4.5 Article

Abnormal degree centrality in lifelong premature ejaculation patients: an fMRI study

Journal

BRAIN IMAGING AND BEHAVIOR
Volume 15, Issue 3, Pages 1412-1419

Publisher

SPRINGER
DOI: 10.1007/s11682-020-00340-4

Keywords

Lifelong premature ejaculation; Degree centrality; Graph theory-based network; Resting-state fMRI

Categories

Funding

  1. China Postdoctoral Science Foundation [2019 M650985]
  2. Development Funds of Shaanxi Science and Technology Agency of China [2018SF/091]
  3. National Natural Science Foundation of China [81,603,631, 81,771,918]
  4. Shaanxi Health and Family Planning Commission Foundation of China for Youths [2016E04]

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This study investigated abnormal brain functional networks in lifelong PE patients and found altered degrees of centrality in regions involved in sensation, motivation, and inhibitory control processing, suggesting a relationship between these functional abnormalities and PE.
Lifelong premature ejaculation (PE) is one of the most prevalent male sexual dysfunctions. It is still not well known about the possible neural mechanisms of lifelong PE. This study tried to investigate the abnormal characteristics of brain functional networks of lifelong PE and to assess relationships of PE-related functional abnormalities with clinical symptoms. Functional magnetic resonance imaging (fMRI) data and clinical symptoms were collected from 45 lifelong PE patients and 37 healthy controls (HCs) since 2016, including disease and sexual life history, intravaginal ejaculatory latency time measured by stopwatch and other scales. The degree centrality (DC) approach were applied to distinguish altered brain functions between the two groups (p < 0.05, false discovery rate corrected). Correlation analysis was then performed to examine relationships between the imaging findings and clinical symptoms (p < 0.05, Bonferroni corrected). Results showed that compared with HCs, lifelong PE patients had increased DC value in the medial prefrontal cortex (mPFC), precuneus and primary somatosensory cortex (SI) as well as decreased DC value in the insula and orbitofrontal cortex. After controlling for anxiety and depression levels, the significant difference in the mPFC was not found. The DC value in the SI positively correlated with premature ejaculation diagnostic tool (PEDT) score in the patients. The present findings indicate that lifelong PE patients have altered DC in brain regions involved in sensation, motivation and inhibitory control processing. Our study may improve our understanding and provide a new sight into the further research of lifelong PE.

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