Evidence map›Paper›PMID 41204157›Full record

ArticleBMC pregnancy and childbirth2025

Mediating role of preterm birth in the relationship between maternal disease and infant development.

Shan Tan, Yiduo Wang, Changshi Tang, Shizhou Li, Jiang Mei

Abstract read
In one paragraph

Article in BMC pregnancy and childbirth, 2025. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Shan TanDepartment of Pediatrics, The Third Xiangya Hospital, Central South University, Changsha, China.
Yiduo WangThe Nick Davey Laboratory, Division of Surgery, Department of Surgery and Cancer, Faculty of Medicine, Sir Michael Uren Hub, Imperial College London, White City Campus, 86 Wood Lane, London, W12 0BZ, UK.
Changshi TangChancellor's Building, University of Edinburgh, Edinburgh, EH16 4SB, UK.
Shizhou LiThe VOC Laboratory, Division of Surgery, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, Commonwealth Building, Hammersmith Campus, London, W12 0NN, UK. shizhou.li22@imperial.ac.uk.
Jiang MeiNursing Department, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China. 2090187550@qq.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPreterm birth is a major adverse perinatal outcome and may act as a mediator linking maternal disease to impaired infant growth and neurodevelopment. However, the mediating role of preterm birth has not been well explored in relation to maternal diseases. This study aimed to investigate whether preterm birth mediates the association between maternal diseases and infant outcomes including Body Mass Index, the Neonatal Behavioral Neurological Assessment, and the Gesell Development Schedule.

methodsThis study recruited a total of 2000 mother-child pairs from the Pediatric Healthcare Centre at the Third Xiangya Hospital. Maternal diseases, including gestational diabetes mellitus, pregnancy-induced hypertension, anaemia, hypothyroidism, hyperthyroidism, and thrombocytopenia, were assessed through hospital records and parental questionnaires verified against medical records. Infant outcomes were evaluated by trained pediatric nurses blinded to maternal conditions, using anthropometric measurements (Body Mass Index) and standardized neurodevelopmental tools (Neonatal Behavioral Neurological Assessment and Gesell Development Schedule). Mediation analysis with 1,000-sample bootstrapping was applied to quantify the indirect effects of preterm birth.

resultsPreterm birth significantly mediated the association between Pregnancy-Induced Hypertension and Neonatal Behavioral Neurological Assessment (Indirect effect = -0.653, 95% CI: -0.98 - -0.36, p < 0.001). Preterm birth also significantly mediated the relationship between Gestational Diabetes Mellitus and Body Mass Index (Indirect effect = - 0.046, 95% CI: -0.08 - -0.01, p = 0.01).

conclusionsPreterm birth may act as a mediator between maternal diseases and infant growth and neurodevelopmental outcomes. The results support the feasibility and value of using mediation analysis in maternal-infant research. Findings highlight the importance of early prenatal screening, prevention, and management of preterm birth in pregnancies complicated by maternal disease. Future research is warranted to employ longitudinal neurodevelopmental monitoring in affected infants.

Indexed as

Child DevelopmentPregnancy ComplicationsPremature BirthAdultBody Mass IndexDiabetes, GestationalFemaleHumansHypertension, Pregnancy-InducedInfantInfant, NewbornMalePregnancyYoung AdultBody mass indexGestational diabetes mellitusMediation analysisNeurodevelopmental impairmentPregnancy-Induced hypertensionPreterm birth

Identifiers

PMID41204157
PMCPMC12595764

What Socratic holds

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LicenceCC BY
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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 Socratic graph.