- Author:
Sung Hoon KANG
1
;
Jee Hyang JEONG
;
Jung-Min PYUN
;
Geon Ha KIM
;
Young Ho PARK
;
YongSoo SHIM
;
Seong-Ho KOH
;
Chi-Hun KIM
;
Young Chul YOUN
;
Dong Won YANG
;
Hyuk-je LEE
;
Han LEE
;
Dain KIM
;
Kyunghwa SUN
;
So Young MOON
;
Kee Hyung PARK
;
Seong Hye CHOI
Author Information
- Publication Type:ORIGINAL ARTICLE
- From:Journal of Clinical Neurology 2025;21(3):182-189
- CountryRepublic of Korea
- Language:English
-
Abstract:
Background:and Purpose We aimed to determine the proportion of Korean patients with early Alzheimer’s disease (AD) who are eligible to receive lecanemab based on the United States Appropriate Use Recommendations (US AUR), and also identify the barriers to this treatment.
Methods:We retrospectively enrolled 6,132 patients with amnestic mild cognitive impairment or mild amnestic dementia at 13 hospitals from June 2023 to May 2024. Among them, 2,058 patients underwent amyloid positron emission tomography (PET) and 1,199 (58.3%) of these patients were amyloid-positive on PET. We excluded 732 patients who did not undergo brain magnetic resonance imaging between June 2023 and May 2024. Finally, 467 patients were included in the present study.
Results:When applying the criteria of the US AUR, approximately 50% of patients with early AD were eligible to receive lecanemab treatment. Among the 467 included patients, 36.8% did not meet the inclusion criterion of a Mini-Mental State Examination (MMSE) score of ≥22.
Conclusions:Eligibility for lecanemab treatment was not restricted to Korean patients with early AD except for those with an MMSE score of ≥22. The MMSE criteria should therefore be reconsidered in areas with a higher proportion of older people, who tend to have lower levels of education.