Evidence map›Paper›PMID 41410730›Full record

ArticleEuropean radiology experimental2025

Assessing neurobiology of lifelong premature ejaculation through brain MRI structural similarity gradient.

Qiming Deng, Qing Hu, Yan Lei, Xin Zhang, Qingqiang Gao, Xiaozhi Zhao, Yutian Dai, Cong Wang, Jiaming Lu, Bing Zhang

Abstract read
In one paragraph

Article in European radiology experimental, 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

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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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Qiming Deng *Department of Radiology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Qing Hu *Department of Radiology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Yan Lei *Department of Radiology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Xin ZhangDepartment of Radiology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Qingqiang GaoDepartment of Andrology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Xiaozhi ZhaoDepartment of Andrology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Yutian DaiDepartment of Andrology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Cong WangDepartment of Radiology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China. wangcong0016@163.com.
Jiaming LuDepartment of Radiology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China. vector_6@163.com.
Bing ZhangDepartment of Radiology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China. zhangbing_nanjing@nju.edu.cn.ORCID http://orcid.org/0000-0001-7592-1195

Funding

National Natural Science Foundation of China 82271965National Natural Science Foundation of China 82330059
6 · The paper itself

Abstract

objectiveThis study explored the gradient changes in structural similarity based on the cortical structure of patients with lifelong premature ejaculation (LPE) and further analyzed the characteristics of the associations between these changes and clinical phenotypes, gene expression profiles, and neurotransmitter distributions. MATERIALS AND

methodsThis study employed a novel method, morphological inverse divergence (MIND), to construct structural similarity gradients for 62 LPE patients and 53 healthy controls. Between-group comparisons were performed to examine the abnormalities in gradients among LPE patients. Partial least squares regression analysis explored the relationships between gene expression profiles and gradient changes, as well as neurotransmitter expression associations with these alterations.

resultsWe found that both groups showed a classic unimodal-to-cross-modal transition along the principal gradient. In LPE patients, the principal gradient increased in the left visual cortex and right prefrontal regions but decreased in the right cingulate gyrus. The secondary gradient also decreased in the right somatosensory cortex and bilateral visual cortices. Notably, changes in these gradients in the right somatosensory and visual cortices were significantly negatively correlated with clinical phenotypes. Connectome-transcriptome analysis revealed that abnormal gradient patterns were linked to whole-brain gene expression profiles, with enriched genes in pathways related to hormone activity and other functions. Additionally, there was a spatial correlation between the gradients and neurotransmitter densities.

conclusionWe identified the biological pathways enriched in genes associated with the pathological process of LPE and characterized the distribution patterns of neurotransmitter receptors and transporters, thereby providing critical insights into the neuroimaging and neurobiological underpinnings of LPE. RELEVANCE STATEMENT: The MIND-based brain structural similarity gradient exhibits a pattern of segregation and integration. We analyzed the association between this structural gradient and the clinical phenotype of primary premature ejaculation, offering novel insights into the neuroimaging and neurobiological mechanisms underlying the disorder. KEY POINTS: We employed a novel approach, morphometric inverse divergence, to construct the brain structural similarity gradient. We provide evidence for abnormal structural similarity gradients in patients with LPE. We found an association between abnormal changes in gradients and clinical phenotypes, gene enrichment pathways, as well as neurotransmitter density.

Indexed as

BrainMagnetic Resonance ImagingPremature EjaculationAdultHumansMaleMiddle AgedMagnetic resonance imagingMicroscale transcriptome profileNeurotransmitterPremature ejaculationStructural similarity gradient

Identifiers

PMID41410730
PMCPMC12715095

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