The discussion of subgroups is important. "Subtypes" seems an
equivalent word (1). Much subgroup research is occurring. FFindings
in cite 8 surprised me. Several subtype cites have already been
posted. The HU pd list will remain fragmented on this topic if and
as individuals keep changing the topic name when subgroups/subtypes
are the person's topic. The topic could become a questionnaire.
Several moderators could screen for topic-related posts and log
them. Is the four-vector subgrouping sufficient? I think not.
1: A
clinico-pathological study of subtypes in Parkinson's disease.
Brain.
2009 Nov;132(Pt 11):2947-57.
academic.oup.com/brain/arti...
2: Rest
tremor revisited: Parkinson's disease and other disorders.
Transl
Neurodegener 2017 Jun 16;6:16.
ncbi.nlm.nih.gov/pubmed/286...
3: Lower
levels of uric acid and striatal dopamine in non-tremor dominant
Parkinson's disease subtype.
PLoS One 2017 Mar
30;12(3):e0174644.
ncbi.nlm.nih.gov/pubmed/283...
4: Common
variant rs356182 near SNCA defines a Parkinson's disease
endophenotype.
Ann Clin Transl Neurol 2016 Nov 25;4(1):15-25.
ncbi.nlm.nih.gov/pubmed/280...
5: Neuropathological
and genetic correlates of survival and dementia onset in
synucleinopathies: a retrospective analysis.
Lancet Neurol
2017 Jan;16(1):55-65.
ncbi.nlm.nih.gov/pubmed/279...
6: A
Personalized Approach to Parkinson's Disease Patients Based on
Founder Mutation Analysis.
Front Neurol
2016 May 10;7:71.
ncbi.nlm.nih.gov/pubmed/272...
7: Genetic
Architecture of MAPT Gene Region in Parkinson Disease Subtypes.
Front
Cell Neurosci 2016 Apr 11;10:96.
ncbi.nlm.nih.gov/pubmed/271...
8. CSF
biomarkers associated with disease heterogeneity in early
Parkinson's disease: the Parkinson's Progression Markers
Initiative study.
Kang JH, Mollenhauer B, Coffey CS, Toledo JB, Weintraub D, Galasko
DR, Irwin DJ, Van Deerlin V, Chen-Plotkin AS, Caspell-Garcia C,
Waligórska T, Taylor P, Shah N, Pan S, Zero P, Frasier M, Marek K,
Kieburtz K, Jennings D, Tanner CM, Simuni T, Singleton A, Toga AW,
Chowdhury S, Trojanowski JQ, Shaw LM; Parkinson’s Progression Marker
Initiative.
Acta Neuropathol
2016 Jun;131(6):935-49.
ncbi.nlm.nih.gov/pubmed/270...
"The level of α-syn, but not other biomarkers, was significantly
lower in PD patients with non-tremor-dominant phenotype compared
with tremor-dominant phenotype. In addition, in PD patients the
lowest Aβ1-42, or highest t-tau/Aβ1-42 and t-tau/α-syn quintile in
PD patients were associated with more severe non-motor dysfunction
compared with the highest or lowest quintiles, respectively. In a
multivariate regression model, lower α-syn was significantly
associated with worse cognitive test performance. APOE ε4 genotype
was associated with lower levels of Aβ1-42, but neither with PD
diagnosis nor cognition."
9: Biomarker-driven
phenotyping in Parkinson's disease: A translational missing link
in disease-modifying clinical trials.
Espay AJ et al: Mov Disord
2017 Mar;32(3):319-324.
ncbi.nlm.nih.gov/pubmed/282...
10: Longitudinal
whole-brain atrophy and ventricular enlargement in nondemented
Parkinson's disease.
Neurobiol Aging
2017 Jul;55:78-90.
ncbi.nlm.nih.gov/pubmed/284...
11: Modelling
idiopathic Parkinson disease as a complex illness can inform
incidence rate in healthy adults: the PR EDIGT score.
Eur
J Neurosci. 2017 Jan;45(1):175-191.
ncbi.nlm.nih.gov/pubmed/278...
"Fifty-five years after the concept of dopamine replacement therapy
was introduced, Parkinson disease (PD) remains an incurable
neurological disorder. To date, no disease-modifying therapeutic has
been approved. The inability to predict PD incidence risk in healthy
adults is seen as a limitation in drug development, because by the
time of clinical diagnosis ≥ 60% of dopamine neurons have been lost.
We have designed an incidence prediction model founded on the
concept that the pathogenesis of PD is similar to that of many
disorders observed in ageing humans, i.e. a complex, multifactorial
disease. Our model considers five factors...."
12: Cerebrospinal
Fluid Amyloid β1-42, Tau, and Alpha-Synuclein Predict the
Heterogeneous Progression of Cognitive Dysfunction in Parkinson's
Disease.
J Mov
Disord 2016 May;9(2):89-96.
ncbi.nlm.nih.gov/pubmed/272...
13: Parkinson's
Disease: Assay of Phosphorylated α-Synuclein in Skin Biopsy for
Early Diagnosis and Association with Melanoma.
Brain Sci 2016 May
26;6(2). pii: E17.
ncbi.nlm.nih.gov/pubmed/272...
14: Age at
onset and Parkinson disease phenotype.
Neurology 2016 Apr
12;86(15):1400-7.
ncbi.nlm.nih.gov/pubmed/268...
15: Association
of Parkinson's Disease and Its Subtypes with Agricultural
Pesticide Exposures in Men: A Case-Control Study in France.
Environ
Health Perspect. 2015 Nov;123(11):1123-9.
ncbi.nlm.nih.gov/pubmed/258...
16: Models
of α-synuclein aggregation in Parkinson's disease.
Acta
Neuropathol Commun 2014 Dec 13;2:176.
ncbi.nlm.nih.gov/pubmed/254...
17: Neural
substrates of cognitive subtypes in Parkinson's disease: a 3-year
longitudinal study.
PLoS One 2014 Oct
20;9(10):e110547.
ncbi.nlm.nih.gov/pubmed/253...
18: Visual
dysfunction in Parkinson's disease.
Brain
2016 Jul 13. pii: aww175.
ncbi.nlm.nih.gov/pubmed/274...
19: Co-morbidity
and polypharmacy in Parkinson's disease: insights from a large
Scottish primary care database.
McLean G, Hindle JV, Guthrie B, Mercer SW.
BMC Neurol 2017 Jul
1;17(1):126.
ncbi.nlm.nih.gov/pubmed/286...
"Parkinson's disease is associated with substantial physical and
mental co-morbidity. Polypharmacy is also a significant issue due to
the complex nature of the disease and associated treatments."