Abstract

The clinical presentation of Human African Trypanosomiasis (HAT) due to Trypanosoma brucei gambiense is well known, but knowledge on long-term sequelae is limited. In the frame of studies conducted between 2004 and 2005 in the Democratic Republic of the Congo (DRC), the prevalence of HAT related signs and symptoms were evaluated before the start of treatment and at the end of treatment. To explore possible long-term sequelae, the same clinical parameters were assessed in 2017 in 51 first stage and 18 second stage HAT patients. Signs and symptoms 12–13 years after treatment were compared to before and immediately after treatment and to controls matched for sex and age (±5 years). In first stage HAT patients, the prevalence of all signs and symptoms decreased compared to before treatment but were still higher after 12–13 years than immediately at the end of treatment and in the control group. In second stage HAT patients, all HAT-specific findings had continuously decreased to the point where they were in the range of the healthy control group. In a selection of oligosymptomatic first stage HAT patients, no trypanosomes were detected in the blood by microscopic examination or PCR. An oligosymptomatic presentation of HAT due to the persistence of parasites in compartments, where first stage HAT medications do not penetrate, could not be ruled out.

Highlights

  • Human African trypanosomiasis (HAT) is caused by the protozoan parasites Trypanosoma brucei gambiense (T.b. gambiense) and Trypanosoma brucei rhodesiense (T.b. rhodesiense), which are transmitted by tsetse flies

  • In the region of Vanga, 96 first stage and 29 second stage HAT patients were recruited into several studies and trials between 2004 and 2005 [12,13,14,15,16]

  • We demonstrated HAT-related signs and symptoms more than 10 years after treatment for the first time in first stage HAT patients without detectable levels of parasites

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Summary

Introduction

Human African trypanosomiasis (HAT) is caused by the protozoan parasites Trypanosoma brucei gambiense (T.b. gambiense) and Trypanosoma brucei rhodesiense (T.b. rhodesiense), which are transmitted by tsetse flies. The disease occurs in two stages, the first, or hemolymphatic, stage without invasion of the central nervous system (CNS) and the second, or neurological, stage with invasion of the CNS by the trypanosomes. According to the last WHO report (WHO interim guidelines for treatment of gambiense human African trypanosomiasis, August 2019) [2], the worldwide number of T.b. gambiense HAT cases dropped from over 25,000 in the year 2000 to below 1000 reported cases worldwide in 2018 [2]. Neuro-psychiatric disorders such as lethargy, aggressive behaviour, logorrhoea, psychotic reactions, mood changes, and sleep disturbances/disorders dominate the clinical presentation.

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