Evidence map›Paper›PMID 39913512›Full record

ArticleThe Indian journal of medical research2024

Recent HCMV infection in early pregnancy associates with congenital transmission & adverse pregnancy outcome: A prospective cohort study.

Harsha Chandrashekhar Palav, Varsha Sakharam Padwal, Shilpa Milind Velhal, Sapna Yadav, Gauri Sanjay Bhonde, Varsha Kalsurkar, Sachee Agrawal, Reena Set, Jayanthi Shastri, Forum Shah and 4 more

Abstract read
In one paragraph

Article in The Indian journal of medical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Harsha Chandrashekhar PalavDepartment of Viral Immunopathogenesis Lab, ICMR - National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, India.
Varsha Sakharam PadwalDepartment of Viral Immunopathogenesis Lab, ICMR - National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, India.
Shilpa Milind VelhalDepartment of Viral Immunopathogenesis Lab, ICMR - National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, India.
Sapna YadavDepartment of Viral Immunopathogenesis Lab, ICMR - National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, India.
Gauri Sanjay BhondeDepartment of Molecular Immunology and Microbiology, ICMR - National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, India.
Varsha KalsurkarDepartment of Viral Immunopathogenesis Lab, ICMR - National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, India.
Sachee AgrawalDepartment of Microbiology, T.N. Medical College & B.Y.L. Nair Hospital, Mumbai, Maharashtra, India.
Reena SetDepartment of Microbiology, T.N. Medical College & B.Y.L. Nair Hospital, Mumbai, Maharashtra, India.
Jayanthi ShastriDepartment of Microbiology, T.N. Medical College & B.Y.L. Nair Hospital, Mumbai, Maharashtra, India.
Forum ShahNowrosjee Wadia Maternity Hospital, Mumbai, Maharashtra, India.
Ira ShahBai Jerbai Wadia Hospital for Children, Mumbai, Maharashtra, India.
Purnima SatoskarNowrosjee Wadia Maternity Hospital, Mumbai, Maharashtra, India.
Vainav PatelDepartment of Viral Immunopathogenesis Lab, ICMR - National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, India.
Vikrant Madhukar BhorDepartment of Molecular Immunology and Microbiology, ICMR - National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & objectives Human Cytomegalovirus (HCMV) infection, leading to >90 per cent seropositivity in women of reproductive age from India, is the largest cause of congenital infections worldwide. HCMV infection status was prospectively monitored together with congenital transmission (cCMV) and adverse pregnancy outcomes (APO) in a public health setting where maternal or neonatal screening was not in practice. Methods Eighty three pregnant women, with (n=45) and without (n=38) bad obstetric history (BOH), were monitored for HCMV infection by ELISA-(IgM, IgG, IgG avidity) for all TORCH (Toxoplasma, Rubella, HCMV, HSV 1 & 2) pathogens along with HCMV-specific chemiluminescent microparticle immunoassay (CMIA) and nested polymerase chain reaction (PCR). Descriptive statistics were applied on data sets to determine associations between maternal infection status, pregnancy outcome and cCMV in 52 mother-neonate dyads. Results Combined avidity, PCR-based and HCMV IgM screening, compared to the latter alone, was successful in identifying incident infection during early pregnancy. Pregnancy loss was associated strongly with BOH and concurrent HCMV infection. Features associated with APO and cCMV, were high PCR positivity (first trimester) and high rates of HCMV-specific IgM and intermediate IgG avidity (P=0.0211, 0.0455). Also, recent HCMV infection (intermediate IgG avidity), observed mainly in the BOH group, but not recurrent infection (IgM positivity), in first and second trimesters, was associated with neonatal saliva positivity and adverse outcomes, including neonatal death (P=0.0762). Exposure to other TORCH pathogens, while detected, did not include IgM positivity or low/intermediate IgG. Conclusion This study highlights the significance of conducting early, multi-pronged screening for maternal HCMV infection during pregnancy, especially in public health settings with high HCMV seroprevalence.

Indexed as

CytomegalovirusCytomegalovirus InfectionsInfectious Disease Transmission, VerticalPregnancy Complications, InfectiousAdultAntibodies, ViralFemaleHumansImmunoglobulin GImmunoglobulin MIndiaInfant, NewbornPregnancyPregnancy OutcomeProspective StudiesToxoplasmaAntibodies, ViralImmunoglobulin GImmunoglobulin MAdverse pregnancy outcomeaviditybad obstetric historycongenital transmissionHCMVnested PCRprospectiveTORCH

Identifiers

PMID39913512
PMCPMC11801775

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

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.