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Association between mitochondrial DNA D-loop region polymorphisms and endometriosis in a Chinese population

  • Genetics
  • Published:
Journal of Assisted Reproduction and Genetics Aims and scope Submit manuscript

Abstract

Objective

To investigate the correlation between endometriosis and mitochondrial DNA (mtDNA) D-loop single nucleotide polymorphisms (SNPs) and haplotype, as well as the predictive power of certain SNPs in reproductive outcomes in a Chinese Han population.

Methods

A case-control study was conducted in which 125 endometriosis patients and 124 controls were recruited from an academic fertility center. The entire 1124-bp D-loop region of mtDNA of whole blood samples from all subjects was amplified, sequenced, and compared with the revised Cambridge Reference Sequence (rCRS) to identify SNPs and haplotypes. The association between D-loop SNPs and embryo quality and clinical outcome following in vitro fertilization (IVF) was also assessed.

Results

A total of 321 polymorphisms were identified by sequencing, allowing comparison of the D-loop between endometriosis patients and controls. The frequency of the AC523–524 del, T16172C, and C16290T variants were significantly higher, while the frequency of polymorphisms T195C, 573XCins, 16036Gins, 16049Gins, T16140C, A16183C, T16189C, and 16193Cins were lower, in the endometriosis group compared with the control group (p < 0.05). Within the endometriosis group, the high-quality blastocyst rate in the 16,290T subgroup was significantly lower than that in the 16290C subgroup (p < 0.05). In the control group, 16519C carriers showed a lower rate of high-quality blastocyst development compared with 16519T (p < 0.05). In endometriosis patients clinical pregnancy rate was significantly lower in the 150T subgroup compared with the 150C subgroup (p < 0.05).

Discussion

Data confirms a correlation between D-loop polymorphisms and endometriosis. The polymorphisms AC523–524 del, T16172C, and C16290T are associated with increased risk of endometriosis, while T195C, 573XCins, 16036Gins, 16049Gins, T16140C, A16183C, T16189C, and 16193Cins are associated with decreased risk of endometriosis. In addition, C16290T and T16519C can be associated with poor quality blastocyst development in population with and without endometriosis, respectively and C150T can be a predictor of poor IVF outcome.

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References

  1. Govatati S, Tipirisetti NR, Perugu S, Kodati VL, Deenadayal M, Satti V, et al. Mitochondrial genome variations in advanced stage endometriosis: a study in south Indian population. PLoS One. 2012;7(7):e40668.

    Article  CAS  Google Scholar 

  2. Creed J, Maggrah A, Reguly B, Harbottle A. Mitochondrial DNA deletions accurately detect endometriosis in symptomatic females of child-bearing age. Biomark Med. 2019;13(4):291–306.

    Article  CAS  Google Scholar 

  3. Kao SH, Huang HC, Hsieh RH, Chen SC, Tsai MC, Tzeng CR. Oxidative damage and mitochondrial DNA mutations with endometriosis. Ann N Y Acad Sci. 2005;1042:186–94.

    Article  CAS  Google Scholar 

  4. Van Langendonckt A, Casanas-Roux F, Donnez J. Oxidative stress and peritoneal endometriosis. Fertil Steril. 2002;77(5):861–70.

    Article  Google Scholar 

  5. Vercellini P, Vigano P, Somigliana E, Fedele L. Endometriosis: pathogenesis and treatment. Nat Rev Endocrinol. 2014;10(5):261–75.

    Article  CAS  Google Scholar 

  6. Greene AD, Lang SA, Kendziorski JA, Sroga-Rios JM, Herzog TJ, Burns KA. Endometriosis: where are we and where are we going? Reproduction. 2016;152(3):R63–78.

    Article  CAS  Google Scholar 

  7. Tanbo T, Fedorcsak P. Endometriosis-associated infertility: aspects of pathophysiological mechanisms and treatment options. Acta Obstet Gynecol Scand. 2017;96(6):659–67.

    Article  Google Scholar 

  8. Matalliotakis M, Zervou MI, Matalliotaki C, Rahmioglu N, Koumantakis G, Kalogiannidis I, et al. The role of gene polymorphisms in endometriosis. Mol Med Rep. 2017;16(5):5881–6.

    Article  CAS  Google Scholar 

  9. Osinski M, Mostowska A, Wirstlein P, Wender-Ozegowska E, Jagodzinski PP, Szczepanska M. The assessment of GWAS - identified polymorphisms associated with infertility risk in polish women with endometriosis. Ginekol Pol. 2018;89(6):304–10.

    Article  Google Scholar 

  10. Shu J, Xing L, Ding G, Luo Q, Liu X, Yan Q, et al. The effect of peritoneal fluid from patients with endometriosis on mitochondrial function and development of early mouse embryos. PLoS One. 2013;8(12):e82334.

    Article  Google Scholar 

  11. Kang D, Hamasaki N. Alterations of mitochondrial DNA in common diseases and disease states: aging, neurodegeneration, heart failure, diabetes, and cancer. Curr Med Chem. 2005;12(4):429–41.

    Article  CAS  Google Scholar 

  12. Stefano GB, Bjenning C, Wang F, Wang N, Kream RM. Mitochondrial Heteroplasmy. Adv Exp Med Biol. 2017;982:577–94.

    Article  CAS  Google Scholar 

  13. Stewart JB, Chinnery PF. The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease. Nat Rev Genet. 2015;16(9):530–42.

    Article  CAS  Google Scholar 

  14. Cheng M, Guo Z, Li H, Li Z, Li C, Geng C. Identification of sequence polymorphisms in the mitochondrial displacement loop as risk factors for sporadic and familial breast cancer. Tumour Biol. 2014;35(5):4773–7.

    Article  CAS  Google Scholar 

  15. Kong D, Shi S, Li Y. Single nucleotide polymorphisms in the D-loop region of mitochondrial DNA are associated with epithelial ovarian cancer prognosis. Mitochondrial DNA. 2015;26(6):848–50.

    Article  CAS  Google Scholar 

  16. Reddy TV, Govatati S, Deenadayal M, Sisinthy S, Bhanoori M. Impact of mitochondrial DNA copy number and displacement loop alterations on polycystic ovary syndrome risk in south Indian women. Mitochondrion. 2019;44:35–40.

    Article  CAS  Google Scholar 

  17. Zhai K, Chang L, Zhang Q, Liu B, Wu Y. Mitochondrial C150T polymorphism increases the risk of cervical cancer and HPV infection. Mitochondrion. 2011;11(4):559–63.

    Article  CAS  Google Scholar 

  18. Tipirisetti NR, Govatati S, Pullari P, Malempati S, Thupurani MK, Perugu S, et al. Mitochondrial control region alterations and breast cancer risk: a study in south Indian population. PLoS One. 2014;9(1):e85363.

    Article  Google Scholar 

  19. Liu VW, Wang Y, Yang HJ, Tsang PC, Ng TY, Wong LC, et al. Mitochondrial DNA variant 16189T>C is associated with susceptibility to endometrial cancer. Hum Mutat. 2003;22(2):173–4.

    Article  CAS  Google Scholar 

  20. Gardner DK, Vella P, Lane M, Wagley L, Schlenker T, Schoolcraft WB. Culture and transfer of human blastocysts increases implantation rates and reduces the need for multiple embryo transfers. Fertil Steril. 1998;69(1):84–8.

    Article  CAS  Google Scholar 

  21. Kumari T, Vachher M, Bansal S, Bamezai R, Kumar B. Meta-analysis of mitochondrial T16189C polymorphism for cancer and type 2 diabetes risk. Clin Chim Acta. 2018;482:136–43.

    Article  CAS  Google Scholar 

  22. Govatati S, Saradamma B, Malempati S, Dasi D, Thupurani MK, Nagesh N, et al. Association of mitochondrial displacement loop polymorphisms with risk of colorectal cancer in south Indian population. Mitochondrial DNA A DNA Mapp Seq Anal. 2017;28(5):632–7.

    CAS  PubMed  Google Scholar 

  23. Hu WX, Ding CM, Li RJ, Fan HY, Guo ZJ, Liu W. Single nucleotide polymorphisms in the mitochondrial displacement loop and age-at-onset of non-small cell lung cancer. Genet Mol Res. 2015;14(1):2512–7.

    Article  CAS  Google Scholar 

  24. Li Z, Deng B, Wang W, Jia Z, Liu X, Li N. Single nucleotide polymorphisms in the mitochondrial displacement loop region predict malignant melanoma outcome: a study in Chinese Han population. Mitochondrial DNA A DNA Mapp Seq Anal. 2016;27(3):1812–6.

    CAS  PubMed  Google Scholar 

  25. Er LM, Wu ML, Gao Y, Wang SJ, Li Y. Identification of sequence polymorphisms in the displacement loop region of mitochondrial DNA as a risk factor for gastroenteropancreatic neuroendocrine neoplasm. J Clin Lab Anal. 2017;31(5):e22078.

  26. Guo Z, Zhao S, Fan H, Du Y, Zhao Y, Wang G. Identification of sequence polymorphisms in the D-loop region of mitochondrial DNA as a risk factor for colon cancer. Mitochondrial DNA A DNA Mapp Seq Anal. 2016;27(6):4244–5.

    CAS  PubMed  Google Scholar 

  27. Bai Y, Guo Z, Xu J, Liu S, Zhang J, Cui L, et al. Single nucleotide polymorphisms in the D-loop region of mitochondrial DNA is associated with renal cell carcinoma outcome. Mitochondrial DNA. 2015;26(2):224–6.

    Article  CAS  Google Scholar 

  28. Xun J, Li Z, Feng J, Gao S, Yang H, Song X. Single nucleotide polymorphisms in the mitochondrial displacement loop region and outcome of malignant fibrous histiocytoma. Mitochondrial DNA A DNA Mapp Seq Anal. 2016;27(1):177–81.

    Article  CAS  Google Scholar 

  29. Wang X, Guo Y, Luan Q. Association of mitochondrial DNA displacement loop polymorphisms and aggressive periodontitis in a Chinese population: a pilot study. Mitochondrial DNA. 2015;26(3):389–95.

    Article  CAS  Google Scholar 

  30. Andres MP, Cardena M, Fridman C, Podgaec S. Polymorphisms of mitochondrial DNA control region are associated to endometriosis. J Assist Reprod Genet. 2018;35(3):533–8.

    Article  Google Scholar 

  31. Cho S, Lee YM, Choi YS, Yang HI, Jeon YE, Lee KE, et al. Mitochondria DNA polymorphisms are associated with susceptibility to endometriosis. DNA Cell Biol. 2012;31(3):317–22.

    Article  CAS  Google Scholar 

  32. Govatati S, Deenadayal M, Shivaji S, Bhanoori M. Mitochondrial displacement loop alterations are associated with endometriosis. Fertil Steril. 2013;99(7):1980–6.e9.

    Article  CAS  Google Scholar 

  33. Bai Y, Guo Z, Xu J, Zhang J, Cui L, Zhang H, et al. Association of sequence polymorphism in the mitochondrial D-loop with chronic kidney disease. Ren Fail. 2014;36(5):781–4.

    Article  CAS  Google Scholar 

  34. Fernandez-Silva P, Enriquez JA, Montoya J. Replication and transcription of mammalian mitochondrial DNA. Exp Physiol. 2003;88(1):41–56.

    Article  CAS  Google Scholar 

  35. Xu K, Hu S. Population data of mitochondrial DNA HVS-I and HVS-II sequences for 208 Henan Han Chinese. Leg Med (Tokyo). 2015;17(4):287–94.

    Article  CAS  Google Scholar 

  36. Yao YG, Kong QP, Bandelt HJ, Kivisild T, Zhang YP. Phylogeographic differentiation of mitochondrial DNA in Han Chinese. Am J Hum Genet. 2002;70(3):635–51.

    Article  CAS  Google Scholar 

  37. Xu B, Guo N, Zhang XM, Shi W, Tong XH, Iqbal F, et al. Oocyte quality is decreased in women with minimal or mild endometriosis. Sci Rep. 2015;5:10779.

    Article  Google Scholar 

  38. Navaglia F, Basso D, Fogar P, Sperti C, Greco E, Zambon CF, et al. Mitochondrial DNA D-loop in pancreatic cancer: somatic mutations are epiphenomena while the germline 16519 T variant worsens metabolism and outcome. Am J Clin Pathol. 2006;126(4):593–601.

    Article  CAS  Google Scholar 

  39. Zhou HY, Shu HY, Dai J, Li HC, Tang L, Wang HW, et al. Maternal genetic backgrounds contribute to the genetic susceptibility of tongue cancer patients in Hunan, central of China. Mitochondrial DNA A DNA Mapp Seq Anal. 2018;29(3):347–52.

    CAS  PubMed  Google Scholar 

  40. Guney O, Ak H, Atay S, Ozkaya AB, Aydin HH. Mitochondrial DNA polymorphisms associated with longevity in the Turkish population. Mitochondrion. 2014;17:7–13.

    Article  CAS  Google Scholar 

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Acknowledgments

We are grateful to Kai Zong (Hefei Customs) for assisting in mtDNA sequencing and analysis.

Funding

This study was supported by the National Key R&D Program of China (2017YFC1001300) and the National Natural Science Foundation of China (81601345, 81871216, 81771653).

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Correspondence to Dongmei Ji or Yunxia Cao.

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Li, X., Ji, D., Marley, J.L. et al. Association between mitochondrial DNA D-loop region polymorphisms and endometriosis in a Chinese population. J Assist Reprod Genet 37, 2171–2179 (2020). https://doi.org/10.1007/s10815-020-01853-z

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  • DOI: https://doi.org/10.1007/s10815-020-01853-z

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