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他汀类药物对急性脑梗死的抗炎作用 被引量:48

Effects of atorvastatin on plasma hypersensitive C-reactive protein and interleukin-6 in patients with acute cerebral infarction
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摘要 目的观察脑梗死急性期阿托伐他汀的抗炎作用。方法131例脑梗死急性期患者随机分为3组,A组为普通治疗组(47例),B组每晚加服阿托伐他汀10mg(42例),C组每晚加服阿托伐他汀20mg(42例),均治疗14d。观察治疗前、治疗后7d、治疗后14d高敏C反应蛋白(hsCRP)、白细胞介素6(IL-6)的变化,比较治疗前、治疗14d后血脂、神经功能缺损评分、生化指标等变化,并调查发病6个月的生存状态。结果(1)各组治疗后hsCRP均有下降,A组、B组、C组hsCRP在治疗后7d分别降低9·1%、33·9%、33·5%,14d分别降低34·3%、56·0%、56·8%,B、C组hsCRP下降百分率较A组明显,差异均有统计学意义(均P<0·05)。(2)治疗7d后,A组、B组、C组IL-6分别下降44·2%、50·8%、49·2%,14d后分别下降48·0%,51·6%、51·4%,下降百分率差异无统计学意义(均P>0·05)。(3)B组hsCRP的降低与总胆固醇下降百分数间无相关关系(r=0·141,P=0·373),与低密度脂蛋白胆固醇(LDL-C)下降百分数间亦无相关关系(r=0·027,P=0·866)。C组hsCRP的降低与总胆固醇、LDL-C下降百分数间也无相关关系(分别为r=0·126,P=0·427;r=0·069,P=0·662)。(4)对神经功能缺损评分,6个月预后无明显影响。结论阿托伐他汀在脑梗死急性期应用,具有不依赖降脂的抗炎作用,有利于减轻脑梗死急性期继发的炎症损伤。 Objective To observe the effects of different doses of atorvastatin on the plasma hypersensitive C-reactive protein (hsCRP) and interleukin-6 (IL-6) in patients with acute cerebral infarction. Methods 131 patients with acute cerebral infarction, 73 males and 58 females, aged 63 ~ 11, were randomly divided into 3 groups : Group A ( n = 47 ), with basal treatment ; Group B ( n = 42 ), atorvastatin 10 mg was added every night; and Group C (n =42), atorvastatin 20 mg was added every night. Before the treatment and 7 and ld days after the treatment the plasma levels of hsCRP and IL-6, fasting plasma levels of lipid, such as total cholesterol (TC) and low density lipoprotein-C (LDL-C), liver functions, such as aspartate aminotransferase (ALT) and alanine transaminase ( ALT), creatine kinase (CK), urea nitrogen, were detected. Neurological function deficit was determined. The survival condition was surveyed 6 months after. Results ( 1 ) The TC and LDL-C decreased after treatment in the 3 groups with significant differences between Group A and Group C, Group B and Group C, and Group B and Group C (all P 〈 0.05 ). (2) The plasma level of hsCRP decreased by 9.1% , 33.9% , and 30.1% respectively 7 days after treatment in Groups A, B, and C with significant differences between Groups A and B and between Groups A and C ( both P 〈 0.05 ), however, without significant difference between Group B and Group C. The level of hsCRP decreased by 34.3% , 56.0% , and 52. 9% respectively 14 days after treatment in the 3 groups with significant differences between Groups A and B and between Groups A and C (both P 〈 0.05 ) , however, without significant difference between Group B and Group C. (3) The level of IL-6 decreased 7 and 14 days after treatment in all 3 groups, however, without significant differences between any 2 groups ( all P 〉 0.05 ). (4) The decrease of hsCRP and decrease of IL-6 were not correlated with the percentage of TC decrease ( both P 〉 0.05 ) in Group B. The decrease of hsCRP was not correlated with the changes of blood lipids in Group C. ( 5 ) Both the plasma hsCRP and IL-6 before treatment were positively correlated with the infection volume and neurological function score ( all P 〈 0.01 ). Conclusion Atorvastatin has an anti-inflammatory action benefiting the alleviation of secondary inflammatory damaged in acute cerebral infarction that is independent of lipid lowering.
出处 《中华医学杂志》 CAS CSCD 北大核心 2005年第40期2841-2845,共5页 National Medical Journal of China
关键词 脑梗死 急相蛋白质类 炎症 Brain infarction Acute-phase proteins Inflammation
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参考文献18

  • 1Kim JS, Yoon SS, Kim YH, et al. Serial measurement of interleukin-6,transforming growth factor-β, and S-100 protein in patients with acute stroke. Stroke,1996, 27: 1553-1557.
  • 2Vila N, Castillo J, Davalos A, et al. Proinflammatory cytokines and early neurological worsening in ischemic stroke. Stroke,2000, 31: 2325-2329.
  • 3Albert MA, Danielson E, Rifai N, et al . Effect of therapy on C-reactive protein levels, the pravastatin inflammation/CRP evaluation (PRINCE) : a randomized trial and cohort study . JAMA,2001,286:64-70.
  • 4Riesen WF, Engler H, Risch M, et al. Short-term effects of atorvastatin on C-reactive protein. European Heart, 2002,23:794-799.
  • 5中华神经科学会 中华神经外科学会.脑血管疾病分类(1995),各类脑血管疾病诊断要点,脑卒中患者临床神经功能缺损程度评分标准(1995)[J].中华神经科杂志,1996,29:376-383.
  • 6Yu H, Rifai N. High-sensitivity C-reactive protein and atherosclerosis:from theory to therapy.Clin Biochem, 2000, 8:601-610.
  • 7周冀英,董为伟.脑梗死患者循环白细胞对内皮细胞金属蛋白酶9表达的影响[J].中华医学杂志,2004,84(12):979-981. 被引量:15
  • 8Suzuki H, Hayashi T, Tojo SJ, et al. Anti-P-selectin antibody attenuates rat brain ischemic injury. Neurosci Lett, 1999, 265:163-166.
  • 9Connolly ES Jr, Winfree CJ, Prestigiacomo CJ, et al. Exacerbation of cerebral injury in mice that express the P-selectin gene: identification of P-selectin blockade as a new target for the treatment of stroke. Circ Res,1997, 81:304-310.
  • 10Di Napoli M, Papa F, Bocola V. C-reactive protein in ischemic stroke, an independent prognostic factor. Stroke,2001, 32:917-924.

二级参考文献16

  • 1Loftus IM,Naylor AR, Bell PR, et al. Matrix metalloproteinases and atherosclerotic plaque instability. Br J Surg,2002,89:680-694.
  • 2Loftus IM, Naylor R, goodall S, et al. Increased matrix metalloproteinase-9 activity in unstable carotid plaques. A potential role in acute plaque disruption. Stroke,2000,31:40-47.
  • 3Chen XZ,Lu BX.Matrix metalloproteinases and cerebrovascular disease. Cerebrovascular Disease Foreign Medical Science,1999,7:197-200.陈兴洲,陆兵勋.基质金属蛋白酶与脑血管病.国外医学脑血管病分册,1999,7:197-200.
  • 4Falke P, Elneihoum AM, Ohlsson K. Leukocyte activation: relation to cardiovascular mortality after cerebrovascular ischemia. Cerebrovasc Dis,2000,10:97-101.
  • 5The diagnosis outlines of cerebrovascular diseases. The 4th chinese conference on cerebrovascular diseases. Chin J of Neurol, 1996,29:381. 各类脑血管病诊断要点. 全国第四届脑血管病学术会议. 中华神经科杂志,1996,29:381.
  • 6Mach F, Schonbeck U, Fabunmi RP, et al. T lymphocytes induce endothelial cell matrix metalloproteinase expression by a CD40L-dependent mechanism: implications for tubule formation. Am J Pathol,1999,154:229-238.
  • 7Xie YQ, Yang QD. Research Developments of MMP-2、MMP-9 and cerebrovascular ischemia. Foreign Medical Sciences Section on Neurol and Neurosurg, 2000,27:172-174.谢逸群,杨期东.MMP-2、MMP-9与脑缺血损伤研究进展.国外医学神经病
  • 8Newby AC, Libby P, van der Wal AC. Plaque instability--the real challenge for atherosclerosis research in the next decade? Cardiovasc Res, 1999,41:321-322.
  • 9Altieri P, Brunelli C, Garibaldi S, et al. Metalloproteinases 2 and 9 are increased in plasma of patients with heart failure. Eur J Clin Invest,2003,33:648-656.
  • 10Reynolds MA, Kirchick HJ, Dahlen JR, et al. Early biomarkers of stroke. Clin Chem,2003,49:1733-1739.

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