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嗜酸性粒细胞趋化因子(CCL11、CCL24、CCL26)在骨质减少和骨质疏松症发病机制中的作用

Involvement of Eotaxins (CCL11, CCL24, CCL26) in Pathogenesis of Osteopenia and Osteoporosis.

作者信息

Ahmadi Hadis, Khorramdelazad Hossein, Hassanshahi Gholamhossein, Abbasi Fard Mitra, Ahmadi Zahra, Noroozi Karimabad Mojgan, Mollahosseini Majid

机构信息

Molecular Medicine Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.

Department of Immunology, Medical School, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.

出版信息

Iran J Public Health. 2020 Sep;49(9):1769-1775. doi: 10.18502/ijph.v49i9.4098.

Abstract

BACKGROUND

The purpose of this study was to investigate the role of eotaxin family members including C-C motif chemokine 11 (CCL11), C-C motif chemokine 24 (CCL24), and C-C motif chemokine 26 (CCL26) as the subgroups of CC-chemokine in patients affected with osteoporosis and osteopenia.

METHODS

Overall, 19 osteoporotic patients, 18 osteopenic individuals, and 20 healthy subjects were recruited in this study. The bone mineral density (BMD) was then measured at the lumbar spine (L1-L4) and the hip (femoral neck and total hip) using dual-energy X-ray absorptiometry for diagnosis of bone density and related disorders. Additionally, enzyme-linked immunosorbent assay (ELISA) technique was employed to measure the serum levels of CCL11, CCL24, and CCL26.

RESULTS

The circulating levels of CCL11, CCL24, and CCL26 had been increased in both groups of patients with osteopenia and osteoporosis compared to those in healthy subjects (<0.05); while no significant difference was observed between serum levels of these chemokines in such patients.

CONCLUSION

Eotaxins can play a role in the pathogenesis of osteoporosis and osteopenia; however, further studies are needed to clarify various roles of eotaxins in the pathophysiology of osteoporosis and osteopenia.

摘要

背景

本研究旨在探讨作为CC趋化因子亚群的嗜酸性粒细胞趋化因子家族成员,包括C-C基序趋化因子11(CCL11)、C-C基序趋化因子24(CCL24)和C-C基序趋化因子26(CCL26)在骨质疏松症和骨质减少患者中的作用。

方法

本研究共招募了19名骨质疏松症患者、18名骨质减少个体和20名健康受试者。然后使用双能X线吸收法测量腰椎(L1-L4)和髋部(股骨颈和全髋)的骨密度(BMD),以诊断骨密度及相关疾病。此外,采用酶联免疫吸附测定(ELISA)技术测量血清中CCL11、CCL24和CCL26的水平。

结果

与健康受试者相比,骨质减少和骨质疏松症患者组中CCL11、CCL24和CCL26的循环水平均升高(<0.05);而这些趋化因子在这些患者血清水平之间未观察到显著差异。

结论

嗜酸性粒细胞趋化因子可在骨质疏松症和骨质减少的发病机制中发挥作用;然而,需要进一步研究以阐明嗜酸性粒细胞趋化因子在骨质疏松症和骨质减少病理生理学中的各种作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c190/7898105/7abf197d589c/IJPH-49-1769-g001.jpg

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