国际医药卫生导报
國際醫藥衛生導報
국제의약위생도보
INTERNATIONAL MEDICINE & HEALTH GUIDANCE NEWS
2012年
2期
250-251
,共2页
何桂儿%王蕴端%黄霜%王晶晶%黄志成
何桂兒%王蘊耑%黃霜%王晶晶%黃誌成
하계인%왕온단%황상%왕정정%황지성
甲胎蛋白%绒毛膜促性腺激素%游离雌三醇%唐氏综合征%产前筛查
甲胎蛋白%絨毛膜促性腺激素%遊離雌三醇%唐氏綜閤徵%產前篩查
갑태단백%융모막촉성선격소%유리자삼순%당씨종합정%산전사사
Alpha fetoprotein%Chorionic gonadotrophin%Unconjugated estriol%Down' s syndrome%Prenatal screening
目的 检测孕中期妇女血清中甲胎蛋白(AFP)、绒毛膜促性腺激素(HCG)和游离雌三醇(uE3)的含量,经试剂配套软件进行发病风险评价,探讨其在唐氏综合征筛查中的应用价值.方法 应用酶联免疫法定量检测孕中期孕妇的血清标志物甲胎蛋白(AFP)、绒毛膜促性腺激素(HCG)和游离雌三醇(uE3),结合孕妇的年龄、孕周、体重等因素,利用配套软件进行对唐氏综合征的风险值进行评估.对筛查结果为高风险的孕妇进行遗传咨询,在知情同意情况下进行羊水细胞染色体检查,并对筛查的孕妇追踪到产后一个月.结果 13736例孕15 ~ 20+6周的妇女进行上述3项血清标记物检测,筛查出各类风险人群1017例,其中DS高风险728例、ONTD高风险138例、18三体高风险151例,在阳性孕妇中发现唐氏综合征5例、18三体4例、脑积水4例、左侧脑室扩张1例,低风险中发现唐氏综合征2例.结论 孕中期应用母血三联生化指标进行产前筛查,对降低唐氏儿和神经管缺陷儿的出生率有着重要意义.
目的 檢測孕中期婦女血清中甲胎蛋白(AFP)、絨毛膜促性腺激素(HCG)和遊離雌三醇(uE3)的含量,經試劑配套軟件進行髮病風險評價,探討其在唐氏綜閤徵篩查中的應用價值.方法 應用酶聯免疫法定量檢測孕中期孕婦的血清標誌物甲胎蛋白(AFP)、絨毛膜促性腺激素(HCG)和遊離雌三醇(uE3),結閤孕婦的年齡、孕週、體重等因素,利用配套軟件進行對唐氏綜閤徵的風險值進行評估.對篩查結果為高風險的孕婦進行遺傳咨詢,在知情同意情況下進行羊水細胞染色體檢查,併對篩查的孕婦追蹤到產後一箇月.結果 13736例孕15 ~ 20+6週的婦女進行上述3項血清標記物檢測,篩查齣各類風險人群1017例,其中DS高風險728例、ONTD高風險138例、18三體高風險151例,在暘性孕婦中髮現唐氏綜閤徵5例、18三體4例、腦積水4例、左側腦室擴張1例,低風險中髮現唐氏綜閤徵2例.結論 孕中期應用母血三聯生化指標進行產前篩查,對降低唐氏兒和神經管缺陷兒的齣生率有著重要意義.
목적 검측잉중기부녀혈청중갑태단백(AFP)、융모막촉성선격소(HCG)화유리자삼순(uE3)적함량,경시제배투연건진행발병풍험평개,탐토기재당씨종합정사사중적응용개치.방법 응용매련면역법정량검측잉중기잉부적혈청표지물갑태단백(AFP)、융모막촉성선격소(HCG)화유리자삼순(uE3),결합잉부적년령、잉주、체중등인소,이용배투연건진행대당씨종합정적풍험치진행평고.대사사결과위고풍험적잉부진행유전자순,재지정동의정황하진행양수세포염색체검사,병대사사적잉부추종도산후일개월.결과 13736례잉15 ~ 20+6주적부녀진행상술3항혈청표기물검측,사사출각류풍험인군1017례,기중DS고풍험728례、ONTD고풍험138례、18삼체고풍험151례,재양성잉부중발현당씨종합정5례、18삼체4례、뇌적수4례、좌측뇌실확장1례,저풍험중발현당씨종합정2례.결론 잉중기응용모혈삼련생화지표진행산전사사,대강저당씨인화신경관결함인적출생솔유착중요의의.
Objective To determine serum contents of maternal serum markers including alpha fetoprotein(AFP),chorionic gonadotrophin(HCG)and unconjugated estriol(uE3)in mid-pregnancy women,and explore its clinical value in screening for Down syndrome(DS).Methods ELISA was used to test the concentrations of AFP,HCG and uE3 in maternal serum.The morbidities of DS were calculated base on the results with supported software combining with factors of the maternal age,gestation age and weight.Hereditary consultation was provided for the high-risk pregnant women,amniocentesis was done under their agreements.Each case was followed till one month after the fetus birth.Results 1017 pregnancies among 13736 women of 15 to 20 plus 6 weeks pregnancy were screen positive,728 pregnancies were detected at high risk for DS,138 pregnancies were detected as high risk for open neural tube defects (ONTD),151 pregnancies were detected as high risk for trisomy 18.In the screening positive pregnancies,we found 5 cases of DS,4 cases of trisomy 18,4 cases of hydrocephalus,1 case of dilatation of ventricle,2 cases of DS were found in the screening negative pregnancies.Conclusion The results in this paper indicate that triple screen test for middle period serum of pregnancy women is important for decreasing the birth rate of DS and neural tube defects.