Evidence map›Paper›PMID 40063133›Full record

Observational studyClinical and experimental medicine2025

Antiphospholipid syndrome in patients with fetal death: a prospective longitudinal cohort study.

Anxia Xie, Ziwei Jin, Changping Li, Chengxiong Li, Gang Luo, Xuecheng Zhang, Shengyan Jian, Deqin Li, Youbang Xie, Ling Xie and 1 more

Abstract readObservational Study
In one paragraph

Observational study in Clinical and experimental medicine, 2025. 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. Review
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

11 authors.

Anxia Xie *Research Center for High Altitude Medicine, Qinghai University, No.251, Ningda Road, Chengbei District, Xining, 810016, People's Republic of China.
Ziwei Jin *Department of Obstetrics, Qinghai Red Cross Hospital, Xining, 810000, People's Republic of China.
Changping Li *Medical College, Qinghai University, No.251, Ningda Road, Chengbei District, Xining, 810016, People's Republic of China.
Chengxiong LiMedical Laboratory Center, Qinghai Provincial People's Hospital, Xining, 810007, People's Republic of China.
Gang LuoCenter for Artificial Intelligence Driven Drug Discovery, Faculty of Applied Sciences, Macao Polytechnic University, Macau SR, Macao.
Xuecheng ZhangDepartment of Pathology, Qinghai Provincial People's Hospital, Xining, 810007, People's Republic of China.
Shengyan JianCentre for Reproductive Medicine, Qinghai Provincial People's Hospital, Xining, 810007, People's Republic of China.
Deqin LiMedical Laboratory Center, Qinghai Provincial People's Hospital, Xining, 810007, People's Republic of China.
Youbang XieDepartment of Hematology and Rheumatology, Qinghai Provincial People's Hospital, Xining, 810007, People's Republic of China.
Ling XieDepartment of Obstetrics, Qinghai Red Cross Hospital, Xining, 810000, People's Republic of China.
Xiaoxing WeiResearch Center for High Altitude Medicine, Qinghai University, No.251, Ningda Road, Chengbei District, Xining, 810016, People's Republic of China. weixiaoxing@qhu.edu.cn.ORCID http://orcid.org/0000-0002-8861-9769

Funding

the Natural Science Foundation of Qinghai Province 2024-ZJ-923
6 · The paper itself

Abstract

To investigate the causes of fetal death, focusing on maternal antiphospholipid syndrome diagnosis, and to follow the patients for changes in antiphospholipid antibodies, subsequent pregnancy outcomes, and thrombotic events. This is a prospective longitudinal cohort study that recruited patients who were hospitalized for fetal death at ≥ 10 weeks of gestation from three tertiary hospitals in China. Antiphospholipid syndrome was diagnosed according to the 2006 Sydney classification criteria. In total, 159 patients were recruited to the study; 3 were excluded and 144 of whom tested for aPLs. Among these, 126 (87.5%) were available for diagnostic analysis of antiphospholipid syndrome, 13 (10.3%) of which carried a diagnosis of antiphospholipid syndrome. Meanwhile, 136 of 156 patients had fetal samples for which copy number variation sequencing was completed, and 12 (8.8%) of which carried a diagnosis of fetal chromosomal abnormalities. During later follow-up, among the 13 patients with antiphospholipid syndrome, seven were persistently positive serostatus of antiphospholipid antibodies, four exhibited fluctuation, and one had negative conversion; four patients with subsequent pregnancies received guideline-based therapy and had term livebirths. None of the participants experienced thrombotic events. Maternal antiphospholipid syndrome was found to be one of the important causes of fetal death, contributing 10.3% of cases of fetal death at ≥ 10 weeks of gestation, slight ahead of fetal chromosomal abnormalities. Follow-up indicated that the serostatus of antiphospholipid antibodies may fluctuate significantly in some patients with antiphospholipid syndrome.Clinical trial registration:As this study was an observational study, we did not register it as a clinical trial.

Indexed as

Antiphospholipid SyndromeFetal DeathPregnancy ComplicationsAdultAntibodies, AntiphospholipidChinaFemaleHumansLongitudinal StudiesPregnancyPregnancy OutcomeProspective StudiesYoung AdultAntibodies, AntiphospholipidAntiphospholipid antibodyCauseChromosomal abnormalityClassification criterionFetal deathSubsequent pregnancy

Identifiers

PMID40063133
PMCPMC11893624

What OpenQuestion holds

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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.