Evidence map›Paper›PMID 40369404›Full record

ArticleThe journal of headache and pain2025

White matter and cortical gray matter microstructural alterations in migraine: a NODDI and DTI analysis.

Zhilei Li, Yanliang Mei, Lei Wang, Tianhua Fan, Cheng Peng, Kaibo Zhang, Shouyi Wu, Tong Chen, Zhenchang Zhang, Binbin Sui and 2 more

Abstract read
In one paragraph

Article in The journal of headache and pain, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

12 authors.

Zhilei Li *Department of Neurology, The Second Hospital of Lanzhou University, Cuiying Gate, No. 82 Linxia Road, Chengguan District, Lanzhou, 730000, China.
Yanliang Mei *Headache Center, Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, No.119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China.
Lei WangDepartment of Neurology, The Second Hospital of Lanzhou University, Cuiying Gate, No. 82 Linxia Road, Chengguan District, Lanzhou, 730000, China.
Tianhua FanDepartment of Neurology, The Second Hospital of Lanzhou University, Cuiying Gate, No. 82 Linxia Road, Chengguan District, Lanzhou, 730000, China.
Cheng PengDepartment of Neurology, The Second Hospital of Lanzhou University, Cuiying Gate, No. 82 Linxia Road, Chengguan District, Lanzhou, 730000, China.
Kaibo ZhangDepartment of Neurology, The Second Hospital of Lanzhou University, Cuiying Gate, No. 82 Linxia Road, Chengguan District, Lanzhou, 730000, China.
Shouyi WuDepartment of Neurology, The Second Hospital of Lanzhou University, Cuiying Gate, No. 82 Linxia Road, Chengguan District, Lanzhou, 730000, China.
Tong ChenTiantan Neuroimaging Center of Excellence, China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, No.119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China.
Zhenchang ZhangDepartment of Neurology, The Second Hospital of Lanzhou University, Cuiying Gate, No. 82 Linxia Road, Chengguan District, Lanzhou, 730000, China.
Binbin SuiTiantan Neuroimaging Center of Excellence, China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, No.119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China. reneesui@163.com.
Yonggang WangDepartment of Neurology, The Second Hospital of Lanzhou University, Cuiying Gate, No. 82 Linxia Road, Chengguan District, Lanzhou, 730000, China. w100yg@gmail.com.
Xueying YuHeadache Center, Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, No.119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China. yuxueying6@aliyun.com.

Funding

the Joint Funds of the National Natural Science Foundation of China U24A20683the National Natural Science Foundation of Beijing Z200024The National Natural Science Foundation of China 32170752, 91849104, and 31770800
6 · The paper itself

Abstract

backgroundThe pathophysiological mechanism of migraine remains elusive, thereby impeding the effective treatment of the disease. Current neuroimaging research focuses on changes in brain functional connectivity, functional networks, and macrostructural alterations, which reflect abnormal neuronal function during the disease process. The plasticity changes in neuronal structures and neurotransmitter system dysregulations potentially play a crucial role in migraine onset and chronicity of migraine. This study utilizes multimodal neuroimaging techniques to investigate the microstructural and neurotransmitter alterations in migraine and provides new insights into its pathological mechanisms and therapeutic method.

methodsMicrostructural alterations in both white matter (WM) and cortical gray matter (GM) were evaluated among 40 chronic migraine (CM) patients, 35 episodic migraine (EM) patients, and 45 healthy controls (HCs) using Diffusion Tensor Imaging (DTI) and Neurite Orientation Dispersion and Density Imaging (NODDI) models. Tract-based spatial statistics (TBSS) and Surface-based analysis (SBA) were performed to compare groupwise differences in white and gray matter microstructure, respectively. Furthermore, the cross-modal toolbox JuSpace was used to analyze the correlation between cortical gray matter neurite alterations and neurotransmitter.

resultsIn the WM, compared to HC, a decrease in neurite density index (NDI) was identified in the migraine group, and both NDI and fractional anisotropy (FA) were decreased in the CM group. No significant alterations were observed in the EM group. An increase in radial diffusivity (RD) was found in the CM group compared to the EM group. In the cortical GM, compared to HC, the migraine group had fewer neurites in the right insula and temporal pole cortex, and the CM group showed a reduction in neurites in the right middle temporal and fusiform cortex. The cortical GM of neurite damage was negatively correlated with neurotransmitters in migraine and CM. There was no correlation between NODDI and DTI metrics of these brain regions and clinical data after the Bonferroni correction.

conclusionOur findings indicated that neurite loss was detected in both WM and cortical GM of migraineurs. As the migraine progresses into chronicity, the axonal damage may become more pronounced. The neurite damage of cortical GM was negatively related to neurotransmitters.

Indexed as

Cerebral CortexDiffusion Tensor ImagingGray MatterMigraine DisordersWhite MatterAdultFemaleHumansMaleMiddle AgedNeuritesYoung AdultDiffusion tensor imagingMicrostructureMigraineNeurite orientation dispersion and density imagingSurface-based analysisTract-based Spatial statistics

Identifiers

PMID40369404
PMCPMC12076971

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

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 Socratic graph.