Javascript must be enabled to continue!
Sex differences in LRRK2 G2019S and idiopathic Parkinson's Disease
View through CrossRef
AbstractObjectiveTo evaluate sex differences and the relative effect of G2019S LRRK2 mutations in Parkinson's disease (PD).Methods530 LRRK2 PD carriers and 759 noncarrier PD (idiopathic, IPD) evaluated as part of the Fox Foundation (MJFF) Consortium were included. All participants completed a study visit including information on clinical features, treatment, examination, and motor and nonmotor questionnaires. Clinical features were compared between men and women separately for IPD and LRRK2 PD; and features were compared between IPD and LRRK2 PD separately for men and women.ResultsAmong IPD: men had higher levodopa equivalency dose (LED), worse activities of daily living and motoric severity but lower complications of therapy (UPDRS‐IV). IPD women had higher olfaction and thermoregulatory scores and were more likely to report family history of PD. Among LRRK2 PD: Male predominance was not observed among G2019S LRRK2 cases. Women had worse UPDRS‐IV but better olfaction. Among same sex: LRRK2 men and women had better olfaction than IPD counterparts. LRRK2 men demonstrated lower motor and higher cognitive, RBD and thermoregulation scores than IPD men and LRRK2 women had greater UDPRS‐IV and rates of dyskinesia.InterpretationThere were clinical differences between sexes with a more severe phenotype in IPD men and more complications of therapy in women. The more severe male phenotype was moderated by LRRK2, with LRRK2 men and women showing less diversity of phenotype. Our study supports that both genetics and sex drive phenotype, and thus trials in LRRK2 and IPD should consider gender stratification in design or analysis.
Title: Sex differences in LRRK2 G2019S and idiopathic Parkinson's Disease
Description:
AbstractObjectiveTo evaluate sex differences and the relative effect of G2019S LRRK2 mutations in Parkinson's disease (PD).
Methods530 LRRK2 PD carriers and 759 noncarrier PD (idiopathic, IPD) evaluated as part of the Fox Foundation (MJFF) Consortium were included.
All participants completed a study visit including information on clinical features, treatment, examination, and motor and nonmotor questionnaires.
Clinical features were compared between men and women separately for IPD and LRRK2 PD; and features were compared between IPD and LRRK2 PD separately for men and women.
ResultsAmong IPD: men had higher levodopa equivalency dose (LED), worse activities of daily living and motoric severity but lower complications of therapy (UPDRS‐IV).
IPD women had higher olfaction and thermoregulatory scores and were more likely to report family history of PD.
Among LRRK2 PD: Male predominance was not observed among G2019S LRRK2 cases.
Women had worse UPDRS‐IV but better olfaction.
Among same sex: LRRK2 men and women had better olfaction than IPD counterparts.
LRRK2 men demonstrated lower motor and higher cognitive, RBD and thermoregulation scores than IPD men and LRRK2 women had greater UDPRS‐IV and rates of dyskinesia.
InterpretationThere were clinical differences between sexes with a more severe phenotype in IPD men and more complications of therapy in women.
The more severe male phenotype was moderated by LRRK2, with LRRK2 men and women showing less diversity of phenotype.
Our study supports that both genetics and sex drive phenotype, and thus trials in LRRK2 and IPD should consider gender stratification in design or analysis.
Related Results
Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Objective: To determine the frequency of common chromosomal aberrations in local population idiopathic determine the frequency of common chromosomal aberrations in local population...
Clinical profiles and outcomes of deep brain stimulation in G2019S LRRK2 Parkinson disease
Clinical profiles and outcomes of deep brain stimulation in G2019S LRRK2 Parkinson disease
OBJECTIVE
The objective of this study was to evaluate clinical features and response to deep brain stimulation (DBS) in G2019S LRRK2-Parkinson disease (LRRK2-PD) and idiopathic PD ...
Membrane traffic defects in Parkinson's disease
Membrane traffic defects in Parkinson's disease
Défauts de trafic membranaire dans la maladie de Parkinson
La maladie de Parkinson (MP) est une maladie neurodégénérative progressive caractérisée par la mort de ne...
Multiple sclerosis in LRRK2 G2019S Parkinson’s disease and isolated nigral degeneration in a homozygous variant carrier
Multiple sclerosis in LRRK2 G2019S Parkinson’s disease and isolated nigral degeneration in a homozygous variant carrier
BackgroundLRRK2 variants have been associated with immune dysregulation as well as immune-related disorders such as IBD. A possible relationship between multiple sclerosis (MS) and...
Fluctuation Imaging of LRRK2 Reveals that the G2019S Mutation Alters Spatial and Membrane Dynamics
Fluctuation Imaging of LRRK2 Reveals that the G2019S Mutation Alters Spatial and Membrane Dynamics
Mutations within the Leucine-Rich Repeat Kinase 2 (LRRK2) gene are the most common genetic cause of autosomal and sporadic Parkinson’s disease (PD). LRRK2 is a large multidomain ki...
LRRK2
expression in normal and pathologic human gut and in rodent enteric neural cell lines
LRRK2
expression in normal and pathologic human gut and in rodent enteric neural cell lines
Abstract
Leucine‐rich repeat kinase 2 (LRRK2)
gene, which is the gene most commonly associated with Parkinson's disease (...
LRRK2/LRRK1 interactions modulate Rab7 activity and inhibit lysosomal exocytosis
LRRK2/LRRK1 interactions modulate Rab7 activity and inhibit lysosomal exocytosis
Abstract
Mutations in the
LRRK2
gene are the most common genetic cause of both familial and sporadic Parkinso...
LRRK2 in Infection:
Friend or Foe?
LRRK2 in Infection:
Friend or Foe?
Abstract
In the field of Parkinson’s disease (PD) research, leucine-rich repeat kinase 2 (LRRK2) remains one of the most enigmatic kinases. LRRK2 pathogenic mutat...

