Dyson Gabby, Barrett Montana, Schlupp Leoni, Prinz Emmaline, Hannebut Nicholas, Szymczak Aleksander, Brawner Cindy Miranda, Jeffries Matlock A
Oklahoma Medical Research Foundation, Arthritis & Clinical Immunology Program and the Oklahoma City Veterans Affairs Medical Center.
Oklahoma Medical Research Foundation, Arthritis & Clinical Immunology Program, Oklahoma City.
ACR Open Rheumatol. 2025 Jan;7(1):e11794. doi: 10.1002/acr2.11794.
Dietary interventions are a potentially powerful treatment option for knee osteoarthritis (OA). The objective of this study was to evaluate a well-formulated ketogenic diet (KD) in the context of knee OA histology and pain using the destabilization of the medial meniscus (DMM) mouse model and correlate with gut microbiome and systemic cytokine levels.
Adult male mice underwent unilateral DMM or sham surgery and were then fed eight weeks of KD or chow. At baseline and every two weeks, mechanical allodynia of the operated and contralateral knees was assessed via analgesiometry. Knee joints were collected for histology, gut microbiome analysis was performed on cecal material via 16S sequencing, and serum cytokines were analyzed via Bio-Plex assay.
KD mice had worse histopathologic OA after DMM (mean ± SEM Osteoarthritis Research Society International score: KD-DMM: 4.0 ± 0.5 vs chow-DMM: 2.7 ± 0.08; P = 0.02). KD mice had increased mechanical allodynia postsurgery (P = 0.005 in mixed-effects model). The gut microbiome changed substantially with KD: 59 clades were altered by KD in DMM and 39 by KD in sham (36 were shared, 25 overlapped with previous murine OA studies). Several clades were correlated on an individual-mouse level with both histology and allodynia (eg, Lactobacillus histology P = 0.004, allodynia P = 1 × 10). Serum analysis showed four cytokines increased with KD (interleukin [IL]-1β, IL-2, IL-3, and IL-13).
KD started immediately after OA induction via DMM is associated with worsened histologic outcomes. KD also worsens mechanical allodynia after either DMM or sham surgery. KD induces significant gut microbiome dysbiosis in clades previously associated with murine OA.
饮食干预是膝骨关节炎(OA)一种潜在的有效治疗选择。本研究的目的是使用内侧半月板不稳定(DMM)小鼠模型,在膝OA组织学和疼痛背景下评估精心设计的生酮饮食(KD),并将其与肠道微生物群和全身细胞因子水平相关联。
成年雄性小鼠接受单侧DMM或假手术,然后喂食8周的KD或普通饲料。在基线时以及每两周,通过镇痛测定法评估手术侧和对侧膝关节的机械性异常性疼痛。收集膝关节进行组织学检查,通过16S测序对盲肠材料进行肠道微生物群分析,并通过Bio-Plex检测分析血清细胞因子。
在DMM后,KD小鼠的组织病理学OA更严重(国际骨关节炎研究学会平均±标准误评分:KD-DMM组:4.0±0.5,而普通饲料-DMM组:2.7±0.08;P = 0.02)。KD小鼠术后机械性异常性疼痛增加(混合效应模型中P = 0.005)。KD使肠道微生物群发生显著变化:在DMM组中,59个进化枝因KD而改变,在假手术组中39个因KD而改变(36个是共同的,25个与先前的小鼠OA研究重叠)。在个体小鼠水平上,几个进化枝与组织学和异常性疼痛均相关(例如,组织学方面乳酸杆菌P = 0.004,异常性疼痛方面P = 1×10)。血清分析显示,有四种细胞因子随KD升高(白细胞介素[IL]-1β、IL-2、IL-3和IL-13)。
通过DMM诱导OA后立即开始的KD与更差的组织学结果相关。KD还会使DMM或假手术后的机械性异常性疼痛恶化。KD在先前与小鼠OA相关的进化枝中诱导显著的肠道微生物群失调。