Premium
Dissecting the Phenotype and Genotype of PLA2G6 ‐Related Parkinsonism
Author(s) -
Magrinelli Francesca,
Mehta Sahil,
Di Lazzaro Giulia,
Latorre Anna,
Edwards Mark J.,
Balint Bettina,
Basu Purba,
Kobylecki Christopher,
Groppa Sergiu,
Hegde Anaita,
Mulroy Eoin,
EstevezFraga Carlos,
Arora Anshita,
Kumar Hrishikesh,
Schneider Susanne A.,
Lewis Patrick A.,
Jaunmuktane Zane,
Revesz Tamas,
Gandhi Sonia,
Wood Nicholas W.,
Hardy John A.,
Tinazzi Michele,
Lal Vivek,
Houlden Henry,
Bhatia Kailash P.
Publication year - 2022
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.28807
Subject(s) - parkinsonism , dystonia , medicine , neurodegeneration , movement disorders , levodopa , myoclonus , parkinson's disease , neuroscience , pathology , pediatrics , psychology , disease , psychiatry
Background Complex parkinsonism is the commonest phenotype in late‐onset PLA2G6 ‐associated neurodegeneration. Objectives The aim of this study was to deeply characterize phenogenotypically PLA2G6 ‐related parkinsonism in the largest cohort ever reported. Methods We report 14 new cases of PLA2G6 ‐related parkinsonism and perform a systematic literature review. Results PLA2G6 ‐related parkinsonism shows a fairly distinct phenotype based on 86 cases from 68 pedigrees. Young onset (median age, 23.0 years) with parkinsonism/dystonia, gait/balance, and/or psychiatric/cognitive symptoms were common presenting features. Dystonia occurred in 69.4%, pyramidal signs in 77.2%, myoclonus in 65.2%, and cerebellar signs in 44.6% of cases. Early bladder overactivity was present in 71.9% of cases. Cognitive impairment affected 76.1% of cases and psychiatric features 87.1%, the latter being an isolated presenting feature in 20.1%. Parkinsonism was levodopa responsive but complicated by early, often severe dyskinesias. Five patients benefited from deep brain stimulation. Brain magnetic resonance imaging findings included cerebral (49.3%) and/or cerebellar (43.2%) atrophy, but mineralization was evident in only 28.1%. Presynaptic dopaminergic terminal imaging was abnormal in all where performed. Fifty‐four PLA2G6 mutations have hitherto been associated with parkinsonism, including four new variants reported in this article. These are mainly nontruncating, which may explain the phenotypic heterogeneity of childhood‐ and late‐onset PLA2G6 ‐associated neurodegeneration. In five deceased patients, median disease duration was 13.0 years. Brain pathology in three cases showed mixed Lewy and tau pathology. Conclusions Biallelic PLA2G6 mutations cause early‐onset parkinsonism associated with dystonia, pyramidal and cerebellar signs, myoclonus, and cognitive impairment. Early psychiatric manifestations and bladder overactivity are common. Cerebro/cerebellar atrophy are frequent magnetic resonance imaging features, whereas brain iron deposition is not. Early, severe dyskinesias are a tell‐tale sign. © 2021 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society