Evidence map›Paper›PMID 34326994›Full record

ArticleJournal of global health2021

Using AMANHI-ACT cohorts for external validation of Iowa new-born metabolic profiles based models for postnatal gestational age estimation.

Sunil Sazawal, Kelli K Ryckman, Harshita Mittal, Rasheda Khanam, Imran Nisar, Elizabeth Jasper, Sayedur Rahman, Usma Mehmood, Sayan Das, Bruce Bedell and 16 more

Abstract read
In one paragraph

Article in Journal of global health, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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.

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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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

26 authors.

Sunil SazawalCenter for Public Health Kinetics, Global Division, New Delhi, India.
Kelli K RyckmanUniversity of Iowa, College of Public Health, Department of Epidemiology, Iowa City, Iowa, USA.
Harshita MittalCenter for Public Health Kinetics, Global Division, New Delhi, India.
Rasheda KhanamDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Imran NisarAga Khan University, Department of Paediatrics and Child Health, Karachi, Sindh, Pakistan.
Elizabeth JasperUniversity of Iowa, College of Public Health, Department of Epidemiology, Iowa City, Iowa, USA.
Sayedur RahmanProjahnmo Research Foundation, Dhaka, Bangladesh.
Usma MehmoodAga Khan University, Department of Paediatrics and Child Health, Karachi, Sindh, Pakistan.
Sayan DasCenter for Public Health Kinetics, Global Division, New Delhi, India.
Bruce BedellUniversity of Iowa, College of Public Health, Department of Epidemiology, Iowa City, Iowa, USA.
Nabidul Haque ChowdhuryProjahnmo Research Foundation, Dhaka, Bangladesh.
Amina BarkatAga Khan University, Department of Paediatrics and Child Health, Karachi, Sindh, Pakistan.
Arup DuttaCenter for Public Health Kinetics, Global Division, New Delhi, India.
Saikat DebCenter for Public Health Kinetics, Global Division, New Delhi, India.
Salahuddin AhmedProjahnmo Research Foundation, Dhaka, Bangladesh.
Farah KhalidAga Khan University, Department of Paediatrics and Child Health, Karachi, Sindh, Pakistan.
Rubhana RaqibInternational Center for Diarrheal Disease Research, Bangladesh, Mohakhali, Dhaka, Bangladesh.
Muhammad IlyasAga Khan University, Department of Paediatrics and Child Health, Karachi, Sindh, Pakistan.
Ambreen NizarAga Khan University, Department of Paediatrics and Child Health, Karachi, Sindh, Pakistan.
Said Mohammed AliPublic Health Laboratory-IDC, Chake Chake, Pemba,Tanzania.
Alexander ManuWorld Health Organization (MCA/MRD), Geneva, Switzerland.
Sachiyo YoshidaWorld Health Organization (MCA/MRD), Geneva, Switzerland.
Abdullah H BaquiDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Fyezah JehanAga Khan University, Department of Paediatrics and Child Health, Karachi, Sindh, Pakistan.
Usha DhingraCenter for Public Health Kinetics, Global Division, New Delhi, India.
Rajiv BahlWorld Health Organization (MCA/MRD), Geneva, Switzerland.

Funding

World Health Organization 001
6 · The paper itself

Abstract

backgroundGlobally, 15 million infants are born preterm and another 23.2 million infants are born small for gestational age (SGA). Determining burden of preterm and SGA births, is essential for effective planning, modification of health policies and targeting interventions for reducing these outcomes for which accurate estimation of gestational age (GA) is crucial. Early pregnancy ultrasound measurements, last menstrual period and post-natal neonatal examinations have proven to be not feasible or inaccurate. Proposed algorithms for GA estimation in western populations, based on routine new-born screening, though promising, lack validation in developing country settings. We evaluated the hypothesis that models developed in USA, also predicted GA in cohorts of South Asia (575) and Sub-Saharan Africa (736) with same precision.

methodsDried heel prick blood spots collected 24-72 hours after birth from 1311 new-borns, were analysed for standard metabolic screen. Regression algorithm based, GA estimates were computed from metabolic data and compared to first trimester ultrasound validated, GA estimates (gold standard).

resultsOverall Algorithm (metabolites + birthweight) estimated GA to within an average deviation of 1.5 weeks. The estimated GA was within the gold standard estimate by 1 and 2 weeks for 70.5% and 90.1% new-borns respectively. Inclusion of birthweight in the metabolites model improved discriminatory ability of this method, and showed promise in identifying preterm births. Receiver operating characteristic (ROC) curve analysis estimated an area under curve of 0.86 (conservative bootstrap 95% confidence interval (CI) = 0.83 to 0.89);

conclusionMetabolic gestational age dating offers a novel means for accurate population-level gestational age estimates in LMIC settings and help preterm birth surveillance initiatives. Further research should focus on use of machine learning and newer analytic methods broader than conventional metabolic screen analytes, enabling incorporation of region-specific analytes and cord blood metabolic profiles models predicting gestational age accurately.

Indexed as

Gestational AgeMetabolomeModels, BiologicalCohort StudiesHumansInfant, NewbornReproducibility of Results

Identifiers

PMID34326994
PMCPMC8285766

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LicenceCC BY
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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.