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The covariates identified as determinants of death in the primary analyses were entered into the model.
Because these data were missing due to systematic causes, and thus missing not at random (MNAR) [45], no methods for imputation of missing data at the visit level were applied in the primary analyses.
Individuals with a mild grade renal insufficiency were considered eligible for the interview but were not included in the primary analyses.
To assess the associations of seropositioning and serosorting with HIV seroconversion, we used the same adaptation of the Cox model previously employed in the primary analyses of this outcome in EXPLORE[11].
Finally, the relationships among DRD4 VNTR genotype, sex, age, sexual behavior, smoking behavior, and impulsivity (DRD) were examined to determine the specificity of the associations in the primary analyses.
Sex is also controlled for in the primary analyses.
We used logistic regression models in the primary analyses.
Results 200 participants were included in the primary analyses.
Randomised controlled trials (RCTs) were included in the primary analyses.
In the primary analyses, none of the associations attained genome-wide significance.
In the primary analyses, we interpreted inconclusive responses as negative ones.
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