Dementia

From Citizendium
Revision as of 10:40, 30 October 2024 by Jack S. Byrom (talk | contribs) (→‎Prevention: making this section into more of a narrative than a list)
Jump to navigation Jump to search
This article is developing and not approved.
 Main Article
 Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
https://en.citizendium.org/wiki/index.php?title=Dementia&printable=yes
This editable Main Article is under development and subject to a disclaimer.

Dementia is a syndrome associated with many neurodegenerative diseases, characterized by a general decline in cognitive abilities that affects a person's ability to perform everyday activities. Dementia may involve problems with memory, thinking, behavior, and motor control. Aside from memory impairment and a disruption in thought patterns, the most common symptoms of dementia include emotional problems, difficulties with language, and decreased motivation. The symptoms may be described as occurring in a continuum over several stages. A diagnosis of dementia requires the observation of a change from a person's usual mental functioning and a greater cognitive decline than might be caused by the normal aging process. Dementia is currently the seventh leading cause of death worldwide and has 10 million new cases reported every year (approximately one every three seconds).

History

Until the end of the 19th century, dementia was a much broader clinical concept. It included mental illness and any type of psychosocial incapacity, including reversible conditions. Dementia at this time simply referred to anyone who had lost the ability to reason, and was applied equally to psychosis, "organic" diseases like syphilis that can destroy the brain, and to the dementia associated with old age, which was attributed to "hardening of the arteries".

In Roman times, philosopher Emperor Marcus Aurelius, who lived from 161 to 180 C.E., feared falling into a state of dementia more than he feared death. He wrote:

"...if we live longer, there is no guarantee that our mind will likewise retain that power to comprehend and study the world which contributes to our experience of things divine and human. If dementia sets in, there will be no failure of such faculties as breathing, feeding, imagination, desire: before these go, the earlier extinction is of one's proper use of oneself, one's accurate assessment of the gradations of duty, one's ability to analyse impressions, one's understanding of whether the time has come to leave this life - these and all other matters which wholly depend on trained calculation. So we must have a sense of urgency, not only for the ever closer approach of death, but also because our comprehension of the world and our ability to pay proper attention will fade before we do." --Meditations 3:1, Marcus Aurelius

Possible causes

Various diseases and injuries to the brain, such as stroke, can give rise to dementia. However, the most common cause is Alzheimer's disease, a neurodegenerative disorder. The Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), has re-described dementia as a mild or major neurocognitive disorder with varying degrees of severity and many causative subtypes. The International Classification of Diseases (ICD-11) also classifies dementia as a neurocognitive disorder (NCD) with many forms or subclasses. Dementia is listed as an acquired brain syndrome, marked by a decline in cognitive function, and is contrasted with neurodevelopmental disorders. It is also described as a spectrum of disorders with causative subtypes of dementia based on a known disorder, such as Parkinson's disease for Parkinson's disease dementia, Huntington's disease for Huntington's disease dementia, vascular disease for vascular dementia, HIV infection causing HIV dementia, frontotemporal lobar degeneration for frontotemporal dementia, Lewy body disease for dementia with Lewy bodies, and prion diseases.[1] Subtypes of neurodegenerative dementias may also be based on the underlying pathology of misfolded proteins, such as synucleinopathies and tauopathies. The coexistence of more than one type of dementia is known as mixed dementia.

Many neurocognitive disorders may be caused by another medical condition or disorder, including brain tumors and subdural hematoma, endocrine disorders such as hypothyroidism and hypoglycemia, nutritional deficiencies including of thiamine and niacin, infections, immune disorders, liver or kidney failure, metabolic disorders such as Kufs disease, some leukodystrophies, and neurological disorders such as epilepsy and multiple sclerosis. Some of the neurocognitive deficits may sometimes show improvement with treatment of the causative medical condition.

Decades of published scientific research strongly implicate long-term exposure to low levels of aluminum in the development of Alzheimer's disease. This dementia was completely unknown to medicine before the proliferation of aluminum throughout industrialized societies beginning in the late 19th century.

Signs and symptoms

The signs and symptoms of dementia are termed as the neuropsychiatric symptoms—also known as the behavioral and psychological symptoms—of dementia. The behavioral symptoms can include agitation, restlessness, inappropriate behavior, sexual disinhibition, and verbal or physical aggression. These symptoms may result from impairments in cognitive inhibition. The psychological symptoms can include depression, hallucinations (most often visual), delusions, apathy, and anxiety. The most commonly affected areas of brain function include memory, language, attention, problem solving, and visuospatial function affecting perception and orientation. The symptoms progress at a continuous rate over several stages, and they vary across the dementia subtypes. Most types of dementia are slowly progressive with some deterioration of the brain well established before signs of the disorder become apparent. There are often other conditions present, such as high blood pressure or diabetes, and there can sometimes be as many as four of these comorbidities.

Signs of dementia include getting lost in a familiar neighborhood, using unusual words to refer to familiar objects, forgetting the name of a close family member or friend, forgetting old memories, and being unable to complete tasks independently, such as paying bills or balancing a checkbook.

People with dementia are more likely to have problems with incontinence than those of a comparable age without dementia; they are three times more likely to have urinary incontinence and four times more likely to have fecal incontinence.

Stages

The course of dementia is often described in four stages – pre-dementia, early, middle, and late, that show a pattern of progressive cognitive and functional impairment. More detailed descriptions can be arrived at by the use of numeric scales. These scales include the Global Deterioration Scale for Assessment of Primary Degenerative Dementia (GDS or Reisberg Scale), the Functional Assessment Staging Test (FAST), and the Clinical Dementia Rating (CDR). Using the GDS, which more accurately identifies each stage of the disease progression, a more detailed course is described in seven stages – two of which are broken down further into five and six degrees. Stage 7(f) is the final stage.

Classification

Vascular dementia can affect both cortical and subcortial locations.

Cortical dementias

Among the many causes of cortical dementia, common causes are:

Subcortical dementias

Among the many causes of subcortical dementia, common causes are Parkinson's disease, vitamin B12 deficiency, and some vascular dementias.

Epidemiology

The number of cases of dementia worldwide in 2021 was estimated at 55 million, with close to 10 million new cases each year.[3] According to a report by the World Health Organization, "In 2021, Alzheimer’s disease and other forms of dementia ranked as the seventh leading cause of death, killing 1.8 million lives." By 2050, the number of people living with dementia is estimated to be over 150 million globally. Around 7% of people over the age of 65 have dementia, with slightly higher rates (up to 10% of those over 65) in places with relatively high life expectancy. In the United States, an estimated 40% of those over the age of 85 years old will eventually develop Alzheimer's dementia. The prevalence of dementia differs in different world regions, ranging from 4.7% in Central Europe to 8.7% in North Africa/Middle East; the prevalence in other regions is estimated to be between 5.6 and 7.6%. The number of people living with dementia is estimated to double every 20 years. In 2016 dementia resulted in about 2.4 million deaths, up from 0.8 million in 1990.

The annual incidence of dementia diagnosis is nearly 10 million worldwide. Almost half of new dementia cases occur in Asia, followed by Europe (25%), the Americas (18%), and Africa (8%). The incidence of dementia increases exponentially with age, doubling with every 6.3-year increase in age.[4] Rates are slightly higher in women than men at ages 65 and greater. The disease trajectory is varied and the median time from diagnosis to death depends strongly on age at diagnosis, from 6.7 years for people diagnosed aged 60–69 to 1.9 years for people diagnosed at 90 or older.

Dementia impacts not only individuals with dementia, but also their carers and the wider society. Among people aged 60 years and over, dementia is ranked the ninth most burdensome condition according to the 2010 Global Burden of Disease (GBD) estimates. The global costs of dementia was around U.S. $818 billion in 2015, a 35.4% increase from U.S. $604 billion in 2010.

A new 2024 study reveals that deaths from dementia in the U.S. have tripled in the past 21 years, rising from around 150,000 in 1999 to over 450,000 in 2020; the likelihood of dying from dementia increased across all demographic groups studied.

Diagnosis

Studies on diagnosing dementia are compromised by the lack of a true reference standard for comparison.[5][6]

A number of systematic reviews, including ones by the U.S. Preventive Services Task Force (USPSTF)[7], Rational Clinical Examination[8], have summarized the diagnostic accuracy of screening tests.

[9]

One minute screening tests, such as the inability to name 15 or more animals in one minute, predicts the presence of dementia.[9]

The single best finding may be disoriented to year.[10]

Four functional symptoms

Diagnosis of dementia is usually based on medical history and cognitive testing with imaging. Blood tests may be taken to rule out other possible causes that may be reversible, such as hypothyroidism, and to determine the dementia subtype. One commonly used cognitive test is the mini–mental state examination. Although the greatest risk factor for developing dementia is aging, dementia is not a normal part of the aging process; many people aged 90 and above show no signs of dementia. Several risk factors for dementia, such as smoking and obesity, are preventable by lifestyle changes.

Deficits in cognitive function contribute to impaired functional status.[11] The deficits in the domains of cognitive function are[8]:

  • Agnosia - "Failure to recognize or identify objects despite intact sensory function"[8]
  • Aphasia - "Deterioration of language function"[8]
  • Apraxia - "Impaired ability to execute motor activities despite intact motor abilities, sensory function, and comprehension of the required task"[8]
  • Disturbance in executive functioning - "The ability to think abstractly and to plan, initiate, sequence, monitor, and stop complex behavior"[8]

Ascertainment of decision-making capacity

Decision making can be assessed with the Aid to Capacity Evaluation (ACE).[12]

Consequences of labeling

In one study, learning of having mild cognitive impairment reduced stress.[13]

Mental status schedules

Systematic reviews have compared the schedules.[14][8]

A separate systematic review has examined decision making capacity.[12]

Temporal disorientation

Among hospitalized geriatric patients, "failure to identify either year or month correctly was 95% sensitive and 86.5% specific for the detection of cognitive impairment".[10]

Diagnostic surveys have been compared.[15]

Sweet 16

The Sweet 16 is available online at http://hospitalelderlifeprogram.org/private/sweet16-disclaimer.php?pageid=01.09.00. Accuracy using a score of less than 14:[16]

Mini-cog

According to the systematic review by the Rational Clinical Examination, regarding the mini-cog "the performance of the Mini-Cog...cannot be determined with confidence because none of these screens were actually administered in their suggested forms. However, the performance suggested by the retrospective analyses reported in these articles is promising."[8] More recent studies[17] and reviews[18] are favorable. The mini-COG is available at http://www.hospitalmedicine.org/geriresource/toolbox/pdfs/clock_drawing_test.pdf and http://geriatrics.uthscsa.edu/tools/MINICog.pdf .

Mini-mental state examination

The Mini-mental state examination (MMSE) is the most studied test.[8] A systematic review concluded that the accuracy of the MMSE is:[7]:

Copies of their MMSE can be purchased (http://www4.parinc.com/Products/Product.aspx?ProductID=MMSE). A copy of the Mini-mental state examination can be found in the appendix of the original publication.[19]

Modified Mini-Mental State examination (3MS)

A meta-analysis concluded that the Modified Mini-Mental State (3MS) examination has:

A copy of the 3MS is online.[20]

Abbreviated mental test score

A meta-analysis concluded:

sensitivity 73% to 100%
specificity 71% to 100%

Clinical Dementia Rating

The Clinical Dementia Rating scale can quantify severity of functional impairment.[21]


St Louis University mental status examination (SLUMS)

The SLUMS has been compared to the MMSE.[22][23] Both evaluations were by the developer of the SLUMS and showed comparable accuracy to the MMSE.

Other examinations

Many other tests have been studied [24][25][26] including the Executive Interview (EXIT)[27].[28]

Investigation of causes

Among rapidly progressive cases, causes include:[29]

  • Sporadic Creutzfeldt-Jakob disease (sCJD)
  • Immunological (vasculitis, encephalomyelitis, and limbic encephalitis)
  • Neoplastic (mainly lymphoma)
  • Infectious (fungal, viral, and parasitic)
  • Metabolic (including Wernicke encephalopathy)

Laboratory tests

Apolipoprotein E4

Although apolipoprotein E4 is an important susceptibility gene for Alzheimer's disease[30], its sensitivity and specificity are insufficient (65 and 68 percent, respectively) to be used as a diagnostic test.[31]

Apolipoprotein E4 does not added to other tests in predicting who will develop Alzheimer's.[32]

Treatment

Approaches to treatment

"Actively involving caregivers in making choices about treatments" my be the most important way to delay institutionalization of patients with dementia.[33]

The use of care managers may help.[34][35]

Non drug treatments

Behavior management techniques (BMT)

Behavior management techniques (BMT) might help.[36] More specifically, " interventions that address behavioral issues and unmet needs" may help.[34]

Exercise

Home-based program of physical activity might benefit according to a randomized controlled trial.[37]


Medications

According to the clinical practice guideline by the American College of Physicians, "the evidence is insufficient to compare the effectiveness of different pharmacologic agents for the treatment of dementia."[38]

"Treatment of dementia with cholinesterase inhibitors and memantine can result in statistically significant but clinically marginal improvement in measures of cognition and global assessment of dementia" according to a systematic review for the clinical practice guideline.[39]

Cholinesterase inhibitors

Available cholinesterase inhibitors drugs are donepezil, galantamine, rivastigmine, and tacrine.

Neuropeptide-modifier

Memantine is a neuropeptide-modifier that acts on the N-Methyl-D-Aspartate (NMDA) cell surface receptors for the neurotransmitter glutamate.

Anti-psychotics

The newer, atypical antipsychotic agents (olanzapine, quetiapine, risperidone), were found to have "adverse effects offset advantages in the efficacy of atypical antipsychotic drugs for the treatment of psychosis, aggression, or agitation in patients with Alzheimer's disease."[40] A more recent randomized controlled trial that compared the second generation anti-psychotic agents found that none improved functioning, care needs, or quality of life with statistical significance[40]; however, olanzapine and risperidone may reduce anger.[41] Regardless, antipsychotic agents may increase mortality.[42]

Withdrawing psychotropics agents may prevent accidental falls.[43]

Melatonin

Melatonin may[44]or may not[45][46][47][48] help with associated sleep and behavior disturbance.

Dietary supplements

Ginkgo biloba has conflicting evidence regarding its efficacy.[49][50][51]

Analgesics

Treating pain may reduce agitation.[52]

Prevention

Risk factors for dementia include high blood pressure, high levels of cholesterol, vision loss, hearing loss, smoking, obesity, depression, inactivity, diabetes, lower levels of education, and low social contact. Overindulgence in alcohol, lack of sleep, anemia, traumatic brain injury, and air pollution can also increase the chance of developing dementia. Many of these risk factors, including the lower level of education, smoking, physical inactivity and diabetes, are modifiable. Several of the group are known as vascular risk factors. Managing these risk factors can reduce the risk of dementia in individuals in their late midlife or older age. A reduction in a number of these risk factors, such as switching to a high-fiber, low-fat, plant-based diet or quitting cigarette smoking, can give a positive outcome. The decreased risk achieved by adopting a healthy lifestyle is seen even in those with a high genetic risk.

The standard American diet high in animal products and dairy and concomitant elevated levels of saturated fat is associated with a greater risk of developing dementia. Population and clinical research studies show that plant-based diets low in animal products and high in starch, fruits, and vegetables are associated with lower risk.

Most,[53][54][55][56] but not all[57] studies find that physical activity is associated with reduced risk of dementia. These observational studies cannot prove cause and effect.

Maintaining activities such as cognitive games and reading, playing musical instruments, and physical activities are associated with reduced the risk of dementia in an observational study.[57]

Various medications have been associated with progression or prevention (cholinesterase inhibitors, N-methyl-D-aspartate receptor antagonists, renin-angiotensin system blockers, and hydroxymethylglutaryl-coenzyme A reductase inhibitors) of dementia.[58]

Observational, non-randomized cohort studies suggest that hydroxymethylglutaryl-coenzyme A reductase inhibitors (statins) may[59][60] or may not[61][62] prevent dementia.

Ginkgo biloba does not prevent dementia according to a large randomized controlled trial[63] and systematic review[51] by the Cochrane Collaboration in spite of earlier studies that were positive[64].

Screening

Practice guidelines

In 2003, a clinical practice guideline by the U.S. Preventive Services Task Force (USPSTF) gave a grade I recommendation, indicating "the evidence is insufficient to recommend for or against routine screening for dementia in older adults".[65]

Evidence

The late-life dementia risk index:[66]

late-life dementia risk index
Risk Score Incidence of dementia
within 6 years
High ≥8 56%
Intermediate 4-7 23%
Low 0-3 4%
Based on Table 3 from Barnes et al.[66]
  • older age (1–2 points)
  • poor cognitive test performance (2–4 points)
  • body mass index <18.5 (2 points)
  • ≥1 apolipoprotein E 4 alleles (1 point)
  • cerebral MRI findings of white matter disease (1 point)
  • cerebral ventricular enlargement (1 point)
  • internal carotid artery thickening on ultrasonography (1 point)
  • history of coronary artery bypass surgery (1 point)
  • slow physical performance (1 point)
  • lack of alcohol consumption (1 point)

Prognosis

Functional Assessment Staging (FAST) scale[67]
Stage 6
6a = inability to dress
6b = inability to bathe
6c = inability to toilet
6d = urinary incontinence at least occasionally
6e = bowel incontinence at least occasionally
Stage 7
7a = speech is limited to less than 5 words
7b = all intelligible vocabulary is lost
7c = nonambulatory
7d = unable to sit independently
7e = unable to smile
7f = unable to hold head up

Mild cognitive impairment

Mortality is increased with mild cognitive impairment.[68] A systematic review of cohort studies concluded that the rate conversion of mild cognitive impairment to dementia is about 4% per year."[69]

Once a patient has advanced dementia, defined as a score of 5 or 6 on the Cognitive Performance Scale from the most recent Minimum Data Set assessment (a score of 5 corresponds to a score of 5.1 (95% CI: ±10) on the Folstein Mini–Mental State Examination, the median survival is about 18 months.[70]

Dementia

Mortality can also be predicted by Medicare guidelines for use of Hospice. If the patients is a stage 7c on the Functional Assessment Staging (FAST) scale and has had a prior complication of dementia such aspiration pneumonia, stage 4 or more pressure ulcer, upper urinary tract infection, or inability to eat, then mortality is predicted at 6 months with accuracy of:[71]

  • Sensitivity 20%
  • Specificity 89%

Similarly, mortality can be predicted by the ADEPT score.[71]

Legal issues

As of 2024, when improved healthcare means that many people are living longer, there is growing concern about dementia, not just in aging patients but as a result of other health challenges. However, physicians often do not agree among themselves on how to detect and define it. And a medical diagnosis of dementia can have serious legal consequences, resulting (just for example) in a patient losing the right to manage their own finances or make their own medical decisions. Thus, in the U.S., physicians "recommend" that Medicare patients (age 65 and over) be given a cognitive test as part of their annual wellness exam, but they stopped short of requiring such a test.

Attribution

Some content on this page may previously have appeared on Wikipedia.


References

  1. ↑ Wilson H, Pagano G, Politis M (March 2019). "Dementia spectrum disorders: lessons learnt from decades with PET research". J Neural Transm (Vienna). 126(3): 233–251. doi:10.1007/s00702-019-01975-4. PMC 6449308. PMID 30762136.
  2. ↑ McKeith IG, Fairbairn AF, Perry RH, Thompson P (September 1994). "The clinical diagnosis and misdiagnosis of senile dementia of Lewy body type (SDLT)". Br J Psychiatry 165 (3): 324–32. PMID 7994501. [e]
  3. ↑ "Dementia". World Health Organization. Retrieved October 29, 2024.
  4. ↑ Alzheimer's Disease International (September 2015). "World Alzheimer Report 2015" (PDF). Retrieved October 29, 2024.
  5. ↑ Erkinjuntti T, Ostbye T, Steenhuis R, Hachinski V (December 1997). "The effect of different diagnostic criteria on the prevalence of dementia". N. Engl. J. Med. 337 (23): 1667–74. PMID 9385127. [e]
  6. ↑ Rockwood K et al. Toward a revision of criteria for the dementias. Alzheimer's and Dementia 3 (4), 428 (2007) DOI:10.1016/j.jalz.2007.07.014
  7. ↑ 7.0 7.1 Boustani, M.; Peterson, B.; Hanson, L.; Harris, R.; & Lohr, K. (2003). "Screening for dementia in primary care: a summary of the evidence for the U.S. Preventive Services Task Force". Ann Intern Med 138 (11): 927-37. PMID 12779304.
  8. ↑ 8.0 8.1 8.2 8.3 8.4 8.5 8.6 8.7 8.8 Holsinger T, Deveau J, Boustani M, Williams JW (2007). "Does this patient have dementia?". JAMA 297 (21): 2391–404. DOI:10.1001/jama.297.21.2391. PMID 17551132. Research Blogging.
  9. ↑ 9.0 9.1 Canning SJ, Leach L, Stuss D, Ngo L, Black SE (2004). "Diagnostic utility of abbreviated fluency measures in Alzheimer disease and vascular dementia.". Neurology 62 (4): 556-62. PMID 14981170. [e]
  10. ↑ 10.0 10.1 O'Keeffe E, Mukhtar O, O'Keeffe ST (2011). "Orientation to time as a guide to the presence and severity of cognitive impairment in older hospital patients.". J Neurol Neurosurg Psychiatry 82 (5): 500-4. DOI:10.1136/jnnp.2010.214817. PMID 20852313. Research Blogging.
  11. ↑ Royall DR, Lauterbach EC, Kaufer D, Malloy P, Coburn KL, Black KJ (2007). "The cognitive correlates of functional status: a review from the Committee on Research of the American Neuropsychiatric Association". The Journal of neuropsychiatry and clinical neurosciences 19 (3): 249–65. DOI:10.1176/appi.neuropsych.19.3.249. PMID 17827410. Research Blogging.
  12. ↑ 12.0 12.1 Sessums LL, Zembrzuska H, Jackson JL (2011). "Does this patient have medical decision-making capacity?". JAMA 306 (4): 420-7. DOI:10.1001/jama.2011.1023. PMID 21791691. Research Blogging.
  13. ↑ Carpenter, B. D., Xiong, C., Porensky, E. K., Lee, M. M., Brown, P. J., Coats, M., et al. (2008). Reaction to a dementia diagnosis in individuals with Alzheimer's disease and mild cognitive impairment, Journal of the American Geriatrics Society, 56(3), 405-412. DOI:doi:10.1111/j.1532-5415.2007.01600.x. doi:10.1111/j.1532-5415.2007.01600.x.
  14. ↑ Lin JS, O'Connor E, Rossom RC, Perdue LA, Eckstrom E (2013). "Screening for cognitive impairment in older adults: A systematic review for the U.S. Preventive Services Task Force.". Ann Intern Med 159 (9): 601-12. DOI:10.7326/0003-4819-159-9-201311050-00730. PMID 24145578. Research Blogging. Review in: Ann Intern Med. 2014 Feb 18;160(4):JC12
  15. ↑ Holsinger T, Plassman BL, Stechuchak KM, Burke JR, Coffman CJ, Williams JW (2012). "Screening for cognitive impairment: comparing the performance of four instruments in primary care.". J Am Geriatr Soc 60 (6): 1027-36. DOI:10.1111/j.1532-5415.2012.03967.x. PMID 22646750. Research Blogging.
  16. ↑ Fong TG, Jones RN, Rudolph JL, Yang FM, Tommet D, Habtemariam D et al. (2011). "Development and validation of a brief cognitive assessment tool: the sweet 16.". Arch Intern Med 171 (5): 432-7. DOI:10.1001/archinternmed.2010.423. PMID 21059967. Research Blogging.
  17. ↑ Hirsch C (2012). "The Mini-Cog had sensitivity similar to the longer 3MS for detecting cognitive impairment or dementia.". Ann Intern Med 157 (8): JC4-8. DOI:10.7326/0003-4819-157-8-201210160-02008. PMID 23070510. Research Blogging.
  18. ↑ Mitchell AJ, Malladi S (2010). "Screening and case finding tools for the detection of dementia. Part I: evidence-based meta-analysis of multidomain tests.". Am J Geriatr Psychiatry 18 (9): 759-82. DOI:10.1097/JGP.0b013e3181cdecb8. PMID 20808118. Research Blogging.
  19. ↑ Folstein MF, Folstein SE, McHugh PR (1975). ""Mini-mental state". A practical method for grading the cognitive state of patients for the clinician". Journal of psychiatric research 12 (3): 189-98. DOI:10.1016/0022-3956(75)90026-6. PMID 1202204. Research Blogging.
  20. ↑ Hogan DB, Ebly EM (2000). "Predicting who will develop dementia in a cohort of Canadian seniors". The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 27 (1): 18–24. PMID 10676583. [e] [Appendix: The Modified Mini-Mental State (3MS)]
  21. ↑ Morris JC (1993). "The Clinical Dementia Rating (CDR): current version and scoring rules.". Neurology 43 (11): 2412-4. PMID 8232972.
  22. ↑ Cummings-Vaughn LA, Chavakula NN, Malmstrom TK, Tumosa N, Morley JE, Cruz-Oliver DM (2014). "Veterans affairs saint louis university mental status examination compared with the montreal cognitive assessment and the short test of mental status.". J Am Geriatr Soc 62 (7): 1341-6. DOI:10.1111/jgs.12874. PMID 24916485. Research Blogging.
  23. ↑ Tariq SH, Tumosa N, Chibnall JT, Perry MH, Morley JE (2006). "Comparison of the Saint Louis University mental status examination and the mini-mental state examination for detecting dementia and mild neurocognitive disorder--a pilot study.". Am J Geriatr Psychiatry 14 (11): 900-10. DOI:10.1097/01.JGP.0000221510.33817.86. PMID 17068312. Research Blogging.
  24. ↑ Sager, M.; Hermann, B.; La Rue, A.; & Woodard, J. (2006). "Screening for dementia in community-based memory clinics". WMJ 105 (7): 25-9. PMID 17163083.
  25. ↑ Fleisher, A.; Sowell B.; Taylor C.; Gamst A.; Petersen R.; & Thal L. (2007). "Clinical predictors of progression to Alzheimer's disease in amnestic mild cognitive impairment". Neurology 68 (19): 1588-95. PMID 17287448.
  26. ↑ Diagnostic evaluation of elderly patients with mild memory problems by Jason H T Karlawish and Christopher M Clark, PMID 12614094 DOI 10.7326/0003-4819-138-5-200303040-00011
  27. ↑ Royall DR, Mahurin RK, Gray KF. Bedside assessment of executive cognitive impairment: the executive interview. J Am Geriatr Soc. 1992;40:1221-6. PMID 1447438
  28. ↑ Carpenter CR, Bassett ER, Fischer GM, Shirshekan J, Galvin JE, Morris JC (2011). "Four sensitive screening tools to detect cognitive dysfunction in geriatric emergency department patients: brief Alzheimer's Screen, Short Blessed Test, Ottawa 3DY, and the caregiver-completed AD8.". Acad Emerg Med 18 (4): 374-84. DOI:10.1111/j.1553-2712.2011.01040.x. PMID 21496140. PMC PMC3080244. Research Blogging.
  29. ↑ Chitravas N, Jung RS, Kofskey DM, Blevins JE, Gambetti P, Leigh RJ et al. (2011). "Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease.". Ann Neurol. DOI:10.1002/ana.22454. PMID 21674591. Research Blogging.
  30. ↑ Skoog I (August 2000). "Detection of preclinical Alzheimer's disease". N. Engl. J. Med. 343 (7): 502–3. PMID 10944568. “The APOE 4 allele is a susceptibility gene for Alzheimer's disease and seems to affect the age of onset of the disease. However, the presence of this allele alone is not sufficient to predict which asymptomatic subjects will ultimately have Alzheimer's disease, and the disease never develops in many subjects with this genotype” [e]
  31. ↑ Kivipelto M, Helkala EL, Laakso MP, et al (August 2002). "Apolipoprotein E epsilon4 allele, elevated midlife total cholesterol level, and high midlife systolic blood pressure are independent risk factors for late-life Alzheimer's disease". Ann. Intern. Med. 137 (3): 149–55. PMID 12160362. [e]
  32. ↑ Devanand DP, Liu X, Tabert MH, et al (November 2008). "Combining early markers strongly predicts conversion from mild cognitive impairment to Alzheimer's disease". Biol. Psychiatry 64 (10): 871–9. DOI:10.1016/j.biopsych.2008.06.020. PMID 18723162. Research Blogging.
  33. ↑ Spijker A et al. Effectiveness of Nonpharmacological Interventions in Delaying the Institutionalization of Patients with Dementia: A Meta-Analysis.J Am Geriatr Soc. 2008 Apr 11. PMID 18410323
  34. ↑ 34.0 34.1 Ayalon L, Gum AM, Feliciano L, Areán PA (2006). "Effectiveness of nonpharmacological interventions for the management of neuropsychiatric symptoms in patients with dementia: a systematic review". Arch. Intern. Med. 166 (20): 2182–8. DOI:10.1001/archinte.166.20.2182. PMID 17101935. Research Blogging.
  35. ↑ Vickrey BG, Mittman BS, Connor KI, et al (2006). "The effect of a disease management intervention on quality and outcomes of dementia care: a randomized, controlled trial". Ann. Intern. Med. 145 (10): 713–26. PMID 17116916. [e]
  36. ↑ Teri L, Gibbons LE, McCurry SM, et al (2003). "Exercise plus behavioral management in patients with Alzheimer disease: a randomized controlled trial". JAMA 290 (15): 2015–22. DOI:10.1001/jama.290.15.2015. PMID 14559955. Research Blogging.
  37. ↑ Lautenschlager NT, Cox KL, Flicker L, Foster JK, van Bockxmeer FM, Xiao J, et al. Effect of Physical Activity on Cognitive Function in Older Adults at Risk for Alzheimer Disease: A Randomized Trial. JAMA. 2008 Sep 3;300(9):1027-1037.
  38. ↑ Qaseem A, Snow V, Cross JT, et al (March 2008). "Current pharmacologic treatment of dementia: a clinical practice guideline from the American College of Physicians and the American Academy of Family Physicians". Ann. Intern. Med. 148 (5): 370–8. PMID 18316755. [e]
  39. ↑ Raina P, Santaguida P, Ismaila A, et al (March 2008). "Effectiveness of cholinesterase inhibitors and memantine for treating dementia: evidence review for a clinical practice guideline". Ann. Intern. Med. 148 (5): 379–97. PMID 18316756. [e]
  40. ↑ 40.0 40.1 Schneider LS, Tariot PN, Dagerman KS, et al (2006). "Effectiveness of atypical antipsychotic drugs in patients with Alzheimer's disease". N. Engl. J. Med. 355 (15): 1525–38. DOI:10.1056/NEJMoa061240. PMID 17035647. Research Blogging.
  41. ↑ Sultzer DL, Davis SM, Tariot PN, Dagerman KS, Lebowitz BD, Lyketsos CG et al. (2008). "Clinical symptom responses to atypical antipsychotic medications in Alzheimer's disease: phase 1 outcomes from the CATIE-AD effectiveness trial.". Am J Psychiatry 165 (7): 844-54. DOI:10.1176/appi.ajp.2008.07111779. PMID 18519523. PMC PMC2714365. Research Blogging. Review in: Evid Based Ment Health. 2009 Feb;12(1):20
  42. ↑ Ballard C, Hanney ML, Theodoulou M, Douglas S, McShane R, Kossakowski K et al. (2009). "The dementia antipsychotic withdrawal trial (DART-AD): long-term follow-up of a randomised placebo-controlled trial.". Lancet Neurol 8 (2): 151-7. DOI:10.1016/S1474-4422(08)70295-3. PMID 19138567. Research Blogging. Review in: Ann Intern Med. 2009 Jun 16;150(12):JC6-8 Review in: Evid Based Med. 2009 Aug;14(4):115
  43. ↑ Campbell AJ, Robertson MC, Gardner MM, Norton RN, Buchner DM (1999). "Psychotropic medication withdrawal and a home-based exercise program to prevent falls: a randomized, controlled trial". J Am Geriatr Soc 47 (7): 850–3. PMID 10404930. [e]
  44. ↑ Dowling GA, Burr RL, Van Someren EJ, Hubbard EM, Luxenberg JS, Mastick J et al. (2008). "Melatonin and bright-light treatment for rest-activity disruption in institutionalized patients with Alzheimer's disease.". J Am Geriatr Soc 56 (2): 239-46. DOI:10.1111/j.1532-5415.2007.01543.x. PMID 18070004. PMC PMC2642966. Research Blogging.
  45. ↑ Gehrman PR, Connor DJ, Martin JL, Shochat T, Corey-Bloom J, Ancoli-Israel S (2009). "Melatonin fails to improve sleep or agitation in double-blind randomized placebo-controlled trial of institutionalized patients with Alzheimer disease.". Am J Geriatr Psychiatry 17 (2): 166-9. DOI:10.1097/JGP.0b013e318187de18. PMID 19155748. PMC PMC2630117. Research Blogging.
  46. ↑ Singer C, Tractenberg RE, Kaye J, Schafer K, Gamst A, Grundman M et al. (2003). "A multicenter, placebo-controlled trial of melatonin for sleep disturbance in Alzheimer's disease.". Sleep 26 (7): 893-901. PMID 14655926.
  47. ↑ Serfaty M, Kennell-Webb S, Warner J, Blizard R, Raven P (2002). "Double blind randomised placebo controlled trial of low dose melatonin for sleep disorders in dementia.". Int J Geriatr Psychiatry 17 (12): 1120-7. DOI:10.1002/gps.760. PMID 12461760. Research Blogging.
  48. ↑ Haffmans PM, Sival RC, Lucius SA, Cats Q, van Gelder L (2001). "Bright light therapy and melatonin in motor restless behaviour in dementia: a placebo-controlled study.". Int J Geriatr Psychiatry 16 (1): 106-10. PMID 11180494.
  49. ↑ Solomon PR, Adams F, Silver A, Zimmer J, DeVeaux R (2002). "Ginkgo for memory enhancement: a randomized controlled trial". JAMA 288 (7): 835–40. PMID 12186600. [e]
  50. ↑ Le Bars PL, Katz MM, Berman N, Itil TM, Freedman AM, Schatzberg AF (1997). "A placebo-controlled, double-blind, randomized trial of an extract of Ginkgo biloba for dementia. North American EGb Study Group". JAMA 278 (16): 1327–32. PMID 9343463. [e]
  51. ↑ 51.0 51.1 Birks J, Grimley Evans J (2009). "Ginkgo biloba for cognitive impairment and dementia". Cochrane Database Syst Rev (1): CD003120. DOI:10.1002/14651858.CD003120.pub3. PMID 19160216. Research Blogging.
  52. ↑ Husebo BS, Ballard C, Sandvik R, Nilsen OB, Aarsland D (2011). "Efficacy of treating pain to reduce behavioural disturbances in residents of nursing homes with dementia: cluster randomised clinical trial.". BMJ 343: d4065. DOI:10.1136/bmj.d4065. PMID 21765198. Research Blogging.
  53. ↑ Byles JE, Sanson-Fisher RW (June 1996). "Mass mailing campaigns to promote screening for cervical cancer: do they work, and do they continue to work?". Aust N Z J Public Health 20 (3): 254–60. PMID 8768414. [e]
  54. ↑ Ravaglia G, Forti P, Lucicesare A, et al (2007). "Physical activity and dementia risk in the elderly. Findings from a prospective Italian study". Neurology. DOI:10.1212/01.wnl.0000296276.50595.86. PMID 18094335. Research Blogging.
  55. ↑ Larson EB, Wang L, Bowen JD, et al (2006). "Exercise is associated with reduced risk for incident dementia among persons 65 years of age and older". Ann. Intern. Med. 144 (2): 73–81. PMID 16418406. [e]
  56. ↑ Abbott RD, White LR, Ross GW, Masaki KH, Curb JD, Petrovitch H (2004). "Walking and dementia in physically capable elderly men". JAMA 292 (12): 1447–53. DOI:10.1001/jama.292.12.1447. PMID 15383515. Research Blogging.
  57. ↑ 57.0 57.1 Verghese J, Lipton RB, Katz MJ, et al (2003). "Leisure activities and the risk of dementia in the elderly". N. Engl. J. Med. 348 (25): 2508–16. DOI:10.1056/NEJMoa022252. PMID 12815136. Research Blogging.
  58. ↑ Ellul J, Archer N, Foy CM, et al (March 2007). "The effects of commonly prescribed drugs in patients with Alzheimer's disease on the rate of deterioration". J. Neurol. Neurosurg. Psychiatr. 78 (3): 233–9. DOI:10.1136/jnnp.2006.104034. PMID 17012333. Research Blogging.
  59. ↑ Cramer C, Haan MN, Galea S, Langa KM, Kalbfleisch JD (July 2008). "Use of statins and incidence of dementia and cognitive impairment without dementia in a cohort study". Neurology 71 (5): 344–50. DOI:10.1212/01.wnl.0000319647.15752.7b. PMID 18663180. Research Blogging.
  60. ↑ Haag MD, Hofman A, Koudstaal PJ, Stricker BH, Breteler MM (January 2009). "Statins are associated with a reduced risk of Alzheimer disease regardless of lipophilicity. The Rotterdam Study". J. Neurol. Neurosurg. Psychiatr. 80 (1): 13–7. DOI:10.1136/jnnp.2008.150433. PMID 18931004. Research Blogging.
  61. ↑ Zandi PP, Sparks DL, Khachaturian AS, et al (February 2005). "Do statins reduce risk of incident dementia and Alzheimer disease? The Cache County Study". Arch. Gen. Psychiatry 62 (2): 217–24. DOI:10.1001/archpsyc.62.2.217. PMID 15699299. Research Blogging.
  62. ↑ Li G, Higdon R, Kukull WA, et al (November 2004). "Statin therapy and risk of dementia in the elderly: a community-based prospective cohort study". Neurology 63 (9): 1624–8. PMID 15534246. [e]
  63. ↑ DeKosky ST, Williamson JD, Fitzpatrick AL, et al (November 2008). "Ginkgo biloba for prevention of dementia: a randomized controlled trial". JAMA 300 (19): 2253–62. DOI:10.1001/jama.2008.683. PMID 19017911. Research Blogging.
  64. ↑ Mix JA, Crews WD (August 2002). "A double-blind, placebo-controlled, randomized trial of Ginkgo biloba extract EGb 761 in a sample of cognitively intact older adults: neuropsychological findings". Hum Psychopharmacol 17 (6): 267–77. DOI:10.1002/hup.412. PMID 12404671. Research Blogging.
  65. ↑ U.S. Preventive Services Task Force (2003). "Screening for dementia: recommendation and rationale". Ann. Intern. Med. 138 (11): 925–6. PMID 12779303. [e]
  66. ↑ 66.0 66.1 Barnes DE et al (2009). "Predicting risk of dementia in older adults. The late-life dementia risk index". Neurology. DOI:10.1212/WNL.0b013e3181a8163. PMID 19439724. Research Blogging.
  67. ↑ Reisberg B (1988). "Functional assessment staging (FAST).". Psychopharmacol Bull 24 (4): 653-9. PMID 3249767. [e]
  68. ↑ Sachs GA, Carter R, Holtz LR, Smith F, Stump TE, Tu W et al. (2011). "Cognitive impairment: an independent predictor of excess mortality: a cohort study.". Ann Intern Med 155 (5): 300-8. DOI:10.1059/0003-4819-155-5-201109060-00007. PMID 21893623. Research Blogging.
  69. ↑ Mitchell AJ, Shiri-Feshki M (December 2008). "Temporal trends in the long term risk of progression of mild cognitive impairment: a pooled analysis". J. Neurol. Neurosurg. Psychiatr. 79 (12): 1386–91. DOI:10.1136/jnnp.2007.142679. PMID 19010949. Research Blogging.
  70. ↑ Mitchell SL, Teno JM, Kiely DK, Shaffer ML, Jones RN, Prigerson HG et al. (2009). "The Clinical Course of Advanced Dementia.". N Engl J Med 361 (16): 1529-1538. DOI:10.1056/NEJMoa0902234. PMID 19828530. Research Blogging.
  71. ↑ 71.0 71.1 Mitchell SL, Miller SC, Teno JM, Kiely DK, Davis RB, Shaffer ML (2010). "Prediction of 6-month survival of nursing home residents with advanced dementia using ADEPT vs hospice eligibility guidelines.". JAMA 304 (17): 1929-35. DOI:10.1001/jama.2010.1572. PMID 21045099. Research Blogging.
Retrieved from "https://citizendium.org/wiki/index.php?title=Dementia&oldid=991561"