Evidence map›Paper›PMID 34935918›Full record

ArticleJAMA network open2021

Association of Maternal Inflammation During Pregnancy With Birth Outcomes and Infant Growth Among Women With or Without HIV in India.

Mehr Shafiq, Jyoti S Mathad, Shilpa Naik, Mallika Alexander, Su Yadana, Mariana Araújo-Pereira, Vandana Kulkarni, Prasad Deshpande, Nathella Pavan Kumar, Subash Babu and 7 more

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.6field-weighted citation impact, top 6% of its field
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

33 citing papers in PubMed, 40 citations in OpenAlex.

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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

17 authors at 7 institutions in 3 countries.

Mehr ShafiqDepartment of Epidemiology, Columbia University Mailman School of Public Health, New York, New York.
Jyoti S MathadDepartment of Medicine, Weill Cornell Medical College, New York, New York.
Shilpa NaikDepartment of Obstetrics and Gynecology, Byramjee Jeejeebhoy Government Medical College, Pune, India.
Mallika AlexanderByramjee Jeejeebhoy Government Medical College-Johns Hopkins University Clinical Research Site, Pune, India.
Su YadanaDepartment of Epidemiology, Columbia University Mailman School of Public Health, New York, New York.
Mariana Araújo-PereiraInstituto Goncalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Vandana KulkarniByramjee Jeejeebhoy Government Medical College-Johns Hopkins University Clinical Research Site, Pune, India.
Prasad DeshpandeByramjee Jeejeebhoy Government Medical College-Johns Hopkins University Clinical Research Site, Pune, India.
Nathella Pavan KumarNational Institutes of Health, National Institute for Research in Tuberculosis, International Center for Excellence in Research, Chennai, India.
Subash BabuNational Institutes of Health, National Institute for Research in Tuberculosis, International Center for Excellence in Research, Chennai, India.
Bruno B AndradeInstituto Goncalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Cheng-Shiun LeuDepartment of Biostatistics, Columbia University Mailman School of Public Health, New York.
Saltanat KhwajaByramjee Jeejeebhoy Government Medical College-Johns Hopkins University Clinical Research Site, Pune, India.
Ramesh BhosaleDepartment of Obstetrics and Gynecology, Byramjee Jeejeebhoy Government Medical College, Pune, India.
Aarti KinikarDepartment of Paediatrics, Byramjee Jeejeebhoy Government Medical College, Pune, India.
Amita GuptaDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Rupak ShivakotiDepartment of Epidemiology, Columbia University Mailman School of Public Health, New York, New York.
Columbia University · USGovernment Medical College · INGovernment Medical College · INJohns Hopkins University · USCornell University · USFaculdade de Tecnologia e Ciências · BRUniversidade Federal da Bahia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: The association of elevated levels of specific inflammatory markers during pregnancy with adverse birth outcomes and infant growth could indicate pathways for potential interventions. Objective: To evaluate whether higher levels of certain inflammatory markers during pregnancy are associated with preterm birth (PTB), low birth weight (LBW), and infant growth deficits. Design, Setting, and Participants: In this cohort study of pregnant women with or without HIV, 218 mother-infant pairs were followed up from pregnancy through 12 months post partum from June 27, 2016, to December 9, 2019. Pregnant women aged 18 to 40 years and between 13 and 34 weeks of gestation who were receiving antenatal care were enrolled in a cohort stratified by HIV status; sampling was based on convenience sampling from women receiving antenatal care at Byramjee Jeejeebhoy Government Medical College. Exposures: Levels of multiple circulating inflammation markers during the third trimester of pregnancy. Main Outcomes and Measures: The primary study outcome was PTB (<37 weeks' gestation). Secondary outcomes were LBW (<2500 g) and repeated measures (delivery; 6 weeks post partum; and 3, 6, and 12 months post partum using multivariable generalized linear models) of infant growth outcomes (length-for-age, weight-for-age, and weight-for-length z scores). Results: The median age of the 218 women at enrollment was 23 years (IQR, 21-27 years). In multivariable models, higher pregnancy levels of interleukin 17A were associated with increased odds of both PTB (adjusted odds ratio [aOR], 2.62; 95% CI, 1.11-6.17) and LBW (aOR, 1.81; 95% CI, 1.04-3.15). Higher levels of interleukin 1β were associated with increased PTB (aOR, 1.47; 95% CI, 1.15-1.89) and infant growth deficits (lower length-for-age z score: adjusted β = -0.10; 95% CI, -0.18 to -0.01; lower weight-for-age z score: adjusted β = -0.07; 95% CI, -0.14 to 0.001). Conclusions and Relevance: This study suggests that increased levels of certain systemic inflammatory markers, including interleukin 1β and interleukin 17A, during pregnancy were associated with adverse birth outcomes and infant growth deficits. Future studies should evaluate whether potential interventions to modulate specific inflammatory pathways during pregnancy could improve birth outcomes and infant growth.

Indexed as

Child DevelopmentPregnancy OutcomeAdultBiomarkersFemaleHIV InfectionsHumansIndiaInfantInfant, Low Birth WeightInfant, NewbornInflammationPregnancyPregnancy Complications, InfectiousPremature BirthRisk FactorsBiomarkers

Identifiers

PMID34935918
PMCPMC8696571
OpenAlexW4200213347

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.