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Introduction: Key populations, including female sex workers (FSW), people who inject drugs (PWID), and people in serodiscordant partnerships, experience higher HIV incidence compared to the general population. Maternal HIV retesting, particularly during late pregnancy, helps detect new infections and prevent vertical HIV transmission, but optimal testing schedules among key populations are unknown.
Methods: We used a Markov model to estimate the health and economic impacts of maternal HIV retesting on vertical HIV transmission outcomes among FSW and PWID in Kenya, South Africa, and pre-war Ukraine as well as among pregnant people in serodiscordant partnerships in Kenya and South Africa. We calculated incremental cost-effectiveness ratios (ICERs) for seven maternal retesting scenarios that included HIV testing during early antenatal care (ANC) and retesting from late ANC through nine months postpartum.
Results: Retesting during late ANC was estimated to avert 16% (Kenya), 14% (South Africa), and 8% (Ukraine) of infant HIV infections among key populations. Retesting during late ANC was cost-saving or cost-effective among all populations included in our model in South Africa and Kenya. In Ukraine, HIV retesting during late ANC was cost-saving for PWID but not cost-effective for FSW. Postpartum retesting was not cost-effective in any population.
Conclusions: Maternal HIV retesting during late ANC is cost-saving or cost-effective for vertical HIV transmission outcomes for pregnant key populations and serodiscordant couples in Kenya and South Africa and is cost-saving for PWID in Ukraine.
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http://dx.doi.org/10.1101/2025.04.08.25325413 | DOI Listing |
J Glob Antimicrob Resist
September 2025
Department of Medical Microbiology & Infectious Diseases, Erasmus University Medical Centre Rotterdam (Erasmus MC), Rotterdam, the Netherlands.
J Crohns Colitis
September 2025
Division of Gastroenterology and Hepatology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Background & Aims: Pregnancy can be a complex and risk-filled event for women with inflammatory bowel disease (IBD). High-quality studies in this population are lacking, with limited data on medications approved to treat IBD during pregnancy. For patients, limited knowledge surrounding pregnancy impacts pregnancy rates, medication adherence, and outcomes.
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September 2025
College of Horticulture, Bioinformatics Center, Academy for Advanced Interdisciplinary Studies, Nanjing Agricultural University, Nanjing 210095, China. Electronic address:
Molecular phylogenetics illustrates the evolution and divergence of green plants by employing sequence data from various sources. Interestingly, phylogenetic reconstruction based on mitochondrial genes tends to exhibit incongruence with those derived from nuclear and chloroplast genes. Although the uniparental inheritance and conservatively retained protein-coding genes of mitochondrial genomes inherently exclude certain potential factors that affect phylogenetic reconstruction, such as hybridization and gene loss, the utilization of mitochondrial genomes for phylogeny and divergence time estimation remains limited.
View Article and Find Full Text PDFMol Psychiatry
September 2025
Department of Child and Adolescent Psychiatry and Psychology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.
Epigenetic processes, such as DNA methylation, show potential as biological markers and mechanisms underlying gene-environment interplay in the prediction of mental health and other brain-based phenotypes. However, little is known about how peripheral epigenetic patterns relate to individual differences in the brain itself. An increasingly popular approach to address this is by combining epigenetic and neuroimaging data; yet, research in this area is almost entirely comprised of cross-sectional studies in adults.
View Article and Find Full Text PDFBlood Rev
August 2025
Department of Medicine, Stellenbosch University, Faculty of Medicine and Health Sciences, Tygerberg Campus, South Africa. Electronic address:
Clinicians need a good understanding of available tools to diagnose iron deficiency (ID). Interpretation of commonly used laboratory tests can be challenging due to the dynamic nature of iron homeostasis and concurrent inflammation, which influence results. The misinterpretation of iron studies, inconsistencies in ID diagnostic guidelines, and low awareness of non-anaemic ID may lead to missed diagnoses and opportunities for treatment.
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