Evidence-Based Medicine

Mild Cognitive Impairment (MCI)

Mild Cognitive Impairment (MCI)

Background

  • Mild cognitive impairment (MCI) is a heterogeneous syndrome in which cognitive impairment leads to no or minimal impairment of activities of daily living and does not meet criteria for dementia.
  • MCI can be subclassified into amnestic MCI (memory impairments dominate) vs. nonamnestic MCI, and single-domain (impairment mostly isolated to 1 cognitive domain) vs. multiple-domain MCI.
  • Prevalence increases with age from 6.7% in patients aged 60-64 years to 37.6% in patients ≥ 85 years old.
  • Risk factors include apolipoprotein E gene (APOE) e4 allele, hormone replacement therapy, lower educational level, male sex, older age, prior critical illness, sleep-disordered breathing, vascular risk factors (such as diabetes and hypertension), and vitamin D deficiency.
  • Dementia within 2 years reported in 14.9% of patients with MCI > 65 years old, with a greater risk for patients with amnestic MCI, APOE e4 allele(s), diabetes, less education, and stroke.

Evaluation

  • Suspect cognitive impairment in patients with concerns over changes in cognition as reported by patient, clinician, or other informant (Strong recommendation).
  • Take careful history from patient and knowledgeable informants and perform physical to help with further assessments.
  • Conduct routine blood work and structural brain imaging to assess for potential causes of symptoms.
  • Perform cognitive assessment using a validated tool.
  • If cognitive assessment suggests cognitive impairment, perform in-depth clinical assessment.
    • Assess for functional impairment to differentiate between MCI (in which function is mostly preserved) and dementia (in which function is impaired) (Strong recommendation).
    • If an impairment in activities of daily function is suspected, consider dementia as a diagnosis (see Dementia Evaluation for details).
    • Otherwise, use established diagnostic criteria to determine diagnosis of MCI.
  • Also attempt to determine etiology and assess for potentially modifiable causes of symptoms and risk factors.

Management

  • Discuss diagnosis and uncertainties regarding prognosis, including advising patients and family members to discuss long-term planning topics (Strong recommendation).
  • Wean patients from medications that can contribute to cognitive impairment (if possible) and address potentially modifiable risk factors (Strong recommendation).
  • Advise general lifestyle strategies associated with reduced risk of poor health.
  • Assess for behavioral and neuropsychiatric symptoms and manage accordingly (Strong recommendation).
  • Advise regular exercise as part of an overall management strategy (Strong recommendation).
  • Consider cognitive interventions (Weak recommendation).
  • Advise patients and families that there are currently no medications or dietary agents shown to have symptomatic cognitive benefits in patients with MCI and that there are no FDA-approved medications for MCI (Strong recommendation).
    • Consider not offering cholinesterase inhibitors (Weak recommendation).
    • If offering a cholinesterase inhibitor, first discuss with the patient that there is no empirical evidence for benefit and that cholinesterase inhibitors are not indicated for MCI (Strong recommendation).
  • Perform serial assessments over time to monitor for changes in cognitive impairment (Strong recommendation).

Published: 01-07-2023 Updeted: 05-07-2023

References

  1. Petersen RC, Lopez O, Armstrong MJ, et al. Practice guideline update summary: Mild cognitive impairment: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology. Neurology. 2018 Jan 16;90(3):126-135, commentary can be found in Ann Intern Med 2018 Apr 17;168(8):JC38
  2. Tangalos EG, Petersen RC. Mild cognitive impairment in geriatrics. Clin Geriatr Med. 2018 Nov;34(4):563-589
  3. Langa KM, Levine DA. The diagnosis and management of mild cognitive impairment: a clinical review. JAMA. 2014 Dec 17;312(23):2551-61

Related Topics