Evidence map›Paper›PMID 40113921›Full record

ArticleScientific reports2025

Comparative analysis of perinatal outcomes in pregnant women with pregestational diabetes mellitus based on diagnostic timing.

Xinyu Shu, Juan Juan, Xin Kang, Mi Yao, Xu Chen, Zhuo Wei, Lingyi Kong, Haitian Chen, Shihong Cui, Fengchun Gao and 7 more

Abstract readMulticenter StudyComparative Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 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

17 authors.

Xinyu Shu *Department of Obstetrics and Gynecology and Reproductive Medicine, Peking University First Hospital, Beijing, China.
Juan Juan *Department of Obstetrics and Gynecology and Reproductive Medicine, Peking University First Hospital, Beijing, China.
Xin KangDepartment of Obstetrics and Gynecology and Reproductive Medicine, Peking University First Hospital, Beijing, China.
Mi YaoDepartment of General Practice, Peking University First Hospital, Beijing, China.
Xu ChenTianjin Key Laboratory of Human Development and Reproductive Regulation, Tianjin Central Hospital of Obstetrics and Gynecology, Tianjin, China.
Zhuo WeiTianjin Key Laboratory of Human Development and Reproductive Regulation, Tianjin Central Hospital of Obstetrics and Gynecology, Tianjin, China.
Lingyi KongDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong Province, China.
Haitian ChenDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong Province, China.
Shihong CuiDepartment of Obstetrics and Gynecology, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.
Fengchun GaoDepartment of Obstetrics, Jinan Maternity and Child Care Hospital, Shandong First Medical University, Jinan, Shandong Province, China.
Ping ZhuDepartment of Obstetrics, Jinan Maternity and Child Care Hospital, Shandong First Medical University, Jinan, Shandong Province, China.
Jianying YanDepartment of Obstetrics and Gynecology, Fujian Provincial Maternity and Child Health Hospital, Fuzhou, Fujian, China.
Xia XuDepartment of Obstetrics and Gynecology, Fujian Provincial Maternity and Child Health Hospital, Fuzhou, Fujian, China.
Li ZhangDepartment of Obstetrics, Nanjing Women and Children's Healthcare Hospital, Nanjing, Jiangsu, China.
Yanxia WangDepartment of Obstetrics, Northwest Women and Children's Hospital, Xian, Shanxi Province, China.
Yang MiDepartment of Obstetrics, Northwest Women and Children's Hospital, Xian, Shanxi Province, China.
Huixia YangDepartment of Obstetrics and Gynecology and Reproductive Medicine, Peking University First Hospital, Beijing, China. yhxktz2018@163.com.

Funding

National High Level Hospital Clinical Research Funding 22cz020401-4811009 and 24cz020204-4803048National Key Research and Development Program of China 2021YFC2700700Youth Program of the National Natural Science Foundation of China 82003528
6 · The paper itself

Abstract

Diabetes is a major concern in healthcare worldwide and is detrimental to mothers and fetuses during pregnancy. However, half of the women were unaware of hyperglycemia before pregnancy, and there is no consensus on their identification during pregnancy. We aim to understand the role that diagnostic timing plays in perinatal outcomes. This was a multicenter retrospective study of all pregestational diabetes mellitus (PGDM) women who delivered from January 2021 to June 2023. Diagnoses were made before or during gestation. Characteristics and outcomes were compared among stages, and logistic regression was performed to explore the relationship between adverse outcomes and the diagnostic timing. This study included 2,818 women; 1188 (42.2%) were self-aware before pregnancy, and 286 (10.1%), 1208 (42.9%), and 136 (4.8%) were diagnosed in the first, second, and third trimesters, respectively. Maternal body mass index, hypertensive disorders during pregnancy, glucose profile, large-for-gestational-age (LGA), etc., differed among stages (all P < 0.05). Logistic regression revealed that PGDM diagnosed during any trimester was significantly associated with an increased risk of macrosomia (aOR = 2.632, 1.502, 2.314; all P < 0.05). However, the risk of LGA decreased if the diagnosis was based on the 2 h value of the oral glucose tolerance test (OGTT) alone in the second trimester (aOR = 0.608, 95% CI: 0.444-0.831). No relationship existed between diagnostic timing and neonatal birth defects or hypoglycemia (both P > 0.05). PGDM identified during pregnancy was significantly associated with an increased risk of fetal overgrowth. The role of the 2 h-OGTT alone in diagnosis warrants further exploration. PGDM screening is essential for the entire gestational period.

Indexed as

Diabetes, GestationalPregnancy in DiabeticsAdultFemaleFetal MacrosomiaHumansInfant, NewbornPregnancyPregnancy OutcomeRetrospective StudiesDiagnostic timingFetal overgrowthLarge for gestational ageMacrosomiaOral glucose tolerance testPregestational diabetes mellitus

Identifiers

PMID40113921
PMCPMC11926075

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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.