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Record W2297719908 · doi:10.1111/jgs.14001

Mild Cognitive Impairment as the Initial Manifestation of Progressive Supranuclear Palsy

2016· letter· en· W2297719908 on OpenAlexaboutno aff
Tsuyoshi Ogata, Ryuji Sakakibara, Fuyuki Tateno, Yohei Tsuyusaki, Hiromi Tateno, Yosuke Aiba, Masahiko Kishi, Tsutomu Inaoka, Hitoshi Terada, Hirokazu Doi, Yasuo Suzuki

Bibliographic record

VenueJournal of the American Geriatrics Society · 2016
Typeletter
Languageen
FieldMedicine
TopicParkinson's Disease Mechanisms and Treatments
Canadian institutionsnot available
Fundersnot available
KeywordsProgressive supranuclear palsyMedicineMontreal Cognitive AssessmentParkinsonismAudiologyNeurological examinationPhysical medicine and rehabilitationCognitionPsychiatryDiseaseCognitive impairmentPathology

Abstract

fetched live from OpenAlex

To the Editor: Progressive supranuclear palsy (PSP) is a major form atypical parkinsonism that should be differentiated from Parkinson's disease. Individuals with PSP typically present with an akinetic rigid syndrome with early postural instability, axial rigidity, and supranuclear gaze palsy.1, 2 Cognitive disorder in PSP is milder than Alzheimer's disease,3 featuring frontal executive dysfunction,4, 5 and appears with motor signs.1, 2 In contrast, it is rare that cognitive disorder occurs without motor disorder in PSP.2, 3 Such a patient was recently seen. A 73-year-old, previously healthy woman began to have memory problems (e.g., forgetful, forgetting to turn lights off, forgetting neighbors’ names) and infrequent delusional episodes (e.g., thinking that someone had stolen her wallet) for which she saw a general physician, who referred her to a memory clinic. She was taking no drugs that might affect cognitive or motor function. She was alert but slightly nervous and irritable. Her speech was fluent, and cranial nerve examinations, including extraocular muscle movement and eyelids, produced normal results. Her posture, including her neck, was normal. She had no tremor, rigidity, or akinesia of the neck, hands, or feet. Her gait was slightly slow for her age. Sensory examinations were unremarkable. She scored 20 out of 30 (normal > 24) on the Mini-Mental state Examination (MMSE) and 8 out of 18 (normal > 16) on the Frontal Assessment Battery (FAB). Laboratory data were normal. Brain magnetic resonance imaging (MRI) (Figure 1A) and brain 99mTc- L,L-ethyl cysteinate dimer single-photon emission computed tomography showed no remarkable changes. Metaiodobenzylguanidine myocardial scintigraphy results were normal (heart to mediastinum ratio on delayed images 3.35, normal > 2.0).6 Although hippocampal atrophy was not remarkable, she was diagnosed with mild cognitive impairment (MCI) due possibly to Alzheimer's disease. She was referred back to the local clinic, where 5 mg/d donepezil hydrochloride was started. Two years later, she was referred to the memory clinic again because of slow, short-stepped gait with assistance that had begun 1 year before. On examination, her cognitive function had deteriorated: MMSE score 14, FAB score 5. Delusions were not significant. Cranial nerve examination showed supranuclear vertical gaze palsy and dysarthria. She had no retropulsion. She had rigidity in her neck and upper extremities and marked akinesia bilaterally. She had no signs of aphasia, apraxia, limb dystonia, or alien hands. Brain MRI showed atrophy of the midbrain tegmentum (humming-bird sign or emperor penguin sign)7 (Figure 1B), and she was diagnosed with PSP1, 2 and referred back to the local clinic with instructions that she needed 300 mg/d of levodopa/carbidopa for gait difficulty. At the first visit, she had MCI alone without motor disorder. At the second visit, 2 years later, she had vertical gaze palsy and axial rigidity and akinesia. She did not have classical corticobasal syndrome during the course of the disease. Repeated brain MRI revealed midbrain atrophy and neurological signs. No similar cases had been previously reported to the knowledge of the authors except for a schizophrenia-like case8 and two cases of behavioral changes.9, 10 At the first memory screening, The woman described herein had marked frontal executive dysfunction as assessed according to the FAB. Prominent frontal dysfunction is a feature of PSP but not of Alzheimer's disease.3 A pathological lesion might have started in the frontal cortex and caused her frontal executive dysfunction. In conclusion, an elderly woman with PSP who presented with MCI without motor disorder is reported. MCI can be listed as a premotor feature of PSP. Conflict of Interest: None of the authors have any conflict of interest. Author Contributions: Ogata, Tateno: data acquisition, analysis, and interpretation. Sakakibara: study concept and design, acquisition of subjects and data, data analysis and interpretation, manuscript preparation. Tsuyusaki, Tateno, Aiba, Kishi, Inaoka, Terada, Doi: acquisition of subjects and data. Suzuki: critical review of data. Sponsor's Role: No sponsors.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.008
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Case report · Consensus signal: Case report
GenreCandidate signal: Empirical · Consensus signal: none
Teacher disagreement score0.008
Threshold uncertainty score0.014

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.008
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0020.001
Science and technology studies0.0010.001
Scholarly communication0.0020.002
Open science0.0030.001
Research integrity0.0080.005
Insufficient payload (model declined to judge)0.0040.002

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.018
GPT teacher head0.308
Teacher spread0.289 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designCase report
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2016
Admission routes1
Has abstractyes

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