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Aberrant interactions of peripheral measures and neurometabolites with lipids in complex regional pain syndrome using magnetic resonance spectroscopy: A pilot study

机译:磁共振波谱法研究复杂区域疼痛综合征中外周血脂和神经代谢产物与脂质的异常相互作用:一项先导研究

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The aim of this study was to assess peripheral measures and central metabolites associated with lipids using magnetic resonance spectroscopy. Twelve patients with complex regional pain syndrome (CRPS) and 11 healthy controls participated. Using magnetic resonance spectroscopy, we measured the levels of lipid 13a (Lip13a) and lipid 09 (Lip09) relative to total creatine (tCr) levels in the right and left thalamus. We found negative correlations of Lip13a/tCr in the right thalamus with red blood cells or neutrophils, but a positive correlation between Lip13a/tCr and lymphocytes in the controls. We found negative correlations between Lip09/tCr and peripheral pH or platelets in the controls. There were positive correlations between Lip09a/tCr and myo-inositol/tCr, between Lip13a/tCr and N-acetylaspartate (NAA)/tCr, and between Lip09/tCr and NAA/tCr in healthy controls. On the other hand, there were positive correlations between Lip13a/tCr and Lip09/tCr and urine pH in CRPS patients. There were significant correlations between Lip13a/tCr or Lip09/tCr and different peripheral measures depending on the side of the thalamus (right or left) in CRPS patients. This is the first report indicating that abnormal interactions of Lip13a and Lip09 in the thalamus with peripheral measures and central metabolites may mediate the complex pathophysiological mechanisms underlying CRPS.
机译:这项研究的目的是使用磁共振波谱技术评估与脂类相关的外周指标和中心代谢产物。参加了12例复杂的局部疼痛综合征(CRPS)和11名健康对照的患者。使用磁共振波谱,我们测量了左右丘脑中脂质13a(Lip13a)和脂质09(Lip09)的水平相对于总肌酸(tCr)的水平。我们发现右丘脑中的Lip13a / tCr与红细胞或中性粒细胞呈负相关,但在对照组中Lip13a / tCr与淋巴细胞之间呈正相关。我们在对照中发现Lip09 / tCr与外周pH或血小板之间呈负相关。在健康对照组中,Lip09a / tCr和肌醇/ tCr之间,Lip13a / tCr和N-乙酰天冬氨酸(NAA)/ tCr之间以及Lip09 / tCr和NAA / tCr之间存在正相关。另一方面,CRPS患者的Lip13a / tCr和Lip09 / tCr与尿液pH呈正相关。在CRPS患者中,根据丘脑的一侧(右侧或左侧),Lip13a / tCr或Lip09 / tCr与不同的周围测量之间存在显着相关性。这是第一个报告,表明丘脑中Lip13a和Lip09与周围环境和中央代谢产物的异常相互作用可能介导了CRPS的复杂病理生理机制。

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