Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 Oct 8:16:60.
doi: 10.1186/s12865-015-0125-9.

Increased levels of interleukin 31 (IL-31) in osteoporosis

Affiliations

Increased levels of interleukin 31 (IL-31) in osteoporosis

Lia Ginaldi et al. BMC Immunol. .

Abstract

Background: Several inflammatory cytokines play a key part in the induction of osteoporosis. Until now, involvement of the Th2 cytokine interleukin-31 (IL-31) in osteoporosis hadn't yet been studied. IL-31 is a proinflammatory cytokine mediating multiple immune functions, whose involvement in a wide range of diseases, such as atopic dermatitis, inflammatory bowel diseases and cutaneous lymphomas, is now emerging. Given the important role of IL-31 in inflammation, we measured its serum levels in postmenopausal osteoporotic patients.

Methods and results: In fifty-six postmenopausal females with osteoporosis and 26 healthy controls, bone mineral density (BMD) measurements were performed by using calcaneal quantitative ultrasound (QUS) technique, confirmed at the lumbar spine and hip by dual energy X-ray absorptiometry (DXA). Both patients and controls were divided according to age (less or more than 65 years) and disease severity (T-score levels and presence of fractures). Serum IL-31 levels were measured by ELISA technique. Osteoporotic patients exhibited elevated levels of serum IL-31 compared with healthy controls (43.12 ± 6.97 vs 29.58 ± 6.09 pg/ml; p < 0.049). IL-31 expression was higher in over 65 years old patients compared to age-matched controls (45 ± 11.05 vs. 17.92 ± 5.92; p < 0.01), whereas in younger subjects no statistically significant differences were detected between patients and controls (37.91 ± 6.9 vs 32.08 ± 8.2). No statistically significant differences were found between IL-31 levels in patients affected by mild (T-score > -3) compared to severe (T-score < -3) osteoporosis (59.17 ± 9.22 vs 37.91 ± 10.52), neither between fractured and unfractured osteoporotic women (33.75 ± 9.16 vs 51.25 ± 8.9).

Conclusions: We showed for the first time an increase of IL-31 serum levels in postmenopausal women with decreased BMD. Although they did not reflect the severity of osteoporosis and/or the presence of fractures, they clearly correlated with age, as reflected by the higher levels of this cytokine in aged patients.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
IL-31 serum levels in osteoporotic patients and controls according to age. a: IL31 serum levels in all patients and controls; lines represent medians. b: IL31 serum levels in patients and controls less than or equal to 65 years; lines represent medians. c: IL31 serum levels in patients and controls older than 65 years; lines represent medians
Fig. 2
Fig. 2
IL31 serum levels in patients divided according to the severity of osteoporosis and controls older than 65 years; lines represent medians
Fig. 3
Fig. 3
IL31 serum levels in patients divided according to the presence or absence of fragility fractures and controls older than 65 years; lines represent medians

References

    1. Rauner M, Sipos W, Thiele S, Pietschmann P. Advances in osteoimmunology: pathophysiologic concepts and treatment opportunities. Int Arch Allergy Immunol. 2013;160:114–25. doi: 10.1159/000342426. - DOI - PubMed
    1. Charles JF, Nakamura MC. Bone and the innate immune system. Curr Osteoporos Rep. 2014;12:1–8. doi: 10.1007/s11914-014-0195-2. - DOI - PMC - PubMed
    1. Zupan J, Jeras M, Marc J. Osteoimmunology and the influence of proinflammatory cytokines on osteoclasts. Biochem Med. 2013;23:43–63. doi: 10.11613/BM.2013.007. - DOI - PMC - PubMed
    1. Deal C. Bone loss in rheumatoid arthritis: systemic, periarticular, and focal. Curr Rheumatol Rep. 2012;14:231–7. doi: 10.1007/s11926-012-0253-7. - DOI - PubMed
    1. Sigl V, Penninger JM: RANKL/RANK-From bone physiology to breast cancer. Cytokine Growth Factor Rev 2014. doi: 10.1016/j.cytogfr.2014.01.002 - PubMed