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Engaging African ancestry participants in SLE clinical trials

SLE is a complex autoimmune disease with genetic and clinical differences between patients that appear to reside along ancestral lines. Over the last 20 years, a preponderance of evidence has shown that SLE is more common and severe in minority populations, particularly in African ancestry (AA) wome...

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Detalles Bibliográficos
Autores principales: Anjorin, Aderike, Lipsky, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307590/
https://www.ncbi.nlm.nih.gov/pubmed/30613420
http://dx.doi.org/10.1136/lupus-2018-000297
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author Anjorin, Aderike
Lipsky, Peter
author_facet Anjorin, Aderike
Lipsky, Peter
author_sort Anjorin, Aderike
collection PubMed
description SLE is a complex autoimmune disease with genetic and clinical differences between patients that appear to reside along ancestral lines. Over the last 20 years, a preponderance of evidence has shown that SLE is more common and severe in minority populations, particularly in African ancestry (AA) women. However, in clinical trials for new therapies of SLE, AA is often under-represented. Without enrolling sufficient AA participants, it is difficult to ascertain the safety and efficacy of new potential therapies among individuals with SLE of different ancestries. Although enrolling minority populations in clinical trials has been a significant challenge for many reasons, the various stakeholders involved in clinical research could act within their own realms to develop new paradigms and policies to bolster the inclusion of AA in the development of new therapies.
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spelling pubmed-63075902019-01-04 Engaging African ancestry participants in SLE clinical trials Anjorin, Aderike Lipsky, Peter Lupus Sci Med Review SLE is a complex autoimmune disease with genetic and clinical differences between patients that appear to reside along ancestral lines. Over the last 20 years, a preponderance of evidence has shown that SLE is more common and severe in minority populations, particularly in African ancestry (AA) women. However, in clinical trials for new therapies of SLE, AA is often under-represented. Without enrolling sufficient AA participants, it is difficult to ascertain the safety and efficacy of new potential therapies among individuals with SLE of different ancestries. Although enrolling minority populations in clinical trials has been a significant challenge for many reasons, the various stakeholders involved in clinical research could act within their own realms to develop new paradigms and policies to bolster the inclusion of AA in the development of new therapies. BMJ Publishing Group 2018-12-11 /pmc/articles/PMC6307590/ /pubmed/30613420 http://dx.doi.org/10.1136/lupus-2018-000297 Text en © Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0
spellingShingle Review
Anjorin, Aderike
Lipsky, Peter
Engaging African ancestry participants in SLE clinical trials
title Engaging African ancestry participants in SLE clinical trials
title_full Engaging African ancestry participants in SLE clinical trials
title_fullStr Engaging African ancestry participants in SLE clinical trials
title_full_unstemmed Engaging African ancestry participants in SLE clinical trials
title_short Engaging African ancestry participants in SLE clinical trials
title_sort engaging african ancestry participants in sle clinical trials
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307590/
https://www.ncbi.nlm.nih.gov/pubmed/30613420
http://dx.doi.org/10.1136/lupus-2018-000297
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