The effect of coagulation factors polymorphisms on abortion
Received date: 19 Apr 2018
Accepted date: 21 May 2018
Published date: 31 Jul 2018
Copyright
OBJECTIVE: Recent studies showed coagulation factors play important role in controlling pregnancy duration in addition to controlling homeostasis. Recent studies showed several polymorphisms of coagulation factors genes increase the clot formation and lead to abortion. In this study, we evaluated the polymorphisms of coagulation factors and their effects on the development of the fetus.
MATERIAL and METHODS: Relevant literature was identified by a PubMed search (1988-2017) of English language papers using the terms Abortion, pregnancy woman, coagulation factor and polymorphism.
RESULT: Several polymorphisms of coagulation factors disturb the exchange of food and other materials between the fetus and the mother, and impairs the formation of the placenta during embryonic stages.
DISCUSSION: Evaluation of functional polymorphisms in coagulation factors gene during fetal development can be used as a prognostic factor in the prevention of the abortion.
Key words: polymorphism; thrombosis; abortion; prognosis
Narjes Feizollahi , Zeinab Deris Zayeri , Najme Moradi , Mahvash Zargar , Hadi Rezaeeyan . The effect of coagulation factors polymorphisms on abortion[J]. Frontiers in Biology, 2018 , 13(3) : 190 -196 . DOI: 10.1007/s11515-018-1500-8
1 |
Aarabi M, Memariani T, Arefi S, Aarabi M, Hantoosh Zadeh S, Akhondi M A, Modarressi M H (2011). Polymorphisms of plasminogen activator inhibitor-1, angiotensin converting enzyme and coagulation factor XIII genes in patients with recurrent spontaneous abortion. J Matern Fetal Neonatal Med, 24(3): 545–548
|
2 |
Abbate R, Sofi F, Gensini F, Fatini C, Sticchi E, Fedi S (2002). Thrombophilias as risk factors for disorders of pregnancy and fetal damage. Pathophysiol Haemost Thromb, 32(5-6): 318–321
|
3 |
Al-Azzawie H F, Sabri S (2014). C677T and A1298C polymorphisms of Methylenetetrahydrofolate Reductase Gene in Iraqi Patients with Recurrent Abortion. Int J, 2(6): 227–234
|
4 |
Aleman M M, Byrnes J R, Wang J G, Tran R, Lam W A, Di Paola J, Mackman N, Degen J L, Flick M J, Wolberg A S (2014). Factor XIII activity mediates red blood cell retention in venous thrombi. J Clin Invest, 124(8): 3590–3600
|
5 |
Anokhin B A, Stribinskis V, Dean W L, Maurer M C (2017). Activation of factor XIII is accompanied by a change in oligomerization state. FEBS J, 284(22): 3849–3861
|
6 |
Antza C, Cifkova R, Kotsis V (2017). Hypertensive complications of pregnancy: A clinical overview. Metabolism: S0026-0495(17)30323-2
|
7 |
Avila-Vergara M, Felipe de Jesús Peraza-Garay, Noemí Meraz-Cruz, Cesar Hernandez-Guerrero, Berenice Palacios-Gonzalez, Felipe Vadillo-Ortega (2018). Association of Intron-2 Variable Numbers of an 86-bp Tandem Repeat-Polymorphisms of Interleukin-1 Receptor Antagonist Gene and Idiopathic Recurrent Spontaneous Abortion. Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion, 70(2): 96–102
|
8 |
Badenhop R F, Wang X L, Wilcken D E (1995). Angiotensin-converting enzyme genotype in children and coronary events in their grandparents. Circulation, 91(6): 1655–1658
|
9 |
Bailey L B, Gregory J F 3rd (1999). Polymorphisms of methylenetetrahydrofolate reductase and other enzymes: metabolic significance, risks and impact on folate requirement. J Nutr, 129(5): 919–922
|
10 |
Barlik M, Seremak-Mrozikiewicz A, Drews K, Klejewski A, Kurzawińska G, Łowicki Z, Wolski H (2016). Correlation between factor VII and PAI-1 genetic variants and recurrent miscarriage. Ginekol Pol, 87(7): 504–509
|
11 |
Ben-Ami I, Fuchs N, Schneider D, Pansky M, Halperin R, the BEN‐AMI (2012). Coagulopathy associated with dilation and evacuation for second-trimester abortion. Acta Obstet Gynecol Scand, 91(1): 10–15
|
12 |
Buchholz T, Lohse P, Rogenhofer N, Kosian E, Pihusch R, Thaler C J (2003). Polymorphisms in the ACE and PAI-1 genes are associated with recurrent spontaneous miscarriages. Hum Reprod, 18(11): 2473–2477
|
13 |
Cardenas J C, Matijevic N, Baer L A, Holcomb J B, Cotton B A, Wade C E (2014). Elevated tissue plasminogen activator and reduced plasminogen activator inhibitor promote hyperfibrinolysis in trauma patients. Shock, 41(6): 514–521
|
14 |
Castoldi E, Simioni P, Kalafatis M, Lunghi B, Tormene D, Girelli D, Girolami A, Bernardi F (2000). Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family. Blood, 96(4): 1443–1448
|
15 |
Chen Z, Xu F, Wei Y, Liu F, Qi H (2012). Angiotensin converting enzyme insertion/deletion polymorphism and risk of pregnancy hypertensive disorders: a meta-analysis. J Renin Angiotensin Aldosterone Syst, 13(1): 184–195
|
16 |
Chodirker B N, Dawson A J (2011). Recurrent miscarriage. N Engl J Med, 364(8): 783–784
|
17 |
Coolman M, de Groot C J M, Steegers E A P, Geurts-Moespot A, Thomas C M G, Steegers-Theunissen R P M, Sweep F C G J (2006). Concentrations of plasminogen activators and their inhibitors in blood preconceptionally, during and after pregnancy. Eur J Obstet Gynecol Reprod Biol, 128(1-2): 22–28
|
18 |
D’Elia P Q, dos Santos A A, Bianco B, Barbosa C P, Christofolini D M, Aoki T (2014). MTHFR polymorphisms C677T and A1298C and associations with IVF outcomes in Brazilian women. Reprod Biomed Online, 28(6): 733–738
|
19 |
Djurovic J, Stojkovic O, Todorovic J, Brajic A, Stankovic S, Obradovic S, Stamenkovic G (2017). Genetics of suspected thrombophilia in Serbian females with infertility, including three cases, homozygous for FII 20210A or FV 1691A mutations. Hum Fertil (Camb), 20(2): 132–139
|
20 |
Dorgalaleh A, Rashidpanah J (2016). Blood coagulation factor XIII and factor XIII deficiency. Blood Rev, 30(6): 461–475
|
21 |
Egerup P, Kolte A M, Larsen E C, Krog M, Nielsen H S, Christiansen O B (2016). Recurrent pregnancy loss: what is the impact of consecutive versus non-consecutive losses? Hum Reprod, 31(11): 2428–2434
|
22 |
ElDanasori N, Abulata N, Shaheen I A, ElGendy A M, El-Khayat W (2017). Thrombin-Activatable Fibrinolysis Inhibitor Gene Polymorphism (TAFI1040C/T) in Women With Recurrent Spontaneous Abortion. Clin Appl Thromb Hemost, 24 (3): 532-535
|
23 |
Elkin A C, Higham J (2000). Folic acid supplements are more effective than increased dietary folate intake in elevating serum folate levels. BJOG, 107(2): 285–289
|
24 |
Festa A, D’Agostino R Jr, Rich S S, Jenny N S, Tracy R P, Haffner S M (2003). Promoter (4G/5G) plasminogen activator inhibitor-1 genotype and plasminogen activator inhibitor-1 levels in blacks, Hispanics, and non-Hispanic whites: the Insulin Resistance Atherosclerosis Study. Circulation, 107(19): 2422–2427
|
25 |
Ford J G, Li Y, O’Sullivan M M, Demopoulos R, Garte S, Taioli E, Brandt-Rauf P W (2000). Glutathione S-transferase M1 polymorphism and lung cancer risk in African-Americans. Carcinogenesis, 21(11): 1971–1975
|
26 |
Franssen M T, Nico J Leschot, Patrick M M Bossuyt, Alida C Knegt, Klasien B J Gerssen-Schoorl, Cokkie H Wouters, Kerstin B M Hansson, Ron Hochstenbach, Kamlesh Madan, Fulco van der Veen, Mariette Goddijn (2005). Selective chromosome analysis in couples with two or more miscarriages: case-control study. BMJ, 331(7509): 137–141
|
27 |
Garlantézec R, Chevrier C, Coiffec I, Celebi C, Cordier S (2012). Combined effect of prenatal solvent exposure and GSTT1 or GSTM1 polymorphisms in the risk of birth defects. Birth Defects Res A Clin Mol Teratol, 94(6): 481–485
|
28 |
Glueck C J, Wang P, Goldenberg N, Sieve L (2004). Pregnancy loss, polycystic ovary syndrome, thrombophilia, hypofibrinolysis, enoxaparin, metformin. Clin Appl Thromb Hemost, 10(4): 323–334
|
29 |
Guerra-Shinohara E M, Bertinato J F, Tosin Bueno C, Cordeiro da Silva K, Burlacchini de Carvalho M H, Pulcineli Vieira Francisco R, Zugaib M, Cerda A, Morelli V M (2012). Polymorphisms in antithrombin and in tissue factor pathway inhibitor genes are associated with recurrent pregnancy loss. Thromb Haemost, 108(4): 693–700
|
30 |
Hayashi Y, Sasaki H, Suzuki S, Nishiyama T, Kitaori T, Mizutani E, Suzumori N, Sugiura-Ogasawara M (2013). Genotyping analyses for polymorphisms of ANXA5 gene in patients with recurrent pregnancy loss. Fertil Steril, 100(4): 1018–1024
|
31 |
James A H (2009). Venous thromboembolism in pregnancy. Arterioscler Thromb Vasc Biol, 29(3): 326–331
|
32 |
Jeddi-Tehrani M, Torabi R, Mohammadzadeh A, Arefi S, Keramatipour M, Zeraati H, Zarnani A H, Akhondi M M, Mahmoudian J, Mahmoudi A R, Zarei S (2010). Investigating association of three polymorphisms of coagulation factor XIII and recurrent pregnancy loss. Am J Reprod Immunol, 64(3): 212–217
|
33 |
Kamimoto Y, Wada H, Ikejiri M, Nakatani K, Sugiyama T, Osato K, Murabayashi N, Habe K, Mizutani H, Matsumoto T, Ohishi K, Ikeda T (2017). Hypofibrinogenemia and the a-Fibrinogen Thr312Ala polymorphism may be risk factors for early pregnancy loss. Clin Appl Thromb Hemost, 23(1): 52–57
|
34 |
Karatas A, Eroz R, Albayrak M, Ozlu T, Cakmak B, Keskin F (2014). Evaluation of chromosomal abnormalities and common trombophilic mutations in cases with recurrent miscarriage. Afr Health Sci, 14(1): 216–222
|
35 |
Karimlo F K, Mashayekhi F, Sorouri Z Z, Bahador M H, Salehi Z (2015). Association of GSTM1 and GSTT1 gene polymorphisms and in-vitro fertilisation outcome in a population in northern Iran. J Obstet Gynaecol, 35(1): 46–48
|
36 |
Kim S Y, Park S Y, Choi J W, Kim D J, Lee S Y, Lim J H, Han J Y, Ryu H M, Kim M H (2011). Association between MTHFR 1298A>C polymorphism and spontaneous abortion with fetal chromosomal aneuploidy. Am J Reprod Immunol, 66(4): 252–258
|
37 |
Kohler H P (2001). Role of blood coagulation factor XIII in vascular diseases. Swiss Med Wkly, 131(3-4): 31–34
|
38 |
Kotze M J, La Grange C, Mansvelt E (2005). Genetics in family practice: rapid thrombophilia genetic test facilitates improved prenatal care for mother and child. S Afr Fam Pract, 47(7): 50–51
|
39 |
Kuhli C, Lüchtenberg M, Scharrer I, Hattenbach L O (2005). Massive subhyaloidal hemorrhage associated with severe PAI-1 deficiency. Graefes Arch Clin Exp Ophthalmol, 243(10): 963–966
|
40 |
Kupferminc M J (2003). Thrombophilia and pregnancy. Reprod Biol Endocrinol, 1(1): 111
|
41 |
Kurzawińska G, Seremak-Mrozikiewicz A, Drews K, Barlik M, Mrozikiewicz P M (2009). (Genetic conditioned changes in activity of 5,10-methylenetetrahydrofolate reductase (MTHFR) and recurrent miscarriages). Ginekol Pol, 80(10): 762–767
|
42 |
López-Jiménez J, Porras-Dorantes Á, Juárez-Vázquez C I, García-Ortiz J E, Fuentes-Chávez C A, Lara-Navarro I J, Jaloma-Cruz A R (2016). Molecular thrombophilic profile in Mexican patients with idiopathic recurrent pregnancy loss. Genet Mol Res, 15(4)
|
43 |
Luo Y, Wang C, Tu H (2014). Impact of the 4G/5G polymorphism in the plasminogen activator inhibitor-1 gene on primary nephrotic syndrome. Mol Med Rep, 9(3): 894–898
|
44 |
Lyall F, Bulmer J N, Duffie E, Cousins F, Theriault A, Robson S C (2001). Human trophoblast invasion and spiral artery transformation: the role of PECAM-1 in normal pregnancy, preeclampsia, and fetal growth restriction. Am J Pathol, 158(5): 1713–1721
|
45 |
MacCallum P, Bowles L, Keeling D (2014). Diagnosis and management of heritable thrombophilias. BMJ, 349(7967): g4387
|
46 |
Masini S, Ticconi C, Gravina P, Tomassini M, Pietropolli A, Forte V, Federici G, Piccione E, Bernardini S (2009). Thrombin-activatable fibrinolysis inhibitor polymorphisms and recurrent pregnancy loss. Fertil Steril, 92(2): 694–702
|
47 |
Matsumoto T, Nogami K, Shima M (2013). Simultaneous measurement of thrombin and plasmin generation to assess the interplay between coagulation and fibrinolysis. Thromb Haemost, 110(4): 761–768
|
48 |
Medicine P C A S R, and the Practice Committee of American Society for Reproductive Medicine (2013). Definitions of infertility and recurrent pregnancy loss: a committee opinion. Fertil Steril, 99(1): 63
|
49 |
Middeldorp S (2007). Pregnancy failure and heritable thrombophilia. in Seminars in hematology. Elsevier
|
50 |
Mowla K, Rajaei E, Jalali M T, Zayeri Z D (2018). Threatening biomarkers in lupus pregnancy: Biochemistry and genetic challenges. Front Biol: 13 (1) : 1–8
|
51 |
Mtiraoui N, Borgi L, Gris J C, Almawi W Y, Mahjoub T (2004). Factor V Leiden, prothrombin G20210A and antibodies against phospholipids in recurrent spontaneous abortion. J Thromb Haemost, 2(8): 1482–1484
|
52 |
Mtiraoui N, Borgi L, Hizem S, Nsiri B, Finan R R, Gris J C, Almawi W Y, Mahjoub T (2005). Prevalence of antiphospholipid antibodies, factor V G1691A (Leiden) and prothrombin G20210A mutations in early and late recurrent pregnancy loss. Eur J Obstet Gynecol Reprod Biol, 119(2): 164–170
|
53 |
Muszbek L, Katona É ( 2016). Diagnosis and management of congenital and acquired FXIII deficiencies. in Seminars in thrombosis and hemostasis. Thieme Medical Publishers
|
54 |
Naderi M, Dorgalaleh A, Tabibian Sh, Alizadeh Sh, Eshghi P, Solaimani G (2013). Current understanding in diagnosis and management of factor XIII deficiency. Iran J Ped Hematol Oncol, 3(4): 164–172
|
55 |
Pereza N, Ostojić S, Kapović M, Peterlin B (2017). Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion. Fertil Steril, 107(1): 150–159
|
56 |
Pickering W, Marriott K, Regan L (2001). G20210A prothrombin gene mutation: prevalence in a recurrent miscarriage population. Clin Appl Thromb Hemost, 7(1): 25–28
|
57 |
Prat M, Morales-Indiano C, Jimenez C, Mas V, Besses C, Checa M A, Carreras R (2014). “20209C-T” a variant mutation of prothrombin gene mutation in a patient with recurrent pregnancy loss. Ann Clin Lab Sci, 44(3): 334–336
|
58 |
Qublan H S, Eid S S, Ababneh H A, Amarin Z O, Smadi A Z, Al-Khafaji F F, Khader Y S (2006). Acquired and inherited thrombophilia: implication in recurrent IVF and embryo transfer failure. Hum Reprod, 21(10): 2694–2698
|
59 |
Rezaeeyan H, Jaseb K, Alghasi A, Asnafi A A, Saki N (2017). Association between gene polymorphisms and clinical features in idiopathic thrombocytopenic purpura patients. Blood Coagul Fibrinolysis, 28(8): 617–622
|
60 |
Rijken D C, Lijnen H R (2009). New insights into the molecular mechanisms of the fibrinolytic system. J Thromb Haemost, 7(1): 4–13
|
61 |
Sata F, Yamada H, Kondo T, Gong Y, Tozaki S, Kobashi G, Kato EH, Fujimoto S, Kishi R (2003). Glutathione S‐transferase M1 and T1 polymorphisms and the risk of recurrent pregnancy loss. MHR: Basic science of reproductive medicine, 9(3): 165–169
|
62 |
Shi Q, Hu M, Luo M, Liu Q, Jiang F, Zhang Y, Wang S, Yan C, Weng Y (2011). Reduced expression of Mad2 and Bub1 proteins is associated with spontaneous miscarriages. Mol Hum Reprod, 17(1): 14–21
|
63 |
Simcox L E, Ormesher L, Tower C, Greer I A (2015). Thrombophilia and pregnancy complications. Int J Mol Sci, 16(12): 28418–28428
|
64 |
Su M T, Lin S H, Chen Y C, Kuo P L (2013). Genetic association studies of ACE and PAI-1 genes in women with recurrent pregnancy loss: a systematic review and meta-analysis. Thromb Haemost, 109(1): 8–15
|
65 |
Tulandi, T. and Al-FozanH., Definition and etiology of recurrent pregnancy loss. Up To Date Last updated, 2011. 16.
|
66 |
Tusskorn O, Khunluck T, Prawan A, Senggunprai L, Kukongviriyapan U, Kukongviriyapan V (2018). Suppression of glutathione S-transferases potentiates the cytotoxic effect of phenethyl isothiocyanate in cholangiocarcinoma cells. Naunyn Schmiedebergs Arch Pharmacol, 391(6): 657–667
|
67 |
Van der Put, N., van der Molen E F, Kluijtmans L A, Heil S G, Trijbels J M, Eskes T K, Van Oppenraaij-Emmerzaal D, Banerjee R, Blom H J (1997). Sequence analysis of the coding region of human methionine synthase: relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease. QJM, 90(8): 511–517
|
68 |
Vívenes-de Lugo M, Alvaro R L, Belsy G, Dinorah C D G (2008). Ethnic/geographic variation of the val34leu polymorphism of coagulation factor XIII and its distribution in American admixed populations. Internet J Biol Anthropol, 2: 1
|
69 |
Vora S, Shetty S, Khare M, Ghosh K (2009). Placental histomorphology in unexplained foetal loss with thrombophilia. Indian J Med Res, 129(2): 144–149
|
70 |
Walton B L, Byrnes J R, Wolberg A S (2015). Fibrinogen, red blood cells, and factor XIII in venous thrombosis. J Thromb Haemost, 13(Suppl 1): S208–S215
|
71 |
Wang H Y, Qiao J, Sun X X, Wang S Y, Liang X Y, Sun Y, Liu F H (2017). Epidemiological Survey and Risk Factor Analysis of Recurrent Spontaneous Miscarriages in Infertile Women at Large Infertility Centers. Chin Med J (Engl), 130(17): 2056–2062
|
72 |
Wolski H, Barlik M, Drews K, Klejewski A, Kurzawińska G, Ożarowski M, Łowicki Z, Seremak-Mrozikiewicz A (2017). Contribution of inherited thrombophilia to recurrent miscarriage in the Polish population. Ginekol Pol, 88(7): 385–392
|
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