Blood leptin levels in patients with osteoarthritis: relation to clinical conditions of diseases

Authors

  • Valerii Novoseletskyi National Pirogov Memorial Medical University Pyrohova str., 56, Vinnytsia, Ukraine, 21000, Ukraine https://orcid.org/0000-0002-7713-6868
  • Mykola Stanislavchuk National Pirogov Memorial Medical University Pyrohova str., 56, Vinnytsia, Ukraine, 21000, Ukraine

DOI:

https://doi.org/10.15587/2519-4798.2018.124136

Keywords:

osteoarthritis of the knee joints, leptin, Lequesne index, body mass index, HAQ

Abstract

Aim of the work: study of the content of leptin in the serum of patients with OA and the study of relationships with clinical manifestations and functional status of patients.

Objects and methods: The determination of blood serum leptin levels and for the evaluation of the Lequesne index, HAQ, and KOOS was performed on 71 female with knee joints OA and 32 healthy women in control group.

Results. There was a significant relationship between serum leptin levels and the HAQ scale (p=0.026) and significant differences in the level of leptin in the X-ray stage of OA (p=0.043). An association of excess body weight with an increase in the level of serum leptin in the level of the tendency is established.

Conlusions: A detailed analysis of the level of leptin in relation to clinical and demographic indicators, clinical manifestations and functional status of patients with OA revealed a significant difference in the level of leptin in the context of the X-ray stage of OA. A reliable link between the level of leptin and the functional status of patients with HAQ was found. In addition, the association of excess body weight with the increase in the level of serum leptin in the bloodstream was observed at the level of the trend.

Author Biographies

Valerii Novoseletskyi, National Pirogov Memorial Medical University Pyrohova str., 56, Vinnytsia, Ukraine, 21000

Assistant

Department of Internal medicine No. 1

Mykola Stanislavchuk, National Pirogov Memorial Medical University Pyrohova str., 56, Vinnytsia, Ukraine, 21000

MD, Proffesor

Department of Internal medicine No. 1

References

  1. Poonpet, T. (2014). Adipokines: Biomarkers for osteoarthritis? World Journal of Orthopedics, 5 (3), 319. doi: 10.5312/wjo.v5.i3.319
  2. Kontny, E., Zielińska, A., Księżopolska-Orłowska, K., Głuszko, P. (2016). Secretory activity of subcutaneous abdominal adipose tissue in male patients with rheumatoid arthritis and osteoarthritis – association with clinical and laboratory data. Reumatologia/Rheumatology, 5, 227–235. doi: 10.5114/reum.2016.63662
  3. DeClercq, V., Cui, Y., Forbes, C., Grandy, S. A., Keats, M., Parker, L. et. al. (2017). Adiposity Measures and Plasma Adipokines in Females with Rheumatoid and Osteoarthritis. Mediators of Inflammation, 2017, 1–9. doi: 10.1155/2017/4302412
  4. Scotece, M., Mobasheri, A. (2015). Leptin in osteoarthritis: Focus on articular cartilage and chondrocytes. Life Sciences, 140, 75–78. doi: 10.1016/j.lfs.2015.05.025
  5. Gualillo, O., Eiras, S., Lago, F., Diéguez, C., Casanueva, F. F. (2000). Elevated serum leptin concentrations induced by experimental acute inflammation. Life Sciences, 67 (20), 2433–2441. doi: 10.1016/s0024-3205(00)00827-4
  6. Ku, J. H., Lee, C. K., Joo, B. S., An, B. M., Choi, S. H., Wang, T. H., Cho, H. L. (2009). Correlation of synovial fluid leptin concentrations with the severity of osteoarthritis. Clinical Rheumatology, 28 (12), 1431–1435. doi: 10.1007/s10067-009-1242-8
  7. Terlain, B., Presle, N., Pottie, P., Mainard, D., Netter, P. (2006). Leptin: A link between obesity and osteoarthritis? Bull. Acad. Natl. Med., 190 (7), 1421–1435.
  8. Junker, S., Krumbholz, G., Frommer, K. W., Rehart, S., Steinmeyer, J., Rickert, M. et. al. (2016). Differentiation of osteophyte types in osteoarthritis – proposal of a histological classification. Joint Bone Spine, 83 (1), 63–67. doi: 10.1016/j.jbspin.2015.04.008
  9. Vuolteenaho, K., Koskinen, A., Moilanen, E. (2013). Leptin – A Link between Obesity and Osteoarthritis. Applications for Prevention and Treatment. Basic & Clinical Pharmacology & Toxicology, 114 (1), 103–108. doi: 10.1111/bcpt.12160
  10. Bassi, M., Furuya, W. I., Menani, J. V., Colombari, D. S. A., do Carmo, J. M., da Silva, A. A. et. al. (2014). Leptin into the ventrolateral medulla facilitates chemorespiratory response in leptin-deficient (ob/ob) mice. Acta Physiologica, 211 (1), 240–248. doi: 10.1111/apha.12257
  11. Kalbe, C., Mau, M., Rehfeldt, C. (2008). Developmental changes and the impact of isoflavones on mRNA expression of IGF-I receptor, EGF receptor and related growth factors in porcine skeletal muscle cell cultures. Growth Hormone & IGF Research, 18 (5), 424–433. doi: 10.1016/j.ghir.2008.03.002
  12. Hampel, U., Sesselmann, S., Iserovich, P., Sel, S., Paulsen, F., Sack, R. (2013). Chemokine and cytokine levels in osteoarthritis and rheumatoid arthritis synovial fluid. Journal of Immunological Methods, 396 (1-2), 134–139. doi: 10.1016/j.jim.2013.08.007
  13. Wen, Y., Li, J., Tan, Y., Qin, J., Xie, X., Wang, L. et. al. (2014). Angelica Sinensis Polysaccharides Stimulated UDP-Sugar Synthase Genes through Promoting Gene Expression of IGF-1 and IGF1R in Chondrocytes: Promoting Anti-Osteoarthritic Activity. PLoS ONE, 9 (9), e107024. doi: 10.1371/journal.pone.0107024
  14. Zhen, G., Wen, C., Jia, X., Li, Y., Crane, J. L., Mears, S. C. et. al. (2013). Inhibition of TGF-β signaling in mesenchymal stem cells of subchondral bone attenuates osteoarthritis. Nature Medicine, 19 (6), 704–712. doi: 10.1038/nm.3143
  15. Chi, Y., Finnson, K., Antoniou, J., Philip, A. (2011). 243 the regulation of TGF-beta signaling in chondrocytes. Osteoarthritis and Cartilage, 19, S118. doi: 10.1016/s1063-4584(11)60270-7
  16. Ludin, A., Sela, J. J., Schroeder, A., Samuni, Y., Nitzan, D. W., Amir, G. (2013). Injection of vascular endothelial growth factor into knee joints induces osteoarthritis in mice. Osteoarthritis and Cartilage, 21 (3), 491–497. doi: 10.1016/j.joca.2012.12.003
  17. Shahmoon, S., Rubinfeld, H., Wolf, I., Cohen, Z. R., Hadani, M., Shimon, I., Rubinek, T. (2014). The aging suppressor klotho: a potential regulator of growth hormone secretion. American Journal of Physiology-Endocrinology and Metabolism, 307 (3), E326–E334. doi: 10.1152/ajpendo.00090.2014
  18. Jiao, K., Zhang, M., Niu, L., Yu, S., Zhen, G., Xian, L. et. al. (2013). Overexpressed TGF-β in Subchondral Bone Leads to Mandibular Condyle Degradation. Journal of Dental Research, 93 (2), 140–147. doi: 10.1177/0022034513513034
  19. Wluka, A. E., Lombard, C. B., Cicuttini, F. M. (2012). Tackling obesity in knee osteoarthritis. Nature Reviews Rheumatology, 9 (4), 225–235. doi: 10.1038/nrrheum.2012.224
  20. Yusuf, E., Nelissen, R. G., Ioan-Facsinay, A., Stojanovic-Susulic, V., DeGroot, J., van Osch, G. et. al. (2009). Association between weight or body mass index and hand osteoarthritis: a systematic review. Annals of the Rheumatic Diseases, 69 (4), 761–765. doi: 10.1136/ard.2008.106930
  21. Ku, J. H., Lee, C. K., Joo, B. S., An, B. M., Choi, S. H., Wang, T. H., Cho, H. L. (2009). Correlation of synovial fluid leptin concentrations with the severity of osteoarthritis. Clinical Rheumatology, 28 (12), 1431–1435. doi: 10.1007/s10067-009-1242-8

Published

2018-02-27

How to Cite

Novoseletskyi, V., & Stanislavchuk, M. (2018). Blood leptin levels in patients with osteoarthritis: relation to clinical conditions of diseases. ScienceRise: Medical Science, (2 (22), 10–14. https://doi.org/10.15587/2519-4798.2018.124136

Issue

Section

Medical Science