A Randomized Double-blind Placebo-controlled Study of Pu'er Tea(普洱茶) Extract on the Regulation of Metabolic Syndrome.pdfVIP

A Randomized Double-blind Placebo-controlled Study of Pu'er Tea(普洱茶) Extract on the Regulation of Metabolic Syndrome.pdf

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A Randomized Double-blind Placebo-controlled Study of Pu'er Tea(普洱茶) Extract on the Regulation of Metabolic Syndrome.pdf

·492· n ORIGINALARTlCLE A RandomizedDouble-blindPlacebo-controlledStudyofPu。er Tea(普洱茶)ExtractontheRegulationofMetabolicSyndrome CHUSong-ling(褚松龄)’,FUHong(富 宏)’,YANGJin.xia(杨金霞)’,LIUGeng-xin(刘庚信)’, DOUPan(窦 攀)’,ZHANGLiang(张 良),TUPeng—fei(屠鹏飞),andWANGXue-mei(王学美)’ ABSTRACT objective:ToexploretheregulativeefficacyofPu。ertea(普洱茶)extractonmetabolicsyndrome. Methods:Ninetypatientswithmetabolicsyndromewererandomlydividedintotwogroups,theinterventiongroup administeredwithPue‘rteaextract,andtheplacebogroupwithplacebocapsules.Afler3months。treatment。 bodymassindex,waisthipratio,bloodlipids,bloodsugar,immuneandinflammatoryindex,andoxidationindex ofthepatientswithmetabolicsyndromeweretestedandanalyzed.Resuits:Intheinterventiongroup.thebody massindex,waist·hipratio,fastingand2hpostprandialbloodglucose,serum totaIcholesterol,triglycerides, Iow density IipoproteinandapolipoproteinB一100alldecreasedinthepatientswithmetabolicsyndrome.and alsothehigh—densitylipoproteinIeveIincreasedandapOIip0pr0teinA一1showedthetendencyto increase. Serum C-reactiveprotein,tumornecrosisfactor— ,andinterleukin一6weredecreasedinthe interventiongroup. Interleukin-10leve1wasincreased.MDA wasdecreasedandsuperoxidedismutasewasincreased.Compared withbeforetreatmentandtheplacebogroup,thereweresignificantdifferences 0.05,PO.01).Conclusions: Pu。erteademonstratedexcellentpotentialinimprovingcentralobesiyt,adjustingbloodlipid,loweringblood sugar.regulatingimmuniytandresistingoxidation.Itcanadjustthemetabolicsyndromeofdifferentclinical phenoytpestodifierentdegrees.andisideallyfitforearlypreventionofmetabolicsyndrome. KEYII,『ORDS tea,metabolicsyndrome,randomizedcontrolledclinicalstudy MetaboIicsyndrome (MS)ischaracterized phenotypesofMS,whichareweightloss,bloodlipids bycentralobesity.diabetes orimpaired glucose r

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