检验医学
檢驗醫學
검험의학
LABORATORY MEDICINE
2013年
11期
1034-1037
,共4页
李友琼%黄慧嫔%覃桂芳%黄春丽
李友瓊%黃慧嬪%覃桂芳%黃春麗
리우경%황혜빈%담계방%황춘려
毛细管电泳%地中海贫血%血红蛋白CS型H病%血红蛋白病
毛細管電泳%地中海貧血%血紅蛋白CS型H病%血紅蛋白病
모세관전영%지중해빈혈%혈홍단백CS형H병%혈홍단백병
Capillary electrophoresis%Thalassemia%Hemoglobin CS-H disease%Hemoglobin disease
目的:探讨毛细管电泳分析仪在诊断血红蛋白(Hb)CS-H病中的应用价值。方法用Sebia Capillar-ys 2型毛细管电泳仪分别对经地中海贫血基因分析确诊的34例Hb CS-H病患者和70例非Hb CS-H病患者(包括42例-SEA/-α3.7、19例-SEA/-α4.2、7例Hb WS-H、2例Hb QS-H)进行Hb电泳。采用缺口聚合酶链反应(Gap-PCR)和反向斑点杂交的方法对2组患者进行地中海贫血基因分析。结果毛细管电泳分析 Hb CS-H组的HbCS带含量为(1.89±1.33)%,HbH带含量为(1.07±0.86)%,HbA2带含量为(1.17±0.68)%;非Hb CS-H组均未能检测到HbCS带,有部分标本未检出HbH带,HbA2带含量为(1.81±1.21)%。2组HbA2带含量比较差异有统计学意义(P<0.05)。毛细管电泳仪诊断Hb CS-H病的敏感性和特异性分别为88.2%和100.0%,阳性预测值为100.0%,阴性预测值为94.6%,诊断效率为96.2%,与地中海贫血基因分析比较差异无统计学意义(P=0.134)。结论毛细管电泳可以用来快速诊断Hb CS-H病,能够为患者减轻部分经济负担。
目的:探討毛細管電泳分析儀在診斷血紅蛋白(Hb)CS-H病中的應用價值。方法用Sebia Capillar-ys 2型毛細管電泳儀分彆對經地中海貧血基因分析確診的34例Hb CS-H病患者和70例非Hb CS-H病患者(包括42例-SEA/-α3.7、19例-SEA/-α4.2、7例Hb WS-H、2例Hb QS-H)進行Hb電泳。採用缺口聚閤酶鏈反應(Gap-PCR)和反嚮斑點雜交的方法對2組患者進行地中海貧血基因分析。結果毛細管電泳分析 Hb CS-H組的HbCS帶含量為(1.89±1.33)%,HbH帶含量為(1.07±0.86)%,HbA2帶含量為(1.17±0.68)%;非Hb CS-H組均未能檢測到HbCS帶,有部分標本未檢齣HbH帶,HbA2帶含量為(1.81±1.21)%。2組HbA2帶含量比較差異有統計學意義(P<0.05)。毛細管電泳儀診斷Hb CS-H病的敏感性和特異性分彆為88.2%和100.0%,暘性預測值為100.0%,陰性預測值為94.6%,診斷效率為96.2%,與地中海貧血基因分析比較差異無統計學意義(P=0.134)。結論毛細管電泳可以用來快速診斷Hb CS-H病,能夠為患者減輕部分經濟負擔。
목적:탐토모세관전영분석의재진단혈홍단백(Hb)CS-H병중적응용개치。방법용Sebia Capillar-ys 2형모세관전영의분별대경지중해빈혈기인분석학진적34례Hb CS-H병환자화70례비Hb CS-H병환자(포괄42례-SEA/-α3.7、19례-SEA/-α4.2、7례Hb WS-H、2례Hb QS-H)진행Hb전영。채용결구취합매련반응(Gap-PCR)화반향반점잡교적방법대2조환자진행지중해빈혈기인분석。결과모세관전영분석 Hb CS-H조적HbCS대함량위(1.89±1.33)%,HbH대함량위(1.07±0.86)%,HbA2대함량위(1.17±0.68)%;비Hb CS-H조균미능검측도HbCS대,유부분표본미검출HbH대,HbA2대함량위(1.81±1.21)%。2조HbA2대함량비교차이유통계학의의(P<0.05)。모세관전영의진단Hb CS-H병적민감성화특이성분별위88.2%화100.0%,양성예측치위100.0%,음성예측치위94.6%,진단효솔위96.2%,여지중해빈혈기인분석비교차이무통계학의의(P=0.134)。결론모세관전영가이용래쾌속진단Hb CS-H병,능구위환자감경부분경제부담。
Objective To investigate the application significance of capillary electrophoresis analyzer in the diagnosis of hemoglobin(Hb)CS-H disease.Methods A total of 34 patients with Hb CS-H disease confirmed by thalassemia genetic analysis and 70 patients with non Hb CS-H disease (including 42 cases of -SEA/-α3.7 ,1 9 cases of-SEA/-α4.2 ,7 cases of Hb WS-H and 2 cases of Hb QS-H)were determined for Hb with Sebia Capillarys 2 capillary electrophoresis.The thalassemia genetic analysis of the 2 groups was conducted by gap-polymerase chain reaction (Gap-PCR)and reverse dot blot hybridization.Results The HbCS and HbH contents of Hb CS-H group were (1 .89 ± 1 .33)% and (1 .07 ±0.86)%,and the HbA2 content was (1 .1 7 ±0.68)%.However,the samples with HbCS and a part of HbH were not detected in non-Hb CS-H group,and the HbA2 content was (1 .81 ±1 .21 )%.Compared with Hb CS-H group and non-Hb CS-H group for HbA2 ,there were significant significance (P<0.05 ).Compared with the thalassemia genetic analysis,the sensitivity of capillary electrophoresis for the diagnosis of Hb CS-H disease was 88.2%, the specificity was 1 00.0%,the positive predictive value was 1 00.0%,the negative predictive value was 94.6%,the diagnosis efficiency was 96.2%,and there was no statistical significance (P=0.1 34).Conclusions The capillary electrophoresis can be used to the rapid diagnosis of Hb CS-H disease,and it will alleviate some of the economic burdens for patients.