TY - JOUR
T1 - The Black and African American Connections to Parkinson’s Disease (BLAAC PD) study protocol
AU - the BLAAC PD Study and the Global Parkinson’s Genetics Program (GP2)
AU - Chahine, Lana M.
AU - Louie, Naomi
AU - Solle, J.
AU - Akçimen, Fulya
AU - Ameri, Andrew
AU - Augenbraun, Samantha
AU - Avripas, Sabrina
AU - Breaux, Sarah
AU - Causey, Christopher
AU - Chandra, Shivika
AU - Dean, Marissa
AU - Disbrow, Elizabeth A.
AU - Fanty, Lauren
AU - Fernandez, Jessica
AU - Voegtli, Erin
AU - Furr Stimming, Erin
AU - Hall, Deborah
AU - Hinson, Vanessa
AU - Johnson-Turbes, Ashani
AU - Jonas, Cabell
AU - Kilbane, Camilla
AU - Norris, Scott
AU - Nguyen, Bao Tran
AU - Padmanaban, Mahesh
AU - Paquette, Kimberly
AU - Parry, Carly
AU - Pessoa Rocha, Natalia
AU - Rawls, Ashley
AU - Shamim, Ejaz A.
AU - Shulman, Lisa M.
AU - Sipma, Rebeka
AU - Staisch, Julia
AU - Traurig, Rami
AU - von Coelln, Rainer
AU - Wild Crea, Peter
AU - Xie, Tao
AU - Fang, Zih Hua
AU - O’Grady, Alyssa
AU - Kopil, Catherine M.
AU - McGuire Kuhl, Maggie
AU - Singleton, Andrew
AU - Blauwendraat, Cornelis
AU - Bandres-Ciga, Sara
AU - Parker, Tanya
AU - Baker, Debbie
AU - Clark, Karen
AU - Alessi-Fox, Christi
AU - Kostrzebski, Melissa
AU - Abdollah Zadegan, Shayan
AU - Woodhouse, Dominique
AU - Williamson, Jared
AU - Williams, Mackenzie
AU - Weimer, Rebecca
AU - Volcy, Magdaline
AU - Vanegas, Jacqueline
AU - Valdez, Olga
AU - Thomas-Dean, Fermine
AU - Thompson, Kristin
AU - Thomas, Hannah
AU - Thomas, Dominique
AU - Terrell, Eileen
AU - Smith, Van
AU - Smith, Jenna
AU - Senette, Terrelle
AU - Sajewski, Kailey
AU - Ruffrage, Lauren
AU - Rosenbaum, Marc
AU - Chamorro, Andrea Rosado
AU - Robinson, Christina
AU - Rizer, Kyle
AU - Richardson, Joseph
AU - Peters, Alexandra
AU - Patel, Davina
AU - Parker, James Ryan
AU - Mesaros, Maysen
AU - Mercado, Crystal
AU - Marathonitis, Sophia
AU - Levenes, Elsa
AU - Krinickas, Nathan
AU - Hudson, Jessica
AU - Hines, Joshua
AU - Heliste, Jennifer
AU - Hawkins, Ashley
AU - Griffin, Christina
AU - Guilluly, Hanna
AU - Franklin, Tenisha
AU - Foli, Randy
AU - Flowers, Jennifer
AU - Delaune, Mariah
AU - Davis, Kandace
AU - Crovetto, Nicolle
AU - Cromer, Candace
AU - Chauppetta, Brian
AU - Bonano, Aidan
AU - Bean, Myeshia
AU - Baskin, Lynae
AU - Toms, Jamie
AU - Tholanikunnel, Tracy
AU - Standaert, David
AU - Kelley, Roger
AU - Javalkar, Vijayakumar
AU - Elkasaby, Mohamed
AU - Coleman, Juliana
AU - Alfradique-Dunham, Isabel
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12
Y1 - 2024/12
N2 - Determining the genetic contributions to Parkinson’s disease (PD) across diverse ancestries is a high priority as this work can guide therapeutic development in a global setting. The genetics of PD spans the etiological risk spectrum, from rare, highly deleterious variants linked to monogenic forms with Mendelian patterns of inheritance, to common variation involved in sporadic disease. A major limitation in PD genomics research is lack of racial and ethnic diversity. Enrollment disparities have detrimental consequences on the generalizability of results and exacerbate existing inequities in care. The Black and African American Connections to Parkinson’s Disease (BLAAC PD) study is part of the Global Parkinson’s Genetics Program, supported by the Aligning Science Across Parkinson’s initiative. The goal of the study is to investigate the genetic architecture underlying PD risk and progression in the Black and/or African American populations. This cross-sectional multicenter study in the United States has a recruitment target of up to 2,000 individuals with PD and up to 2,000 controls, all of Black and/or African American ancestry. The study design incorporates several strategies to reduce barriers to research participation. The multifaceted recruitment strategy aims to involve individuals with and without PD in various settings, emphasizing community outreach and engagement. The BLAAC PD study is an important first step toward informing understanding of the genetics of PD in a more diverse population.
AB - Determining the genetic contributions to Parkinson’s disease (PD) across diverse ancestries is a high priority as this work can guide therapeutic development in a global setting. The genetics of PD spans the etiological risk spectrum, from rare, highly deleterious variants linked to monogenic forms with Mendelian patterns of inheritance, to common variation involved in sporadic disease. A major limitation in PD genomics research is lack of racial and ethnic diversity. Enrollment disparities have detrimental consequences on the generalizability of results and exacerbate existing inequities in care. The Black and African American Connections to Parkinson’s Disease (BLAAC PD) study is part of the Global Parkinson’s Genetics Program, supported by the Aligning Science Across Parkinson’s initiative. The goal of the study is to investigate the genetic architecture underlying PD risk and progression in the Black and/or African American populations. This cross-sectional multicenter study in the United States has a recruitment target of up to 2,000 individuals with PD and up to 2,000 controls, all of Black and/or African American ancestry. The study design incorporates several strategies to reduce barriers to research participation. The multifaceted recruitment strategy aims to involve individuals with and without PD in various settings, emphasizing community outreach and engagement. The BLAAC PD study is an important first step toward informing understanding of the genetics of PD in a more diverse population.
KW - African admixed
KW - African American ancestry
KW - Genetics
KW - Parkinson’s disease
KW - Racial health disparities
KW - Risk
UR - http://www.scopus.com/inward/record.url?scp=85206962500&partnerID=8YFLogxK
U2 - 10.1186/s12883-024-03914-7
DO - 10.1186/s12883-024-03914-7
M3 - Article
C2 - 39434044
AN - SCOPUS:85206962500
SN - 1471-2377
VL - 24
JO - BMC Neurology
JF - BMC Neurology
IS - 1
M1 - 403
ER -