Literature DB >> 24280773

Perceptions regarding genetic testing in populations at risk for nephropathy.

Barry I Freedman1, Alison J Fletcher, Vivek R Sanghani, Mitzie Spainhour, Angelina W Graham, Gregory B Russell, Jessica N Cooke Bailey, Ana S Iltis, Nancy M P King.   

Abstract

BACKGROUND: Population ancestry-based differences exist in genetic risk for many kidney diseases. Substantial debate remains regarding returning genetic test results to participants. African-Americans (AAs) and European-Americans (EAs) at risk for end-stage kidney disease were queried for views on the value and use of genetic testing in research.
METHODS: A standardized survey regarding attitudes toward genetic testing was administered to 130 individuals (64 AA, 66 EA) with first-degree relatives on dialysis. Fisher's exact test was used to assess differences in participant attitudes between population groups.
RESULTS: Mean (SD) age of surveyed AAs and EAs was 45.5 (12.8) and 50.5 (14.4) years, respectively (p = 0.04), with similar familial relationships (p = 0.22). AAs and EAs wished to know their test results if risk could be: (1) reduced by diet or exercise (100 and 98%, p = 0.99); (2) reduced by medical treatment (100 and 98%, p = 0.99), or (3) if no treatments were available (90 and 82%, p = 0.21). If informed they lacked a disease susceptibility variant, 87% of AAs and 88% of EAs would be extremely or pretty likely to inform family members (p = 0.84). If informed they had a disease susceptibility variant, 92% of AAs and 89% of EAs would be extremely or pretty likely to inform their family (p = 0.43).
CONCLUSIONS: Attitudes toward obtaining and using genetic test results for disease in research contexts were similar in AAs and EAs at risk for end-stage kidney disease. A substantial majority would want information regardless of available treatments and would share the information with the family. These results have important implications for patient care, study design and the informed consent process.
© 2013 S. Karger AG, Basel.

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Year:  2013        PMID: 24280773      PMCID: PMC3914164          DOI: 10.1159/000356244

Source DB:  PubMed          Journal:  Am J Nephrol        ISSN: 0250-8095            Impact factor:   3.754


  21 in total

1.  Racial and ethnic variations in knowledge and attitudes about genetic testing.

Authors:  Eleanor Singer; Toni Antonucci; John Van Hoewyk
Journal:  Genet Test       Date:  2004

2.  Association of trypanolytic ApoL1 variants with kidney disease in African Americans.

Authors:  Giulio Genovese; David J Friedman; Michael D Ross; Laurence Lecordier; Pierrick Uzureau; Barry I Freedman; Donald W Bowden; Carl D Langefeld; Taras K Oleksyk; Andrea L Uscinski Knob; Andrea J Bernhardy; Pamela J Hicks; George W Nelson; Benoit Vanhollebeke; Cheryl A Winkler; Jeffrey B Kopp; Etienne Pays; Martin R Pollak
Journal:  Science       Date:  2010-07-15       Impact factor: 47.728

3.  Public perspectives on returning genetics and genomics research results.

Authors:  J O'Daniel; S B Haga
Journal:  Public Health Genomics       Date:  2011-05-07       Impact factor: 2.000

4.  Attitudes of urban American Indians and Alaska Natives regarding participation in research.

Authors:  Dedra Buchwald; Veronica Mendoza-Jenkins; Calvin Croy; Helen McGough; Marjorie Bezdek; Paul Spicer
Journal:  J Gen Intern Med       Date:  2006-06       Impact factor: 5.128

Review 5.  The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans.

Authors:  Barry I Freedman; Jeffrey B Kopp; Carl D Langefeld; Giulio Genovese; David J Friedman; George W Nelson; Cheryl A Winkler; Donald W Bowden; Martin R Pollak
Journal:  J Am Soc Nephrol       Date:  2010-08-05       Impact factor: 10.121

6.  Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study.

Authors:  Samantha A Streicher; Saskia C Sanderson; Ethylin Wang Jabs; Michael Diefenbach; Meg Smirnoff; Inga Peter; Carol R Horowitz; Barbara Brenner; Lynne D Richardson
Journal:  J Community Genet       Date:  2011-06-07

7.  Regional differences in awareness and attitudes regarding genetic testing for disease risk and ancestry.

Authors:  Charles R Jonassaint; Eunice R Santos; Crystal M Glover; Perry W Payne; Grace-Ann Fasaye; Nefertiti Oji-Njideka; Stanley Hooker; Wenndy Hernandez; Morris W Foster; Rick A Kittles; Charmaine D Royal
Journal:  Hum Genet       Date:  2010-06-13       Impact factor: 4.132

8.  Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.

Authors:  Shay Tzur; Saharon Rosset; Revital Shemer; Guennady Yudkovsky; Sara Selig; Ayele Tarekegn; Endashaw Bekele; Neil Bradman; Walter G Wasser; Doron M Behar; Karl Skorecki
Journal:  Hum Genet       Date:  2010-07-16       Impact factor: 4.132

9.  Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis.

Authors:  Krzysztof Kiryluk; Yifu Li; Simone Sanna-Cherchi; Mersedeh Rohanizadegan; Hitoshi Suzuki; Frank Eitner; Holly J Snyder; Murim Choi; Ping Hou; Francesco Scolari; Claudia Izzi; Maddalena Gigante; Loreto Gesualdo; Silvana Savoldi; Antonio Amoroso; Daniele Cusi; Pasquale Zamboli; Bruce A Julian; Jan Novak; Robert J Wyatt; Krzysztof Mucha; Markus Perola; Kati Kristiansson; Alexander Viktorin; Patrik K Magnusson; Gudmar Thorleifsson; Unnur Thorsteinsdottir; Kari Stefansson; Anne Boland; Marie Metzger; Lise Thibaudin; Christoph Wanner; Kitty J Jager; Shin Goto; Dita Maixnerova; Hussein H Karnib; Judit Nagy; Ulf Panzer; Jingyuan Xie; Nan Chen; Vladimir Tesar; Ichiei Narita; Francois Berthoux; Jürgen Floege; Benedicte Stengel; Hong Zhang; Richard P Lifton; Ali G Gharavi
Journal:  PLoS Genet       Date:  2012-06-21       Impact factor: 5.917

10.  Attitudes of African American premedical students toward genetic testing and screening.

Authors:  Sara L Laskey; Joseph Williams; Jacqui Pierre-Louis; MaryAnn O'Riordan; Anne Matthews; Nathaniel H Robin
Journal:  Genet Med       Date:  2003 Jan-Feb       Impact factor: 8.822

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  12 in total

Review 1.  Practical Considerations for APOL1 Genotyping in the Living Kidney Donor Evaluation.

Authors:  Alejandra M Mena-Gutierrez; Amber M Reeves-Daniel; Colleen L Jay; Barry I Freedman
Journal:  Transplantation       Date:  2020-01       Impact factor: 4.939

2.  Motivation, Perception, and Treatment Beliefs in the Myocardial Infarction Genes (MI-GENES) Randomized Clinical Trial.

Authors:  Sharma Kattel; Tochukwu Onyekwelu; Sherry-Ann Brown; Hayan Jouni; Erin Austin; Iftikhar J Kullo
Journal:  J Genet Couns       Date:  2017-04-06       Impact factor: 2.537

3.  Race, Genomics and Chronic Disease: What Patients with African Ancestry Have to Say.

Authors:  Carol R Horowitz; Kadija Ferryman; Rennie Negron; Tatiana Sabin; Mayra Rodriguez; Randi F Zinberg; Erwin Böttinger; Mimsie Robinson
Journal:  J Health Care Poor Underserved       Date:  2017

Review 4.  Clinical Genetic Testing for APOL1: Are we There Yet?

Authors:  Bessie A Young; Stephanie Malia Fullerton; James G Wilson; Kerri Cavanaugh; Erika Blacksher; Clarence Spigner; Jonathan Himmelfarb; Wylie Burke
Journal:  Semin Nephrol       Date:  2017-11       Impact factor: 5.299

Review 5.  Apolipoprotein L1 Gene Effects on Kidney Transplantation.

Authors:  Barry I Freedman; Jayme E Locke; Amber M Reeves-Daniel; Bruce A Julian
Journal:  Semin Nephrol       Date:  2017-11       Impact factor: 5.299

6.  Attitudes Toward Genetic Testing for Celiac Disease.

Authors:  Abhik Roy; Michele Pallai; Benjamin Lebwohl; Annette K Taylor; Peter H Green
Journal:  J Genet Couns       Date:  2015-08-02       Impact factor: 2.537

7.  African American Living Donors' Attitudes About APOL1 Genetic Testing: A Mixed Methods Study.

Authors:  Elisa J Gordon; Daniela Amόrtegui; Isaac Blancas; Catherine Wicklund; John Friedewald; Richard R Sharp
Journal:  Am J Kidney Dis       Date:  2018-10-22       Impact factor: 8.860

8.  Willingness to Participate in a National Precision Medicine Cohort: Attitudes of Chronic Kidney Disease Patients at a Cleveland Public Hospital.

Authors:  Jessica N Cooke Bailey; Dana C Crawford; Aaron Goldenberg; Anne Slaven; Julie Pencak; Marleen Schachere; William S Bush; John R Sedor; John F O'Toole
Journal:  J Pers Med       Date:  2018-06-26

9.  Opinions of African American adults about the use of apolipoprotein L1 (ApoL1) genetic testing in living kidney donation and transplantation.

Authors:  Margaret Berrigan; Jasmine Austrie; Aaron Fleishman; Kenneth P Tercyak; Martin R Pollak; Martha Pavlakis; Vinayak Rohan; Prabhakar K Baliga; Liise K Kayler; Thomas H Feeley; James R Rodrigue
Journal:  Am J Transplant       Date:  2020-08-29       Impact factor: 8.086

10.  APOL1 Long-term Kidney Transplantation Outcomes Network (APOLLO): Design and Rationale.

Authors:  Barry I Freedman; Marva M Moxey-Mims; Amir A Alexander; Brad C Astor; Kelly A Birdwell; Donald W Bowden; Gordon Bowen; Jonathan Bromberg; Timothy E Craven; Darshana M Dadhania; Jasmin Divers; Mona D Doshi; Elling Eidbo; Alessia Fornoni; Michael D Gautreaux; Rasheed A Gbadegesin; Patrick O Gee; Giselle Guerra; Chi-Yuan Hsu; Ana S Iltis; Nichole Jefferson; Bruce A Julian; David K Klassen; Patrick P Koty; Carl D Langefeld; Krista L Lentine; Lijun Ma; Roslyn B Mannon; Madhav C Menon; Sumit Mohan; J Brian Moore; Barbara Murphy; Kenneth A Newell; Jonah Odim; Mariella Ortigosa-Goggins; Nicholette D Palmer; Meyeon Park; Afshin Parsa; Stephen O Pastan; Emilio D Poggio; Nishadi Rajapakse; Amber M Reeves-Daniel; Sylvia E Rosas; Laurie P Russell; Deirdre Sawinski; S Carrie Smith; Mitzie Spainhour; Robert J Stratta; Matthew R Weir; David M Reboussin; Paul L Kimmel; Daniel C Brennan
Journal:  Kidney Int Rep       Date:  2019-12-13
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