EXPLORING BIOLOGIC PREDICTORS OF RESPONSE DISPARITIES TO ATYPICAL ANTIPSYCHOTICS AMONG BLACKS: A QUASI-SYSTEMATIC REVIEW

被引:9
作者
Jerome, Rebecca N. [1 ]
Pulley, Jill M. [1 ]
Sathe, Nila A. [2 ,3 ]
Krishnaswami, Shanthi [2 ]
Dickerson, Alyssa B. [1 ]
Worley, Katherine J. [1 ,2 ]
Wilkins, Consuelo H. [4 ,5 ]
机构
[1] Vanderbilt Univ, Vanderbilt Inst Clin & Translat Res, Med Ctr, 2525 West End Ave,Suite 600, Nashville, TN 37203 USA
[2] Vanderbilt Univ, Inst Med & Publ Hlth, Med Ctr, Vanderbilt Evidence Based Practice Ctr, Nashville, TN 37203 USA
[3] Vanderbilt Univ, Inst Med & Publ Hlth, Med Ctr, Vanderbilt Dept Hlth Policy, Nashville, TN 37203 USA
[4] Vanderbilt Univ, Dept Med, Med Ctr, Nashville, TN 37203 USA
[5] Meharry Med Coll, Dept Internal Med, Nashville, TN 37208 USA
关键词
Atypical Antipsychotics; Schizophrenia; Blacks; Disparities; Pharmacogenetics; INDUCED WEIGHT-GAIN; RECEPTOR GENE VARIANTS; DOUBLE-BLIND; TARDIVE-DYSKINESIA; AFRICAN-AMERICANS; CLOZAPINE; SCHIZOPHRENIA; ASSOCIATION; POLYMORPHISMS; CHILDREN;
D O I
10.18865/ed.30.S1.229
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Purpose: Management of schizophrenia among Blacks in the United States is affected by persistent disparities. This review explored response to atypical antipsychotics among Blacks compared with other groups to assess systematic variation that may contribute to disparities. Methods: We conducted a quasi-systematic review of studies reporting response to atypical antipsychotics among Blacks compared with other groups, including effects of genetic variation. Results: Of 48 identified research articles, 29 assessed differences in outcomes without inclusion of genetic variation and 20 explored effects of genetic variation; of note: one article included both types of data. Analysis of the 29 papers with clinical outcomes only suggests that while data on efficacy and risk of movement disorders were heterogeneous, findings indicate increased risk of metabolic effects and neutropenia among Blacks. Of the 20 articles exploring effects of genetic variation, allelic or genotypic variations involving several genes were associated with altered efficacy or safety among Blacks but not Whites, including risk of decreased response involving variation in DRD4 and DRD1, and improved efficacy associated with variants in DRD2, COMT, and RGS4. Others showed significant improvement in treatment response only among Whites, including variation in DTNBP1, DRD4, and GNB3. Conclusions: The current analysis can help tailor management among Blacks using an atypical antipsychotic. Heterogeneity in genetic variation effects and response allele frequency suggests that pharmacogenetics approaches for atypical antipsychotics will need to explicitly incorporate race and ethnicity.
引用
收藏
页码:229 / 240
页数:12
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