Clinical indication | Alzheimer’s Association’s appropriate use criteria |
Meeting core clinical criteria for probable AD dementia with typical age of onset | Appropriate |
Symptoms suggesting possible AD dementia* | |
Dementia with onset age below 65 years* | |
Mild cognitive impairment with onset age below 65 years | |
Persistent, progressing or unexplained mild cognitive impairment | |
Subjective cognitive decline but considered to be at high risk of AD (persistent decline in memory rather than other cognitive domains; onset in the last 5 years, age at onset >60 years, worries associated with subjective cognitive decline, feeling of worse performance than others of the same age group, confirmation of cognitive decline by an informant; carriage of APOE ε 4) | |
Dominant symptom of change in behaviour, where AD diagnosis is being considered* | |
Determining disease severity in patients who have already received a diagnosis of AD | Inappropriate |
Subjective cognitive decline not considered to be at high risk of AD | |
Symptoms of rapid eye movement sleep behaviour disorder | |
Carriers of autosomal dominant AD mutations, with or without symptoms | |
In lieu of genotyping for suspected carriers of autosomal dominant AD mutations | |
Carriers of APOE ε 4 with no cognitive impairment | |
Cognitively unimpaired on objective testing and no subjective cognitive decline but considered as high risk due to family history of AD | |
Cognitively unimpaired on objective testing, no subjective cognitive decline, no expressed concern about developing AD and no condition suggesting high risk |
Reproduced with minor reformatting from Shaw et al 7 with the publisher’s permission.
*Indications that would be considered appropriate according to the current NICE guideline.6
AD, Alzheimer’s disease; APOE, apolipoprotein E gene; NICE, National Institute for Health and Care Excellence.