尼日利亚东北部恶性疟原虫临床分离株对 4-氨基喹啉类药物的体外敏感性。

MalariaWorld journal Pub Date : 2016-07-29 eCollection Date: 2016-01-01 DOI:10.5281/zenodo.10818088
Sulayman T Balogun, Umar K Sandabe, Isah A Waziri, Justus Jibrin, Fatai A Fehintola
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引用次数: 0

摘要

背景:恶性疟原虫耐药菌株广泛存在,这对包括氯喹(CQ)在内的4-氨基喹啉类药物所发挥的关键作用提出了挑战。本研究评估了尼日利亚东北部恶性疟原虫临床分离株(PfCIs)对阿莫地喹(AQ)和氯喹(CQ)的体外敏感性:在获得知情同意后,从包奇州阿扎雷和博尔诺州迈杜古里的无并发症恶性疟原虫疟疾患者身上采集了 PfCIs。体外敏感性用微量测试(MarkIII)法进行评估,AQ 和 CQ 的 IC50 用 HN-NonLin Version VI.1 软件测定。体外 AQ 和 CQ 抗药性的参考标准临界值分别为 80 和 160 nmol/l。被较低浓度的 AQ 和 CQ 抑制的分离菌被称为敏感菌:88.9%(80/90)的 PfCIs 获得了有效的体外检测结果;Azare 为 93.3%(28/30),Maiduguri 为 86.7%(52/60)[χ2 = 0.35; df = 1; p = 0.486]。AQ 和 CQ 的 IC50 几何平均(GM)值分别为 24.2 nmol/l(95% CI,10.5 - 49.6 nmol/l)和 39.5 nmol/l(95% CI,34.5 - 49.6 nmol/l)。Azare和Maiduguri PfCIs的AQ(p = 0.922)和CQ(p = 0.085)GM IC50相似。只有一种分离物对 AQ 具有体外抗药性,敏感性为 98.8%(79/80),而 17 种 PfCIs 对 CQ 具有体外抗药性,敏感性为 78.8%(63/80)。阿扎雷(67.9%;19/28)和迈杜古里(84.6%;44/52)的 PfCIs 对 CQ 的敏感性相似(χ2 = 3.05;df = 1;p = 0.081):研究结果可能表明,AQ 的体外敏感性仍然很高,尼日利亚东北部的分离株可能比其他地区的分离株对 CQ 更敏感。这些发现可能会影响尼日利亚的疟疾治疗和控制政策。
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In vitro sensitivity of Plasmodium falciparum clinical isolates to 4-aminoquinolines in Northeast Nigeria.

Background: Widespread dr ug-resistant Plasmodium falciparum strains have challenged the pivotal role played by 4-aminoquinolines, including chloroquine (CQ), which has been delisted for the treatment of malaria in most parts of the world. This study assessed the in vitro sensitivity of P. falciparum clinical isolates (PfCIs) to amodiaquine (AQ) and CQ in Northeast Nigeria.

Materials and methods: PfCIs were collected from subjects with uncomplicated P. falciparum malaria in Azare, Bauchi State and Maiduguri, Borno State following an informed consent. The in vitro sensitivity was assessed by micro-test (MarkIII) method and the IC50 of AQ and CQ was determined using HN-NonLin Version VI.1 software. The reference standard cut-off values for in vitro AQ and CQ resistance of 80 and 160 nmol/l, respectively, were used. Isolates that were inhibited by lower AQ and CQ concentrations were referred to as sensitive.

Results: Valid in vitro assay r esults were obtained for 88.9% (80/90) of the PfCIs; Azare had 93.3% (28/30) and Maiduguri had 86.7% (52/60) [χ2 = 0.35; df = 1; p = 0.486]. The geometric mean (GM) IC50 of AQ and CQ were 24.2 nmol/l (95% CI, 10.5 - 49.6 nmol/l) and 39.5 nmol/l (95% CI, 34.5 - 49.6 nmol/l), respectively. The AQ (p = 0.922) and CQ (p = 0.085) GM IC50 were similar between Azare and Maiduguri PfCIs. Only one isolate showed in vitro resistance to AQ giving a sensitivity of 98.8% (79/80) while 17 PfCIs showed in vitro resistance to CQ giving a sensitivity of 78.8% (63/80). The CQ sensitivity was similar between Azare (67.9%; 19/28) and Maiduguri (84.6%; 44/52) PfCIs (χ2 = 3.05; df = 1; p = 0.081).

Conclusions: The findings may suggest that the AQ in vitro sensitivity remains high and the isolates in Northeast Nigeria may appear more sensitive to CQ than isolates from other parts. These findings may affect malaria treatment and control policy in Nigeria.

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