ImageVerifierCode 换一换
格式:PPTX , 页数:43 ,大小:4.54MB ,
资源ID:875097      下载积分:11 金币
验证码下载
登录下载
邮箱/手机:
验证码: 获取验证码
温馨提示:
支付成功后,系统会自动生成账号(用户名为邮箱或者手机号,密码是验证码),方便下次登录下载和查询订单;
特别说明:
请自助下载,系统不会自动发送文件的哦; 如果您已付费,想二次下载,请登录后访问:我的下载记录
支付方式: 支付宝    微信支付   
验证码:   换一换

开通VIP
 

温馨提示:由于个人手机设置不同,如果发现不能下载,请复制以下地址【https://www.zixin.com.cn/docdown/875097.html】到电脑端继续下载(重复下载【60天内】不扣币)。

已注册用户请登录:
账号:
密码:
验证码:   换一换
  忘记密码?
三方登录: 微信登录   QQ登录  
声明  |  会员权益     获赠5币     写作写作

1、填表:    下载求助     留言反馈    退款申请
2、咨信平台为文档C2C交易模式,即用户上传的文档直接被用户下载,收益归上传人(含作者)所有;本站仅是提供信息存储空间和展示预览,仅对用户上传内容的表现方式做保护处理,对上载内容不做任何修改或编辑。所展示的作品文档包括内容和图片全部来源于网络用户和作者上传投稿,我们不确定上传用户享有完全著作权,根据《信息网络传播权保护条例》,如果侵犯了您的版权、权益或隐私,请联系我们,核实后会尽快下架及时删除,并可随时和客服了解处理情况,尊重保护知识产权我们共同努力。
3、文档的总页数、文档格式和文档大小以系统显示为准(内容中显示的页数不一定正确),网站客服只以系统显示的页数、文件格式、文档大小作为仲裁依据,个别因单元格分列造成显示页码不一将协商解决,平台无法对文档的真实性、完整性、权威性、准确性、专业性及其观点立场做任何保证或承诺,下载前须认真查看,确认无误后再购买,务必慎重购买;若有违法违纪将进行移交司法处理,若涉侵权平台将进行基本处罚并下架。
4、本站所有内容均由用户上传,付费前请自行鉴别,如您付费,意味着您已接受本站规则且自行承担风险,本站不进行额外附加服务,虚拟产品一经售出概不退款(未进行购买下载可退充值款),文档一经付费(服务费)、不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。
5、如你看到网页展示的文档有www.zixin.com.cn水印,是因预览和防盗链等技术需要对页面进行转换压缩成图而已,我们并不对上传的文档进行任何编辑或修改,文档下载后都不会有水印标识(原文档上传前个别存留的除外),下载后原文更清晰;试题试卷类文档,如果标题没有明确说明有答案则都视为没有答案,请知晓;PPT和DOC文档可被视为“模板”,允许上传人保留章节、目录结构的情况下删减部份的内容;PDF文档不管是原文档转换或图片扫描而得,本站不作要求视为允许,下载前自行私信或留言给上传者【胜****】。
6、本文档所展示的图片、画像、字体、音乐的版权可能需版权方额外授权,请谨慎使用;网站提供的党政主题相关内容(国旗、国徽、党徽--等)目的在于配合国家政策宣传,仅限个人学习分享使用,禁止用于任何广告和商用目的。
7、本文档遇到问题,请及时私信或留言给本站上传会员【胜****】,需本站解决可联系【 微信客服】、【 QQ客服】,若有其他问题请点击或扫码反馈【 服务填表】;文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“【 版权申诉】”(推荐),意见反馈和侵权处理邮箱:1219186828@qq.com;也可以拔打客服电话:4008-655-100;投诉/维权电话:4009-655-100。

注意事项

本文(从抑制胆固醇吸收谈如何减少血液中胆固醇.pptx)为本站上传会员【胜****】主动上传,咨信网仅是提供信息存储空间和展示预览,仅对用户上传内容的表现方式做保护处理,对上载内容不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知咨信网(发送邮件至1219186828@qq.com、拔打电话4008-655-100或【 微信客服】、【 QQ客服】),核实后会尽快下架及时删除,并可随时和客服了解处理情况,尊重保护知识产权我们共同努力。
温馨提示:如果因为网速或其他原因下载失败请重新下载,重复下载【60天内】不扣币。 服务填表

从抑制胆固醇吸收谈如何减少血液中胆固醇.pptx

1、Reduce Blood Cholesterol by Targeting Cholesterol AbsorptionLiqing Yu,M.D.,Ph.D.Department of Pathology-Lipid SciencesWake Forest University School of MedicineWinston-Salem,NC,USABeijing,October 26,2008Plasma Cholesterol and CoronaryHeart Disease(CHD)CHD DeathsPer 1000 patients per 10 yrSerum Choles

2、terol Level(mg/dl)MRFIT:Multiple Risk Factor Intervention Trial ShanghaiFrom Dr.John M.Dietschy(USA)Mean LDL-CholesterolAGE(YEARS)Lifetime Exposure to LDL-Cholesterol American vs.Chinese MenLifetime LDL Exposure IndexSMOKINGHTNDIABETESCHR.9etc.FEMALEFrom Dr.Helen H.HobbsElbow Tuberous Xanthoma(15Ys

3、Chinese Girl,FH?)From Dr.Luya Wang in BeijingFluid-Mosaic Model of Cell Membrane:Cholesterol is a structural component of mammalian cell membranes“Cholesterol Is Good”Net Cholesterol Balance in Humans 700 mg 375 mgHepatic andExtrahepaticSynthesis Total Body Cholesterol750 mgDietary+BiliaryCholestero

4、l 400 mg Bile FC 375 mgFeces 300 mg Bile acidsVon Bergmann K,Grundy SM,Gastroenterology 1979:77:1183 50%50 mg Steroids 100 mg Skin sloughIntestinal absorption:50%100 mg Intestine sloughMolecular Mechanisms of Cholesterol Transport in Liver and IntestinePCSK9,ARHABC transportersApoBApoBMonogenic Hype

5、rcholesterolemiaAutosomal Familial LDLR Familial Defective APOB ApoB-100 Inheritance Disease Gene DefectDominant Hypercholesterolemia Autosomal Autosomal Recessive ARHHypercholesterolemia Sitosterolemia ABCG5/G8RecessiveAutosomal DominantHypercholesterolemia PSCK9Targets of Cholesterol Lowering Drug

6、s1.Inhibit cholesterol synthesis:HMG-CoA reductase inhibitors statins2.Inhibit cholesterol absorption:Ezetimibe,bile acid resins,plant sterols3.Reduce lipoprotein-cholesterol production:ApoB antisense oligos(ISIS)4.Raise LDLR:statins,PCSK9 inhibition(drugs and antisense oligos)Targets of Cholesterol

7、 Lowering Drugs(continue)HDL-C is controversial.Just a marker or a real cause?The body does not need HDL to get rid of cholesterol.Consequence of raising HDL:Why did CETP inhibitor fail?Does reverse cholesterol transport(RCT)quantitatively important?Anti-inflammation may delay heart attack,but when

8、your LDL-C is below 70 mg/dL,your chance to develop atherosclerotic lesions is very,very low.Why as low as 70?Because what matters is“Not Just How Low,But Also How Long”.(PCSK9 mutants,Framingham study)How to get there?GlucuronidationZetiaIntestinal Sterol Absorption and ExcretionDietarySterolsBilia

9、ry SterolsBA,PLSterolsMixedmicellesABCG5ABCG8NPC1L1LymphEzetimibe(Zetia)GUT LUMENChFecesReduce Blood Cholesterol Levels by Ezetimibe and Statin in HumansBays HE,et al.Clin Ther 2004:26:1758Switching to Ezetimibe/Simvastatin vs Doubling Statin Doses in Patients with CHD and/or DiabetesThe Ezetimibe A

10、nd Simvastatin vs doublE statin reach new lipid treatment GOals(EASEGO)StudySwitching to Ezetimibe/Simvastatin More Effective Than Doubling Statin DoseAdapted from Roeters van Lennep HWO,et al.Curr Med Res Opin.2008;24(3):685694.Patients at LDL-C Goal at Week 12,%Ezetimibe/simvastatinDoubling to ato

11、rvastatin 20 mg or simvastatin 40 mgPatients at LDL-C Goal at Week 12,%Doubling to Simvastatin 40 mg GroupDoubling to Atorvastatin 20 mg Group02040608002040608024%(n=115)73%(n=110)28%(n=74)57%(n=68)LDL-C Goal Attainment to 2.5 mmol/LSwitching to Ezetimibe/Simvastatin Superior to Doubling Statin Dose

12、 Across Most Lipid SubfractionsAdapted from Roeters van Lennep HWO,et al.Curr Med Res Opin.2008;24(3):685694.Mean Change From Statin Baseline at Week 12,%Total Cholesterol353015105052520LDL-CHDL-CTriglyceridesTotal Cholesterol/HDL-Capo B17.76.611.529.12.61.00.12.813.56.119.77.2Ezetimibe/simvastatin(

13、n=178)Doubling to atorvastatin 20 mg or simvastatin 40 mg(n=189)The Best Option?Start early and start aggressively,particularly on hypercholesterolemic patients with other risk factors and previous heart eventsWith the new goal for blood LDL-C,combined therapies may be the best option.For example:a

14、statin+ezetimibe;VytorinDont forget regular exercise,healthy diet,blood pressure control,and a“happy heart”Say no to smokeClinical Trial:ENHANCEEzetimibe and Simvastatin in Hypercholesterolemia Enhances Atherosclerosis Regression18 Center study in United States,Canada,South Africa,Spain,Denmark,Norw

15、ay,Sweden,and the NetherlandsAugust 2002 April 20062 Year study720 participants with Heterozygous Familial HypercholesterolemiaSimvastatin 80 mg+Placebo vs+EzetimibeLDL C=318+65 mg/dl80%previously on a statin.Baseline IMT=.70 vs.69(S+P vs S+E)2 year change in IMT=.006 vs.011(S+P vs S+E)(NS)ENHANCE T

16、RIALKastelein JJP et al.NEJM 2008Mean(SE)Intima-Media Thickness of the Carotid ArteryKastelein JJP et al.NEJM 2008B-mode ultrasound techniqueTRIALBaselineCommonAggregateCmnAggCompTestCompTestASAP .86 .93-.010-.020.015-.015ARBITER 1 .61 .025-.034ARBITER 2 .88 .044 .014RADIANCE 11.00 1.15-.004 .004 .0

17、05 .005RADIANCE 21.15 1.30 .008 .013.030 .025METEOR1.02 1.16 .008-.004.013 -.001ENHANCE.68 .70 .001 .001.003 .005SANDS.80 .013-.004Baseline wall thickness(mm)and progression rate(mm/yr)TRIALBaselineCommonAggregateCmnAggCompTestCompTestARBITER 2.88 .044 .014CAIUS.881.05 .008-.003.009-.004ASAP.86 .93-

18、.010-.020.015-.015LIPID.80 .048-.014SANDS.80 .013-.004MARS.70 .015-.028ENHANCE.68 .70 .001 .001.003 .005CLAS.65 .013-.013ARBITER 1.61 .025-.034Baseline wall thickness(mm)and progression rate(mm/yr)TRIALBaselineCommonAggregateCmnAggCompTestCompTestKAPS1.66.031.017RADIANCE 21.15 1.30.008 .013.030 .025

19、ACAPS1.141.31.006-.009METEOR1.02 1.16.008-.004.013-.001PLAC-II1.011.32.046 .030.068 .060RADIANCE 11.00 1.15-.004 .004 .005 .005Baseline wall thickness(mm)and progression rate(mm/yr)From Dr.John R.CrouseProblems with ENHANCE1.Baseline wall thickness:at the low end of multiple trials that showed some

20、differences2.Long-term high dose statin treatment history:not much lipids left?collagen-rich plaque?3.Short duration of treatment:Only 2 years4.Limited subjects:7205.Data against the well established correlation between LDL-C levels and CVDComments from Dr.Helen H.Hobbs:The ENHANCE work is“just a te

21、rrible paper from beginning to end”Relative Risk of Onset of Cancer in the SEAS Trial and in SHARP and IMPROVE-ITPeto R,et al.NEJM 2008Effects of Ezetimibe on SitosterolemiaCholesterolPlant Sterols 400 mg 200 mg 200 mg 400 mgDaily Intake of Dietary SterolsCholesterolHOSitosterolHO 1 mg/dL 200 mg/dLS

22、terol Levels in Normal Humans200 mg/Day 400 mg/DayDietary:Plasma:Major Features of SitosterolemiaInheritanceRecessiveXanthomasPremature CAD+Plasma sitosterol 15-30 mg/dLDiet-responsiveness+Plasma cholesterol 100-800 mg/dL Ezetimibe Reduces Blood Sitosterol in Sitosterolemic HumansLutjohann D,et al.I

23、nt J Clin Pract 2008:62:1499Campesterol050100150Day 0Day 15Day 30%of the value on day 0KO/ZetiaSitosterol050100150Day 0Day 15Day 30KO/ChowEzetimibe Reduces Plasma Plant Sterol Levelsin the Absence of ABCG5/8Genetic Ablation of NPC1L1 Prevents Sitosterolemia in Mice Lacking ABCG5/G8Tang W,et al.JLR 2

24、008Other Potential Beneficial Effects of Ezetimibe1.On fatty liver?WT-T 3.40.4a 2.30.4a 12.30.7a 241.829.1bL1KO-V 4.10.3a 3.60.2a 18.80.5a 48.07.5aL1KO-T 3.00.3a 2.90.3a 19.10.5a 110.827.3a Genotype TC FC PL TGMean SEM(mg/g wet liver)WT-V 4.40.3a 2.90.1a 19.34.0a 36.07.9a Hepatic Lipid Content of WT

25、 and L1-KO Mice Treated with T0901317Other Potential Beneficial Effects of Ezetimibe2.On obesity?NPC1L1 deficiency prevents a high fat diet-induced obesity in pure C57BL/6 miceNPC1L1 deficiency prevents a high fat diet-induced obesity in pure C57BL/6 micePromoting fat storage during evolution?Why do

26、 we have intestinal cholesterol absorption while the body can synthesize cholesterol?Is Ezetimibe a Solution of Modern Diseases(High Fat Diet-Induced Obesity,Insulin Resistance,Diabetes,Dyslipidemia,and Nonalcoholic Fatty Liver Diseases)?AcknowledgmentsWake Forest UniversityDepartment of PathologyJo

27、hn R.CrouseYinyan MaWeiqing TangJia LinLawrence L.RudelUT SouthwesternDepartment of Cell BiologyHelen H.HobbsJonathan C.CohenMount Sinai School of MedicineDepartment of Human GeneticsJoanna P.DaviesYiannis A.IoannouSwitching to Ezetimibe/Simvastatin Superior to Doubling Statin DoseAdapted from Roeters van Lennep HWO,et al.Curr Med Res Opin.2008;24:685Ezetimibe/simvastatinDoubling to atorvastatin 20 mg or simvastatin 40 mgLDL-C 2.5 mmol/LLDL-C 2.0 mmol/L26%(n=189)67%(n=178)0204060800102030403%(n=189)30%(n=178)Patients at LDL-C Goal at Week 12,%Patients at LDL-C Goal at Week 12,%

移动网页_全站_页脚广告1

关于我们      便捷服务       自信AI       AI导航        获赠5币

©2010-2024 宁波自信网络信息技术有限公司  版权所有

客服电话:4008-655-100  投诉/维权电话:4009-655-100

gongan.png浙公网安备33021202000488号   

icp.png浙ICP备2021020529号-1  |  浙B2-20240490  

关注我们 :gzh.png    weibo.png    LOFTER.png 

客服