Hu Xin, Lin Ruhai, Yan Jinyao, Wang Dan, Liu Yazhuo, Fu Deqiang, Huang Yinqiong
Department of Endocrinology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
School of Electronics and Communicaiton Engineering, Quanzhou University of Information Engineering, Quanzhou, China.
Sci Rep. 2025 Aug 5;15(1):28642. doi: 10.1038/s41598-025-13537-8.
Evidence indicates a relationship between osteoporosis and nutritional factors. Nevertheless, the correlation between fatty acids and bone health remains not fully elucidated. This research sought to explore the potential associations between fatty acids (FAs) and osteoporosis. This study enrolled 248 patients in total. Basic demographic characteristics, serum phospholipid FAs, and bone mineral density were assessed. There were differences in arachidonic acid (AA) and docosapentaenoic acid (DPA) levels among the groups (P < 0.05). In the greatest quartile of docosahexaenoic acid (DHA) levels, the odds ratio (OR) in osteoporosis was 0.23 (0.05, 0.99); the corresponding value for AA was 0.2 (0.06, 0.64). In contrast, the risk of osteoporosis increased with elevated serum DPA; the highest quartile was associated with an OR of 13.44 for osteoporosis (4.82, 74.61). Receiver operating characteristic analysis showed that fatty acids have diagnostic value for osteoporosis (area under the curve 0.814; 0.751-0.867). Fatty acids are associated with bone mineral density. AA and DHA showed an inverse association with osteoporosis risk, while DPA was positively associated with osteoporosis risk. Therefore, the fatty acids metabolism profile might be a potential therapeutic target for osteoporosis.
有证据表明骨质疏松症与营养因素之间存在关联。然而,脂肪酸与骨骼健康之间的相关性仍未完全阐明。本研究旨在探讨脂肪酸(FAs)与骨质疏松症之间的潜在关联。本研究共纳入248例患者。评估了基本人口统计学特征、血清磷脂脂肪酸和骨密度。各组之间花生四烯酸(AA)和二十二碳五烯酸(DPA)水平存在差异(P < 0.05)。在二十二碳六烯酸(DHA)水平最高的四分位数中,骨质疏松症的优势比(OR)为0.23(0.05,0.99);AA的相应值为0.2(0.06,0.64)。相反,骨质疏松症的风险随着血清DPA升高而增加;最高四分位数与骨质疏松症的OR为13.44相关(4.82,74.61)。受试者工作特征分析表明,脂肪酸对骨质疏松症具有诊断价值(曲线下面积0.814;0.751 - 0.867)。脂肪酸与骨密度相关。AA和DHA与骨质疏松症风险呈负相关,而DPA与骨质疏松症风险呈正相关。因此,脂肪酸代谢谱可能是骨质疏松症的一个潜在治疗靶点。