gagnon, France ;

von Elm, Erik ;

Khoury, Muin J. ;

Cohen, Barbara ;

Davey-Smith, George ;

Grimshaw, Jeremy ;

Scheet, Paul ;

Gwinn, Marta ;

Williamson, Robin E. ;

Zou, Guang Yong ;

Hutchings, Kim ;

Johnson, Candice Y. ;

Tait, Valerie ;

Wiens, Miriam ;

Golding, Jean ;

van Duijn, Cornelia ;

McLaughlin, John ;

Paterson, Andrew ;

Wells, George ;

Fortier, Isabel ;

Freedman, Matthew ;

Zecevic, Maja ;

King, Richard ;

Infante-Rivard, Claire ;

Stewart, Alex F. R. ;

Birkett, Nick .

PLOS MEDICINE, 2009, 6 (02) :151-163

[42]

Little R. J. A., 1987, STAT ANAL MISSING DA

[43] Eye color and the prediction of complex phenotypes from genotypes [J].

Liu, Fan ;

van Duijn, Kate ;

Vingerling, Johannes R. ;

Hofman, Albert ;

Uitterlinden, Andre G. ;

Janssens, A. Cecile J. W. ;

Kayser, Manfred .

CURRENT BIOLOGY, 2009, 19 (05) :R192-R193

[44] Overinterpretation of Clinical Applicability in Molecular Diagnostic Research [J].

Lumbreras, Blanca ;

Parker, Lucy A. ;

Porta, Miquel ;

Pollan, Marina ;

Ioannidis, John P. A. ;

Hernandez-Aguado, Ildefonso .

CLINICAL CHEMISTRY, 2009, 55 (04) :786-794

[45] Genetic prediction of future type 2 diabetes [J].

Lyssenko, V ;

Almgren, P ;

Anevski, D ;

Orho-Melander, M ;

Sjögren, M ;

Saloranta, C ;

Tuomi, T ;

Groop, L .

PLOS MEDICINE, 2005, 2 (12) :1299-1308

[46] Clinical Risk Factors, DNA Variants, and the Development of Type 2 Diabetes. [J].

Lyssenko, Valeriya ;

Jonsson, Anna ;

Almgren, Peter ;

Pulizzi, Nicolo ;

Isomaa, Bo ;

Tuomi, Tiinamaija ;

Berglund, Goran ;

Altshuler, David ;

Nilsson, Peter ;

Groop, Leif .

NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (21) :2220-2232

[47] The NCBI dbGaP database of genotypes and phenotypes [J].

Mailman, Matthew D. ;

Feolo, Michael ;

Jin, Yumi ;

Kimura, Masato ;

Tryka, Kimberly ;

Bagoutdinov, Rinat ;

Hao, Luning ;

Kiang, Anne ;

Paschall, Justin ;

Phan, Lon ;

Popova, Natalia ;

Pretel, Stephanie ;

Ziyabari, Lora ;

Lee, Moira ;

Shao, Yu ;

Wang, Zhen Y. ;

Sirotkin, Karl ;

Ward, Minghong ;

Kholodov, Michael ;

Zbicz, Kerry ;

Beck, Jeffrey ;

Kimelman, Michael ;

Shevelev, Sergey ;

Preuss, Don ;

Yaschenko, Eugene ;

Graeff, Alan ;

Ostell, James ;

Sherry, Stephen T. .

NATURE GENETICS, 2007, 39 (10) :1181-1186

[48] Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration [J].

Maller, Julian ;

George, Sarah ;

Purcell, Shaun ;

Fagerness, Jes ;

Altshuler, David ;

Daly, Mark J. ;

Seddon, Johanna M. .

NATURE GENETICS, 2006, 38 (09) :1055-1059

[49] New models of collaboration in genome-wide association studies: the Genetic Association Information Network [J].

Manolio, Teri A. ;

Rodriguez, Laura Lyman ;

Brooks, Lisa ;

Abecasis, Goncalo ;

Ballinger, Dennis ;

Daly, Mark ;

Donnelly, Peter ;

Faraone, Stephen V. ;

Frazer, Kelly ;

Gabriel, Stacey ;

Gejman, Pablo ;

Guttmacher, Alan ;

Harris, Emily L. ;

Insel, Thomas ;

Kelsoe, John R. ;

Lander, Eric ;

McCowin, Norma ;

Mailman, Matthew D. ;

Nabel, Elizabeth ;

Ostell, James ;

Pugh, Elizabeth ;

Sherry, Stephen ;

Sullivan, Patrick F. ;

Thompson, John F. ;

Warram, James ;

Study, GoKinD ;

Wholley, David ;

Milos, Patrice M. ;

Collins, Francis S. .

NATURE GENETICS, 2007, 39 (09) :1045-1051

[50]

McShane LM, 2005, NAT CLIN PRACT GASTR, V2, pA416, DOI 10.1038/ncponc0252

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