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February 19, 2026Open Life Sciences0 citationsOpen Access

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

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XQXuan QiHebei Medical UniversityFZFeifei ZhangHebei Medical UniversityXLXiaomeng LiHebei Medical University

Key Points

  • To develop a diagnostic nomogram for obstetric antiphospholipid syndrome, including both criteria- and non-criteria-defined cases.
  • Retrospective analysis of clinical and laboratory data from 182 subjects, including both OAPS types and healthy controls.
  • Use of logistic regression to identify significant risk factors for OAPS.
  • Development of a nomogram based on identified risk factors and validation using standard performance metrics.
  • Nomogram achieved an AUC of 0.97 in the training set and 0.99 in the validation set.
  • Sensitivity and specificity reached 89% and 94% in the training set; 100% and 88% in the validation set respectively.
  • Identified independent risk factors: antinuclear antibody titer, complement C3, anti-β2 glycoprotein I, thrombin-antithrombin complex, and Von Willebrand factor.

Abstract

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.

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Cite This Study

Qi et al. (2026) studied this question.

synapsesocial.com/papers/6996a7a5ecb39a600b3ed8bahttps://doi.org/10.1515/biol-2025-1252
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