实用医学杂志
實用醫學雜誌
실용의학잡지
THE JOURNAL OF PRACTICAL MEDICINE
2014年
7期
1151-1153
,共3页
谢丽%易珍%王建%邓燕%陈志坚%徐涓娟%李山%秦雪
謝麗%易珍%王建%鄧燕%陳誌堅%徐涓娟%李山%秦雪
사려%역진%왕건%산연%진지견%서연연%리산%진설
存储时间%巨细胞病毒%DNA%稳定性
存儲時間%巨細胞病毒%DNA%穩定性
존저시간%거세포병독%DNA%은정성
Prolong period%Cytomegalovirus%DNA%Stability
目的:了解4℃条件下储存21 d后血浆中巨细胞病毒(cytomegalovirus,CMV)DNA的稳定性。方法:收集CMV载量300~100000拷贝/mL 的30份造血干细胞移植后患者血浆,并分为低载量组、中载量组、高载量组。标本采集后立即分离血浆并进行基线(0 d)载量检测,其余血浆于4℃存储,分别在第1、2、3、7、14和21天进行实时荧光定量PCR测定。结果:将30份样本进行不同时间点的配对t检验,CMV载量均差异无显著性:第1天与第0天比较,t=1.654,P=0.109;第2天与第0天比较,t=1.487,P=0.148;第3天与第0天比较,t =1.609,P =0.118;第7天与第0天比较,t=0.831,P=0.413;第14天与第0天比较, t=1.721,P=0.096;第21天与第0天比较,t=0.244,P=0.244。分组比较中,第21天与第0天比较CMV载量差异无显著性(低载量组P=0.485;中载量组P=0.858;高载量组P=0.949)。结论:4℃储存21 d中,血浆标本CMV载量未出现连续下降或上升趋势,且不同时间点与第0天的基线载量比较差异无显著性。
目的:瞭解4℃條件下儲存21 d後血漿中巨細胞病毒(cytomegalovirus,CMV)DNA的穩定性。方法:收集CMV載量300~100000拷貝/mL 的30份造血榦細胞移植後患者血漿,併分為低載量組、中載量組、高載量組。標本採集後立即分離血漿併進行基線(0 d)載量檢測,其餘血漿于4℃存儲,分彆在第1、2、3、7、14和21天進行實時熒光定量PCR測定。結果:將30份樣本進行不同時間點的配對t檢驗,CMV載量均差異無顯著性:第1天與第0天比較,t=1.654,P=0.109;第2天與第0天比較,t=1.487,P=0.148;第3天與第0天比較,t =1.609,P =0.118;第7天與第0天比較,t=0.831,P=0.413;第14天與第0天比較, t=1.721,P=0.096;第21天與第0天比較,t=0.244,P=0.244。分組比較中,第21天與第0天比較CMV載量差異無顯著性(低載量組P=0.485;中載量組P=0.858;高載量組P=0.949)。結論:4℃儲存21 d中,血漿標本CMV載量未齣現連續下降或上升趨勢,且不同時間點與第0天的基線載量比較差異無顯著性。
목적:료해4℃조건하저존21 d후혈장중거세포병독(cytomegalovirus,CMV)DNA적은정성。방법:수집CMV재량300~100000고패/mL 적30빈조혈간세포이식후환자혈장,병분위저재량조、중재량조、고재량조。표본채집후립즉분리혈장병진행기선(0 d)재량검측,기여혈장우4℃존저,분별재제1、2、3、7、14화21천진행실시형광정량PCR측정。결과:장30빈양본진행불동시간점적배대t검험,CMV재량균차이무현저성:제1천여제0천비교,t=1.654,P=0.109;제2천여제0천비교,t=1.487,P=0.148;제3천여제0천비교,t =1.609,P =0.118;제7천여제0천비교,t=0.831,P=0.413;제14천여제0천비교, t=1.721,P=0.096;제21천여제0천비교,t=0.244,P=0.244。분조비교중,제21천여제0천비교CMV재량차이무현저성(저재량조P=0.485;중재량조P=0.858;고재량조P=0.949)。결론:4℃저존21 d중,혈장표본CMV재량미출현련속하강혹상승추세,차불동시간점여제0천적기선재량비교차이무현저성。
Objective To analyze CMV DNA stability of 30 EDTA plasma samples in the order of magnitude between 300 and 100 000 copies/mL over a 21 day period. Methods Thirty plasma samples were grouped into three categories according to the CMV DNA loads , including low CMV DNA contents , intermediate CMV DNA loads and high CMV DNA loads. Ten milliliters of whole blood was freshly collected from each patient. Plasma samples without hemolysis were divided into 1-ml aliquots. One aliquot was processed immediately (Day 0) for baseline PCR assays. The remaining aliquots were then processed after one , two, three, seven, 14 or 21 day of storage at 4℃. Results There was no significant difference between the mean of the difference time point in viral loads following storage at 4 ℃ by paired-samples t test, including Day 1 compared to Day 0 (t = 1.654, P =0.109), Day 2 compared to Day 0 (t = 1.487, P = 0.148), Day 3 compared to Day 0 (t = 1.609, P = 0.118), Day 7 compared to Day 0 (t=0.831, P=0.413), Day 14 compared to Day 0 (t=1.721, P=0.096), and Day 21 compared to Day 0 (t=0.244, P=0.810). Conclusion The concentration of CMV DNA in all samples stored at 4 ℃ for 21 days did not differ significantly from the baseline viral load ,and it was not observed the trend in continued degradation in different time point (Day 1, 2, 3, 7 and 14).