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慢性腹痛患者早期不良生活事件与静息态神经网络:性别差异的证据。

Early adverse life events and resting state neural networks in patients with chronic abdominal pain: evidence for sex differences.

机构信息

From the Oppenheimer Family Center for Neurobiology of Stress and Pain and Interoception Network (PAIN) (A.G., L.K., J.L., K.T., A.B., J.-Y.H., C.A.-M., B.N., E.A.M.), Los Angeles, California; Departments of Medicine (L.K., J.L., K.T., B.N., E.A.M.) and Psychiatry (J.L., K.T., B.N., E.A.M.) and Division of Digestive Diseases (A.G., L.K. J.L., K.T., B.N., E.A.M.), David Geffen School of Medicine at UCLA, Los Angeles, California; and Ahmanson-Lovelace Brain Mapping Center (E.A.M.), UCLA, Los Angeles, California.

出版信息

Psychosom Med. 2014 Jul-Aug;76(6):404-12. doi: 10.1097/PSY.0000000000000089.


DOI:10.1097/PSY.0000000000000089
PMID:25003944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4113723/
Abstract

BACKGROUND: Early adverse life events (EALs) and sex have been identified as vulnerability factors for the development of several stress-sensitive disorders, including irritable bowel syndrome (IBS). We aimed to identify disease and sex-based differences in resting state (RS) connectivity associated with EALs in individuals with IBS. METHOD: A history of EALs before age 18 years was assessed using the early trauma inventory. RS functional magnetic resonance imaging was used to identify patterns of intrinsic brain oscillations in the form of RS networks in 168 people (58 people with IBS, 28 were female; 110 healthy controls, 72 were female). Partial least squares, a multivariate analysis technique, was used to identify disease and sex differences and possible correlations between EALs and functional connectivity in six identified RS networks. RESULTS: Associations between EALs and RS networks were observed. Although a history of EALs was associated with altered connectivity in the salience/executive control network to a similar extent in male and female patients with IBS (bootstrap ratio = 3.28-5.61; p = .046), male patients with IBS demonstrated additional EAL-related alterations in the cerebellar network (bootstrap ratio = 3.92-6.79; p = .022). CONCLUSIONS: This cross sectional study identified correlations between RS networks and EALs in individuals with IBS. These results suggest that exposure to EALs before age 18 years can shape adult RS in both male and female patients in the salience/executive control network, a brain network that has been implicated in the pathophysiology of central pain amplification.

摘要

背景:早期不良生活事件(EALs)和性别已被确定为易患几种应激敏感障碍的危险因素,包括肠易激综合征(IBS)。我们旨在确定与 IBS 个体 EALs 相关的静息状态(RS)连接的疾病和性别差异。 方法:使用早期创伤清单评估 18 岁之前的 EALs 病史。RS 功能磁共振成像用于识别以 RS 网络形式存在的内在大脑振荡模式,共涉及 168 人(58 名 IBS 患者,28 名女性;110 名健康对照者,72 名女性)。偏最小二乘法(一种多变量分析技术)用于识别疾病和性别差异,以及 EALs 与六个鉴定的 RS 网络中功能连接之间的可能相关性。 结果:观察到 EALs 与 RS 网络之间的关联。尽管 EALs 病史与 IBS 男性和女性患者的显着/执行控制网络连接改变有关(bootstrap ratio = 3.28-5.61;p =.046),但 IBS 男性患者还表现出与小脑网络有关的额外 EAL 相关改变(bootstrap ratio = 3.92-6.79;p =.022)。 结论:这项横断面研究确定了 IBS 个体中 RS 网络与 EALs 之间的相关性。这些结果表明,18 岁之前暴露于 EALs 可以塑造男性和女性患者显着/执行控制网络中的成年 RS,该大脑网络与中枢疼痛放大的病理生理学有关。

相似文献

[1]
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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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J Neurogastroenterol Motil. 2022-4-30

[10]
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本文引用的文献

[1]
Update on irritable bowel syndrome program of research.

J Korean Acad Nurs. 2013-10

[2]
Irritable bowel syndrome in female patients is associated with alterations in structural brain networks.

Pain. 2014-1

[3]
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PLoS One. 2013-9-5

[4]
Patients with chronic visceral pain show sex-related alterations in intrinsic oscillations of the resting brain.

J Neurosci. 2013-7-17

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Sex differences in emotion-related cognitive processes in irritable bowel syndrome and healthy control subjects.

Pain. 2013-6-20

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Diffusion tensor imaging detects microstructural reorganization in the brain associated with chronic irritable bowel syndrome.

Pain. 2013-4-8

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Altered fronto-striatal and fronto-cerebellar circuits in heroin-dependent individuals: a resting-state FMRI study.

PLoS One. 2013-3-6

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Gastroenterology. 2013-3-6

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Altered cerebellar-cerebral resting-state functional connectivity reliably identifies major depressive disorder.

Brain Res. 2012-12-7

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Proc Natl Acad Sci U S A. 2012-11-26

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