急性大脑中动脉供血区脑梗死与同型半胱氨酸、氢质子磁共振波谱的相关性研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
【目的】
     研究脑梗死患者血清同型半胱氨酸(Hcy)、氢质子磁共振波谱(1H-MRS)与脑梗死的关系及二者间的相互关系。探讨Hcy及1H-MRS在判定脑梗死患者功能障碍及预后中的价值,以利于在脑梗死早期对其严重程度及预后作出确切的判断,制定合理的治疗方案。
     【方法】
     对30例发病时间在3天以内,并经头部MRI检查证实诊断的脑梗死(大脑中动脉供血区)患者,在入院后24h内测定静脉血Hcy水平,根据Hcy水平,分为正常组(≤15umol/L)4例,轻度升高组(15~20umol/L)8例,中度升高组(20~25 umol/L)10例,重度升高组(>25umol/L)8例;同时对所有患者病灶中心区及对侧镜像正常脑组织行1H-MRS分析,主要检测物化学位移定位,N-乙酞天门冬氨酸(NAA)2.0ppm、乳酸(Lac)1.32ppm。应用美国国立卫生研究院卒中量表(NIHSS)在患者入院及治疗后3个月时进行神经功能缺损程度评分,分别记作NIHSS1、NIHSS2。对患者的Hcy、NIHSS1、NIHSS2及1H-MRS代谢物的值进行相关性分析。
     【结果】
     1、1H-MRS在脑梗死中的变化:⑴除2例患者外,28例患者的梗死灶中均可见到不同程度增高的Lac峰;对侧镜像区3例患者出现轻微升高的Lac峰,其余27名患者未见到Lac峰。⑵除1例患者外,29例患者梗死灶中心NAA峰较对侧镜像区均有不同程度的下降,配对样本t检验证实病灶侧NAA低于对侧镜像区有统计学意义(P<0.001)。
     2、脑梗死患者中Hcy升高者占86.7%,且Hcy水平越高,1H-MRS中NAA值越低, NAA值的各组间两两比较差异均有统计学意义(P<0.001)。
     3、对各指标的相关分析得出:⑴Hcy与NIHSS1、NIHSS2呈正相关关系(r=0.880 P<0.01;r=0.924 P<0.01)。⑵梗死灶中心的NAA与NIHSS1、NIHSS2呈负相关关系(r=-0.842 P<0.01;r=-0.818 P<0.01)。⑶梗死灶中心的Lac与NIHSS1、NIHSS2呈正相关关系(r=0.776 P<0.01;r=0.796 P<0.01)。⑷Hcy与NAA病侧呈负相关关系(r=-0.748 P<0.01)。
     【结论】
     Hcy与1H-MRS中的NAA、Lac均可对脑梗死病情及预后作出判断,且二者之间具有统计学相关性。
[Objective]
     The purpose of our research is first, to study the relation between Homocysteine and Proton magnetic reasonance spectroscopy,then the correlation between them and Cerebral infarction. Second,to detect all the index of 1H-MRS and Hcy in acute cerebral infarction patients, and concentrate on the relation between the changes of the index and the prognosis of the patience, so as to evaluate the application value of 1H-MRS and Hcy in cerebral infarction.
     [Methods]
     Thirty patients presenting within 3 days of the onset and diagnosed as the cerebral infarction by the brain MRI inspection, were studied. Each patient's Hcy level in the venous blood is assayed. According to the Hcy level, these patients were classified into four groups: the normal group(≤15umol/L), including 4 cases, the mildly increased group(15~20umol/L), including 8 cases, the moderately increased group(20~25umol/L), including 10 cases and the seriously increased group(≥25umol/L), including 8 cases. Meanwhile, we did the 1H-MRS analysis on the infarction area and the opposite normal brain tissue and mainly detected the chemical shift position and the level of NAA (2.0ppm) and Lac (1.32ppm). All the patients’NIHSS scores were determined when they were on admission or treated after three months, and these two scores were noted as NIHSS1、NIHSS2, respectively. At last, we did the correlation analysis to the value of Hcy、NIHSS1、NIHSS2 and 1H-MRS, and drew the conclusion.
     [Results]
     (1)Changes of 1H-MRS in cerebral infarction: (1) in the infarction area, increased Lactic acid peak in varying degrees was detected in all the patients except two cases; in the mirror imaging normal area, the Lactic acid peak was seemed to mildly increase in only three cases, and the other 27 cases were not. (2) The NAA peak in the center of the infarct area showed deceases in varying degrees compared to the opposite mirror image area on the other 29 cases, except one case, and this resut was confirmed by compared t test with significance(P<0.01).
     2. Increased Hcy in varying degrees can be seen in 86.7% of the cerebral infarction patients and the higher the Hcy is, the lower the NAA level of 1H-MRS is. And the accumulated NAA level in the various groups was significant different.
     3.Correlative analysis of metabolism changes in infarct center and NIHSS score, NIHSS prognosis showed that :(1)the vary of Hcy in infarct center had positive correlation with NIHSS1、NIHSS2(r=0.880 P<0.01;r=0.924 P<0.01). (2) the vary of NAA in the infarct center has obvious negative correlation with NIHSS1 and NIHSS2(r=-0.842 P<0.01;r=-0.818 P<0.01).⑶the vary of Lac has positive correlation with NIHSS1、NIHSS2 (r=0.776 P<0.01;r=0.796 P<0.01).(4) the vary of NAA in the infarct center has obvious negative correlation with Hcy(r=-0.748 P<0.01).
     [Conclusions]
     The level of Hcy and NAA、Lac in 1H-MRS all could contribute to the judgement of severity and prognosis of the cerebral infarction patients and there is significant correlation between them.
引文
[1]彭洪娟,赵斌.1H-MRS基本原理及成像技术.医学影像学杂志2004,14(12):1033
    [2]Lanefmrann H,Kugel H,Heindelw,et al.Metbaolic changes in aeute and subacute Cerebralinfarctiongs:findings at proton MR spectroscopic imaging.Radiology1995,196:203一210
    [3]Bakrer PB,Gillard JH,vna Zijl PCM,et al.Acute Stroke:evaluation with serial proton MR spectroscopie imaging.Radiology1994,192:723一732
    [4]Parsons Mw,LI T,Barber PA,et al.combined I-HMR spectroscopy and Diffusion-weighted MRI improves the prediction of stroke outcome.Neurology2000,55(4):498一505
    [5]Grhama GD,Kalvoah P,Blamire AM,et al.Clinical correlates of proton magnetic resonance spectroscopy findings after acute cerebral inarfetion.stroke1995,26(2):225一9
    [6]Perry TT,Refsum H,Morris RN,et al.Prosrtctive study of serum total homocysteine concentration and risk of stroke in middle-age British men〔J〕.Lancel,1995,346:1395~1398
    [7]Kittner SJ,Giles WH,Macko RF,et al.Homocysteine and risk of cerebral infarction in a biralial population:the stroke prevention in young wmoma study〔J〕.Stroke,1999,30:1554~1560
    [8]中华神经科学会,中华神经外科学会.各类脑血管疾病诊要点.中华神经科杂志1996,29:379一380.
    [9]Audebert HJ,Rott MM ,Eek T,et al.Systemie inflammatory response depends on initial stroke severity but is attenuated by sueeessful thrombolysis.Srtoke2004,35(9):2128一33
    [10]王维治主编.神经病学.第5版.北京:人民卫生出版社,2004,126
    [11]De Koning ABL , Werstuck GH , Zhou J , et al. Hyperhomocysteinemia and its role in the development of atherosclerosis[J ]. Clin Biochem , 2003 , 36 : 431-441
    [12]Fortin LJ , Genest J.Measurement of homocysteine in the prediction ofarteriosclerosis[J ]. Clin Biochem , 1995 , 28 : 1552-1621
    [13]孙娟,谭红梅,程超,等.高同型半胱氨酸诱导血管内皮功能障碍促进微循环障碍和微血栓形成[ J ].中国病理生理杂志2007, 23 (12) : 2336-2340.
    [14]Vermeulen EG, Rauwerda JA, van den Berg M, et al . Homocysteine lowering treatmentwith folic acid plus vitamin B6 owers urinary albumin excreti on but not plas ma markers of endothelial function or Creactive protein: further analysis of secondary end-point of a randomized clinical trial[ J ]. Eur J Clin I nvest, 2003, 33 (3) :209-215.
    [15]Geisel J, Hennen B, HubnerU, et al . The impact of hyperhomocys teinemia as a cardiovascular risk factor in the prediction of coronar heart disease[ J ]. Clin Chem LabMed, 2003, 41 (11) : 1513-1517.
    [16]Kartal OzerN,Negis Y,Aytan N. Molecularmechanisms of choles terol or homocysteine effect in the development of ather osclerosis :Role of vitamin E[ J ]. Biofactors, 2003, 19 (1 /2) : 63-70.
    [17]范伯丽,董会奕,蒋宝琦,等.同型半胱氨酸血症血小板及内皮细胞活性的体内研究[ J ].中华心血管杂志, 2004, 32 ( 2 ) :126-130.
    [18]Schroecksnadel K, Frick B,Winkler C, et al . Hyperhomocysteine mia and immune activati on [ J ]. Clin Chem Lab Med, 2003, 41(11) : 1438-1443.
    [19]Mujumdar VS, Tummalapalli CM, Aru G M, et al . Mechanism of constrictive vascular remodeling by homocysteine: role of PPAR[ J ]. Cell physiology, 2002, 282 (5) : C1009-C1015.
    [20]李红伟,李焰生.同型半胱氨酸与神经系统疾病的研究进展[ J ].临床神经病学杂志, 2006, 19: 474.
    [21]McCully KS . Vascular pathology of homocysteinemia: implicati ons for the pathogenesis of arteriosclerosis [ J ]. Am J Pathol, 1969,56: 111.
    [22] Falk E,Zhou J,Moller J.Homocysteine and atherothrombosis,Lipids,2001;36:3~11
    [23] Yoo TH,Chung CS,Kang SS.Relation of piasma homocysteine to cerebral infaction and cerebral atherosclerosis,Stroke,1998;29(12):2478~2483
    [24]高海凤,张哲成.高同型半胱氨酸血症与缺血性脑卒中.医学综述,2003;9(3):174~175
    [25]Perry TT,Refsum H,Morris RN,et al.Prosrtctive study of serum total homocysteine concentration and risk of stroke in middle-age British men〔J〕.Lancel,1995,346:1395~1398
    [26]Kittner SJ,Giles WH,Macko RF,et al.Homocysteine and risk of cerebral infarction in a biralial population:the stroke prevention in young wmoma study〔J〕.Stroke,1999,30:1554~1560
    [27]Sager TN,Laursen H,Corralation between N-acetylasparatelevel and h istopathologic in cortical infarcts of mice after middle cerebral artery occlusion,J Cereb Blood Metab,2000,20(7);780~788
    [28]Beauchamp NJ,Barker PB,Wang PY,et al.Imagine of acute cerebral ischemic.Radiology,1999,212(2):307~324
    [29]Castillo M,K wock L,Mukherji SK.Clinical applications of proton MR spectroscopy.AJNR,1996,17(1):1~15
    [30]Saunders DE,Howe FA,vanden Boogaart A,et al.Continuing ischemic damage after acute middle cerebra lartery infarction in humans demonstrated by short-echoproton spectroscopy.Stroke,1995,26(6):1007~1013
    [31]Saunders DE.MR spectroscopy in stroke.BritishMedical Bulleti,2000,56 (2):334~345
    [32]Lanfermann H,Kugel H,Heindel W,et al.Metabolic changes in acute and subacute cerebral infarctions:findings at proton MR spectroscopic imaging.Radiology,1995,196:203~210
    [33]Monsein LH,Mathews VP,Barker PB,et al.Irreversible regional cerebral ischemia:serial MR imaging and proton MR spectroscopy in a nonhuman primate model Mathews.AJNR,1993,14:963~970
    [34]Sauder DE,Howe FA,Bogart A,et al.Discrimination of metabolite from lipid and macro molecule resonance in cerebral infarction in human using short echo proton spectroscopy.Magn Reason Imaging,1997,7:1116
    [35] Pereira AC,Sauders DE,Doyle VL,et al.Measurement of initial N-acetylaspattateconcentration by magnetic resonance spectroscopy and initial infarct volume by MRI predicts outcome in patients with middle cerebral arteryterritory infarction.Stroke,1999,30(8):1577
    [36]Igarashi H,K wee IL,Okubo S,et al.Predicting the pathological fate of focal cerebral ischemia using 1H-magnetic resonance spectroscopic imaging.International Congress Series,2003,1252:341~344
    [37]Gillard JH,Barker PB,van Zijl PCM,et al.Proton MR spectroscopy in acute middle cerebral artery stroke.AJNR,1996,17(5):873~886
    [38]Federico F,Simone IL,Conte C,et al.Prognostic significance of metabolic changes detected by proton magnetic resonance spectroscopy in ischemic stroke.Neurol,1996,243:241~247
    [39]Ward law J M,Marshall I Wild J,et al.Studies of acute ischemic stroke with proton magnetic resonancespectroscopy:relation between time from onset,neurologicaldeficit,metabolite abnormalities in the infarct,blood flow,and clinical outcome.Stroke 1998;29(8):1618~24
    [41]Myers RE.Lactic acid accumulation as cause brain edema and cerebral necrosis resulting from oxygen deprivation.In:Korobkin R,Guilleminault C,eds.Advances in Perinatal Neurology.New York,NY:Spectrum;1979:85~114
    [42]Graham GD,Kalvach P,Blamire AM,et al.Clinical correlates of proton magnetic reso nancespectroscopy findingsafter acute cerebral infarction.Stroke,1995,26:225~229
    [1] Castillo M , Kwock L , Mukherji SK. Clinical applications of proton MR spectroscopy [J ] . AJNR , 1996 ,17 (1) :1215.
    [2] Tien RD , Lai PH , Smith J S , et al. Single voxel proton brain spectroscopy exam( PROBE/ SV ) in patients with primary brain tumors [J ] . AJR ,1996 ,167 (1) :201-209.
    [3] Burtscher IM , Holtas S , et al. Proton MR spectroscopy in clinical routine [J ] . J Magn Reson Imaging , 2001 , 13 (2) :560-567.
    [4] Martin RC ,Sawrie S ,Hugg J , et al. Cognitive correlates of 1 H MRSI2detected hippocampal abnormalities in temporal lobeepilepsy [ J ] . Neurology , 1999 , 53 ( 11 ) :2052-2058.
    [5] Nelson SJ , Graves E , Pirzkall A , et al. Invivo molecular imaging for planning radiation therapy of gliomas : an application of 1 HMRSI [J ] . J Magn Reson Imaging , 2002 ,16 :464-476.
    [6] Dowling C ,Bollen A ,Noworolski SM. Preoperative proton MR spectroscopy imaging of brain tumors : Correlation with histopathologic analysis of resection specimens[J ] . AJNR ,2001 ,22 :604-612
    [7] Bendszus M,Warmuth2Metz M.MR spectroscopy in gliomatosis cerebri [J] .AJNR ,2000 ,21 :375-380
    [8] Shimizu H, Kumabe T, Shirane T, et al. Correlation between choline level measured by proton MR spectroscopy and Ki一67 labeling index in gliomas. AJNR一Am一J一Neuroradiol. 2000, 21:659一65
    [9] Robinson SP , Barton SJ , Mcsheeny PMJ ,et al. Nuclear magnetic resonance spectroscopy of cancer [ J ] . British Journal of Radiology , 1997 ,70 :60-69.
    [10] Burtscher IM , Holtas S , et al. Proton MR spectroscopy in clinical routine [J ] . J Magn Reson Imaging , 2001 , 13 (2) :560-567.
    [11] Major C , Cucurella G, Aguilera C ,et al.Intraventricular meningomas : MR imaging and MR spectrospopic findings in two cases [J ] . AJNR ,1999 ,20 :882-885.
    [12]吴光耀,孙骏谟,田志雄,等.质子磁共振波谱在脑肿瘤中的应用研究[J] .临床放射学杂志,2001 ,20 (4) :271-275.
    [13]周正华,王玖华,刘宜春,等.颅脑肿瘤质子磁共振研究,中国临床神经学,2002,10:33一37:
    [14] Law M , Cha S , Knopp EA , et al. High grade gliomas and solitary metastases : differentiation by using perfusion and proton spectroscopic MR imaging [J ] . Radiology ,2002 , 222 (3) :715-721.
    [15] Ishimaru H , Morikawa M , Iwanaga S , etal. Differetiation between high grade glioma and metastatic brain tumor usingsingle voxel proton MR spectroscopy [ J ] .Eur Radiol , 2001 ,11 (9) :1784-1791.
    [16]鱼博浪,王,斐,郭世萍,等.实用放射学杂志,2005,21(6):572—575
    [17]鱼博浪.中枢神经系统CT和MR鉴别诊断.西安:陕西科学技术出版社,2005.116—119
    [18]赵喜平.磁共振成像系统的原理及其应用.北京:科学出版社,2O00.12
    [19]朱文珍,等.放射学实践,2002,17(3):266—268 [20 ]陈增爱,耿道颖.沈天真.等.中国医学计算机成像杂志,2001,7(4):217—221
    [21] Alberto Cifelli,Marzena Arridge,Peter jezzard,et al,Ann neurol,2002,52:650
    [22] Moller Harlmann W ,Henninghaus S.Neuroradiology,2002,44(5):371—381
    [23] Quan D , Hackney DB , Pruitt AA , et al.Transient MRI enhencement in a patient with seizures and previously resected glioma : use of MRS [ J ] . Neurology ,1999 ,53 (1) :211-213.
    [24] Duncan JS,Epliepsia,1996,37(7):598—605
    [25] Cross JH,Connelly A,Jackson GD,et a1.Ann Neurol,1996;39(1):1O7—113

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700