Genetic risk factors for the development of vibration disease (literature review)
- Authors: Mukhammadiyeva G.F.1, Shaihlislamova E.R.1,2, Karimov D.D.1, Karimov D.O.1,3
-
Affiliations:
- Ufa Research Institute of Occupational Health and Human Ecology
- Bashkir State Medical University
- N.A. Semashko National Research Institute of Public Health»
- Issue: Vol 104, No 3 (2025)
- Pages: 340-347
- Section: OCCUPATIONAL HEALTH
- Published: 15.12.2025
- URL: https://ruspoj.com/0016-9900/article/view/678769
- DOI: https://doi.org/10.47470/0016-9900-2025-104-3-340-347
- EDN: https://elibrary.ru/jueqrw
- ID: 678769
Cite item
Abstract
About the authors
Guzel F. Mukhammadiyeva
Ufa Research Institute of Occupational Health and Human Ecology
Email: ufniimt@mail.ru
PhD (Biology), Senior Researcher at the Department of Toxicology and Genetics with the Experimental Clinics for Laboratory Animals, Ufa Research Institute of Occupational Health and Human Ecology, Ufa, 450106, Russian Federation
Elmira R. Shaihlislamova
Ufa Research Institute of Occupational Health and Human Ecology; Bashkir State Medical University
Email: fbun@uniimtech.ru
PhD (Medicine), Director, Ufa Research Institute of Occupational Health and Human Ecology, Ufa, 450106, Russian Federation
Denis D. Karimov
Ufa Research Institute of Occupational Health and Human Ecology
Email: lich-tsar@mail.ru
PhD (Biology), Senior Researcher at the Department of Toxicology and Genetics with the Experimental Clinics for Laboratory Animals, Ufa Research Institute of Occupational Health and Human Ecology, Ufa, 450106, Russian Federation
Denis O. Karimov
Ufa Research Institute of Occupational Health and Human Ecology; N.A. Semashko National Research Institute of Public Health»
Email: karimovdo@gmail.com
PhD (Medicine), Head of the Department of Toxicology and Genetics with the Experimental Clinics for Laboratory Animals, Ufa Research Institute of Occupational Health and Human Ecology, Ufa, 450106, Russian Federation
References
- Мухина Н.А., Бабанова С.А. Профессиональные болезни. М.: ГЭОТАР-Медиа; 2018.
- Шайхлисламова Э.Р., Валеева Э.Т., Волгарева А.Д., Кондрова Н.С., Галимова Р.Р., Масягутова Л.М. Профессиональные заболевания от воздействия физических факторов в Республике Башкортостан. Медицина труда и экология человека. 2018; (4): 63–9. https://elibrary.ru/ypnmfv
- Бабанов С.А., Азовскова Т.А., Вакурова Н.В., Бараева Р.А. О современных аспектах классификации вибрационной болезни. Терапевт. 2019; (4): 21–7. https://elibrary.ru/zcqfgh
- Бабанов С.А., Азовскова Т.А., Кирюшина Т.М., Лотков В.С., Агар-кова А.С., Безшанова А.Е. и др. Вибрационная болезнь: эволюция классификационных представлений, диагностика, вопросы экспертизы. Врач. 2023; 34(4): 11–7. https://doi.org/10.29296/25877305-2023-04-02 https://elibrary.ru/ezyjlk
- Скоромец А.А. Туннельные компрессионно-ишемические моно- и мультиневропатии. М.: ГЭОТАР-Медиа; 2022.
- Бабанов С.А., Азовскова Т.А., Бараева Р.А. Влияние производственной вибрации на организм работников всех отраслей. Охрана труда и техника безопасности в сельском хозяйстве. 2020; (2): 35–44. https://elibrary.ru/bczcbh
- Morioka M., Whitehouse D.J., Griffin M.J. Vibrotactile thresholds at the fingertip, volar forearm, large toe, and heel. Somatosens Mot. Res. 2008; 25(2): 101–12. https://doi.org/10.1080/08990220802045574
- Thompson A.M., House R., Krajnak K., Eger T. Vibration-white foot: a case report. Occup. Med (Lond.). 2010; 60(7): 572–4. https://doi.org/10.1093/occmed/kqq107
- House R., Jiang D., Thompson A., Eger T., Krajnak K., Sauvé J., et al. Vasospasm in the feet in workers assessed for HAVS. Occup. Med (Lond). 2011; 61(2): 115–20. https://doi.org/10.1093/occmed/kqq191
- Eger T., Thompson A., Leduc M., Krajnak K., Goggins K., Godwin A., et al. Vibration induced white-feet: overview and field study of vibration exposure and reported symptoms in workers. Work. 2014; 47(1): 101–10. https://doi.org/10.3233/WOR-131692
- Pyykkö I., Färkkilä M., Inaba R., Starck J., Pekkarinen J. Effect of hand-arm vibration on inner ear and cardiac functions in man. Nagoya J. Med. Sci. 1994; 57(Suppl.): 113–9.
- Harada N. Autonomic nervous function of hand-arm vibration syndrome patients. Nagoya J. Med. Sci. 1994; 57(Suppl.): 77–85.
- Жукова А.Г., Горохова Л.Г. Ретроспектива молекулярно-генетических исследований производственно обусловленной патологии. Медицина в Кузбассе. 2020; 20(3): 5–11. https://doi.org/10.24412/2687-0053-2021-3-5-11 https://elibrary.ru/xwxgem
- Баранов В.С. Геномика и предиктивная медицина. Сибирский журнал клинической и экспериментальной медицины. 2021; 36(4): 14–28. https://doi.org/10.29001/2073-8552-2021-36-4-14-28 https://elibrary.ru/kkkzma
- Ядыкина Т.К., Коротенко О.Ю., Семенова Е.А., Бугаева М.С., Жукова А.Г. Исследование генов глутатион-S-трансфераз (GST) T1 и M1 у работников алюминиевой промышленности с коморбидной кардио-васкулярной патологией. Медицина труда и промышленная экология. 2023; 63(8): 519–27. https://doi.org/10.31089/1026-9428-2023-63-8-519-527 https://elibrary.ru/vfnyqa
- Mattagajasingh I., Kim C.S., Naqvi A., Yamamori T., Hoffman T.A., Jung S.B., et al. SIRT1 promotes endothelium-dependent vascular relaxation by activating endothelial nitric oxide synthase. Proc. Natl. Acad Sci. USA. 2007; 104(37): 14855–60. https://doi.org/10.1073/pnas.0704329104
- Voelter-Mahlknecht S., Rossbach B., Schleithoff C., Dransfeld C.L., Letzel S., Mahlknecht U. Sirtuin1 single nucleotide polymorphism (A2191G) is a diagnostic marker for vibration-induced white finger disease. Clin. Epigenetics. 2012; 4(1): 18. https://doi.org/10.1186/1868-7083-4-18
- Спицын В.А., Кузьмина Л.П., Макаров С.В., Карапетян М.К., Попова М.В., Бычковская Л.С. и др. Особенности распространения полиморфизма генов ACE, CHIT1, PON1, SIRT1 и NOS3 у больных вибрационной болезнью. Медицинская генетика. 2015; 14(5): 23–7. https://elibrary.ru/unuhoz
- Ahmad A., Dempsey S.K., Daneva Z., Azam M., Li N., Li P.L., et al. Role of nitric oxide in the cardiovascular and renal systems. Int. J. Mol. Sci. 2018; 19(9): 2605. https://doi.org/10.3390/ijms19092605
- Oliveira-Paula G.H., Lacchini R., Tanus-Santos J.E. Endothelial nitric oxide synthase: From biochemistry and gene structure to clinical implications of NOS3 polymorphisms. Gene. 2016; 575(2 Pt. 3): 584–99. https://doi.org/10.1016/j.gene.2015.09.061
- Yao Y.S., Chang W.W., Jin Y.L., He L.P. An updated meta-analysis of endothelial nitric oxide synthase gene: three well-characterized polymorphisms with ischemic stroke. Gene. 2013; 528(2): 84–92. https://doi.org/10.1016/j.gene.2013.06.047
- Rai H., Parveen F., Kumar S., Kapoor A., Sinha N. Association of endothelial nitric oxide synthase gene polymorphisms with coronary artery disease: an updated meta-analysis and systematic review. PLoS One. 2014; 9(11): e113363. https://doi.org/10.1371/journal.pone.0113363
- Герасименко О.Н., Шпагина Л.А., Горбунова А.М., Шпагин И.С., Сергеева Я.С. Клинико-функциональная и молекулярная характеристика коморбидной патологии (вибрационная болезнь в сочетании с артериальной гипертензией). Атеросклероз. 2022; 18(1): 68–75. https://elibrary.ru/ydjovz
- Потеряева Е.Л., Смирнова Е.Л., Максимов В.Н., Колесник К.Н., Никифорова Н.Г., Песков С.А. Роль индивидуальных факторов риска в формировании особенностей течения основных форм профессиональных заболеваний в послеконтактном периоде. Сибирский научный медицинский журнал. 2017; 37(1): 41–7. https://elibrary.ru/xuwewx
- Шпагина Л.А., Герасименко О.Н., Дробышев В.А., Кузнецова Г.В. Полиморфизм генов-предикторов высокого риска сосудистых осложнений при вибрационной болезни в сочетании с артериальной гипертензией. Санитарный врач. 2017; (5–6): 60–3. https://elibrary.ru/zmdufj
- Blanquart S., Borowiec A.S., Delcourt P., Figeac M., Emerling C.A., Meseguer A.S., et al. Evolution of the human cold/menthol receptor, TRPM8. Mol. Phylogenet. Evol. 2019; 136: 104–18. https://doi.org/10.1016/j.ympev.2019.04.011
- Wang M., Gu Y., Meng S., Kang L., Yang J., Sun D., et al. Association between TRP channels and glutamatergic synapse gene polymorphisms and migraine and the comorbidities anxiety and depression in a Chinese population. Front. Genet. 2023; 14: 1158028. https://doi.org/10.3389/fgene.2023.1158028
- He J., Kelly T.N., Zhao Q., Li H., Huang J., Wang L., et al. Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese. Circ. Cardiovasc. Genet. 2013; 6(6): 598–607. https://doi.org/10.1161/CIRCGENETICS.113.000307
- Смирнова Е.Л., Потеряева Е.Л., Максимов В.Н., Несина И.А. Концепция индивидуального риска в формировании и особенностях течения вибрационной болезни. Медицина в Кузбассе. 2020; 19(1): 35–41. https://elibrary.ru/ddazub
- Abd El-Aziz T.A., Mohamed R.H. Influence of MTHFR C677T gene polymorphism in the development of cardiovascular disease in Egyptian patients with rheumatoid arthritis. Gene. 2017; 610: 127–32. https://doi.org/10.1016/j.gene.2017.02.015
- Luo Z., Lu Z., Muhammad I., Chen Y., Chen Q., Zhang J., et al. Associations of the MTHFR rs1801133 polymorphism with coronary artery disease and lipid levels: a systematic review and updated meta-analysis. Lipids Health Dis. 2018; 17(1): 191. https://doi.org/10.1186/s12944-018-0837-y
- Zhu J., Wang Z., Tao L., Han L., Huang Q., Fang X., et al. MTHFR gene polymorphism association with psoriatic arthritis risk and the efficacy and hepatotoxicity of methotrexate in psoriasis. Front. Med. (Lausanne). 2022; 9: 869912. https://doi.org/10.3389/fmed.2022.869912
- Liu Y., Xu C., Wang Y., Yang C., Pu G., Zhang L., et al. Association analysis of MTHFR (rs1801133 and rs1801131) and MTRR (rs1801394) gene polymorphisms towards the development of hypertension in the Bai population from Yunnan, China. Clin. Exp. Hypertens. 2023; 45(1): 2206066. https://doi.org/10.1080/10641963.2023.2206066
- Zhao L., Li T., Dang M., Li Y., Fan H., Hao Q., et al. Association of methylenetetrahydrofolate reductase (MTHFR) rs1801133 (677C>T) gene polymorphism with ischemic stroke risk in different populations: An updated meta-analysis. Front. Genet. 2023; 13: 1021423. https://doi.org/10.3389/fgene.2022.1021423
- Rigat B., Hubert C., Alhenc-Gelas F., Cambien F., Corvol P., Soubrier F. An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. J. Clin. Invest. 1990; 86(4): 1343–6. https://doi.org/10.1172/JCI114844
- Patel D.D., Parchwani D.N., Dikshit N., Parchwani T. Analysis of the pattern, alliance and risk of rs1799752 (ACE I/D Polymorphism) with essential hypertension. Indian J. Clin. Biochem. 2022; 37(1): 18–28. https://doi.org/10.1007/s12291-020-00927-0
- Luo S., Shi C., Wang F., Wu Z. Association between the Angiotensin-Converting Enzyme (ACE) genetic polymorphism and diabetic retinopathy-a meta-analysis comprising 10,168 subjects. Int. J. Environ. Res. Public Health. 2016; 13(11): 1142. https://doi.org/10.3390/ijerph13111142
- Gouissem I., Midani F., Soualmia H., Bouchemi M., Ouali S., Kallele A., et al. Contribution of the ACE (rs1799752) and CYP11B2 (rs1799998) gene polymorphisms to atrial fibrillation in the Tunisian population. Biol. Res. Nurs. 2022; 24(1): 31–9. https://doi.org/10.1177/10998004211029376
- Ramanathan B., Nagarajan G., Velayutham K. Association of angiotensin‑converting enzyme gene polymorphism (rs1799752) with type 2 diabetes mellitus, hypertension, and chronic kidney disease and its clinical relevance: A preliminary study from South India. Chron. Diabetes Res. Pract. 2022; 1(2): 51–7. https://doi.org/10.4103/cdrp.cdrp_6_22
- Коляскина М.М., Анварул Н.А., Ликонцева А.С. Роль полиморфизмов генов Cyp1A1 и ЕРНХ1 в механизмах окислительного стресса у больных вибрационной болезнью. Медицина труда и промышленная экология. 2019; 59(9): 652. https://doi.org/10.31089/1026-9428-2019-59-9-652-653 https://elibrary.ru/qppogo
- Кононыхина Н.В., Бачинский О.Н., Бабкина В.И., Трубникова Е.В., Иванов В.П. Вовлеченность полиморфных вариантов гена EPHX1 в формирование хронической патологии легких профессионального и непрофессионального генеза в популяции жителей Курской области. Пульмонология. 2011; (5): 25–8. https://elibrary.ru/okmtvn
- Безрукавникова Л.М., Анохин Н.Н., Цидильковская Э.С. Ассоциация молекулярно-генетических маркеров и показателей оксидативного стресса у работающих в контакте с пылью асбеста. Медицина труда и промышленная экология. 2019; 59(9): 560. https://doi.org/10.31089/1026-9428-2019-59-9-560-561 https://elibrary.ru/znsclh
- Zhang M., Wu J.M., Zhang Q.S., Yan D.W., Ren L.J., Li W.P. The association of CYP1A1 genetic polymorphisms and additional gene-gene interaction with ischemic stroke in the eastern Han of China. Neurol. Sci. 2016; 37(10): 1679–84. https://doi.org/10.1007/s10072-016-2652-4.
- Peng D.D., Xie W., Yu Z.X. Impact of interaction between CYP1A1 genetic polymorphisms and smoking on coronary artery disease in the Han of China. Clin. Exp. Hypertens. 2017; 39(4): 339–43. https://doi.org/10.1080/10641963.2016.1259326
- Sun T., Gao Y., Tan W., Ma S., Shi Y., Yao J., et al. A six-nucleotide insertion-deletion polymorphism in the CASP8 promoter is associated with susceptibility to multiple cancers. Nat. Genet. 2007; 39(5): 605–13. https://doi.org/10.1038/ng2030
- Максимов В.Н., Пархоменко О.М., Ложкина Н.Г., Гуражева А.А., Максимова С.В., Иванова А.А. Некоторые молекулярно-генетические маркеры прогрессирующего атеросклероза у пациентов с ишемической болезнью сердца. Атеросклероз. 2022; 18(1): 6–13. https://elibrary.ru/fivrqv
- Gundapaneni K.K., Shyamala N., Galimudi R.K., Kupsal K., Gantala S.R., Padala C., et al. Polymorphic variants of Caspase genes (8 & 3) in the risk prediction of coronary artery disease. Gene. 2017; 627: 278–83. https://doi.org/10.1016/j.gene.2017.06.035
- Brown K.L., Seale K.B., El Khoury L.Y., Posthumus M., Ribbans W.J., Raleigh S.M., et al. Polymorphisms within the COL5A1 gene and regulators of the extracellular matrix modify the risk of Achilles tendon pathology in a British case-control study. J. Sports Sci. 2017; 35(15): 1475–83. https://doi.org/10.1080/02640414.2016.1221524
- Rahim M., Mannion S., Klug B., Hobbs H., van der Merwe W., Posthumus M., et al. Modulators of the extracellular matrix and risk of anterior cruciate ligament ruptures. J. Sci. Med. Sport. 2017; 20(2): 152–8. https://doi.org/10.1016/j.jsams.2016.07.003
- Смирнова Е.Л., Потеряева Е.Л., Иванова А.А., Максимов В.Н., Фунтикова И.С., Несина И.А. Ассоциация ID полиморфизма гена CASP8 с вибрационной болезнью. Медицина труда и промышленная экология. 2022; 62(12): 809–13. https://doi.org/10.31089/1026-9428-2022-62-12-809-813 https://elibrary.ru/srspyj
- Rey J., Cretel E., Jean R., Pastor M.J., Durand J.M. Serotonin reuptake inhibitors, Raynaud’s phenomenon and erythromelalgia. Rheumatology (Oxford). 2003; 42(4): 601–2. https://doi.org/10.1093/rheumatology/keg137
- Chen Q., Lang L., Xiao B., Lin H., Yang A., Li H., et al. HTR1B gene variants associate with the susceptibility of Raynauds’ phenomenon in workers exposed hand-arm vibration. Clin. Hemorheol. Microcirc. 2016; 63(4): 335–47. https://doi.org/10.3233/CH-152021
- Herrick A.L. Pathogenesis of Raynaud’s phenomenon. Rheumatology (Oxford). 2005; 44(5): 587–96. https://doi.org/10.1093/rheumatology/keh552
- Vos M.J., Hageman J., Carra S., Kampinga H.H. Structural and functional diversities between members of the human HSPB, HSPH, HSPA, and DNAJ chaperone families. Biochemistry. 2008; 47(27): 7001–11. https://doi.org/10.1021/bi800639z
- Srivastava K., Narang R., Bhatia J., Saluja D. Expression of heat shock protein 70 gene and its correlation with inflammatory markers in essential hypertension. PLoS One. 2016; 11(3): e0151060. https://doi.org/10.1371/journal.pone.0151060
- Hrira M.Y., Chkioua L., Slimani A., Chahed H., Mosbah H., Khaldoun H.B., et al. Hsp70-2 gene polymorphism: susceptibility implication in Tunisian patients with coronary artery disease. Diagn. Pathol. 2012; 7(1): 88. https://doi.org/10.1186/1746-1596-7-88
- Mehramiz M., Hassanian S.M., Mardan-Nik M., Pasdar A., Jamialahmadi K., Fiuji H., et al. The interaction between a HSP-70 gene variant with dietary calories in determining serum markers of inflammation and cardiovascular risk. Clin. Nutr. 2018; 37(6 Pt. A): 2122–6. https://doi.org/10.1016/j.clnu.2017.10.006
- Черняк Ю.И., Меринова А.П. Полиморфные локусы генов-кандидатов у пациентов с профессиональными болезнями. Гигиена и санитария. 2023; 102(7): 689–94. https://doi.org/10.47470/0016-9900-2023-102-7-689-694 https://elibrary.ru/glwiya
- Chernyak Y.I., Kudaeva I.V. Analysis of HSPA1B (+1267A>G) genetic polymorphism in patients with vibration disease in combination with metabolic syndrome. Bull. Exp. Biol. Med. 2021; 171(3): 375–8. https://doi.org/10.1007/s10517-021-05231-2
- Virtanen I.M., Karppinen J., Taimela S., Ott J., Barral S., Kaikkonen K., et al. Occupational and genetic risk factors associated with intervertebral disc disease. Spine (Phila Pa 1976). 2007; 32(10): 1129–34. https://doi.org/10.1097/01.brs.0000261473.03274.5c
- Solovieva S., Leino-Arjas P., Saarela J., Luoma K., Raininko R., Riihimäki H. Possible association of interleukin 1 gene locus polymorphisms with low back pain. Pain. 2004; 109(1-2): 8–19. https://doi.org/10.1016/j.pain.2003.10.020
- Noponen-Hietala N., Virtanen I., Karttunen R., Schwenke S., Jakkula E., Li H., et al. Genetic variations in IL6 associate with intervertebral disc disease characterized by sciatica. Pain. 2005; 114(1–2): 186–94. https://doi.org/10.1016/j.pain.2004.12.015
- Zayed N., Afif H., Chabane N., Mfuna-Endam L., Benderdour M., Martel-Pelletier J., et al. Inhibition of interleukin-1beta-induced matrix metalloproteinases 1 and 13 production in human osteoarthritic chondrocytes by prostaglandin D2. Arthritis Rheum. 2008; 58(11): 3530–40. https://doi.org/10.1002/art.23958
- Dinarello C.A. Immunological and inflammatory functions of the interleukin-1 family. Annu. Rev. Immunol. 2009; 27: 519–50. https://doi.org/10.1146/annurev.immunol.021908.132612
- Dinarello C.A. Interleukin-1 in the pathogenesis and treatment of inflammatory diseases. Blood. 2011; 117(14): 3720–32. https://doi.org/10.1182/blood-2010-07-273417
- Gabay C., Lamacchia C., Palmer G. IL-1 pathways in inflammation and human diseases. Nat. Rev. Rheumatol. 2010; 6(4): 232–41. https://doi.org/10.1038/nrrheum.2010.4
- Le Maitre C.L., Hoyland J.A., Freemont A.J. Catabolic cytokine expression in degenerate and herniated human intervertebral discs: IL-1beta and TNFalpha expression profile. Arthritis Res. Ther. 2007; 9(4): R77. https://doi.org/10.1186/ar2275
- Le Maitre C.L., Freemont A.J., Hoyland J.A. The role of interleukin-1 in the pathogenesis of human intervertebral disc degeneration. Arthritis Res. Ther. 2005; 7(4): R732–45. https://doi.org/10.1186/ar1732
- Burke J.G., Watson R.W., McCormack D., Dowling F.E., Walsh M.G., Fitzpatrick J.M. Intervertebral discs which cause low back pain secrete high levels of proinflammatory mediators. J. Bone Joint Surg. Br. 2002; 84(2): 196–201. https://doi.org/10.1302/0301-620x.84b2.12511
- Risbud M.V., Shapiro I.M. Role of cytokines in intervertebral disc degeneration: pain and disc content. Nat. Rev. Rheumatol. 2014; 10(1): 44–56. https://doi.org/10.1038/nrrheum.2013.160
- Ye W., Ma R.F., Su P.Q., Huang D.S., Liu S.L., Chen W.J., et al. Association of single nucleotide polymorphisms of IL-1b with lumbar disc disease. Yi Chuan. 2007; 29(8): 923–8. (in Chinese)
- Kim S.H., Mok J.W., Kim H.S., Joo C.K. Association of –31T>C and –511 C>T polymorphisms in the interleukin 1 beta (IL1B) promoter in Korean keratoconus patients. Mol. Vis. 2008; 14: 2109–16.
- Choi J., Choi S.A., Kim S.Y., Kim H., Lim B.C., Hwang H., et al. Association analysis of interleukin-1β, interleukin-6, and HMGB1 variants with postictal serum cytokine levels in children with febrile seizure and generalized epilepsy with febrile seizure plus. J. Clin. Neurol. 2019; 15(4): 555–63. https://doi.org/10.3988/jcn.2019.15.4.555
- Rong H., He X., Wang L., Bai M., Jin T., Wang Y., et al. Association between IL1B polymorphisms and the risk of rheumatoid arthritis. Int. Immunopharmacol. 2020; 83: 106401. https://doi.org/10.1016/j.intimp.2020.106401
- Wang Z., Song X., Fang Q., Xia W., Luo A. Polymorphism of IL-1β rs16944(T/C) associated with serum levels of IL-1β and subsequent stimulation of extracellular matrix degradation affects intervertebral disk degeneration susceptibility. Ther. Clin. Risk Manag. 2021; 17: 453–61. https://doi.org/10.2147/TCRM.S308653
- Kishimoto T. Interleukin-6: from basic science to medicine – 40 years in immunology. Annu. Rev. Immunol. 2005; 23: 1–21. https://doi.org/10.1146/annurev.immunol.23.021704.115806
- Fishman D., Faulds G., Jeffery R., Mohamed-Ali V., Yudkin J.S., Humphries S., et al. The effect of novel polymorphisms in the interleukin-6 (IL-6) gene on IL-6 transcription and plasma IL-6 levels, and an association with systemic-onset juvenile chronic arthritis. J. Clin. Invest. 1998; 102(7): 1369–76. https://doi.org/10.1172/JCI2629
- Guan Y., Wang S., Wang J., Meng D., Wu H., Wei Q., et al. Gene polymorphisms and expression levels of interleukin-6 and interleukin-10 in lumbar disc disease: a meta-analysis and immunohistochemical study. J. Orthop. Surg. Res. 2020; 15(1): 54. https://doi.org/10.1186/s13018-020-01588-8
- Amr K., El-Awady R., Raslan H. Assessment of the –174G/C (rs1800795) and –572G/C (rs1800796) interleukin 6 gene polymorphisms in Egyptian patients with rheumatoid arthritis. Open Access Maced. J. Med. Sci. 2016; 4(4): 574–7. https://doi.org/10.3889/oamjms.2016.110
- Dar S.A., Haque S., Mandal R.K., Singh T., Wahid M., Jawed A., et al. Interleukin-6-174G > C (rs1800795) polymorphism distribution and its association with rheumatoid arthritis: A case-control study and meta-analysis. Autoimmunity. 2017; 50(3): 158–69. https://doi.org/10.1080/08916934.2016.1261833
- Sun G., Ba C.L., Gao R., Liu W., Ji Q. Association of IL-6, IL-8, MMP-13 gene polymorphisms with knee osteoarthritis susceptibility in the Chinese Han population. Biosci. Rep. 2019; 39(2): BSR20181346. https://doi.org/10.1042/BSR20181346
- Kroeger K.M., Carville K.S., Abraham L.J. The -308 tumor necrosis factor-alpha promoter polymorphism effects transcription. Mol. Immunol. 1997; 34(5): 391–9. https://doi.org/10.1016/s0161-5890(97)00052-7
- Lee S., Yoo J.I., Kang Y.J. Integrative analyses of genes related to femoral head osteonecrosis: an umbrella review of systematic reviews and meta-analyses of observational studies. J. Orthop. Surg. Res. 2022; 17(1): 182. https://doi.org/10.1186/s13018-022-03079-4
- Malysheva I.E., Topchieva L.V., Balan O.V., Marusenko I.M., Barysheva O.Y., Kurbatova I.V. Analysis of the association of TNF –238G>A gene polymorphism with the risk of rheumatoid arthritis development in Russian population in the Republic of Karelia. Bull. Exp. Biol. Med. 2018; 165(5): 674–7. https://doi.org/10.1007/s10517-018-4239-y
- Loures M.A.R., Alves H.V., de Moraes A.G., Santos T.D.S., Lara F.F., Neves J.S.F., et al. Association of TNF, IL12, and IL23 gene polymorphisms and psoriatic arthritis: meta-analysis. Expert Rev. Clin. Immunol. 2019; 15(3): 303–13. https://doi.org/10.1080/1744666X.2019.1564039
- Krajnak K., Dong R.G., Flavahan S., Welcome D., Flavahan N.A. Acute vibration increases alpha2C-adrenergic smooth muscle constriction and alters thermosensitivity of cutaneous arteries. J. Appl. Physiol. (1985). 2006; 100(4): 1230–7. https://doi.org/10.1152/japplphysiol.00761.2005
- Welcome D.E., Krajnak K., Kashon M.L., Dong R.G. An investigation on the biodynamic foundation of a rat tail vibration model. Proc. Inst. Mech. Eng. H. 2008; 222(7): 1127–41. https://doi.org/10.1243/09544119JEIM419
- Krajnak K., Miller G.R., Waugh S., Johnson C., Li S., Kashon M.L. Characterization of frequency-dependent responses of the vascular system to repetitive vibration. J. Occup. Environ. Med. 2010; 52(6): 584–94. https://doi.org/10.1097/JOM.0b013e3181e12b1f
- Wu J.Z., An K.N., Cutlip R.G., Krajnak K., Welcome D., Dong R.G. Analysis of musculoskeletal loading in an index finger during tapping. J. Biomech. 2008; 41(3): 668–76. https://doi.org/10.1016/j.jbiomech.2007.09.025
- Xu X.S., Riley D.A., Persson M., Welcome D.E., Krajnak K., Wu J.Z., et al. Evaluation of anti-vibration effectiveness of glove materials using an animal model. Biomed. Mater. Eng. 2011; 21(4): 193–211. https://doi.org/10.3233/BME-2011-0669
- Krajnak K., Miller G.R., Waugh S. Contact area affects frequency-dependent responses to vibration in the peripheral vascular and sensorineural systems. J. Toxicol. Environ. Health A. 2018; 81(1–3): 6–19. https://doi.org/10.1080/15287394.2017.1401022
- Afonso V., Champy R., Mitrovic D., Collin P., Lomri A. Reactive oxygen species and superoxide dismutases: role in joint diseases. Joint Bone Spine. 2007; 74(4): 324–9. https://doi.org/10.1016/j.jbspin.2007.02.002
- Xie Y.G., Mu H.J., Li Z., Ma J.H., Wang Y.L. Supression of chronic central pain by superoxide dismutase in rats with spinal cord injury: Inhibition of the NMDA receptor implicated. Exp. Ther. Med. 2014; 8(4): 1137–41. https://doi.org/10.3892/etm.2014.1878
- Wan X.S., Devalaraja M.N., St Clair D.K. Molecular structure and organization of the human manganese superoxide dismutase gene. DNA Cell Biol. 1994; 13(11): 1127–36. https://doi.org/10.1089/dna.1994.13.1127
- Hernandez-Saavedra D., McCord J.M. Association of a new intronic polymorphism of the SOD2 gene (G1677T) with cancer. Cell Biochem. Funct. 2009; 27(4): 223–7. https://doi.org/10.1002/cbf.1560
- Işikli A., Kubat-Üzüm A., Satman İ., Matur Z., Öge A.E., Küçükali C.İ., et al. A SOD2 polymorphism is associated with abnormal quantitative sensory testing in type 2 diabetic patients. Noro Psikiyatr. Ars. 2018; 55(3): 276–9. https://doi.org/10.29399/npa.23027
- Sutton A., Khoury H., Prip-Buus C., Cepanec C., Pessayre D., Degoul F. The Ala16Val genetic dimorphism modulates the import of human manganese superoxide dismutase into rat liver mitochondria. Pharmacogenetics. 2003; 13(3): 145–57. https://doi.org/10.1097/01.fpc.0000054067.64000.8f
- Fujimoto H., Taguchi J., Imai Y., Ayabe S., Hashimoto H., Kobayashi H., et al. Manganese superoxide dismutase polymorphism affects the oxidized low-density lipoprotein-induced apoptosis of macrophages and coronary artery disease. Eur. Heart J. 2008; 29(10): 1267–74. https://doi.org/10.1093/eurheartj/ehm500
- Valenti L., Conte D., Piperno A., Dongiovanni P., Fracanzani A.L., Fraquelli M., et al. The mitochondrial superoxide dismutase A16V polymorphism in the cardiomyopathy associated with hereditary haemochromatosis. J. Med. Genet. 2004; 41(12): 946–50. https://doi.org/10.1136/jmg.2004.019588
- Santl Letonja M., Letonja M., Ikolajević-Starcević J.N., Petrovic D. Association of manganese superoxide dismutase and glutathione S-transferases genotypes with carotid atherosclerosis in patients with diabetes mellitus type 2. Int. Angiol. 2012; 31(1): 33–41.
- Souiden Y., Mallouli H., Meskhi S., Chaabouni Y., Rebai A., Chéour F., et al. MnSOD and GPx1 polymorphism relationship with coronary heart disease risk and severity. Biol. Res. 2016; 49: 22. https://doi.org/10.1186/s40659-016-0083-6
- Xu M., Xu M., Han L., Yuan C., Mei Y., Zhang H., et al. Role for functional SOD2 polymorphism in pulmonary arterial hypertension in a Chinese population. Int. J. Environ. Res. Public Health. 2017; 14(3): 266. https://doi.org/10.3390/ijerph14030266
- Synowiec E., Wigner P., Cichon N., Watala C., Czarny P., Saluk-Bijak J., et al. Single-nucleotide polymorphisms in oxidative stress-related genes and the risk of a stroke in a Polish population – a preliminary study. Brain Sci. 2021; 11(3): 391. https://doi.org/10.3390/brainsci11030391
- Потеряева Е.Л., Смирнова Е.Л., Никифорова Н.Г. Прогнозирование формирования и течения вибрационной болезни на основе изучения геннометаболических маркеров. Медицина труда и промышленная экология. 2015; (6): 19–22. https://elibrary.ru/ubemit
- Govindaraju S.R., Curry B.D., Bain J.L., Riley D.A. Comparison of continuous and intermittent vibration effects on rat-tail artery and nerve. Muscle Nerve. 2006; 34(2): 197–204. https://doi.org/10.1002/mus.20578
- Krajnak K., Riley D.A., Wu J., McDowell T., Welcome D.E., Xu X.S., et al. Frequency-dependent effects of vibration on physiological systems: experiments with animals and other human surrogates. Ind. Health. 2012; 50(5): 343–53. https://doi.org/10.2486/indhealth.ms1378
- Krajnak K., Raju S.G., Miller G.R., Johnson C., Waugh S., Kashon M.L., et al. Long-term daily vibration exposure alters current perception threshold (CPT) sensitivity and myelinated axons in a rat-tail model of vibration-induced injury. J. Toxicol. Environ. Health A. 2016; 79(3): 101–11. https://doi.org/10.1080/15287394.2015.1104272
- Krajnak K., Waugh S. Systemic Effects of segmental vibration in an animal model of hand-arm vibration syndrome. J. Occup. Environ. Med. 2018; 60(10): 886–95. https://doi.org/10.1097/JOM.0000000000001396
- Cauwe B., Van den Steen P.E., Opdenakker G. The biochemical, biological, and pathological kaleidoscope of cell surface substrates processed by matrix metalloproteinases. Crit. Rev. Biochem. Mol. Biol. 2007; 42(3): 113–85. https://doi.org/10.1080/10409230701340019
- Zeng G.Q., Chen A.B., Li W., Song J.H., Gao C.Y. High MMP-1, MMP-2, and MMP-9 protein levels in osteoarthritis. Genet. Mol. Res. 2015; 14(4): 14811–22. https://doi.org/10.4238/2015.November.18.46
- Zhang C., Chen L., Gu Y. Polymorphisms of MMP-1 and MMP-3 and susceptibility to rheumatoid arthritis. A meta-analysis. Z. Rheumatol. 2015; 74(3): 258–62. https://doi.org/10.1007/s00393-014-1537-2
- Milaras C., Lepetsos P., Dafou D., Potoupnis M., Tsiridis E. Association of matrix metalloproteinase (MMP) gene polymorphisms with knee osteoarthritis: a review of the literature. Cureus. 2021; 13(10): e18607. https://doi.org/10.7759/cureus.18607
- Luo Y., Wang J., Pei J., Rong Y., Liu W., Tang P., et al. Interactions between the MMP-3 gene rs591058 polymorphism and occupational risk factors contribute to the increased risk for lumbar disk herniation: A case-control study. J. Clin. Lab. Anal. 2020; 34(7): e23273. https://doi.org/10.1002/jcla.23273
- Lesauskaite V., Sinkūnaite G., Benetis R., Grabauskas V., Vaskelyte J., Smalinskiene A., et al. Matrix metalloproteinase-3 gene polymorphism and dilatative pathology of ascending thoracic aorta. Medicina (Kaunas). 2008; 44(5): 386–91.
- Chakraborti S., Mandal M., Das S., Mandal A., Chakraborti T. Regulation of matrix metalloproteinases: an overview. Mol. Cell Biochem. 2003; 253(1–2): 269–85. https://doi.org/10.1023/a:1026028303196
- Malemud C.J. Matrix metalloproteinases (MMPs) in health and disease: an overview. Front. Biosci. 2006; 11: 1696–701. https://doi.org/10.2741/1915
- Eser B., Eser O., Yuksel Y., Aksit H., Karavelioglu E., Tosun M., et al. Effects of MMP-1 and MMP-3 gene polymorphisms on gene expression and protein level in lumbar disc herniation. Genet. Mol. Res. 2016; 15(3). https://doi.org/10.4238/gmr.15038669
- McCann M.R., Patel P., Pest M.A., Ratneswaran A., Lalli G., Beaucage K.L., et al. Repeated exposure to high-frequency low-amplitude vibration induces degeneration of murine intervertebral discs and knee joints. Arthritis Rheumatol. 2015; 67(8): 2164–75. https://doi.org/10.1002/art.39154
- McCann M.R., Veras M.A., Yeung C., Lalli G., Patel P., Leitch K.M., et al. Whole-body vibration of mice induces progressive degeneration of intervertebral discs associated with increased expression of Il-1β and multiple matrix degrading enzymes. Osteoarthritis Cartilage. 2017; 25(5): 779–89. https://doi.org/10.1016/j.joca.2017.01.004
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