National surveillance of hookworm disease in China: A population study

Background Hookworm disease is endemic in China and is widespread globally. The disease burden to humans is great. Methods The study described the national surveillance of hookworm implemented in 31 provinces/autonomous regions/municipalities (P/A/Ms) of China in 2019. Each P/A/M determined the number and location of surveillance spots (counties). A unified sampling method was employed, and at least 1000 subjects were investigated in each surveillance spot. The modified Kato-Katz thick smear method was employed for stool examination. Fifty samples positive with hookworm eggs were cultured in each surveillance spot to discriminate species between A. duodenale and N. americanus. Twenty-five soil samples were collected from each surveillance spot and examined for hookworm larva. The 2019 surveillance results were analyzed and compared with that of 2016–2018. Results A total of 424766 subjects were investigated in 31 P/A/Ms of China in 2019, and the overall hookworm infection rate was 0.85% (3580/424766). The weighted infection and standard infection rates were 0.66% (4288357/648063870) and 0.67% (4343844/648063870), respectively. Sichuan province had the highest standard infection rate (4.75%) in 2019, followed by Chongqing (2.54%) and Hainan (2.44%). The standard infection rates of other P/A/Ms were all below 1%, with no hookworm detected in 15 P/A/Ms. The standard hookworm infection rate in the males and the females were 0.61% (2021216/330728900) and 0.71% (2267141/317334970), respectively, with a significant difference between different genders (χ2 = 17.23, P<0.0001). The highest standard hookworm infection rate (1.97%) was among age ≥ 60 years, followed by 45~59 years (0.77%), 15~44 years (0.37%), and 7~14 years (0.20%). The lowest standard infection rate was among the 0~6 years age group (0.12%). A significant difference was observed among different age groups (χ2 = 2 305.17, P<0.0001). The constitute ratio for N. americanus, A. duodenale, and coinfection was 78.70% (1341/1704), 2.03% (346/1704), and 1.00% (17/1704), respectively. The detection rate of hookworm larva from soil was 3.45% (71/2056). Conclusion The national surveillance showed that the hookworm infection rate has been decreasing annually from 2016 to 2019, and it is now below 1%. China has made significant progress in controlling hookworm. The national surveillance system is an important way to understand the endemic status and provide important information in this process and thus needs to be continually optimized.

[1]  Jun Cao,et al.  Multi-intervention integrated deworming strategy for sustained control of soil-transmitted helminths infections: a case study in Jiangsu Province, China , 2021, Infectious Diseases of Poverty.

[2]  M. Malecela,et al.  A road map for neglected tropical diseases 2021–2030 , 2021, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[3]  Shizhu Li,et al.  Soil-Transmitted Helminthiasis — China, 2018 , 2020, China CDC weekly.

[4]  Xiaonong Zhou,et al.  National surveillance on soil-transmitted helminthiasis in the People's Republic of China. , 2020, Acta tropica.

[5]  Xiaonong Zhou,et al.  Engagement of the National Institute of Parasitic Diseases in control of soil-transmitted helminthiasis in China. , 2020, Advances in parasitology.

[6]  J. Utzinger,et al.  Neglected tropical diseases in the People’s Republic of China: progress towards elimination , 2019, Infectious Diseases of Poverty.

[7]  A. C. D. de Faria,et al.  Hookworm infection aggravates metabolic disorder in obesity. , 2019, Molecular and biochemical parasitology.

[8]  M. Mutignani,et al.  Intestinal hookworm infestation causing chronic anaemia , 2019, BMJ Case Reports.

[9]  X. Long-qi,et al.  [Interpretation of Detection of Intestinal Helminthes-The Kato-Katz Method (WS/T 570-2017)]. , 2018, Zhongguo xue xi chong bing fang zhi za zhi = Chinese journal of schistosomiasis control.

[10]  Berhanu ELFU FELEKE Epidemiology of Hookworm Infection in the School-age Children: A Comparative Cross-sectional Study , 2018, Iranian journal of parasitology.

[11]  D. Bhasin,et al.  Hookworm-Induced Obscure Overt Gastrointestinal Bleeding. , 2017, Clinical Gastroenterology and Hepatology.

[12]  Bruce Y. Lee,et al.  The Global Economic and Health Burden of Human Hookworm Infection , 2016, PLoS neglected tropical diseases.

[13]  Xing-Quan Zhu,et al.  Major parasitic diseases of poverty in mainland China: perspectives for better control , 2016, Infectious Diseases of Poverty.

[14]  N. Nagelkerke,et al.  Concerted Efforts to Control or Eliminate Neglected Tropical Diseases: How Much Health Will Be Gained? , 2016, PLoS neglected tropical diseases.

[15]  A. Kontoleon,et al.  Influence of Schistosoma mansoni and Hookworm Infection Intensities on Anaemia in Ugandan Villages , 2015, PLoS neglected tropical diseases.

[16]  Dan J Stein,et al.  Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013 , 2015, The Lancet.

[17]  S. Brooker,et al.  Sensitivity of diagnostic tests for human soil-transmitted helminth infections: a meta-analysis in the absence of a true gold standard , 2014, International journal for parasitology.

[18]  B. Erko,et al.  Comparison of the Kato-Katz and FLOTAC techniques for the diagnosis of soil-transmitted helminth infections. , 2011, Parasitology international.

[19]  A. Loukas,et al.  Developing vaccines to combat hookworm infection and intestinal schistosomiasis , 2010, Nature Reviews Microbiology.

[20]  Stefanie Knopp,et al.  Comparing Diagnostic Accuracy of Kato-Katz, Koga Agar Plate, Ether-Concentration, and FLOTAC for Schistosoma mansoni and Soil-Transmitted Helminths , 2010, PLoS neglected tropical diseases.

[21]  Peter J Hotez,et al.  Soil-transmitted helminth infections: ascariasis, trichuriasis, and hookworm , 2006, The Lancet.

[22]  S. Brooker,et al.  Global epidemiology, ecology and control of soil-transmitted helminth infections. , 2006, Advances in parasitology.

[23]  [A national survey on current status of the important parasitic diseases in human population]. , 2005, Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases.

[24]  Dirk Engels,et al.  Soil-transmitted helminth infections: updating the global picture. , 2003, Trends in parasitology.

[25]  S. Brooker,et al.  Hookworm and anaemia prevalence , 2000, The Lancet.

[26]  J. Horton Albendazole: a review of anthelmintic efficacy and safety in humans , 2000, Parasitology.

[27]  Xu Shuhui,et al.  Distribution and pathogenic impact of human parasites in China. , 2000 .

[28]  S. Brooker,et al.  The potential of geographical information systems and remote sensing in the epidemiology and control of human helminth infections. , 2000, Advances in parasitology.

[29]  D. Pritchard,et al.  Hookworm infection. , 2020, Scientific American.

[30]  Z. Jiang,et al.  Soil-transmitted helminthiases: nationwide survey in China. , 1995, Bulletin of the World Health Organization.

[31]  P. Smith,et al.  A randomized controlled trial comparing mebendazole and albendazole against Ascaris, Trichuris and hookworm infections. , 1994, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[32]  K. Alawi,et al.  Efficacy of a single dose of mebendazole on prevalence and intensity of soil-transmitted nematodes in Zanzibar. , 1994, Tropical and geographical medicine.

[33]  G. Medley,et al.  The epidemiology and population biology of Necator americanus infection in a rural community in Zimbabwe. , 1992, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[34]  U. Premaratne,et al.  Comparative efficacy of single dose anthelmintics in relation to intensity of geohelminth infections. , 1991, The Ceylon medical journal.

[35]  P. Dekumyoy,et al.  Effect of single-dose albendazole and single-dose mebendazole on Necator americanus. , 1989, Southeast Asian Journal of Tropical Medicine and Public Health.

[36]  J. Sc Albendazole, a broad-spectrum anthelmintic, in the treatment of intestinal nematode and cestode infection: a multicenter study in 480 patients. , 1986 .

[37]  B. Sinniah,et al.  Albendazole, an effective single dose, broad spectrum anthelmintic drug. , 1983, The American journal of tropical medicine and hygiene.

[38]  D. Stürchler Chemotherapy of human intestinal helminthiases: a review, with particular reference to community treatment. , 1982, Advances in pharmacology and chemotherapy.

[39]  N Katz,et al.  A simple device for quantitative stool thick-smear technique in Schistosomiasis mansoni. , 1972, Revista do Instituto de Medicina Tropical de Sao Paulo.