Literature DB >> 10795342

Risk estimation and value-of-information analysis for three proposed genetic screening programs for chronic beryllium disease prevention.

S M Bartell1, R A Ponce, T K Takaro, R O Zerbe, G S Omenn, E M Faustman.   

Abstract

Genetic differences (polymorphisms) among members of a population are thought to influence susceptibility to various environmental exposures. In practice, however, this information is rarely incorporated into quantitative risk assessment and risk management. We describe an analytic framework for predicting the risk reduction and value-of-information (VOI) resulting from specific risk management applications of genetic biomarkers, and we apply the framework to the example of occupational chronic beryllium disease (CBD), an immune-mediated pulmonary granulomatous disease. One described Human Leukocyte Antigen gene variant, HLA-DP beta 1*0201, contains a substitution of glutamate for lysine at position 69 that appears to have high sensitivity (approximately 94%) but low specificity (approximately 70%) with respect to CBD among individuals occupationally exposed to respirable beryllium. The expected postintervention CBD prevalence rates for using the genetic variant (1) as a required job placement screen, (2) as a medical screen for semiannual in place of annual lymphocyte proliferation testing, or (3) as a voluntary job placement screen are 0.08%, 0.8%, and 0.6%, respectively, in a hypothetical cohort with 1% baseline CBD prevalence. VOI analysis is used to examine the reduction in total social cost, calculated as the net value of disease reduction and financial expenditures, expected for proposed CBD intervention programs based on the genetic susceptibility test. For the example cohort, the expected net VOI per beryllium worker for genetically based testing and intervention is $13,000, $1,800, and $5,100, respectively, based on a health valuation of $1.45 million per CBD case avoided. VOI results for alternative CBD evaluations are also presented. Despite large parameter uncertainty, probabilistic analysis predicts generally positive utility for each of the three evaluated programs when avoidance of a CBD case is valued at $1 million or higher. Although the utility of a proposed risk management program may be evaluated solely in terms of risk reduction and financial costs, decisions about genetic testing and program implementation must also consider serious social, legal, and ethical factors.

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Year:  2000        PMID: 10795342     DOI: 10.1111/0272-4332.00009

Source DB:  PubMed          Journal:  Risk Anal        ISSN: 0272-4332            Impact factor:   4.000


  5 in total

1.  Quantifying the advantages and disadvantages of pre-placement genetic screening.

Authors:  K T Palmer; J Poole; R G Rawbone; D Coggon
Journal:  Occup Environ Med       Date:  2004-05       Impact factor: 4.402

Review 2.  Genetic screening and occupational and environmental exposures.

Authors:  P Vineis; H Ahsan; M Parker
Journal:  Occup Environ Med       Date:  2005-09       Impact factor: 4.402

3.  A practical guide to value of information analysis.

Authors:  Edward C F Wilson
Journal:  Pharmacoeconomics       Date:  2015-02       Impact factor: 4.981

4.  Impact of negatively charged patches on the surface of MHC class II antigen-presenting proteins on risk of chronic beryllium disease.

Authors:  James A Snyder; Eugene Demchuk; Erin C McCanlies; Christine R Schuler; Kathleen Kreiss; Michael E Andrew; Bonnie L Frye; James S Ensey; Marcia L Stanton; Ainsley Weston
Journal:  J R Soc Interface       Date:  2008-07-06       Impact factor: 4.118

5.  MyD88 dependence of beryllium-induced dendritic cell trafficking and CD4⁺ T-cell priming.

Authors:  A S McKee; D G Mack; F Crawford; A P Fontenot
Journal:  Mucosal Immunol       Date:  2015-03-11       Impact factor: 7.313

  5 in total

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