Abnormal cortical surface-based spontaneous and functional connectivity in the whole brain in lifelong premature ejaculation patients.
- Author:
Si-Yan XING
1
;
Jia-Ming LU
2
;
Yue-Hui JIANG
3
;
Tong WANG
3
;
Guang-Jun DU
1
;
Bai-Bing YANG
1
;
Qing-Qiang GAO
1
;
Bin WANG
1
;
Ning WU
1
;
Chun-Lu XU
1
;
Tao SONG
1
;
Yu-Tian DAI
1
Author Information
- Publication Type:Journal Article
- MeSH: Male; Humans; Premature Ejaculation; Brain Mapping/methods*; Brain; Cerebral Cortex; Magnetic Resonance Imaging/methods*
- From: Asian Journal of Andrology 2023;25(6):699-703
- CountryChina
- Language:English
- Abstract: Recent research has highlighted structural and functional abnormalities in the cerebral cortex of patients with premature ejaculation (PE). These anomalies could play a pivotal role in the physiological mechanisms underlying PE. This study leveraged functional magnetic resonance imaging (fMRI), a noninvasive technique, to explore these neural mechanisms. We conducted resting-state fMRI scans on 36 PE patients and 22 healthy controls (HC), and collected data on Premature Ejaculation Diagnostic Tool (PEDT) scores and intravaginal ejaculation latency time (IELT). Employing a surface-based regional homogeneity (ReHo) approach, we analyzed local neural synchronous spontaneous activity, diverging from previous studies that utilized a volume-based ReHo method. Areas with significant ReHo differences between PE and HC groups underwent surface-based functional connectivity (FC) analysis. Significant discrepancies in ReHo and FC across the cortical surface were observed in the PE cohort. Notably, PE patients exhibited decreased ReHo in the left triangular inferior frontal gyrus and enhanced ReHo in the right middle frontal gyrus. The latter showed heightened connectivity with the left lingual gyrus and the right orbital superior frontal gyrus. Furthermore, a correlation between ReHo and FC values with PEDT scores and IELT was found in the PE group. Our findings, derived from surface-based fMRI data, underscore specific brain regions linked to the neurobiological underpinnings of PE.
