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重复序列DNA扩增——IS 6110在肺外结核病早期诊断中的应用

DNA AMPLIFICATION OF A REPETITIVE SEQUENCE - IS 6110 IN THE EARLY DIAGNOSIS OF EXTRA PULMONARY TUBERCULOSIS.

作者信息

Lahiri K K, Goorha Y K

机构信息

Classified Specialist (Path & Micro), Command Hospital (Western Command), Chandimandir.

Commandant, AFMSD, Delhi 110 010.

出版信息

Med J Armed Forces India. 2001 Jan;57(1):12-5. doi: 10.1016/S0377-1237(01)80081-2. Epub 2011 Jul 21.

Abstract

DNA amplification by Polymerase Chain Reaction (PCR) of a repetitive sequence specific for Mycobacterium tuberculosis, from clinical samples of extra pulmonary origin were evaluated. The 123 base pair fragment of the insertion element IS 6110 in Mycobacterium tuberculosis was amplified. A total of 50 samples were analysed by PCR and compared with culture on Lowenstein-Jensen medium (LJ) and the clinical findings of the patient. Out of the total 26 samples were positive by PCR, while only seven grew the bacilli in culture. 24 samples were negative by PCR and culture. All the seven samples that grew the bacilli on culture were positive by PCR. In remaining 19 cases that were positive by PCR but did not grow the bacilli clinical features, radiological findings and Mantoux test were strongly suggestive of M. tuberculosis. All the amplification negative cases had no positive evidence of tuberculosis but were being followed up. When correlated with culture and clinical history the sensitivity of PCR for the diagnosis of active tuberculosis was 100%. However, the specifity was only 55.8% as culture on LJ (Gold Standard) was positive in only 7 samples out of 26 samples that were positive by PCR.

摘要

对来自肺外来源临床样本的结核分枝杆菌特异性重复序列进行聚合酶链反应(PCR)DNA扩增评估。扩增了结核分枝杆菌插入元件IS 6110的123个碱基对片段。通过PCR共分析了50个样本,并与罗氏培养基(LJ)培养结果及患者的临床发现进行比较。在总共50个样本中,26个样本PCR结果为阳性,而只有7个样本在培养中培养出杆菌。24个样本PCR和培养均为阴性。所有7个在培养中培养出杆菌的样本PCR结果均为阳性。在其余19例PCR结果为阳性但未培养出杆菌的病例中,临床特征、影像学表现和结核菌素试验强烈提示为结核分枝杆菌。所有扩增阴性的病例均无结核病的阳性证据,但正在进行随访。与培养和临床病史相关时,PCR诊断活动性结核病的敏感性为100%。然而,特异性仅为55.8%,因为在26个PCR阳性样本中,只有7个样本在罗氏培养基(金标准)上培养结果为阳性。

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