Alzheimer diseaseAD; Dementia
An in-depth report on the causes, diagnosis, and treatment of Alzheimer disease.
Dementia is significant loss of cognitive functions such as memory, judgment, attention, and abstract thinking. Alzheimer disease is the most common form of dementia. It is a progressive brain disease. It affects more than 5 million Americans, and millions more worldwide.
Age is the greatest risk factor for Alzheimer disease. Most people who develop Alzheimer disease are 65 years old or older, and the risk increases with age. People age 85 years and older are especially at risk for Alzheimer disease.
Early symptoms of Alzheimer disease may include:
- Loss of concentration
- Language problems
- Confusion about time and place
- Impaired judgment
- Loss of insight
- Impaired movement and coordination
- Mood and behavior changes
- Apathy and depression
There is no cure for Alzheimer disease. Drug therapy aims to slow disease progression and treat symptoms associated with the disease. The benefit from drugs used to treat Alzheimer disease is typically small. Patients and their families may not notice any benefit.
Patients and their families need to discuss with their doctors whether drug therapy can help improve behavior or functional abilities. They also need to discuss whether or not drugs should be prescribed early in the course of the disease or delayed.
The following drugs are commonly prescribed for treatment of Alzheimer disease:
- Donepezil (Aricept, generic)
- Rivastigmine (Exelon, generic)
- Galantamine (Razadyne, generic)
- Memantine (Namenda)
Alzheimer disease (AD) is the most common cause of dementia among older people. Dementia is the medical term for loss of cognitive functions including memory, judgment, attention, and abstract thinking
Alzheimer disease is a progressive and incurable degenerative disease of the brain. AD begins slowly. It first involves the parts of the brain that control thought, memory and language.
The disease slowly attacks nerve cells in all parts of the cortex of the brain and some surrounding structures, thereby impairing a person's abilities to govern emotions, recognize errors and patterns, coordinate movement, and remember. The changes in the brain may begin to develop more than 20 years before symptoms develop. Ultimately, a person with AD loses memory and many other mental functions.
There are three brain abnormalities that are the hallmarks of the Alzheimer disease process:
- Plaques. A protein called beta-amyloid accumulates and forms sticky clumps of amyloid plaque between nerve cells (neurons). High levels of beta amyloid are associated with reduced levels of the neurotransmitter acetylcholine. (Neurotransmitters are chemical messengers in the brain.) Acetylcholine is part of the cholinergic system, which is essential for memory and learning.
- Tangles. Neurofibrillary tangles are the damaged remains of a protein called tau, which in its normal version helps maintain microtubules within healthy neurons. (Microtubules are hollow rods within cells that support their shape and structure.).
- Loss of nerve cell connections. The tangles and plaques cause neurons to lose their connection to one another and die off. As the neurons die, brain tissue shrinks (atrophies).
Stages of Alzheimer Disease
Although no cure has been found for Alzheimer, scientists are making advances in better understanding the disease and how it progresses. The U.S. National Institute on Aging and the Alzheimer's Association has criteria for defining and diagnosing Alzheimer. It classifies the disease into three stages:
- Preclinical. In this stage, brain changes including amyloid buildup and nerve cell disruption are beginning to occur but symptoms are not yet evident. Researchers are studying various tests for biomarkers to better understand what these changes mean and what type of risk they may pose for progression to Alzheimer dementia.
- Mild Cognitive Impairment (MCI). MCI is marked by symptoms of memory problems but they are not severe enough to interfere with a person's functioning or independence. People with MCI may or may not go on to develop Alzheimer dementia. Biomarker tests to better identify this stage are currently being developed.
- Alzheimer Dementia. This stage encompasses the spectrum of dementia severity from mild to severe. Symptoms are apparent and have gradually become worse over months or years. They are now significant enough to affect daily functional abilities. The most typical symptom is memory loss, particularly the learning and recall of recent information. Other symptoms may include difficulties in finding words, identifying and locating objects and faces, and problems with judgment and reasoning.
Scientists do not know what causes Alzheimer disease. It may be a combination of various genetic and environmental factors that trigger the process in which brain nerve cells are destroyed.
Genetics certainly plays a role in early-onset Alzheimer, a rare form of the disease that usually runs in families. Scientists are also investigating genetic targets for late-onset Alzheimer, which is the more common form.
Apolipoprotein E (ApoE) is the main gene that has been definitively linked to late-onset Alzheimer disease. However, only a small percentage of people carry the form of ApoE (ApoE e4) that increases the risk of late-onset Alzheimer. Other genes or combinations of genes may be involved. Researchers have made some preliminary identifications of other possible gene variants.
Researchers have investigated various environmental factors that may play a role in Alzheimer disease or may trigger the disease process in people who have a genetic susceptibility. Some studies have suggested an association between serious head injuries in early adulthood and Alzheimer development. Lower educational level, which may decrease mental and activity and neuron stimulation, has also been investigated. To date, there does not appear to be any evidence that infections, metals, or industrial toxins cause Alzheimer disease.
Alzheimer disease is the fifth leading cause of death in American adults age 65 and older. It affects more than 5 million Americans and millions more people worldwide.
Age is the primary risk factor for Alzheimer disease. The number of cases of Alzheimer disease doubles every 5 years beyond age 65. According to the U.S. Alzheimer's Association, nearly 1 in 3 people age 85 years and older have the disease. While less common, Alzheimer disease can also affect younger people. About 200,000 Americans younger than age 65 have early-onset Alzheimer disease.
More women than men develop Alzheimer disease but this is most likely because women tend to live longer than men. According to the Alzheimer's Association, nearly two-thirds of patients with Alzheimer disease are women. Women in their 60s are more likely to develop Alzheimer disease during their lifetimes than breast cancer.
Race and Ethnicity
African Americans and Hispanics are at greater risk for developing Alzheimer disease than whites. This may be in part because they have a higher prevalence of medical conditions such as high blood pressure and diabetes, which are associated with increased risk for Alzheimer. Genetic factors may also play a role.
Having a first-degree relative (parent, brother, sister) with Alzheimer disease increases your risk for the disease. Having more than one first-degree relative with Alzheimer disease further increases risk.
Mild Cognitive Impairment (MCI)
People who have memory problems and other early symptoms that suggest mild cognitive impairment (MCI) may be at increased risk for later developing Alzheimer disease. However, not everyone who has MCI goes on to have Alzheimer disease.
Serious Head Injury
A history of traumatic brain injury, including a concussion, is a risk factor for Alzheimer disease.
Heart and Vascular Diseases
There is growing evidence that diseases that affect the heart and vascular (blood vessel) system increase the risk of Alzheimer disease. The brain requires a steady supply of oxygen-rich blood, which is supplied by a healthy pumping heart and adequate blood flow throughout the body. Conditions associated with heart and circulatory problems include high blood pressure, unhealthy cholesterol levels, and type 2 diabetes. There is some evidence that controlling these conditions may help prevent Alzheimer disease.
Blood pressure is the force applied against the walls of the arteries as the heart pumps blood through the body. The pressure is determined by the force and amount of blood pumped and the size and flexibility of the arteries.
Clinical trials have evaluated numerous substances for preventing Alzheimer disease but have not found any of them to be helpful. They included nonsteroidal anti-inflammatory drugs (NSAIDs), statin drugs, estrogen replacement therapy, folic acid supplementation, vitamin E, fish oil supplements, and herbal remedies such as ginkgo biloba.
However, certain lifestyle changes may help in Alzheimer disease prevention:
- Stay mentally active. Participating in intellectually engaging activity (such as doing crossword puzzles or learning a new language) may help reduce the risk of Alzheimer disease.
- Stay physically active. Exercise and regular physical activity of at least moderate intensity is important for heart and vascular health and may help preserve cognitive function.
- Stay socially active. Personal relations and connections may help protect against Alzheimer disease.
- Eat a heart-healthy and brain-healthy diet. While no specific dietary factors have been found to prevent Alzheimer disease, a low-fat, low-cholesterol diet is healthy for the heart and the brain. Replace saturated fats and trans-fatty acids with unsaturated fats from plant and fish oils. Fish oil's omega-3 fatty acids, which contain docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) are an excellent source of unsaturated fat. Eat lots of darkly colored fruits and vegetables, which are the best source for antioxidant vitamins and other nutrients. (Although there has been much research, there is no evidence that vitamin B or E supplements, or fish oil supplements, are protective. Food is the best source for these nutrients.) The Mediterranean Diet is an example of an eating plan that includes many of these recommendations.
- Maintain a healthy weight. Obesity is associated with a more sedentary lifestyle, which is a risk factor for Alzheimer disease. Obesity also increases the risk for heart and metabolic conditions that may be associated with Alzheimer disease development.
The early symptoms of Alzheimer disease (AD) may be overlooked because they resemble signs of natural aging. However, extreme memory loss or other cognitive changes that disrupt normal life are not typical signs of aging. In addition, the symptoms of Alzheimer disease do not begin abruptly; they develop gradually and worsen over the course of months or years.
Older adults who begin to notice a persistent mild memory loss of recent events may have a condition called mild cognitive impairment (MCI). MCI may be a sign of early-stage Alzheimer disease in older people. Studies suggest that some, although not all, older individuals who experience such mild memory abnormalities can later develop Alzheimer disease.
Patients may be aware of their symptoms or may be unaware that anything is wrong. The Alzheimer's Association recommends that everyone learn these 10 warning signs of Alzheimer disease:
- Memory changes that disrupt daily life. Forgetfulness, particularly of recent events or information, or repeatedly asking for the same information.
- Challenges in planning or solving problems. Loss of concentration (having trouble planning or completing familiar tasks, difficulty with abstract thinking such as simple arithmetic problems).
- Difficulty completing familiar tasks at home, at work, or at leisure.
- Confusion about time or place. Difficulty recognizing familiar neighborhoods or remembering how you arrived at a location, confusion about months or seasons.
- Trouble understanding visual images and spatial relationships. Difficulty reading, figuring out distance, or determining color.
- Language problems. Forgetting the names of objects, mixing up words, difficulty completing sentences or following conversations.
- Misplacing things and losing the ability to retrace steps. Putting objects back in unusual places, losing things, accusing others of hiding or stealing.
- Impaired judgment and decision making. Dressing inappropriately or making poor financial decisions.
- Withdrawal from work or social activities. No longer participating in familiar hobbies and interests.
- Mood and personality changes. Confusion, increased fear or suspicion, apathy and depression, anxiety. Signs can be loss of interest in activities, increased sleeping, sitting in front of the television for long periods of time.
Alzheimer disease can only be definitely diagnosed after death when an autopsy of the brain is performed. However, Alzheimer diagnosis is a very active area of research. The goal is to diagnose Alzheimer disease while it is still in its early stages.
Researchers are making progress studying biomarkers, chemical substances that signal changes in the brain associated with Alzheimer disease. In a recent study of biomarkers, scientists found that measuring levels of amyloid beta and tau proteins in brain imaging scans and spinal fluid may help predict the development of Alzheimer disease many years before symptoms begin.
The scientific community is working on standardizing the use of biomarkers to aid in the early detection of Alzheimer disease while it is in its preclinical or mild cognitive impairment stages. Biomarkers may also eventually help doctors evaluate how the disease progresses.
At this time, there is no one test that confirms a diagnosis of Alzheimer disease. Doctors use a variety of tests to make a probable diagnosis of Alzheimer disease.
Medical History and Physical Examination
The doctor will ask about the patient's health history, including other medical conditions the patient has, recent or past illnesses, and progressive changes in mental function, behavior, or daily activities. The doctor will ask about use of prescription drugs (it is helpful to bring a complete list of the patient's medications) and lifestyle factors, including diet and use of alcohol. The doctor will evaluate the patient's hearing and vision, and check blood pressure and other physical signs. A neurological test will also be conducted to check reflexes, coordination, and eye movement.
Blood and urine samples may be collected. They can help the doctor evaluate other possible causes of dementia, such as thyroid imbalances or vitamin deficiencies. Researchers are studying measuring levels of amyloid beta and tau proteins in spinal fluid samples to help identify patients with memory problems who may be at risk for developing Alzheimer disease.
Several psychological tests are used to assess difficulties in attention, perception, memory, language, problem-solving, social, and language skills. These tests can also be used to evaluate mood problems such as depression. Because depression may mimic symptoms of dementia, neuropsychological testing may be useful in determining if symptoms are due to depression, dementia, or both.
One commonly used test is the Mini-Mental State Exam (MMSE), which uses a series of questions and tasks to evaluate cognitive function. For example, the patient is given a series of words and asked to recall and repeat them a few minutes later. In the clock-drawing test, the patient is given a piece of paper with a circle on it and is asked to write the numbers in the face of a clock and then to show a specific time on the clock.
Imaging tests are useful for ruling out blood clots, tumors, or other structural abnormalities in the brain that may be causing signs of dementia. These tests include magnetic resonance imaging (MRI), computed tomography (CT), or positron-emission testing (PET) scans.
Researchers are using MRIs and PET scans to study new approaches to diagnosing Alzheimer disease in earlier stages of the disease. Methods include measuring the volume and shrinkage (atrophy) of brain tissue with MRI and evaluating the brain's use of glucose with PET.
Since 2012, the Food and Drug Administration (FDA) has approved three radioactive diagnostic drugs that are used with PET scans to evaluate beta amyloid density. They are florbetapir (Amyvid), flutemetamol (Vizamyl), and florbetaben (Neuraceq). Patients with Alzheimer disease have a high build-up of amyloid plaques in the brain. However, high amyloid plaque density is also found in some patients with normal cognitive function as well as those who have dementias not related to Alzheimer disease. If PET scans using these drugs do not show amyloid accumulation in the brain, a person's symptoms are unlikely due to Alzheimer disease.
Ruling out Other Causes of Memory Loss or Dementia
Alzheimer disease is the most common cause of dementia. Other causes of dementia in the elderly can include:
- Vascular dementia (abnormalities in the vessels that carry blood to the brain)
- Lewy bodies variant (LBV), also called dementia with Lewy bodies
- Parkinson disease
- Frontotemporal dementia
Vascular Dementia. Vascular dementia is primarily caused by either multi-infarct dementia (multiple small strokes) or Binswanger's disease (which affects tiny arteries in the midbrain).
Lewy Bodies Variant. Lewy bodies are abnormalities found in the brains of patients with both Parkinson and Alzheimer disease. They can also be present in the absence of either disease; in such cases, the condition is called Lewy bodies variant (LBV). In all cases, the presence of Lewy bodies is highly associated with dementia.
Parkinson Disease. Some of the symptoms of Parkinson and Alzheimer disease can be similar and the diseases may coexist.
Parkinson disease is a slowly progressive disorder that affects movement, muscle control, and balance. Part of the disease process develops as cells are destroyed in certain parts of the brain stem, particularly the crescent-shaped cell mass known as the substantia nigra. Nerve cells in the substantia nigra send out fibers to tissue located in both sides of the brain. There the cells release essential neurotransmitters that help control movement and coordination. About a third of people with Parkinson disease will develop dementia. However, unlike Alzheimer disease, language is not usually affected in Parkinson dementia.
Frontotemporal Dementia. Frontotemporal dementia (FTD) is a term used to describe a group of disorders that affect the frontal and temporal lobes of the brain. Although some of the symptoms can overlap with Alzheimer disease, people who develop this condition tend to be younger than most patients with Alzheimer disease.
Other Conditions. A number of conditions, including many medications, can produce symptoms similar to Alzheimer. These conditions include severe depression, drug abuse, thyroid disease, vitamin deficiencies, blood clots, infections, brain tumors, and various neurological or vascular disorders.
There is no cure for Alzheimer disease or treatment to stop its progression or reverse the symptoms. Most drugs used to treat Alzheimer are aimed at slowing the rate at which symptoms become worse, and prolonging a person's ability to remain independent. The benefit from these drugs is generally small, and patients and their families may not even notice any benefit.
Alzheimer disease is classified into various stages that range from mild to moderate to severe. In the final stages of Alzheimer disease, the patient is unable to communicate and is completely dependent on others for care.
The lifespan of patients with Alzheimer disease is generally reduced, although a patient may live anywhere from 4 to 20 years after diagnosis. The final phase of the disease may last from a few months to several years, during which time the patient becomes increasingly immobile and dysfunctional.
Most people with Alzheimer disease are cared for at home, especially during the early stages of the disease. Caregiving is an enormous commitment. Support services can greatly improve the quality of life for both caretakers and their patients and make it easier for people to continue caring for patients in their homes. These services include home healthcare aides and adult day care.
As Alzheimer disease progresses, round-the-clock care is usually required. At this point, the family needs to decide whether in-home treatment can be continued or whether placement in a nursing home or assisted living facility is a feasible option. In choosing a facility, it is best to select one that is specialized in the care of people with Alzheimer disease and equipped to meet their needs.
Most drugs used to treat Alzheimer disease, and those under investigation, are aimed at slowing progression. At this time, there is no cure. In addition, the improvements from some of these drugs may be so modest that patients and their families may not notice any benefit.
The FDA has approved two drug classes to treat the cognitive symptoms of Alzheimer disease:
- Cholinesterase inhibitors (generally used to treat mild-to-moderate Alzheimer disease; donepezil is also approved for treatment of severe dementia)
- N-methyl-D-aspartate (NMDA) receptor antagonists (used to treat moderate-to-severe Alzheimer disease)
While these drugs do not have generally serious risks, they can cause a number of bothersome side effects, including indigestion, nausea, vomiting, diarrhea, loss of appetite, muscle cramps, and fatigue.
Patients and caregivers should ask their doctors the following questions about when and if to use these drugs:
- Will there be a noticeable change in behavior or function of the patient? The published studies that enabled approval of these drugs for treatment of Alzheimer disease demonstrated modest benefit when evaluating patients using cognitive and functional scales. While these scales are important for consistency of recording and performing studies, the benefit demonstrated in clinical trials does not necessarily translate into any significant change in how patients function in their daily lives. There is, in fact, no evidence that use of these medications extends the time before a person requires care in an institutional setting, such as a nursing home.
- Is it better to use these drugs early in the course of Alzheimer disease? Treating people with mild cognitive impairment (persistent mild memory loss of recent events but no diagnosis of Alzheimer disease) does not seem to prevent them from developing Alzheimer disease.
- If there are no signs of improvement, when should a drug be discontinued? Define goals with the patient's doctor, and establish a timeline for how long a drug should be tried and when it should be stopped.
Cholinesterase Inhibitors (Donepezil, Rivastigmine, Galantamine)
Cholinesterase inhibitors are designed to protect the cholinergic system, which is essential for memory and learning and is progressively destroyed in Alzheimer disease. These drugs work by preventing the breakdown of the brain chemical acetylcholine.
The three most commonly prescribed cholinesterase inhibitors for Alzheimer disease are donepezil, rivastigmine, and galantamine:
- Donepezil. Donepezil (Aricept, generic) is the only Alzheimer disease drug approved for all stages of dementia, from mild to severe. It is taken once a day and has only modest benefits at best.
- Rivastigmine. Rivastigmine (Exelon, generic) targets two enzymes: Acetylcholinesterase and butyrylcholinesterase. It is available in pill form and also available as a skin patch. It is approved for mild-to-moderate Alzheimer disease. A higher-dose skin patch is approved for patients with severe Alzheimer disease.
- Galantamine. Galantamine (Razadyne, generic) in addition to inhibiting acetylcholinesterase, also directly stimulates acetylcholine receptors. It is approved to treat mild-to-moderate Alzheimer disease.
Side Effects. Common side effects of cholinesterase inhibitors, especially when taken at higher doses, may include nausea, vomiting, diarrhea, and upset stomach. Rivastigmine and galantamine tend to have more side effects than donepezil, and may also cause weight loss and loss of appetite. Cholinesterase inhibitors may increase the risk for gastrointestinal bleeding or ulcers, especially when used with NSAIDs (which can also cause gastric irritation).
Some drugs known as anticholinergics may offset the effects of the Alzheimer disease pro-cholinergic drugs. Such drugs include antihistamines, antipsychotic drugs, and some antidepressants and anti-incontinence drugs.
Effectiveness. Comparative studies have reported little difference in effectiveness among these drugs. In any case, the benefits of these drugs may often not be noticeable in everyday life. Many doctors have reservations about developing additional drugs that affect the cholinergic system since, at best, they only slow progression and do not appear to affect the basic destructive disease process or even the quality of a patient's life.
N-methyl-D-aspartate (NMDA) Receptor Antagonist (Memantine)
Memantine (Namenda) is approved for treatment of moderate-to-severe Alzheimer disease. (It does not appear to be effective for mild Alzheimer disease. Cholinesterase inhibitors are used to treat mild-to-moderate stages of the disease.) By blocking NMDA receptors, memantine protects against the overstimulation of glutamate, an amino acid that excites nerves and, in excess, is a powerful nerve-cell killer.
Memantine is prescribed either alone or in combination with donepezil. Studies indicate that memantine may help modestly improve cognitive function and delay the progression of Alzheimer disease for up to 1 year. Side effects are generally mild but may include dizziness, drowsiness, or fainting.
Treating Symptoms Associated with Alzheimer Disease
Depression. Antidepressants known as selective serotonin reuptake inhibitors (SSRIs), including fluoxetine (Prozac, generic) and sertraline (Zoloft, generic), may help reduce depression, irritability, and restlessness associated with Alzheimer in some patients.
Apathy. Depression is often confused with apathy. An apathetic patient lacks emotions, motivation, interest, and enthusiasm while a depressed patient is generally very sad, tearful, and hopeless. Apathy may respond to stimulants, such as methylphenidate (Ritalin, generic), rather than antidepressants.
Psychosis. Antipsychotic drugs are used to treat verbally or physically aggressive behavior and hallucinations. Because older antipsychotic drugs, such as haloperidol (Haldol, generic), have severe side effects, most doctors now prescribe newer atypical antipsychotics, such as risperidone (Risperdal, generic) or olanzapine (Zyprexa).
However, these newer antipsychotic drugs can cause serious side effects, including confusion, sleepiness, and Parkinsonian-like symptoms. In addition, studies indicate that their safety risks may outweigh any possible benefits. Studies show that both atypical and older antipsychotics produce a slightly increased rate of death in patients with Alzheimer disease or dementia and that atypical antipsychotics work no better than placebo in controlling psychosis, aggression, and agitation in patients with Alzheimer disease.
The American Psychiatric Association and the American Geriatrics Society recommend against prescribing antipsychotic medication to patients with dementia unless absolutely necessary. They recommend first trying behavioral treatments and controlling changes in the patient's environment and routine.
Disturbed Sleep. Patients with Alzheimer disease commonly experience disturbances in their sleep/wake cycles. Moderately short-acting sleeping drugs, such as temazepam (Restoril, generic), zolpidem (Ambien, generic), or zaleplon (Sonata, generic), or sedating antidepressants, such as trazodone (Desyrel, generic), may be useful in managing insomnia. However, these drugs increase the risk of falling, confusion, and abnormal behavior and must be used with considerable caution and restraint.
Some research suggests that exposure to brighter-than-normal artificial light during the day for patients with normal vision may help reset wake/sleep cycles and prevent nighttime wandering and sleeplessness. Sleep hygiene methods (regular times for meal and bed, exercise, avoiding caffeine) can also be helpful.
Caregivers of people with Alzheimer disease face enormous challenges. Few diseases disrupt patients and their families so completely or for so long a period of time as Alzheimer disease. The following tips may help caregivers better cope with some of the issues and behaviors associated with this disease.
Personality Changes and Communication
There is no single Alzheimer disease personality, just as there is no single human personality. All patients must be treated as the individuals they continue to be, even after their social self has vanished.
Patients with Alzheimer disease often display abrupt mood swings, and some become aggressive and angry. Some of this erratic behavior is caused by chemical changes in the brain. But it may also be due to the experience of losing knowledge and understanding of one's surroundings, causing fear and frustration that patients can no longer express verbally.
The following recommendations for caregivers may help soothe patients and avoid agitation:
- Establish a daily routine for getting up, meal times, bathing, activities to help patients have a sense of comfort and familiarity.
- Keep environmental distractions and noise (television, radio) at a minimum if possible. (Even normal noises, such as people talking outside a room, may seem threatening and trigger agitation or aggression.)
- Speak clearly in a gentle tone of voice using simple words and short sentences. Allow enough time for a response.
- Offer diversions, such as a snack or car ride, if the patient starts shouting or exhibiting other disruptive behavior.
- Maintain as natural an attitude as possible. Patients with Alzheimer disease can be highly sensitive to the caregiver's underlying emotions and react negatively to patronization or signals of anger and frustration.
- Showing movies or videos of family members and events from the patient's past may be comforting.
Although much attention is given to the negative emotions of patients with Alzheimer disease, some patients become extremely gentle, retaining an ability to laugh at themselves or appreciate simple visual jokes even after their verbal abilities have disappeared. Some patients may seem to be in a drug-like or "mystical" state, focusing on the present experience as their past and future slip away. Encouraging and even enjoying such states may bring comfort to both the patient and the caregiver.
Bathing and Dressing
Hygiene and grooming can be major challenges for caregivers. Many patients resist bathing or taking a shower. Some patients find bathing confusing or frightening. Some spouses find that showering with their afflicted mate can solve the problem for a while. Establishing a daily and familiar routine can be helpful.
Often patients with Alzheimer disease lose their sense of color and design and will put on odd or mismatched clothing. It is important to maintain a sense of humor and perspective and to learn which battles are worth fighting and which ones are best abandoned. Caregivers can pick a selection of outfits and allow the patient to select a favorite. Try to choose clothes that are easy to put on and take off.
Eating and Drinking
Weight loss and the gradual inability to swallow are two major related problems in late-stage Alzheimer disease and are associated with an increased risk of death. As Alzheimer disease progresses, patients may change their food preferences or find some kinds of foods more difficult to eat. Try different foods and be sure to allow enough time for the patient to eat. Limit distractions around mealtimes. Because choking is a danger, you should learn how to administer the Heimlich maneuver. Dehydration can also become a problem. It is important to encourage fluid intake equal to 8 glasses of water daily. Coffee and tea are mild diuretics that may deplete fluid.
Patients at any stage of dementia, including mild, are at high risk for unsafe driving. Typical Alzheimer disease symptoms, such as difficulty remembering and navigating locations, poor judgment, and slow decision making, all pose dangers for driving. A history of recent citations, crashes, or aggressive or reckless driving are specific warning signs. As soon as Alzheimer disease is diagnosed, the patient should be prevented from driving. This includes hiding car keys.
Wandering is a common problem. As memory problems worsen, patients may become easily confused, disoriented, and lost. The following precautions are recommended:
- Locks should be installed outside the door, which the caregiver can open, but the patient cannot.
- Alarms may be installed at exits.
- Plan daily activities and distractions to coincide with the times of day that the patient seems prone to wandering. This can be as simple as giving the patient a household task like folding towels.
- Daily exercise can help give the patient a chance to burn off energy and sleep better at night.
- Make sure the patient is not wandering due to hunger, thirst, or need to use bathroom.
- Consider enrolling the patient in a program such as the Alzheimer's Association's Medic Alert and Safe Return, which provides identification supplies and procedures that help locate patients who wader away from home and become lost.
Incontinence (loss of control of bowel or urine function) is one of the main reasons why many caregivers decide to seek nursing home placement. When the patient first shows signs of incontinence, the doctor should make sure that it is not caused by an infection. Urinary incontinence may be controlled for some time by trying to monitor times of liquid intake, feeding, and urinating. Once a schedule has been established, the caregiver may be able to anticipate incontinent episodes and get the patient to the toilet before they occur.
Urinary tract infections (UTIs) are a common cause of urinary incontinence. UTIs can also cause behavioral changes, and worsen aggression and confusion symptoms. Antibiotics are used to treat UTIs.
As the disease progresses to later stages, patients become immobile, literally forgetting how to move. Eventually, they become almost entirely wheelchair-bound or bedridden. Bedsores can be a major problem. Sheets must be kept clean, dry, and free of food. The patient's skin should be washed frequently, gently blotted thoroughly dry, and moisturizers applied. Try to move the patient every few hours and keep their feet raised with pillows or pads. Manipulation exercises can help keep legs and arms flexible.
Care for the Caregiver
Caregiving for a loved one with Alzheimer disease is undoubtedly stressful. Most patients with Alzheimer disease are cared for at home by family members, who often lack adequate support, finances, or training for this difficult job.
It is important for caregivers to recognize and take care of their own physical and emotional needs. Depression, exhaustion, guilt, and anger can lead to caregiver burnout as well as poor health.
Seek out support from family, friends, and professional associations. Such support includes individual and family counseling, support groups, and stress management and problem-solving techniques.
- www.nia.nih.gov/alzheimers -- Alzheimer's Disease Education and Referral Center (U.S. National Institute on Aging)
- www.alz.org -- Alzheimer's Association
- www.alzfdn.org -- Alzheimer's Foundation of America
- www.alz.co.uk -- Alzheimer's Disease International
- www.aan.com -- American Academy of Neurology
- www.medicalert.org -- Medic Alert
- www.clinicaltrials.gov -- Find clinical trials
- www.medicare.gov/NHCompare/Home.asp -- Find a nursing home
ADAPT Research Group; Lyketsos CG, Breitner JC, Green RC, et al. Naproxen and celecoxib do not prevent AD in early results from a randomized controlled trial. Neurology. 2007;68(21):1800-8.
AGS Choosing Wisely Workgroup. American Geriatrics Society identifies another five things that healthcare providers and patients should question. J Am Geriatr Soc. 2014;62(5):950-60.
AGS Choosing Wisely Workgroup. American Geriatrics Society identifies five things that healthcare providers and patients should question. J Am Geriatr Soc. 2013;61(4):622-31.
Albert MS, Dekosky ST, Dickson D, et al. The diagnosis of mild cognitive impairment due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimer's Dement. 2011;7(3):270-9.
Alzheimer's Association. 2014 Alzheimer's disease facts and figures. Alzheimer's Dement. 2014;10(2):e47-e92.
Ayalon L, Gum AM, Feliciano L, Arean PA. Effectiveness of nonpharmacological interventions for the management of neuropsychiatric symptoms in patients with dementia: a systematic review. Arch Intern Med. 2006;166(20):2182-8.
Ballard C, Gauthier S, Corbett A, Brayne C, Aarsland D, Jones E. Alzheimer's disease. Lancet. 2011;377(9770):1019-31.
Bateman RJ, Xiong C, Benzinger TL, et al. Clinical and biomarker changes in dominantly inherited Alzheimer's disease. N Engl J Med. 2012;367(9):795-804. Erratum in N Engl J Med. 2012;367(8):780.
Crane PK, Walker R, Hubbard RA, et al. Glucose levels and risk of dementia. N Engl J Med. 2013;369(6):540-8.a
Daviglus ML, Bell CC, Berrettini W, et al. National Institutes of Health State-of-the-Science Conference statement: preventing alzheimer disease and cognitive decline. Ann Intern Med. 2010;153(3):176-81.
De Meyer G, Shapiro F, Vanderstichele H, et al. Diagnosis-independent Alzheimer disease biomarker signature in cognitively normal elderly people. Arch Neurol. 2010;67(8):949-56.
Gu Y, Nieves JW, Stern Y, Luchsinger JA, Scarmeas N. Food combination and Alzheimer disease risk: a protective diet. Arch Neurol. 2010;67(6):699-706.
Iverson DJ, Gronseth GS, Reger MA, Classen S, Dubinsky RM, Rizzo M; Quality Standards Subcommittee of the American Academy of Neurology. Practice parameter update: evaluation and management of driving risk in dementia: report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2010;74(16):1316-24.
Jack CR Jr, Albert MS, Knopman DS, et al. Introduction to the recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimer's Dement. 2011;7(3):257-62.
Jonsson T, Stefansson H, Steinberg S, Jonsdottir I, Jonsson PV, Snaedal J, Variant of TREM2 associated with the risk of Alzheimer's disease. N Engl J Med. 2013;368(2):107-16.
Knopfman DS. Alzheimer's disease and other dementias. In: Goldman L, Schafer AI, eds. Goldman's Cecil Medicine. 24th ed. Philadelphia, PA: Elsevier Saunders; 2011:c2274-83.
Lautenschlager NT, Cox KL, Flicker L, et al. Effect of physical activity on cognitive function in older adults at risk for Alzheimer disease: a randomized trial. JAMA. 2008;300(9):1027-37.
Mayeux R. Early Alzheimer's disease. N Engl J Med. 2010;362(4):2194-201.
McKhann GM, Knopman DS, Chertkow H, et al. The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimer's Dement. 2011;7(3):263-9.
Querfurth HW, LaFerla FM. Alzheimer's disease. N Engl J Med. 2010;362(4):329-44.
Quinn JF, Raman R, Thomas RG, et al. Docosahexaenoic acid supplementation and cognitive decline in Alzheimer disease: a randomized trial. JAMA. 2010;304(17):1903-11.
Reitz C, Jun G, Naj A, et al. Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E epsilon-4,and the risk of late-onset Alzheimer disease in African Americans. JAMA. 2013;309(14):1483-92.
Roe CM, Fagan AM, Grant EA, et al. Amyloid imaging and CSF biomarkers in predicting cognitive impairment up to 7.5 years later. Neurology. 2013;80(19):1784-91.
Scarmeas N, Luchsinger JA, Schupf N, et al. Physical activity, diet, and risk of Alzheimer disease. JAMA. 2009;302(6):627-37.
Schneider LS, Dagerman KS, Higgins JP, McShane R. Lack of evidence for the efficacy of memantine in mild Alzheimer disease. Arch Neurol. 2011;68(8):991-8.
Seshadri S, Fitzpatrick AL, Ikram MA, et al. Genome-wide analysis of genetic loci associated with Alzheimer disease. JAMA. 2010 May 12;303(18):1832-40.
Snitz BE, O'Meara ES, Carlson MC, et al. Ginkgo biloba for preventing cognitive decline in older adults: a randomized trial. JAMA. 2009;302(24):2663-70.
Sperling RA, Aisen PS, Beckett LA, et al. Toward defining the preclinical stages of Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimer's Dement. 2011;7(3):280-92.
Vellas B, Coley N, Ousset PJ, Berrut G, Dartigues JF, Dubois B, et al. Long-term use of standardised Ginkgo biloba extract for the prevention of Alzheimer's disease (GuidAge): a randomised placebo-controlled trial. Lancet Neurol. 2012;11(10):851-9.
Review Date: 10/7/2014
Reviewed By: Joseph V. Campellone, MD, Division of Neurology, Cooper University Hospital, Camden, NJ. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team. Author: Julia Mongo, MS.