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We therefore investigated the effects of both age of <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> initiation and duration of <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> interruption on <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> decay in children.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>We investigated <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> decay in three groups of children on <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content>: Group<jats:bold>\u2010<\/jats:bold>1 (n\u00a0=\u00a07) started uninterrupted <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> within eight days of life; Group\u20102 (n\u00a0=\u00a08) started uninterrupted <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> at a median of five months of age; and Group\u20103 (n\u00a0=\u00a023) started <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> at a median age of 1.8\u00a0months for either 40 or 96\u00a0weeks, then interrupted <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> (median of seven months), and restarted <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> based on <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4 count and clinical criteria. Total <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> was assayed using a sensitive <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 subtype C\u2010adapted quantitative <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content> for <jats:italic>integrase<\/jats:italic>. The duration of <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> was square root transformed to fit the observed slowing of <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> decay rate. For each group, point estimates for decay rates were determined after six months of continuous suppressive <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> in groups 1 and 2 or six months after restarting <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> in Group\u20103. Groups\u20102 and 3 were combined using a mixed effect regression model to investigate covariates of <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> decay rate.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results and Discussion<\/jats:title><jats:p>At six months of continuous suppressive <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content>, the <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> t\u00bd (95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>) was shorter in Group\u20101 (n\u00a0=\u00a07): 2.7\u00a0months (2.1 to 3.8), than 9.2\u00a0months (7.4 to 12.1) in Group\u20102 (n\u00a0=\u00a08); and 9.6\u00a0months (7.6 to 12.6) in Group\u20103 (n\u00a0=\u00a023) (<jats:italic>p\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.01). In multivariable analyses, <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> before treatment (<jats:italic>p\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.001) and the change in <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> during interruption (<jats:italic>p\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.01) were independent predictors of slower <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> decay.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>These data suggest that <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> initiation within the first week of life can reduce the persistence of long\u2010lived infected cells. Delaying <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> is associated with slower decay of infected cells.<\/jats:p><\/jats:sec>","DOI":"10.1002\/jia2.25368","type":"journal-article","created":{"date-parts":[[2019,8,23]],"date-time":"2019-08-23T07:54:53Z","timestamp":1566546893000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":25,"title":["<scp>HIV<\/scp>\u20101 <scp>DNA<\/scp> decay is faster in children who initiate <scp>ART<\/scp> shortly after birth than later"],"prefix":"10.1002","volume":"22","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6796-1787","authenticated-orcid":false,"given":"Kirsten A","family":"Veldsman","sequence":"first","affiliation":[{"name":"Division of Medical Virology Stellenbosch University Faculty of Medicine and Health Sciences Cape Town South Africa"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anita","family":"Janse van 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