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   <subfield code="a">10.12688/wellcomeopenres.14683.1</subfield>
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   <subfield code="a">(SERVAL)BIB_147F5B316B25</subfield>
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   <subfield code="a">Effect of high-intensity versus low-intensity praziquantel treatment on HIV disease progression in HIV and &lt;i&gt;Schistosoma mansoni&lt;/i&gt; co-infected patients: a randomised controlled trial</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[A. Abaasa, G. Asiki, A. Obuku Ekii, J. Wanyenze, P. Pala, G. J van Dam, P. L A M Corstjens, P. Hughes, S. Ding, G. Pantaleo, P. Kaleebu, A. M Elliott, A. Kamali]</subfield>
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   <subfield code="a">&amp;lt;b&amp;gt;Background:&amp;lt;/b&amp;gt; It has been hypothesised that &amp;lt;i&amp;gt;Schistosoma&amp;lt;/i&amp;gt; co-infection exacerbates HIV progression, and hence anthelminthic intervention in co-infected individuals will delay it. We evaluated effects of high-intensity versus low-intensity praziquantel treatment of schistosomiasis on HIV disease progression among co-infected patients from fishing populations around Lake Victoria, Uganda. &amp;lt;b&amp;gt;Methods&amp;lt;/b&amp;gt; : Between August 2012 and September 2015, we conducted an open-label randomised, controlled trial. Adults, antiretroviral therapy-naïve, CD4 counts ≥350 cells/μl, HIV and &amp;lt;i&amp;gt;S. mansoni&amp;lt;/i&amp;gt; co-infected, were randomised 1:1 to praziquantel (40mg/kg) given quarterly (starting at enrolment) or annually (starting 12 weeks after enrolment; such that low-intensity participants were still untreated when sampled at 12 weeks). A non-randomised HIV-positive &amp;lt;i&amp;gt;S. mansoni-&amp;lt;/i&amp;gt; negative comparison group was recruited. The primary outcome was mean change in plasma viral load at 12 and 60 weeks. &amp;lt;b&amp;gt;Results:&amp;lt;/b&amp;gt; In total 363 participants (high-intensity 113, low-intensity 113, comparison group 137) were recruited; 96 (85.0%), 97 (85.8%) and 107 (78.1%) completed 60 weeks of follow up, respectively. Adjusting for baseline age and viral load, the geometric mean ratio (aGMR [95%CI]) viral load for high-intensity vs low-intensity groups at 12 weeks was 0.90 [0.65, 1.25] p=0.55 and at 60 weeks 1.88 [0.78, 4.53] p=0.16. Results in the comparison group were similar to trial arms. High-intensity, compared to low-intensity, treatment resulted in substantially lower &amp;lt;i&amp;gt;S. mansoni&amp;lt;/i&amp;gt; prevalence at all follow up visits (p&amp;lt;0.05). &amp;lt;b&amp;gt;Conclusions:&amp;lt;/b&amp;gt; In communities with a high burden of both &amp;lt;i&amp;gt;S. mansoni&amp;lt;/i&amp;gt; and HIV infection, high-intensity treatment of &amp;lt;i&amp;gt;S. mansoni&amp;lt;/i&amp;gt; does not delay HIV progression despite relevant benefit for parasite clearance. &amp;lt;b&amp;gt;Trial registration:&amp;lt;/b&amp;gt; ISRCTN15371662 (17/11/2016).</subfield>
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   <subfield code="a">Abaasa</subfield>
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