Journals / Sakarya University Journal of Science / 2016 / Cilt: 20 Sayı: 1

Detection of the relationship between thrombophilia disease with genetic disorders by adaptive neuro-fuzzy inference system (ANFIS)

Trombofili hastalığı ile genetik bozukluklar arasındaki ilişkinin adaptif ağ tabanlı bulanık mantık çıkarım sistemi (ANFIS) ile tespit edilmesi

Pages
13–21
Publication Date
2016-04-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Simulation results showed that the results from using ANFIS were more successful than those obtained from considered classification algorithms.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Thrombosis is a condition involving the clotting of bloods in the veins or in an organ, whereas thrombophilia is a term used to describe a predisposition for thrombosis.
📊
Key Findings & Data:In diseases causing major health problems that are related to thrombosis, people may even lose their lives in many cases.
💡
Conclusion & Impact:Simulation results showed that the results from using ANFIS were more successful than those obtained from considered classification algorithms.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:ANFIS · bulanık mantık · Trombofili

Abstract

Thrombosis is a condition involving the clotting of bloods in the veins or in an organ, whereas thrombophilia is a term used to describe a predisposition for thrombosis. In diseases causing major health problems that are related to thrombosis, people may even lose their lives in many cases. Thrombosis is multifactorial, it is known to cause a number of acquired and hereditary factors which lead to thrombosis formation through various mechanisms. Therefore, many difficulties are experienced in the diagnosis of thrombophilia. In this context, traditional statistical methods are often inadequate for the evaluation of clinical and laboratory data. In this study, in order to determine the relationship between genetic disorders and thrombophilic disease, the Adaptive Neuro-Fuzzy Inference System (ANFIS) is used and our results are compared to the results of some of the commonly-used classification algorithms. Simulation results showed that the results from using ANFIS were more successful than those obtained from considered classification algorithms.

Özet

Kanın damar içinde ya da bir organda pıhtılaşması olan Tromboz’a yol açan hastalıklarda önemli sağlık sorunları ortaya çıkmakta ve hatta birçok vakada insanlar hayatını kaybedebilmektedir. Tromboz gelişimi multifaktoriyel olup,çok sayıda edinsel ve kalıtsal faktörün değişik mekanizmalarla tromboz oluşumuna neden olduğu bilinmekte ise de tromboza yatkınlık olarak bilinen Trombofili tanısının konmasında önemli zorluklar yaşanmaktadır. Bu kapsamda,geleneksel sınıflandırma yöntemlerinin klinik, laboratuvar ve genetik tetkiklere ait verilerin değerlendirilmesindeki başarımları ise çoğunlukla sınırlı kalabilmektedir. Bu çalışmada, Trombofili hastalığı ile genetik bozukluklar arasındaki ilişkinin tespit edilebilmesi için Adaptif Ağ Tabanlı Bulanık Mantık Çıkarım Sistemi (ANFIS) kullanılmış ve elde edilen sonuçlar literatürde yaygın olarak kullanılan bazı sınıflandırma algoritmalarına ait sonuçlarla karşılaştırılmıştır. Elde edilen sonuçlardan, ANFIS ile elde edilen sonuçların daha başarılı olduğu görülmüştür.

🔖

Cite This Article

Haznedar, B., Kalınlı, A. (2016). Detection of the relationship between thrombophilia disease with genetic disorders by adaptive neuro-fuzzy inference system (ANFIS). Sakarya University Journal of Science, Cilt: 20 Sayı: 1, 13–21. https://ajindex.com/articles/942397

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (16)

  1. Küçükkaya, R., Aydın, M., “Trombofili Genetiği”, Türk Hematoloji Derneği - Moleküler Hematoloji, Klinik Hematoloji için Pratik Genetik Yaklaşım Kursu, Antalya, 39-43, 11 Kasım 2006.
  2. De Stefano, V., Finazzi, G., Mannucci, M., “Inherited thrombophilia: Pathogenesis, clinical syndromes and management”. Blood, Cilt 87, No 9, 3531-3544, 1996.
  3. Lane, D.A., Manucci, P.M., Bauer, K.A., ”Inherited thrombophilia: Part-1.”, Thromb Haemost, Cilt 76, 1996.
  4. Dahlback, B., Carlsson, M., Svensson, P.J., “Familial thrombophilia due to a previously unrecognised mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C.”, Proc Natl Acad Sci USA, Cilt 90, 1004-1008, 1993.
  5. Bertina, R.M., Koeleman, B.P.C., Koster, T., Rosendaal, F.R., Dirven, R.J., de Ronde, H., van der Velden, P.A., Reitsma, P.H., “Mutation in blood coagulation factor V associated with resistance to activated protein C.”, Nature, Cilt 369, 64, 1994.
  6. Falcon, C.R., Cattaneo, M., Panzeri, D., Martinelli, I., Manucci, P.M., “High prevalanve of hyperhomocyst(e)inemia in patients with juvenile venous thrombosis”, Arterioscler Thromb, Cilt 14, 1080, 1994.
  7. Poort, S.R., Rosendaal, F.R., Reitsma, P.H., Bertina, R.M., “A common genetic variation in the 3’-untranslated region of the protrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis”, Blood, Cilt 88, 3698, 1996.
  8. Makris, M., Rosendaal, F.R., Preston, F.E., “Familial thrombophilia: Genetic risk factors and management”, J Int Med, Cilt 242, 9, 1997.
  9. Kolodziej, M., Comp, P.C., “Hypercoagulable states due to natural anticoagulant deficiencies”, Curr Op Hematol, Cilt 301, 1993.
  10. Rodgers, G.M., “Thrombosis and antithrombotic therapy. In: Wintrobe’s Clinical Hematology,10th Edition”, Williams and Wilkins Comp, 1781-1818, 1998.
  11. Bauer, K.A., “The Hypercagulable state. In: Williams Hematology 5th edition”, McGraw Hill inc, 1531-1549, 1995.
  12. Lane, D.A., Manucci, P.M., Bauer, K.A., “Inherited thrombophilia: Part-2.”, Thromb Haemost, Cilt 76, 824, 1996.
  13. Bick, R.L., Kaplan, H., “Syndromes of thrombosis and hypercoagulability”, Med Clin North Am., Cilt 82, 409, 1998.
  14. Hultin, M.B., “Antithrombin III assays. In: Williams Hematology 5th edition”, McGraw Hill inc., 101, 1995.
  15. Comp, P.C., “Protein C and protein S. In: Williams Hematology 5th edition”, McGraw Hill inc., 99, 1995.
  16. Welch, G.N., Loscalzo, J., “Homocysteine and atherothrombosis”, N Engl J Med, Cilt 338, 1042, 19