Dementia is a major neurocognitive disorder involving deficits that interfere with daily function. Age is the greatest risk factor for developing the disease. Other risk factors include family history, cardiovascular disease, uncontrolled diabetes, and lower education levels. The initial evaluation for dementia involves recognizing subtle signs that are often missed or mistaken for normal aging. Screening tools include the Mini-Cog, Memory Impairment Screen (MIS), and questionnaires that are completed by caregivers or friends. If cognitive impairment is suspected, a more detailed evaluation should be performed using tools such as the Montreal Cognitive Assessment (MoCA), Saint Louis University Mental Status (SLUMS), or Rowland Universal Dementia Assessment Scale (RUDAS). A thorough history should be taken and a medication review and physical examination should be performed for the assessment of vision; hearing; cardiovascular, nutritional, and functional status; neurologic function; and psychiatric status. Laboratory testing, such as vitamin B12 and folate levels, thyroid function, complete blood cell count, and comprehensive metabolic panel, may be necessary to rule out underlying conditions. Brain imaging with noncontrast magnetic resonance imaging (or non-contrast computed tomography of the head if magnetic resonance imaging is unavailable or contraindicated) can rule out secondary causes. Differentiating dementia from potentially reversible conditions such as depression and delirium is essential. Referral to a neurologist is recommended for early-onset symptoms (before 60 years of age), for severe behavioral disturbances, or if the diagnosis is unclear.
The Diagnostic and Statistical Manual of Mental Disorders, 5th ed., defines dementia as a major neurocognitive disorder that requires evidence of decline in at least one of six cognitive domains that interfere with daily function.1 Mild cognitive impairment (MCI) is defined as cognitive impairment without functional impact.1 In the United States, the prevalence of dementia is rising as the population ages, affecting 6.9 million individuals older than 65 years. Age is the strongest risk factor for developing dementia2 (Table 12–4).
WHAT'S NEW ON THIS TOPIC

| The 2024 Lancet Commission report identified 14 potentially modifiable risk factors associated with dementia: less education, traumatic brain injury, physical inactivity, smoking, excessive alcohol intake, hypertension, obesity, uncontrolled diabetes, hearing loss, depression, social isolation, untreated vision loss, high low-density lipoprotein cholesterol, and air pollution. |
| Clinical trials are underway to evaluate serum and cerebrospinal fluid biomarkers for predicting cognitive decline and Alzheimer disease progression in patients with mild cognitive impairment. However, the use of routine biomarkers for progressive dementias in mild cognitive impairment is not recommended due to the risks of overdiagnosis and overtreatment. |
SORT: KEY RECOMMENDATIONS FOR PRACTICE

| Clinical recommendation | Evidence rating | Comments |
|---|---|---|
| Validated instruments, such as the Mini-Cog or the Memory Impairment Screen, should be used for screening patients at risk for dementia.9,18–21 | C | Expert opinion, consensus guidelines, systematic review, and studies on accuracy of screening tools |
| If initial testing indicates potential cognitive impairment or there is high suspicion for impairment despite normal testing, a more detailed evaluation should be performed using tools such as MoCA, SLUMS, or RUDAS.21–27 | B | Expert opinion and consensus guidelines, systematic review, and comparative studies on cognitive testing |
| Laboratory testing for the evaluation of cognitive or behavioral symptoms should be tailored to the patient's medical risks and profile. Initial laboratory studies include complete blood cell count, comprehensive metabolic panel, thyroid-stimulating hormone (thyrotropin), and folate and vitamin B12 levels.28 | C | Expert opinion and consensus guideline in the absence of clinical trials |
| Structural neuroimaging with noncontrast MRI (or noncontrast head CT if MRI is unavailable) is appropriate to rule out secondary causes.28,35 | C | Expert opinion and consensus guideline in the absence of clinical trials |
CT = computed tomography; MoCA = Montreal Cognitive Assessment; MRI = magnetic resonance imaging; RUDAS = Rowland Universal Dementia Assessment Scale; SLUMS = Saint Louis University Mental Status.
A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, go to https://www.aafp.org/afpsort.
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