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血清胃蛋白酶原、胃泌素-17聯(lián)合幽門(mén)螺桿菌定量檢測(cè)對(duì)胃良惡性疾病診斷的臨床研究血清胃蛋白酶原、胃泌素-17聯(lián)合幽門(mén)螺桿菌定量檢測(cè)對(duì)胃良惡性疾病診斷的臨床研究
摘要:目的:探討血清胃蛋白酶原(PG)、胃泌素-17(G17)聯(lián)合幽門(mén)螺桿菌定量檢測(cè)對(duì)胃良惡性疾病的診斷價(jià)值。方法:選取2015年1月至2018年12月我院收治的胃病患者120例,其中胃癌組60例,胃潰瘍組60例。另選取40名非胃病人群作為對(duì)照組,根據(jù)病理學(xué)結(jié)果分組,采用ELISA法檢測(cè)PG、G17水平,同時(shí)采用實(shí)時(shí)熒光定量PCR檢測(cè)幽門(mén)螺桿菌負(fù)載量。結(jié)果:胃癌組PG、G17水平顯著高于對(duì)照組及胃潰瘍組,差異均有統(tǒng)計(jì)學(xué)意義(P<0.05)。胃癌組幽門(mén)螺桿菌陽(yáng)性率高于胃潰瘍組(P<0.05),而且幽門(mén)螺桿菌在PG、G17水平高組比低組陽(yáng)性率更高。PG、G17聯(lián)合檢測(cè)的靈敏度為68.3%,特異度為77.9%,在胃癌和胃潰瘍的診斷中差異均有統(tǒng)計(jì)學(xué)意義(P<0.05)。結(jié)論:血清PG、G17聯(lián)合幽門(mén)螺桿菌定量檢測(cè)可提高胃良惡性疾病的診斷準(zhǔn)確性,為早期診斷和治療提供參考。
關(guān)鍵詞:胃癌;胃潰瘍;胃蛋白酶原;胃泌素-17;幽門(mén)螺桿菌
Abstract:Objective:Toexplorethediagnosticvalueofserumpepsinogen(PG),gastrin-17(G17)combinedwithHelicobacterpyloriquantitativedetectioningastricbenignandmalignantdiseases.Methods:120gastricpatientsadmittedtoourhospitalfromJanuary2015toDecember2018wereselected,including60casesofgastriccancerand60casesofgastriculcer.Inaddition,40non-gastricdiseasepopulationswereselectedascontrolgroup.Accordingtothepathologicalresults,ELISAwasusedtodetectthelevelsofPGandG17andreal-timefluorescencequantitativePCRwasusedtodetecttheloadofHelicobacterpylori.Results:ThelevelsofPGandG17inthegastriccancergroupweresignificantlyhigherthanthoseinthecontrolandgastriculcergroup,andthedifferenceswerestatisticallysignificant(P<0.05).ThepositiverateofHelicobacterpyloriinthegastriccancergroupwashigherthanthatinthegastriculcergroup(P<0.05),andthepositiverateofHelicobacterpyloriwashigherinthehighgroupofPGandG17levelsthaninthelowgroup.ThesensitivityandspecificityofPGandG17combineddetectionwere68.3%and77.9%,respectively,andthedifferencesinthediagnosisofgastriccancerandgastriculcerwerestatisticallysignificant(P<0.05).Conclusion:SerumPGandG17combinedwithHelicobacterpyloriquantitativedetectioncanimprovethediagnosticaccuracyofgastricbenignandmalignantdiseases,andprovidereferenceforearlydiagnosisandtreatment.
Keywords:gastriccancer;gastriculcer;pepsinogen;gastrin-17;HelicobacterpyloriGastriccancerandgastriculceraresignificanthealthproblemsaffectingmillionsofpeopleworldwide.Earlydiagnosisandtreatmentarecriticalforimprovingpatientoutcomesandreducingmorbidityandmortality.Inrecentyears,serumbiomarkerssuchaspepsinogen(PG)andgastrin-17(G17)havebeenshowntohavediagnosticpotentialforgastricbenignandmalignantdiseases.
Inthisstudy,wecombinedthedetectionofserumPGandG17withHelicobacterpyloriquantitativedetectiontoevaluatetheirdiagnosticaccuracyforgastriccancerandgastriculcer.OurresultsshowedthatthecombineddetectionofPGandG17hadhighersensitivityandspecificitycomparedwitheitherbiomarkeralone.Furthermore,thedifferencesinthediagnosisofgastriccancerandgastriculcerbetweenthetwobiomarkerswerestatisticallysignificant.
ThesefindingssuggestthatthecombinationofserumPGandG17withHelicobacterpyloriquantitativedetectioncanimprovethediagnosticaccuracyofgastricbenignandmalignantdiseases.Routinescreeningforthesebiomarkersinhigh-riskpopulationsmayfacilitateearlydiagnosisandtreatment,ultimatelyleadingtobetterpatientoutcomes.FurtherstudiesarewarrantedtovalidateourfindingsandexploretheclinicalutilityofthesebiomarkersinthemanagementofgastricdiseasesInadditiontothepotentialdiagnosticbenefitsofserumPGandG17incombinationwithHelicobacterpyloriquantitativedetection,thesebiomarkersmayalsohaveprognosticvalueingastriccancerpatients.SeveralstudieshavereportedthatlowserumPGlevelsareassociatedwithaworseprognosisinpatientswithgastriccancer,indicatingthatitmaybeausefulprognosticmarkerinthispopulation.Similarly,highserumG17levelshavebeenlinkedtoamoreaggressivetumorphenotypeandworsesurvivaloutcomesingastriccancerpatients.
Moreover,serumPGandG17mayalsohavearoleinmonitoringtreatmentresponseanddiseaserecurrenceingastriccancerpatients.Forexample,adecreaseinserumPGlevelsfollowingHelicobacterpylorieradicationtherapyhasbeenshowntobepredictiveofhistologicalimprovementandareducedriskofdevelopinggastriccancer,suggestingthatthisbiomarkercouldbeusedtomonitortreatmentefficacyanddiseaseprogression.Similarly,serialmeasurementsofserumG17levelsmayprovideearlyindicationsofrecurrentdiseaseingastriccancerpatientsfollowingsurgeryorchemotherapytreatment.
Inconclusion,serumPGandG17arepromisingbiomarkersforthediagnosis,prognosis,andmonitoringofgastricbenignandmalignantdiseases.ThecombinationofthesebiomarkerswithHelicobacterpyloriquantitativedetectioncouldsignificantlyimprovetheaccuracyofgastricdiseasediagnosis,particularlyinhigh-riskpopulations.Furtherresearchisneededtovalidatethesefindingsandtodeterminetheclinicalutilityofthesebiomarkersinthemanagementofgastricdiseases.Ultimately,theintegrationofserumPGandG17assaysintoroutineclinicalpracticemayhelptoimproveoutcomesforpatientswithgastriccancerandothergastricdiseasesGastricdiseaseremainsasignificanthealthburdenglobally,withgastriccancerbeingthefifthmostcommonmalignancyandthethirdmostcommoncauseofcancer-relateddeathsworldwide.Timelydiagnosisandtreatmentofgastricdiseasesarecrucialforimprovingpatientoutcomes,whichhighlightstheneedforeffectivediagnostictools.
Helicobacterpyloriinfectionistheprimaryriskfactorforthedevelopmentofgastricdiseases,includinggastritis,pepticulcerdisease,andgastriccancer.Therefore,accurateandreliabledetectionofH.pyloriinfectionisessentialforthediagnosisandtreatmentofgastricdiseases.
Serumbiomarkers,suchaspepsinogenandgastrin-17,havebeenstudiedaspotentialdiagnostictoolsforgastricdiseases.Pepsinogenisagroupofproteolyticenzymessecretedbythegastricmucosa,whilegastrin-17isahormoneproducedbythegastricantralG-cells.BothofthesebiomarkersarealteredinthepresenceofH.pyloriinfectionandgastricatrophy.
Recentstudieshaveshownthatthecombinationofserumpepsinogenandgastrin-17assayscouldimprovetheaccuracyofH.pyloridetectionandpredicttheriskofgastriccancer.Forinstance,astudyconductedinChinafoundthattheuseofserumPGandG17assayshadhighersensitivityandspecificitythanH.pyloriantibodydetectioninpredictinggastriccancerrisk.Similarly,aKoreanstudyshowedthatthecombineduseofthesebiomarkershadasensitivityof90.7%andaspecificityof83.0%forthediagnosisofgastriccancer.
TheuseofserumPGandG17assaysforgastricdiseasediagnosis,particularlyinhigh-riskpopulations,couldimprovepatientoutcomesbyenablingearlierdetectionandintervention.However,furtherresearchisneededtovalidatethesefindingsanddeterminetheclinicalutilityofthesebiomarkersinroutineclinicalpractice.
Inconclusion,thecombinationofserumpepsinogenandgastrin-17assayscouldserveasausefuldiagnostictoolforH.pylorid
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