Araştırma Makalesi

Pregnancy outcomes in patients with MTHFR gene polymorphism: A case series

Cilt: 4 Sayı: 7 1 Temmuz 2020
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Pregnancy outcomes in patients with MTHFR gene polymorphism: A case series

Abstract

Aim: Based on the literature, MTHFR polymorphism is common among the general population and is controversial in terms of treatment, as it is poorly associated with pregnancy complications. In this study, we aimed to investigate the relationship between treatment and pregnancy outcomes in patients with MTHFR polymorphism.
Methods: The data of 48 patients who were diagnosed with MTHFR C677T and A1298C polymorphism between June 2012 and April 2020 and followed up during their pregnancy were reviewed retrospectively. Demographic and clinical features of patients, pregnancy history, diagnosis, and perinatal complications were examined. Pre- and post-treatment clinical features of the patients were compared.
Results: Comparison of pre- and post-treatment pregnancy data of the patients revealed that live birth rates were significantly higher (pre-treatment: 9.4% post-treatment: 68.7%, P=0.001) and abortion rates were significantly lower after treatment (pre-treatment: 81.2%, post-treatment: 32.1%, P=0.001). Pregnancy complications were observed in 9 (18.3%) patients. It was observed that among patients with MTHFR gene mutation, live birth rates increased by 24.12-fold and by 3.76-fold for each year of decrease in the age of conception following treatment.
Conclusion: In pregnant women with MTHFR polymorphism, methionine-poor diet and medical treatment had a positive effect on pregnancy outcomes. It was also observed that among those with MTHFR gene polymorphism, young patients with MTHFR A1298C heterozygotes had the best treatment results.

Keywords

Destekleyen Kurum

yok

Proje Numarası

Alaaddin Keykubat University Ethics Committee of Clinical Research (Date: 05/06/2020-No. 19-23).

Kaynakça

  1. 1. Ueland PM, Hustad S, Schneede J, Refsum H, Vollset SE. Biological and clinical implications of the MTHFR C677T polymorphism. Trends in Pharmacological Sciences. 2001;22(4):195-201. doi: 10.1016/s0165-6147(00)01675-8.
  2. 2. Weisberg I, Tran P, Christensen B, Sibani S, Rozen R. A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Molecular genetics and metabolism. 1998;64(3):169-72.
  3. 3. Rozen R. Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR). Thrombosis and haemostasis. 1997;78(01):523-6.
  4. 4. Klerk M, Verhoef P, Clarke R, Blom HJ, Kok FJ, Schouten EG. MTHFR 677C→ T polymorphism and risk of coronary heart disease: a meta-analysis. JAMA. 2002;288(16):2023-31. doi: 10.1001/jama.288.16.2023.
  5. 5. Grandone E, Margaglione M, Colaizzo D, Cappucci G, Paladini D, Martinelli P, et al. Factor V Leiden, C> T MTHFR polymorphism and genetic susceptibility to preeclampsia. Thrombosis and Haemostasis. 1997;77(06):1052-4.
  6. 6. Blount BC, Mack MM, Wehr CM, MacGregor JT, Hiatt RA, Wang G, et al. Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. Proceedings of the National Academy of Sciences. 1997;94(7):3290-5.
  7. 7. Amin S, Issa H, Ramzy A. Prevalence/Incidence of Hereditary and Acquired Thrombophilia Markers among Egyptian Females with Recurrent Pregnancy Loss or IVF Failure. J Blood Disord Transfus. 2018;10(412):2.
  8. 8. Zappacosta B, Mastroiacovo P, Persichilli S, Pounis G, Ruggeri S, Minucci A, et al. Homocysteine lowering by folate-rich diet or pharmacological supplementations in subjects with moderate hyperhomocysteinemia. Nutrients. 2013;5(5):1531-43. doi: 10.3390/nu5051531.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Kadın Hastalıkları ve Doğum

Bölüm

Araştırma Makalesi

Yayımlanma Tarihi

1 Temmuz 2020

Gönderilme Tarihi

11 Temmuz 2020

Kabul Tarihi

3 Ağustos 2020

Yayımlandığı Sayı

Yıl 2020 Cilt: 4 Sayı: 7

Kaynak Göster

APA
Deniz, A. (2020). Pregnancy outcomes in patients with MTHFR gene polymorphism: A case series. Journal of Surgery and Medicine, 4(7), 536-539. https://doi.org/10.28982/josam.768231
AMA
1.Deniz A. Pregnancy outcomes in patients with MTHFR gene polymorphism: A case series. J Surg Med. 2020;4(7):536-539. doi:10.28982/josam.768231
Chicago
Deniz, Alparslan. 2020. “Pregnancy outcomes in patients with MTHFR gene polymorphism: A case series”. Journal of Surgery and Medicine 4 (7): 536-39. https://doi.org/10.28982/josam.768231.
EndNote
Deniz A (01 Temmuz 2020) Pregnancy outcomes in patients with MTHFR gene polymorphism: A case series. Journal of Surgery and Medicine 4 7 536–539.
IEEE
[1]A. Deniz, “Pregnancy outcomes in patients with MTHFR gene polymorphism: A case series”, J Surg Med, c. 4, sy 7, ss. 536–539, Tem. 2020, doi: 10.28982/josam.768231.
ISNAD
Deniz, Alparslan. “Pregnancy outcomes in patients with MTHFR gene polymorphism: A case series”. Journal of Surgery and Medicine 4/7 (01 Temmuz 2020): 536-539. https://doi.org/10.28982/josam.768231.
JAMA
1.Deniz A. Pregnancy outcomes in patients with MTHFR gene polymorphism: A case series. J Surg Med. 2020;4:536–539.
MLA
Deniz, Alparslan. “Pregnancy outcomes in patients with MTHFR gene polymorphism: A case series”. Journal of Surgery and Medicine, c. 4, sy 7, Temmuz 2020, ss. 536-9, doi:10.28982/josam.768231.
Vancouver
1.Alparslan Deniz. Pregnancy outcomes in patients with MTHFR gene polymorphism: A case series. J Surg Med. 01 Temmuz 2020;4(7):536-9. doi:10.28982/josam.768231