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

article OA: green CC0 ⤵ 2 in-corpus citations
AI-generated summary by claude@2026-06+body, 2026-06-07

This study investigated mitochondrial DNA D-loop polymorphisms and haplotypes in Chinese endometriosis patients, identifying specific variants associated with increased or decreased risk and reproductive outcomes.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-06, 2026-06-07 · read from full text

This Chinese Han case-control study evaluated whether mitochondrial DNA (mtDNA) D-loop region single-nucleotide polymorphisms and haplotypes are associated with endometriosis and whether specific variants relate to reproductive outcomes after IVF. Whole blood mtDNA from 125 endometriosis patients and 124 controls was sequenced across the full 1124-bp D-loop region, and D-loop variants were tested for association with clinical outcome measures including blastocyst quality and pregnancy rate; the paper does not state a major limitation such as sample-size power, but the findings are based on a single-population, academic fertility-center cohort. The endometriosis group showed higher frequencies of AC523–524 del, T16172C, and C16290T and lower frequencies of multiple other variants, while within patients certain subgroups had altered high-quality blastocyst rates and clinical pregnancy rates. Relevance to endometriosis: the central finding is that specific mtDNA D-loop polymorphisms are associated with endometriosis risk and are also linked to IVF outcomes in endometriosis patients. This paper is centrally about endometriosis — it tests associations between mtDNA D-loop polymorphisms and endometriosis susceptibility and related IVF outcomes.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Full text 10,772 characters · extracted from oa-doi-fallback · 5 sections · click to expand

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. Similar content being viewed by others

References

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. 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. 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. Van Langendonckt A, Casanas-Roux F, Donnez J. Oxidative stress and peritoneal endometriosis. Fertil Steril. 2002;77(5):861–70. Vercellini P, Vigano P, Somigliana E, Fedele L. Endometriosis: pathogenesis and treatment. Nat Rev Endocrinol. 2014;10(5):261–75. 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. Tanbo T, Fedorcsak P. Endometriosis-associated infertility: aspects of pathophysiological mechanisms and treatment options. Acta Obstet Gynecol Scand. 2017;96(6):659–67. 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. 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. 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. 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. Stefano GB, Bjenning C, Wang F, Wang N, Kream RM. Mitochondrial Heteroplasmy. Adv Exp Med Biol. 2017;982:577–94. Stewart JB, Chinnery PF. The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease. Nat Rev Genet. 2015;16(9):530–42. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. Govatati S, Deenadayal M, Shivaji S, Bhanoori M. Mitochondrial displacement loop alterations are associated with endometriosis. Fertil Steril. 2013;99(7):1980–6.e9. 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. Fernandez-Silva P, Enriquez JA, Montoya J. Replication and transcription of mammalian mitochondrial DNA. Exp Physiol. 2003;88(1):41–56. 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. 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. 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. 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. 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. 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. 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). Author information Authors and Affiliations Corresponding authors Ethics declarations Competing interests The authors declare that there are no conflicts of interest. Additional information Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Electronic supplementary material ESM 1 (download DOCX ) (DOCX 39 kb) Rights and permissions About this article Cite this article 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 Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s10815-020-01853-z

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Condition tags

mesh:D004715endometriosis

MeSH descriptors

DNA, Mitochondrial DNA, Mitochondrial Endometriosis Endometriosis Endometriosis Genetic Association Studies Genetic Predisposition to Disease Adult Blastocyst Blastocyst Female Haplotypes Haplotypes Humans Mitochondria Mitochondria Polymorphism, Single Nucleotide Polymorphism, Single Nucleotide

Citation neighborhood

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

References (40)

Cited by (2)

Source provenance

europepmc
last seen: 2026-06-04T01:30:01.192114+00:00
openalex
last seen: 2026-06-04T00:00:01.174412+00:00
pubmed
last seen: 2026-05-13T22:21:59.141895+00:00
License: CC0 · commercial use OK