Evidence map›Paper›PMID 39994172›Full record

ArticleTranslational psychiatry2025

Alzheimer's disease with depression: clinical characteristics and potential mechanisms involving orexin and brain atrophy.

Jing Li, Tenghong Lian, Jinghui Li, Ning Wei, Peng Guo, Mingyue He, Yanan Zhang, Yue Huang, Jing Qi, Dongmei Luo and 4 more

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Jing LiDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Tenghong LianCenter for Cognitive Neurology, Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Jinghui LiDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Ning WeiChina National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Peng GuoDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Mingyue HeDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Yanan ZhangDepartment of Blood Transfusion, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Yue HuangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.ORCID http://orcid.org/0000-0001-6051-2241
Jing QiDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Dongmei LuoDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Weijia ZhangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Ruidan WangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Mingwei WangThe First Hospital of Hebei Medical University; Brain Aging and Cognitive Neuroscience Laboratory of Hebei Province, Shijiazhuang, Hebei, China.
Wei ZhangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China. ttyyzw@163.com.ORCID http://orcid.org/0000-0002-9056-5675

Funding

Natural Science Foundation of Hebei Province (Hebei Provincial Natural Science Foundation) H2021206416
6 · The paper itself

Abstract

This study aimed to explore the clinical characteristics and alteration of orexinergic level in cerebrospinal fluid (CSF) and the volumes of brain grey and white matters, and investigate the roles of orexinergic level on the association between brain atrophy and depression in Alzheimer's disease (AD) patients. The demographic variables of 156 participants were collected. Orexinergic level in CSF and the volumes of brain grey and white matters were evaluated. The correlations of orexinergic level in CSF with depression and brain volume in AD patients were analyzed. The mediating effect of orexinergic level in CSF on the association between brain atrophy and depression in AD patients was investigated. The joint predictive value of orexinergic level in CSF and brain volume for depression in AD patients was established. AD with depression patients showed significantly elevated levels of orexin A and orexin B in CSF; orexin A level in CSF was positively correlated with HAMD score in AD patients. The elevated orexin A level in CSF mediated 49.6% of total association between the decreased grey matter volume of right dorsal medial thalamic nucleus and depression, and 50.3% of total association between the reduced white matter volume of left amygdala and depression. Combinations of above parameters could predict depression in AD patients with a significantly high area under the curve (AUC = 0.841). Therefore, the elevated orexin A level in CSF mediates its effect on the atrophy of the right dorsal medial thalamic nucleus and the white matter of the left amygdala, eventually alleviating depression in AD.

Indexed as

Alzheimer DiseaseBrainDepressionGray MatterOrexinsWhite MatterAgedAtrophyFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedOrexins

Identifiers

PMID39994172
PMCPMC11850912

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