Literature DB >> 31038731

The Advantages and Challenges of Diversity in Pharmacogenomics: Can Minority Populations Bring Us Closer to Implementation?

Honghong Zhang1, Tanima De1, Yizhen Zhong1, Minoli A Perera1.   

Abstract

Health disparities exist among minorities in the United States, with differences seen in disease prevalence, mortality, and responses to medications. These differences are multifactorial with genetic variation explaining a portion of this variability. Pharmacogenomics aims to find the effect of genetic variations on drug response, with the goal of optimizing drug therapy and development. Although genome-wide association studies have been useful in unbiasedly surveying the genome for genetic drivers of clinically relevant phenotypes, most of these studies have been conducted in mainly participants of European and Asian descent, contributing to a growing health disparity in precision medicine. Diversity is important to pharmacogenomic studies, and there may be real advantages to the use of these complex genomes in pharmacogenomics. In this review we will outline some of the advantages and confounders of pharmacogenomics in minorities, describe the role of genetic variation in pharmacologic pathways, and highlight a number of population-specific findings.
© 2019 The Authors Clinical Pharmacology & Therapeutics © 2019 American Society for Clinical Pharmacology and Therapeutics.

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Year:  2019        PMID: 31038731      PMCID: PMC6663589          DOI: 10.1002/cpt.1491

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  90 in total

1.  What causes intracerebral hemorrhage during warfarin therapy?

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Journal:  Neurology       Date:  2000-10-10       Impact factor: 9.910

2.  Control of confounding of genetic associations in stratified populations.

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Journal:  Am J Hum Genet       Date:  2003-06       Impact factor: 11.025

3.  Prevention of cardiovascular events with an antihypertensive regimen of amlodipine adding perindopril as required versus atenolol adding bendroflumethiazide as required, in the Anglo-Scandinavian Cardiac Outcomes Trial-Blood Pressure Lowering Arm (ASCOT-BPLA): a multicentre randomised controlled trial.

Authors:  Björn Dahlöf; Peter S Sever; Neil R Poulter; Hans Wedel; D Gareth Beevers; Mark Caulfield; Rory Collins; Sverre E Kjeldsen; Arni Kristinsson; Gordon T McInnes; Jesper Mehlsen; Markku Nieminen; Eoin O'Brien; Jan Ostergren
Journal:  Lancet       Date:  2005 Sep 10-16       Impact factor: 79.321

Review 4.  CYP2C9 gene variants, drug dose, and bleeding risk in warfarin-treated patients: a HuGEnet systematic review and meta-analysis.

Authors:  Simon Sanderson; Jon Emery; Julian Higgins
Journal:  Genet Med       Date:  2005-02       Impact factor: 8.822

Review 5.  Genetic contribution to variable human CYP3A-mediated metabolism.

Authors:  Jatinder K Lamba; Yvonne S Lin; Erin G Schuetz; Kenneth E Thummel
Journal:  Adv Drug Deliv Rev       Date:  2002-11-18       Impact factor: 15.470

Review 6.  Linkage disequilibrium in humans: models and data.

Authors:  J K Pritchard; M Przeworski
Journal:  Am J Hum Genet       Date:  2001-06-14       Impact factor: 11.025

7.  The influence of ethnicity on warfarin dosage requirement.

Authors:  Mai-Trang N Dang; Julie Hambleton; Steven R Kayser
Journal:  Ann Pharmacother       Date:  2005-04-26       Impact factor: 3.154

8.  Codeine intoxication associated with ultrarapid CYP2D6 metabolism.

Authors:  Yvan Gasche; Youssef Daali; Marc Fathi; Alberto Chiappe; Silvia Cottini; Pierre Dayer; Jules Desmeules
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9.  Mutations in PCSK9 cause autosomal dominant hypercholesterolemia.

Authors:  Marianne Abifadel; Mathilde Varret; Jean-Pierre Rabès; Delphine Allard; Khadija Ouguerram; Martine Devillers; Corinne Cruaud; Suzanne Benjannet; Louise Wickham; Danièle Erlich; Aurélie Derré; Ludovic Villéger; Michel Farnier; Isabel Beucler; Eric Bruckert; Jean Chambaz; Bernard Chanu; Jean-Michel Lecerf; Gerald Luc; Philippe Moulin; Jean Weissenbach; Annick Prat; Michel Krempf; Claudine Junien; Nabil G Seidah; Catherine Boileau
Journal:  Nat Genet       Date:  2003-06       Impact factor: 38.330

10.  Serum uric acid and risk for development of hypertension and impaired fasting glucose or Type II diabetes in Japanese male office workers.

Authors:  N Nakanishi; M Okamoto; H Yoshida; Y Matsuo; K Suzuki; K Tatara
Journal:  Eur J Epidemiol       Date:  2003       Impact factor: 8.082

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  16 in total

1.  Pharmacogenetics: Chasing Perfection.

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Journal:  Clin Pharmacol Ther       Date:  2019-08       Impact factor: 6.875

2.  Genetic Variations of the DPYD Gene and Its Relationship with Ancestry Proportions in Different Ecuadorian Trihybrid Populations.

Authors:  Camila Farinango; Jennifer Gallardo-Cóndor; Byron Freire-Paspuel; Rodrigo Flores-Espinoza; Gabriela Jaramillo-Koupermann; Andrés López-Cortés; Germán Burgos; Eduardo Tejera; Alejandro Cabrera-Andrade
Journal:  J Pers Med       Date:  2022-06-10

3.  Multi-Omic Approaches to Identify Genetic Factors in Metabolic Syndrome.

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Journal:  Compr Physiol       Date:  2021-12-29       Impact factor: 8.915

Review 4.  Health Disparities of Cardiometabolic Disorders Among Filipino Americans: Implications for Health Equity and Community-Based Genetic Research.

Authors:  Gerald Coronado; Jacqueline Chio-Lauri; Rosheanne Dela Cruz; Youssef M Roman
Journal:  J Racial Ethn Health Disparities       Date:  2021-11-26

Review 5.  PharmVar GeneFocus: CYP2D6.

Authors:  Charity Nofziger; Amy J Turner; Katrin Sangkuhl; Michelle Whirl-Carrillo; José A G Agúndez; John L Black; Henry M Dunnenberger; Gualberto Ruano; Martin A Kennedy; Michael S Phillips; Houda Hachad; Teri E Klein; Andrea Gaedigk
Journal:  Clin Pharmacol Ther       Date:  2019-12-09       Impact factor: 6.875

6.  Phenotype prediction and characterization of 25 pharmacogenes in Thais from whole genome sequencing for clinical implementation.

Authors:  John Mauleekoonphairoj; Monpat Chamnanphon; Apichai Khongphatthanayothin; Boosamas Sutjaporn; Pharawee Wandee; Yong Poovorawan; Koonlawee Nademanee; Monnat Pongpanich; Pajaree Chariyavilaskul
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Review 7.  PharmVar GeneFocus: CYP2C19.

Authors:  Mariana R Botton; Michelle Whirl-Carrillo; Andria L Del Tredici; Katrin Sangkuhl; Larisa H Cavallari; José A G Agúndez; Jorge Duconge; Ming Ta Michael Lee; Erica L Woodahl; Karla Claudio-Campos; Ann K Daly; Teri E Klein; Victoria M Pratt; Stuart A Scott; Andrea Gaedigk
Journal:  Clin Pharmacol Ther       Date:  2020-07-22       Impact factor: 6.875

Review 8.  A Tutorial for Pharmacogenomics Implementation Through End-to-End Clinical Decision Support Based on Ten Years of Experience from PREDICT.

Authors:  Michelle Liu; Cindy L Vnencak-Jones; Bartholomew P Roland; Cheryl L Gatto; Janos L Mathe; Shari L Just; Josh F Peterson; Sara L Van Driest; Asli O Weitkamp
Journal:  Clin Pharmacol Ther       Date:  2020-11-15       Impact factor: 6.903

Review 9.  DPYD and UGT1A1 Pharmacogenetic Testing in Patients with Gastrointestinal Malignancies: An Overview of the Evidence and Considerations for Clinical Implementation.

Authors:  Lisa A Varughese; Kelsey S Lau-Min; Christine Cambareri; Nevena Damjanov; Ryan Massa; Nandi Reddy; Randall Oyer; Ursina Teitelbaum; Sony Tuteja
Journal:  Pharmacotherapy       Date:  2020-10-19       Impact factor: 6.251

Review 10.  Digital Health Applications for Pharmacogenetic Clinical Trials.

Authors:  Hetanshi Naik; Latha Palaniappan; Euan A Ashley; Stuart A Scott
Journal:  Genes (Basel)       Date:  2020-10-26       Impact factor: 4.096

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