Trough Melatonin Levels Differ between Early and Late Phases of Alzheimer Disease
Chieh-Hsin Lin1,2,3, Chih-Chiang Chiu4,5, Hsien-Yuan Lane2,6,7
1Department of Psychiatry, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Kaohsiung, 2Graduate Institute of Biomedical Sciences, China Medical University, Taichung, 3School of Medicine, Chang Gung University, Taoyuan, 4Department of Psychiatry, Taipei City Psychiatric Center, 5Department of Psychiatry, School of Medicine, Taipei Medical University, Taipei, 6Department of Psychiatry and Brain Disease Research Center, China Medical University Hospital, 7Department of Psychology, College of Medical and Health Sciences, Asia University, Taichung, Taiwan
Correspondence to: Hsien-Yuan Lane Department of Psychiatry, China Medical University Hospital, No. 2, Yuh-Der Road, Taichung 404, Taiwan
Received: May 7, 2020; Revised: July 22, 2020; Accepted: July 30, 2020; Published online: February 28, 2021.
© The Korean College of Neuropsychopharmacology. All rights reserved.

Objective: Melatonin has been considered to have an essential role in the pathophysiology of Alzheimer’s disease (AD) for its regulatory function on circadian rhythm and interaction with glutamate for the modulation of learning and memory. Previous studies revealed that melatonin levels decreased in patients with AD. However, melatonin supplement didn’t show promising efficacy for AD. This study compared trough melatonin levels among elderly people with different severities of cognitive deficits.
Methods: We enrolled 270 elder individuals (consisting four groups: healthy elderly, amnestic mild cognitive impairment [MCI], mild AD, and moderate-severe AD) in the learning cohort. Trough melatonin levels in plasma were measured using ELISA. Cognitive function was evaluated by Clinical Dementia Rating Scale (CDR) and Mini-Mental State Examination (MMSE). An independent testing cohort, also consisting of four groups, was enrolled for ascertainment.
Results: In the learning cohort, trough melatonin levels decreased in the MCI group but elevated in the mild and moderate to severe AD groups. Trough melatonin levels were associated with CDR and MMSE in MCI or AD patients significantly. In the testing cohort, the results were similar to those in the learning cohort.
Conclusion: This study demonstrated that trough melatonin levels in the peripheral blood were decreased in MCI but increased with the severity of AD. The finding supports the trials indicating that melatonin showed efficacy only in MCI but not in AD. Whether trough melatonin level has potential to be a treatment response biomarker for AD, especially its early phase needs further studies.
Keywords: Melatonin; Alzheimer’s disease; Mild cognitive impairment; Cognitive function; Clinical dementia rating scale; Mini-mental state examination

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