TY - JOUR
T1 - Postencephalitic Parkinsonism
T2 - Unique Pathological and Clinical Features—Preliminary Data
AU - Strobel, Sabrina
AU - Sian-Hulsmann, Jeswinder
AU - Tappe, Dennis
AU - Jellinger, Kurt
AU - Riederer, Peter
AU - Monoranu, Camelia Maria
PY - 2024/9
Y1 - 2024/9
N2 - Postencephalitic parkinsonism (PEP) is suggested to show a virus-induced pathology, which is different from classical idiopathic Parkinson’s disease (PD) as there is no α-synuclein/Lewy body pathology. However, PEP shows a typical clinical representation of motor disturbances. In addition, compared to PD, there is no iron-induced pathology. The aim of this preliminary study was to compare PEP with PD regarding iron-induced pathology, using histochemistry methods on paraffin-embedded post-mortem brain tissue. In the PEP group, iron was not seen, except for one case with sparse perivascular depositions. Rather, PEP offers a pathology related to tau-protein/neurofibrillary tangles, with mild to moderate memory deficits only. It is assumed that this virus-induced pathology is due to immunological dysfunctions causing (neuro)inflammation-induced neuronal network disturbances as events that trigger clinical parkinsonism. The absence of iron deposits implies that PEP cannot be treated with iron chelators. The therapy with L-Dopa is also not an option, as L-Dopa only leads to an initial slight improvement in symptoms in isolated cases.
AB - Postencephalitic parkinsonism (PEP) is suggested to show a virus-induced pathology, which is different from classical idiopathic Parkinson’s disease (PD) as there is no α-synuclein/Lewy body pathology. However, PEP shows a typical clinical representation of motor disturbances. In addition, compared to PD, there is no iron-induced pathology. The aim of this preliminary study was to compare PEP with PD regarding iron-induced pathology, using histochemistry methods on paraffin-embedded post-mortem brain tissue. In the PEP group, iron was not seen, except for one case with sparse perivascular depositions. Rather, PEP offers a pathology related to tau-protein/neurofibrillary tangles, with mild to moderate memory deficits only. It is assumed that this virus-induced pathology is due to immunological dysfunctions causing (neuro)inflammation-induced neuronal network disturbances as events that trigger clinical parkinsonism. The absence of iron deposits implies that PEP cannot be treated with iron chelators. The therapy with L-Dopa is also not an option, as L-Dopa only leads to an initial slight improvement in symptoms in isolated cases.
KW - cognitive disturbances
KW - iron pathology
KW - Lewy bodies
KW - neurofibrillary tangles
KW - Parkinson’s disease
KW - postencephalitic parkinsonism
KW - tau protein
KW - α-synuclein
U2 - 10.3390/cells13181511
DO - 10.3390/cells13181511
M3 - Journal article
C2 - 39329695
AN - SCOPUS:85205151577
SN - 2073-4409
VL - 13
JO - Cells
JF - Cells
IS - 18
M1 - 1511
ER -