Department of Morphological Studies, Adelson School of Medicine, Ariel University, 40700, Ariel, Israel.
Department of Nursing, The Max Stern Yezreel Valley College, 19300, Yezreel Valley, Israel.
Arch Osteoporos. 2023 Nov 10;18(1):132. doi: 10.1007/s11657-023-01343-6.
In this cross-sectional study, we observed a strong, age-independent association of circulating interleukin-34 (IL-34) levels with osteoporosis.
The reported capacity of IL-34 to induce and enhance osteoclastogenesis suggests its potential involvement in the pathogenesis of osteoporosis. Our study aimed to evaluate whether there is an association between IL-34 expression and osteoporosis.
We enrolled 30 women with osteoporosis and 230 age-matched non-osteoporotic women as a control group. Osteoporosis diagnosis was based on dual-energy X-ray absorptiometry (DXA) of the lumbar spine and femoral neck. Body composition parameters were assessed by the bioimpedance method. Plasma IL-34 levels were measured by ELISA.
In comparison with the control group, the mean plasma IL-34 levels were significantly higher in osteoporotic women (164.61 ± 36.40 pg/ml vs. 665.43 ± 253.67 pg/ml, p = 0.0002), whereas basal metabolic rate (BMR) was significantly lower (1422.03 ± 6.80 kcal vs. 1339.39 ± 17.52 kcal, p = 0.00007). Both variables remained statistically significant after adjustment for age (p < 0.001). We did not observe correlations between plasma IL-34 levels and body composition parameters in osteoporotic and control groups. Multiple logistic regression analysis with osteoporosis status as a dependent variable clearly showed that age, BMR and IL-34 levels were independently and significantly associated with osteoporosis. The calculated odds ratios (OR) were 1.66 (95% CI = 1.16-2.38) for IL-34 levels and 0.22 (95% CI = 0.07-0.65) for BMR.
The significant (fourfold) elevation of IL-34 plasma levels in osteoporosis patients suggests that circulating IL-34 could be used as a biomarker for osteoporosis.
已有研究表明白细胞介素 34(IL-34)能够诱导和增强破骨细胞生成,提示其可能参与骨质疏松症的发病机制。本研究旨在评估 IL-34 表达与骨质疏松症之间是否存在关联。
我们纳入了 30 名骨质疏松症患者和 230 名年龄匹配的非骨质疏松症患者作为对照组。骨质疏松症的诊断基于腰椎和股骨颈的双能 X 射线吸收法(DXA)。通过生物阻抗法评估身体成分参数。通过 ELISA 法测定血浆 IL-34 水平。
与对照组相比,骨质疏松症患者的平均血浆 IL-34 水平显著升高(164.61 ± 36.40 pg/ml 比 665.43 ± 253.67 pg/ml,p = 0.0002),而基础代谢率(BMR)显著降低(1422.03 ± 6.80 kcal 比 1339.39 ± 17.52 kcal,p = 0.00007)。在校正年龄后,这两个变量仍然具有统计学意义(p < 0.001)。我们未观察到骨质疏松症组和对照组中血浆 IL-34 水平与身体成分参数之间的相关性。将骨质疏松症状态作为因变量的多元逻辑回归分析清楚地表明,年龄、BMR 和 IL-34 水平与骨质疏松症独立且显著相关。计算出的优势比(OR)分别为 IL-34 水平的 1.66(95%可信区间= 1.16-2.38)和 BMR 的 0.22(95%可信区间= 0.07-0.65)。
骨质疏松症患者血浆中 IL-34 水平显著升高(四倍),提示循环中的 IL-34 可作为骨质疏松症的生物标志物。