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Mielke, Michelle M.

https://orcid.org/0000-0001-7177-1185

A5090710393 | I4405269449

Mayo Clinic

Wake Forest University Health Sciences

Citations 530

P2‐169: Slow gait predicts cognitive decline: A population‐based cohort study

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_9 | Pages: No page available

10.1016/j.jalz.2012.05.875

IC‐P‐038: Identification of noninvasive screening variables for the prediction of amyloid accumulation in a population‐based study of cognitively normal elderly individuals

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_1 | Pages: No page available

10.1016/j.jalz.2012.05.070

O2‐06‐03: Identification of non‐invasive screening variables for the prediction of amyloid accumulation in a population‐based study of cognitively normal elderly individuals

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_7 | Pages: No page available

10.1016/j.jalz.2012.05.656

P2‐040: Plasma ceramide concentrations are associated with change in verbal memory performance in patients undertaking cardiac rehabilitation

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_8 | Pages: No page available

10.1016/j.jalz.2012.05.743

O1‐10‐01: Clinical outcomes for stages of NIA‐AA preclinical Alzheimer's disease

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_3 | Pages: No page available

10.1016/j.jalz.2012.05.257

P1‐057: Neuropsychiatric symptoms at baseline predict shorter time to severe dementia in a population‐based sample of incident Alzheimer's disease: The Cache County Dementia Progression Study

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_4 | Pages: No page available

10.1016/j.jalz.2012.05.333

O4‐04‐04: NIA‐AA MCI criteria applied to the Mayo Clinic Study of Aging

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_17 | Pages: No page available

10.1016/j.jalz.2012.05.1655

Biomarker development: A population‐level perspective

Alzheimer's & Dementia | June 28, 2012 | Volume: 8 | Issue: 4 | Pages: 247-249

10.1016/j.jalz.2012.06.002 | PMID 22748935

Shifting Our Focus to blood-based Biomarkers of Alzheimer’s Disease: the Promise of Ceramides and Sphingomyelins

Neurodegenerative Disease Management | March 12, 2012 | Volume: 2 | Issue: 1 | Pages: 91-94

10.2217/nmt.11.87

The association of psychotropic medication use with the cognitive, functional, and neuropsychiatric trajectory of Alzheimer's disease

International Journal of Geriatric Psychiatry | February 29, 2012 | Volume: 27 | Issue: 12 | Pages: 1248-1257

10.1002/gps.3769 | PMID 22374884

ObjectiveThe use of psychotropic medications in Alzheimer's disease (AD) has been associated with both deleterious and potentially beneficial outcomes. We examined the longitudinal association of psychotropic medication use with cognitive, functional, and neuropsychiatric symptom (NPS) trajectories among community‐ascertained incident AD cases from the Cache County Dementia Progression Study.MethodsA total of 230 participants were followed for a mean of 3.7 years. Persistency index (PI) was calculated for all antidepressants, selective serotonin reuptake inhibitors (SSRIs), antipsychotics (atypical and typical), and benzodiazepines as the proportion of observed time of medication exposure. Mixed‐effects models were used to examine the association between PI for each medication class and Mini‐Mental State Exam (MMSE), Clinical Dementia Rating Sum of Boxes (CDR‐Sum), and Neuropsychiatric Inventory – Total (NPI‐Total) trajectories, controlling for appropriate demographic and clinical covariates.ResultsAt baseline, psychotropic medication use was associated with greater severity of dementia and poorer medical status. Higher PI for all medication classes was associated with a more rapid decline in MMSE. For antidepressant, SSRI, benzodiazepine, and typical antipsychotic use, a higher PI was associated with a more rapid increase in CDR‐Sum. For SSRIs, antipsychotics, and typical antipsychotics, a higher PI was associated with more rapid increase in NPI‐Total.ConclusionsPsychotropic medication use was associated with more rapid cognitive and functional decline in AD, and not with improved NPS. Clinicians may tend to prescribe psychotropic medications to AD patients at risk of poorer outcomes, but one cannot rule out the possibility of poorer outcomes being caused by psychotropic medications. Copyright © 2012 John Wiley & Sons, Ltd.