Evidence map›Paper›PMID 40796698›Full record

ArticleMolecular psychiatry2025

Plasma neurofilament light reflects more severe manifestation of Alzheimer's disease in men.

Xiaoqin Cheng, Zhenghong Wang, Kun He, Yingfeng Xia, Ying Wang, Qihao Guo, Fang Xie, Peng Yuan

Abstract read
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In one paragraph

Article in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Review
  2. 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

8 authors.

Xiaoqin Cheng *Department of Neurology, Zhongshan Hospital, Fudan University, Shanghai, China.
Zhenghong Wang *Department of Rehabilitation Medicine, Huashan Hospital, State Key Laboratory of Medical Neurobiology, Institute for Translational Brain Research, MOE Frontiers Center for Brain Science, MOE Innovative Center for New Drug Development of Immune Inflammatory Diseases, Fudan University, Shanghai, China.
Kun He *Department of Nuclear Medicine & PET Center, Huashan Hospital, Fudan University, Shanghai, China.ORCID http://orcid.org/0000-0002-6969-3488
Yingfeng Xia *Department of Neurology, Zhongnan Hospital, Wuhan University, Wuhan, China.
Ying WangDepartment of Gerontology, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai, China.
Qihao GuoDepartment of Gerontology, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai, China.
Fang XieDepartment of Nuclear Medicine & PET Center, Huashan Hospital, Fudan University, Shanghai, China. fangxie@fudan.edu.cn.ORCID http://orcid.org/0000-0003-2667-281X
Peng YuanDepartment of Rehabilitation Medicine, Huashan Hospital, State Key Laboratory of Medical Neurobiology, Institute for Translational Brain Research, MOE Frontiers Center for Brain Science, MOE Innovative Center for New Drug Development of Immune Inflammatory Diseases, Fudan University, Shanghai, China. pyuan@fudan.edu.cn.ORCID http://orcid.org/0000-0003-4051-4447

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32371036
6 · The paper itself

Abstract

Plasma neurofilament light (NfL) protein is a promising non-invasive biomarker for detecting neuronal damage in Alzheimer's disease (AD). However, its clinical utility is limited by the lack of standardized threshold values. Sex is an important factor that should be considered when setting these thresholds, but only a few studies have examined sex differences in plasma NfL levels in AD, with inconsistent findings. Even fewer have explored whether sex influences the relationship between plasma NfL levels and disease severity. To investigate this, we first analyzed data from 860 participants in the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Linear regression models were used to assess sex differences in the correlation between plasma NfL levels, cognitive deficits, and neuroimaging metrics. A Cox model with bootstrap resampling was used to evaluate sex differences in dementia risk, calculating the hazard ratio for men versus women for a given increase in plasma NfL. Our results showed that, compared to women, men with higher plasma NfL levels exhibited more severe cognitive defects and brain hypometabolism, along with smaller hippocampal volume. These findings were validated using data from 619 participants in the Chinese Preclinical Alzheimer's Disease Study (C-PAS) cohort and 86 participants from a publicly available dataset. In addition, we found that increase in plasma NfL levels were predictive of faster cognitive decline and a higher likelihood of AD progression in men compared to women. In conclusion, sex differences influence the relationship between plasma NfL levels and AD symptoms. Men exhibit greater cognitive and neuropathological defects with rising plasma NfL levels, underscoring the need for considering sex when using NfL as a biomarker for neuronal damage in AD.

Indexed as

Alzheimer DiseaseNeurofilament ProteinsAgedAged, 80 and overBiomarkersBrainCognitive DysfunctionFemaleHippocampusHumansMaleNeuroimagingSex CharacteristicsSex FactorsBiomarkersneurofilament protein LNeurofilament Proteins

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.