Table 1.
Models used | Causative agents* | Mode of transmission | Main clinical manifestations in endemic settings | Number of people affected worldwide | 2030 target: EPHP or EOT | |
---|---|---|---|---|---|---|
Soil-transmitted helminths | Erasmus MC;22, 23, 24 Imperial College London25 | Roundworm (Ascaris lumbricoides), whipworm (Trichuris trichiura), hookworms (Necator americanus and Ancylostoma duodenale) | Primarily faecal–oral transmission (also skin penetration of larvae in hookworm) | Diarrhoea, abdominal pain, stunting, general malaise, and weakness | Approximately 1·5 billion people are infected worldwide26 | EPHP: ≤2% prevalence of moderate-to-heavy-intensity infections among school-aged children |
Schistosomiasis | Imperial College London;27 Oxford and SCHISTOX;28 only for intestinal schistosomiasis in sub-Saharan Africa | Parasitic worm, Schistosoma mansoni | Transmission via contact with water containing aquatic snail intermediate host | Anaemia, stunting, diarrhoea, hepatomegaly, portal hypertension, and periportal fibrosis | 229 million school-aged children and adults requiring preventive chemotherapy26 | EPHP: ≤1% prevalence of heavy-intensity infections among school-aged children |
Lymphatic filariasis | Warwick (TRANSFIL);29, 30 Erasmus MC, LYMFASIM31 and University of South Florida, and EPIFIL32 | Parasitic worm, Wuchereria bancrofti | Mosquito vector | Hydrocele (scrotal swelling), acute lymphoedema, and chronic lymphoedema (elephantiasis) affecting limbs and genitals | Affects over 120 million people worldwide, with 593 million at risk, and is a leading cause of permanent disability26 | EPHP: defined as passing three transmission assessment surveys; operationally equivalent to 1% prevalence of infective stages (microfilariae) |
Onchocerciasis | Erasmus MC (ONCHOSIM); 33, 34 Imperial College London, and EPIONCHO35 | Parasitic worm, Onchocerca volvulus | Blackfly vector | Skin disease (eg, severe itching), visual Impairment, and permanent blindness | 2·9 million O volvulus infections worldwide26 | EOT |
Trachoma | Oxford36 | Bacterial eye infection, Chlamydia trachomatis | Predominantly direct personal contact | Repeated episodes of conjunctivitis, which can lead to scarring, entropion (in-turning of eyelids), trichiasis (abrasion of cornea by the eyelashes), and eventual blindness | Responsible for blindness or visual impairment of 1·9 million people; 137 million at risk of blindness26 | EPHP: reduction of trachomatous inflammation—follicular in children aged 1–9 years to less than 5%; prevalence of trachomatous trichiasis unknown to health system <0·2% (trichiasis not modelled here) |
Visceral leishmaniasis | Erasmus MC;37, 38 only for India | Protozoa, Leishmania donovani | Sandfly vector | Persistent fever, enlarged liver and spleen, death if untreated | 50 000–90 000 new cases per year globally26 | EPHP: <1 per 10 000 inhabitants per year at subdistrict level in India |
Gambiense human African trypanosomiasis | Warwick;39, 40 Swiss TPH;41 specified for DR Congo | Protozoa, Trypanosoma brucei gambiense | Tsetse fly vector | Stage 1: mild symptoms (eg, fever and headaches); stage 2: neurological disorders resulting in death if untreated | 51 million people estimated to be at risk of infection26 | EPHP: <1 case per 10 000 inhabitants per year averaged over a 5-year period by 2020; EOT: zero reported cases by 2030 |
Further details on transmission, epidemiology, control strategies, and elimination targets for each disease are available in the WHO NTD factsheets26 and the WHO 2021–30 NTD roadmap.5 For more information on the models used see figure 1 and the appendix (pp 5–33). NTD=neglected tropical disease. EPHP=elimination as a public health problem. EOT=elimination of transmission. SCHISTOX=schistosomiasis Oxford model. TRANSFIL=transmission model of filariasis. LYMFASIM=lymphatic filariasis simulation model. EPIFIL=epidemiological model of filariasis. ONCHOSIM=onchocerciasis simulation model. EPIONCHO=epidemiological model of onchocerciasis.
Causative agents considered in this study.