Editors' Note: Risk of Hospitalization and Death Associated With Pimavanserin Use in Older Adults With Parkinson Disease

Neurology ◽  
2021 ◽  
Vol 98 (1) ◽  
pp. 48-48
Author(s):  
Aravind Ganesh ◽  
Steven Galetta
Neurology ◽  
2017 ◽  
Vol 88 (9) ◽  
pp. 920.1-920
Author(s):  
Nicolaas I. Bohnen ◽  
Martijn Muller

2017 ◽  
Author(s):  
Rajesh R Tampi ◽  
Deena J Tampi

Major neurocognitive disorder is the most common neurodegenerative condition in the world and the leading cause of dependence and disability among older adults worldwide. There are numerous etiologies for major neurocognitive disorder, of which Alzheimer disease (AD) is the most common. Available evidence indicates that the risk factors for major neurocognitive disorder include older age, female sex, lower educational attainment, obesity, and vascular risk factors, including smoking, hypertension, diabetes mellitus, and hyperlipidemia. Certain etiologies for major neurocognitive disorder are heritable, especially those due to AD and frontotemporal lobar degeneration. The pathophysiologic changes associated with the various etiologies of major neurocognitive disorder include neuronal loss, senile plaques, neurofibrillary tangles, vascular pathology, and α-synuclein neuronal inclusions. Major neurocognitive disorder remains a clinical diagnosis with a thorough history, appropriate laboratory tests, and standardized rating scales assisting in determining the etiology and severity of the condition. In older adults, major neurocognitive disorder must be differentiated from depression and delirium as these three conditions may have similar clinical presentations or may coexist. Current data indicate that approximately a third of the cases of major neurocognitive disorder, especially those due to AD, may be prevented by controlling potentially modifiable risk factors, including diabetes, depression, smoking, physical inactivity, midlife hypertension, midlife obesity, and low educational attainment. Currently, the only Food and Drug Administration–approved medications are acetylcholinesterase inhibitors and memantine for use in major neurocognitive disorder due to AD and rivastigmine (an acetylcholinesterase inhibitor) for major neurocognitive disorder due to Parkinson disease.   Key words: acetylcholinesterase inhibitors, Alzheimer disease, amyloid precursor protein, frontotemporal lobar degeneration, Lewy body disease, major neurocognitive disorder, memantine, Parkinson disease, tau proteins, vascular disease


2019 ◽  
Vol 100 (10) ◽  
pp. e58
Author(s):  
Sean Miller ◽  
Andrzej Remaisz ◽  
Brad Johnson ◽  
Jenna Tarran ◽  
Hamid Bateni

2019 ◽  
Vol 76 (1) ◽  
pp. 41 ◽  
Author(s):  
Sneha Mantri ◽  
Michelle Fullard ◽  
Shelly L. Gray ◽  
Daniel Weintraub ◽  
Rebecca A. Hubbard ◽  
...  

2019 ◽  
Vol 35 (3) ◽  
pp. 224-230
Author(s):  
Rosemary Gallagher ◽  
Michelle Farella-Accurso ◽  
Dara Johnson ◽  
Ramanjit Kang ◽  
Angel Rodriguez ◽  
...  

Neurology ◽  
2017 ◽  
Vol 89 (14) ◽  
pp. 1441-1447 ◽  
Author(s):  
Honglei Chen ◽  
Srishti Shrestha ◽  
Xuemei Huang ◽  
Samay Jain ◽  
Xuguang Guo ◽  
...  

Objective:To investigate olfaction in relation to incident Parkinson disease (PD) in US white and black older adults.Methods:The study included 1,510 white (mean age 75.6 years) and 952 black (75.4 years) participants of the Health, Aging, and Body Composition study. We evaluated the olfaction of study participants with the Brief Smell Identification Test (BSIT) in 1999–2000. We retrospectively adjudicated PD cases identified through August 31, 2012, using multiple data sources. We used multivariable Cox models to estimate hazard ratios (HRs) and 95% confidence intervals (CIs).Results:During an average of 9.8 years of follow-up, we identified a total of 42 incident PD cases, including 30 white and 12 black participants. Overall, poor sense of smell, as indicated by a lower BSIT score, was associated with higher risk of PD. Compared with the highest tertile of BSIT (t3), the HR was 1.3 (95% CI 0.5–3.6) for the second tertile (t2) and 4.8 (95% CI 2.0–11.2) for the lowest tertile (t1) (ptrend < 0.00001). Further analyses revealed significant associations for incident PD in both the first 5 years of follow-up (HRt1/[t2+t3] 4.2, 95% CI 1.7–10.8) and thereafter (HRt1/[t2+t3] 4.1, 95% CI 1.7–9.8). This association appeared to be stronger in white (HRt1/[t2+t3] 4.9, 95% CI 2.3–10.5) than in black participants (HRt1/[t2+t3] 2.5, 95% CI 0.8–8.1), and in men (HRt1/[t2+t3] 5.4, 95% CI 2.3–12.9) than in women (HRt1/[t2+t3] 2.9, 95% CI 1.1–7.8).Conclusions:Poor olfaction predicts PD in short and intermediate terms; the possibility of stronger associations among men and white participants warrants further investigation.


2003 ◽  
Vol 27 (1) ◽  
pp. 2-7 ◽  
Author(s):  
Curt M. Campbell ◽  
Jennifer L. Rowse ◽  
Marcia A. Ciol ◽  
Anne Shumway-Cook

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