国际医药卫生导报
國際醫藥衛生導報
국제의약위생도보
INTERNATIONAL MEDICINE & HEALTH GUIDANCE NEWS
2011年
19期
2410-2414
,共5页
梅敏%帅虎%朱甫津%谭尚华
梅敏%帥虎%硃甫津%譚尚華
매민%수호%주보진%담상화
Mentzer指数%轻型α地中海贫血%缺铁性贫血%红细胞体积分布宽度%ROC曲线
Mentzer指數%輕型α地中海貧血%缺鐵性貧血%紅細胞體積分佈寬度%ROC麯線
Mentzer지수%경형α지중해빈혈%결철성빈혈%홍세포체적분포관도%ROC곡선
Mentzer index%Alpha thalassemia%Iron deficiency anemia%Red cell distribution width%Receiver operating characteristic curve
目的 评估Mentzer指数(Mentzer index,MI)在鉴别HbA2减低中轻型α地中海贫血与缺铁性贫血中的价值.方法 回顾本院3年来血红蛋白电泳中HbA2减低的151例人群的α地贫基因、血常规、铁蛋白、血清铁数据,根据地贫基因分析和铁蛋白、血清铁水平将其分成2组:轻型α地中海贫血组(n=90),缺铁性贫血组(n=61).结果 缺铁组与地中海贫血无缺铁组、地中海贫血合并缺铁组、轻型α地中海贫血组三者比较中,MI有明显差异(P<0.01),而在地中海贫血无缺铁组与地中海贫血合并缺铁组比较差异无显著性(P> 0.05).MI在缺铁组与轻型α地中海贫血组的ROC曲线下面积为0.849,并确定MI的截断点为13.1;以MI≥13.1时,缺铁性贫血检出的敏感度为96.7%,特异度为61.1%,尤登指数为0.58;若联合RDW、MI对两者进行鉴别,缺铁性贫血检出的敏感度为100%.结论 MI在鉴别HbA2减低中轻型α地中海贫血与缺铁性贫血有一定的准确性,MI与RDW两者均小于截断点可排除缺铁性贫血的可能.
目的 評估Mentzer指數(Mentzer index,MI)在鑒彆HbA2減低中輕型α地中海貧血與缺鐵性貧血中的價值.方法 迴顧本院3年來血紅蛋白電泳中HbA2減低的151例人群的α地貧基因、血常規、鐵蛋白、血清鐵數據,根據地貧基因分析和鐵蛋白、血清鐵水平將其分成2組:輕型α地中海貧血組(n=90),缺鐵性貧血組(n=61).結果 缺鐵組與地中海貧血無缺鐵組、地中海貧血閤併缺鐵組、輕型α地中海貧血組三者比較中,MI有明顯差異(P<0.01),而在地中海貧血無缺鐵組與地中海貧血閤併缺鐵組比較差異無顯著性(P> 0.05).MI在缺鐵組與輕型α地中海貧血組的ROC麯線下麵積為0.849,併確定MI的截斷點為13.1;以MI≥13.1時,缺鐵性貧血檢齣的敏感度為96.7%,特異度為61.1%,尤登指數為0.58;若聯閤RDW、MI對兩者進行鑒彆,缺鐵性貧血檢齣的敏感度為100%.結論 MI在鑒彆HbA2減低中輕型α地中海貧血與缺鐵性貧血有一定的準確性,MI與RDW兩者均小于截斷點可排除缺鐵性貧血的可能.
목적 평고Mentzer지수(Mentzer index,MI)재감별HbA2감저중경형α지중해빈혈여결철성빈혈중적개치.방법 회고본원3년래혈홍단백전영중HbA2감저적151례인군적α지빈기인、혈상규、철단백、혈청철수거,근거지빈기인분석화철단백、혈청철수평장기분성2조:경형α지중해빈혈조(n=90),결철성빈혈조(n=61).결과 결철조여지중해빈혈무결철조、지중해빈혈합병결철조、경형α지중해빈혈조삼자비교중,MI유명현차이(P<0.01),이재지중해빈혈무결철조여지중해빈혈합병결철조비교차이무현저성(P> 0.05).MI재결철조여경형α지중해빈혈조적ROC곡선하면적위0.849,병학정MI적절단점위13.1;이MI≥13.1시,결철성빈혈검출적민감도위96.7%,특이도위61.1%,우등지수위0.58;약연합RDW、MI대량자진행감별,결철성빈혈검출적민감도위100%.결론 MI재감별HbA2감저중경형α지중해빈혈여결철성빈혈유일정적준학성,MI여RDW량자균소우절단점가배제결철성빈혈적가능.
Objective To evaluates the value of Mentzer index ( MI ) in differentiating alpha thalassemia carriers from iron deficiency anemia.Methods The data on alpha thalassemia gene,blood cell count,and serum levels of iron and ferritin were retrospectively analyzed in 151 patients with reduced hemoglobin A2( HbA2 )levels on hemoglobin electrophoresis.Based on α -globin gene analysis and levels of iron and ferritin,the patients were assigned to alpha thalassemia carriers group ( n =90 ),or iron deficiency anemia group ( n =61 ).Results MI differed significantly between iron deficiency anemia group and alpha thalassemia carriers with normal iron group ( P < 0.01 ),iron deficiency anemia group and alpha thalassemia carriers with iron deficiency group ( P< 0.01 ),iron deficiency anemia group and alpha thalassemia carriers group ( P < 0.01 ); but did not differ significantly between alpha thalassemia carriers with normal iron group and alpha thalassemia carriers with iron deficiency group ( P> 0.05 ).The area under the curve ( AUC ) for MI of receiver operating characteristic curve ( ROC ) was 0.849 between iron deficiency anemia group and alpha thalassemia carriers group,and the cut-off point was 13.1.As MI was -- 13.1,the sensitivity for detecting iron deficiency anemia was 96.7%,specificity 61.1%,and Youden index 0.58.If MI combined with RDW,the sensitivity was 100%.Conclusions Mentzer index has certain accuracy in differentiating alpha thalassemia carriers with reduced HbA2 levels from iron deficiency anemia.Both MI and RDW under the cut-off point can exclude the possibility of iron deficiency anemia.