Ethnic Variation in the Manifestation of Parkinson’s Disease: A Narrative Review DOI Creative Commons
Aaron Ben-Joseph, Charles R. Marshall, Andrew J. Lees

et al.

Journal of Parkinson s Disease, Journal Year: 2019, Volume and Issue: 10(1), P. 31 - 45

Published: Dec. 17, 2019

The global prevalence of Parkinson's disease is increasing, yet the characteristics, risk factors and genetics PD in Black, Asian Hispanic populations little understood.In this paper we review published literature on clinical variation symptoms signs different ethnic groups responses to treatment.We included any study that sampled patients with from distinct backgrounds.We conclude whilst there evidence for features disease, are substantial limitations gaps current literature, which mean does necessarily not fit observation.Possible explanations expected differences manifestation include genetic determinants, co-existence cerebrovascular and/or Alzheimer's pathology, healthcare inequalities socio-cultural factors.

Language: Английский

Parkinson's disease DOI
Bastiaan R. Bloem, Michael S. Okun, Christine Klein

et al.

The Lancet, Journal Year: 2021, Volume and Issue: 397(10291), P. 2284 - 2303

Published: April 11, 2021

Language: Английский

Citations

2162

Diagnosis and Treatment of Parkinson Disease DOI
Melissa J. Armstrong, Michael S. Okun

JAMA, Journal Year: 2020, Volume and Issue: 323(6), P. 548 - 548

Published: Feb. 11, 2020

Importance

Parkinson disease is the most common form of parkinsonism, a group neurological disorders with disease–like movement problems such as rigidity, slowness, and tremor. More than 6 million individuals worldwide have disease.

Observations

Diagnosis based on history examination. History can include prodromal features (eg, rapid eye sleep behavior disorder, hyposmia, constipation), characteristic difficulty tremor, stiffness, slowness), psychological or cognitive decline, depression, anxiety). Examination typically demonstrates bradykinesia both. Dopamine transporter single-photon emission computed tomography improve accuracy diagnosis when presence parkinsonism uncertain. has multiple variants different prognoses. Individuals diffuse malignant subtype (9%-16% disease) prominent early motor nonmotor symptoms, poor response to medication, faster progression. mild motor-predominant (49%-53% good dopaminergic medications carbidopa-levodopa, dopamine agonists), slower Other an intermediate subtype. For all patients disease, treatment symptomatic, focused improvement in bradykinesia) constipation, cognition, mood, sleep) signs symptoms. No disease-modifying pharmacologic treatments are available. Dopamine-based therapies help initial Nonmotor symptoms require nondopaminergic approaches selective serotonin reuptake inhibitors for psychiatric cholinesterase cognition). Rehabilitative therapy exercise complement treatments. experiencing complications, worsening functional impairment medication dose wears off ("off periods"), medication-resistant dyskinesias, benefit from advanced levodopa-carbidopa enteral suspension deep brain stimulation. Palliative care part management.

Conclusions Relevance

heterogeneous rapidly slowly progressive forms. Treatment involves (typically levodopa preparations prescribed without other medications) nonpharmacologic (such physical, occupational, speech therapies). Approaches stimulation off, dyskinesias.

Language: Английский

Citations

2087

Parkinson’s disease: etiopathogenesis and treatment DOI Open Access
Joseph Jankovic,

Eng King Tan

Journal of Neurology Neurosurgery & Psychiatry, Journal Year: 2020, Volume and Issue: 91(8), P. 795 - 808

Published: June 23, 2020

The concept of ‘idiopathic’ Parkinson’s disease (PD) as a single entity has been challenged with the identification several clinical subtypes, pathogenic genes and putative causative environmental agents. In addition to classic motor symptoms, non-motor manifestations (such rapid eye movement sleep disorder, anosmia, constipation depression) appear at prodromic/premotor stage evolve, along cognitive impairment dysautonomia, progresses, often dominating advanced stages disease. key molecular mechanisms include α-synuclein misfolding aggregation, mitochondrial dysfunction, protein clearance (associated deficient ubiquitin-proteasome autophagy-lysosomal systems), neuroinflammation oxidative stress. involvement dopaminergic well noradrenergic, glutamatergic, serotonergic adenosine pathways provide insights into rich variable phenomenology associated PD possibility alternative therapeutic approaches beyond traditional dopamine replacement therapies. One biggest challenges in development potential neuroprotective therapies lack reliable sensitive biomarkers progression. Immunotherapies such use vaccination or monoclonal antibodies directed against aggregated, toxic α-synuclein.as anti-aggregation strategies are currently investigated trials. application glucagon-like peptide one receptor agonists, specific gene target agents GBA LRRK2 modifiers) other modifying drugs cautious optimism that more effective on horizon. Emerging therapies, new symptomatic drugs, innovative drug delivery systems novel surgical interventions give hope patients about their future outcomes prognosis.

Language: Английский

Citations

785

Parkinson disease-associated cognitive impairment DOI Open Access
Dag Aarsland, Lucia Batzu, Glenda M. Halliday

et al.

Nature Reviews Disease Primers, Journal Year: 2021, Volume and Issue: 7(1)

Published: July 1, 2021

Language: Английский

Citations

779

New evidence on the management of Lewy body dementia DOI
John‐Paul Taylor, Ian G. McKeith, David J. Burn

et al.

The Lancet Neurology, Journal Year: 2019, Volume and Issue: 19(2), P. 157 - 169

Published: Sept. 10, 2019

Language: Английский

Citations

267

Microbiota Composition and Metabolism Are Associated With Gut Function in Parkinson's Disease DOI
Mihai Cirstea, Adam C. Yu,

Ella Golz

et al.

Movement Disorders, Journal Year: 2020, Volume and Issue: 35(7), P. 1208 - 1217

Published: May 1, 2020

Abstract Background Parkinson's disease is characterized by a high burden of gastrointestinal comorbidities, especially constipation and reduced colonic transit time, gut microbiota alterations. The diverse metabolites produced the are broadly relevant to host health. How composition metabolism relate function in largely unknown. objectives current study were assesses associations between composition, stool consistency, constipation, systemic microbial better understand how intestinal microbes contribute disturbances commonly observed patients. Methods Three hundred participants (197 patients 103 controls) recruited for this cross‐sectional cohort study. Participants supplied fecal samples sequencing (n = 300) serum untargeted metabolomics 125). Data collected on motor nonmotor symptoms, medications, diet, demographics. Results Significant taxonomic differences patients, even when controlling function. was carbohydrate fermentation butyrate synthesis capacity increased proteolytic production deleterious amino acid metabolites, including p‐cresol phenylacetylglutamine. Taxonomic shifts elevated strongly associated with consistency (a proxy time) among Conclusions Compositional metabolic alterations highly function, suggesting plausible mechanistic links altered bacterial health disease. detection suggests mechanism whereby dysbiosis contributes etiology pathophysiology. © 2020 International Parkinson Movement Disorder Society

Language: Английский

Citations

247

Sleep in Parkinson’s disease DOI Open Access
Ambra Stefani, Birgit Högl

Neuropsychopharmacology, Journal Year: 2019, Volume and Issue: 45(1), P. 121 - 128

Published: June 24, 2019

Language: Английский

Citations

200

Treatment Options for Motor and Non-Motor Symptoms of Parkinson’s Disease DOI Creative Commons
Frank Church

Biomolecules, Journal Year: 2021, Volume and Issue: 11(4), P. 612 - 612

Published: April 20, 2021

Parkinson’s disease (PD) usually presents in older adults and typically has both motor non-motor dysfunctions. PD is a progressive neurodegenerative disorder resulting from dopaminergic neuronal cell loss the mid-brain substantia nigra pars compacta region. Outlined here an integrative medicine health strategy that highlights five treatment options for people with (PwP): rehabilitate, therapy, restorative, maintenance, surgery. Rehabilitating begins following diagnosis throughout any additional processes, especially vis-à-vis consulting physical, occupational, and/or speech pathology therapist(s). Therapy uses daily administration of either dopamine precursor levodopa (with carbidopa) or agonist, compounds preserve residual dopamine, other specific motor/non-motor-related compounds. Restorative strenuous aerobic exercise programs can be neuroprotective. Maintenance complementary alternative substances potentially support protect brain microenvironment. Finally, surgery, including deep stimulation, pursued when PwP fail to respond positively options. There currently no cure PD. In conclusion, best treating hope slow progression strive achieve stability neuroprotection. The ultimate goal management program improve quality-of-life person disease.

Language: Английский

Citations

171

Sex differences in movement disorders DOI
Sara Meoni, Antonella Macerollo, Elena Moro

et al.

Nature Reviews Neurology, Journal Year: 2020, Volume and Issue: 16(2), P. 84 - 96

Published: Jan. 3, 2020

Language: Английский

Citations

162

Probiotics for Constipation in Parkinson Disease DOI
Ai Huey Tan, Shen‐Yang Lim, Kah Kian Chong

et al.

Neurology, Journal Year: 2020, Volume and Issue: 96(5)

Published: Oct. 13, 2020

To determine whether probiotics are effective for constipation, a common and often difficult-to-treat problem, in Parkinson disease (PD).

Language: Английский

Citations

161