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Sexual role and HIV-1 set point viral load among men who have sex with men
[Display omitted] •Set-point viral load is higher in insertive than receptive men who have sex with men.•This difference is limited to men presumed to be infected in longer relationships.•This pattern is predicted by mathematical models and confirmed in empirical analysis. HIV-1 set point viral load...
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Published in: | Epidemics 2019-03, Vol.26, p.68-76 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Set-point viral load is higher in insertive than receptive men who have sex with men.•This difference is limited to men presumed to be infected in longer relationships.•This pattern is predicted by mathematical models and confirmed in empirical analysis.
HIV-1 set point viral load (SPVL) is a highly variable trait that influences disease progression and transmission risk. Men who are exclusively insertive (EI) during anal intercourse require more sexual contacts to become infected than exclusively receptive (ER) men. Thus, we hypothesize that EIs are more likely to acquire their viruses from highly infectious partners (i.e., with high SPVLs) and to have higher SPVLs than infected ERs.
We used a one-generation Bernoulli model, a dynamic network model, and data from the Multicenter AIDS Cohort Study (MACS) to examine whether and under what circumstances MSM differ in SPVL by sexual role.
Both models predicted higher SPVLs in EIs than role versatile (RV) or ER men, but only in scenarios where longer-term relationships predominated. ER and RV men displayed similar SPVLs. EI men remained far less likely than ER men to become infected, however. When the MACS data were limited by some estimates of lower sex partner counts (a proxy for longer relationships), EI men had higher SPVLs; these differences were clinically relevant (>0.3 log10 copies/mL) and statistically significant (p |
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ISSN: | 1755-4365 1878-0067 |
DOI: | 10.1016/j.epidem.2018.08.006 |