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脑白质结构变化与泌尿科慢性盆腔疼痛综合征(UCPPS)尿液蛋白有关:MAPP 网络研究。

Changes in brain white matter structure are associated with urine proteins in urologic chronic pelvic pain syndrome (UCPPS): A MAPP Network study.

机构信息

Department of Radiological Science, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, CA, United States of America.

Department of Biomedical Physics, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, CA, United States of America.

出版信息

PLoS One. 2018 Dec 5;13(12):e0206807. doi: 10.1371/journal.pone.0206807. eCollection 2018.


DOI:10.1371/journal.pone.0206807
PMID:30517112
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6281196/
Abstract

The Multidisciplinary Approach to the Study of Chronic Pelvic Pain (MAPP) Research Network has yielded neuroimaging and urinary biomarker findings that highlight unique alterations in brain structure and in urinary proteins related to tissue remodeling and vascular structure in patients with Urological Chronic Pelvic Pain Syndrome (UCPPS). We hypothesized that localized changes in diffusion tensor imaging (DTI) measurements might be associated with corresponding changes in urinary protein levels in UCPPS. To test this hypothesis, we created statistical parameter maps depicting the linear correlation between DTI measurements (fractional anisotropy (FA) and apparent diffusion coefficient (ADC)) and urinary protein quantification (MMP2, MMP9, NGAL, MMP9/NGAL complex, and VEGF) in 30 UCPPS patients from the MAPP Research Network, after accounting for clinical covariates. Results identified a brainstem region that showed a strong correlation between both ADC (R2 = 0.49, P<0.0001) and FA (R2 = 0.39, P = 0.0002) with urinary MMP9 levels as well as a correlation between both ADC (R2 = 0.42, P = 0.0001) and FA (R2 = 0.29, P = 0.0020) and urinary MMP9/NGAL complex. Results also identified significant correlations between FA and urinary MMP9 in white matter adjacent to sensorimotor regions (R2 = 0.30, P = 0.002; R2 = 0.36, P = 0.0005, respectively), as well as a correlation in similar sensorimotor regions when examining ADC and urinary MMP2 levels (R2 = 0.42, P<0.0001) as well as FA and urinary MMP9/NGAL complex (R2 = 0.33, P = 0.0008). A large, diffuse cluster of white matter was identified as having a strong correlation between both ADC (R2 = 0.35, P = 0.0006) and FA (R2 = 0.43, P<0.0001) with urinary NGAL levels. In contrast, no significant association between DTI measurements and VEGF was observed. Results suggest that elevated MMP9 or MMP9/NGAL in UCPPS may be related to degenerative neuronal changes in brainstem nuclei through excitotoxicity, while also facilitating synaptic plasticity in sensorimotor regions.

摘要

多学科方法研究慢性盆腔疼痛(MAPP)研究网络产生了神经影像学和尿生物标志物的研究结果,这些结果突出了与尿蛋白相关的组织重塑和血管结构的改变,这些改变与泌尿系统慢性盆腔疼痛综合征(UCPPS)患者的大脑结构有关。我们假设,弥散张量成像(DTI)测量的局部变化可能与 UCPPS 患者尿液蛋白水平的相应变化有关。为了验证这一假设,我们创建了统计参数图,描述了弥散张量成像(DTI)测量值(各向异性分数(FA)和表观扩散系数(ADC))与尿液蛋白定量(MMP2、MMP9、NGAL、MMP9/NGAL 复合物和 VEGF)之间的线性相关性,该研究纳入了 MAPP 研究网络中的 30 名 UCPPS 患者,并考虑了临床协变量。研究结果确定了一个脑干区域,该区域在 ADC(R2=0.49,P<0.0001)和 FA(R2=0.39,P=0.0002)与尿 MMP9 水平之间以及在 ADC(R2=0.42,P=0.0001)和 FA(R2=0.29,P=0.0020)与尿 MMP9/NGAL 复合物之间均显示出与尿 MMP9 水平之间存在强烈的相关性。研究结果还表明,FA 与感觉运动区周围白质中的尿 MMP9 之间存在显著相关性(R2=0.30,P=0.002;R2=0.36,P=0.0005),当检查 ADC 和尿 MMP2 水平时,在类似的感觉运动区中也存在相关性(R2=0.42,P<0.0001),以及 FA 和尿 MMP9/NGAL 复合物(R2=0.33,P=0.0008)。确定了一个较大的、弥散性的白质簇,其 ADC(R2=0.35,P=0.0006)和 FA(R2=0.43,P<0.0001)与尿 NGAL 水平之间存在强烈相关性。相比之下,没有观察到 DTI 测量值与 VEGF 之间存在显著关联。研究结果表明,UCPPS 中 MMP9 或 MMP9/NGAL 的升高可能与通过兴奋毒性导致脑干核神经元退行性变化有关,同时也促进了感觉运动区的突触可塑性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/6633a13c2c50/pone.0206807.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/2deffc2ad3c9/pone.0206807.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/5af9406c9555/pone.0206807.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/540afd82cc7c/pone.0206807.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/7522bce2c43a/pone.0206807.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/7a13af623f7b/pone.0206807.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/6633a13c2c50/pone.0206807.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/2deffc2ad3c9/pone.0206807.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/5af9406c9555/pone.0206807.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/540afd82cc7c/pone.0206807.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/7522bce2c43a/pone.0206807.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/7a13af623f7b/pone.0206807.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf6/6281196/6633a13c2c50/pone.0206807.g006.jpg

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