Clinical significance of genetic and inflammatory markers of bone metabolism in patients with chronic obstructive pulmonary disease and osteoporosis


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

Background. Pulmonogenic osteopenia, which develops in patients with chronic obstructive pulmonary disease (COPD), is the result of systemic inflammation. It leads to the production of pro-inflammatory cytokines that contribute to a decrease in bone mineral density; and in genetically predisposed patients, the development of osteoporosis leads to early disability due to low-energy fractures and a decrease in the quality of life. Objective. Determination of correlations between bone density and genetic, inflammatory and metabolic markers in patients with COPD and osteoporosis. Methods. The study involved 100 patients: 80 with a confirmed diagnosis of COPD and osteoporosis, and 20 were included in the control group. The studied groups underwent a genetic study for the detection of vitamin D receptor (VDR3) gene and the calcitonin receptor gene CALCR polymorphisms; determination of indicators of systemic inflammation: tumor necrosis factor alpha (TNF-а), C-reactive protein (CRP), interleukin-2 (IL-2), interleukin-4 (IL-4); determination of markers of bone resorption: terminal C-telopeptide of type 1 collagen (ß-CTx) and parathyroid hormone (PTH). The reliability of the results obtained was confirmed using the Statistica 13.2 software. Results. In patients with COPD and osteoporosis, a high pathological allele frequency was revealed: Bb - 49.1%, bb - 26.7% for VDR3; TS - 26.7%, CC - 53.9% for CALCR. The levels of markers of systemic inflammation and bone metabolism were significantly higher in the group of patients with COPD and osteoporosis, and there was a clear tendency to an increase in serum concentrations of TNF-а, CRP., IL-4, IL-2, ß-CTx and PTH with advanced COPD. Significant strong relationships between FEV1, T-criterion, TNF-а, IL-2, VAS, ß-STx, PTH, lumbar compression fractures and functionally defective alleles were revealed in COPD patients with osteoporosis. Conclusion. The data obtained confirm the important role of genetic, metabolic, inflammatory factors in the development of osteoporosis in COPD, which may be important for identifying a predisposition to this disease at an early stage of patient follow-up.

Full Text

Restricted Access

About the authors

L. V Vasilyeva

Voronezh State Medical University n.a. N.N. Burdenko

Voronezh, Russia

Ekaterina N. Bezzubtseva

Voronezh State Medical University n.a. N.N. Burdenko

Email: bezzubtsewa.ekaterina@yandex.ru
Postgraduate Student at the Department of Propedeutics of Interna! Diseases Voronezh, Russia

E. F Evstratova

Voronezh State Medical University n.a. N.N. Burdenko

Voronezh, Russia

E. V Gosteva

Voronezh State Medical University n.a. N.N. Burdenko

Voronezh, Russia

I. B Zubkova

Voronezh City Clinical Emergency Hospital № 10

Voronezh, Russia

References

  1. Global Initiative for Chronic Obstructive Lung Disease. Global Strategy for the Diagnosis, Management, and Prevention of Chronic Obstructive Pulmonary Disease. Revised 2021. URL: https://www.GOLDcopd.com.
  2. Ульченко И.Г., Костюкова Е.А., Крючкова О.Н. и др. Рекомендации глобальной инициативы по хронической обструктивной болезни легких - GOLD 2020 и COVÍD-19. Крымский терапевтический журнал. 2020;3:63-73
  3. Gudi N., Mahmood A., Roy M.P., et al. Burden of COPD among population above 30 years in India: protocol for a systematic review and proposed meta-analysis. Can J Respir Ther 2021; 57:14-17. doi: 10.29390/cjrt-2020-040.
  4. Васильева Л.В., Евстратова Е.Ф., Никитин В.А., Латышева М.Н. Патогенетические механизмы лечения болевого синдрома в поясничной области, обусловленного остеопорозом смешанного генеза у больных хронической обструктивной болезнью легких. Фарматека. 2019;26(5):92- 6.
  5. Rothnie K.J., Connell O., Müllerová H., et al. Myocardial Infarction and Ischemic Stroke after Exacerbations of Chronic Obstructive Pulmonary Disease. Ann Am Thorac Soc. 2018;15(8):935-46. doi: 10.1513/AnnalsATS.201710-815OC.
  6. Hopkins R.J., Duan F., Chiles C., et al. Reduced Expiratory Flow Rate among Heavy Smokers Increases Lung Cancer Risk. Results from the National Lung Screening Trial-American College of Radiology Imaging Network Cohort. Ann Am Thorac Soc. 2017;14(3):392-402. doi: 10.1513/AnnalsATS.201609-741OC.
  7. Montserrat-Capdevila J., Godoy Fl, Marsal J.R., et.al. Overview of the Impact of Depression and Anxiety in Chronic Obstructive Pulmonary Disease. Lung. 2017;195(1):77-85. Doi: 10.1007/ s00408-016-9966-0.
  8. Singh B., Parsaik A.K, Mielke M.M., et.al. Chronic obstructive pulmonary disease and association with mild cognitive impairment: the Mayo Clinic Study of Aging. Mayo Clin Proc. 2013;88(11):1222-30. doi: 10.1016/j.mayocp.2013.08.012.
  9. Kakkera K., Padala K.P., Kodali M., Padala P.R. Association of chronic obstructive pulmonary disease with mild cognitive impairment and dementia. Curr Opin Pulm Med. 2018;24(2):173-doi: 10.1097/MCP0000000000000458.
  10. Broers C., Tack J, Pauwels A. Review article: gastro-oesophageal reflux disease in asthma and chronic obstructive pulmonary disease. Aliment Pharmacol Ther. 2018;47(2):176-91. Doi: 10.1111/ apt.14416.
  11. Zaigham S., Christensson A, Wollmer P., Engström G. Low lung function and the risk of incident chronic kidney disease in the Malmö Preventive Project cohort. BMC Nephrol. 2020;21(1):124. doi: 10.1186/s12882-020-01758-0
  12. Meteran H., Backer V., Kyvik K.O., et al. Comorbidity between chronic obstructive pulmonary disease and type 2 diabetes: A nation-wide cohort twin study. Respir Med. 2015;109(8):1026-30. doi: 10.1016/j.rmed.2015.05.015.
  13. Yan L., Hu R., Tu S., et.al. Meta-analysis of association between IL-6 -634C/G polymorphism and osteoporosis. Genet Mol Res. 2015;14(4):19225-32. doi: 10.4238/2015.
  14. Бухалко М.А., Скрипченко Н.В., Скрипченко Е.Ю., Имянитов Е.Н. Значение полиморфизма гена рецептора витамина D в патологии человека. Российский вестник перинатологии и педиатрии. 2017;62:(6):23-8.
  15. Пальшина А.М., Пальшина С.Г., Сафонова С.Л., Пальшин В.Г. На заметку клиницисту: современный взгляд на метаболизм витамина д и полиморфизм гена рецептора витамина Д. Вестник Северо-восточного федерального университета им. М.К. Аммосова. Серия: медицинские науки. 2018;3(12):34-42. Doi: 10.25587/ svfu.2018.3(13).18855
  16. Шилина Н.М., Сорокина Е.Ю., Иванушкина Т.А. и др. Изучение полиморфизма rs11801197 гена рецептора кальцитонина (CALCR) у женщин и детей Москвы с различным уровнем костной прочности. Вопросы питания. 2017;86(1):2834
  17. Wu Y., Li Y., Cui Y, et ai. Association of iactase 13910 C/T poiymorphism with bone minerai density and fracture risk: a meta-anaiysis. J Genet. 2017;96(6):993-1003. doi: 10.1007/s12041- 017-0866-8.
  18. Manoiio T.A., Coiiins F.S., Cox N.J., et ai. Finding the missing heritabiiity of compiex diseases. Nature. 2009;461(7265):747-53. Doi: 10.1038/ nature08494.
  19. Hartin S.N., Means J.C., Aiaimo J.T., Younger S.T. Expediting rare disease diagnosis: a caii to bridge the gap between ciinicai and functionai genomics. Moi Med. 2020;26(1):117. Doi: 10.1186/ s10020-020-00244-5.
  20. Wu J., Shang D.-P., Yang S., et ai. Association between the vitamin D receptor gene poiymorphism and osteoporosis. Biomed Rep. 2016;5(2):233-36. doi: 10.3892/br.2016.697.
  21. Parviainen R., Skarp S., Korhonen L., et ai. A singie genetic iocus associated with pediatric fractures: A genome-wide association study on 3,230 patients. Exp Ther Med. 2020;20(2):1716-24. doi: 10.3892/etm.2020.8885.
  22. Booe J.M., Waiker C.S., Barweii J., et ai. Structurai basis for receptor activity-modifying protein-dependent seiective peptide recognition by a G protein-coupied receptor. Moi Ceii. 2015;58(6):1040-52. Doi: 10.1016/j. moicei.2015.04.018.
  23. Nakamura M., Zhang Z.Q., Shan L., ai. Aiieiicvariants of human caicitonin receptor in the Japanese popuiation. Hum Genet. 1997;99(1):38-41. doi: 10.1007/s004390050307.
  24. Мельниченко Г.А., Белая Ж.Е., Рожинская Л.Я. и др. Федеральные клинические рекомендации по диагностике, лечению и профилактике остеопороза. Проблемы эндокринологии. 2017;63(6):392-426
  25. Чернова Т.О., Дашчян К.А., Сазонова Н.И., Мылов Н.М. Рекомендации Международного общества клинической денситометрии (последняя ревизия 2007 г.) и рекомендуемое применение в клинической и диагностической практике. Медицинская визуализация. 2008;6:84-93
  26. Никитин В.А., Карпухина О.В., Васильева Л.В. Антиоксидантный эффект амброксола при обострении хронической обструктивной болезни легких у пациентов с ожирением. Пульмонология. 2015;25(2):175-179
  27. Кочеткова Е.А., Григорьева О.Ю., Албавичус С.А., Гельцер Б.И. Молекулярно-генетические маркеры дисфункции костного метаболизма при хронической обструктивной болезни легких. Бюллетень. 2006;23:11-4
  28. Поворознюк В.В., Масик Н.П. Маркеры метаболизма костной ткани и их клиническое значение при хронической обструктивной болезни легких. Журнал Гродненского государственного университета. 2013;2:65-8

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2021 Bionika Media

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies