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作 者:魏虹[1] 应艳琴[1] 梁雁[1] 王光惠[1] 罗小平[1]
机构地区:[1]华中科技大学同济医学院附属同济医院儿科,湖北武汉430030
出 处:《临床儿科杂志》2005年第8期519-522,共4页Journal of Clinical Pediatrics
基 金:卫生部临床重点学科项目;"十五"国家科技攻关计划项目(编号:2004BA720A01);973计划项目(编号:2005CB522507)
摘 要:目的通过建立血浆极长链脂肪酸(VLCFAs)气相色谱-质谱(GC-MS)方法,确立实验室血浆VLCFAs正常参比值,为以脑白质营养不良为表现的过氧化酶体病研究提供检测手段。方法对血浆中VLCFAs进行提取、酯化,并应用GC-MS检测,用选择离子扫描进行定量。检测47例正常人血浆VLCFAs和60例经临床和影像学(脑CT或MRI)初步诊断为脑白质营养不良者,并对9例X_连锁肾上腺脑白质营养不良(X_ALD)中的6例进行头颅氢质子磁共振波谱检测。结果正常对照组血浆C22∶0、C24∶0、C26∶0分别为(32.20±9.39)μmol/L、(24.82±7.20)μmol/L和(0.51±0.13)μmol/L;C24∶0/C22∶0和C26∶0/C22∶0分别为0.883±0.277和0.017±0.006。60例脑白质营养不良患者中有9例血浆C22∶0下降,C24∶0、C26∶0、C24∶0/C22∶0和C26∶0/C22∶0均明显高于正常对照组,结合影像学检查可确诊为X_ALD。结论应用GC-MS法检测血浆VLCFAs的方法,灵敏度、准确性均得到提高,且用血量较少,稳定性好,能为临床诊断提供重要的生化依据。影像学检查和血浆VLCFAs测定相结合是诊断X_ALD的可靠方法。Objective To establish the normal reference range of plasma very long chain fatty acids (VLCFAs) with gas chromatography-mass spectrometry(GC- MS) and provide chemical diagnostic evidence for inherited disorders of peroxisome. Methods VLCFAs were extracted from blood samples and esterifled. Quantitative analysis was performed using selected ion scan on GC-MS. Sixty patients diagnosed as leukoencephalopathy by brain CT or MRI and 47 normal controls involved in our study. 6 of 9 patients with X-link adrenoleukodystrophy(X-ALD) were examined with 1^H-magnetic resonance spectrum(1^HMRS) . Resuits Plasma C22 : 0, C24 : 0, C26 : 0 values in normal group were (32.20±9.39)mol/L, (24.82±7.20)mol/ L and (0.51 ± 0.13) mol/L respectively, and the ratios of C24 : 0/C22 : 0 and C26 : 0/C22 : 0 were 0.883± 0.277,0. O17±0. 006, respectively. C22:0 decreased and C24: 0, C26 : 0,C24 : 0/C22 : 0, C26 : 0/C22:0 increased significantly in 9 confirmed X-ALD patients. Conclusions Determination of plasma very long fatty acid using GC-MS is stable,reliable and helpful for the chemical diagnosis of leukoencephalopathy.
关 键 词:气相色谱-质谱 极长链脂肪酸 肾上腺脑白质营养不良 氢质子磁共振波谱
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