TY - JOUR
T1 - Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry
AU - for the Michael J. Fox LRRK2 Cohort Consortium
AU - Lee, Annie J.
AU - Wang, Yuanjia
AU - Alcalay, Roy N.
AU - Mejia-Santana, Helen
AU - Saunders-Pullman, Rachel
AU - Bressman, Susan
AU - Corvol, Jean Christophe
AU - Brice, Alexis
AU - Lesage, Suzanne
AU - Mangone, Graziella
AU - Tolosa, Eduardo
AU - Pont-Sunyer, Claustre
AU - Vilas, Dolores
AU - Schüle, Birgitt
AU - Kausar, Farah
AU - Foroud, Tatiana
AU - Berg, Daniela
AU - Brockmann, Kathrin
AU - Goldwurm, Stefano
AU - Siri, Chiara
AU - Asselta, Rosanna
AU - Ruiz-Martinez, Javier
AU - Mondragón, Elisabet
AU - Marras, Connie
AU - Ghate, Taneera
AU - Giladi, Nir
AU - Mirelman, Anat
AU - Marder, Karen
N1 - Publisher Copyright:
© 2017 Internationalnternational Parkinson and Movement Disorder Society
PY - 2017/10/1
Y1 - 2017/10/1
N2 - Background: Penetrance estimates of the leucine-rich repeat kinase 2 (LRRK2) p.G2019S mutation for PD vary widely (24%-100%). The p.G2019S penetrance in individuals of Ashkenazi Jewish ancestry has been estimated as 25%, adjusted for multiple covariates. It is unknown whether penetrance varies among different ethnic groups. The objective of this study was to estimate the penetrance of p.G2019S in individuals of non-Ashkenazi Jewish ancestry and compare penetrance between Ashkenazi Jews and non-Ashkenazi Jews to age 80. Methods: The kin-cohort method was used to estimate penetrance in 474 first-degree relatives of 69 non-Ashkenazi Jewish LRRK2 p.G2019S carrier probands at 8 sites from the Michael J. Fox LRRK2 Cohort Consortium. An identical validated family history interview was administered to assess age at onset of PD, current age, or age at death for relatives in different ethnic groups at each site. Neurological examination and LRRK2 genotype of relatives were included when available. Results: Risk of PD in non-Ashkenazi Jewish relatives who carry a LRRK2 p.G2019S mutation was 42.5% (95% confidence interval [CI]: 26.3%-65.8%) to age 80, which is not significantly higher than the previously estimated 25% (95% CI: 16.7%-34.2%) in Ashkenazi Jewish carrier relatives. The penetrance of PD to age 80 in LRRK2 p.G2019S mutation carrier relatives was significantly higher than the noncarrier relatives, as seen in Ashkenazi Jewish relatives. Conclusions: The similar penetrance of LRRK2 p.G2019S estimated in Ashkenazi Jewish carriers and non-Ashkenazi Jewish carriers confirms that p.G2019S penetrance is 25% to 42.5% at age 80 in all populations analyzed.
AB - Background: Penetrance estimates of the leucine-rich repeat kinase 2 (LRRK2) p.G2019S mutation for PD vary widely (24%-100%). The p.G2019S penetrance in individuals of Ashkenazi Jewish ancestry has been estimated as 25%, adjusted for multiple covariates. It is unknown whether penetrance varies among different ethnic groups. The objective of this study was to estimate the penetrance of p.G2019S in individuals of non-Ashkenazi Jewish ancestry and compare penetrance between Ashkenazi Jews and non-Ashkenazi Jews to age 80. Methods: The kin-cohort method was used to estimate penetrance in 474 first-degree relatives of 69 non-Ashkenazi Jewish LRRK2 p.G2019S carrier probands at 8 sites from the Michael J. Fox LRRK2 Cohort Consortium. An identical validated family history interview was administered to assess age at onset of PD, current age, or age at death for relatives in different ethnic groups at each site. Neurological examination and LRRK2 genotype of relatives were included when available. Results: Risk of PD in non-Ashkenazi Jewish relatives who carry a LRRK2 p.G2019S mutation was 42.5% (95% confidence interval [CI]: 26.3%-65.8%) to age 80, which is not significantly higher than the previously estimated 25% (95% CI: 16.7%-34.2%) in Ashkenazi Jewish carrier relatives. The penetrance of PD to age 80 in LRRK2 p.G2019S mutation carrier relatives was significantly higher than the noncarrier relatives, as seen in Ashkenazi Jewish relatives. Conclusions: The similar penetrance of LRRK2 p.G2019S estimated in Ashkenazi Jewish carriers and non-Ashkenazi Jewish carriers confirms that p.G2019S penetrance is 25% to 42.5% at age 80 in all populations analyzed.
KW - LRRK2
KW - Parkinson's disease
KW - penetrance
UR - http://www.scopus.com/inward/record.url?scp=85021200907&partnerID=8YFLogxK
U2 - 10.1002/mds.27059
DO - 10.1002/mds.27059
M3 - Article
AN - SCOPUS:85021200907
SN - 0885-3185
VL - 32
SP - 1432
EP - 1438
JO - Movement Disorders
JF - Movement Disorders
IS - 10
ER -