Welhaven Hope D, Viles Ethan, Starke Jenna, Wallace Cameron, Bothner Brian, June Ronald K, Hahn Alyssa K
Department of Chemistry & Biochemistry, Montana State University, Bozeman, MT, 59717, United States.
Department of Mechanical & Industrial Engineering, Montana State University, Bozeman, MT, 59717, United States.
Biochem Biophys Res Commun. 2024 Apr 9;703:149683. doi: 10.1016/j.bbrc.2024.149683. Epub 2024 Feb 13.
Osteoarthritis is the most common chronic joint disease, characterized by the abnormal remodeling of joint tissues including articular cartilage and subchondral bone. However, there are currently no therapeutic drug targets to slow the progression of disease because disease pathogenesis is largely unknown. Thus, the goals of this study were to identify metabolic differences between articular cartilage and subchondral bone, compare the metabolic shifts in osteoarthritic grade III and IV tissues, and spatially map metabolic shifts across regions of osteoarthritic hip joints. Articular cartilage and subchondral bone from 9 human femoral heads were obtained after total joint arthroplasty, homogenized and metabolites were extracted for liquid chromatography-mass spectrometry analysis. Metabolomic profiling revealed that distinct metabolic endotypes exist between osteoarthritic tissues, late-stage grades, and regions of the diseased joint. The pathways that contributed the most to these differences between tissues were associated with lipid and amino acid metabolism. Differences between grades were associated with nucleotide, lipid, and sugar metabolism. Specific metabolic pathways such as glycosaminoglycan degradation and amino acid metabolism, were spatially constrained to more superior regions of the femoral head. These results suggest that radiography-confirmed grades III and IV osteoarthritis are associated with distinct global metabolic and that metabolic shifts are not uniform across the joint. The results of this study enhance our understanding of osteoarthritis pathogenesis and may lead to potential drug targets to slow, halt, or reverse tissue damage in late stages of osteoarthritis.
骨关节炎是最常见的慢性关节疾病,其特征是包括关节软骨和软骨下骨在内的关节组织异常重塑。然而,目前尚无治疗药物靶点来减缓疾病进展,因为疾病发病机制很大程度上尚不清楚。因此,本研究的目的是确定关节软骨和软骨下骨之间的代谢差异,比较骨关节炎III级和IV级组织中的代谢变化,并在空间上绘制骨关节炎髋关节各区域的代谢变化图谱。全关节置换术后获取9例人类股骨头的关节软骨和软骨下骨,匀浆后提取代谢物进行液相色谱 - 质谱分析。代谢组学分析表明,骨关节炎组织、晚期分级以及患病关节区域之间存在不同的代谢内型。对这些组织间差异贡献最大的途径与脂质和氨基酸代谢相关。分级之间的差异与核苷酸、脂质和糖代谢相关。特定的代谢途径,如糖胺聚糖降解和氨基酸代谢,在空间上局限于股骨头的更上区域。这些结果表明,经X线片确认的III级和IV级骨关节炎与不同的整体代谢相关,且代谢变化在整个关节中并不均匀。本研究结果增进了我们对骨关节炎发病机制的理解,并可能导致在骨关节炎晚期减缓、阻止或逆转组织损伤的潜在药物靶点。