EngelsF., Anti-Durhing (Moscow: Progress Publishers, 1878 [1975]): at 333.
2.
HollyB. and PettyN., “Not Fade Away,”1957.
3.
DusterT., “The Molecular Reinscription of Race: Unanticipated Issues in Biotechnology and Forensic Science,”Patterns of Prejudice40, nos. 4/5 (2006): 427–441. See also, FullwileyD., “The Biologistical Construction of Race: ‘Admixture’ Technology and the New Genetic Medicine,”Social Studies of Science38, no. 5 (2008): 695–735. IssaA., “Ethical Perspectives on Pharmacogenomics Profiling in the Drug Development Process,”Nature Reviews Drug Discovery1, no. 4 (2002): 300–301; RothsteinM. and EppsP., “Ethical and Legal Implications of Pharmacogenomics,”Nature Reviews Genetics2, no. 3 (2001): 228–231; RothsteinM. and EppsP., “Pharmacogenomics and the (Ir)relevance of Race,”Pharmacogenomics Journal1, no. 2 (2001): 104–108, at 105. On the promissory nature of genomics see, FortunM., Promising Genomics: Iceland and deCODE Genetics in a World of Speculation (Berkeley: University of California Press, 2008); and HedgecoeA., The Politics of Personalised Medicine (New York: Cambridge University Press, 2004). On the use of race as a crude surrogate, see, e.g., KaufmanJ. and CooperR., “Race in Epidemiology: New Tools, Old Problems,”Annals of Epidemiology18, no. 2 (2007): 119–123.
AlbainK. S., “Racial Disparities in Cancer Survival among Randomized Clinical Trials Patients of the Southwest Oncology Group,”Journal of the National Cancer Institute101, no. 14 (2009): 984–992.
7.
See Elton, supra note 4 (emphasis added).
8.
Id.
9.
AlbainK. S., “Racial Disparities in Cancer Survival Among Randomized Clinical Trials Patients of the Southwest Oncology Group,”Journal of the National Cancer Institute101, no. 14 (2009): 984–992, at 985.
10.
TriversK. F.MesserL. C., and KaufmanJ. S., “Re: Racial Disparities in Cancer Survival among Randomized Clinical Trials of the Southwest Oncology Group,”Journal of the National Cancer Institute102, no. 4 (2010): 278–279.
11.
GravleeC. C. and MulliganC. J., “Re: Racial Disparities in Cancer Survival Among Randomized Clinical Trials of the Southwest Oncology Group,”Journal of the National Cancer Institute102, no. 4 (2010): 280.
12.
See Elton, supra note 4. Or as the article itself concluded, “Our findings suggest that unrecognized interactions of tumor biological, hormonal, and/or inherited host factors must be contributing to differential survival outcomes by race in sex-specific malignancies.” See Albain, supra note 9, at 991 (emphasis added).
ParadiesY.MontoyaM., and FullertonS., “Racialized Genetics and the Study of Complex Diseases,”Perspectives in Biology and Medicine50, no. 2 (2007): 203–227, at 216.
17.
I am indebted to Karen-Sue Taussig for the idea of considering the “unknown” and “potential” as spaces for the production of meaning and assignment of value.
18.
HuangS.-M. and TempleR., “Is This the Drug or Dose for You? Impact and Consideration of Ethnic Factors in Global Drug Development, Regulatory Review, and Clinical Practice,”Clinical Pharmacology & Therapeutics84, no. 3 (2008): 287–294, at 291 (emphasis added).
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21.
Id.
22.
TempleR. and StockbridgeN. L., “BiDil for Heart Failure in Black Patients: The U.S. Food and Drug Administration Perspective,”Annals of Internal Medicine146, no. 1 (2007): 57–62, available at <http://www.annals.org/cgi/content/full/146/1/57#R11-10> (last visited November 30, 2012).
23.
HartyL.JohnsonK., and PowerA., “Race and Ethnicity in the Era of Emerging Pharmacogenomics,”Journal of Clinical Pharmacology46, no. 4 (2006): 405–407, at 405.
24.
Yen-RevolloJ.AumanJ. T., and McLeodH. L., “Race Does Not Explain Genetic Heterogeneity in Pharmacogenomic Pathways,”Pharmacogenomics9, no. 11 (2008): 1639–1645, at 1639.
25.
Id., at 1644 (emphasis added).
26.
Id., at 1643 (emphasis added).
27.
Id.
28.
KimM.-J., “A Regulatory Science Perspective on Warfarin Therapy: A Pharmacogenomic Opportunity,”Journal of Clinical Pharmacology49, no. 2 (2009): 138–146.
29.
GageB. F., “Use of Pharmacogenetic and Clinical Factors to Predict the Therapeutic Dose of Warfarin,”Clinical Pharmacology & Therapeutics84, no. 3 (2008): 326–331, at 328.
The International Warfarin Pharmacogenetics Consortium, “Estimation of the Warfarin Dose with Clinical and Pharmacogenetic Data,”New England Journal of Medicine360, no. 8 (2009): 753–764, at 754.
U.S. Food and Drug Administration, “Pharmacogenomics and Its Role in Drug Safety,”FDA Drug Safety Newsletter1, no. 2 (Winter 2008), available at <http://www.fda.gov/Drugs/DrugSafety/DrugSafetyNewsletter/ucm119991.htm> (last visited November 30, 2012); DalyA. K., “Pharmacogenomics of Anticoagulants: Steps toward Personal Dosage,”Genome Medicine1, no. 1 (2009): 10.1–10.4; U.S. Food and Drug Administration, “The Critical Path: Making Medical Products Better, Faster, and Cheaper,”available at <http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm061234.htm> (last visited December 5, 2012).
JohnsonJ. A., “Ethnic Differences in Cardiovascular Drug Response: Potential Contribution of Pharmacogenetics,”Circulation118, no. 13 (2008): 1383–1393, at 1383. See also, TakahashiH. and EchizenH., “Pharmacogenetics of Warfarin Elimination and Its Clinical Implications,”Clinical Pharmacokinetics40, no. 8 (2001): 587–603, El RoubyS.MestresC. A.LaDucaF. M., and ZuckerM. L., “Racial and Ethnic Differences in Warfarin Response,”Journal of Heart Valve Disease13, no. 1 (2004): 15–21.
38.
See supra note 36.
39.
See, e.g., NguyeA.DestaZ., and FlockhartD. A., “Enhancing Race-Based Prescribing Precision with Pharmacogenomics,”Clinical Pharmacology & Therapeutics81 (2007): 323–324, at 324.
40.
DangM. T.HambletonJ., and KayserS. R., “The Influence of Ethnicity on Warfarin Dosage Requirement,”Annals of Pharmacotherapy39, no. 6 (2005): 1008–1012.
41.
MathewsA., “In Milestone, FDA Pushes Genetic Tests Tied to Drug,”Wall Street Journal, August 16, 2007, available at <http://online.wsj.com/article/SB118722561330199147.html> (last visited November 30, 2012; restricted access).
42.
TeichertM., “Genotypes Associated with Reduced Activity of VKORC1 and CYP2C9 and Their Modification of Acenocoumarol Anticoagulation during the Initial Treatment Period,”Clinical Pharmacology & Therapeutics85, no. 4 (2009): 379–386, at 379.
43.
WuA., “Dosing Algorithm for Warfarin Using CYP2C9 and VKORC1 Genotyping from a Multi-Ethnic Population: Comparison with Other Equations,”Pharmacogenomics9, no. 2 (2008): 169–78, at 169–170.
44.
See Kim, supra note 28, at 140.
45.
See Wu, supra note 43.
46.
See, e.g., id.
47.
TakeuchiF., “A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose,”PLoS Genetics5, no. 3 (2009): E1000433; ChoH.-J., “Factors Affecting the Interindividual Variability of Warfarin Dose Requirement in Adult Korean Patients,”Pharmacogenomics8, no. 4 (2007): 329–337; GhadamP., “VKORC1 Gene Analysis in an Iranian Warfarin Resistant Patient,”Journal of Biological Sciences8, no. 3 (2007): 691–692; NakaiK., “Ethnic Differences in the VKORC1 Gene Polymorphism and an Association with Warfarin Dosage Requirements in Cardiovascular Surgery Patients,”Pharmacogenomics8, no. 7 (2007): 713–719.
48.
American Medical Association, Critical Path Institute, and the Arizona Center for Education and Research on Therapeutics, “Personalized health care report 2008: Warfarin and genetic testing,”2008, at 1, available at <http://www.ama-assn.org/resources/doc/genetics/warfarin-brochure.pdf> (last visited December 5, 2012).
The International Warfarin Pharmacogenetics Consortium, “Estimation of the Warfarin Dose with Clinical and Pharmacogenetic Data,”New England Journal of Medicine360 (2009): 753–764.
ChoM. and SankarP., “Forensic Genetics and Ethical, Legal and Social Implications beyond the Clinic,”Nature Genetics36, no. 11, Supp. (2004): S8–S12 at S9, citing LeechK. A., “A Question in Dispute: The Debate about an ‘Ethnic’ Question in the Census,” in Runnymeade Research Report (1989).
62.
ConditC.TempletonA.BatesB. R.BevanJ. L., and HarrisT. M., “Attitudinal Barriers to Delivery of Race-Targeted Pharmacogenomics among Informed Lay Persons,”Genetic Medicine5, no. 5 (2003): 385.
63.
Id.
64.
See, e.g., HahnR., “The State of Federal Health Statistics on Racial and Ethnic Groups,”JAMA267, no. 2 (1992): 268–271; HahnR.MulinareR. J., and TeutschS., “Inconsistencies in Coding of Race and Ethnicity between Birth and Death in U.S. Infants,”JAMA267, no. 2 (1992): 259–263; HahnR.TrumanB. I., and BarkerN., “Identifying Ancestry: The Reliability of Ancestral Identification in the United States by Self, Proxy, Interviewer, and Funeral Director,”Epidemiology7, no. 1 (1996): 75–80.
65.
See supra note 57.
66.
Id.
67.
Id., at 753.
68.
Id., at 758.
69.
Id., at 758 (emphasis added).
70.
Id., at 759 (emphasis added).
71.
For an excellent discussion of racial categories and “kinds,” see RootM., “How We Divide the World,”Philosophy of Science67, no. 3 (Proceedings) (2000): S628–S639.
72.
Supplementary Appendix to the International Warfarin Pharmacogenetics Consortium, “Estimation of the Warfarin Dose with Clinical and Pharmacogenetic Data,”New England Journal of Medicine360, no. S15 (2009): 753–764. My thanks to Jay Kaufman for pointing this out and helping me interpret the statistical data.
73.
Id., at S5.
74.
Id., at S6.
75.
BowserR., “Racial Profiling in Health Care: An Institutional Analysis of Medical Treatment Disparities,”Michigan Journal of Race & Law7 (Fall 2001): 79–133, at 111. For a broader analysis of the operation of the “white norm” in American law, see CrenshawK. W., “Race, Reform, and Retrenchment: Transformation and Legitimation in Antidiscrimination Law,”Harvard Law Review101, no. 7 (1988): 1331–1387, especially at 1377–1379.
76.
See supra note 72, at S6.
77.
GageB.F., “Use of Pharmacogenetic and Clinical Factors to Predict the Therapeutic Dose of Warfarin,”Clinical Pharmacology and Therapeutics84, no. 3 (2008): 326–331, at 326.