ArticleHaematologica2014
Distinct frequencies and mutation spectrums of genetic thrombophilia in Korea in comparison with other Asian countries both in patients with thromboembolism and in the general population.
Article in Haematologica, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.
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31 citing papers in PubMed, 54 citations in OpenAlex.
- Protein S Levels to Guide Exon-Level Copy Number Variant Analysis ofAnnals of laboratory medicine · 2026Article
- Association of the PROC rs146922325 variant with venous thrombosis in a Taiwanese population.Blood research · 2026Article
- A pedigree analysis of deep venous thrombosis caused by rare compound heterozygous PROC mutations combined with a heterozygous THBD mutation.Thrombosis journal · 2025Article
- Unraveling the Molecular Pathogenesis of Protein C Deficiency-Associated VTE: Insights from Protein C Mutations C238G and R189W in Thai Patients.Thrombosis and haemostasis · 2025Article
- Compound heterozygous congenital protein C deficiency: a challenging management with recurrent purpura fulminans treated with protein C concentrations.BMJ case reports · 2025Article
- Identification of two point mutations associated with inherited antithrombin deficiency.Thrombosis journal · 2024Article
- The risk profiles of pregnancy-related cerebral venous thrombosis: a retrospective study in a comprehensive hospital.BMC neurology · 2024Article
- Article
- Congenital thrombophilia in East-Asian venous thromboembolism population: a systematic review and meta-analysis.Research and practice in thrombosis and haemostasis · 2023Article
- Surgical treatment of traction retinal detachment associated with compound heterozygous congenital protein C deficiency.American journal of ophthalmology case reports · 2023Article
- Analysis of phenotype and gene mutation in three pedigrees with inherited antithrombin deficiency.Journal of clinical laboratory analysis · 2022Article
- Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing.Diagnostics (Basel, Switzerland) · 2022Article
- Utility of theFrontiers in neurology · 2022Article
- Severe protein C deficiency in a newborn caused by a homozygous pathogenic variant in the PROC gene: a case report.BMC pediatrics · 2021Article
- A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1.Thrombosis journal · 2021Article
- Heritable Thrombophilia in Venous Thromboembolism in Northern Pakistan: A Cross-Sectional Study.Advances in hematology · 2021Article
- Protein S Deficiency and the Risk of Venous Thromboembolism in the Han Chinese Population.Frontiers in cardiovascular medicine · 2021Article
- Association ofFrontiers in genetics · 2019Article
- Protein S deficiency in patients from the French Basque Country with various thrombotic conditions: a rarer inherited trait in autochthonous individuals?Journal of thrombosis and thrombolysis · 2018Article
- Distinctive regional-specific PROS1 mutation spectrum in Southern China.Journal of thrombosis and thrombolysis · 2018Article
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10 authors at 2 institutions in 2 countries.
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No grant is acknowledged in the PubMed record.
Abstract
Hereditary natural anticoagulant deficiencies are the major cause of genetic thrombophilia in Asia. Given the growing acknowledgment of the risk of venous thromboembolism in Asian populations, we investigated the frequency and mutation spectrums of natural anticoagulant deficiency in Korea. The group of patients consisted of consecutive patients with venous thromboembolism screened for thrombophilia. Genetic tests were performed on suspicion of natural anticoagulant deficiency. For the population group, >3,000 individuals were screened from routine check-ups, and those with a low level (<1(st) percentile) of natural anticoagulant underwent genetic tests. Mutations were detected by direct sequencing of PROC, PROS1, and SERPINC1, followed by additional multiplex ligation-dependent probe amplification for PROS1 and SERPINC1 for dosage mutations. Among 500 patients screened, 127 were suspected of having a natural anticoagulant deficiency, and this was genetically confirmed in 71: protein C deficiency in 36 (50.7%), antithrombin deficiency in 21 (29.6%), and protein S deficiency in 14 (19.7%). Among 3,129 individuals from the population who were screened, the frequency of natural anticoagulant deficiency was ~1.0%: antithrombin deficiency 0.49%, protein C deficiency 0.35%, and protein S deficiency 0.16%. Two PROC mutations causing type I protein C deficiency were prevalent (Arg211Trp and Met406Ile in patients and Arg211Trp in the population). Two SERPINC1 mutations causing type II antithrombin deficiency, Arg79Cys and Ser158Pro, were prevalent in the population group. This is the first study on the genetic epidemiology of natural anticoagulant deficiencies in Korea. The results demonstrated that the frequencies and spectrum of mutations underlying genetic thrombophilia in Korea are different not only from those in Caucasians but also those in other Asian populations.
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