Ghimire Prakash, Singh Nihal, Ortega Leonard, Rijal Komal Raj, Adhikari Bipin, Thakur Garib Das, Marasini Baburam
World Health Organization, Country Office Nepal, UN House, Pulchowk, Lalitpur, Nepal.
Global Malaria Programme, World Health Organization, Geneva, Switzerland.
Malar J. 2017 May 23;16(1):214. doi: 10.1186/s12936-017-1864-2.
Glucose-6-phosphate dehydrogenase (G6PD) is a rate limiting enzyme of the pentose phosphate pathway and is closely associated with the haemolytic disorders among patients receiving anti-malarial drugs, such as primaquine. G6PD deficiency (G6PDd) is an impending factor for radical treatment of malaria which affects the clearance of gametocytes from the blood and subsequent delay in the achievement of malaria elimination. The main objective of this study was to assess the prevalence of G6PD deficiency in six malaria endemic districts in Southern Nepal.
A cross-sectional population based prevalence survey was conducted in six malaria endemic districts of Nepal, during April-Dec 2013. A total of 1341 blood samples were tested for G6PDd using two different rapid diagnostic test kits (Binax-Now and Care Start™). Equal proportions of participants from each district (n ≥ 200) were enrolled considering ethnic and demographic representation of the population groups.
Out of total 1341 blood specimens collected from six districts, the overall prevalence of G6PDd was 97/1341; 7.23% on Binax Now and 81/1341; 6.0% on Care Start test. Higher prevalence was observed in male than females [Binax Now: male 10.2%; 53/521 versus female 5.4%; 44/820 (p = 0.003) and Care Start: male 8.4%; 44/521 versus female 4.5%; 37/820 (p = 0.003)]. G6PDd was higher in ethnic groups Rajbanshi (11.7%; 19/162) and Tharu (5.6%; 56/1005) (p = 0.006), major inhabitant of the endemic districts. Higher prevalence of G6PDd was found in Jhapa (22/224; 9.8%) and Morang districts (18/225; 8%) (p = 0.031). In a multivariate analysis, male were found at more risk for G6PDd than females, on Binax test (aOR = 1.97; CI 1.28-3.03; p = 0.002) and Care Start test (aOR = 1.86; CI 1.16-2.97; p = 0.009).
The higher prevalence of G6PDd in certain ethnic group, gender and geographical region clearly demonstrates clustering of the cases and ascertained the risk groups within the population. This is the first study in Nepal which identified the vulnerable population groups for G6PDd in malaria endemic districts. The finding of this study warrants the need for G6PDd testing in vulnerable population groups in endemic districts, and also facilitates use of primaquine in mass supporting timely progress for malaria elimination.
葡萄糖-6-磷酸脱氢酶(G6PD)是磷酸戊糖途径的限速酶,与接受抗疟药物(如伯氨喹)治疗的患者中的溶血性疾病密切相关。G6PD缺乏症(G6PDd)是疟疾根治的一个潜在因素,它会影响配子体从血液中的清除,进而延迟疟疾消除目标的实现。本研究的主要目的是评估尼泊尔南部六个疟疾流行区中G6PD缺乏症的患病率。
2013年4月至12月期间,在尼泊尔六个疟疾流行区进行了一项基于人群的横断面患病率调查。使用两种不同的快速诊断试剂盒(Binax-Now和Care Start™)对总共1341份血样进行G6PDd检测。考虑到人群的种族和人口统计学代表性,从每个区纳入了相等比例的参与者(n≥200)。
在从六个区采集的总共1341份血样中,G6PDd的总体患病率为97/1341;Binax Now检测为7.23%,Care Start检测为81/1341;6.0%。男性患病率高于女性[Binax Now:男性10.2%;53/521,女性5.4%;44/820(p = 0.003),Care Start:男性8.4%;44/521,女性4.5%;37/820(p = 0.003)]。在拉杰班西族(11.7%;19/162)和塔鲁族(5.6%;56/1005)(p = 0.006)中G6PDd患病率较高,这两个族是流行区的主要居民。在贾帕(22/224;9.8%)和莫朗区(18/225;8%)中发现G6PDd患病率较高(p = 0.031)。在多变量分析中,Binax检测显示男性患G6PDd的风险高于女性(调整后比值比[aOR]=1.97;可信区间[CI] 1.28 - 3.03;p = 0.002),Care Start检测也显示如此(aOR = 1.86;CI 1.16 - 2.97;p = 0.009)。
G6PDd在特定种族、性别和地理区域的较高患病率清楚地表明了病例的聚集性,并确定了人群中的风险群体。这是尼泊尔首次在疟疾流行区确定G6PDd的脆弱人群组的研究。本研究结果表明有必要在流行区的脆弱人群组中进行G6PDd检测,也有助于在大规模使用伯氨喹时支持及时推进疟疾消除工作。