The site of the Media Sphera Publishers contains materials intended solely for healthcare professionals.
By closing this message, you confirm that you are a certified medical professional or a student of a medical educational institution.

Andreeva E.N.

Endocrinology Research Centre;
Moscow State University of Medicine and Dentistry

Sheremetyeva E.V.

A.I. Evdokimov Moscow State University of Medicine and Dentistry

Grigoryan O.R.

A.I. Evdokimov Moscow State University of Medicine and Dentistry

Environmental factors and menopause

Authors:

Andreeva E.N., Sheremetyeva E.V., Grigoryan O.R.

More about the authors

Journal: Russian Journal of Human Reproduction. 2020;26(4): 14‑21

Read: 2200 times


To cite this article:

Andreeva EN, Sheremetyeva EV, Grigoryan OR. Environmental factors and menopause. Russian Journal of Human Reproduction. 2020;26(4):14‑21. (In Russ.)
https://doi.org/10.17116/repro20202604114

Recommended articles:
Myokines — the cardiometabolic risk pote­ntial biomarkers. Russian Journal of Preventive Medi­cine. 2025;(7):119-126
Cardiogenic deme­ntia. S.S. Korsakov Journal of Neurology and Psychiatry. 2025;(8):43-49
The fundamental foundations of periodontal aging. Part 2. Russian Journal of Operative Surgery and Clinical Anatomy. 2025;(3):62-69
Staffing resources solu­tions for patients with obesity healthcare enha­ncement. Russian Journal of Preventive Medi­cine. 2025;(9):42-46

References:

  1. Berestyanaya AN. Epigenome: parallel reality inside the cell. Nauka i zhizn’. 2017;8:69-75. (In Russ.).
  2. Waddington C.H. Canalization of development and the inheritance of acquired characters. Nature. 1942;150:563-565.  https://doi.org/10.1038/150563a0
  3. Gurdon JB, Elsdale TR, Fischberg M. Sexually mature individuals of Xenopus laevis from the transplantation of single somatic nuclei. Nature. 1958;182(4627):64-65.  https://doi.org/10.1038/182064a0
  4. Vanyushin BF, Tkacheva SG, Belozersky AN. Rare bases in animal DNA. Nature. 1970;225:948-949.  https://doi.org/10.1038/225948a0
  5. Soubry A, Schildkraut JM, Murtha A, Wang F, Huang Z, Bernal A, Kurtzberg J, Jirtle RL, Murphy SK, Hoyo C. Paternal obesity is associated with IGF2hypomethylation in newborns: results from a Newborn Epigenetics Study (NEST) cohort. BMC Medicine. 2013; 11:29.  https://doi.org/10.1186/1741-7015-11-29
  6. Spork P. Chitaya mezhdu strok DNK. M.: Lomonosov; 2013. (In Russ.).
  7. Meaney MJ, Szyf M, Seckl JR. Epigenetic mechanisms of perinatal programming of hypothalamic pituitary adrenal function and health. Trends in Molecular Medicine. 2007;13(7):269-277.  https://doi.org/10.1016/j.molmed.2007.05.003
  8. Nieratschker V, Batra A, Fallgatter A. Genetics and epigenetics of alcohol dependence. Journal of Molecular Psychiatry. 2013;1(1):11.  https://doi.org/10.1186/2049-9256-1-11
  9. Nielsen DA, Utrankar A, Reyes JA, Simons DD, Kosten TR. Epigenetics of drug abuse: predisposition or response. Pharmacogenomics. 2012;13(10):1149-1160. https://doi.org/10.2217/pgs.12.94
  10. Labonte B, Turecki G. The epigenetics of suicide: explaining the biological effects of early life environmental adversity. Archives of Suicide Research. 2010;14(4):291-310.  https://doi.org/10.1080/13811118.2010.524025
  11. Johnson AA, Akman K, Calimport SR, Wuttke D, Stolzing A, de Magalhães JP. The role of DNA methylation in aging, rejuvenation, and age-related disease. Rejuvenation Research. 2012;15(5):483-494.  https://doi.org/10.1089/rej.2012.1324
  12. Nikitin AG, Shmookler Reis RJ. Role of transposable elements in agerelated genomic instability. Genetics Research. 1997;69(3):183-195.  https://doi.org/10.1017/s0016672397002772
  13. Vayserman AM, Voitenko VP, Mekhova LV. Epigenetic epidemiology of age-related diseases. Ontogenez. 2011;42(1):1-21. (In Russ.).
  14. Kim YR, Kim CS, Naqvi A, Kumar A, Kumar S, Hoffman TA, Irani K. Epigenetic upregulation of p66shc mediates low-density lipoprotein cholesterol-induced endothelial cell dysfunction. American Journal of Physiology: Heart and Circulatory Physiology. 2012;303: 189-196.  https://doi.org/10.1152/ajpheart.01218.2011
  15. Remely M. Therapeutic perspectives of epigenetically active nutrients. British Journal of Pharmacology. 2015;172(11):2756-2768. https://doi.org/10.1111/bph.12854
  16. Wei YH, Lee HC. Oxidative stress, mitochondrial DNA mutation, and impairment of antioxidant enzymes in aging. Experimental Biology and Medicine. 2002;227:671-682.  https://doi.org/10.1177/153537020222700901
  17. Murakoshi Y, Sueoka K, Takahashi K, Sato S, Sakurai T, Tajima H, Yoshimura Y. Embryo developmental capability and pregnancy outcome are related to the mitochondrial DNA copy number and ooplasmic volume. Journal of Assisted Reproduction and Genetics. 2013; 30:1367-1375. https://doi.org/10.1007/s10815-013-0062-6
  18. Meyne J, Ratliff R, Moyzis R. Conservation of the human telomere sequence (TTAGGG)n among vertebrates. Proceedings of the National Academy of Sciences. 1989;86(18):7049-7053. https://doi.org/10.1073/pnas.86.18.7049
  19. Bonda DJ, Wang X, Perry G, Nunomura A, Tabaton M, Zhu X, Smith MA. Oxidative stress in Alzheimer disease: a possibility for prevention. Neuropharmacology. 2010;59(4-5):290-294.  https://doi.org/10.1016/j.neuropharm.2010.04.005
  20. Dalgård C, Benetos A, Verhulst S, Labat C, Kark J, Christensen K, Kimura M, Kyvik KO, Aviv A. Leukocyte telomere length dynamics in women and men: menopause vs age effects. International Journal of Epidemiology. 2015;44(5):1688-1695. https://doi.org/10.1093/ije/dyv165
  21. Gray K, Schiff M, Fitzpatrick A, Kimura M, Aviv A, Starr J. Leukocyte Telomere Length and Age at Menopause. Epidemiology. 2014;25(1):139-146.  https://doi.org/10.1097/EDE.0000000000000017
  22. Lopatina OV, Balan VE, Tkacheva ON, Sharashkina NV, Zhuravel AS. Features of cell aging in women at different periods of life. Rossijskij vestnik akushera-ginekologa. 2015;15(2):62-67. (In Russ.). https://doi.org/10.17116/rosakush201515262-67
  23. Lopatina OV, Balan VE, Tkacheva ON, Sharashkina NV, Zhuravel’ AS. Factors of women’s health from the perspective of reproductive ageing and risk of cardiovascular disorders. Al’manah klinicheskoj mediciny. 2015;37:111-117. (In Russ.). https://doi.org/10.18786/2072-0505-2015-37-111-117
  24. Sayban S, Mirfakhraie R, Omrani M, Ghaedi H, Heidary H, Yaghoobi H, Azizi F, Pouresmaeili F. Idiopathic Premature Ovarian Failure and its association to the abnormal longitudinal changes of telomere length in a population of Iranian Infertile Women: A pilot study. Meta Gene. 2018;18:58-61.  https://doi.org/10.1016/j.mgene.2018.07.005
  25. Khalyavkin AV, Yashin AI. Starenie: rol’ upravlyayushchih signalov. Gerontologiya in Silico: stanovlenie novoj discipliny. Matematicheskie modeli, analiz dannyh i vychislitel’nye eksperimenty. Glava 4. Starenie: rol’ upravlyayushchih signalov. M.: BINOM. Laboratoriya znanij; 2014. (In Russ.).
  26. Murabito JM. Findings from the ReproGen Consortium. MaryFran Sowers Memorial Lecture. April 3, 2018. Accessed May 25, 2020. https://pdfslide.net/documents/genetics-of-menopause-genetics-of-menopause-timing-findings-from-the-reprogen-consortium.html
  27. Liu Z, Chen BH, Assimes TL, Ferrucci L, Horvath S, Levine ME. The role of epigenetic aging in education and racial/ethnic mortality disparities among older U.S. Women. Psychoneuroendocrinology. 2019;104:18-24.  https://doi.org/10.1016/j.psyneuen.2019.01.028
  28. Levine ME, Lu AT, Chen BH, Hernandez DG, Singleton AB, Ferrucci L, Bandinelli S, Salfati E, Manson JE, Quach A, Kusters CD, Kuh D, Wong A, Teschendorff AE, Widschwendter M, Ritz BR, Absher D, Assimes TL, Horvath S. Menopause accelerates biological aging. Proceedings of the National Academy of Sciences of the United States of America. 2016;113(33):9327-9332. https://doi.org/10.1073/pnas.1604558113
  29. Moreau KL, Hildreth KL. Vascular Aging across the Menopause Transition in Healthy Women. Advances in Vascular Medicine. 2014; 204390. https://doi.org/10.1155/2014/204390
  30. Maffei S, Guiducci L, Cugusi L, Cadeddu C, Deidda M, Gallina S, Sciomer S, Gastaldelli A, Kaski JC; Working Group on «Gender difference in cardiovascular disease» of the Italian Society of Cardiology. Women-specific predictors of cardiovascular disease risk — new paradigms. International Journal of Cardiology. 2019;286:190-197.  https://doi.org/10.1016/j.ijcard.2019.02.005
  31. Zhuravel AS, Balan VE, Tkacheva ON, Sharashkina NV, Lopatina OV, Ananyev VA, Orlova SA. Vascular aging in women in climacteria and the risk of cardiovascular diseases. Rossijskij vestnik akushera-ginekologa. 2015;15(2):56-61. (In Russ.). https://doi.org/10.17116/rosakush201515256-61
  32. Repina MA. Menopausal Metabolic Syndrome and Obesity. Obzory po klinicheskoj farmakologii i lekarstvennoj terapii. 2003;2(3):35-43. (In Russ.).
  33. Komulainen K, Pulkki-Råback L, Jokela M, Lyytikäinen LP, Pitkänen N, Laitinen T, Hintsanen M, Elovainio M, Hintsa T, Jula A, Juonala M, Pahkala K, Viikari J, Lehtimäki T, Raitakari O, Keltikangas-Järvinen L. Education as a moderator of genetic risk for higher body mass index: Prospective cohort study from childhood to adulthood. International Journal of Obesity. 2018;42(4):866-871.  https://doi.org/10.1038/ijo.2017.174
  34. Chedraui P, Pérez-López FR. Metabolic syndrome during female midlife: what are the risks? Climacteric. 2019;22(2):127-132.  https://doi.org/10.1080/13697137.2018.1561666
  35. Ward E, Gold EB, Johnson WO, Ding F, Chang PY, Song P, El Khoudary SR, Karvonen-Gutierrez C, Ylitalo KR, Lee JS. Patterns of Cardiometabolic Health as Midlife Women Transition to Menopause: A Prospective Multiethnic Study. Journal of Clinical Endocrinology and Metabolism. 2019;104(5):1404-1412. https://doi.org/10.1210/jc.2018-00941
  36. Mancuso P, Bouchard B. The Impact of Aging on Adipose Function and Adipokine Synthesis. Frontiers in Endocrinology. 2019;10:137.  https://doi.org/10.3389/fendo.2019.00137
  37. Ambikairajah A, Walsh E, Tabatabaei-Jafari H, Cherbuin N. Fat mass changes during menopause: a meta-analysis. American Journal of Obstetrics and Gynecology. 2019;221(5):393-409.e50.  https://doi.org/10.1016/j.ajog.2019.04.023
  38. Kresovich JK, Xu Z, O’Brien KM, Weinberg CR, Sandler DP, Taylor JA. Methylation-based biological age and breast cancer risk. Journal of the National Cancer Institute. 2019;111(10):1051-1058. https://doi.org/10.1093/jnci/djz020
  39. Ryan J, Scali J, Carrière I, Amieva H, Rouaud O, Berr C, Ritchie K, Ancelin ML. Impact of a premature menopause on cognitive function in later life. BJOG. 2014;121(13):1729-1739. https://doi.org/10.1111/1471-0528.12828
  40. Gilsanz P, Lee C, Corrada MM, Kawas CH, Quesenberry CP Jr, Whitmer RA. Reproductive period and risk of dementia in a diverse cohort of health care members. Neurology. 2019;92(17):2005-2014. https://doi.org/10.1212/WNL.0000000000007326
  41. Lahdenpera M, Lummaa V, Helle S, Tremblay M, Russell AF. Fitness benefits of prolonged post-reproductive lifespan in women. Nature. 2004;428:178-181.  https://doi.org/10.1038/nature02367
  42. Kuningas M, Altmae S, Uitterlinden AG, Hofman A, van Duijn CM, Tiemeier H. The relationship between fertility and lifespan in humans. Age. 2011;33(4):615-622.  https://doi.org/10.1007/s11357-010-9202-4
  43. Perls TT, Fretts RC. The evolution of menopause and human life span. Annals of Human Biology. 2001;28:237-245.  https://doi.org/10.1080/030144601300119052
  44. McArdle PF, Pollin TI, O’Connell JR, Sorkin JD, Agarwala R, Schäffer AA, Streeten EA, King TM, Shuldiner AR, Mitchell BD. Does having children extend life span? A genealogical study of parity and longevity in the Amish. The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences. 2006;61:190-195.  https://doi.org/10.1007/s11357-010-9202-4
  45. Muller HG, Chiou JM, Carey JR, Wang JL. Fertility and life span: late children enhance female longevity. The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences. 2002;57:202-206.  https://doi.org/10.1093/gerona/57.5.b202
  46. Murabito JM, Yang Q, Fox C, Wilson PW, Cupples LA. Heritability of age at natural menopause in the Framingham Heart Study. The Journal of Clinical Endocrinology and Metabolism. 2005;90:3427-3430. https://doi.org/10.1210/jc.2005-0181
  47. Aschheim P. Aging in the hypothalamic-hypophyseal-ovarian axis in the rat. Hypothalamus, Pituitary and Aging. Springfield: Ch. C. Thomas. 1976;376-418. 
  48. Klinicheskie rekomendacii. Menopauza i klimaktericheskoe sostoyanie u zhenshchiny. 2016 (In Russ.). Accessed May 25, 2020. https://www.ulsu.ru/media/uploads/nina-baratyuk%40mail.ru/2017/11/02.pdf
  49. Lin J, Kroenke C, Epel E, Kenna H, Wolkowitz O, Blackburn E, Rasgon N. Greater endogenous estrogen exposure is associated with longer telomeres in postmenopausal women at risk for cognitive decline. Brain Research. 2010;1379:224-231.  https://doi.org/10.1016/j.brainres.2010.10.033
  50. Lee D, Im, J, Kim J, Lee H, Shim J. Effect of Long-Term Hormone Therapy on Telomere Length in Postmenopausal Women. Yonsei Medical Journal. 2005;46(4):471.  https://doi.org/10.3349/ymj.2005.46.4.471

Email Confirmation

An email was sent to test@gmail.com with a confirmation link. Follow the link from the letter to complete the registration on the site.

Email Confirmation

We use cооkies to improve the performance of the site. By staying on our site, you agree to the terms of use of cооkies. To view our Privacy and Cookie Policy, please. click here.