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- Publisher Website: 10.1159/000319192
- Scopus: eid_2-s2.0-77956467624
- PMID: 20838054
- WOS: WOS:000283613000005
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Article: Effect size measures in genetic association studies and age-conditional risk prediction
Title | Effect size measures in genetic association studies and age-conditional risk prediction | ||||||||
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Authors | |||||||||
Keywords | Association study Competing risks Genetic counseling Genetic risk prediction Hazard ratio Odds ratio Relative risk | ||||||||
Issue Date | 2010 | ||||||||
Publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/HHE | ||||||||
Citation | Human Heredity, 2010, v. 70 n. 3, p. 205-218 How to Cite? | ||||||||
Abstract | The interest in risk prediction using genomic profiles has surged recently. A proper interpretation of effect size measures in association studies is crucial to accurate risk prediction. In this study, we clarified the relationship between the odds ratio (OR), relative risk and incidence rate ratios in the context of genetic association studies. We demonstrated that under the common practice of sampling prevalent cases and controls, the resulting ORs approximate the incidence rate ratios. Based on this result, we presented a framework to compute the disease risk given the current age and follow-up period (including lifetime risk), with consideration of competing risks of mortality. We considered two extensions. One is correcting the incidence rate to reflect the person-years alive and disease-free, the other is converting prevalence to incidence estimates. The methodology was applied to an example of breast cancer prediction. We observed that simply multiplying the OR by the average lifetime risk estimates yielded a final estimate >100% (101%), while using our method that accounts for competing risks produces an estimate of 63% only. We also applied the method to risk prediction of Alzheimer's disease in Hong Kong. We recommend that companies offering direct-to-consumer genetic testing employ more rigorous prediction algorithms considering competing risks. © 2010 S. Karger AG, Basel. | ||||||||
Persistent Identifier | http://hdl.handle.net/10722/137516 | ||||||||
ISSN | 2023 Impact Factor: 1.1 2023 SCImago Journal Rankings: 0.483 | ||||||||
ISI Accession Number ID |
Funding Information: The work was supported by the Hong Kong Research Grants Council General Research Fund grants HKU 766906M and HKU 774707M and the University of Hong Kong Strategic Research Theme of Genomics. H.-C.S. was supported by a Croucher Foundation Scholarship. | ||||||||
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DC Field | Value | Language |
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dc.contributor.author | So, HC | en_HK |
dc.contributor.author | Sham, PC | en_HK |
dc.date.accessioned | 2011-08-26T14:26:53Z | - |
dc.date.available | 2011-08-26T14:26:53Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Human Heredity, 2010, v. 70 n. 3, p. 205-218 | en_HK |
dc.identifier.issn | 0001-5652 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/137516 | - |
dc.description.abstract | The interest in risk prediction using genomic profiles has surged recently. A proper interpretation of effect size measures in association studies is crucial to accurate risk prediction. In this study, we clarified the relationship between the odds ratio (OR), relative risk and incidence rate ratios in the context of genetic association studies. We demonstrated that under the common practice of sampling prevalent cases and controls, the resulting ORs approximate the incidence rate ratios. Based on this result, we presented a framework to compute the disease risk given the current age and follow-up period (including lifetime risk), with consideration of competing risks of mortality. We considered two extensions. One is correcting the incidence rate to reflect the person-years alive and disease-free, the other is converting prevalence to incidence estimates. The methodology was applied to an example of breast cancer prediction. We observed that simply multiplying the OR by the average lifetime risk estimates yielded a final estimate >100% (101%), while using our method that accounts for competing risks produces an estimate of 63% only. We also applied the method to risk prediction of Alzheimer's disease in Hong Kong. We recommend that companies offering direct-to-consumer genetic testing employ more rigorous prediction algorithms considering competing risks. © 2010 S. Karger AG, Basel. | en_HK |
dc.language | eng | en_US |
dc.publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/HHE | en_HK |
dc.relation.ispartof | Human Heredity | en_HK |
dc.rights | Human Heredity. Copyright © S Karger AG. | - |
dc.subject | Association study | en_HK |
dc.subject | Competing risks | en_HK |
dc.subject | Genetic counseling | en_HK |
dc.subject | Genetic risk prediction | en_HK |
dc.subject | Hazard ratio | en_HK |
dc.subject | Odds ratio | en_HK |
dc.subject | Relative risk | en_HK |
dc.subject.mesh | Genetic Association Studies | - |
dc.subject.mesh | Genetic Counseling | - |
dc.subject.mesh | Genetic Testing | - |
dc.subject.mesh | Odds Ratio | - |
dc.subject.mesh | Risk Assessment - methods | - |
dc.title | Effect size measures in genetic association studies and age-conditional risk prediction | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Sham, PC: pcsham@hku.hk | en_HK |
dc.identifier.authority | Sham, PC=rp00459 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1159/000319192 | en_HK |
dc.identifier.pmid | 20838054 | - |
dc.identifier.scopus | eid_2-s2.0-77956467624 | en_HK |
dc.identifier.hkuros | 189824 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77956467624&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 70 | en_HK |
dc.identifier.issue | 3 | en_HK |
dc.identifier.spage | 205 | en_HK |
dc.identifier.epage | 218 | en_HK |
dc.identifier.isi | WOS:000283613000005 | - |
dc.publisher.place | Switzerland | en_HK |
dc.relation.project | Genome-wide association study of schizophrenia | - |
dc.identifier.scopusauthorid | So, HC=37031934700 | en_HK |
dc.identifier.scopusauthorid | Sham, PC=34573429300 | en_HK |
dc.identifier.citeulike | 8125509 | - |
dc.identifier.issnl | 0001-5652 | - |