Evidence map›Paper›PMID 42210125›Full record

ArticleBMC infectious diseases2026

Congenital cytomegalovirus and associations with maternal HIV serostatus and child health outcomes in Uganda.

Julian Adong, Nitin Arora, Elias Kumbakumba, Adeline A Boatin, Anacret Byamukama, Ingrid V Bassett, Stephen Asiimwe, Lynn T Matthews, Suresh Boppana, Joseph Ngonzi and 1 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

11 authors.

Julian AdongDepartment of Paediatrics and Child Health, Mbarara University of Science and Technology, Mbarara, Uganda. jadong@must.ac.ug.ORCID http://orcid.org/0000-0001-9314-5257
Nitin AroraUniversity of Alabama at Birmingham, Heersink School of Medicine, Birmingham, USA.
Elias KumbakumbaDepartment of Paediatrics and Child Health, Mbarara University of Science and Technology, Mbarara, Uganda.
Adeline A BoatinDepartment of Obstetrics and Gynecology, Massachusetts General Hospital, Boston, USA.
Anacret ByamukamaKabwohe Clinical Research Centre, Kabwohe, Uganda.
Ingrid V BassettHarvard Medical School, Boston, MA, USA.
Stephen AsiimweKabwohe Clinical Research Centre, Kabwohe, Uganda.
Lynn T MatthewsUniversity of Alabama at Birmingham, Heersink School of Medicine, Birmingham, USA.
Suresh BoppanaUniversity of Alabama at Birmingham, Heersink School of Medicine, Birmingham, USA.
Joseph Ngonzi *Department of Obstetrics and Gynecology, Mbarara University of Science and Technology, Mbarara, Uganda.
Lisa M Bebell *Harvard Medical School, Boston, MA, USA.

Funding

Mentoring in patient-oriented research on HIV prevention in the US and South AfricaK24AI141036 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Ingrid Valerie Bassett · 2019 to 2026
$1.1M
HIV Infection, Placental Inflammation, and Early Childhood Outcomes in HIV-exposed, Uninfected Infants in UgandaK23AI138856 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI BEBELL, LISA M · 2019 to 2023
$1.1M
Mentoring in patient-oriented research on HIV prevention in the U.S. and Global SouthK24AI184259 · NIAID · YALE UNIVERSITY · PI Lynn T Matthews · 2025 to 2026
$361k
NIAID NIH HHS K23 AI138856NIAID NIH HHS K24 AI141036NIH HHS K23AI138856NIH HHS K24AI141036NIH HHS K24AI184259
6 · The paper itself

Abstract

introductionCytomegalovirus (CMV) is the most common congenital infection globally, and the leading cause of non-genetic hearing loss and neurodevelopmental disability. The burden is highest in low- and middle-income countries where HIV is also highly prevalent. Women living with HIV have a higher prevalence of CMV and are more likely to transmit CMV to their infants. Despite this, congenital CMV (cCMV) and newborn hearing screening are not routinely available in sub-Saharan Africa (sSA) resulting in missed diagnoses and delayed treatment. Additionally, data comparing cCMV prevalence in HIV-exposed and non-exposed infants is limited. We aimed to determine cCMV prevalence among HIV-exposed and -unexposed neonates in Uganda, describe associated clinical characteristics, and assess infant hearing outcomes.

methodsThis study was nested within a prospective cohort of pregnant women with and without HIV, followed with their infants through early childhood. Eligible participants were 18 years or older, pregnant, and planned to deliver at one of two clinics. We tested newborn saliva for CMV using a real-time PCR. Hearing screening was performed using a pre-approved screening algorithm. Maternal and neonatal medical characteristics and diagnoses were abstracted from clinical records.

resultsA total of 793 women and their newborns were enrolled. Mean maternal age was 28 (standard deviation [SD] 6) years, and parity was 3 (SD, 2.0). The mean birth weight was 3.0 (SD, 0.5) kilograms and gestational age was 37 (SD, 2.0) weeks. Overall, 677 out of 793 (84.7%) neonatal saliva samples were tested for cCMV, 23 out of 677 (3.4%) were positive with no difference by maternal HIV status. cCMV was not associated with failed hearing screen. However, lower one-minute Apgar and jaundice were associated with cCMV.

conclusioncCMV prevalence was high in this Ugandan cohort and did not differ by HIV exposure. Hearing outcomes were similar by cCMV status. Future studies should include a comprehensive clinical and audiological assessment for both HIV-exposed and -unexposed neonates, and longitudinal follow-up to detect hearing loss and other cCMV-associated sequelae.

Indexed as

Cytomegalovirus InfectionsHIV InfectionsHIV SeropositivityPregnancy Complications, InfectiousAdolescentAdultCytomegalovirusFemaleHumansInfantInfant, NewbornInfectious Disease Transmission, VerticalMaleNeonatal ScreeningPregnancyPrevalenceCMVHearing screenHIV-exposed infantSub-Saharan Africa

Identifiers

PMID42210125
PMCPMC13411582

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.