# Coagulation parameter-based nomogram for the diagnosis of obstetric antiphospholipid syndrome and its subtypes

**Authors:** Xuan Qi, Feifei Zhang, Xiaomeng Li, Yan Han, Yue Zhang, Huifang Guo

PMC · DOI: 10.1515/biol-2025-1252 · Open Life Sciences · 2026-02-12

## TL;DR

This study creates a new diagnostic tool for obstetric antiphospholipid syndrome using coagulation parameters to improve detection beyond current criteria.

## Contribution

A novel nomogram is developed to diagnose OAPS and its subtypes using clinical and laboratory parameters.

## Key findings

- The nomogram achieved high accuracy with an area under the curve of 0.97 in the training set and 0.99 in the validation set.
- Key risk factors included antinuclear antibody titer, complement C3, anti-β2 glycoprotein I, and thrombin-antithrombin complex levels.
- The nomogram improved diagnostic sensitivity and specificity for both criteria and non-criteria-defined OAPS.

## Abstract

Currently available classification criteria for obstetric antiphospholipid syndrome (OAPS) are often overly strict and may miss a considerable number of patients with so-called “non-criteria-defined OAPS”. We aimed to establish a diagnostic nomogram based on clinical and laboratory parameters to facilitate the diagnostic efficacy for OAPS by incorporating both criteria – and non-criteria – defined OAPS. We retrospectively analyzed the clinical and laboratory data of 45 patients with criteria-defined OAPS, 57 with non-criteria-defined OAPS, and 80 age-matched healthy controls between September 2023 and March 2024. We established a nomogram for OAPS based on the risk factors identified through logistic regression and evaluated its performance using the receiver-operating characteristic curve, calibration curve, and decision curve analysis. Antinuclear antibody titer, as well as levels of complement C3, anti-β2 glycoprotein I, thrombin-antithrombin complex, and Von Willebrand factor were independent risk factors for OAPS (P < 0.05). In the training set, the nomogram established using these variables exhibited an area under the curve of 0.97, a sensitivity of 89 %, and a specificity of 94 %. In the validation set, these values were 0.99, 100 % and 88 %, respectively. The nomogram demonstrated enhanced diagnostic capabilities and facilitated more precise treatment guidance for OAPS.

## Full-text entities

- **Genes:** F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, SERPINC1 (serpin family C member 1) [NCBI Gene 462] {aka AT3, AT3D, ATIII, ATIII-R2, ATIII-T1, ATIII-T2}, BTG3 (BTG anti-proliferation factor 3) [NCBI Gene 10950] {aka ANA, ANA/BTG3, APRO4, TOB5, TOB55, TOFA}, TAT (tyrosine aminotransferase) [NCBI Gene 6898], VWF (von Willebrand factor) [NCBI Gene 7450] {aka F8VWF, VWD}, F5 (coagulation factor V) [NCBI Gene 2153] {aka FVL, PCCF, RPRGL1, THPH2, fV}, PROC (protein C, inactivator of coagulation factors Va and VIIIa) [NCBI Gene 5624] {aka APC, PC, PROC1, THPH3, THPH4}, C3 (complement C3) [NCBI Gene 718] {aka AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1}
- **Diseases:** chromosomal or genetic abnormalities (MESH:D025063), developmental delay (MESH:D002658), fetal death (MESH:D005313), heart disease (MESH:D006331), premature delivery (MESH:C536271), thromboembolic (MESH:D013923), miscarriage (MESH:D000022), stillbirth (MESH:D050497), uterine malformations (MESH:D014591), APS (MESH:D016736), deep vein thrombosis (MESH:D020246), ischemic stroke (MESH:D002544), eclampsia (MESH:D004461), immune abnormalities (MESH:D007154), abortions (MESH:D000026), preterm birth (MESH:D047928), antinuclear antibody (MESH:D007153), hypertension (MESH:D006973), hematologic disorders (MESH:D006402), Thrombosis (MESH:D013927), placental insufficiency (MESH:D010927), lupus anticoagulant (MESH:C531622), placental abruption (MESH:D000037), systemic lupus erythematosus (MESH:D008180), fetal loss (MESH:D005315), hypercoagulable (MESH:D019851), Von Willebrand (MESH:D014842), autoimmune (MESH:D001327), obstetric (MESH:D048949), chronic kidney disease (MESH:D051436), preeclampsia (MESH:D011225), malignancy (MESH:D009369), diabetes mellitus (MESH:D003920), endometriosis (MESH:D004715), fetal growth restriction (MESH:D005317), platelet aggregation (MESH:D001791), liver disease (MESH:D008107), thrombo-inflammation (MESH:D007249), trauma (MESH:D014947)
- **Chemicals:** GPI (MESH:D017261), 25-hydroxyvitamin D (MESH:C104450), silica (MESH:D012822), abeta2 (-), phospholipid (MESH:D010743)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12917551/full.md

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Source: https://tomesphere.com/paper/PMC12917551