Soltani Azin, Aghakhani Amirhossein, Dehghanbanadaki Hojat, Majidi Ziba, Rezaei-Tavirani Mostafa, Shafiee Gita, Ostovar Afshin, Mir Moeini Seyed Amirhossein, Bandarian Fatemeh, Larijani Bagher, Nabipour Iraj, Fahimfar Noushin, Razi Farideh
Metabolomics and Genomics Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
School of Medicine, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
J Diabetes Metab Disord. 2025 Feb 6;24(1):65. doi: 10.1007/s40200-025-01574-z. eCollection 2025 Jun.
Both liver fibrosis and osteoporosis share inflammatory pathways, with liver fibrosis potentially contributing to decreased bone mineral density (BMD). The rising prevalence of non-alcoholic fatty liver disease (NAFLD) and associated liver fibrosis, especially in older populations, may increase the risk of osteoporosis, but evidence remains inconclusive. This study aims to investigate the relationship between liver fibrosis and osteoporosis in individuals over 50 years old.
This cross-sectional study used data from the Bushehr Elderly Health Program (BEHP), a cohort of 2,000 participants aged 50 and older, selected through multistage stratified random sampling. BMD and trabecular bone score (TBS) measurements were assessed. The Fibrosis-4 (FIB-4) index, a surrogate marker for liver fibrosis, was also calculated to examine its association with these bone health indicators. Multiple linear regression was applied to assess the relationship between FIB-4 and lumbar, hip, femoral neck BMD, and TBS scores, while logistic regression was used to evaluate osteoporosis as the dependent variable.
A total of 1,959 participants with adequate data were included in our analysis. 538 participants had osteoporosis, 936 participants had osteopenia, and 485 participants had normal bone density. FIB-4 index was higher in osteoporotic groups (1.45 ± 0.90) than in osteopenic (1.26 ± 0.58, < 0.001) and normal groups (1.17 ± 0.48, < 0.001). After controlling for confounders, FIB-4 index was negatively associated with hip BMD (β=-0.0162; 95% CI: -0.0313, -0.0012 and β=-0.0221; 95% CI: -0.0340, -0.0102), femoral neck BMD (β=-0.0216; 95% CI: -0.0356, -0.0076 and β=-0.0233; 95% CI: -0.0342, 0.0124), and TBS (β=-0.0154; 95% CI: -0.0264, -0.0043 and β=-0.0244; 95% CI: -0.0338, -0.0149) in both genders and with lumbar BMD in women (β=-0.0176; 95% CI: -0.0307, -0.0045). An increase in the FIB-4 index was associated with more than a twofold rise in the risk of developing osteoporosis in women (OR = 2.123; 95% CI: 1.503, 3.000; < 0.001) and a 36% higher risk in men (OR = 1.366; 95% CI: 1.012, 1.844; = 0.042).
Liver fibrosis is associated with decreased bone density and attenuated bone architecture. Elevated FIB-4 index has been identified as a risk factor for osteoporosis, indicating a potential link between liver fibrosis and deteriorating bone health.
肝纤维化和骨质疏松症具有共同的炎症途径,肝纤维化可能导致骨密度(BMD)降低。非酒精性脂肪性肝病(NAFLD)及其相关肝纤维化的患病率不断上升,尤其是在老年人群中,这可能会增加骨质疏松症的风险,但证据仍不确凿。本研究旨在调查50岁以上人群中肝纤维化与骨质疏松症之间的关系。
这项横断面研究使用了布什尔老年健康项目(BEHP)的数据,该队列由2000名年龄在50岁及以上的参与者组成,通过多阶段分层随机抽样选取。评估了骨密度和骨小梁骨评分(TBS)测量值。还计算了肝纤维化的替代标志物纤维化-4(FIB-4)指数,以检查其与这些骨骼健康指标的关联。应用多元线性回归评估FIB-4与腰椎、髋部、股骨颈骨密度和TBS评分之间的关系,同时使用逻辑回归将骨质疏松症作为因变量进行评估。
共有1959名有足够数据的参与者纳入我们的分析。538名参与者患有骨质疏松症,936名参与者患有骨质减少症,485名参与者骨密度正常。骨质疏松症组的FIB-4指数(1.45±0.90)高于骨质减少症组(1.26±0.58,<0.001)和正常组(1.17±0.48,<0.001)。在控制混杂因素后,FIB-4指数与髋部骨密度(β=-0.0162;95%置信区间:-0.0313,-0.0012和β=-0.0221;95%置信区间:-0.0340,-0.0102)、股骨颈骨密度(β=-0.0216;95%置信区间:-0.0356,-0.0076和β=-0.0233;95%置信区间:-0.0342,0.0124)和TBS(β=-0.0154;95%置信区间:-0.0264,-0.0043和β=-0.0244;95%置信区间:-0.0338,-0.0149)在男女中均呈负相关,在女性中与腰椎骨密度也呈负相关(β=-0.0176;95%置信区间:-0.0307,-0.0045)。FIB-4指数的升高与女性患骨质疏松症风险增加两倍以上相关(比值比[OR]=2.123;95%置信区间:1.503,3.000;<0.001),男性患骨质疏松症风险高36%(OR=1.366;95%置信区间:1.012,1.844;P=0.042)。
肝纤维化与骨密度降低和骨结构减弱有关。FIB-4指数升高已被确定为骨质疏松症的一个危险因素,表明肝纤维化与骨骼健康恶化之间存在潜在联系。