{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,21]],"date-time":"2026-09-21T22:52:54Z","timestamp":1790031174076,"version":"4.0.1"},"reference-count":28,"publisher":"Wiley","issue":"S1","license":[{"start":{"date-parts":[[2015,2,25]],"date-time":"2015-02-25T00:00:00Z","timestamp":1424822400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/100000060","name":"National Institute of Allergy and Infectious Diseases","doi-asserted-by":"crossref","award":["UM1-AI068641"],"award-info":[{"award-number":["UM1-AI068641"]}],"id":[{"id":"10.13039\/100000060","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100000098","name":"NIH Clinical Center","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100000098","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100000054","name":"National Cancer Institute","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100000054","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100000050","name":"National Heart, Lung, and Blood Institute","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100000050","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100000025","name":"National Institute of Mental Health","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100000025","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100000065","name":"National Institute of Neurological Disorders and Stroke","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100000065","id-type":"DOI","asserted-by":"crossref"}]},{"name":"National Institute of Arthritis and Musculoskeletal Disorders"},{"name":"French Agence Nationale de Recherches sur le SIDA et les H\u00e9patites Virales (ANRS)"},{"name":"German Ministry of Education and Research"},{"name":"European AIDS Treatment Network (NEAT)"},{"name":"Australian National Health and Medical Research Council"},{"DOI":"10.13039\/501100000265","name":"UK Medical Research Council","doi-asserted-by":"crossref","id":[{"id":"10.13039\/501100000265","id-type":"DOI","asserted-by":"crossref"}]},{"name":"National Institute for Heath Research"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["HIV Medicine"],"published-print":{"date-parts":[[2015,4]]},"abstract":"<jats:sec><jats:title>Objectives<\/jats:title><jats:p>A small subset of <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u2010positive adults have low <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content> in the absence of therapy, sometimes for years. Clinical factors associated with low <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content> in early infection have not been well defined.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>We assessed factors associated with low plasma <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content> level at study entry in the <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>trategic <jats:styled-content style=\"fixed-case\">T<\/jats:styled-content>iming of <jats:styled-content style=\"fixed-case\">AntiRetroviral T<\/jats:styled-content>reatment (<jats:styled-content style=\"fixed-case\">START<\/jats:styled-content>) trial. All <jats:styled-content style=\"fixed-case\">START<\/jats:styled-content> participants had a baseline <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content> assessment within 60 days prior to randomization. The key covariables considered for this analysis were race, and hepatitis <jats:styled-content style=\"fixed-case\">B<\/jats:styled-content> virus (<jats:styled-content style=\"fixed-case\">HBV<\/jats:styled-content>) and hepatitis <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content> virus (<jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content>) status. We assessed factors associated with <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content> \u2264\u200950 and \u2264\u2009400 <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content> copies\/mL using logistic regression. Because of the strong association between region of randomization and baseline low <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content>, analyses were stratified by region.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>We found that, of 4676 eligible participants randomized in <jats:styled-content style=\"fixed-case\">START<\/jats:styled-content> with a baseline <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content> assessment, 113 (2.4%) had <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content> \u2264\u200950\u2009copies\/mL at baseline, and a further 257 (5.5%) between 51 and 400\u2009copies\/mL. We found that <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content> exposure routes other than male homosexual contact, higher high\u2010density lipoprotein (<jats:styled-content style=\"fixed-case\">HDL<\/jats:styled-content>) cholesterol levels, higher <jats:styled-content style=\"fixed-case\">CD4<\/jats:styled-content> cell counts, and higher <jats:styled-content style=\"fixed-case\">CD4<\/jats:styled-content>:<jats:styled-content style=\"fixed-case\">CD8<\/jats:styled-content> ratio were associated with increased odds of low <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content>. <jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content> antibody positivity was borderline statistically significantly associated with low <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content>. Race and <jats:styled-content style=\"fixed-case\">HBV<\/jats:styled-content> surface antigen positivity were not significantly associated with low <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>In a modern cohort of individuals with early untreated <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content> infection, we found that <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content> exposure routes other than male homosexual contact and higher <jats:styled-content style=\"fixed-case\">HDL<\/jats:styled-content> cholesterol were associated with increased odds of low <jats:styled-content style=\"fixed-case\">HIV RNA<\/jats:styled-content>.<\/jats:p><\/jats:sec>","DOI":"10.1111\/hiv.12232","type":"journal-article","created":{"date-parts":[[2015,2,25]],"date-time":"2015-02-25T09:55:37Z","timestamp":1424858137000},"page":"37-45","source":"Crossref","is-referenced-by-count":11,"title":["Clinical and demographic factors associated with low viral load in early untreated <scp>HIV<\/scp> infection in the <scp>INSIGHT S<\/scp>trategic <scp>T<\/scp>iming of <scp>AntiRetroviral T<\/scp>reatment (<scp>START<\/scp>) trial"],"prefix":"10.1111","volume":"16","author":[{"given":"MG","family":"Law","sequence":"first","affiliation":[{"name":"The Kirby Institute University of New South Wales  Sydney Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A","family":"Achhra","sequence":"additional","affiliation":[{"name":"The Kirby Institute University of New South Wales  Sydney 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