{"title":"患有类风湿性关节炎的非肥胖妇女血清脂肪因子的增加与肌肉疏松症有关","authors":"Tzu‐Jung Fang, Min‐Hsi Chiu, Ming‐Shyan Huang, Chia‐Yen Dai, Yao‐Tsung Yeh, Jeng‐Hsien Yen","doi":"10.1002/kjm2.12823","DOIUrl":null,"url":null,"abstract":"Large cohort studies have disclosed the association between obesity and rheumatoid arthritis (RA) risk. The sarcopenia prevalence in RA patients can be up to 31%. However, there is little information linking adipokines to sarcopenia in RA, so this study aimed to investigate whether adipokines were indeed involved in secondary sarcopenia in RA with a focus on non‐obese females. Sixty‐four female patients and 36 controls were included in this study. The serum adipokine levels (leptin and adiponectin) were determined by ELISA kits. The impacts of adipokines on muscle atrophy and potential autophagy were examined in mouse myoblasts, C2C12, upon treatment with recombinant leptin and adiponectin agonist (AdipoRan). Interestingly, serum adiponectin was significantly increased but the ratio of leptin/adiponectin was dramatically decreased in the RA patients with sarcopenia. After normalization by body mass, serum leptin was positively associated but adiponectin was negatively associated with muscle mass respectively, even after adjustment for fat mass. Treating C2C12 cells with leptin and AdipoRan inhibited proliferation of mature myotube respectively, as did treatment with the serum from RA patients. A combination of low leptin and high AdipoRan greatly decreased myogenin, but instead increased MAFbx and MuRF‐1 as well as increased Beclin 1, Atg5, and LC3β. Taken together, our study reveals that secondary sarcopenia of RA females may be an imbalance of RA‐related, but not obesity‐related, increase in adipokine production; additionally, the reduced leptin/adiponectin ratio could be a better indicator in monitoring sarcopenia in non‐obese RA females. Moreover, adipokine imbalance may promote muscle atrophy through inducing autophagy.","PeriodicalId":94244,"journal":{"name":"The Kaohsiung journal of medical sciences","volume":"56 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Increased serum adipokines are associated with sarcopenia in non‐obese women with rheumatoid arthritis\",\"authors\":\"Tzu‐Jung Fang, Min‐Hsi Chiu, Ming‐Shyan Huang, Chia‐Yen Dai, Yao‐Tsung Yeh, Jeng‐Hsien Yen\",\"doi\":\"10.1002/kjm2.12823\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Large cohort studies have disclosed the association between obesity and rheumatoid arthritis (RA) risk. The sarcopenia prevalence in RA patients can be up to 31%. 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Treating C2C12 cells with leptin and AdipoRan inhibited proliferation of mature myotube respectively, as did treatment with the serum from RA patients. A combination of low leptin and high AdipoRan greatly decreased myogenin, but instead increased MAFbx and MuRF‐1 as well as increased Beclin 1, Atg5, and LC3β. Taken together, our study reveals that secondary sarcopenia of RA females may be an imbalance of RA‐related, but not obesity‐related, increase in adipokine production; additionally, the reduced leptin/adiponectin ratio could be a better indicator in monitoring sarcopenia in non‐obese RA females. 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引用次数: 0
摘要
大型队列研究揭示了肥胖与类风湿性关节炎(RA)风险之间的关联。类风湿性关节炎患者的肌肉疏松症发病率高达 31%。因此,本研究旨在以非肥胖女性为重点,调查脂肪因子是否真的与类风湿性关节炎继发性肌肉疏松症有关。本研究共纳入了 64 名女性患者和 36 名对照组患者。血清脂肪因子水平(瘦素和脂肪连蛋白)由 ELISA 试剂盒测定。在使用重组瘦素和促脂肪生成素激动剂(AdipoRan)处理小鼠 C2C12 肌母细胞时,检测了脂肪因子对肌肉萎缩和潜在自噬的影响。有趣的是,在患有肌肉疏松症的 RA 患者中,血清中的脂肪连通素明显增加,但瘦素/脂肪连通素的比率却急剧下降。按体重归一化后,血清瘦素与肌肉质量呈正相关,但脂肪连通素与肌肉质量呈负相关,即使在调整脂肪质量后也是如此。用瘦素和AdipoRan处理C2C12细胞可分别抑制成熟肌管的增殖,用RA患者的血清处理也是如此。低瘦素和高 AdipoRan 的组合大大降低了肌生成素,反而增加了 MAFbx 和 MuRF-1,并增加了 Beclin 1、Atg5 和 LC3β。综上所述,我们的研究揭示了女性 RA 继发性肌肉疏松症可能是与 RA 相关而非与肥胖相关的脂肪因子分泌增加失衡所致;此外,瘦素/脂联素比值的降低可能是监测非肥胖 RA 女性肌肉疏松症的更好指标。此外,脂肪因子失衡可能会通过诱导自噬作用促进肌肉萎缩。
Increased serum adipokines are associated with sarcopenia in non‐obese women with rheumatoid arthritis
Large cohort studies have disclosed the association between obesity and rheumatoid arthritis (RA) risk. The sarcopenia prevalence in RA patients can be up to 31%. However, there is little information linking adipokines to sarcopenia in RA, so this study aimed to investigate whether adipokines were indeed involved in secondary sarcopenia in RA with a focus on non‐obese females. Sixty‐four female patients and 36 controls were included in this study. The serum adipokine levels (leptin and adiponectin) were determined by ELISA kits. The impacts of adipokines on muscle atrophy and potential autophagy were examined in mouse myoblasts, C2C12, upon treatment with recombinant leptin and adiponectin agonist (AdipoRan). Interestingly, serum adiponectin was significantly increased but the ratio of leptin/adiponectin was dramatically decreased in the RA patients with sarcopenia. After normalization by body mass, serum leptin was positively associated but adiponectin was negatively associated with muscle mass respectively, even after adjustment for fat mass. Treating C2C12 cells with leptin and AdipoRan inhibited proliferation of mature myotube respectively, as did treatment with the serum from RA patients. A combination of low leptin and high AdipoRan greatly decreased myogenin, but instead increased MAFbx and MuRF‐1 as well as increased Beclin 1, Atg5, and LC3β. Taken together, our study reveals that secondary sarcopenia of RA females may be an imbalance of RA‐related, but not obesity‐related, increase in adipokine production; additionally, the reduced leptin/adiponectin ratio could be a better indicator in monitoring sarcopenia in non‐obese RA females. Moreover, adipokine imbalance may promote muscle atrophy through inducing autophagy.