Extrapyramidal Signs Before and After Diagnosis of Incident Alzheimer Disease in a Prospective Population Study
Open accessAbstract
BACKGROUND: Extrapyramidal signs (EPSs) are commonly accepted as a feature of Alzheimer disease (AD) and may influence both the profile of impairment and prognosis. OBJECTIVE: To examine rates of occurrence and risk factors for all types of EPSs and to describe the impact of EPSs over time on the clinical course of AD. DESIGN: Longitudinal study. SETTING: The Washington Heights Hamilton Heights Inwood Columbia Aging Project. Patients A total of 388 patients with incident AD (mean age, 79 years; 71.4% female). MAIN OUTCOME MEASURES: Extrapyramidal signs rated by means of a standardized portion of the Unified Parkinson's Disease Rating Scale; prevalence and incidence rates and cumulative risk for non-drug-induced EPSs; and rates of change in EPSs over time, taking into account potential covariates. RESULTS: Extrapyramidal signs were detected in 12.3% of patients at first evaluation and 22.6% at last evaluation. In a multivariate-adjusted generalized estimating equation model of change, total EPS score increased at an annual rate of 1.3%. Women (relative risk [RR], 1.57; P = .03), older patients (RR, 1.03; P = .02), and those with EPSs at baseline (RR, 2.07; P = .001) had greater rates of cognitive decline. CONCLUSIONS: Extrapyramidal signs occur frequently and progress significantly in AD. Patients with incident AD and concomitant EPSs have a greater rate of cognitive decline than do patients with incident AD but without EPSs.
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Parkinsonian features may be present in up to 30% of patients with AD, and these appear later in the disease course.
“While parkinsonian features may be present in up to 30% of patients with AD, [32] these appear later in the disease course [32].”
From Diagnosing the frontal variant of Alzheimer’s disease: a clinician’s yellow brick road (2017) · cites this paper as [32]
The Discussion says extrapyramidal signs were present in very early AD, even before the diagnosis was confirmed, contrary to the claim that they appear later in the disease course. The Abstract Results report 12.3% at first evaluation and 22.6% at last evaluation, supporting their presence in a substantial minority but not the claimed timing. Our copy provides no page numbers for these passages. (LLM, conf=0.87)
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References 36 · Cited by 79
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- Authors
- Portet, F., Scarmeas, N., Cosentino, S., Helzner, E. P., & Stern, Y.
- Affiliations
- Inserm (FR)
- Venue
- Archives of Neurology
- Publisher
- American Medical Association (AMA)
- Published
- 2009-09-01
- Volume
- 66
- Issue
- 9
- Pages
- 1120-6
- ISSN
- 0003-9942 (ISSN-L)
- PMC
- PMC2896248
- OpenAlex
- W2134181639
- Cited by
- 79
- References
- 36
- Citations by year
- 2025: 1 · 2024: 1 · 2023: 1 · 2022: 3 · 2021: 15 · 2020: 2 · 2019: 9 · 2018: 7 · 2017: 7 · 2016: 3 · 2015: 6 · 2014: 5 · 2013: 4 · 2012: 1
- FWCI
- 3.09
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Archives of Neurology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- JAMA Neurology
- Funders
- National Institute on Aging (P01AG007232, AG 07232, P01AG07232)
- National Institute of Neurological Disorders and Stroke (T32NS007153)
- National Center for Research Resources (RR 00645, M01RR000645)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
- Keywords
- extrapyramidal signs, Alzheimer's disease, cognitive decline, Unified Parkinson's Disease Rating Scale, disease progression, risk factors, sex differences, older adults
- MeSH terms
- Alzheimer Disease, Basal Ganglia Diseases, Brain, Cognition Disorders, Disability Evaluation, Neuropsychological Tests, Prospective Studies, Severity of Illness Index, Time Factors, Cohort Studies, Comorbidity, Incidence, Prevalence, Multivariate Analysis, Age Distribution, Sex Distribution, Disease Progression, Risk Assessment
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