CURRENT STATE OF THE PROBLEM OF MENSTRUAL CYCLE DISORDERS IN WOMEN OF REPRODUCTIVE AGE WITH UNDIFFERENTIATED CONNECTIVE TISSUE DYSPLASIA (LITERATURE REVIEW)

In: Bulletin of Problems Biology and Medicine · 2024 · vol. 1(1) , pp. 69 · doi:10.29254/2077-4214-2024-1-172-69-75 · W4393170122
article OA: diamond CC0
AI-generated summary by claude@2026-06, 2026-06-09

This literature review explores the current state of menstrual cycle disorders in women with undifferentiated connective tissue dysplasia, aiming to improve diagnosis and treatment for enhanced reproductive health.

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, 2026-06-09 · read from full text

This literature review analyzes the current state of menstrual cycle disorders in women of reproductive age with undifferentiated connective tissue dysplasia (UCTD), drawing on studies identified via PubMed, Medline, and the Cochrane Library over the prior 10 years. It synthesizes evidence that menstrual dysfunction in this population—most commonly dysmenorrhea and abnormal uterine bleeding—is linked to proposed interactions between sex hormones and immune dysregulation, including autoimmune changes and inflammation, while noting that it is difficult to determine whether hormonal abnormalities result from disease versus treatment and that hormone measurements before disease are often unavailable. The review further summarizes available findings that UCTD is associated with worse pregnancy outcomes, including higher rates of miscarriage and pregnancy complications, and that women with connective tissue disorders may exhibit phenotypic signs in the maternal context. The paper states limitations including UCTD’s clinical heterogeneity, lack of uniform terminology and diagnostic criteria, and incomplete standardization of diagnostic methods. Relevance to endometriosis: the review explicitly mentions that menstrual cycle disorders can present alongside uterine fibroids, endometriosis, and adenomyosis, though its main focus is UCTD-related menstrual dysfunction.

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

Abstract

improve the process of diagnosis and treatment of the specified category of patients, which will contribute to the improvement of the reproductive health of the future generation.
Full text 46,349 characters · extracted from oa-pdf · 2 sections · click to expand

Methods

that will contribute to strengthening the reproductive health of young women.

References

1. Brantelid IE, Nilvér H, Alehagen S. Menstruation during a lifespan: A qualitative study of women’s experiences. Health Care Women Int. 2014;35(6):600–16. DOI: 10.1080/07399332.2013.868465. 2. Odongo E, Byamugisha J, Ajeani J, Mukisa J. Prevalence and effects of menstrual disorders on quality of life of female undergraduate students in Makerere University College of health sciences, a cross sectional survey. BMC Womens Health. 2023;23(1):152. DOI: 10.1186/ s12905-023-02290-7. 3. Anikwe CC, Mamah JE, Okorochukwu BC, Nnadozie UU, Obarezi CH, Ekwedigwe KC. Age at menarche, menstrual characteristics, and its associated morbidities among secondary school students in Abakaliki, southeast Nigeria. Heliyon. 2020;6(5):e04018. DOI: 10.1016/j. heliyon.2020. e04018. 4. Lebduska E, Beshear D, Spataro BM. Abnormal Uterine Bleeding. Med Clin North Am. 2023;107(2):235–246. DOI: 10.1016/j. mcna.2022.10.014. 5. Zeru AB, Gebeyaw ED, Ayele ET. Magnitude and associated factors of menstrual irregularity among undergraduate students of Debre Berhan University, Ethiopia. Reprod Health. 2021;18(1):101. DOI: 10.1186/s12978–021–01156–1. 6. Rajiwade SR, Sagili H, Soundravally R, Subitha L. Endocrine Abnormalities in Adolescents with Menstrual Disorders. J Obstet Gynaecol India. 2018;68(1):58–64. DOI: 10.1007/s13224–017–1035-y. 7. Nyirenda T, Nyagumbo E, Murewanhema G, Mukonowenzou N, Kagodora SB, Mapfumo C, et al. Prevalence of dysmenorrhea and associated risk factors among university students in Zimbabwe. Womens Health (Lond). 2023;19:17455057231189549. DOI: 10.1177/17455057231189549. 8. Maybin JA, Critchley HO. Menstrual physiology: implications for endometrial pathology and beyond. Hum Reprod Update. 2015;21(6):748– 761. DOI: 10.1093/humupd/dmv038. 9. Marwa K, Anjum F. Undifferentiated Connective Tissue Disease [Internet]. Treasure Island (FL): StatPearls Publishing; 2023 [updated 2023 Apr 27]. Available from: https://www.ncbi.nlm.nih.gov/books/NBK572061/. 10. Wiśniewski M, Zabłocka-Żytka L. Sexual and mental health of woman suffering from selected connective tissue diseases: an original paper. Clin Rheumatol. 2021;40(8):3319–3327. DOI: 10.1007/s10067–021–05611-z. 11. Alia F, Rim BS, Miladi S, Ouenniche K, Kassab S, Chekili S, et al. Comparison of sexual function in Tunisian women with rheumatoid arthritis and healthy controls. Clin Rheumatol. 2019;38(12):3361–3365. DOI: 10.1007/s10067–019–04726–8. ISSN 2077-4214. Вісник проблем біології і медицини – 2024 – Вип. 1 (172) / Bulletin of problems in biology and medicine – 2024 – Issue 1 (172) 73 ОГЛЯДИ ЛІТЕРАТУРИ / LITERATURE REVIEWS 12. Østensen M. Sexual and reproductive health in rheumatic disease. Nat Rev Rheumatol. 2017;13(8):485–493. DOI: 10.1038/ nrrheum.2017.102. 13. Desai MK, Brinton RD. Autoimmune Disease in Women: Endocrine Transition and Risk Across the Lifespan. Front Endocrinol (Lausanne). 2019;10:265. DOI: 10.3389/fendo.2019.00265. 14. Kronzer VL, Bridges SL Jr, Davis JM 3rd. Why women have more autoimmune diseases than men: An evolutionary perspective. Evol Appl. 2020;14(3):629–633. DOI: 10.1111/eva.13167. 15. Cutolo M, Straub RH. Sex steroids and autoimmune rheumatic diseases: state of the art. Nat Rev Rheumatol. 2020;16:628–44. DOI: 10.1038/s41584–020–0503–4. 16. Fuentes N, Silveyra P. Estrogen receptor signaling mechanisms. Adv Protein Chem Struct Biol. 2019;116:135–170. DOI: 10.1016/ bs.apcsb.2019.01.001. 17. Buendía-González FO, Legorreta-Herrera M. The Similarities and Differences between the Effects of Testosterone and DHEA on the Innate and Adaptive Immune Response. Biomolecules. 2022;12(12):1768. DOI: 10.3390/biom12121768. 18. Tang J, Chen LR, Chen KH. The Utilization of Dehydroepiandrosterone as a Sexual Hormone Precursor in Premenopausal and Postmenopausal Women: An Overview. Pharmaceuticals (Basel). 2021;15(1):46. DOI: 10.3390/ph 15010046. 19. Xing E, Billi AC, Gudjonsson JE. Sex Bias and Autoimmune Diseases. J Invest Dermatol. 2022;142(3.B):857–866. DOI: 10.1016/j. jid.2021.06.008. 20. Zucchi D, Tani C, Monacci F, Elefante E, Carli L, Parma A, et al. Pregnancy and undifferentiated connective tissue disease: outcome and risk of flare in 100 pregnancies. Rheumatology (Oxford). 2020;59(6):1335–1339. DOI: 10.1093/rheumatology/kez440. 21. Spinillo A, Beneventi F, Epis OM, Montanari L, Mammoliti D, Ramoni V, et al. Prevalence of undiagnosed autoimmune rheumatic diseases in the first trimester of pregnancy. Results of a two-steps strategy using a self-administered questionnaire and autoantibody testing. BJOG. 2008;115(1):51–57. DOI: 10.1111/j.1471–0528.2007.01530.x. 22. Shavazi NN, Nurmukhamedova DU. Menstrual function disorders in adolescent girls with dysplasia of connective tissues. Galaxy int. interdiscip. res. j. 2022;10(4):206–211. Available from: https://internationaljournals.co. in/index.php/giirj/article/view/1649. 23. Beneventi F, Locatelli E, Ramoni V, Caporali R, Montecucco CM, Simonetta M, et al. Uterine artery Doppler velocimetry and obstetric outcomes in connective tissue diseases diagnosed during the first trimester of pregnancy. Prenat Diagn. 2012;32(11):1094–101. DOI: 10.1002/pd.3964. 24. Spinillo A, Beneventi F, Locatelli E, Ramoni V, Caporali R, Alpini C, et al. Early, Incomplete, or Preclinical Autoimmune Systemic Rheumatic Diseases and Pregnancy Outcome. Arthritis Rheumatol. 2016;68(10):2555–62. DOI: 10.1002/art.39737. 25. Veglia M, D’Ippolito S, Marana R, Di Nicuolo F, Castellani R, Bruno V, et al. Human IgG Antinuclear Antibodies Induce Pregnancy Loss in Mice by Increasing Immune Complex Deposition in Placental Tissue: In Vivo Study. Am J Reprod Immunol. 2015;74(6):542–52. DOI: 10.1111/aji.12429. 26. Pietropolli A, Bruno V, Capogna MV, Bernardini S, Piccione E, Ticconi C. Uterine blood flow indices, antinuclear autoantibodies and unexplained recurrent miscarriage. Obstet Gynecol Sci. 2015;58(6):453–460. DOI: 10.5468/ogs.2015.58.6.453. 27. Ferreira AM, Pires CR, Moron AF, Araujo Júnior E, Traina E, Mattar R. Doppler assessment of uterine blood flow in recurrent pregnancy loss. Int J Gynaecol Obstet. 2007;98(2):115–119. DOI: 10.1016/j.ijgo.2007.05.006. 28. Nakken B, Bodolay E, Szodoray P. Cytokine Milieu in Undifferentiated Connective Tissue Disease: a Comprehensive Review. Clin Rev Allergy Immunol. 2015;49(2):152–162. DOI: 10.1007/s12016–014–8452–9. 29. Yang S, Ni R, Lu Y, Wang S, Xie F, Zhang C, et al. A three-arm, multicenter, open-label randomized controlled trial of hydroxychloroquine and low-dose prednisone to treat recurrent pregnancy loss in women with undifferentiated connective tissue diseases: protocol for the Immunosuppressant regimens for LIving FEtuses (ILIFE) trial. Trials. 2020;21(1):771. DOI: 10.1186/s13063–020–04716–1. 30. Marder W, Littlejohn EA, Somers EC. Pregnancy and autoimmune connective tissue diseases. Best Pract Res Clin Rheumatol. 2016;30(1):63-80. DOI: 10.1016/j.berh.2016.05.002. 31. Klimaszyk K, Wender-Ożegowska E, Kędzia M. Maternal and foetal outcome of pregnancy in women with connective tissue diseases. Journal of Medical Science. 2021;90(3):e525. DOI: 10.20883/medical.e525. 32. Critchley HOD, Babayev E, Bulun SE, Clark S, Garcia-Grau I, Gregersen PK, et al. Menstruation: science and society. Am J Obstet Gynecol. 2020;223(5):624–664. DOI: 10.1016/j.ajog.2020.06.004. 33. López-Liria R, Torres-Álamo L, Vega-Ramírez FA, García-Luengo AV, Aguilar-Parra JM, Trigueros-Ramos R, et al. Efficacy of Physiotherapy Treatment in Primary Dysmenorrhea: A Systematic Review and Meta-Analysis. Int J Environ Res Public Health. 2021;18(15):7832. DOI: 10.3390/ijerph18157832. 34. Bakhsh H, Algenaimi E, Aldhuwayhi R, AboWadaan M. Prevalence of dysmenorrhea among reproductive age group in Saudi Women. BMC Womens Health. 2022;22(1):78. DOI: 10.1186/s12905–022–01654–9. 35. Kural M, Noor NN, Pandit D, Joshi T, Patil A. Menstrual characteristics and prevalence of dysmenorrhea in college going girls. J Family Med Prim Care. 2015;4(3):426–431. DOI: 10.4103/2249–4863.161345. 36. Ali A, Ali A, Eldalo AS, Alotaibi NS, Alsufyan MS i, Alotaibi AJ, et al. Prevalence, impact, and management perception of dysmenorrhea among university students: A cross-sectional study. Braz. J. Pharm. Sci. 2022;58:e20458. DOI: 10.1590/s2175–97902022e20458. 37. Serrahima C, Martínez M. The Experience of Dysmenorrhea. Synthese. 2023;201(173):1–22. DOI: 10.1007/s11229–023–04148–9. 38. Yakubova O, Ayupova F, Kamalov Z, Negmatshaeva K, Mamarasulova D. Role of Col1a1 and G2046t genes in Uzbeks with juvenile dysmenorrhea in the presence of criteria for undifferentiated connective tissue dysplasia. Journal of Critical Reviews. 2020;7(2):391–394. Available from: https://annalsofrscb.ro/index.php/journal/article/view/832. 39. Orlandi M, Vannuccini S, El Aoufy K, Melis MR, Lepri G, Sambataro G, et al. Menstruation-Related Disorders-Dysmenorrhea and Heavy Bleeding-as Significant Epiphenomena in Women With Rheumatic Diseases. Front Pharmacol. 2022;13:807880. DOI: 10.3389/ fphar.2022.807880. 40. Shigesi N, Kvaskoff M, Kirtley S, Feng Q, Fang H, Knight JC, et al. The association between endometriosis and autoimmune diseases: a systematic review and meta-analysis. Hum Reprod Update. 2019;25(4):486–503. DOI: 10.1093/humupd/dmz014. 41. Chapron C, Marcellin L, Borghese B, Santulli P. Rethinking mechanisms, diagnosis and management of endometriosis. Nat Rev Endocrinol. 2019;15(11):666–682. DOI: 10.1038/s41574–019–0245-z. 42. Yakubova O, Isakova D, Rizakova D, Farmankulova Y, Usmanova M, Umarova M. The Relationship of Changes in the State of Connective Tissue and Hypomagnesemia in Juvenile Dysmenorrhea. Nat. Volatiles & Essent. Oils, 2021;8(5):6805–6810. Available from: https://www. nveo.org/index. php/journal/article/view/1893. 43. Bourdon M, Santulli P, Jeljeli M, Vannuccini S, Marcellin L, Doridot L, et al. Immunological changes associated with adenomyosis: a systematic review. Hum Reprod Update. 2021;27(1):108–129. DOI: 10.1093/humupd/dmaa038. 44. Králíčková M, Fiala L, Losan P, Tomes P, Vetvicka V. Altered Immunity in Endometriosis: What Came First? Immunol Invest. 2018;47(6):569– 582. DOI: 10.1080/08820139.2018.1467926. 45. Critchley HOD, Babayev E, Bulun SE, Clark S, Garcia-Grau I, Gregersen PK, et al. Menstruation: science and society. Am J Obstet Gynecol. 2020;223(5):624–664. DOI: 10.1016/j.ajog.2020.06.004. 46. Lavadi RS, Venkatachalaiah R, Prasad M. Double Trouble: A Case Report of Abnormal Uterine Bleeding due to Both Central and Peripheral Pathology. Int J Appl Basic Med Res. 2022;12(2):134–136. DOI: 10.4103/ijabmr. ijabmr_500_21. 47. Ueno A, Yoshida T, Yamamoto Y, Hayashi K. Successful control of menstrual cycle-related exacerbation of inflammatory arthritis with GnRH agonist with add-back therapy in a patient with rheumatoid arthritis. J Obstet Gynaecol Res. 2022;48(7):2005–2009. DOI: 10.1111/ jog.15287. 48. Rosenblum E, Wilkinson LD, Brady PH, Gin GT. Female Pelvic Conditions: Abnormal Uterine Bleeding. FP Essent. 2022;515:20–25. ISSN 2077-4214. Вісник проблем біології і медицини – 2024 – Вип. 1 (172) / Bulletin of problems in biology and medicine – 2024 – Issue 1 (172) 74 ОГЛЯДИ ЛІТЕРАТУРИ / LITERATURE REVIEWS 49. Bofill Rodriguez M, Lethaby A, Farquhar C. Non-steroidal anti-inflammatory drugs for heavy menstrual bleeding. Cochrane Database Syst Rev. 2019;9(9):CD000400. DOI: 10.1002/14651858.CD000400.pub4. 50. Roy SN, Bhattacharya S. Benefits and risks of pharmacological agents used for the treatment of menorrhagia. Drug Saf. 2004;27(2):75– 90. DOI: 10.2165/00002018–200427020–00001. 51. Kontogiannis A, Matsas A, Valsami S, Livanou ME, Panoskaltsis T, Christopoulos P. Primary Hemostasis Disorders as a Cause of Heavy Menstrual Bleeding in Women of Reproductive Age. J Clin Med. 2023;12(17):5702. DOI: 10.3390/jcm12175702. 52. Leminen H, Hurskainen R. Tranexamic acid for the treatment of heavy menstrual bleeding: efficacy and safety. Int J Womens Health. 2012;4:413–21. DOI: 10.2147/IJWH.S13840. 53. Marjoribanks J, Lethaby A, Farquhar C. Surgery versus medical therapy for heavy menstrual bleeding. Cochrane Database Syst Rev. 2016;2016(1):CD003855. DOI: 10.1002/14651858.CD003855.pub3. 54. Shalaby MA, Maged AM, Al-Asmar A, El Mahy M, Al-Mohamady M, Rund NMA. Safety and efficacy of preoperative tranexamic acid in reducing intraoperative and postoperative blood loss in high-risk women undergoing cesarean delivery: a randomized controlled trial. BMC Pregnancy Childbirth. 2022;22(1):201. DOI: 10.1186/s12884–022–04530–4. 55. American College of Obstetricians and Gynecologists’ Committee on Clinical Consensus–Gynecology. General Approaches to Medical Management of Menstrual Suppression: ACOG Clinical Consensus No. 3. Obstet Gynecol. 2022;140(3):528–541. DOI: 10.1097/ AOG.0000000000004899. 56. Shoupe D. The Progestin Revolution: progestins are arising as the dominant players in the tight interlink between contraceptives and bleeding control. Contracept Reprod Med. 2021;6(1):3. DOI: 10.1186/s40834–020–00142–5. 57. Shoupe D. The progestin revolution 2: progestins are now a dominant player in the tight interlink between contraceptive protection and bleeding control-plus more. Contracept Reprod Med. 2023;8(1):48. DOI: 10.1186/s40834–023–00249–5. 58. Buhur A, Ünal Ö. Treatment of abnormal uterine bleeding using levonorgestrel-releasing intrauterine devices: experience from a Turkish tertiary hospital. Eur Rev Med Pharmacol Sci. 2023;27(3):1045–1050. DOI: 10.26355/eurrev_202302_31200. 59. Bryant-Smith AC, Lethaby A, Farquhar C, Hickey M. Antifibrinolytics for heavy menstrual bleeding. Cochrane Database Syst Rev. 2018;4(4):CD000249. DOI: 10.1002/14651858.CD000249.pub2. 60. Zou J, Thornton C, Chambers ES, Rosser EC, Ciurtin C. Exploring the Evidence for an Immunomodulatory Role of Vitamin D in Juvenile and Adult Rheumatic Disease. Front Immunol. 2021;11:616483. DOI: 10.3389/fimmu. 2020.616483. 61. Benito PJ, Alfaro-Magallanes VM, Rael B, Castro EA, Romero-Parra N, Rojo-Tirado MA, et al. Effect of Menstrual Cycle Phase on the Recovery Process of High-Intensity Interval Exercise-A Cross-Sectional Observational Study. Int J Environ Res Public Health. 2023;20(4):3266. DOI: 10.3390/ijerph20043266. 62. Purslow PP. The Structure and Role of Intramuscular Connective Tissue in Muscle Function. Front Physiol. 2020;11:495. DOI: 10.3389/ fphys.2020. 004952023. СУЧАСНИЙ СТАН ПРОБЛЕМИ ПОРУШЕНЬ МЕНСТРУАЛЬНОГО ЦИКЛУ У ЖІНОК РЕПРОДУКТИВНОГО ВІКУ З НЕДИФЕРЕНЦІЙОВАНОЮ СПОЛУЧНОТКАНИННОЮ ДИСПЛАЗІЄЮ (ОГЛЯД ЛІТЕРАТУРИ) Ракитянський І. Ю. Резюме. На основі аналізу доступних джерел наукової літератури представлено огляд проблеми пору- шень менструального циклу у жінок репродуктивного віку та впливу на них захворювань сполучної тканини. Порушення менструального циклу вражають 75 % молодих жінок у розвинених країнах і країнах, що розви- ваються, та становлять більшість захворювань жінок дітородного віку. Патогенез цих станів можна описати як статево-гормонально-імунну асоціацію. Добре відомо, що недиференційована дисплазія сполучної тканини (НДСТ) має негативний вплив на перебіг вагітності та можливий розвиток уражень плода. Ця проблема є в центрі уваги більшості досліджень. Виявлено зв’язок між патологічним перебігом вагітності та фенотипічни - ми ознаками захворювань сполучної тканини в матерів, чиї доньки мають порушення менструальної функції. У молодих жінок із захворюваннями сполучної тканини дисменорея та аномальні маткові кровотечі є най - поширенішими порушеннями менструального циклу, які зумовлені імунною дисрегуляцією, аутоімунними процесами та запаленням. Сучасний підхід до лікування таких пацієнток полягає в розробці індивідуального плану лікування, зважаючи на супутні захворювання, поточні лабораторні показники, патологічні особливос- ті дебюту захворювання та перебігу порушень менструального циклу. Лікування складається з призначення гормональних (синтетичних і природних естрогенів, гонадотропін-рилізинг-гормонів, аналогів прогестерону та гонадотропін-рилізинг-гормону) та негормональних засобів (нестероїдних протизапальних препаратів, транексамової кислоти), а також немедикаментозного лікування (модифікація способу життя, фізична актив- ність, раціональне харчування). На сьогодні відсутня єдина термінологія та загальноприйняті критерії діагнос- тики та оцінки тяжкості НДСТ. Діагностичні методи та критерії НДСТ не стандартизовано порівняно з іншими захворюваннями сполучної тканини. Ведення пацієнтів із захворюваннями сполучної тканини та менстру- альною дисфункцією є комплексним питанням, відповідь на яке базується на оцінці гінекологічних проблем (менструація, фертильність, сексуальність) та мультидисциплінарному підході із залученням фахівців інших спеціальностей. Ключові слова: порушення менструального циклу, жінки репродуктивного віку, недиференційована дис- плазія сполучної тканини, аномальні маткові кровотечі, дисменорея. CURRENT STATE OF THE PROBLEM OF MENSTRUAL CYCLE DISORDERS IN WOMEN OF REPRODUCTIVE AGE WITH UNDIFFERENTIATED CONNECTIVE TISSUE DYSPLASIA (LITERATURE REVIEW) Rakytianskyi I. Yu. Abstract. Based on the analysis of available sources of scientific literature, an overview of the problem of menstrual cycle disorders in women of reproductive age and the impact of connective tissue diseases on them is presented. Menstrual disorders affect 75% of young women in developed and developing countries and constitute the majority of diseases in women of childbearing age. The pathogenesis of these conditions can be described as a sex-hormonal-immune association. Undifferentiated connective tissue dysplasia (UCTD) is known to exert a negative impact on the course of pregnancy and the possible development of fetal impairment. This problem is the focus of most research. The relationship between the pathological course of pregnancy and phenotypic signs of connective tissue diseases in mothers whose daughters have menstrual disorders was revealed. In young women with connective ISSN 2077-4214. Вісник проблем біології і медицини – 2024 – Вип. 1 (172) / Bulletin of problems in biology and medicine – 2024 – Issue 1 (172) 75 ОГЛЯДИ ЛІТЕРАТУРИ / LITERATURE REVIEWS tissue diseases, dysmenorrhea and abnormal uterine bleeding are the most common menstrual disorders, caused by immune dysregulation, autoimmune processes, and inflammation. The modern approach to the treatment of such patients consists in the development of an individual treatment plan, taking into account concomitant diseases, current laboratory findings, pathological features of the onset of the disease and the course of menstrual cycle disorders. Treatment consists of prescribing hormonal (synthetic and natural estrogens, gonadotropin-releasing hormones, progesterone and gonadotropin-releasing hormone analogues) and non-hormonal agents (nonsteroidal anti-inflammatory drugs, tranexamic acid), as well as non-drug treatment (lifestyle modification, physical activity, rational nutrition). To date, there is no unified terminology and generally accepted criteria for diagnosing and assessing the severity of UCTD. Diagnostic methods and criteria for UCTD are not standardized compared to other connective tissue diseases. Management of patients with connective tissue diseases and menstrual dysfunction is a complex issue, the answer to which is based on the assessment of gynecological problems (menstruation, fertility, sexuality) and a multidisciplinary approach involving specialists from other branches. Key words: menstrual cycle irregularities, women of reproductive age, undifferentiated connective tissue dysplasia, abnormal uterine bleeding, dysmenorrhea. ORCID and contributionship: Rakytianskyi I. Yu.: https://orcid.org/0009-0009-5986-6988 ABCDEF ________________________________________________________________ Corresponding author Rakytianskyi Igor Yuriyovych Kharkiv National Medical University Ukraine, 61000, Kharkiv, 4 Nauky Avenue Tel.: +380678033564 E-mail: [email protected] ________________________________________________________________ A – Work concept and design, B – Data collection and analysis, C – Responsibility for statistical analysis, D – Writing the article, E – Critical review, F – Final approval of the article. Received 02.09.2023 Accepted 14.02.2024 DOI 10.29254/2077-4214-2024-1-172-75-81 UDC 616.61:591.3:546.48:612.6 Shatorna V. F. INFLUENCE OF HEAVY METALS ON MORPHO-FUNCTIONAL STATE OF BONE TISSUE Dnipro State Medical University (Dnipro, Ukraine) [email protected] Connection of the publication with planned re- search works. The work was carried out in accordance with the sci- entific theme of DSMU “Morphological and functional features of organs and tissues under the influence of external and internal factors”, state registration number 0120U105219. Introduction. Increasing rates of environmental pollution in indus- trialised countries require studying the impact of envi- ronmental factors on human health. One of the most widespread and dangerous environmental pollutants is heavy metals, which, when ingested by the human body, lead to acute and delayed complications, change the balance of trace element systems, cause diseases or The article presents an analysis of scientific literature on the impact of heavy metal compounds on bone and cartilage tissue. The most common environmental toxicants in the group of heavy metals are mercury, cadmium and lead salts, which, when ingested, accumulate in the body, provoke a hypoxic state and compete with biogenic metals for binding to the active site of many proteins and enzymes, causing a violation of their functions. Modern scientific research has shown that chronic cadmium intoxication creates an imbalance in the process of bone remodelling, in- ducing the development of osteopenia and osteoporosis. The ability of the toxicant to accumulate in the extracellular bone matrix has been experimentally determined, leading to its bioaccumulation and an increase in the half-life of the metal from the body. The accumulation of cadmium in bone tissue leads to a decrease in calcium and zinc levels, which disrupts the basic processes of ossification and negatively affects cartilage and joint tissue. Understanding the mechanisms of osteo- and chondrotoxicity of cadmium will help to find adequate therapy methods for cadmium- induced osteoporosis and prevent the negative impact of the toxicant on bone and cartilage tissue. Studies of the accumulation level of trace elements in bones and their changes under the influence of negative factors are also relevant. It is perspective not only to determine the accumulation level of heavy metal salts but also to search for possible bioantagonists of heavy metal salt accumulation. Key words: bone tissue, femur, lower jaw, microelements, dyselementoses, cartilage tissue, rats, heavy metals, cadmium, zinc, iron, influence, accumulation.

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-pdf

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

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 (59)

Source provenance

openalex
last seen: 2026-06-10T17:14:06.276822+00:00
License: CC0 · commercial use OK