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用于麻风病检测及麻风病化疗疗效评估的DNA扩增技术

DNA amplification for detection of leprosy and assessment of efficacy of leprosy chemotherapy.

作者信息

Kampirapap K, Singtham N, Klatser P R, Wiriyawipart S

机构信息

Swellengrebel Laboratory of Tropical Hygiene, Royal Tropical Institute, Amsterdam, The Netherlands.

出版信息

Int J Lepr Other Mycobact Dis. 1998 Mar;66(1):16-21.

PMID:9614835
Abstract

Polymerase chain reaction (PCR) for the detection of Mycobacterium leprae was applied to fresh skin biopsies and slit-skin smears from 122 untreated leprosy patients. The PCR positivity rates in biopsies were 95.6% in multibacillary (MB) cases and 44.2% in paucibacillary (PB) cases. Following 1 month of treatment, MB cases declined by 54.3% and PB cases by 61.8% of initial values. Six-month values also declined from initial positivity rates to 50.3% and 53.8% of initial values in MB and PB, respectively. Larger declines in the rate of positivity were seen for skin-smear samples at 1 and 6 months in both MB and PB, but overall PCR positivity rates were lower than biopsy rates for M. leprae.

摘要

采用聚合酶链反应(PCR)检测122例未经治疗的麻风患者的新鲜皮肤活检组织和皮肤刮片。多菌型(MB)病例活检组织的PCR阳性率为95.6%,少菌型(PB)病例为44.2%。治疗1个月后,MB病例下降至初始值的54.3%,PB病例下降至初始值的61.8%。6个月时,MB和PB病例的阳性率也分别从初始阳性率下降至初始值的50.3%和53.8%。MB和PB病例在1个月和6个月时,皮肤涂片样本的阳性率下降幅度更大,但总体上麻风杆菌的PCR阳性率低于活检组织的阳性率。

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