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_第1頁(yè)
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_第2頁(yè)
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_第3頁(yè)
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_第4頁(yè)
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_第5頁(yè)
已閱讀5頁(yè),還剩3頁(yè)未讀 繼續(xù)免費(fèi)閱讀

下載本文檔

版權(quán)說(shuō)明:本文檔由用戶提供并上傳,收益歸屬內(nèi)容提供方,若內(nèi)容存在侵權(quán),請(qǐng)進(jìn)行舉報(bào)或認(rèn)領(lǐng)

文檔簡(jiǎn)介

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

溫馨提示

  • 1. 本站所有資源如無(wú)特殊說(shuō)明,都需要本地電腦安裝OFFICE2007和PDF閱讀器。圖紙軟件為CAD,CAXA,PROE,UG,SolidWorks等.壓縮文件請(qǐng)下載最新的WinRAR軟件解壓。
  • 2. 本站的文檔不包含任何第三方提供的附件圖紙等,如果需要附件,請(qǐng)聯(lián)系上傳者。文件的所有權(quán)益歸上傳用戶所有。
  • 3. 本站RAR壓縮包中若帶圖紙,網(wǎng)頁(yè)內(nèi)容里面會(huì)有圖紙預(yù)覽,若沒(méi)有圖紙預(yù)覽就沒(méi)有圖紙。
  • 4. 未經(jīng)權(quán)益所有人同意不得將文件中的內(nèi)容挪作商業(yè)或盈利用途。
  • 5. 人人文庫(kù)網(wǎng)僅提供信息存儲(chǔ)空間,僅對(duì)用戶上傳內(nèi)容的表現(xiàn)方式做保護(hù)處理,對(duì)用戶上傳分享的文檔內(nèi)容本身不做任何修改或編輯,并不能對(duì)任何下載內(nèi)容負(fù)責(zé)。
  • 6. 下載文件中如有侵權(quán)或不適當(dāng)內(nèi)容,請(qǐng)與我們聯(lián)系,我們立即糾正。
  • 7. 本站不保證下載資源的準(zhǔn)確性、安全性和完整性, 同時(shí)也不承擔(dān)用戶因使用這些下載資源對(duì)自己和他人造成任何形式的傷害或損失。

最新文檔

評(píng)論

0/150

提交評(píng)論