中华妇产科杂志
中華婦產科雜誌
중화부산과잡지
CHINESE JOUNAL OF OBSTETRICS AND GYNECOLOGY
2014年
3期
193-198
,共6页
谢言信%徐艳文%苗本郁%曾艳红%王静%周灿权
謝言信%徐豔文%苗本鬱%曾豔紅%王靜%週燦權
사언신%서염문%묘본욱%증염홍%왕정%주찬권
易位,遗传%植入前诊断%微阵列分析%核酸杂交%原位杂交,荧光
易位,遺傳%植入前診斷%微陣列分析%覈痠雜交%原位雜交,熒光
역위,유전%식입전진단%미진렬분석%핵산잡교%원위잡교,형광
Translocation,genetic%Preimplantation diagnosis%Microarray analysis%Nucleic acid hybridization%In situ hybridization,fluorescence
目的 探讨微阵列芯片比较基因组杂交(aCGH)技术用于染色体易位携带者胚胎植入前遗传学诊断(PGD)的效果.方法 2012年1月至2013年6月在中山大学附属第一医院生殖中心共对151对染色体相互易位和62对罗氏易位携带者夫妇进行220个周期的PGD,其中应用aCGH技术对染色体相互易位和罗氏易位携带者行PGD的周期数分别为33和22个周期,应用荧光原位杂交(FISH)技术对染色体相互易位和罗氏易位携带者行PGD的周期数分别为119和46个周期.比较两种检测方法的诊断率.结果 应用aCGH技术对染色体相互易位和罗氏易位携带者易位染色体正常或平衡胚胎检出率分别为38.20% (123/322)及67.20% (127/189),FISH技术分别为15.39%(195/1 267)及30.75% (202/657),aCGH技术的检出率均显著高于FISH技术(P均<0.05).应用aCGH技术对染色体相互易位和罗氏易位携带者易位染色体的异常胚胎检出率分别为59.32%(191/322)及30.69% (58/189),FISH技术分别为83.03%(1 052/1 267)及67.43% (443/657),aCGH技术均显著低于FISH技术(P均<0.05).aCGH技术检测的染色体相互易位携带者胚胎中,易位染色体正常或平衡、而非易位染色体发生非整倍体改变的异常胚胎检出率为20.19%(65/322),明显低于罗氏易位携带者的38.62% (73/189),两者比较,差异有统计学意义(P<0.01).结论 aCGH技术进行染色体易位携带者PGD的易位染色体正常或平衡检出率较FISH技术更高,而相互易位携带者的胚胎中非易位染色体发生非整倍体改变的异常胚胎检出率较罗氏易位携带者低.
目的 探討微陣列芯片比較基因組雜交(aCGH)技術用于染色體易位攜帶者胚胎植入前遺傳學診斷(PGD)的效果.方法 2012年1月至2013年6月在中山大學附屬第一醫院生殖中心共對151對染色體相互易位和62對囉氏易位攜帶者伕婦進行220箇週期的PGD,其中應用aCGH技術對染色體相互易位和囉氏易位攜帶者行PGD的週期數分彆為33和22箇週期,應用熒光原位雜交(FISH)技術對染色體相互易位和囉氏易位攜帶者行PGD的週期數分彆為119和46箇週期.比較兩種檢測方法的診斷率.結果 應用aCGH技術對染色體相互易位和囉氏易位攜帶者易位染色體正常或平衡胚胎檢齣率分彆為38.20% (123/322)及67.20% (127/189),FISH技術分彆為15.39%(195/1 267)及30.75% (202/657),aCGH技術的檢齣率均顯著高于FISH技術(P均<0.05).應用aCGH技術對染色體相互易位和囉氏易位攜帶者易位染色體的異常胚胎檢齣率分彆為59.32%(191/322)及30.69% (58/189),FISH技術分彆為83.03%(1 052/1 267)及67.43% (443/657),aCGH技術均顯著低于FISH技術(P均<0.05).aCGH技術檢測的染色體相互易位攜帶者胚胎中,易位染色體正常或平衡、而非易位染色體髮生非整倍體改變的異常胚胎檢齣率為20.19%(65/322),明顯低于囉氏易位攜帶者的38.62% (73/189),兩者比較,差異有統計學意義(P<0.01).結論 aCGH技術進行染色體易位攜帶者PGD的易位染色體正常或平衡檢齣率較FISH技術更高,而相互易位攜帶者的胚胎中非易位染色體髮生非整倍體改變的異常胚胎檢齣率較囉氏易位攜帶者低.
목적 탐토미진렬심편비교기인조잡교(aCGH)기술용우염색체역위휴대자배태식입전유전학진단(PGD)적효과.방법 2012년1월지2013년6월재중산대학부속제일의원생식중심공대151대염색체상호역위화62대라씨역위휴대자부부진행220개주기적PGD,기중응용aCGH기술대염색체상호역위화라씨역위휴대자행PGD적주기수분별위33화22개주기,응용형광원위잡교(FISH)기술대염색체상호역위화라씨역위휴대자행PGD적주기수분별위119화46개주기.비교량충검측방법적진단솔.결과 응용aCGH기술대염색체상호역위화라씨역위휴대자역위염색체정상혹평형배태검출솔분별위38.20% (123/322)급67.20% (127/189),FISH기술분별위15.39%(195/1 267)급30.75% (202/657),aCGH기술적검출솔균현저고우FISH기술(P균<0.05).응용aCGH기술대염색체상호역위화라씨역위휴대자역위염색체적이상배태검출솔분별위59.32%(191/322)급30.69% (58/189),FISH기술분별위83.03%(1 052/1 267)급67.43% (443/657),aCGH기술균현저저우FISH기술(P균<0.05).aCGH기술검측적염색체상호역위휴대자배태중,역위염색체정상혹평형、이비역위염색체발생비정배체개변적이상배태검출솔위20.19%(65/322),명현저우라씨역위휴대자적38.62% (73/189),량자비교,차이유통계학의의(P<0.01).결론 aCGH기술진행염색체역위휴대자PGD적역위염색체정상혹평형검출솔교FISH기술경고,이상호역위휴대자적배태중비역위염색체발생비정배체개변적이상배태검출솔교라씨역위휴대자저.
Objective To investigate the clinical use of array comparative genomic hybridization (aCGH) with fluorescence in situ hybridization (FISH) in preimplantion genetic diagnosis (PGD)for reciprocal and Robertsonian translocation carriers.Methods From Jan.2012 to Jun.2013,a total of 220 PGD cycles from 151 reciprocal translocation and 62 Robertsonian translocation carrier couples,including 33 cycles for reciprocal translocation carriers and 22 cycles for Robertsonian translocation carriers performed using array CGH,and 119 cycles for reciprocal translocation carriers and 46 cycles for Robertsonian translocation carriers performed using FISH were retrospectively studied.The rate of accurate diagnosis was compared between two methods.Results Normal and/or balance rates of the two translocated chromosomes detected by aCGH for both reciprocal and Robertsonian translocation carriers were 38.20% (123/322) and 67.20% (127/189),significantly higher than 15.39% (195/1 267) and 30.75% (202/657) by FISH (all P <0.05).Abnormal rates of the two translocated chromosomes detected by aCGH for both reciprocal and Robertsonian translocation carriers were 59.32% (191/322) and 30.69% (58/189),significantly lower than 83.03% (1 052/1 267) and 67.43% (443/657) by FISH (all P < 0.05).And the rate of aneu ploidy in non-translocated chromosome from reciprocal translocation embryos was 20.19% (65/322),which was significantly lower than 38.62% (13/189) from Robertsonian translocation embryos (P < 0.01).Conclusions Normal and/or balance rates of the two translocated chromosomes detected by array CGH were significantly higher than FISH.And the rate of aneuploidy in non-translocated chromosomes from reciprocal translocation embryos was significantly lower than that from Robertsonian translocation embryos.